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This individual will provide program Quality Engineering support for assigned contracted programs spanning the lifecycle of the program including design, development, production, test and supplier support. Utilizes engineering background and expertise to ensure customer requirement flow-down and har

L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers’ mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, dedication to our communities, and commitment to excellence in everything we do. L3Harris Technologies is the Trusted Disruptor in the defense industry. With customers’ mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security. Job Title: Lead, Quality Process Engineer - Factory Lead Job Code: 28508 Job Location: Onsite at our Canoga Park, CA facility Job Schedule: 9/80 Employees work 9 out of every 14 days – totaling 80 hours worked – and have every other Friday off Job Description: Aerojet Rocketdyne segment of L3Harris, is seeking a a Lead Quality Engineer to join our Space Propulsion and Power Systems (SP&PS) team. This individual will drive quality processes and procedural compliance across the factory floor encompassing multiple product lines, collaborating with quality and operations leadership, and working closely with the Sr. Manager – Product Acceptance. Essential Functions: • Champion, lead, and support the execution of flow-down strategic initiatives., • Utilizes engineering background and expertise to ensure customer requirement flow-down and hardware is compliant to specifications. Handles and communicates deviations/non-conformances at different levels within the organization and at customer level as applicable. Prepares comprehensive analyses, procedures, reports and presentations for both internal and external customers., • Actively participates in improvement teams to reduce risk through the application of six sigma tools. Applies zero defects quality principles, concepts and methods, including Lean Manufacturing to continuously improve processes, reduce cost and ensure the quality of our products and services., • Drives corrective and preventative action activity both in-house and at the Supplier, and provides corrective action board support to manage timely and effective problem closure and recurrence control., • Interprets engineering drawings and specifications, customer quality requirements and company quality requirements to ensure compliance with the customer's requirements. Participates in design reviews to identify and correct inspectability and producibility issues and opportunities early in the product life cycle. Provides a clear and concise flow down of product definition and Quality requirements to Suppliers., • Actively participates in the Material Review Board, including segregation and control of nonconforming hardware to preclude inadvertent processing, disposition nonconforming hardware, preparing for and conducting board meetings, and implementing disposition decisions. Qualifications: • Bachelor's degree and a minimum of 9 years of prior related quality experience. Graduate Degree and a minimum of 7 years of prior related quality experience. In lieu of a degree, minimum of 13 years of prior related quality experience. Preferred Additional Skills: * • Technical Skills:, • Familiarity with AS9100, ISO9001, or other quality management systems., • Proficient in reading and interpreting engineering drawings and specifications., • Experienced in investigating technical issues and nonconformance’s to determine root causes and implement effective corrective actions, including familiarity with 8D analysis or similar tools, • Communication Skills:, • Excellent leadership, communication, and interpersonal skill., • Self-Starter:, • Ability to hit the ground running and make an immediate impact with minimal supervision., • Deal with multiple tasks and deadlines set by management, • Strong analytical and problem-solving abilities., • Advanced business knowledge, general management, and leadership capabilities., • Proven experience in developing and implementing quality assurance programs and systems., • Relevant experience supporting the production of high-complexity aerospace products., • Experience interfacing with US government agencies and/or aerospace prime customers., • CQE and/or CSSBB certification., • APQP and/or Zero Defect Planning experience., • EVM and BOE experience., • Proficient in MS Office, business analytics software such as Qlik and PowerBI, and tools like Microsoft Visio and Minitab. In compliance with pay transparency requirements, the salary range for this role in California, Massachusetts, New Jersey, Washington, and the Greater D.C, Denver, or NYC areas is $114,000 - $212,000. The salary range for this role in Colorado state, Hawaii, Illinois, Maryland, Minnesota, New York state, and Vermont is $99,000 - $184,000. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. L3Harris also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements. #LI-HJ1 L3Harris Technologies is proud to be an Equal Opportunity Employer. L3Harris is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. L3Harris maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Please be aware many of our positions require the ability to obtain a security clearance. Security clearances may only be granted to U.S. citizens. In addition, applicants who accept a conditional offer of employment may be subject to government security investigation(s) and must meet eligibility requirements for access to classified information. By submitting your resume for this position, you understand and agree that L3Harris Technologies may share your resume, as well as any other related personal information or documentation you provide, with its subsidiaries and affiliated companies for the purpose of considering you for other available positions. L3Harris Technologies is an E-Verify Employer. Please click here for the E-Verify Poster in ___ or ___. For information regarding your Right To Work, please click here for ___ or ___.

