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Description Medical Device Sales - Paid Internship Looking for a rewarding and lucrative career in the medical sales industry? Our paid Internship may be the right path for you! Here are just some of the reasons a career in Orthopaedic Surgical Sales is fulfilling: Average entry level income of over

Job Description Akkodis is seeking a Production Artwork Technician for a contract with a client in Temecula, CA. The ideal candidate will be responsible for creating and updating product artwork, managing labeling formats, and ensuring compliance with corporate standards. Rate Range: $22/hour to 24/hour; The rate may be negotiable based on experience, education, geographic location, and other factors. Production Artwork Technician job responsibilities include: * Create, update, and distribute product artwork using design tools such as QuarkXpress, Adobe Illustrator, Photoshop, and InDesign. * Support artwork routing and approval processes, ensuring timely reviews and compliance with internal standards. * Attend product launch meetings and communicate artwork priorities to meet project timelines. * Ensure artwork compliance with corporate and divisional policies, including proofreading and pre-flight checks. * Collaborate with production sites and third-party suppliers to ensure artwork meets graphic standards and release requirements. * Manage computer-generated labeling formats and validate production readiness before release. Required Qualifications: * Associate or bachelor’s degree in graphic design, Visual Communications, or a related field. * Minimum 2 years of production graphics experience, preferably in a medical device or regulated environment. * Proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign) and QuarkXpress on both Mac and PC platforms. * Strong attention to detail with excellent proofreading skills and the ability to manage multiple tasks under tight deadlines. If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Pay Details: $22.00 to $24.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: • The California Fair Chance Act, • Los Angeles City Fair Chance Ordinance, • Los Angeles County Fair Chance Ordinance for Employers, • San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Company DescriptionGlobal Footprint, Local Impact: As part of the world's second-largest ER&D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level. Diverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set. Commitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish. Continuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career. Inclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard. Our Evolution and Your Role in It Akkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success. Empowering the Future We're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering. Join the Akkodis Community At Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.Global Footprint, Local Impact: As part of the world's second-largest ER&D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level.\r\n\r\nDiverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set.\r\n\r\nCommitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish.\r\n\r\nContinuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career.\r\n\r\nInclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard.\r\n\r\nOur Evolution and Your Role in It\r\n\r\nAkkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success.\r\n\r\nEmpowering the Future\r\n\r\nWe're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering.\r\n\r\nJoin the Akkodis Community\r\n\r\nAt Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.

Job Description Job description We are looking for Medical Device Assemblers for a large medical device manufacturing company. Location - Temecula, CA Day Shift: 5am to 6am - 1:30pm to 2:30pm Pay Rate: Operator I $19.25 Operator II $20.00 Operator III $20.75 Job Duties: • This position is responsible for the production of high quality medical devices within a manufacturing cell., • Follow safety guidelines and utilize appropriate safety devices when performing all operations., • Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics. Benefits include: -MEC/ACP Medical -Voluntary Dental, Vision, Life, Supplemental Income -401k (must meet requirements) -sick leave as required by state/county

Job Description Bindery Operator: 2nd Shift Location: Temecula, CA Base Pay: $20 - $30 per hour (based on experience) Employment Type: Full-Time Industry: Offset Lithographic Printing / Manufacturing Education: Minimum High School Diploma or equivalent Experience: 3+ years Saddle Stitcher experience preferred About Steven Label Founded in 1954, Steven Label is a trusted name in the manufacturing of high-quality labels, overlays, membrane switches, sensors, instructions for use (IFUs), and folding cartons—primarily serving the medical device industry. With over 70 years of experience, our customer-focused team delivers precision, innovation, and world-class service. We offer a broad range of capabilities including screen, flexographic, offset, and digital printing. Our value-added services include: At Steven Label, we are committed to helping our customers succeed by providing dependable, high-performance solutions with unmatched service. Compensation & Benefits: • Health Insurance, • Paid Vacation, • 5 Sick Days, • 9 Paid Holidays, • 401(k) Plan, • Flexible Spending Account, • Life Insurance, • Long-Term Disability, • Employee Assistance Program Job Summary: The Bindery Operator is responsible for setting up and operating bindery equipment such as saddle stitchers, cutters, and folders. This role requires strong mechanical skills, attention to detail, and the ability to assist team members as needed. Essential Job Duties & Responsibilities: • Set up and fine-tune machine pockets to minimize drops and stoppages., • Adjust and monitor machine calipers to ensure product quality., • Set up, adjust, and repair stitcher heads for smooth operation., • Change and adjust trimmer knives as required., • Inspect and identify machine parts that need replacement., • Setup, monitor, and maintain inkjet systems when applicable., • Continuously monitor product quality and adjust machines accordingly., • Perform general maintenance and lubrication of machines., • Maintain cleanliness and organization of the bindery area., • Ensure compliance with safety procedures, including PPE usage, ergonomics, and chemical hazard protocols., • Maintain accurate production charts and records., • Provide guidance to machine crew during production and downtime., • Assist supervisors with evaluations and provide feedback as needed., • Perform other duties as assigned. Physical Requirements: • Ability to lift up to 50 pounds occasionally, up to 20 pounds frequently, and up to 10 pounds constantly., • Frequent reaching, standing for long periods, walking, lifting, grasping, and repetitive hand/wrist movements. Qualifications & Skills: • Strong mechanical aptitude and troubleshooting abilities., • Effective communication skills., • Organizational skills., • Team collaboration skills., • Computer skills. Steven Label is an equal-opportunity employer. We do not discriminate on the basis of race, color, religion, creed, national origin or ancestry, sex, age, physical or mental disability, veteran or military status, genetic information, sexual orientation, gender identity, marital status, military status, order of protection status, or any other legally recognized protected basis under federal, state, or local law. 2nd Shift: Mon - Thur 12:45 PM - 11:15 PM

