Offres technical support à Carlsbad, California - Page 3Create job alerts

Job Description Veridiam is a strategic manufacturing partner with over 60 years of experience serving the aerospace, industrial, medical, and nuclear markets. Our roots were formed in the exacting nuclear and aerospace industries, expanded into Medical where we have supplied critical components to a global customer base. We currently provide elegant solutions across a broad range of customers and diverse markets. At Veridiam we recognize that talent is at the forefront of our organization and define who we are in today's industry. POSITION SUMMARY Provide generalist support to the Human Resources department, including but not limited to involvement in all the functional areas of the department. Partner with leadership and supervisory personnel to provide guidance and advise on workplace issues, conflict resolution and policy interpretation. ESSENTIAL DUTIES AND RESPONSIBILITIES • Partner with hiring managers and lead initiatives on employment life cycle including recruitment, onboarding, employee relations and offboarding activities., • Perform and support training development initiatives, including preparation and administration of programs such as new hire orientation., • Maintain leave of absence programs, including coordination of appropriate and applicable leave eligibility., • May assist with conducting investigations into employee concerns and recommending resolutions., • Assist with facilitating performance management processes and communication., • Administer human resources programs, policies and procedures ensuring compliance with regulations., • Support change management processes., • May assist with department metrics and reporting updates and/or changes., • Provide guidance and support of benefit enrollment activities including annual open enrollment and communication., • Participate and plan employee relations activities, including but not limited to monthly newsletter creation and distribution., • May assist in administrative tasks involving human resources functions and maintain appropriate documentation., • May participate in job analysis and documentation, job posting, searching and reviewing resumes, screening candidates and scheduling/coordinating interviews., • May conduct and coordinate applicant interviews for all levels of positions, including but not limited to technical, managerial, clerical and production employees., • Maintain and keep up to date physical and/or digital employee personnel files and their documents, including medical and benefits information., • Provide assistance with benefits administration and/or enrollment activities., • Works with cross functional teams and collaborates with members of management and contributes to a team effort., • Demonstrates ability to appear for work on time, follow directions from a supervisor, interact well with co-workers, understand and follow work rules and procedures, comply with company policies and procedures, goals and objectives, and accepts constructive feedback. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. Education and Experience: • Bachelor’s degree in related field., • Ability to work at a high level of accuracy and attention to detail., • Ability and tolerance to meet due dates and deadlines and/or time constraints., • Proficient with human resource information systems and software., • Knowledge of and ability to utilize Microsoft office applications., • Ability to communicate with all levels of employee., • Time management and organizational skills. Pay Rate: The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience with the industry, education, geographic location, etc. Veridiam is an Equal Employment Opportunity/Affirmative Action Employer. Veridiam will recruit, hire, train and promote persons into all jobs without regard to age, race, color, religion, ancestry, medical condition, sex, sexual orientation, gender identity, national origin, status as a veteran or status as an individual with a disability or any other characteristic or classification protected by law. Access to our facility (and, therefore, employment) is restricted under the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR) to U.S. Citizens, lawful permanent residents of the United States and properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes.

Job Description About the Role: The Vice President Bioinformatics and Software Engineering will provide strategic and technical leadership for computational biology, software development, and data infrastructure in support of whole genome sequencing (WGS), multi-omics analysis, and clinical diagnostics. This executive role requires deep expertise in de novo algorithm development, data modeling, and scalable bioinformatics methods for genomic discovery and precision medicine. The successful candidate will lead a multidisciplinary team of bioinformaticians and engineers, advancing both production-ready clinical pipelines and cutting-edge computational research to enable next-generation diagnostics. Responsibilities: * Develop and execute the strategic roadmap for bioinformatics and software engineering, with emphasis on de novo method development and novel algorithm design. * Lead the design, validation, and deployment of NGS pipelines for WGS, RNA-seq, and multi-omics applications, ensuring compliance with CLIA, CAP, and FDA standards. * Drive innovation in data modeling, statistical methods, and computational frameworks to address large-scale genomic and structural variation analysis. * Oversee end-to-end software engineering efforts including cloud infrastructure, APIs, automation tools, and scalable production systems. * Establish and enforce engineering best practices in version control, testing, reproducibility, and audit-ready documentation. * Recruit, mentor, and manage a high-performing team spanning bioinformatics, machine learning, software engineering, and data science. * Collaborate with R&D, Clinical, Regulatory, and Product teams to integrate novel computational methods into diagnostic product development. * Shape the data strategy to support AI/ML applications, real-world evidence generation, and advanced data integration across omics modalities. * Ensure compliance with data security, privacy, and regulatory frameworks across all systems and workflows. * Foster partnerships with academic, industry, and open-source communities to accelerate innovation in bioinformatics methods and software solutions. Qualifications: * PhD or MS in Bioinformatics, Computational Biology, Computer Science, or a related discipline. * At least 10 years of experience in bioinformatics and software engineering, with proven expertise in algorithm development for NGS and large-scale genomics. * Demonstrated success in developing de novo methods for genome assembly, structural variant detection, or advanced computational modeling. * Strong track record building cloud-based platforms and production-grade pipelines for regulated diagnostics. * Leadership experience managing cross-functional teams across bioinformatics, engineering, and clinical domains. * Deep understanding of regulatory compliance frameworks including CLIA, CAP, and FDA submissions. * Hands-on expertise with cloud infrastructure, distributed computing, and data-intensive systems, preferably AWS. * Exceptional communication skills, with the ability to influence technical, scientific, and executive stakeholders. Desired Qualifications: * Experience with multi-omics integration, statistical modeling, and advanced algorithmic methods in computational biology. * Background in genome assembly, haplotype phasing, structural variant calling, or other de novo discovery pipelines. * Familiarity with LIMS, clinical reporting systems, and laboratory automation workflows. * Experience leading FDA submissions and developing QMS-aligned software systems for diagnostics. * Knowledge of AI/ML applications in bioinformatics, including predictive modeling and real-world data analysis. * Proven ability to translate computational innovations into clinically validated products.

Job DescriptionCompany Description The sky's not the limit at Nearmap We’re a SaaS company, with proprietary hardware and software that’s continuously advancing through our commitment to innovation. The sky’s the limit when it comes to what we can and plan to do for our customers. Our imagery is just the starting point. Our impact comes from our people, applying complex analysis, interpretation and artificial intelligence that opens up all sorts of possibilities for our customers. Job Description The Senior Solution Engineer, Insurance will be a technical expert and key contributor within the Solutions Engineering team at Nearmap, specifically focused on supporting clients in the property & casualty (P&C) insurance industry. This role will involve deep technical knowledge of Nearmap’s platform, including 2D, 3D, and AI technologies, to help clients solve business challenges related to underwriting, claims, and risk management. Working alongside cross-functional teams such as Product, Engineering, and Technology, the Senior Solution Engineer will develop tailored solutions and deliver compelling product demonstrations to showcase the value of Nearmap's content and technology in driving better decision-making and operational efficiency. Key Responsibilities: Client Engagement and Insurance-Specific Support: • Lead technical discussions with P&C insurance clients to understand their unique workflows in underwriting, claims, and risk mitigation., • Conduct customized product demonstrations showcasing Nearmap’s geospatial solutions, focusing on applications in claims assessment, risk scoring, and underwriting decisions., • Drive Proof of Concept (POC) processes to demonstrate the value of Nearmap’s solutions in specific insurance use cases, such as post-catastrophe analysis, risk profiling, and claims triage., • Respond to insurance-specific RFIs/RFPs, tailoring technical responses to address client pain points and regulatory requirements., • Collaborate with Sales, Product, and Engineering teams to create custom workflows that align with insurance customer requirements, leveraging Nearmap’s AI, 3D, and imagery capabilities., • Design and deliver workflows that support faster claims resolution, improved risk selection, and accurate property condition assessment., • Develop solutions that integrate Nearmap’s data into insurance client systems for use in applications like underwriting automation, claims automation, and geospatial risk modeling., • Support insurance clients with best practices for integrating Nearmap’s data with their systems, including underwriting platforms, GIS, and policy management systems., • Educate internal teams and clients on Nearmap’s roadmap with a specific focus on new features and enhancements relevant to insurance applications., • Provide training for Solutions Engineers and other technical staff on insurance-focused use cases, products, and best practices., • Create industry-specific technical content, such as whitepapers and presentations, to support customer onboarding and engagement in the insurance space., • Cultivate strong relationships with insurance clients, acting as a trusted advisor on how Nearmap’s technology can address their business goals in claims, underwriting, and risk assessment., • Regularly gather feedback from clients to ensure Nearmap’s solutions are delivering value in insurance-specific applications., • Act as the voice of the customer within Nearmap, advocating for product improvements that directly benefit insurance workflows.Qualifications 5+ years of experience in a technical role, with a strong preference for candidates with experience in technical presales or solution engineering in the insurance industry. • Bachelor’s degree in Geography, Engineering, or a related STEM field., • Direct experience supporting the insurance industry, particularly in property underwriting, claims processes, or risk analysis is preferred., • Proficiency in Python or another programming language (e.g., JavaScript, SQL) to build and support custom solutions., • Strong technical understanding of SaaS products, REST APIs, and geospatial data integration., • Experience in enterprise selling., • Expertise in geospatial data and remote sensing, with the ability to apply these to insurance-specific use cases., • Exceptional presentation skills, with the ability to communicate technical details to both insurance and non-technical audiences., • Familiarity with insurance-relevant technologies and datasets, such as condition scoring, damage detection, and AI-based risk modeling., • Self-driven, organized, and capable of managing multiple projects., • Customer-focused with strong interpersonal skills and a commitment to delivering value in every client interaction., • Ability to thrive in a fast-paced, dynamic environment and adapt to the changing needs of insurance clients., • Willingness to travel to meet with clients and attend industry events as needed. Additional Information Why you'll love working at Nearmap: We move fast and work smart; often wearing multiple hats. We adapted to remote working with ease and are continually looking at ways to improve. We’re proud of our inclusive, supportive culture, and maintain a safe environment where everyone feels a sense of belonging and can be themselves. At Nearmap, you can chart your own career path and see where our journey together might take you. With complex and fascinating work to challenge and inspire you, you might be surprised by the opportunities you discover. We've got so much more to share—come and explore with us! Nearmap does not accept unsolicited resumes from recruitment agencies and search firms. Please do not email or send unsolicited resumes to any Nearmap employee, location or address. Nearmap is not responsible for any fees related to unsolicited resumes.

Job DescriptionCompany Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description NO Experience Needed AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $17.00 - $18.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Label Operator you will: Label, ink stamp, overcoat and etch outlined information on detail components and assemblies using general shop tools and equipment. What will my responsibilities include? • Perform label, ink stamp and etch duties on components and assemblies., • Use general shop and hand tools., • Where special PPE required to do the Job (Respirators, Safety Glasses), • Follow documented manufacturing processes and procedures., • Produce quality parts and meet individual productivity goals., • Clean and maintain work areas as part of 5s program., • Comply with all safety requirements., • Follow all Steico Policies including Attendance, • Communicate well with leads and coworkers to achieve the department goals, • Other reasonable duties as business and operational needs dictate Qualifications What key skills and experience do I need? • Requires the ability communicate verbally and in writing in a clear, easily understood manner, • Requires English verbal and written skills, • High School diploma / General Education Completion., • NO Experience Needed, • Basic math skills to perform basic calculations such as addition and subtraction, • General understanding of manufacturing processes and use of hand tools Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor

Job DescriptionCompany Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $21.00 - $24.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Fabrication Planner you will: Create manufacturing instructions/shop travelers compliant to STEICO Industries Inc. quality processes and procedures. Review customer Quality, Engineering and Specification requirements to include in the manufacturing instructions. Generating data packages to accompany the shop travelers. Generate aides to assist manufacturing departments. What will my responsibilities include? • Interpret customer drawings/ specifications/ Quality Manual/ PO clauses and Terms and Conditions while creating manufacturing work instructions/ shop travelers to ensure we are meeting requirements., • Generate Engineering drawing packets, coordinate data sheets, Weld schedule aides, Masking Drawings, Label drawings., • Plot X,Y,Z intersection points, label locations and masking locations from CAD models., • Creates Bill of Materials using customer provided parts lists, drawings and models., • Creates manufacturing operation sequencing., • Validating tooling, machinery and process capabilities., • Verifying and Scheduling part manufacturing based off Customer purchase order/forecast., • Perform document control of Engineering drawing packets, customer specifications and industry specifications in data retention system., • Other reasonable duties as business and operational needs dictate. Qualifications What key skills and experience do I need? • 3-5 years’ manufacturing industry experience, • Blueprint/drawing interpretation, 3D modeling experience, fabrication and assembly experience, • Requires basic math skills. A strong understanding of Geometry is preferred, • Working knowledge of MS Word, PowerPoint and Excel spreadsheets – formulas, graphs and charts, • Requires ability to assess facts and develop conclusions, • High School Diploma or equivalent Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor

Job Description Davis Farr LLP is searching for a Staff Auditor(s) to join a flourishing company who is routinely included in Orange County Business Journals Best Places to Work. You will support the development and implementation of accounting policies, take part in compliance and communicate with other auditors relating to annual audits along with reviewing schedules for the reporting process. About: Davis Farr LLP is a rapidly growing, full-service CPA firm with its main office located in Irvine, California and two additional offices located in Carlsbad, California and Tacoma, Washington. We have provided expert professional experience in audit, tax, and consulting services to federal, state, and local governments, special purpose governments, non-profit organizations, service organizations and commercial entities for over 30 years. Responsibilities: · Assist in carrying out quality and other assurance services to clients in various industries · Demonstrate a solid understanding of accounting principles, internal control standards and technology implementation · Identify and communicate audit issues, technical matters and improvement opportunities to resolve client issues discovered during the audit process · Perform other accounting, auditing, and consulting duties as assigned · Draft annual financial statements, including footnote disclosures · Develop and maintain an excellent working relationship with all levels of client staff to increase client satisfaction and strengthen client relationships · Comply with and maintain the highest degree of professional standards, client confidentiality and person conduct · Ad-hoc tasks and special projects as needed Requirements · BA/BS in Accounting; advanced certification highly desirable o Eligible to sit for the CPA exam/plan to sit for the exam OR interested in pursuing compliance auditing · 1+ years of public accounting preferred and/or experience with governmental, non-profit, and commercial sector audits · Well-rounded knowledge of GAAP; GAAS, GAS and GAGAS a plus but not required · Highly proficient with Excel, Word and PowerPoint, Audit software experience a plus · Strong oral, written and interpersonal skills · Strong attention to detail and exceptional analytical and research skills · Ability to multi-task, think independently and problem solve in a team-oriented environment · Some travel required Benefits $68,700-$80,000 plus excellent benefits package including generous PTO, medical, dental, vision, life insurance, 401(k) with company match. Company-paid licenses, professional dues and continued professional education.

Job DescriptionCompany Description Vuori is re-defining what athletic apparel looks like: built to move and sweat in but designed with a casual aesthetic to transition into everyday life. We draw inspiration from an active coastal California lifestyle; an integration of fitness, creative expression and life. Our high energy fast paced retail environment is reflected in the clothes we make. We aim to inspire others to take on all aspects of their lives with clarity, enthusiasm and purpose…while having a lot of fun along the way. We are proud to be an outlet for opportunity and for personal growth and success. Job Description As we grow and evolve our analytics capabilities, we’re investing in operationalizing advanced data science to fuel smarter decisions across merchandising, inventory, customer experience, and supply chain. We're looking for an experienced Director of Data Science to lead our applied data science team, focused on delivering scalable, production-grade solutions that drive measurable business outcomes — with a strong emphasis on consumer intelligence and personalization. This is a hands-on leadership role that balances technical depth with organizational influence and plays a key role in the day-to-day execution of our analytics roadmap. What you'll get to do: Operational Leadership • Translate the analytics strategy into an actionable data science roadmap, working closely with the technology and business leaders., • Own execution of predictive and prescriptive analytics use cases across business functions, with emphasis on customer intelligence, retention, and personalization., • Collaborate with Marketing, CRM, Digital Product, and product teams to develop customer-facing data products and segmentation strategies., • Support lifecycle marketing, acquisition, and retention through predictive modeling (e.g., churn prediction, next-best-action, lookalike modeling)., • Work closely with merchandising, planning, and eCommerce to deliver customer-informed product recommendations, channel strategy, and pricing decisions., • Lead and mentor a team of data scientists focused on both customer and operational use cases., • Drive best practices for feature engineering, model development, and reproducibility., • Define and track business impact of consumer analytics initiatives: customer retention uplift, increase in average order value, reactivation rates, etc., • Implement A/B and multivariate testing to validate personalization and targeting strategies., • Ensure transparency, governance, and ethical use of customer data in all modeling efforts. Qualifications Who you are: • 12+ years of experience in data science or advanced analytics, with at least 3 years leading teams., • Demonstrated success applying data science to consumer behavior, personalization, and lifecycle marketing in a B2C or retail apparel context., • Experience delivering models such as:, • Customer segmentation (RFM, behavioral, ML-based), • Customer lifetime value (CLV) modeling, • Personalized recommendations, • Churn prediction & win-back targeting, • Multi-touch attribution or media mix modeling, • Strong hands-on ability in Python, SQL, and tools like Pandas, scikit-learn, or Spark., • Business acumen and the ability to translate complex analysis into practical, audience-tailored recommendations., • Bachelor’s or Master’s in a quantitative discipline (e.g., Statistics, Applied Math, Computer Science)., • Apparel or fashion retail experience where brand affinity, style preferences, and return behavior play key roles., • Experience with modern marketing stacks (e.g., CDPs (hightouch), Attentive, Braze etc)., • Familiarity with real-time data applications for web/app personalization., • Working knowledge of data privacy regulations and ethical AI practices related to customer data. Additional Information Our investment in you: At Vuori, we’re proud to offer the following to our employees: • Health Insurance, • Savings and Retirement Plan, • Employee Assistance Program, • Generous Vuori Discount & Industry Perks, • Paid Time Off Vuori is proud to be an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. All your information will be kept confidential according to EEO guidelines.