This individual develops, implements and analyzes manufacturing engineering plans and projects and communicates them to internal and external customers. Defines and transfers manufacturing and engineering tools, strategies and systems. Experience working as a weld engineer or weld technician in aero

L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers’ mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, dedication to our communities, and commitment to excellence in everything we do. L3Harris Technologies is the Trusted Disruptor in the defense industry. With customers’ mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security. Job Title: NDT Level III RT/DR/UT/PT, Quality Engineering Specialist Job Code: 28124 Job Location: Canoga Park, CA Job Schedule: 9/80: Employees work 9 out of every 14 days – totaling 80 hours worked – and have every other Friday off Aerojet Rocketdyne, an L3Harris company, is seeking a NDT Level III RT/DR/UT/PT, Quality Engineering Specialist to join our team in Canoga Park, California. Essential Functions: • Review supplier-submitted NDT technique sheets for compliance to AR-Los Angeles specifications and drawing requirements. Coordinate with suppliers on the development and approval of these technique sheets. Prepare necessary reports., • Manage site NDT supply base by monitoring suppliers to ensure flow down of AR requirements to sub-tier suppliers, audit existing NDT suppliers and assess potential new NDT suppliers for their ability to meet site requirements., • Review process specifications, in-house technique sheets, etc. as noted above under job responsibilities., • Provide training and testing to L I and L II., • Develop, review and approve NDT techniques with L II personnel., • Write, review and approve specifications pertinent to NDT., • Support review boards for inspectability of product., • Prepare NDT for customer and internal audits., • Develop and Lead Corrective action reviews on audit/NCR findings., • Maintain own L III certifications., • Participate in the direction of the NDT department., • Requires NDT LVL III RT (Radiography), DR (Digital Radiography), UT (Ultrasonic), or PT (Penetrant) certifications., • Needs to have direct experience with the testing of Aerospace Metallic products, • Must have Level 3 ASNT Certification and/ or currently active NAS410 Level III certifications, • Hands-on working experience in a manufacturing environment and a corresponding understanding of manufacturing processes is essential., • Experience with auditing practices and Process Certification is desired., • A demonstrated proficiency with a variety of NDT inspection techniques and equipment along with a working knowledge of blueprint reading and interpretation is required., • Knowledge of industry NDT standards (ex. NAS410, ASTM 1742, ASTM 1417, ASTM 1444, AMS-STD-2154, etc...) is required., • Candidate must meet requirements of NAS-410., • Must have demonstrated excellent interpersonal, written and verbal communication skills, as well as the ability to work well in a team environment., • Must possess strong computer skills and be well-organized., • Position requires responding to customer needs and may include weekend work., • Auditing experience/certification desired. In compliance with pay transparency requirements, the salary range for this role in California, Massachusetts, New Jersey, Washington, and the Greater D.C, Denver, or NYC areas is $114,000 - $212,000. The salary range for this role in Colorado state, Hawaii, Illinois, Maryland, Minnesota, New York state, and Vermont is $99,500 - $184,500. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. L3Harris also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements. L3Harris Technologies is proud to be an Equal Opportunity Employer. L3Harris is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. L3Harris maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Please be aware many of our positions require the ability to obtain a security clearance. Security clearances may only be granted to U.S. citizens. In addition, applicants who accept a conditional offer of employment may be subject to government security investigation(s) and must meet eligibility requirements for access to classified information. By submitting your resume for this position, you understand and agree that L3Harris Technologies may share your resume, as well as any other related personal information or documentation you provide, with its subsidiaries and affiliated companies for the purpose of considering you for other available positions. L3Harris Technologies is an E-Verify Employer. Please click here for the E-Verify Poster in ___ or ___. For information regarding your Right To Work, please click here for ___ or ___.

Our client is seeking a Senior R&D Project Engineer to oversee projects from concept to post-market surveillance. The role requires deep expertise in developing and launching implantable Class II and III devices, navigating stringent regulatory pathways (FDA 21 CFR 820, ISO 13485, PMA/510(k)). Duties and Responsibilities: • Lead the entire product development lifecycle for Class II and III implantable devices., • Manage project plans (timelines, budgets, resources) and ensure on-time product launches aligned with strategic goals., • Ensure strict adherence to design control and regulatory requirements., • Translate user needs into technical specifications in collaboration with clinical, marketing, and regulatory teams., • Oversee design, development, and testing of implantable mesh products, including material selection and prototyping., • Manage verification/validation and draft reports to support regulatory submissions (PMA and 510(k))., • Conduct and document risk management activities (e.g., FMEA)., • Provide technical guidance and serve as the primary liaison with external vendors. Required Knowledge, Skills, and Abilities: • Bachelor's degree in Biomedical, Mechanical, Electrical Engineering, or a related field., • 7+ years of product development, program/project management, or engineering experience., • Proven experience developing and launching Class II and Class III devices., • Direct experience with FDA regulatory processes (PMA and 510(k) submissions) is required., • Experience with implantable devices, particularly surgical mesh for pelvic floor disorders, is highly desirable.

Job Title: Process Development Engineer Location: Thousand Oaks, CA Duration: 12 Months Description: Note: Fully onsite - Monday - Friday Master's Degree - 0 -2 years industry experience Bachelor's Degree - minimum of 2 years industry experience Nice to have: Tech transfer experience Preferably from BioPharma Industry Ideal candidate: The ideal candidate for this role should have a bachelor’s degree in any scientific or engineering discipline with 1 – 3 years professional working experience. Candidates with recent Master degree are also suitable if they bring strong soft skills. The candidate should possess solid working experience with standard software tools such as Microsoft Office. Experience with specialized software such as like SAP or Smartsheets is desirable but can be learned on the job. Biologic drug product knowledge is favorable. The candidate must excel in group management, deadline adherence, and meticulous documentation skills. This position leans heavily on project development (PD) and project management (PM) skills, with technical expertise expected to develop over time. Professional working experience outside of an academic setting is preferred. As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple Amgen products to the aseptic fill finish manufacturing plants at Amgen Thousand Oaks which includes various production lines. The candidate will support senior staff in the planning, execution, and documentation of characterization, process validation and technology transfer projects. The candidate will be primarily responsible for supporting execution of characterization studies to generate technical data packages using complex technology, organization of data and analysis of results, and compiling information in concise summaries while under supervision of senior staff. The candidate will be responsible for interfacing with various drug product teams to ensure successful technology transfer and completion of associated technical documentation for Amgen products. The candidate will assist with experimental design, develop and execute protocols, obtain reproducible and reliable results, analyze and document experimental results, and communicate results to cross-functional groups. Preferred Qualifications: • B.S. in scientific or engineering discipline with 1‒3 years’ relevant professional experience or M.S. in scientific or engineering discipline with 0‒2 years’ relevant professional experience, • Familiarity with cGxP and experience in drug product / drug substance manufacturing or process development, • Knowledge of and hands-on experience with various drug product technologies, • Displays critical thinking, problem solving and independent research skills, • Ability to learn new techniques, perform multiple tasks, keep accurate records, follow instructions, and comply with company policies, • Excellent project management skills and ability to escalate relevant issues to project lead and line-management, • Strong cross functional team player with good communication skills (oral and written), • Ability to work independently and as part of a team with internal and external partners, • Good computer and organizational skills with strong attention to detail, • Self-motivated with a positive attitude

R&D Sustaining Engineer | Medical Devices Location: Westlake Village, CA (100% Onsite) Compensation: $100k–$120k + bonus + benefits Employment: Full Time (This role is not eligible for visa sponsorship.) We are seeking an R&D Engineer who thrives in solving problems, improving products, and collaborating cross-functionally. This role focuses on supporting and improving existing medical device products — ensuring they remain reliable, compliant, and cost-effective throughout their lifecycle. You’ll work closely with Manufacturing, Quality, Supply Chain, and Regulatory teams to troubleshoot issues, implement design changes, and drive continuous improvement efforts. What You’ll Do • Lead sustaining engineering projects focused on product improvements, cost reductions, and component updates, • Serve as a primary R&D partner to Manufacturing for troubleshooting and root cause analysis, • Implement and document design & process changes in compliance with regulated environments, • Support V&V testing, documentation, and engineering evaluations, • Contribute to change orders, labeling/IFU updates, and competitive product testing What You Bring • Bachelor’s degree in Mechanical, Biomedical, Electrical, or related engineering field, • 4+ years in a regulated industry; medical device experience strongly preferred, • Understanding of FDA, ISO, and GMP requirements, • Experience with design controls, risk management, and validation, • Strong problem-solving and project leadership skills, • Proficiency with SolidWorks and Microsoft Office / MS Project, • Familiarity with lean manufacturing or continuous improvement methodologies