Job DescriptionSalary: 70,000-110,000$/hr Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and other Consulting services. MMR Consulting has offices in Canada, USA, and Australia. This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers and specialists involved in project management, commissioning and qualification, of equipment, systems and facilities. The role will require working out of the clients facilitiesin San Diego Area. The ideal candidate should possess leadership skills to lead/mentor intermediate/junior engineers. Responsibilities • Provide technical guidance into the commissioning, qualification and start-up of various pharmaceutical / biopharmaceutical cGMP process equipment, utilities & facilities., • Lead the development (for example, write test cases) of key qualification deliverables such as DQ, FAT, SAT, IQ, OQ and PQ during the project lifecycle, • Able to perform field execution of qualification test cases and protocols, • Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant., • Lead qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met., • Possess knowledge of relevant regulatory requirements and industry best practices on all or any of the following: Process equipment, clean utilities, automation systems, laboratory equipment, building & facilities., • Responsible for document generation, execution, data evaluation and overall documentation support to close out C&Q activities., • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates., • Engage other departments, as required, into design reviews and decisions., • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs)., • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification and validation phases., • Visit construction and installation sites, wearing necessary safety PPE., • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc., • Supervise contractors during critical testing of system and equipment., • Other duties as assigned by client, and/or MMR, based on workload and project requirements., • Lead/Mentor a team of validation engineers/specialists. Qualifications • 8+ years of experience in commissioning, qualification, validation of various systems within the pharmaceutical/biotech industry., • Experience with validation of equipment & facilities is required., • Experience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ., • Write, investigate and implement solutions to protocol deviations and change requests., • Experience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems are considered an asset., • Experience with preparation and execution of URSs, DQs, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs, • Lead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset, but not required., • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity., • Possess mentorship skills, to coach and develop junior and intermediate employees., • Engineering degree, preferably in Mechanical, Electrical or Chemical., • Travel may be required on occasion., • Ability to handle multiple projects and work in a fast-paced environment. Strong multi-tasking skills Salary range: 70,000$ -110,000$ based on experience. Equal Employment Opportunity and Reasonable Accommodations MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request. *

Job Description Compensation Package • The approximate base salary range is $90,000 - $120,000 (Incumbent’s final compensation is determined on experience, knowledge, abilities, etc.)., • Performance Bonus & Profit-Sharing Bonus., • 401k + Company Match., • Open Vacation Policy., • Paid Holidays., • Paid Parental Leave., • Health, Vision, Dental, Life Insurance, Disability. The Building Electrical Group is responsible for all building electrical systems including lighting, fire protection and low voltage for our design-build, industrial projects. We design and build food and beverage production facilities. Our building electrical team is involved with designing the electrical systems, calculating power loads, determining, and selecting equipment sizes, and vetting and selecting suitable vendors, suppliers, and sub-contractors. The professional will have technical responsibility for scoping, performing, and delivering multiple concurrent project assignments. His/her specific responsibilities will include, but not limited to: Responsibilities • Designing electrical systems for building power, i.e. normal, emergency, and standby power distribution systems for 208v, 480v, and medium voltage for industrial facilities., • Documenting all necessary calculations for the design such as short circuit, selective coordination, arc flash, generator sizing, steady state and transient voltage drops, load calculations, conductor sizing, raceway fills, etc., • Maintaining project document organization, • Managing time and meeting commitments, • Understanding Ohms Law, AC/DC, Electric and magnetic fields, • Understanding power system theory – 3-phase vector math, power factor, symmetrical components, • Understanding capacitors, inductors, and resonance, • Designing lighting for food processing spaces, including lighting calculations for emergency and inspection lighting level needs. Coordinating fixture placement/mounting with other trades., • Designing fire alarm systems per NFPA 72, 101, and local building code., • Code expertise – NEC, NFPA 72/101/, IBC, • Specifying means and methods, • Specifying other common work – grounding, start-up, LV & MV Cables, • Specifying equipment, • Designing low voltage systems such as LAN, phones, PA, Wi-Fi, access control, cameras, etc., • Creating power plans, • Creating power one-line and panel schedules, • Defining fire alarm requirements per IBC and NFPA 101, • Defining Low Voltage Systems, • Reviewing scope with client – creating and managing needs list, • Producing bid documents consisting of layout drawings, one-line, riser, schedules, details, and specifications., • CAD – add 2D & 3D devices to Xrefs, • Procuring long lead light fixtures and power distribution equipment such as switchgear, switchboards, panelboards, transformers, MCC’s, generators, variable speed drives, and UPS’s., • Transformer configurations, • Performing short circuit calculations identifying deficiencies or series ratings, • Estimating weights of main tray/trapezes and equipment needing support, • Assisting in managing electrical bid process for clients, observing construction, and assisting with startup., • Project planning and feasibility studies., • Actively participating in and supporting department-wide standard development, updates, and maintenance., • Researching electrical building/power materials and best practices, • Bachelor of Science in Electrical Engineering or related field, • 4-7 years of work experience in electrical systems for building power., • 4-7 years of work experience in designing lighting, fire alarm systems, and low voltage systems for building spaces, including lighting calculations, and coordinating fixture placement with trades., • 4-7 years of work experience in electrical bid documents and procuring electrical materials and equipment., • 4-7 years of work experience in AutoCAD, Revit or other related design programs., • Relevant work experience in a manufacturing or construction setting preferred., • PE tracked desirable., • Prolonged periods sitting at a desk and working on a computer. We plan, design, engineer, and build food plants for major brands across the country and the world. For the past three decades, we’ve focused exclusively on the food and beverage industry, helping your favorite brands put your favorite foods in the grocery store. Simply put, food isn’t one thing we do, it’s all we do. Dennis Group offers competitive compensation packages commensurate with experience. We provide comprehensive employee benefits including medical, dental, vision, life and disability insurance, paid time off including an open vacation policy, as well as bonus, profit-sharing, and retirement plans. Dennis Group is proud to provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or genetics.

Job Description Compensation Package • The approximate base salary range is $85,000 - $115,000 (Incumbent’s final compensation is determined on experience, knowledge, abilities, etc.)., • Performance Bonus & Profit-Sharing Bonus., • 401k + Company Match., • Open Vacation Policy., • Paid Holidays., • Paid Parental Leave., • Health, Vision, Dental, Life Insurance, Disability. Dennis Group’s Mechanical Engineers design and implement mechanical systems as part of a broad engineering and architectural team in designing and building food and beverage production facilities. Specifically, HVAC, plumbing / utility, and fire suppression systems. Our mechanical team is involved with designing the mechanical systems, calculating space heat and cooling loads, determining and selecting equipment sizes, and vetting and selecting suitable vendors, suppliers, and sub-contractors. Mechanical Engineers will have technical responsibility for scoping, performing, and delivering multiple concurrent project assignments. You will be a member of our mechanical department and your responsibilities will include, but not be limited to: Responsibilities • May work independently or with other ME’s, depending on project size, • Execute all tasks necessary to complete the engineering on a project from design through execution, • Perform heating and cooling load calculations, • Code reviews for HVAC/plumbing/fire protection designs, • Perform mass energy balance calculations, • Perform drainage and line loss calculation, • Perform flow test (hydrant or other) analysis, • Sanitary design considerations (layouts, process exhaust), • PID drafting & design, • Bid package: equipment and sub-contractor – bid list, scope of work, milestone schedule, • Provide cost estimation and scheduling to PMs, • Bid Review, • Peer design review, • Scheduling – MS Project, • Discipline lead for commissioning activities, • Equipment selection, • Vendor and Sub-contractor selection, • Controls functional description development, • Create mechanical schedules, • Present engineering findings to client, • Building code familiarity, compliance & review, • Insurance carrier requirements – familiarity and review, • Vendor shop inspection / FAT, • Develop HVAC, plant utility, plumbing, and fire suppression systems, • Assist in mechanical system design development and coordinating with other internal and external team members, • Develop Mechanical / Utility equipment and construction specifications, • Develop P&ID’s, equipment layout plans, plant / process utility distribution plans, and system details, • Size and develop layouts for ductwork and piping plans, • Assist with the development of the building management system (BMS) controls, details, and plans with electrical and controls engineers, • Create project documents such as calculations, reports, and construction drawings and specifications, etc., • Fixture selection, • Perform construction administration in the form of submittal reviews, RFI responses, and field visits to verify construction scope is proceeding per the intent of the design, • Research mechanical / utility materials and best practices, • Support talent growth within our organization, • Bachelor of Science in Mechanical Engineering or related field, • 3-5 years of work experience in heat transfer, fluid dynamics, and thermodynamics, • 3-5 years of work experience with HVAC/plumbing/fire protection designs and specifications., • 3-5 years of work experience performing calculations in areas of energy, drainage, line loss, etc., • 3-5 years of experience working with computer operations for engineering design programs and computer aided drafting (AutoCAD, Revit, etc.), • Basic report writing and communication skills, • Relevant work experience in an industrial manufacturing setting preferred, • FE/EIT certificate preferred, • Strong technical writing skills, • Prolonged periods sitting at a desk and working on a computer. We plan, design, engineer, and build food plants for major brands across the country and the world. For the past three decades, we’ve focused exclusively on the food and beverage industry, helping your favorite brands put your favorite foods in the grocery store. Simply put, food isn’t one thing we do, it’s all we do. Dennis Group offers competitive compensation packages commensurate with experience. We provide comprehensive employee benefits including medical, dental, vision, life and disability insurance, paid time off including an open vacation policy, as well as bonus, profit-sharing, and retirement plans. Dennis Group is proud to provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or genetics.

Job DescriptionWho We Are Dudek is a leading environmental, planning, and engineering firm that help public and private clients plan, design, and build projects that improve communities’ built and natural infrastructure. Founded in 1980, Dudek has grown steadily to more than 800 professionals across the U.S. and received the Top Workplace Award for 2024. As a 100% employee-owned company, Dudek’s culture rewards smart, productive team members with ownership, professional development, and financial benefits. We seek creative, pragmatic problem-solvers working at the intersection of science, engineering, regulations, and multiple stakeholders’ interest to help clients achieve project goals. We encourage collaboration, sustainability, and innovation. At Dudek, we abide by shared values: Trust: We trust each other to use good judgment. Respect: We act professionally and treat each other fairly. Teamwork: We come together, share openly, and apply diverse perspectives. Fun: We take our work seriously…not ourselves. Well-Being: We care about each other’s health, safety, and total wellness. Our culture is the foundation of who we are and how we work. We empower our employee-owners to invest in our local communities and themselves through initiatives that make Dudek a great place to work! Our cultural programs include: • DuGreen: Our sustainability initiative, which works to improve our environmental footprint, • DuGood: Our philanthropic initiative, which seeks to support the communities in which we live and work through fundraising challenges, office-based giving and opportunity to take a paid volunteer day each year., • eDUcate: Our educational outreach program where we aim to foster interest in our work and careers in the environmental and engineering field by participating in educational events in our communities., • DuWell: Our wellness initiative, aimed at providing education on wellness, benefit resources, and preventive care.At Dudek, we recognize that different perspectives, inclusivity, trust and belonging build a stronger culture and add value to our firm. Dudek's Employee Resource (ERGs) operate as diversity champions within Dudek and create a safe space for underrepresented employees and their allies to support, collaborate, network, and brainstorm ways to make Dudek’s work community more inclusive. We proudly support our 4 Employee Resource Groups (ERG’s):, • Women at Dudek, • Members of the Lesbian, Gay, Bisexual, Transgender, Queer (LGBTQ+) community, • Black, Indigenous, and People of Color (BIPOC) employees, • Disabled employees (all disabilities, seen / unseen)Learn more about our culture. About The Job We are seeking a talented and experienced CAD Designer to join our environmental and engineering consulting firm. The ideal candidate will be responsible for the preparation of construction bid documents for public sector water-related infrastructure design projects. This role involves working on a variety of projects, including mechanical pump station design, water storage facilities, water/wastewater treatment plant design and rehabilitation, and linear pipeline installation and rehabilitation. Learn more about the projects you will have the opportunity to shape. Who You Are To thrive at Dudek, you should be comfortable with accountability, collaboration, flexibility while being a resourceful and independent thinker. We look for curious, solution-focused people who can adapt quickly to an ever-changing industry. There is no single way to solve a problem, so we encourage innovation. Duties and Responsibilities (may include some or all of the below): • Assist in the proposal stage of projects by estimating CAD related workload and opportunities for increased efficiency and development of CAD deliverables., • Utilize AutoCAD and Civil 3D to develop detailed CAD drawings for public sector construction bid documents., • Work closely with project managers and engineers to ensure accurate and timely completion of design projects., • Research client/agency CAD design requirements and confirm design files to the requirements, for example structured layering, pen tables, line weights, line types, etc., • Set up backgrounds, existing utility research, record drawing review, plotting and base mapping., • Utilize existing design details, templates, tools as needed to efficiently develop plans, • Coordinate with other design team members to ensure consistency and accuracy in project documentation., • Review and revise drawings as needed based on feedback from engineers and clients., • Ensure all designs comply with relevant codes, standards, and project specifications., • At project completion, transfer client supplied red-line markups to the final record drawing CAD files., • Maintain organized project files and documentation., • Full understanding and highly proficient in latest version of AutoCAD and Civil 3d, • Familiarity with civil and mechanical engineering symbols, plans, and other related drawings, • Strong understanding of construction bid documents and public sector project requirements., • Familiarity with relevant codes and standards in water infrastructure design., • Excellent attention to detail and accuracy in drafting and design., • Ability to work collaboratively in a team environment., • Strong communication and interpersonal skills., • Ability to work effectively in a multi-deadline changing environment, • Exercise good quality control philosophy, • On rare occasions, able to work overtime if required, • Highly motivated, self-starter, and willingness to learn, • Exceptional written and verbal communication skillsMinimum Requirements, • 8+ years of CAD experience in Civil and Mechanical disciplines, • Graduation from certified CAD training program or a technical/Associates degree in engineering or related field, • As a federal contractor, successful candidates are required to pass the following pre-employment requirements prior to beginning employment: pre - employment drug test and background check. Preferred Qualifications • Knowledge of California Mechanical Code, • Knowledge of water/wastewater industry, • Knowledge of the design/layout of electrical design plans, • Experience with GIS Software, • Interest in guidance, mentoring, training of other staff in CAD design., • This job operates in a remote or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc., • This job requires occasional project site visits-based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, moving vehicles and equipment.Physical Requirements: The physical demands described here are representative of those that must be met in order to successfully perform the essential functions of the job., • This job requires working on a computer, sitting or standing for long periods of time in an office or remote office setting., • This job requires attending meetings, both in person and virtually as well as speaking on the phone with peers, clients, etc. Speaking, hearing and listening are required. Proposed Salary Range: $79,000-$99,500 annually* *Final agreed upon compensation will be based on a variety of factors including but not limited to an individual’s related experience, education, certifications, skills, and work location. Perks of Being a Dudekian At Dudek we will provide you with a competitive salary in an environment that promotes growth, career development, and a flexible work–life balance. Dudek offers an array of benefits, from medical, dental, and vision coverage, to the discretionary bonuses, based on firmwide, divisional, and individual performance. We also offer a yearly merit review, an employee stock ownership program, and dog friendly offices! To honor our key value of well-being, Dudek provides generous Paid Time Off (PTO) packages for both salaried and hourly employees. If you’re tired of an overly bureaucratic decision-making process and want to be part of a work culture that puts its employees first, speak with your recruiter to learn more about the great perks of being a Dudekian. Dudek is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, disability, protected veteran status, or other characteristics protected by applicable law. Dudek is a U.S.-based employer. All positions are based in the U.S. and require U.S. work authorization. Powered by JazzHR qG5ZkgAO3B