Enterprise Identity Architect Location: Westlake Village CA Duration: 5 months contract (potential to go PERM eventually) Work from Office Responsibilities: The Vice President Architect is responsible for providing strategic guidance, designs, and solution patterns to team members, and is the "chief architect” for a sub product/s. As the Architect, you will serve as a driver and collaborator throughout the development life cycle, partnering with business analysts and customers to review and optimize requirements. The VP Architect will: Lead the architectural design and initial development and/or major revision of business software solutions Identify and solve systemic architectural problems at the product or multiple subproducts / teams / technical area levels Define product requirements and create high-level architectural specifications, ensuring feasibility, functionality and integration with existing systems and platforms Solve a variety of very open-ended and complex (even to the PM, TLs and Sr. TLs who presented them) problems Provide technical guidance across several scrum teams Perform other related duties as required and assigned Demonstrate behaviors which are aligned with the organization's desired culture and values Qualifications: Bachelor's degree in computer science, engineering or similar major 7+ years of experience with software development Demonstrated track record of anticipating technical problems that will fall out of major subproducts/products and designing solutions to overcome them. Financial Services and, if possible, mortgage industry experience preferred

An employer sitting in Simi Valley, CA is looking to hire a Manufacturing Engineering Manager who will be managing the Manufacturing Engineering Department (5-9 team members consisting of Engineers, Tooling etc. This role will be responsible to shape the strategy, provide strategic leadership, and g

Lead and mentor a multidisciplinary team of analysts, engineers, and data stewards to deliver high-quality outcomes. Knowledge of industry trends and best practices in data engineering. Tech Consulting - Palantir Data Engineer - Manager.

Familiarity with Windows and Linux interoperability with identity systems is a plus. Enterprise Atchitect for one of its clients in the financial domain. Experience with federated identity systems is valuable.

This position leads the Quality group for a subset of product families within Energetic Assemblies and is a supervisor of Quality Engineers (QEs) and Quality Assurance Technicians (QATs). Interfaces and communicates with a variety of personnel including Technicians, Quality Engineers, Mater Schedule

Experience with hardware debugging tools (oscilloscopes, logic analyzers, multimeters, etc. Knowledge of industry standards and best practices related to hardware design, testing, and quality assurance. If you're a dynamic, hands-on leader who can guide a team while actively contributing to cutting-

Pay Range : $24 to $25/hr on W2 (This pay includes mileage).Must have own Vehicle and comfortable using it.As a Field Service Technician, you will: represent the Client brand, problem-solve at a basic module (FRU) level, organize and plan your time effectively, and know when and to whom to escalate

Collaborating with client engineering, R&D, operations, and technical services teams to understand challenges related to process development, scale-up, catalyst evaluation, formulation chemistry, and manufacturing optimization.

Proven leadership of a multi-disciplined engineering organization (aero, electrical, video processing, remote sensing, embedded/software, mechanical-design, CAD, systems, configuration/data management). Coordinates R&D and Sustaining projects with customer-facing organizations (Business Unit) an

Signal Delivery Design: High‑speed interconnects, probing technologies, and test interface hardware. Hardware Engineering Manager – Semiconductor Test Platform (Teradyne, Agoura Hills, CA).

Supplier Quality Assurance experience. Host customer quality audits and participates in internal quality audits. Develops, modifies, coordinates and documents the implementation, evaluation and maintenance of quality assurance programs and systems.

Engineering background - but not computer engineering background (Looking for mechanical / material engineering background with coding experience). No Engineering Background (NOT SOFTWARE ENGINEERING). Data Scientist Associate, mechanical / material engineering background - (JP12135).

Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13348). Applies basic engineering principles to troubleshoot, design and implement system modifications, perform function tests for small projects. Organizes, analyzes and presents interpretation of results for engineering pr

Director of Engineering, Product Engineering page is loaded## Director of Engineering, Product Engineeringlocations: Simi Valley, CAtime type: Full timeposted on: Posted Yesterdayjob requisition id: 5866Worker TypeRegularJob DescriptionThe Director of Engineering leads a

Working cross-functionally with individuals and project teams in Analytical, Engineering, Instrumentation, and Manufacturing. BS in Engineering, Biotech, Chemistry, or Equivalent.

Key Consulting is hiring! We are recruiting an Engineer, Upstream Drug Development Facilities & Engineering for a consulting engagement with our direct client, a leading global biotechnology company. Seeking an Engineer at our client’s main headquarters in Thousand Oaks, CA to join the GMP Facilit

This role has the potential to grow into a more encompassing Program Manager leading a team of Project Managers on complex, large-scale programs with significant business opportunity and impact.