Job Description H2O is a smart water treatment solutions company. We simplify water treatment by integrating state-of-the-art technologies to solve water challenges for good with our team of trusted experts. Our mission is to provide services on an international scale, in a people-oriented, caring environment that fosters professional and personal growth. Be part of our talent pool and grow with H2O. The Senior Process Engineer will mainly be in charge of application engineering/sales support; development of preliminary treatment process designs; develop of standard UF/RO packages; and the overall development of technical and commercial proposals related to the Company’s treatment systems sales process. The Benefits Overall remuneration including: • Profit sharing program;, • Group Insurance plan including dental, vision & telemedicine;, • 401k plan with employer's contribution;, • A minimum of three (3) weeks of paid vacation per year;, • Twelve (12) paid wellness days per year., • Flexible working hours & hybrid working; The Day-to-Day • Perform preliminary design of water treatment plants based on membrane projections and other accepted calculations in accordance with established criteria;, • Collaborate closely with sales managers and engineering discipline teams;, • Prepare budget, preliminary and final (bid) cost estimates including bill of materials, equipment, and controls;, • Prepare formal proposals for submittal to potential clients;, • Develop drawings of equipment and plant playouts as requested and oversee designers;, • Create process drawings such as P&IDs and PFDs;, • Select equipment (pumps, valves, membranes, etc.);, • Develop and present technical presentations/papers on in-house projects to promote Company and water technologies at conferences and clients meetings;, • Continuous investigation into improving design of current equipment and treatment processes, and development or acquisition of new equipment or processes to complement existing portfolio;, • Prepare engineering documents such as functional descriptions, process control narratives, etc.;, • Maintain an excellent working knowledge of state, provincial and federal regulations, as well as current design processes;, • Maintain contact with current installations to obtain performance, operation and maintenance data and provide operational assistance as requested;, • Maintain records of actual costs and provide comparison and analysis of discrepancies between estimated and actual costs;, • Advance the development of standard treatment packages for UF and NF/RO systems;, • Travel to project sites and perform treatment process audits;, • Other duties as assigned. The Skills We Are Looking for • A degree in chemical, environmental, civil or mechanical engineering or equivalent;, • Minimum 7 years experience as a process engineer in the water industry;, • Experience with membrane filtration treatment, • The ability to work efficiently on multiple assignments simultaneously;, • Excellent written and oral communication skills in English;, • Experience with Ion Exchange (IE), an asset;, • Knowledge of drinking and wastewater treatment, an asset. #ZR

Job Description Since 1996, RQC, LLC. has been a leading player in Southern California's robust commercial and governmental Design-Build economy. Headquartered in beautiful Carlsbad, CA, we are a full-service Design-Build company. We offer management of projects throughout the United States and Caribbean. We are seeking a licensed Project Architect to join our established Architecture Department within an integrated Design/Build (DB) construction company that focuses on military construction projects. The Project Architect will actively manage multiple projects and provide oversight across a variety of key disciplines including fire protection/life safety, civil, landscape architecture, structural, interior design, mechanical/plumbing, electrical, and telecommunications/audio visual/security. The Project Architect will work closely with other engineers and architects to provide strong client management and representation for the duration of the projects. The Project Architect will be a technical leader within the design team with technical expertise in architectural design, construction documents, construction, building codes, and project coordination issues associated with diverse project types ideally with the delivery of DoD military constructions projects. This position is based out of our office in Carlsbad, CA. RESPONSIBILITIES: • Assist in leading a multidiscipline team, • Perform schematic layouts and preliminary design, • Construction documentation/detailing on architectural projects, • Participate in owner/client and internal meetings, and participate in design reviews with various governing agencies, • Coordinate workload of architecture team members through multiple phases to complete documents on schedule, • Review architectural documents for areas of conflict with all disciplines, • Write and edit architectural specifications utilizing SpecsIntact software, • Coordinate with and assist affected disciplines with addenda, RFIs, and change orders, • Assist in the project design schedules, • Perform QA/QC and technical reviews, • Perform Independent Technical Reviews (ITR) on projects within the department, • Assist in the management of various projects through all phases of the design process., • Be the point person for coordination of multi-million-dollar projects, • Registered Architect, required, • NCARB certificate, preferred, • Bachelor's or Master's Degree in Architecture, required, • 15 or more years of experience in construction documentation with projects valued at $30-$150 million, • Strong understanding of civil, structural, mechanical, plumbing, electrical, and low voltage systems, • Strong understanding of architectural construction detailing and technical expertise, • Department of Defense (DoD) experience, preferred, • Proficiency with and experience using Revit software, • Strong technical competence and proven experience in schematic design through construction documentation, • Demonstrated understanding of code implementation, construction practices and methodologies, • Strong leadership, written and verbal communication, and organizational skills, • Understanding and experience in Unified Facilities criteria (UFC) and building codes PAY & BENEFITS The approximate pay range for this position is $100,000 to $130,000 per year. This compensation range is a good faith estimate for the position at the time of the posting. Actual compensation is dependent upon factors such as education, qualifications, experience, and skillset. • Hybrid work schedule that consists of a Monday-Wednesday in the office and optional work-from-home days on Thursday and Friday, • Comprehensive Health Coverage: Medical, dental, and vision insurance plans to keep you and your family healthy, • 401(k) Retirement Plan: Competitive employer matching to help you plan for the future, • Paid Time Off: Generous vacation, holidays, and personal days to recharge and enjoy life outside of work All candidates considered for hire must provide evidence of identity and U.S. work authorization at the time of hire. Additionally, all candidates must successfully pass a drug screening and commercial criminal background check, including a stricter Department of Defense background check, for access to job site at military base (if applicable for position being hired for). Job Posted by ApplicantPro

Job Description Mechanical Quality Engineer supporting new product development. Develop, improve, and implement quality methods and systems, working on cross functional teams in a regulated environment to ensure the safety, reliability and efficacy of products and processes. Essential Duties and Responsibilities • Support New Product Development as primary QE for mechanical implants and instruments. Manage multiple concurrent major and minor projects., • Support Design Controls to ensure efficient, effective, and compliant new product launches., • Support the qualification of legal manufacturers (OEM) for distributed products., • Lead Material Review Board (MRB), own Non-Conformance (NC) development and resolution, lead reworks and deviations, participate in Supplier Review Board (SRB)., • Develop inspection plans and custom gauging based upon required measurement and tolerances., • Support Change Order review for drawings, considering Design for Manufacturing (DFM) and Design for Inspection (DFI)., • Act as liaison between supplier and company for quality related concerns or issues. Technical interface with contract manufacturers., • Support cleaning and sterilization validations of implantable devices; basic understanding of tests such as bioburden, BET, and dose audit testing., • Support validation (IQ, OQ, and PQ) development and execution internally and at suppliers., • Apply statistical techniques to analyze manufacturing processes and recommend appropriate process controls., • Support Risk Management efforts in accordance with ISO 14971; conduct preliminary risk assessments for projects. Support Failure Mode and Effects Analysis (FMEA) for designs and processes., • Support Field Retrieval Assessment (FRA) and Health Hazard Evaluation (HHE) as needed., • Support MDSAP, FDA, ISO, and other regulatory audits., • Apply external standards and guidance documents to project / product specific application., • Own Supplier Corrective Actions (SCARs) and Corrective and Preventive Actions (CAPAs). The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Good understanding of the FDA Quality System Regulations (21 CFR Part 820), ISO 13485, MDSAP, and ISO 19227., • Direct experience with implantable devices, instrumentation, and disposables in a regulated environment., • Knowledge of mechanical inspection methods and equipment., • Knowledge of SPC, DOE, probability, and statistics., • Ability to read, analyze, and interpret blueprints, including GD&T., • Ability to solve complex problems to root cause and prevent re-occurrence (CAPA)., • Ability to process data, interpret data trends, and make basic recommendations based on findings., • Ability to troubleshoot and manage priorities across multiple projects based upon ATEC business priorities., • Strong technical writing skills, including ability to write protocols, reports, and procedures., • Ability to effectively interact with all levels of the organization., • Shows desire and ability to take on small leadership roles within projects, effective communication and collaboration with team members., • Ability to develop and maintain strong working relationships with internal and external customers and suppliers., • Excellent verbal and written communication, ability to resolve minor conflicts, collaborative teamwork., • Demonstrates tenacity in overcoming obstacles; proactive in taking initiative., • Knowledge of SolidWorks or other CAD software preferred., • Manufacturing Engineering experience preferred, including knowledge of metal and plastic part production and processing. Process knowledge including milling, turning, EDM, 3D printing, and secondary processing., • Detail oriented., • Good decision-making skills and judgment., • Ability to develop plans and strategies and execute to completion., • Must be able to travel up to 5% of the time. Education and Experience • Minimum Bachelor’s degree (BS) from a four-year college or university, preferably in Mechanical, Industrial, Biomedical, or Manufacturing Engineering., • 2+ years related experience and/ or training; or equivalent combination of education and experience. For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $91,000 to $108,000 Full-Time Annual Salary

Job DescriptionSalary: Position Description We are seeking a highly skilled and motivated Surgical Planning and Data Intelligence Specialist with a solid foundation in spinal surgery, radiographic interpretation, research, and a strong proficiency in analytics. This role bridges clinical insight with advanced analytics and plays a central role in supporting our intelligent surgical planning tools and research initiatives. The ideal candidate brings a unique blend of clinical knowledge, imaging proficiency, and experience in working with large datasets and predictive models. This position offers a dynamic opportunity to work cross-functionally with clinical, engineering, and AI teams to enhance surgical planning, analyze surgical outcomes, and drive innovation across the Carlsmed platform. Responsibilities • Develop expertise in using Carlsmeds AI-enabled systems to analyze large amounts of spinal imaging data (X-ray, CT, MRI), to document consistency, accuracy, and quality in radiographic interpretation and measurements., • Evaluate radiographic outcomes to assess alignment against preoperative plans and provide recommendations to help optimize surgeon specific planning., • Identify and extract clinical insights from internal datasets to support research, education, and support R&D., • Provide guidance into data inputs in collaboration with Engineering, Data Science, and Software teams to ensure clinical relevance in AI-based workflows., • Collaborate with Data Science to provide clinically relevance input for AI/ML models to support continuous improvement in preoperative planning based on postoperative data. Support ongoing optimization of models to predict radiographic outcomes., • Contribute to abstract submissions, publications, and evidence generation., • Develop dashboards and tools to monitor model performance and accuracy across large patient cohorts. Qualifications • Bachelors degree in health sciences, biomedical informatics, computational science, biostatistics, bioengineering, or a related field., • Minimum 5 years of experience in orthopedic or spine settings, with either a graduate-level clinical degree or substantial clinical research/imaging experience, including collaboration with engineering or data science teams on AI/ML or software-based clinical tools., • Strong understanding of spinal alignment parameters, surgical planning workflows, and radiographic measurements is a plus., • Proficiency with imaging software (e.g., PACS, Surgimap, Mimics) and familiarity with DICOM-based imaging analysis., • Experience with data interpretation, outcomes analysis, or collaboration with AI/ML teams in a healthcare setting., • Experience and fluency in Python, R, and SQL or similar., • Scientific publication or abstract authorship experience is highly desirable., • Excellent verbal and written communication skills and a proven ability to work cross-functionally with clinical, product, and technical teams. Equal Opportunity Employer Carlsmed is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Carlsmed is committed to providing reasonable accommodation for candidates with disabilities in our recruitment process. If you need assistance or accommodation due to a disability, please let us know. Compensation We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families, including paying 100% of monthly healthcare, dental and vision insurance premiums, a 401(k) plan with employer matching, and unlimited PTO. The expected pay range is $120,000 - $140,000. Compensation may vary based on related skills, experience, and relevant key attributes.

Job Description JOB DESCRIPTION Position Title: Client Development Executive Reporting Relationship: Client Development Leader Location: Remote Company Overview Solecta plays a globally impactful role in the development of novel and critical separation technologies for high value process feed streams that directly support the improvement of people’s lives. Whether it be advancements in the production of nutritionally sound food, materials for everyday life, or mitigation of environmental footprint, our team is driven to provide thoughtful and meaningful leadership in advanced separations. With a deep focus on understanding our clients’ industries and applications, Solecta strives to deliver superior value and agility to navigate today’s complex business environment. Solecta maintains manufacturing facilities and an R&D center in Oceanside, CA, as well as commercial offices in San Francisco, Boston, Minneapolis, and Chicago. Solecta is a wholly owned subsidiary of True North Venture Partners. Position Summary As a member of Solecta’s commercial team, the Client Development Executive is responsible for the execution of the sales plan in accordance to company vision and strategy. In this position, the Client Development Executive will work with leaders and influencers across a variety of companies within the dairy, food ingredients, life sciences, and manufacturing market segments to help them solve unique and real issues. This role will work collaboratively with the Market Segment Managers, Product Managers, Applications Engineering and Operations leadership to ensure financial goals are met while upholding our company values and culture of teamwork. Essential Functions • Finds and develops new opportunities at targeted prospects., • Identifies and nurtures valuable and relevant leads., • Cultivates existing client relationships and evolve them into further business opportunities and client partnerships that ensure a healthy pipeline., • Accelerates complex sales cycles from prospect to close and beyond., • Identifies client needs and success criteria to advance the sales process. Develops value propositions leveraging products and services core to Solecta., • Creates long-term trust and client partnerships at multiple decision-making levels through a genuine consultative and problem-solving approach., • Investigates and discovers client purchasing and usage data to inform sales planning and market strategy development., • Develops and executes sales targets at all stages and orchestrate compelling interactions with prospective and existing clients., • Plans activity in accordance with commercial milestones., • Establishes aggressive yet realistic plans to achieve the desired sales plan objectives, anticipate risks, and have contingency plans to manage them., • Utilizes CRM to manage a sales portfolio, pipeline metrics, analytics, share information with commercial team, monitor sales cycles and stages, maintain pipeline to meet metrics., • Participates in the development of the sales annual operating budget and maintains expenses within the plan., • Partners with marketing and sales team to execute strategy, demand generation, lead development and communication to drive sales efforts., • Engages customers and creates personal brand using social media in accordance with Solecta guidelines., • Remains current on industry, market trends, developments, and technology trends within the membrane and element industry, while continuously learning about Solecta, its vision, culture and people., • Consistently improves knowledge of all products and services provided by competitors., • Learn all aspects of customer operations. Continuous development of technical and commercial skills., • Other duties as assigned. Position Qualifications • Bachelor’s degree in Science, Business Administration or other related field; MBA preferred., • 5 years of sales, and business development experience with complex global manufacturing clients., • 5+ years of experience in company providing technical products and/or services, preferred., • Process membrane separations experience, preferred., • Proven track record of interpersonal skills with ability to cross-functionally interface with and positively influence other departments., • Strong leadership skills, independent thinking, proven organizational and planning abilities, and excellent analytical and problem-solving skills., • Ability to develop strategic relationships; strong verbal and written communication skills; excellent presentation skills., • Thrives in a fast-moving environment., • 50-75% travel required., • Remote worker position located near a major metropolitan area. The salary range for this position is $115,500 to $214,500. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, job-related knowledge, experience and location. EOE

Job DescriptionCompany Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description AM Shift: Monday - Thursday 5:00AM - 3:30PM Pay: $18.00 - $19.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Fabricator / Assembly you will: The Fabricator is responsible for manufacturing and preparing detail components and assemblies using general shop tools that meet the customer and STEICO drawings/specifications manufactured within the documented manufacturing processes provided by STEICO. What will my responsibilities include? • Operating Chop saws for trimming of Metal tubes and ducts., • Operating Manual Mills and Lathes for drilling and coping of tubes and ducts., • Operating Pneumatic Tools such as die grinders, Dynabrade belt sanders and pencil grinders., • Operating bench buffers, bench grinders, tube expanders and 20” disk sanders., • Using hand tools such as deburring tools, and rubber mallets., • Using calibrated tools such as dial calipers, depth gauges, snap gauges and height gauges., • Follow company policies and procedures., • Other reasonable duties as business and operational needs dictate. Qualifications What key skills and experience do I need? • Communication skills, • High School diploma / General Education Completion., • Experience in custom cabinet and fine woodworking trades highly beneficial, • Working with aluminum, stainless steel and titanium is a plus, • Experience reading blueprints and using measuring devices is a plus, • Understanding of chop saws, manual drills and general hand tools, • Knowledge of grinders and sanders, • Manual mill and lathe knowledge Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor

Job DescriptionCompany Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description Shift: Monday - Friday 7:00AM - 3:30PM Pay: $30.76 - $33.65 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Buyer you will: This position will be responsible for maintaining supply inventory levels required for effective company operations. This position will be accountable for negotiating agreements with potential vendors as well as being charged with conducting regular price comparisons to ensure that STEICO is being provided with the best price for each product purchased. What will my responsibilities include? • Develop, maintain, and qualify suppliers following STEICO active processes for necessary support of raw material, fittings, and outside services., • Regular visits to suppliers to ensure quality and delivery standards, • Generate, review and action vendor delivery reports also working along with Quality Dept for vendor quality reports, • Maintain accurate reports and current database of vendor information and open order reports, • Send RFQ’s to vendors identifying special requirements by generating and reviewing purchasing demand reports, • Evaluate bids as well as negotiate prices and terms for purchased goods and services., • Create purchase orders for spot buys and long lead materials, supplies and services at the most favorable terms for STEICO., • Verify with vendors orders are ready for pickup. Prepare Drivers Logs for scheduled pickups., • Create RPO documentation for return shipments including replacements or credit memos., • Work with Accounting for updating or correcting PO’s from suppliers or outside processors., • Communicate and participate in meetings between STEICO and vendors regarding open order reports and priority items. Update MRP system to ensure proper alignment and accurately update notes., • When necessary as backup, review blue prints and specifications ensuring correct revisions and Manufacturer are being used prior to procurement of fittings and hardware., • Follow active process for measuring supply inventory and determining purchasing needs based on quarterly and annual numbers and customer forecasts., • Other reasonable duties as business and operational needs dictate.Qualifications What key skills and experience do I need? Requires high school diploma, or equivalent * 5 years in manufacturing environment with at least 4 years in a purchasing role in that environment * Requires working knowledge of computer, scanner, facsimile machine, copier and any other standard office equipment * Basic math skills and the ability to utilize a calculator * Intermediate working knowledge in the MS Office suite: Word, Excel, and Outlook * Requires ability to assess facts and develop conclusions Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor

Job Description Job Title: Quality Technician I Number of Openings: 1 Positions Pay Rate: Position Summary: The Quality Technician I, under direct supervision, ensures the quality processes and products by performing audits, inspections, and tests. The role supports defect investigations, first article sample submission (AS9102), and maintains detailed documentation for internal processes and Source Inspection Items presented to customers. Key Responsibilities: • Assist with product audits, inspections, and final shipment audits based on AS9100 standards., • Support system and process audits (supplier certification, internal system, subcontractor audits, etc.)., • Investigate and resolve quality issues with support from the Quality Engineer., • Maintain accurate ERP System/product transactions to ensure inventory accuracy., • Interpret internal and customer specifications to identify acceptable and rejectable products., • Develop and maintain inspection record filing systems for manufactured products., • Ensure proper inspection documentation accompanies shipments, especially for Source Inspections., • Support calibration of measurement equipment when needed., • Assist Quality Assurance Engineers and Managers as required., • Adhere to quality and safety systems and maintain safety standards., • Familiarity with AS9100 Aerospace Standard (knowledge of TS16949 or other related standards is a plus)., • Experience with First Article documentation and preparation (AS9102)., • Ability to read and interpret blueprints with strong attention to detail., • Skilled in using precision measuring instruments (e.g., calipers, micrometers, optical comparators, Faro Arm CMM, pin gauges, drop gauges)., • Experience operating inspection/lab test equipment (OGP, hardness testers, etc.)., • Proficient in computer skills, including spreadsheet, word processing, and database management., • Strong data analysis and problem-solving skills using 8-Discipline techniques., • Effective written and verbal communication skills, and strong interpersonal and organizational skills., • Background in RF and/or electrical field preferred., • Basic mathematical knowledge., • High school diploma required; additional technical courses, CQT or CMI preferred., • Minimum of 3-4 years of Quality Inspector experience in manufacturing

Job Description Evolve Treatment Centers is hiring for a LVN based out of our Encinitas locations. Our team provides cutting edge residential and outpatient treatment to adolescents struggling with addiction and mental illness. Our rapidly growing company is looking for those who are highly qualified and passionate mental health professionals to join our team! Our ideal candidate is passionate about working with teens and has strong communication skills, time management skills, and organizational skills. Candidates must be eager to participate in an environment that promotes continuous learning and works as a member of a team. We are looking for candidates that can stay calm during stressful situations, those that take initiative and maintains appropriate boundaries with clients. Essential Functions: • Direct patient care and assessment; including the reporting of observed changes in mental status and/or physical condition, response to emergencies, and safety risks, • Completes documentation in an efficient and timely manner, including nursing assessments, transcription of M.D.s' phone orders, • Knowledge of medication administration records, vital sign monitoring, • Attendance and participation in terms of treatment planning and professional staff meetings, • Call in medications to pharmacy and pick up, • Provides in service training to technical staff on medications, documentation, and monitoring of vital signs, • Provides ongoing patient education on all aspects of medications and other health issues including hygiene, • Monitors supplies and reports needs to Facility Manager, • Establishes a compassionate environment by providing emotional, psychological, and educational support to patients and families, • Resolves patient problems and needs by utilizing multidisciplinary team strategies, • Maintains safe and clean working environment by complying with procedures, rules, and regulations; calling for assistance from health care support personnel, • Protects patients and employees by adhering to infection-control policies and protocols, medication administration and storage procedures, • Psychiatric medications and their side effects, • Speak with clients and parents in a compassionate and patient manner, • Maintain professional boundaries with clients and staff, • Assess emergency situations and delegate responsibilities to staff, • Work with a multi-disciplinary team, • Exercise independent judgment and leadership, analyze situations accurately and take effective action, • Valid California Nursing License LVN/LPT, • Current CPR/ BLS card, • Minimum of one year experience as a working nurse. Psych or chemical dependence background preferred Medical/Dental/Vision Insurance * Paid Time Off - We understand a healthy work/life balance is crucial for our success, so we maintain a flexible Paid Time Off policy. Employees start accruing PTO immediately upon hire. In addition, employees receive paid holidays, paid sick days, and time off for bereavement and religious observances. * Flexible Spending Accounts (FSA)/Healthcare Flexible Spending Accounts (HSA) * Employee Assistance Program (EAP) - As a mental health treatment provider, we understand the importance of maintaining the emotional health and personal well-being of each member of our staff. * Retirement Planning * Professional Training - We invest in professional growth, offering quarterly continued education, ongoing training, and professional development courses for all employees. • Free Meals – Employees working at our Residential Treatment Centers are offered free meals provided by our in-house chef. bVBDLYaWti

Job Description The Senior Site Reliability Engineer (SRE) will be responsible for ensuring the availability, performance, scalability, and operational efficiency of the Informatix cloud platform. This role is focused on reducing manual operations work (toil), automating system reliability, and ensuring production-grade observability. The ideal candidate is a systems-focused engineer who is passionate about uptime, incident response, and continuous improvement through engineering solutions. Essential Duties and Responsibilities • Serve as a primary contributor to the on-call rotation to maintain 24/7 uptime for production systems., • Proactively, monitor, and continuously improve SLAs, SLOs, and SLIs across critical services., • Develop and maintain robust observability tooling including logging, metrics, and tracing (e.g., Azure Monitor, OpenTelemetry, Prometheus)., • Proactively conduct postmortems and root cause analysis; implement fixes to prevent repeat incidents., • Identify and eliminate manual operational toil through scripting and automation., • Design and maintain automated incident detection and response systems., • Establish and maintain runbooks, playbooks, and escalation protocols for system support., • Contribute to chaos testing and failure injection to proactively uncover weaknesses., • Promote a culture of operational excellence through data-driven reliability practices. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • 5+ years of experience in Site Reliability Engineering, systems engineering, or DevOps roles., • Expertise in monitoring and observability platforms (e.g., Grafana, Prometheus, ELK, Azure Monitor)., • Solid background in incident response, root cause analysis, and on-call rotations., • Deep knowledge of Microsoft Azure, including containerized services (AKS), networking, and storage., • Strong automation and scripting experience (e.g., Python, Bash, PowerShell)., • Familiarity with IaC tools such as Terraform, Bicep, or ARM templates., • Experience implementing SLIs/SLOs, operational dashboards, and error budgets., • Comfortable designing for resiliency, failover, and graceful degradation., • Knowledge of compliance frameworks (e.g., SOC 2, HITRUST, IEC 62304) is a plus., • BS/MS in Computer Science, Engineering, or related technical field preferred., • 5+ years in production engineering roles with direct ownership of critical systems., • Microsoft certifications a plus For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $135,000 to $145,000 Full-Time Salary Range

Job DescriptionCompany Description All Care Therapies provides speech, occupational, and physical therapy—virtually and in person. With clinics in California, Texas, and Nevada, we support clients of all ages and backgrounds. Our team is made up of passionate clinicians who value flexibility, collaboration, and meaningful care. Whether we’re helping a client communicate or supporting recovery after injury, we meet people where they are. Job Description We are hiring in all 50 states to provide services for clients in California & Nevada. We are also offering reimbursement for California and/or Nevada licensure! We are actively seeking part-time Speech Language Pathologists (SLPs) to join our Provider Network. You will have the opportunity to conduct treatment with our diverse client population of children and adults. We deliver skilled speech therapy services and interventions tailored to the unique needs of our clients with receptive and expressive language disorders, fluency, voice, and apraxia of speech. Responsibilites • Provide remote speech-language therapy services to clients, • Conduct online speech-language assessments to determine eligibility for speech services, • Develop, coordinate, implement, and monitor an individual's plan of care via teletherapy, • Maintain a caseload of kids, adults, and the geriatric population, • Keep appropriate and daily documentationQualifications, • Master's degree in Speech-Language Pathology, • Active CA State Speech Language Pathologist License or able to obtain a CA license, • Experience in a clinic or school setting or successful clinical interview, • Technical proficiency to conduct teletherapy through our all-inclusive platform, • Should be comfortable working with children (18 months+) This is a 100% remote opportunity, requiring a minimum commitment of 12 hours per week for part-time. Compensation W2 | $43.00 - $56.00 per hour commensurate with experience, qualifications, and bilingualism. *Reimbursement for licensure(s) will be paid out after 145 hours of work. Why Join Us? Experience the difference of working with a close-knit team of dedicated therapists who value collaboration, mentorship, and shared professional growth. • Competitive compensation that recognizes your expertise, • Flexible scheduling that empowers you to maintain work-life balance, • A referral bonus program to reward your network Additional Information All your information will be kept confidential according to EEO guidelines. All Care Therapies is an equal opportunity employer. All aspects of employment, including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job DescriptionCompany Description All Care Therapies provides speech, occupational, and physical therapy—virtually and in person. With clinics in California, Texas, and Nevada, we support clients of all ages and backgrounds. Our team is made up of passionate clinicians who value flexibility, collaboration, and meaningful care. Whether we’re helping a client communicate or supporting recovery after injury, we meet people where they are. Job Description We are hiring in all 50 states to provide services for clients in California. We are also offering reimbursement for California licensure! We are actively seeking part-time Speech Language Pathologists (SLPs) to join our Provider Network. You will have the opportunity to conduct treatment with our diverse client population of children and adults. We deliver skilled speech therapy services and interventions tailored to the unique needs of our clients with receptive and expressive language disorders, fluency, voice, and apraxia of speech. Responsibilities • Provide remote speech-language therapy services to clients, • Conduct online speech-language assessments to determine eligibility for speech services, • Develop, coordinate, implement, and monitor an individual's plan of care via teletherapy, • Maintain a caseload of kids, adults, and the geriatric population, • Keep appropriate and daily documentationQualifications, • Master's degree in Speech-Language Pathology, • Active CA State Speech Language Pathologist License or able to obtain a CA license, • Experience in a clinic or school setting or successful clinical interview, • Technical proficiency to conduct teletherapy through our all-inclusive platform, • Should be comfortable working with children (18 months+), • Bilingual in Spanish required Location and Hours This is a 100% remote opportunity, requiring a minimum commitment of 12-29 hours per week for part-time. Compensation W2 | $43.00 - $56.00 per hour commensurate with experience, qualifications, and bilingualism. *Reimbursement for licensure(s) will be paid out after 145 hours of work. Why Join Us? Experience the difference of working with a close-knit team of dedicated therapists who value collaboration, mentorship, and shared professional growth. • Competitive compensation that recognizes your expertise, • Flexible scheduling that empowers you to maintain work-life balance, • A referral bonus program to reward your network Additional Information All your information will be kept confidential according to EEO guidelines. All Care Therapies is an equal opportunity employer. All aspects of employment, including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (), Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp () with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under strategic leadership, sustain the improvement of the Quality Management Systems (QMS) and manage the development of quality assurance & systems staff. Utilize the following industry standards to drive high-quality products: Current Good Manufacturing Practice (cGMP), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH), and International Organization for Standardization (ISO). Facilitate employee relations issues including coaching, mentoring, and disciplining including performance evaluation of employees. Provide strong leadership to motivate, guide and inspire employees to meet the organization’s business objectives with production.Lead the implementation phase of MasterControl, ensuring successful implementation, and post-implementation management. ESSENTIAL DUTIES and/or RESPONSIBILITIES: • Partners with leadership to develop the Quality Management System (QMS) and ensure it is compliant with relevant regulations, including ISO 9001, 21 CFR Part 210 and 211, ICH, and other applicable national and international regulatory guidelines.Ensure the QMS always remains in an auditable state., • Leads the transition of QMS programs, such as Document Control, Training, Quality Events (Deviation, CAPA, Change Control), Audits and Supplier Qualification transition into Master Control, and serves as the System Administrator., • Leads post-implementation management of MasterControl, including, but not limited to, system optimization, performing troubleshooting support, managing software updates, and continuously improving system functionality to meet evolving regulatory needs., • Oversees the daily operations of the QMS, ensuring it runs efficiently and in compliance with quality standards. This includes managing critical quality systems processes such as Document Control, Training, Customer questionnaires and tracking and reporting key metrics for Quality Events, including Deviation, CAPA, Change, Control, Audit, and Supplier Management., • Manages the execution of internal and external audits, ensuring the company is always prepared for audits. Ensures compliance to the internal audit program. Lead audit preparations by ensuring that quality management system documentation is up-to-date and readily available for inspections; including external inspections, serving as the primary point of contact for inspectors, and provide the necessary documentation to support the audit process. Manage post-audit responses and tracking of audit action items., • Ensures proper documentation and records management in compliance with relevant requirements, including batch production records, testing records, and compliance documentation. Monitor the retention and archiving of records in compliance with requirements to ensure traceability and access during audits., • Contributes to the continuous improvement initiatives related to the QMS, collaborating with cross-functional teams to optimize quality processes. Analyze quality data and metrics to identify trends, root causes, and areas for process improvement within manufacturing and quality control activities., • Develops standard operations and other quality documents related to QMS and ensure all documents meet regulatory requirements and internal standards., • Supervises and develop a team of Quality Systems specialists, providing guidance, training, and support to ensure compliance with regulatory standards and best practices., • Mentors and develop a team of Quality Systems specialists, fostering an environment of accountability and growth. Ensure cross-functional collaboration and provide effective leadership managing the QMS processes and ensures effective employee relations., • Directs training initiatives to ensure that team members are adequately prepared to handle QMS functions and sustain a flexible workforce., • Fosters a culture of continuous improvement, supporting staff development and efficiency improvements within the quality systems team., • Conducts performance evaluations of direct reports.Institutes timely corrective actions and interfaces with Leadership and HR in developing disciplinary actions up to and including terminations., • Administers time-keeping functions to track absenteeism; approves timecards on a bi-weekly basis., • Other duties as assigned. SUPERVISORY RESPONSIBILITES: • Quality Systems Specialist, • Sr Quality Systems Specialist MINIMUM EDUCATION and/or EXPERIENCE: • Bachelor’s degree in a scientific discipline; and five (5) years’ directly related experience in a Good Practice (GXP) or ISO manufacturing-controlled environment or equivalent combination of education and experience., • Experience with internal and external audits and processes, including corrective action implementation., • Experience in transitioning from paper based to electronic QMS. KNOWLEDGE, SKILLS and/or ABILITIES: • Working knowledge of pharmaceutical industry concepts, as well as analytical methods and writing skills, including documenting manufacturing processes, a plus. Familiarity in Lean or Six Sigma, a plus., • Strong Knowledge of quality management principles and practices, including ISO and cGMP standards., • Proficient in the use of quality management software with experience in implementing or managing MasterControl being highly desirable., • Experience conducting internal and/or external audits., • Prior supervisory experience, preferred., • Knowledgeable of change control, validation/qualification, and method development and tech transfer., • Strong knowledge of formal root cause analysis and risk assessment tools. Ability to lead or facilitate investigations and/or risk assessments., • Strong application of critical thinking skills along with problem solving and creative skills to identify manufacturing issues for continuous improvement., • Strong multi-tasking skills, flexibility in responding to rapidly changing, dynamic processes and demands/pressures in a fast-paced environment., • Strong ability to verbally communicate across functional organizational groups, provide high-level customer service through effective interpersonal skills and conflict resolution, including communicating with equipment suppliers to obtain input on equipment modification and improvement., • Microsoft Office Suite software applications such as Excel, Word, Power Point, and other enterprise software applications such as Net Suite, LIMS, and Familiarity with statistical analysis tools., • Strong language skills with the ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or government regulations., • Write clear processes, manuals and reports for management review and present technical information in understandable terms and respond to questions from groups of customers, employees and/or public., • Work independently as well as in a small and/or large group and foster cooperation in a team environment using interpersonal skills to document working knowledge., • Work in a detail-oriented environment with strong follow-up, follow-through, and organizational skills. CERTIFICATES and/or LICENSES: • American Society for Quality Certified, a plus., • Certified Quality Engineer, a plus., • Certified Quality Auditor, preferred. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) • Works in a typical office environment with prolonged periods in front a computer entering or researching data., • Regularly required to sit; use hands to finger, handle or feel and talk or hear., • Availability and willingness to travel if required for audits, inspection, vendor management or if requested to visit or attend a business transaction as legal agent of the company., • Must be able to work extended hours per the demands of the business.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Job Summary The Engineer will be a key contributor to the design and development of a therapeutic medical device, from concept to early human use to commercialization. The Engineering Lead will work closely with the team to drive all aspects of the development process including conceptualizing, prototyping, analysis (physical and simulation), researching manufacturing techniques, go-to-market implementation, and manufacturing support. The ideal candidate will possess some knowledge of balloon catheters (i.e., PTA, PTCA). Responsibilities: • Utilize research and experience to develop new product and processes to increase performance., • Manage multiple projects simultaneously, on time, well documented and within budget to meet business objectives., • Collaborate with external suppliers for component and process design and identify outsourcing opportunities., • Provide technical leadership and maintain the engineering staff’s knowledge on technology and engineering areas associated with instrument and mechanism design and manufacturing processes., • Understand the technology and key product features that ensure clinical and commercial success, • Manage research and development activities from Concept Phase through Commercialization, • Make data driven decisions using appropriate analytical methodologies, • Prepare for and conduct various design reviews in accordance with product development, • Demonstrate deep insight regarding design intent and uses insight to drive product requirements and specifications. Develop processes necessary to fabricate devices. Develop and implement test methods for assessing the quality of in-process and finished products., • Develop, execute, and analyze design verification and validation studies, culminating in a design history file., • Prepare documentation to support quality system for design functions (project plans, concept document, FMEA, design input, test results, drawings, etc.), • Provide technical leadership along with technical subject matter expertise to product development team., • Conduct preclinical build operations as necessary., • Initiate, define, perform and execute verification and validation activities., • Prepare technical documentation, including manufacturing instructions, test methods, drawings, BOMs, protocols, and reports to support design control activities., • Perform risk analysis activities and develop product testing plans and protocols; set up and run product testing and protocols in accordance with project plans, • Research and recommend vendor and material choices for product, • Identify hazards and mitigates risk associated with identified hazards in Design and Process FMEA. Assess failure modes and conduct technical risk analysis., • Comply and analyzes data, identifies causes, draws conclusions, generates reports., • Create and managing a schedule of technical deliverables in coordination with a project manager., • Translate highly technical results into easily understood recommendations that will influence cross-functional and senior stakeholders., • Identify hazards and mitigates risk associated with identified hazards in Design and Process FMEA. Assess failure modes and conduct technical risk analysis., • Comply and analyzes data, identifies causes, draws conclusions, generates reports., • Create and managing a schedule of technical deliverables in coordination with a project manager., • Translate highly technical results into easily understood recommendations that will influence cross-functional and senior stakeholders. Qualifications: Education: • MS/PhD degree in Materials Science, or Mechanical Engineering w/emphasis on materials engineering preferred. BS in one of those fields will be considered but will be weighed heavily on work experience., • Polymer knowledge along with extrusion, injection molding experience and metallurgy., • Knowledge of and exposure to product testing and data collection, • Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, and the MDD, • Working knowledge of mechanical design principles and FDA class 3 Agrregulated medical device design controls., • Medical Device experience in new product development with successful design from concept to commercialization is strongly preferred. This includes experience with medical device materials 12+ years product development, preferably in medical device industry., • Proficient in CAD software, preferably SolidWorks., • Familiarity with statistical analysis of raw data is required, proficiency in Minitab is preferred., • Experience with mechanical and/or electrical design, mechanical/electrical drawings, tolerance analysis, and computer-aided design (CAD), • Track record of strong cross-functional collaboration, influence without authority, and project management enabling highly effective project team Knowledge, Skills, and Abilities: • Excellent hands-on mechanical prototyping, verification, and failure analysis skills., • Proficient in Risk Management according to ISO 14971., • Knowledge of ASME Y14.5 GD&T., • Proven self-starter who runs towards critical issues, ambiguous requirements, or loosely defined challenges with a demonstrated ability to rally teams to achieve business results., • Familiarity with design control according to 21 CFR 820 or ISO 13485, engineering change orders (ECO), Corrective Actions and Preventive Actions (CAPA)., • Strong leadership skills and mentoring capabilities, • Strong quantitative analysis and problem-solving skills and methodologies, • Strong interpersonal and communication skills (oral/presentation and written), • A flexible team player, focusing on shared goals with a positive results‐oriented attitude.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Overview: Position Overview: Catheter R&D Engineer will be a key contributor to the design and development of next generation Intravascular Lithotripsy (IVL) devices. Contribute as part of a cross‐functional team in product design and development, process development and optimization, and testing to support new product development. Responsibilities: • Provide technical leadership for projects in the coronary vascular space., • Provide mentorship to other engineers and assignments to technicians as required., • Collaborate cross-functionally to gather and define user needs for new products, • Prototype and develop proof of concept designs, disease models and test methods based on the defined user needs and requirements., • Solve challenging and complex technical problems during the new product development process., • Work with clinical and scientific advisors as well as Key Opinion Leaders in translating clinical needs into design solutions while utilizing these resources to develop and optimize product design., • Analyze, evaluate, source, and coordinate the procurement of new materials to support prototyping and pilot operation., • Develop protocols, test methods, and reports, and perform product assessments on benchtop, in-situ, and in-vivo to prove and de-risk viability and feasibility of new product designs., • Identify suppliers and maintain relationships to ensure the delivery of superior components and services., • Enhance the intellectual property position of the company via invention disclosures and patent applications., • Participate as SME on product development team(s) that manage projects from concept through transfer to PDP team., • Design and develop product(s) in compliance with the company’s Design Control requirements and consistent with applicable regulatory requirements., • Ensure proper documentation consistent with the company’s quality system., • Responsible for knowing and planning activities consistent with the company’s quality policy and quality objectives., • Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company’s products., • Responsible for component and assembly documentation for new products being developed., • Support company goals and objectives, policies and procedures, Quality Systems, and FDA regulations., • Bachelor’s Degree in Mechanical or Biomedical (or similar) Engineering and minimum 5 years’ experience in engineering OR a Master’s Degree/PhD and 3 years’ experience in engineering, • 3 years experience in early-stage (pre-design freeze) catheter and/or leads-based cardiovascular device development, preferred., • Knowledge of coronary and vascular anatomy, physiology, and model development is a strong plus., • Minimum 1 year as team or project technical lead., • Strong understanding of engineering materials, component selection, and design for reliability and manufacturability., • Strong understanding of data analysis and statistics including design of experiments, Gage R&R, capability, etc. is a strong plus., • Strong teamwork skills and demonstrated ability to work closely with cross functional partners., • Effective communication skills with all levels of management and organizations., • Operate independently and adaptability to changing requirements., • Ability to work in a fast-paced environment, managing multiple priorities., • Occasional travel up to 10%, • Employee may be required to lift objects up to 25 lbs.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Position overview: The Senior Quality Engineer will be responsible for providing quality engineering support and leadership for Manufacturing Process development and implementation. This position will work closely Manufacturing in the manufacture of disposable medical catheters in compliance with applicable regulatory and statutory requirement. Essential Duties and Responsibilities: • Oversee EO sterilization validation processes and ensure routine sterilization activities meet regulatory standards., • Support environmental monitoring and clean room verifications according to schedule and assist with excursion investigations., • Review and approve manufacturing validation test plans, protocols, and test reports., • Lead the completion of risk management deliverables, including process Failure Mode and Effects Analysis (pFMEA) and Control Plans., • Support and lead test method validation activities to ensure accurate and reliable testing processes., • Develop, review, and approve inspection plans, Device History Records (DHR), and product drawings for new products., • Create and implement quality plans as needed to ensure product and process compliance., • Develop activities aimed at preventing and detecting defects during the manufacturing process., • Recommend and provide statistical support, expertise, and analytical problem-solving for process validations and Engineering Protocols., • Support activities related to Management Reviews, internal and external audits, deviations, Corrective and Preventive Actions (CAPA), Non-Conformance Reports (NCR), Supplier Management, and Returned Goods Authorization (RGA)., • Provide support to the New Product Development team activities., • Lead the resolution of quality issues related to NCRs and CAPAs., • Ensure compliance with quality system procedures and all regulatory requirements. Technical Expertise • Provide technical expertise regarding component schematics and component inspection requirements., • Identify improvement opportunities related to the quality system and product., • Ensure the contents of Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are accurately developed and verified., • As needed oversee the calibration and preventive maintenance program to ensure equipment accuracy and reliability., • As needed be responsible for managing supplier quality activities, including supplier audits, performance assessments, and quality agreements. Required Education/Training/ & Experience: • Bachelor's degree in a scientific/engineering discipline; or equivalent combination of education and experience., • Minimum 5 years of relevant work experience in either pharmaceutical, medical device, or other highly regulated industry. Knowledge, skills, and abilities: • Experience in catheter design and production, or with similar medical devices, while working within Quality is required., • GMP experience working within ISO 13485, ISO 14976 and FDA 21 CFR Part 820 environments., • Capable of reviewing and interpreting drawings, • Experience in Risk Management Records and Risk Analysis., • Experience in performing test method validation and Gage R&Rs, • Understanding of statistical techniques such as normality analysis, tolerance analysis, and should be able to analyze and interpret data with high confidence., • Must know how to use Minitab or other statistical software, • Expertise in Sterilization (EO) is preferred (ISO 11135), • Knowledge in biocompatibility is preferred (ISO 10993 and associated variants), • Strong analytical, planning and organizational skills, • Strong interpersonal and communications skills (oral & written), • Self-starter with ability to work independently under pressure and react quickly to changing priorities, • Proficient in MS Office Word, Excel, Power Point, Project, Visio.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Position Overview: The Sr. Manufacturing Supervisor coordinates and supervises the daily activities and sets priorities for the production team. Primarily in charge of ensuring the production line is operational and maintaining the ongoing production of products. They are also responsible for troubleshooting any issues that arise, provide technical expertise for complex issues, ensures effective, and efficient production flow. Responsibilities: • Supervise and lead Production Assemblers, • In collaboration with department management and R&D, plans and executes the transfer of products from Research and Development into Manufacturing, • Identifies skill, knowledge and resource needs. Provides input to department management for workforce planning, staff development and performance management activities., • Supervise and coordinate the activities of production and operations workers as assigned, • Assist line personnel in resolving job related problems, • Maintain an organized, safe, and efficient work area at all times, • Monitor work being produced to make sure it meets all specifications, • Monitor workflow and control output through work order distribution, • Ensure production goals are met, • Train assemblers on the proper use of work instructions, • Identifies training gaps and needs. Develops and delivers training to assemblers on the proper use of Manufacturing Instructions, • Sets work schedules and develops training schedules for new employees and evaluates performance, • Coordinate with Quality, Engineering, Shipping, and Manufacturing to deliver results, • Ensures that production personnel carry out all daily duties, • Builds Quality into all aspects of work by maintaining compliance to all quality requirements., • Support Manufacturing and Quality Engineers in product investigations, • Owns Capacity and Output tools if Manufacturing Line, • Collects and analyzes data, prepares, and presents reports and recommendations to improve production output and achieve business goals., • Promotes team compliance with applicable Inova SOPs, ISO, FDA and other Quality System Regulations, as well as applicable Environmental, Health & Safety, Human Resources and all other regulatory and administrative policies., • Support inventory counts by owning Work Order Open/Closing on ERP System Qualifications: Education: • 5+ years of supervising manufacturing production, operations experience in medical device, laboratory, diagnostics, or related industry experience., • Demonstrated leadership abilities, • Continual improvement process experience, • Strong communication and organizational skills, • A thorough understanding of Clean Room requirements, • Ability to create and adhere to effective schedules

Suja Life was founded in 2012 with a shared dream to transform people's lives through mindful nutrition. To address the lack of clean, nutritious, and convenient beverages available, the founders created a line of organic cold-pressed juices made from the freshest and most powerful ingredients imaginable, in a form closest to the living plants they originated from. What began as a local cold-pressed juice delivery service on skateboards in SoCal, has since evolved into a nationwide leader in organic juices and wellness shots. Today, Suja Life boasts an expanding range of portfolio of brands, including Suja Organic, Vive Organic, and Slice. Role Description: Suja Life is seeking a Packaging and Production Designer with strong creative and technical expertise to bring our brands to life across packaging touchpoints. This role blends concept development and design execution with production precision. You’ll be responsible for ideating packaging concepts (across bottles, cans, cartons and labels) that align with brand identities across the Suja Life portfolio, as well as preparing accurate, print-ready files that meet production, sustainability and regulatory standards. Job Title: Packaging & Production Designer Department: Marketing – Suja Studio Direct Reports: n/a Reports To: Senior Graphic Designer Location: Oceanside, CA Classification: Exempt Essential Duties and Responsibilities The primary responsibilities of this role include: • Concept Development: Create original packaging concepts that reflect brand positioning and resonate with consumers across retail, e-commerce, and promotional channels., • Design Execution: Prepare accurate and print-ready dielines, mockups, and final artwork for various packaging formats (boxes, labels, cartons, bags, etc.) ensuring consistency across SKUs and product lines., • Brand Consistency: Maintain visual alignment with brand guidelines while pushing creative boundaries within the packaging space., • Cross-Functional Collaboration: While this role is dedicated towards production, will work closely with the Associate Manager, Innovation to ensure packaging meets functional, aesthetic, and compliance requirements., • Production Support: Manage pre-press, proof reviews, troubleshoot design/production challenges, and ensure quality standards are upheld during printing and manufacturing to maintain design integrity. This will occur onsite at Suja's HQ in Oceanside, CA., • Asset Management: Organize and maintain a central repository for all packaging assets within DAM, ensuring easy access for the team and ensuring brand consistency across all materials. Qualifications, Education & Experience: • Bachelor’s degree(s) in Design preferred but not required, • 3-5+ years of experience in packaging design or print production, • Prior CPG experience is a must. Knowledge of the food & beverage industry is strongly preferred, along with can and/or bottle expertise., • Proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign), • Experience with packaging software and 3D mockup tools would be a plus (but not mandatory), • Strong understanding of prepress, print production processes, color management and materials, • Attention to detail, typography, and layout precision, • Knowledge of packaging compliance and labeling regulations, • Strong organizational skills with the ability to manage multiple projects simultaneously., • Knowledge of project management methodologies and tools (Asana, Bynder) would be preferred. Language Skills: • Excellent verbal and written communication skills. Other Skills: • Ability to work well under pressure and meet tight deadlines., • Enthusiastic about learning and growing within a creative environment. Other Abilities: • Highly creative with a keen eye for detail., • Ability to work under pressure, meet tight deadlines, and adapt to changing priorities., • A passion for content creation and brand storytelling. Working and Environmental Conditions • Typically functions in a home office environment with occasional travel for events and meetings., • Regular use of computer, keyboard, and video conferencing tools., • May involve occasional work on nights and weekends, depending on project timelines. Physical Demands • Sitting/standing for extended periods, extensive computer use, and occasional lifting of up to 15 lbs., • Ability to travel as needed for content production and meetings.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Responsibilities: Overview: Provides technical support to R&D Engineers and performs catheter assembly, prototyping, testing, and helps create assembly procedures. Assists engineers in new product development in all aspects of designs, manufacturability, and quality. Flexibility to adapt sudden changes to different kind of work schedules and task. Responsibilities: • Performs general catheter assembly using laboratory tools and microscopes., • Support R&D catheter builds and production build catheter as necessary., • Build early-stage prototyping catheters and provide inputs to engineers as necessary., • Assists with development of manufacturing processes and corresponding design transfer to production., • Supports R&D in device testing to inform design and/or process updates., • Participate in the development and testing of new concepts., • Sets up and operates test equipment. Records data with limited supervision., • Provides technical support to engineers on a variety of technical tasks., • Conduct tests of completed units or components under operational conditions to investigate designs or to obtain data for development. Qualifications: Education & Experience: • High school or equivalent with six months or more years of relevant experience. Required Experience: • 6+ months experience in medical device industry., • Hands-on experience in medical device manufacturing / production environment or prototyping experience., • Working knowledge of catheters and microscopes in medical device laboratory., • The candidate should have good organizational skills, personal skills, and a strong follow-through “can do” attitude., • Monitors own work to ensure quality.

Position Overview: The Manufacturing Engineer II plans and designs manufacturing processes for a production facility. Maximizes efficiency by analyzing layout of equipment, workflow, assembly methods, and work force utilization. Being a Manufacturing Engineer II determines the parts, equipment, and tools needed to achieve manufacturing goals according to product specifications. Responsibilities: • Evaluate current catheter manufacturing practices and identify those needing improvement., • Lead operations to increase production capacity and implement new efficient processes., • Analyze and design sequence of operations and workflow to improve efficiencies and establish methods for maximum utilization of production facilities and personnel., • Use Lean Manufacturing Methodology, including Value Stream Mapping and Kaizen events., • Use Six Sigma Methodology (DMAIC or DMADV) and tools including Minitab, FMEA, Fishbone, Process Mapping, etc., • Responsible for manufacturing process development, implementation, and continuous improvement to enhance yield, reduce cost and improve productivity., • Represent Process Engineering in assigned R&D and Project Team meetings for technology transfers and provide technical expertise and support in analytical method development, validation and process scale, and current production capabilities in manufacturing., • Performs or manages process validations (IQ, OQ, PQ)., • Troubleshoot production line issues related to yield, quality, and throughput., • Leads scaling up processes from development to full scale manufacturing., • Supports evaluation of NCR, CAPA, SCAR, Failure investigation and Deviation requests arising from Contract Manufacturers/Suppliers., • Creates/Updates manufacturing instructions, routings, bills of materials and SOPs. Qualifications: Education: • Engineering degree desired or equivalent experience in related job field. Required Experience: • 2+ yrs Biomedical product or medical device development experience., • Working knowledge of mechanical design principles and FDA regulated medical device design controls a plus., • Proficient in CAD software, preferably SolidWorks., • Familiarity with statistical analysis of raw data is required, proficiency in Minitab is preferred., • Hands-on experience managing suppliers and/or contract manufacturers a plus., • Familiarity with design control according to 21 CFR 820 or ISO 13485, engineering change orders (ECO), Corrective Actions and Preventive Actions (CAPA) preferred. Knowledge, Skills, and Abilities: • Knowledge of ASME Y14.5 GD&T., • Excellent interpersonal, communication, and documentation skills are required., • Takes initiative and acts quickly to drive solutions., • Strong interpersonal, organizational and communication skills., • A flexible team player, focusing on shared goals with a positive results‐oriented attitude.