Engineer, Process Equipment and analytical support (JP12181). Engineer, Process Equipment and Analytical Support for. Specialized equipment/process expertise.

We are looking for a manager to lead our Mixed-Signal Circuit Design Group at HRL Laboratories. As a manager to a group of technical staff, the candidate will guide team members' careers by providing opportunities for development while engaging in regular formal and informal feedback discussions. El

Shaping the Future with AI Agents:.Architect, develop, and deploy AI agentic systems and multi-agent frameworks that automate complex workflows and enable intelligent decision-making.You will focus on building robust, scalable solutions using cutting-edge AI orchestration tools.Own the entire lifecy

JLL empowers you to shape a brighter way.Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients.We are committed to hiring the best, most talented people and empowering them to thrive,

The Quality Engineer may work in laboratory settings running tests and duplicating real-world conditions, using tools such as micrometers, calipers, gauges, volt meters, ammeters, ohmmeters, and electronic inspection equipment to aid in quality inspections and assessments. Description: Job Title: Qu

The Senior DevOps Engineer on the Cloud Engineering team will be responsible for designing, automating, and optimizing cloud infrastructure and deployment pipelines to ensure scalability, security, and operational efficiency.

Co-Leads the cross-functional Program Core Team to establish an integrated plan for resources and materials to deliver the new product program per the Product Delivery Team commitment. Develop, execute, and review architecture documents, design documents, specifications, development plans, character

Job Description: Manufacturing Engineering Technician. The Senior Manufacturing Engineering Technician provides manufacturing expertise while setting up and conducting complex product evaluation, creating process documentation, operations support, and small scale process development. Support Manufac

Degree in Electrical Engineering or Computer Science, Chemical Engineering, Biotech Engineering, or related life science engineering. Emerson Delta-V DCS Programming Experience, Rockwell Automation SCADA and PLC Experience, Compliance with regulatory requirements such as 21 CFR Part 11Minimum of Bac

Seeking a student for a Summer/Fall Co-op with analytical and programming skills to work as part of process engineering team in the manufacture of GaAs power amplifier circuits. Nearest Major Market:VenturaNearest Secondary Market:Oxnard Job Segment: Process Engineer, Summer Internship, Entry Level

Consulting - Tech Consulting - Sector Tech - Oil & Gas Reservoir Engineer - Senior Manager. Technology - Systems Implementation and Engineering - Technical Engineering - Senior Manager. As a Senior Manager in Technical Engineering, you will lead the delivery of complex processes and solutions while

May 18 - August 7, 2025 (~12 weeks).Milwaukee, WI (MCS Building / HQ).Radford, VA (Rock Road & Main Street.At Regal Rexnord, we're driven by innovation, excellence, and sustainability.As a $6 billion global manufacturer, we're committed to reducing our environmental footprint and investing in the co

Performs electrical/mechanical troubleshooting to determine problems in non-functioning electro-mechanical production equipment used in the Fab. Nearest Major Market:VenturaNearest Secondary Market:Oxnard Job Segment: Network, Telecom, Telecommunications, Electrical, Engineer, Technology, Engineerin

Strong expertise with GitHub Actions, Azure DevOps, and/or Jenkins. The DevOps Engineer will lead the design, implementation, and maintenance of secure, scalable, and reliable CI/CD pipelines to accelerate software delivery across development teams. The position can be 100% remote, but if located in

Experience with ML NLP & AI libraries. Experience with NER and Search technology such BM25, BM42 is a plus. Experience with Gen AI, Agentic AI , LLM training is a plus.

If you are looking for a challenging and exciting career in the world of technology, then look no further.Skyworks is an innovator of high-performance analog semiconductors whose solutions are powering the wireless networking revolution.Through our broad technology expertise and one of the most exte

Provide coaching and development guidance to delivery team members. Work closely with Product / Business Owner and Project Manager to provide progress updates and ensure the management of any delivery risks or issues. Identify environment strategy and conduct environment refreshes if necessary.