The Senior Supply Chain Specialist manages the procurement process for Nalu’s product portfolio and ensures the timely and cost-effective acquisition of requisite products and services. This individual is an expert in strategic sourcing, supplier relationship management, and collaboration with cross-functional teams to support the company’s operational and financial goals. This is an in-office position, which requires candidate to be within a commutable distance to the Carlsbad, CA office. RESPONSIBILITIES: • Develops and implements procurement strategies for raw materials and assemblies required for Nalu’s medical devices, • Makes decisions that consider internal & external constraints and needs of other groups with the ability to communicate those strategies vertically and horizontally across the organization, • Identifies, evaluates, and selects suppliers based on quality, cost, and delivery performance, • Negotiates contracts, terms, and pricing with suppliers to achieve optimal value, • Monitors supplier performance and manage relationships to ensure compliance with contractual obligations and company standards., • Collaborates with internal stakeholders such as R&D, Quality Assurance, and Regulatory Affairs to align procurement and inventory activities with business needs, • Builds bridges across teams to improve product deliverables and elevate the technical standard of the Operations department, • Develops a deep understanding of product needs and recommend solutions for competing technical choices, • Manages inventory levels and coordinate with logistics to ensure timely delivery of products, • Maintains accurate procurement records and generates reports for management review. QUALIFICATIONS: • Minimum of 7 years of experience in procurement, preferably in the medical devices industry, • Bachelor’s degree in Supply Chain Management, Business Administration, or a related field, • Strong negotiation, communication, and interpersonal skills, • Ability to deliver technically relevant communications to functional groups in an easy-to-understand format, • Proven ability to manage supplier relationships and break new ground within supply base to achieve cost and reliability improvements, • Knowledge of regulatory requirements and quality standards for Class II medical devices, • Proficiency in MRP procurement software and lean Supply Chain principles (e.g. kanban, statistics-based supply planning), • Proficiency in Microsoft Office Suite and modern ERP systems, NetSuite experience a plus, • Available to travel up to 5-8% of the calendar year for business purposes

Job Title: Architectural CAD/Revit Drafter II Pay Range: $26 – $32 per hour (commensurate with experience) Schedule: Full-Time or Part-Time (flexible based on availability) Work Environment: Hybrid (Office/Home) | Monday through Friday Start Date: ASAP About the Role Are you a detail-oriented drafter with a passion for turning architectural visions into reality? Join our dynamic team as an Architectural CAD/Revit Drafter II, where you’ll play a key role in designing and drafting innovative structures and interiors. This is a fantastic opportunity to work in a collaborative, hybrid environment that values creativity, precision, and professional growth. What You’ll Do As an Architectural CAD/Revit Drafter II, you’ll: • Create Detailed Designs: Use CAD and BIM software to produce full-scale, detailed architectural designs based on the Design Director’s schematics., • Ensure Compliance: Study building codes and regulations to ensure designs meet all requirements., • Collaborate Across Disciplines: Organize and integrate structural, electrical, and mechanical designs into cohesive plans., • Draft Plans: Develop plans for right-of-way (ROW) work, grading, buildings, and structures based on input from engineers and design professionals., • Conduct Site Visits: Gather data from job sites to inform and refine your designs., • Coordinate with Officials: Interact with city and county officials to address permit plan-check comments and clarifications., • Problem-Solve: Identify design flaws and make revisions as needed., • Technical Expertise: Proficiency in REVIT, CAD, and other architectural drafting tools., • Problem-Solving Skills: A knack for identifying and resolving design challenges., • Communication Skills: Strong written and verbal communication abilities to collaborate effectively with team members and stakeholders., • Attention to Detail: A meticulous approach to drafting and design.Qualifications, • Education: Associate’s degree in Drafting or equivalent., • Experience: At least 3 years of related drafting experience., • Physical Requirements:, • Ability to sit at a desk and work on a computer for extended periods., • Capability to navigate construction sites as needed., • Ability to lift up to 15 pounds occasionally.Why Join Us?, • Flexible Work Options: Enjoy a hybrid schedule that balances office collaboration with the convenience of working from home., • Growth Opportunities: Be part of a team that values professional development and innovation.

Job DescriptionSalary: $100,000.00 - $140,000.00 About Us: Anaergia (TSX: ANRG) is a global leader in offering sustainable solutions to produce clean energy and the conversion of waste streams to resources. Through a proven portfolio of proprietary technological solutions, Anaergia maximizes the generation of renewable energy, diversion of waste from landfills, and reduction of greenhouse gases for customers across the municipal, industrial, commercial, and agricultural sectors. Headquartered in Burlington, ON, and through its multiple subsidiaries across North America, Europe, Africa, and Asia, Anaergia is trusted at more than 1,600 installations globally. Job Overview: Be Anaergias main point of contact on site with the customer, subcontractors, and Anaergia personnel.Consistently manage the assigned jobs by managing all the Site Activity from the site establishment until the handover to the commissioning team, meeting, and possibly improving timing and costing. This role will be site-based in the US, with the primary location in Carlsbad, CA. Job Responsibilities: Goals • Daily morning feedback discussions with the client on activities completed and planned for the day, as well as any cooperation needed from the client., • Coordinate with the Project Manager to ensure that the project timelines, scope, and budget are being adhered to as per the contract., • Ensure the application meets the highest safety standards in the erection and start-up phase, as well as full compliance with the safety rules., • Maintain and improve the project budget, • Maintain and improve the job schedule, • Achieve the Customer Satisfaction rate, • Fulfill the agreed daily reporting with reliable data and within the requested deadline., • Regarding the erection, provide risk analysis, develop, and manage a mitigation plan., • Identify an opportunity to increase revenues and GM, to be pursued in cooperation with the P.M, • Ensure the consistent "hand-over" to the Customer, deliver an effective, safe, and reliable "product" Tasks, Authority, and Liability • Manage all the activities from the site establishment until the handover to the end user, • Read, analyze, and understand the contract, meeting Anaergia's obligations, • Estimate, develop, and agree on the job schedule and budget with the PMs, • Manage, meet, and possibly improve the budget and the timing, • Monitor and plan the delivery of supplies and services (expediting & logistics) unless it is not covered by the supply chain, • Manage directly and/or via contractors the Quality Assurance / Quality Control, • Coordinate all resources involved in site activities, both internal and external (outsourcers/sub-contractors), either through the updating and distributing of a detailed schedule and/or setting regular site meetings, • Early identification of project risks and early adoption ofappropriate countermeasures, • Within the limits of site-related matters (erection and start-up) and with respect to the agreed project communication plan, manage the relationship with the Customers project leader, • Manage relationship with vendor and sub-contractor for what is concerning technical issues and organization of tasks, including technical correspondence, leaving to the PM the management of contract-related communication, • Ensure the plant and all the supplies in general, comply with the applicable codes and regulations, • Support the tests of components, • Collect and deliver to the PE the whole set of documents with red mark-up to enable the production of the as-built release, • Feedback to the office-based team (PE/EE&AUT/DM/PM/AE) with lessons learnt for continuous improvement, • Create, update, and deliver the reporting as per the agreed-upon reporting plan. The CM/SM is authorized to: • Sign correspondence to customers and vendors within the limits agreed (communication plan), • Instruct the sub-contractor for the extra-order task and request the PO regularization within the limits of Anaergia's scope of supply and within the limits of the allowed and agreed field budget, • Manage T&L expenses within the project-related assigned budget Safety and Quality-related responsibilities The CM/SM is responsible for the rigorous application of the company rules regarding the project development, the accuracy of reported data, and the respect of the contractual/agreed deadlines. Compliance with Safety is priority one for Anaergia. The erection and start-up represent two of the most critical phases with respect to the safety risks. The Industrial CM/SM is called to respect all general and project-specific safety rules, applying and ensuring their application to all. It is also CMs/SMs responsibility to ensure that all the people involved and engaged in site activities are adequately trained regarding the activity they are called to perform. The Industrial CM/SM is responsible for notifying all misses and eventually claiming to stop the activity in case of severe negligence/risks. Competencies/Qualifications: Education Holds a technical diploma in one of the following fields: Civil Engineering, Mechanical Engineering, Electrical Engineering, Chemical Engineering, or equivalent;five years of experience in construction management will be considered in lieu of a degree. Experience Minimum 3 years experience as a Construction/Site manager in the Industrial Plant construction. Technical/Special Competencies • Deeply understands and can manage contracts for supplying complex plants, • Is fully skilled in reading and understanding technical drawings, documents, and specifications, • Is knowledgeable in all the disciplines involved with the erection (civil, mechanical, electrical, instrumental, etc.), • Is knowledgeable in construction codes and regulations, • Is knowledgeable in the quality control of all supplies, • Experienced in training resources on safety and technical matters, • Is experienced in managing relationships with Customers, • Is experienced in leading and coordinating the assigned resources, • Is knowledgeable in site project administration, • It is used to manage detailed job schedules, • Some experience in purchasing, • Fluent in English Cross-functional competencies Act with professionalism and with the right sense of priority, the CM/SM must understand how activities affect other functions as well as how other functions can influence either positively or negatively the achievement of the goals. Competences include, but are not limited to: • Strong leadership based on technical competencies to gain the discipline and respect from the managed resources, • Some knowledge of company management and how the projects results, either forecasted and actual, do affect overall company management with reference to structural growth, and other investments, • Have some biogas-specific competences. Hierarchy The CM/SM reports into the Director of Operations at an organizational level, has a wide autonomy with organizing field activity, but reports into the PM for: • Consistency of the delivered scope of supply, • Compliance with the project budget, • Compliance with the job schedule For additional information on Anaergia, please visit. As an Equal Opportunity Employer, Anaergia provides equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Anaergia will provide reasonable accommodations for qualified individuals with disabilities.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Job Summary Perform and support a variety of development and engineering activities, which mainly focus on device's design, prototyping, fabrication, product requirements and verification testing. Will work directly with other R&D technicians and R&D engineers to complete various assignments. Assists engineers in developing methods and procedures to control or improve product design processes. Responsibilities: • Builds prototypes devices in accordance with engineering instructions, or drawings and specifications., • Assists with development of manufacturing processes and corresponding design transfer to production., • Supports R&D catheter assembly, manufacturing, and prototyping., • Performs assembly and failure analysis using laboratory microscopes., • Participate in the design and development of new concepts., • Interact with Engineers to understand product requirements., • Sets up and operates manufacturing and/or test equipment. Records data with limited supervision., • Provides technical support to engineers on a variety of technical tasks, • Gathers, maintains, formats, compiles, and manipulates technical data, such as laboratory or material test results and engineering design changes., • Plans and performs tests and evaluations of systems equipment or components., • Conduct tests of completed units or components under operational conditions to investigate designs or to obtain data for development and standardization., • Partners with engineering staff on project needs (e.g., supports test method development), • Documents all analysis and testing completed for R&D and new product development projects working closely with the cognizant engineer. Records and analyzes test procedures and results, numerical and graphical data., • Assist engineers with product and process design, development, and optimization. Partners with engineers to design and assemble functional prototypes and provide feedback on assembly process and design., • Assist with the development of new and existing test protocols., • Independently identifies processes improvements, generates ideas and qualifies through builds and testing., • Lead and mentor other technicians to reach departmental and company objectives. Qualifications: Education: • High School or equivalent with five or more years’ experience as R&D technician (or relevant experience), • Required Experience:, • 5+ years development experience in medical device/clinical environment., • Hands-on experience in medical device manufacturing /production environment or prototyping experience., • Ability to quickly interpret and comprehend engineering drawings and specifications., • Working knowledge of catheters and microscopes. Working knowledge of word processing and spreadsheet software., • Use of measurement devices., • Use of required safety equipment when performing lab work., • Knowledge, Skills, and Abilities:, • The candidate should have team building skills, organizational skills, personal skills, and a strong follow-through “can do” attitude., • Monitors own work to ensure quality., • Must also verbally communicate work to engineers and other staff in a clearly understood, organized and logical manner., • Familiar with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and laboratory practices.

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Responsibilities: Overview: The R&D Engineer will use engineering knowledge to design, develop, verify and validate product designs in support of company’s strategic plan. Contribute as part of a cross‐functional team in product design and development, process development and optimization, and verification & validation testing to support product transfer to manufacturing. Responsibilities: • Prepare documentation to support quality system for design functions (project plans, concept document, FMEA, design input, test results, drawings, etc.), • Prepare technical documentation, including manufacturing instructions, test methods, drawings, BOMs, protocols, and reports to support design control activities., • Perform Verification and Validation (V&V) and may draft protocols/reports for approval., • Work with engineers & QA to create new components, assemblies, or tools., • Conducts testing to verify that the design meets the engineering specifications., • Document engineering work in compliance with the company's quality system., • Identifies hazards and mitigates risk associated with identified hazards in Design and Process FMEA. Assess failure modes and conduct technical risk analysis., • Compiles and analyzes data, identifies causes, draws conclusions, generates reports., • Provide hands‐on, technical execution in the prototyping and development of devices., • Manages processes and ensures that activity goals are achieved., • Training and/or providing work direction to technicians and less experienced engineers., • Support the development of specifications for tooling and fixturing according to company quality standards. Qualifications: Education & Experience: • Engineering degree desired or equivalent experience in related job field., • 2+ yrs Biomedical product or medical device development experience (catheter experience desirable)., • Working knowledge of mechanical design principles and FDA regulated medical device design controls a plus., • Proficient in CAD software, preferably SolidWorks., • Familiarity with statistical analysis of raw data is required, proficiency in Minitab is preferred., • Understanding of IEC60601 requirements/constraints for mechanical system design is preferred., • Experience managing suppliers and/or contract manufacturers a plus., • Hands-on mechanical prototyping, verification, and failure analysis skills., • Familiarity with design control according to 21 CFR 820 or ISO 13485, engineering change orders (ECO), Corrective Actions and Preventive Actions (CAPA) preferred. Skills & Abilities: • Proficient in Risk Management according to ISO 14971., • Knowledge of ASME Y14.5 GD&T., • Excellent interpersonal, communication, and documentation skills are required., • Proven self-starter who runs towards critical issues, ambiguous requirements, or loosely defined challenges with a demonstrated ability to rally teams to achieve business results., • Takes initiative and acts quickly to drive solutions., • Strong interpersonal, organizational and communication skills., • A flexible team player, focusing on shared goals with a positive results‐oriented attitude.