Job Description A Simi Valley heavy civil/underground utilities contractor is looking for a highly organized, professional, driven, and energetic Office/Project Engineer/Assistant PM and a project manger to join our team for immediate hire. Primary Responsibilities: • Review project plans, requirements, and specifications, • Generate RFI’s, • Prepare submittals, • Review documents and prepare change orders, • Understand project logistics and schedule, • Research for material and issue purchase orders, • Experience in the construction industry (a plus), • Advanced computer skills (experience with PlanSwift or Procore, a plus), • Well organized, flexible, detail oriented, and have the ability to multi-task, • Punctual and reliable, • Self-motivated and able to take responsibility, • Must be able to work primarily out of Simi Valley based office during normal business hours, • Available for immediate hire, • Will require travel to job sites (must provide own transportation, at times), • Looking to hire full-time a in long-term position Company DescriptionSubzero Excavating is an Underground Utilities contractor specializing in both Wet & Dry Underground Utilities that has expanded into Site and Structural Concrete.Subzero Excavating is an Underground Utilities contractor specializing in both Wet & Dry Underground Utilities that has expanded into Site and Structural Concrete.

Job Description Quality/Process Engineer Summary of Job Duties: The Quality Engineer has multiple responsibilities to ensure that the manufacturing process produces product that meets or exceeds customer expectations. To assist with the implementation of a comprehensive quality management system, and to support quality objectives of the company. The ideal candidate is a fast learner who can handle multiple projects and work well as part of a team. Develop processes, control plans, PPAP plans, first article processes, and metrics. Responsibilities: • Establish and define Standards and Procedure of development requirements for the product., • Participate in risk and hazard assessment during the new product Implementation phase of production., • Establish and maintain high quality test procedures and methods to be used in present and future software and hardware testing and development that comply with the company quality standards and deliverables., • Work with Contract Manufacturer customers to specify and qualify the reliability and testing requirements for components and/or assembled parts of the incoming inspections., • Coordinate on the quality trends, including the corrective and preventive actions., • Oversee the resolution of quality-related problems in the development and manufacturing environment resulting from supply or production imperfections., • Ensure the proper maintenance of document control processes and devices., • Confer with Engineering Manager on production and personnel issues. Also assist with preparation of various quality reports., • Participate on/with continuous improvement teams., • Randomly examine production documents (router/Traveler) to ensure that all assembly, inspecting and testing steps were performed according to EMLinQ's practices., • Provide Supplier Quality Engineering support to the Procurement function by auditing Supplier facilities and monitoring supplier performance data., • Follow-up on supplier corrective actions submitted., • Monitor and analyze product non-compliance on assemblies to reduce defects., • Monitor ESD compliance through production., • Analyze customer returns to determine cause and prevention., • Perform follow-up on corrective actions to determine effective implementation., • Perform periodic audits of production processes against procedures., • Monitor and support receiving inspection activities., • Minimum of 5-10 years of Quality Engineer Experience, • Experience working in ISO 9000, AS9100 and ISO-14001 requirements., • Must have strong computer skills and proficiency in Microsoft Office., • Knowledge of Process Analysis: process measurements, process flow diagrams., • Experience interpreting blueprints, Bill-of-Materials, data sheets and test reports., • Excellent communication skills and ability to communicate with all levels of management., • Diploma/Degree in Engineering (preferably Quality Engineering), • Experience working in a production environment with practical process control experience., • Possess strong statistical and analytical skills., • Proactive, independent and self-motivated., • Functional/Technical Certifications that would be an added advantage:, • Certified Internal Auditor ISO 9001-2008, AS9100, • Six Sigma Black Belt is a plus. Company DescriptionEMLinQ LLC is a leading provider of advanced electronics manufacturing services to original equipment manufacturers (OEMs) in the telecommunications, networking, computer, aerospace, military, consumer electronics, and medical device industries.EMLinQ LLC is a leading provider of advanced electronics manufacturing services to original equipment manufacturers (OEMs) in the telecommunications, networking, computer, aerospace, military, consumer electronics, and medical device industries.