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (), Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp () with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here. Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under general supervision, oversee the operations and maintenance of facilities, including buildings, manufacturing suites, labs , tank farm and utilities, ensuring compliance to applicable (GMP, ISO, OSHA, NFPA, etc.) internal and external standards and regulatory requirements. Schedule, prioritize repairs and assign work to maintenance crews and projects. Direct multiple-level maintenance technicians (internal and external) engaged in operating, repairing, maintaining, and installing machines, tools, and equipment. Provide day-to-day guidance and leadership to staff comprising of recruitment, selection, training, disciplining and employee conflict resolution. Partner with contractors to ensure projects are kept on schedule and within budget. Execute various technical tasks related to building maintenance and upkeeping and equipment maintenance; provide general and technical assistance to the department head. ESSENTIAL DUTIES and/or RESPONSIBILITIES: 1. Provides day-to-day leadership to staff including but not limited to recruiting, selecting, orienting, training, disciplining employees including conflict resolution, developing personal growth opportunities., 2. Oversees operation of tank farm, ensuring the equipment is maintained and operated according to KLS procedures and regulatory requirements., 3. Schedules repairs, maintenance, and installation of machines, tools, and equipment to ensure continuous production operations, as well as maintenance and remodeling projects of building and facility (tank farm, HVAC, Air Compressors, DI water System, etc.) to order to provide a clean, safe, efficient, environmentally friendly environment and ensure continuous production operations., 4. Plans budgets and schedules facility modifications, including cost estimates as well as inspect construction and installation progress., 5. Evaluates work orders to determine priorities and assignments based on technical expertise., 6. Confers with engineers, quality control, production, and senior management to resolve maintenance issues and recommend measures to improve the conditions of machines, equipment and building., 7. Develops preventive maintenance program in conjunction with maintenance staff to ensure optimum capital utilization., 8. Identifying areas for improvement in facility operations and implementing changes to enhance efficiency and compliance., 9. Develops and reviews Standard Operating Procedures for process and equipment under the responsibilities of the Facilities department., 10. Analyzes production, quality control, and maintenance reports and statistics to plan and modify maintenance activities., 11. Inspects operating machines and equipment for conformance with operational standards. Research alternative suppliers and technology methods to perform maintenance work with cost and quality. Requisitions tools, equipment, and supplies required for projects., 12. Identifies and selects suitable automated systems necessary to control critical process and facility parameters., 13. Directs training and indoctrination of contractors to improve work performance and acquaint employees with company policies and procedures. Evaluates and proposes changes to documentation, new programs, training, and cost reductions associated with manufacturing/production tools., 14. Utilizes Enterprise Resources Planning (ERP) and Computerized Maintenance Management System (CMMW) software tools to improve performance and resolve issues such as unplanned maintenance, downtime, and variation in equipment performance., 15. Champions the cleaning and maintenance of facility and monitors contractor’s performance., 16. Prepares budget and monitors expenditures of funds in the budget., 17. Other duties as assigned. SUPERVISORY RESPONSIBILITIES: 1. Facilities Lead, 2. Facilities Associate MINIMUM EDUCATION and EXPERIENCE: 1. Bachelor of Science degree in Mechanical or Electrical Engineering and eight (8) years’ experience or equivalent combination of education and experience., 2. Highly regulated industries such as pharmaceutical, chemical or medical device experience, a plus. KNOWLEDGE, SKILLS, and ABILITIES: 1. Principles of management, training, employee relations, and performance management, including basic principles and practices of budget preparation and administration., 2. Working knowledge of materials, methods, terminology, equipment, and tools used in the maintenance and repair of manufacturing equipment, including installation of programmable equipment and safety management practices., 3. Working knowledge of NFPA, OSHA, GMP and ISO principles and requirements., 4. Ability to work independently and in small or large groups and foster cooperation in a team environment using interpersonal skills to influence others., 5. Ability to apply critical thinking skills and create a repeatable thought process to questions and provide solutions. Ability to solve complex technical problems with minimal oversight., 6. Intermediate to advanced ability in reading, analyzing, and interpreting standard scientific and technical journals. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or business community members. Ability to effectively present information to staff across the organization in non-technical terms for understanding. Ability to draft well-written technical reports to communicate with staff, management, and external customers and suppliers. 7. Intermediate to advanced ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret various technical instructions in mathematical or diagram form and deal with abstract and concrete variables., 8. Ability to use software applications such as Microsoft Office Suite (Excel, Word, PowerPoint) and understand Programmable Logic Controller (PLC) and Computerized Automated Design (CAD)/Electrical CAD software, Parts & Instrumentation Diagram (P&ID), and SolidWorks software., 9. Exposure and working knowledge of Hazardous Materials storage and tank farm operations., 10. Working experience with Bulk chemical transportation and tanker truck loading and offloading operations., 11. Strong ability to read schematics, blueprints, technical drawings, etc., 12. Working knowledge of electrical and electronic control systems, including troubleshooting and root cause analysis., 13. Working knowledge of mechanical, electrical, and electronics integration systems design related to production equipment such as Fanuc or Robotics and instrumentation engineerings such as air and liquid distribution equipment and systems controls., 14. Understanding manufacturing processes or procedures (e.g., raw material, work-in-process, and finished goods). PHYSICAL DEMANDS and WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the job’s essential functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) 8. Ability to occasionally (up to 3 hours) push/pull carts with equipment., 9. Ability to drive a forklift occasionally (up to 3 hours/day), 10. Fine hand manipulation of light-moderate strength is required to operate touch screen displays on machinery., 11. Must be able to see/focus for close eye work (small figures) and discriminate colors., 12. Requires close (clear vision at 20 inches or less) and distance (clear vision at 20 feet or more) vision., 13. Peripheral vision (ability to observe an area that can be seen up/down or left/right while eyes are fixed on a point) and depth vision (three-dimensional vision, ability to judge distances and spatial relationships) are required to troubleshoot and correct machine issues and operate a forklift., 14. Must be able to speak/hear verbal communications and respond to machine alarms/buzzers., 15. Occasional exposure to noise, gas/fumes/mists, and chemicals or hazardous materials while using personal protective equipment when required., 16. May drive a company or personal vehicle while on company business., 17. Must wear safety shoes in required areas., 18. Must be able to work extended hours per the demands of the business., 19. Travel, up to 5% as required, to support the needs of the business., 20. Must possess a valid driver’s license and remain qualified as a Driver under the company Driver Policy.

Summary: This individual will successfully manage all preventative maintenance and repair activities to effectively support plant operations. This individual will also coordinate and direct the design, planning, construction, maintenance, and alteration of equipment, machinery, buildings, and other-facilities by performing the following duties personally or through subordinates. Essential Duties and Responsibilities: • Maintenance: The Maintenance Manager's duty includes the maintenance, cleaning, and sanitation of the manufacturing areas, general building and office areas. The focus for this role will be establishing a robust preventative maintenance program focused on maximizing equipment uptime and extending asset life. The Maintenance manager is required to understarnd the basic knowledge of building construction such as wiring, basic plumbing works etc., • Planning, Directing, budgeting and coordinating: Plan, direct, coordinate the activities of a facility or several small facilities within the organization; required to hire the needed personnel for carrying out the above mentioned activities., • Preparing and maintaining annual budgets of the facility: Prepare budget that is required for usage of the facilities for the smooth running of the organization; required to approve and authorize budgeted expenditures for operating expenses up to authorized levels. Effectively control and maintain the department's spare parts inventory., • Administrative Duties: Oversee a team of employees from several different areas that include maintenance and janitorial personnel, as well as independent contractors., • Ensure all machinery is up to acceptable working standards, • Assess current maintenance work processes, to optimize efficiency, • Use data analysis to help prepare for and prevent future problems, • Create and implement measures to minimize breakdowns and repairs (performing quality checks of all machinery, tools, equipment etc.), • Troubleshoot problem areas and create a clear plan of action for permanently resolving the problem, • Oversee repairs and manage quality of work, • Train new employees in maintenance work processes and procedures, • Create a work environment with safety as a high priority, • Perform evaluations of employees to ensure quality of work, • Record and track daily progress/error reports, • Maintain vendor relationships and order new materials as needed, • Create and adhere to maintenance budgets, • Perform evaluations of employees to ensure quality of work, • Record and track daily progress/error reports, • Maintain vendor relationships and order new materials as needed, • Create and adhere to maintenance budgets, • Enforce all health and safety rules and regulations according to state/federal laws and company protocol (e.g., Lockout/Tagout, Arc Flash, GMP's and OSHA) Educational Qualification: • Bachelor's Degree in Engineering or related field required. Experience Qualifications: • Requires at least 4 years' experience in a maintenance management or similar role, dietary supplement or food industry preferred., • An equivalent combination of work experience and education will be considered for the above. Required Skills: • Proven experience as maintenance manager or other managerial role, • Experience in planning maintenance operations, • Solid understanding of technical aspects of plumbing, carpentry, electrical systems etc., • Working knowledge of facilities machines and equipment, • Ability to keep track of and report on activity, • Excellent communication and interpersonal skills, • Outstanding organizational and leadership abilities, • Ability to manage complex and varied projects and workloads, • Customer and client management skills,, • Technical knowledge in construction methods, architectural and engineering drawings,, • Project management skills,, • Experience with Computerized Maintenance Managements Systems (CMMS), • Travel as required to support business needs Supervisory Responsibilities: • There are supervisory duties; up to 16 direct reports. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to fumes or airborne particles. The employee is frequently exposed to work near moving mechanical parts and work in high, precarious places. The employee is occasionally exposed to toxic or caustic chemicals; outdoor weather conditions; extreme cold (non-weather); extreme heat (non-weather) and risk of electrical shock. The noise level in the work environment is usually loud. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee must regularly lift and /or move up to 100 pounds, frequently lift and/or move up to 50 pounds and occasionally lift and/or move more than 100 pounds. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus. While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear and taste or smell. The employee is occasionally required to sit.

Job Description Join Our Team and Keep Moving Forward with Breg! At Breg, we are dedicated to advancing orthopedic solutions that enhance the lives of patients and support healthcare professionals. As a leader in the orthopedic industry, we provide innovative products, consulting, technology, and services that help people move forward with confidence. We are currently seeking a Supervisor, Order Entry and Authorizations to join our team in Carlsbad, CA. If you thrive in a dynamic environment where innovation and impact go hand in hand, this is the opportunity for you. Who You Are You are a forward-thinking professional who values collaboration, innovation, and making a meaningful difference. You bring expertise in the ability to communicate effectively both written and verbally and are eager to contribute to a team that is committed to delivering exceptional patient outcomes. What You’ll Do As a Supervisor, Order Entry and Authorizations, you will: • Supervise and oversee all aspects to Breg's vendor engagements responsible for order entry and coding. Managing the process of accurately entering order information into billing systems, verifying patient eligibility, obtaining prior authorizations , ensuring that claims are submitted correctly to payors, leading to timely and accurate reimbursement driving the achievement of KPI's., • Analyze reports to prioritize claim finalization and determine appropriate actions to be taken to achieve key results., • Act as an individual contributor as needed and provide coverage for coding (on/offshore) and will work alongside the Order Entry team and authorization teams, assisting with claim volume processing when necessary., • Serve as the subject matter expert and escalation resource for order entry and coding., • Partner with Revenue Cycle Management leaders, Field Operations, HIMS, Quality, Payor Contracts, and other leaders to develop and implement strategies to reduce pending claims ( first-time finalization) and expedite accurate claim submission to secure reimbursement without additional intervention ( first-time realization)., • Collaborate with Manager and other leaders to recommend process improvements and contribute to the development of new procedures and work instructions., • Collaborate with the Manager to put together and communicate ( orally and in written form) strategies, plans, performance outcomes, and business conditions to ensure understanding of the current state of claims processing and opportunities for process improvement., • Monitor audit reports for quality and process adherence, communicate identified areas requiring additional training or documented business processes/work instructions., • Leadership responsibilities include selection, development, performance management and continuous recalibration of staff; ensures appropriate staffing levels and resource allocation; performs administrative tasks associated with timekeeping, pay, performance, policy administration and other matters related to employment., • Assesses staff and provides timely and consistent feedback regarding technical proficiency and effectiveness. Provides constructive feedback, guidance, and reinforcement to employees regarding job performance. Works with staff to identify work goals and create individual development plans. Evaluates training programs to ensure content meets staff needs., • Partner with Breg Training Personnel on new and/or revised processes, policies, procedures and training documents specific to order entry and authorization., • Assesses staff and provides timely and consistent feedback regarding technical proficiency and effectiveness. Provides constructive feedback, guidance, and reinforcement to employees regarding job performance. Works with staff to identify work goals and create individual development plans., • Evaluates training programs. Supports vendor's training of new and existing teammates to increase order entry and authorization efficiency and overall company profitability., • Performs duties in compliance with applicable HIPPA, FDA, CMS, ACHC, and other appropriate state and federal regulations., • Responsible for behaving in a professional manner both internally and externally in relationships that positively impact the company's reputation and comply with the company's policies and practices. Responsible for bring accountable and committed to demonstrating Breg's cultural beliefs and achieving the key results of the company., • Associated degree in an applicable field of study or 2-3 years of relevant experience, or equivalent combination. Relevant experience includes healthcare management with DMEPOS/other company that performs Medicare Part B and other health insurance reimbursement functions., • Certified Medical Coder required ( AHIMA or AAPC credentials accepted), • Experience managing or supervising people; Experience with offshore vendor engagement is a plus., • Proficient in reimbursement principles, medical terminology, payer groups and networks, including Medicare, worker's compensation, and private insurance., • Computer proficient to include web browser/internet search, MS Outlook, Word, Excel and PowerPoint capabilities. At Breg, we invest in our people and culture. We offer: • Comprehensive Benefits: Medical, dental, vision, disability, and life insurance, effective the first of the month after hire., • Work-Life Balance: Paid Time Off (PTO) and company-paid holidays., • Growth & Development: Opportunities for professional advancement within a company that values your contributions., • Commitment to Diversity & Inclusion: Breg is proud to be an Equal Employment Opportunity employer, fostering a diverse and inclusive workplace. Salary Range: $58,800.00 - $78,600.00. Actual compensation is determined by factors such as experience, skills, and business needs. This range reflects the minimum and maximum target range for new hire base salary/pay across all US locations. Actual pay is based on many factors unique to each candidate, including but not limited to geographical location, work experience, skill set, relevant trainings and certifications, and business needs. The base pay range is subject to change and may be modified in the future. This role may also be eligible for a bonus. Ready to Move Forward? If you’re ready to be part of a company that is redefining orthopedic care, apply today at . Breg is an Equal Employment Opportunity Employer and dedicated to a diverse work force and Drug Free work environment. EOE/Minorities/Females/Vet/Disabled are encouraged to apply. Applicants must be currently authorized to work in the United States on a full-time basis. The Company will not sponsor applicants for work visas for this position. #LI-KB1

Job DescriptionPosition Summary The HVAC Sales and Comfort Advisor is responsible for driving sales of heating, ventilation, and air conditioning systems and services. This role involves identifying customer needs, developing tailored solutions, and managing the sales process from lead generation through closing. The ideal candidate has strong technical knowledge of HVAC systems, exceptional communication skills, and a proven ability to meet or exceed sales targets. Key Responsibilities * Customer Consultation: Conduct site visits and assess client HVAC needs; provide expert recommendations on system design, installation, or replacement. * Proposal & Quoting: Prepare accurate and timely quotes, proposals, and presentations to customers, outlining technical details and value propositions. * Sales Process Management: Follow up on leads, negotiate pricing, handle objections, and close sales while maintaining high customer satisfaction. * Collaboration: Work with project managers, technicians, and installers to ensure customer requirements are met and projects are delivered on schedule. * Reporting & Forecasting: Maintain records of sales activities in Service Titan CRM, track progress toward goals, and provide accurate forecasts to management. * After-Sales Support: Ensure client satisfaction post-installation and identify opportunities for ongoing maintenance contracts or system upgrades. Qualifications * Education: High school diploma or equivalent required; associate’s or bachelor’s degree in business, mechanical engineering, or a related field preferred. * Experience: 2+ years of proven HVAC sales experience (B2C preferred); familiarity with HVAC systems, installation, and service processes. * Skills: * Strong customer based understanding of HVAC systems and controls (we will train!). * Excellent communication, negotiation, and presentation skills. * Customer-focused with strong relationship-building ability. * Proficiency in CRM software (e.g., Service Titan, Salesforce, HubSpot). * Valid driver’s license. Performance Metrics * Sales revenue generated (monthly/quarterly targets) * Conversion rate of leads to closed deals * Customer satisfaction and retention * Growth of maintenance agreement portfolio Compensation * GENEROUS - Base salary plus commission * Bonus opportunities for exceeding sales goals * Benefits package including Company Vehicle and Fuel, health, dental, vision, 401k, PTO TdzRGeep1b

Director of Quality & Regulatory Affairs – Medical Devices 📍 Location: North San Diego | 💼 Full-time | 🏥 Medical Device Industry We are seeking a Director of Quality & Regulatory Affairs to provide strategic leadership and oversight of compliance, regulatory, and quality activities for our breakthrough medical technologies. This is a high-impact role responsible for ensuring patient safety, regulatory success, and operational excellence as we bring innovative devices to market. Compliance & Risk Management • Act as Management Representative of the Quality Management System (QMS), ensuring compliance with ISO 13485, FDA Quality System Regulation (QSR), and global standards for sterile implantable and electronic devices., • Lead Risk Management activities per ISO 14971, guiding the Risk Management Team in assessing product changes and monitoring design/development activities for compliance with design controls., • Manage internal audits, post-market surveillance, regulatory notifications, and customer communications related to complaints and investigations. Regulatory Affairs • Define regulatory pathways for new products and product changes (e.g., Letter to File, 510(k) submissions)., • Coordinate with regulatory consulting partners to prepare and execute 510(k) submissions for Class II devices., • Maintain oversight of labeling, documentation, and regulatory assessments throughout the product lifecycle. Design Verification & Validation (V&V) • Review design documentation & support development of V&V protocols to confirm conformance to specifications, standards, and process controls using statistically valid methods., • Oversee data collection and reporting for V&V results, software validation, hardware testing, and performance testing protocols. Quality Assurance & Operations • Oversee management of Nonconforming Materials (NCMR), Corrective and Preventive Actions (CAPA), and supplier qualification metrics., • Guide creation and implementation of inspection and test methods, improving manufacturing quality, product assembly, and inspection integrity., • Contribute to building and maintaining the Design History File (DHF) and Device Master Record (DMR)., • Lead document control and change order management across the organization. Qualifications • Bachelor’s degree in engineering, life sciences, or related field (advanced degree preferred)., • 10+ years in the medical device industry, with at least 5 years in a leadership role., • Deep knowledge of FDA/QSR, ISO 13485, ISO 14971 and related international standards., • Experience leading 510(k) preparation and submissions for Class II devices., • Technical proficiency in MS Office, Matlab, PLM systems (Agile), and application of statistical techniques., • Strong interpersonal, leadership, and communication skills to influence across departments and drive compliance.