Job Description$83k-115k/year + Bonus 1st Shift POSITION SUMMARY: The Quality Engineer 2 with a certain degree of creativity and latitude, monitors, tests, and inspects products to ensure they meet specified standards, are free of flaws, and function as designed. RESPONSIBILITIES: • The Quality Engineer may work in laboratory settings running tests and duplicating real-world conditions, using tools such as micrometers, calipers, gauges, volt meters, ammeters, ohmmeters, and electronic inspection equipment to aid in quality inspections and assessments., • Participates in the development of testing and inspection activities associated with product development and all stages of manufacturing., • Defines and conducts both systematic/methodical and random/arbitrary tests to ensure proper performance of our products., • Reviews and creates inspection forms, records, techniques, and procedures for accuracy and relevance and provides changes when necessary., • Lead/Facilitate Shop Floor Quality Improvement activities that include conducting Floor audits and training inspection team or operators on how to inspect their in-process parts effectively and efficiently., • Material Review Board (MRB) investigation/disposition process that include Root Cause/Corrective Action activities, • Facilitate Corrective & Preventive Action (CPA) activities that include monitoring/tracking open corrective action activities assigned to others while working with owners to rapid closure and escalating when necessary., • Read and interpret drawings that include GD&T and multi-level Bills of Materials., • Demonstrate effective interpersonal skills, including Team building and Collaboration., • Review and modify Manufacturing Work Instructions and Quality Inspection plans., • Review and approve First Article, Final inspection reports and drawing/specification change requests., • Collaborate with Manufacturing and Design Engineering to create Process Failure Mode Effects Analysis (PFMEA) and Control Plans., • Lead Customer escapes containments and Root Cause Corrective Action utilizing advanced problem-solving techniques., • Provide training to employees on Quality related topics., • Interface with Customer Quality, Engineering and Government Reps for source surveillance activities., • Performs internal audits of processes using inspection results and statistical techniques to provide timely, accurate product analysis., • Participates in root cause analysis initiatives for process-related concerns. Analyzes audit results and determines proper corrective and preventative action., • Makes the final decision on the acceptability of the product., • Review Customer Purchase Orders/ Contracts for Quality requirements and generate a Compliance Matrix., • Performs additional responsibilities as assigned.QUALIFICATIONS:, • Minimum 3-7 years of experience in quality or manufacturing-related discipline and 5 years supervisory experience preferred., • Experience and familiarity with quality industry standards such as AS9100, ISO 9001, and NQA-1 preferred., • Strong knowledge of quality engineering processes and regulatory requirements., • Strong ability to apply a systematic, disciplined, and analytical approach to problem-solving., • Strong customer orientation., • Demonstrated analytical skills to proactively identify and solve problems., • Ability to interpret internal/external business challenges and make recommendations for improvements to products, processes, or services., • Ability to explain a range of complex technical information., • Ability to gather data, to compile information, and prepare reports., • Effective interpersonal, verbal, and written communication skills., • Well-organized, detail-oriented, and ability to multi-task., • Strong prioritization skills., • Strong computer skills, including proficiency with Microsoft Word, Excel, PowerPoint, Access, Outlook, and database management tool., • Maintain the highest degree of customer service, throughput, quality, cost reduction, and people productivity.EDUCATION:, • Education: Bachelor's Degree in Quality or Engineering (Required) | Master’s is preferred.CONDITIONS OF EMPLOYMENT: “This position is subject to meeting U.S. export compliance and/or U.S. Government contracting citizenship eligibility requirements”

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position • Serve as the primary technical lead for all packaging line engineering activities across capital projects and site initiatives., • Oversee URS/BOD/Design Review development for vial, syringe, and/or combination-product packaging lines (e.g., filling, labeling, cartoning, serialization, aggregation, palletizing)., • Coordinate vendor selection, FAT/SAT, IOQ/PQ readiness, and integration with upstream manufacturing, utilities, and warehouse systems., • Ensure packaging equipment design and installation comply with cGMP, GAMP 5, corporate engineering standards, and safety/ergonomic guidelines.Commissioning & Qualification, • Lead cross-functional teams to execute Cx/Qx protocols for equipment, utilities, and automated control systems, ensuring full 21 CFR Part 11 compliance., • Support resolution of punch-list items, deviations, and CAPAs during start-up and ramp-up phases., • Oversee the development of SOPs, maintenance plans, and spare-parts strategies for packaging assets.Technical Support & Continuous Improvement, • Provide technical troubleshooting for equipment reliability, product quality, and automation interfaces (e.g., SCADA/BAS/MES, serialization systems)., • Drive OEE improvements, line balancing, and changeover optimization to support high-volume biotech packaging operations., • Champion sustainability and energy-efficient design of packaging areas, aligned with LEED v4 energy & atmosphere credits., • Ensure robust data integrity, safety, and regulatory compliance throughout the equipment lifecycle.Team & Stakeholder Engagement, • Act as the primary liaison among Engineering, Validation, Automation, EHS, Quality, Manufacturing, and external suppliers., • Mentor junior engineers and collaborate with Cx Agents/Consultants, Validation Leads, and Reliability teams to ensure knowledge transfer and operational readiness., • Bachelor’s degree in Mechanical, Electrical, Chemical, or Industrial Engineering (Master’s preferred)., • 8+ years of engineering experience in pharmaceutical/biotech packaging lines, including installation and startup of automated filling, labeling, and cartoning equipment., • Strong knowledge of GMP, FDA/EMA regulations, ISO 13485 (for combination products), serialization/aggregation, and GAMP 5 automation standards., • Demonstrated success leading multidisciplinary project teams through design, construction, and qualification phases., • Familiarity with BAS/MES/serialization platforms (e.g., PAS-X, Rockwell, Siemens, Systech, Antares)., • Excellent problem-solving, communication, and vendor-management skills., • Lean Six Sigma Green Belt or equivalent continuous improvement training.Core Competencies:, • Technical Leadership & Decision-Making, • GMP Compliance & Documentation Rigor, • Cross-Functional Teamwork & Vendor Coordination, • Problem Solving under Tight Timelines, • Commitment to Safety, Quality, and Sustainability