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (), Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp () with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under strategic leadership, sustain the improvement of the Quality Management Systems (QMS) and manages the development of quality assurance & systems staff. Utilize the following industry standards to drive high-quality products: Current Good Manufacturing Practice (cGMP), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH), and International Organization for Standardization (ISO). Facilitate employee relations issues including coaching, mentoring, and disciplining including performance evaluation of employees. Provides strong leadership to motivate, guide and inspire employees to meet the organization’s business objectives with production. Lead the implementation phase of MasterControl, ensuring successful implementation, and post-implementation management. ESSENTIAL DUTIES and/or RESPONSIBILITIES: • Partners with leadership to develop the Quality Management System (QMS) and ensure it is compliant with relevant regulations, including ISO 9001, 21 CFR Part 210 and 211, ICH, and other applicable national and international regulatory guidelines.Ensure the QMS always remains in an auditable state., • Oversees the daily operations of the QMS, ensuring it runs efficiently and in compliance with quality standards. This includes managing critical quality systems processes such as Incoming Raw Material Receipt, Raw Material Review/Disposition, Final Product Review/Disposition., • Manages quality events and investigations including but not limited to Deviations, CAPA, Change Control, OOS, OOT, Customer Complaints, including leading and facilitating cross-functional meetings to ensure proper assessments and actions., • Ensures QA review of Validation/Qualification activities including protocols, execution, and reports., • Upholds timely response to events and on-the-floor QA support(MQA), including ensuring the MQA program is tracked and measurable., • Leads the transition of QMS programs, such as Quality Events (Deviation, CAPA, Change Control, OOS, OOT), Audits and Supplier Qualification transition into Master Control, and serves as the System Administrator., • Administers post-implementation management of MasterControl, including, but not limited to, system optimization, performing troubleshooting support, managing software updates, and continuously improving system functionality to meet evolving regulatory needs., • Reports key metrics for QA Operations turnaround times and Quality Events., • Contributes to the continuous improvement initiatives related to the QMS, collaborating with cross-functional teams to optimize quality processes. Analyze quality data and metrics to identify trends, root causes, and areas for process improvement within manufacturing and quality control activities., • Develops standard operations and other quality documents related to QMS and ensure all documents meet regulatory requirements and internal standards., • Supervises and develops a team providing guidance, training, and support to ensure compliance with regulatory standards and best practices., • Mentors and develops a team of the QA team, fostering an environment of accountability and growth. Ensures cross-functional collaboration and provide effective leadership managing the QMS processes and ensures effective employee relations., • Facilitates training initiatives to ensure that team members are adequately prepared to handle QMS functions and sustain a flexible workforce., • Fosters a culture of continuous improvement, supporting staff development and efficiency improvements within the quality systems team., • Conducts performance reviews for direct reports. Institutes timely corrective actions and interfaces with Leadership and HR in developing disciplinary actions up to and including terminations., • Administers time-keeping functions to track absenteeism; approves timecards on a bi-weekly basis. SUPERVISOR RESONSIBLITIES: • Quality Assurance Associate, • Quality Assurance Specialist, • Sr. Quality Assurance Specialist MINIMUM EDUCATION and/or EXPERIENCE: • Bachelor’s degree in a scientific discipline; and five (5) years’ directly related experience in a Good Practice (GXP) or ISO manufacturing-controlled environment or equivalent combination of education and experience., • Experience in transitioning from paper based to electronic QMS. KNOWLEDGE, SKILLS and/or ABILITIES: • Working knowledge of pharmaceutical industry concepts, as well as analytical methods and writing skills, including documenting manufacturing processes, a plus. Familiarity in Lean or Six Sigma, a plus., • Strong Knowledge of quality management principles and practices, including ISO and cGMP standards., • Proficient in the use of quality management software with experience in implementing or managing MasterControl being highly desirable., • Experience conducting technical investigations with formal root cause analysis tools., • Prior supervisory experience, preferred., • Knowledgeable of change control, validation/qualification, and method development and tech transfer., • Strong knowledge of formal root cause analysis and risk assessment tools. Ability to lead or facilitate investigations and/or risk assessments., • Strong application of critical thinking skills along with problem solving and creative skills to identify manufacturing issues for continuous improvement., • Strong multi-tasking skills, flexibility in responding to rapidly changing, dynamic processes and demands/pressures in a fast-paced environment., • Strong ability to verbally communicate across functional organizational groups, provide high-level customer service through effective interpersonal skills and conflict resolution, including communicating with equipment suppliers to obtain input on equipment modification and improvement., • Microsoft Office Suite software applications such as Excel, Word, Power Point, and other enterprise software applications such as Net Suite, LIMS, and Familiarity with statistical analysis tools., • Strong language skills with the ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or government regulations., • Write clear processes, manuals and reports for management review and present technical information in understandable terms and respond to questions from groups of customers, employees and/or public., • Work independently as well as in a small and/or large group and foster cooperation in a team environment using interpersonal skills to document working knowledge., • Work in a detail-oriented environment with strong follow-up, follow-through, and organizational skills. CERTIFICATES and/or LICENSES: • American Society for Quality Certified, a plus., • Certified Quality Engineer, a plus., • Certified Quality Auditor, preferred. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) • Works in a typical office environment with prolonged periods in front a computer entering or researching data., • Regularly required to sit; use hands to finger, handle or feel and talk or hear., • Availability and willingness to travel if required for audits, inspection, vendor management or if requested to visit or attend a business transaction as legal agent of the company., • Must be able to work extended hours per the demands of the business.

Job Description HVAC General Maintenance Worker - Marine Corp Base Camp PendletonCompetitive Wages and an INSURANCE ALLOWANCE! Top reasons to work at EMI Services, a subsidiary of TechFlow: • Paid Time Off - Vacation, Sick & Federal Holidays, • Non-seasonal- Always steady work, • Tuition Reimbursement, • Career growth and advancement potential HVAC General Maintenance Workers on Camp Pendleton perform general maintenance, preventive maintenance, and repairs of various types of commercial HVAC equipment to ensure that machines continue to run smoothly is the primary responsibility. You may also assist workers and journeyman by performing general duties of lesser skill, such as keeping them supplied with materials and tools; holding materials and tools; and cleaning working area, machines, or equipment. The ideal EMI HVAC General Maintenance Worker performs any task as instructed while following all health and safety standards. Salary $23.23/ hr. plus $4.93 fringe benefits used towards insurance and 401k! See ALL the fantastic benefits you receive as an employee of EMI below!! Key Responsibilities • Inspect, operate, or test machinery or equipment to diagnose machine malfunctions, • Inspect drives, motors, pulleys and belts, check fluid levels, replace filters, or perform other maintenance actions, following checklists, • Clean or lubricate shafts, bearings, gears, or other parts of machinery, • Dismantle devices to access and remove defective parts, • repair or replace parts and reassemble equipment, • Inspect used parts to determine changes in dimensional requirements, • Record type and cost of maintenance or repair work, • Order parts, supplies, and equipment from catalogs and suppliers, or obtain them from storerooms, • Performs other related duties as assigned Essential Skills • Knowledge of methods, materials, tools and equipment used in HVAC in a COMMERCIAL/INDUSTRAL setting, • Operate cutting torches or welding equipment to cut or join metal parts, • Use hand tools, measuring instruments and electrical and electronic testing devices such as meters, • Use rules, calipers, micrometers, or other measuring instruments., • Adaptable and flexible in work situations, • Prioritizes tasks to ensure completion in a timely manner, • PRACTICES WORKPLACE SAFETY in the use of tools, equipment, and supplies used in repair of HVAC equipment., • Including proper use of personal protective equipment (PPE). Requirements • High school diploma or equivalent, • 2+ years related experience and/or formal vocational/technical training in a variety of building and/or utility trades, • Valid driver’s license compliant with REAL ID Act or are you willing and able to obtain one, • Pass a pre-employment drug screening and background check, • Regular, dependable attendance, • U.S. citizenship to obtain and maintain access to military installations Physical Requirements • Must be able to lift up to 50lbs unassisted, • Use of hands, reaching with hands and arms, talking, and walking, • Prolonged periods of sitting, bending, squatting, standing, twisting, or stooping, • Climbing ladders and entering confined spaces, • Lifting and adjusting heavy objects, contact with sharp, hot and/or very cold supplies and equipment., • Work both indoors and outdoors in various temperatures (some extreme) and weather conditions., • Physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Preferred Qualifications • CFC License or ability to obtain CFC License (minimum Type 2) within 90 days of employment Click here to follow EMI Services on Facebook Benefits As a team member at EMI, you’ll enjoy: • Generous benefits package consistent with Service Contract Agreement, • Insurance Allowance, • Health Care Plan (Medical, Dental & Vision), • Retirement Plan (401k, IRA), • Life Insurance (Basic, Voluntary & AD&D), • Paid Time Off (Vacation, Sick & Federal Holidays), • Employee Stock Ownership Plan (ESOP), • Short Term and Long Term Disability, • Term Life Insurance, • Safety Allowance, • Uniforms, • Tuition Reimbursement, • Non-seasonal- always steady work!, • Referral program- Join our team then bring your friends What Sets EMI Apart EMI is an industry-leading provider of DOD base operation support services, facilities maintenance, and logistics. Our goal is to contribute to the repair and maintenance of buildings and equipment. EMI consistently delivers cost-saving through best value innovations and quality service that exceeds our clients’ expectations. The Right Partner: EMI has grown by gaining our customers’ trust and our employees’ loyalty. We’ve successfully performed over 60 service contracts and we understand the unique challenges facing today’s military. We offer exceptional responsiveness and a strong commitment to customer satisfaction. We demonstrate this commitment by consistently earning some of the highest customer satisfaction ratings in the industry. The Right Team: The EMI team includes over 250 high-achieving professionals, administrative and trades personnel deployed in various locations throughout the United States. At times, we augment our in-house capabilities with proven and capable business partners. The Right Approach: EMI brings vast expertise and proven solutions to augment our clients’ operations. We provide a platform that delivers seamless mission support and exceptional customer service in a very cost-effective and repeatable solution. #emiservices

$2,500 Signing Bonus for Part Time; $5,000 Signing Bonus for Full Time \n Pay is a combination of hourly rate between $55 and $60 per hour plus an uncapped bonus plan \n At Gentle Dental, we value our teammate’s smile as much as our patient’s smile. \n Our vision is to provide exceptional, lifelong, integrated oral healthcare services. We enhance the quality of our patients’ lives by providing accessible oral healthcare, which is paramount to overall health and wellbeing. \n Our culture is based on innovation and providing a wellness approach to Dentistry to improve clinical results and consistently generate predictable treatment outcomes. We focus on a commitment to patient care, operational and clinical excellence, personal accountability, building relationships, and seeking out innovative and creative approaches to support our patients and teams. \n It’s the whole idea of group dentistry, reimagined to provide Doctors and Clinicians with the right balance of autonomy and support for all stages of their career, focused on the best interests of patients. \n We are hiring immediately for full and part time staff. Come join our team and make a difference in the lives of the people in your community! \n Location: \n\nGentle Dental Carlsbad 2620 El Camino Real Suite A Carlsbad, CA 92008\n \nSchedule:\n \nFull Time or Part-time\n \n\n We offer the following benefits for Part Time employees: \n\n\n\n • Employee Assistance Program\n, • Basic life, AD&D, and long-term disability insurance\n, • 401k plan with company match\n, • CE credits\n, • Malpractice\n, • Medical, dental, vision, and life benefits\n, • PTO\n, • Registered Dental Hygienist License required\n, • Accredited Hygiene Technical School or College\n, • Current applicable State Dental License (or the ability to acquire one by time of employment)\n, • Other licenses/certifications such as CPR, local certified anesthesia\n\n \n Equal Opportunity Employer \nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. \nFor further information, please review the Know Your Rights notice from the Department of Labor.

Customer Service / Fully Remote] - Anywhere in U. Competitive Pay - As a Customer Support Rep you'll: Help customers with technical and non-technical inquiries across multiple channels (Email and Live Chat); Engage in meaningful conversations with customers and problem-solve when things don't go qui

Job DescriptionCompany Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description Shift: Monday - Friday 7:00AM - 4:00PM Pay: $31.44 - $33.65 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As an IT Service Agent you will: IT Service Agent performs various functions to keep computer systems in top working condition. This position will be responsible for keeping internal users active and addressing production concerns as well as monitoring information security solutions to ensure compliance and protection of keys systems and data. What will my responsibilities include? • Talk to users over the phone, via email or face-to-face to provide solutions to technical problems, • Perform diagnostic tests and troubleshooting to identify issues, • Develop and implement technical procedures effective in quickly addressing users’ problems to minimize downtime, • Carry out assessments to determine the need for changes in hardware/software configurations, • Educate users on procedures for resolving or preventing recurrence of a technical problem, • Explain and provide IT solutions to users in non-technical and comprehensible terms, • Prepare and present reports to update management on IT support operations, • Operate and work with equipment such as smartboards, external storage devices, computer diagnostic tools, printers etc., • Respond to inquiries about hardware or software issues, • Perform scheduled maintenance on computer systems to ensure efficient operations, • Repair or replace faulty components of a computer/network system, • Monitor systems and infrastructure to ensure no anomalies and address any that occur, • Develop solutions to address internal situations that may arise within operations, office functions, or general IT/IS infrastructure., • Other reasonable duties as business and operational needs dictate Qualifications What key skills and experience do I need? Associate’s degree in computer science, networking or a related discipline or equivalent experience. Bachelor’s is preferred. * Two years’ experience in the IT Industry. Some experience in the manufacturing industry is preferred. * Requires working knowledge of computer, scanner, facsimile machine, copier and any other standard office equipment * Requires basic arithmetic skills to perform basic calculations * High understanding of computer systems, functions, and operation * Requires ability to assess facts and develop conclusions Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor

Being a Manufacturing Engineer II determines the parts, equipment, and tools needed to achieve manufacturing goals according to product specifications. Represent Process Engineering in assigned R&D and Project Team meetings for technology transfers and provide technical expertise and support in anal

Job DescriptionDescription: Perform radiological duties in compliance with x-ray department and legal requirements. Help patients feel comfortable during the entire process. Perform selected nursing and administrative/clerical duties that assist in the delivery of primary health care and patient care management under the direction of a physician. These duties are delegated in relation to the individual's degree of training, in accordance with the objectives and policies of the organization and respective state laws governing such action and activities. Essential Duties and Responsibilities X-Ray Technician: · Prepare patients for radiological procedures and take X-rays following established procedures for patient care and safety. · Protect patients, yourself and staff from radiation exposure by practicing sound procedures which meet or exceed recommended industry standards. · Develop and process radiological film. · Obtain quality diagnostic radiographs as requested by physicians. Maintain a repeat rate of two percent or less. · Ensure that all equipment is in good working condition and in compliance with applicable laws and regulations. · Report immediately any equipment malfunctions to Supervisor. · Log completed radiological procedures. Complete paperwork accurately and on time. · Identify and file reports as required. · Maintain examination rooms. Stock necessary office and radiological supplies. · Request, retrieve and track films to and from other departments or centers. · Work closely with the physician to receive guidance and instruction for treating patients. Medical Assistant: · Perform selected nursing and administrative duties. · Prepare patients for examination and treatment. Take patient histories and vital signs. · Prepare exam and treatment rooms with necessary instruments. · Administer injections and apply dressings as instructed. · Prepare and maintain supplies and equipment for treatments, including sterilization. · Assist physicians in preparing for minor surgeries and exams. · Assist with scheduling of tests and treatments. · Order and maintain clinical and office supplies and equipment. · Maintain patient files, records and other information. · Work closely with the physician to receive guidance and instruction for treating patients. · Perform direct patient care as instructed by the physician. · Adjust to quality assurance policies and procedures concerning all physical therapy issues. · Maintain equipment for use at all times, in a clean and safe condition. General: · Compile and condense technical and statistical data for reports and records. · Attend required meetings and participate in committees as requested. · Complete appropriate documentation on all patients examined. · Maintain appropriate communication and good interpersonal skills with Supervisors, staff and patients to ensure coordinated efforts and provision of high quality service. · Utilize formal channels of communication to report concerns, personal requests and patient issues. · Respect patients' right to privacy and confidentiality. · Maintain an orderly and professional working atmosphere. · Report to work properly dressed according to the approved dress code. · Adhere to guidelines concerning working hours and break periods. · Manage time effectively to complete all patient treatments and related activities as assigned. · Maintain professional standards and procedures ensuring compliance with corporate policies and with applicable regulations. · Perform related administrative duties as required. · Take all necessary precautions to protect center assets and property against loss or waste through negligence or dishonesty. · Demonstrate support to other co-workers by offering help. · Assist in the solution of problems as directed by Supervisor. · Perform related work as required. Requirements: Knowledge, Skills and Abilities X-Ray Technician: · Knowledge of anatomy and physiology sufficient to perform x-ray testing. · Knowledge of radiology equipment. · Skill in properly positioning patients. · Skill in identifying equipment problems. · Knowledge of safety hazards common to radiology including equipment, body mechanics, and patient movement. Medical Assistant: · Knowledge of medical practice and organizational policies to administer patient care. · Knowledge of examination, diagnostic and treatment room procedures. · Knowledge of use and maintenance of medical equipment and instruments to administer patient care. · Knowledge of common safety hazards and precautions to establish a safe work environment. · Excellent people skills. Ability to work well and effectively with others. General: · Skill in establishing and maintaining effective working relationships with patients, medical staff and the public. · Knowledge of medical practice and organizational policies to administer patient care. · Knowledge of examination and diagnostic procedures. · Knowledge of use and maintenance of radiological equipment and instruments. · Knowledge of common safety hazards and precautions to establish a safe work environment. · Skill in documenting and maintaining patient care records. · Skill in identifying and communicating problems to the supervisor. · Skill in following medical quality assurance and quality control standards. · Skill in establishing and maintaining effective working relationships with patients and other staff. · Ability to understand and follow verbal and written instructions. · Ability to communicate clearly with patients and other staff. · Good oral and written communication skills in English. · Ability to react calmly and effectively in emergency situations and to work under high pressure situations. · Good telephone manners and etiquette. · Detail orientation and organization. · Flexibility in working hours to handle variation in the inflow of patients and cover the needs of the department. Education, Licenses/Certification · High School Diploma or equivalent; completion of course in limited-scope/basic/LMRT/NCT radiological course; completion of medical assistant program. · Limited/Basic/NCT/LMRT certification in Radiology preferred; certification obtained from an accredited Medical Assistant program preferred. NOTE: This job description may not include all of the duties assigned to the employee and may be updated and modified by the department supervisor, according to the operations at any given time. The base salary is determined on the candidate's education, qualifications, and experience, and is subject to change based on various internal and external factors. Akeso is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.