Job Description We are seeking a Contract Quality Engineer to support our quality team with a focus on Root Cause and Corrective Action (RCCA) and Corrective and Preventive Action (CAPA) investigations. This role will be responsible for leading problem-solving efforts, conducting investigations, and driving corrective actions to closure in compliance with aerospace quality standards. Responsibilities: • Lead RCCA and CAPA investigations for nonconformances, audit findings, and customer issues., • Perform root cause analysis using structured problem-solving methodologies (5 Whys, Fishbone, etc.)., • Develop and implement corrective and preventive action plans to prevent recurrence., • Collaborate with engineering, manufacturing, and supply chain teams to resolve quality issues., • Ensure compliance with AS9100, customer, and regulatory requirements., • Document findings and maintain accurate records of investigations and actions., • Bachelor’s degree in Engineering or related field (or equivalent experience)., • 3+ years of quality engineering experience, preferably in aerospace/defense., • Strong knowledge of RCCA, CAPA, and structured problem-solving tools., • Familiarity with AS9100, ISO 9001, and customer quality requirements., • Excellent communication and documentation skills., • Contract position (12+ months, with potential for extension)., • Competitive hourly rate., • Opportunity to work on high-impact quality initiatives within the aerospace industry.

Job Description Essel is seeking an Operations Engineer to join our team. As an Operations Engineer, you will be responsible for ensuring the smooth operation of our projects and identifying opportunities for process improvement. They are responsible for resolving operational issues, enhancing system efficiency, and maintaining accurate system information. This role collaborates with district management and engineering teams to oversee system modifications, water loss control, and energy efficiency initiatives. Your primary duties will include: • Analyze system operations to identify opportunities for enhancing service quality and efficiency., • Assist in forecasting water demands, analyzing operations using hydraulic models and relevant software., • Prepare recommendations to address operational challenges within the water system., • Develop operational memos and update system documentation, including plans and schematics., • Analyze treatment system operations to optimize processes and maintain efficiency., • Generate technical reports and coordinate with superintendents on supply forecasts and budgets., • Select replacement equipment such as pumps, motors, and control valves., • Review and approve work conducted by subordinates, ensuring compliance with standards., • Evaluate system additions, upgrades, and modifications within the district., • Prioritize and oversee system water audits and leak detection activities to ensure regulatory compliance., • Review and approve work conducted by third-party providers offering water loss control services. Requirements Requirements: • Bachelor’s Degree in Civil or Mechanical Engineering or related field., • Strong written and verbal communication skills., • Minimum of six (6) years of experience in water supply, distribution operations, engineering, or construction., • Professional registration as a Civil or Mechanical Engineer in California is preferred., • Proficiency in Microsoft Word, Access, Excel, Outlook, PowerPoint, and relevant software., • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Life insurance, • Paid time off, • Vision insurance

Job DescriptionUS CITIZENS & PERMANENT RESIDENTS ONLY Excellent contract-to-hire job opportunity Looking for a Sr. Chatbot Engineer to join an Artificial Intelligence team. Join our Tech hub and work in a collaborative environment where talent is valued and creativity is encouraged. Description: Work on state of the art Machine Learning, Natural Language Processing and Gen AI projects. Learn new technologies and focus on what you're passionate about. Requirements:: 2+ years experience with Chatbot and RAG Application Development 2+ years experience with Machine Learning and Natural Language Processing 4+ years experience with Python Experience with AWS services. Experience with SQL. Compiler development experience is plus Experience with chat platforms Dialogflow, Connect-Q, etc is a plus Experience with Hybrid RAG Agents, Trainable LLMs is a plus BS in Computer Science or equivalent degree (MS in ML is preferred).. Ability to work in an agile collaborative environment. Excellent communication skills are required.