Job Description NOW HIRING: Nurse Practitioner (NP) or Physician Assistant (PA) Location: Temecula, CA (occasional cross-coverage in San Marcos) Clinic: BFF Medical Wellness Clinic Integrative, preventive medicine first. BFF Medical Wellness Clinic delivers proactive, root-cause care that blends functional medicine, hormone optimization, metabolic health, and device-based aesthetics to prevent disease, improve longevity, and elevate quality of life. We are hiring a high-performing, adaptable clinician who learns quickly on the job, executes with excellence, and thrives in a results-driven environment. Position Summary We seek an NP or PA with at least 3 years of clinical experience to provide comprehensive, longitudinal care across service lines including, but not limited to: hormone optimization (BHRT, TRT), medical weight loss and metabolic health, peptide therapy, device-based aesthetic medicine, and holistic lifestyle coaching. Core Responsibilities Hormone Optimization * Evaluate and manage Bioidentical Hormone Replacement Therapy (BHRT) and Testosterone Replacement Therapy (TRT). * Order/interpret labs; design and adjust individualized protocols; track outcomes. * Educate patients on physiology, expectations, and long-term prevention. Medical Weight Loss & Metabolic Health * Conduct metabolic and lifestyle assessments; create personalized, lab-informed plans. * Prescribe and monitor GLP-1 therapy (e.g., semaglutide). * Address root contributors such as insulin resistance and chronic inflammation. Peptide Therapy * Prescribe and monitor peptides including, but not limited to agents supporting hormone balance, metabolic function, tissue repair, recovery, and performance. * Maintain current knowledge of evolving protocols and safety considerations. Device-Based Medical Aesthetics (experience preferred) * Perform non-invasive procedures including, but not limited to: * Diode laser hair removal * IPL (Intense Pulsed Light) and DPL (Dynamic Pulsed Light) * CO₂ laser resurfacing for texture and photodamage * Ensure rigorous safety, documentation, and patient education. * Note: We do not offer neurotoxins or dermal fillers. Functional & Holistic Wellness * Apply systems-based, preventive frameworks to fatigue, weight resistance, gut issues, and hormonal dysregulation. * Integrate nutrition, supplementation, sleep, stress, and activity prescriptions. * Coordinate care within a physician-led, multidisciplinary team. What Success Looks Like * You are curious, ask incisive questions, and translate new knowledge into action quickly. * You are adaptable under changing protocols and technologies. * You are accountable, organized, and consistently deliver measurable patient outcomes. * You build trust through clear communication and education. Required Qualifications * Active California NP or PA license. * 3+ years of clinical practice. * Demonstrated interest or experience in any of the following: BHRT/TRT, metabolic/weight management, peptide therapy, device-based aesthetics, or functional medicine. * Excellent clinical judgment, communication, and follow-through. * Comfort working both independently and collaboratively. What We Offer * Competitive compensation with performance incentives. * Structured training and mentorship in hormone health, peptide therapy, metabolic care, and aesthetic platforms. * A growth-oriented culture focused on prevention, outcomes, and patient experience. * Advancement opportunities within a multi-location wellness practice.

Job DescriptionBFF Medical Wellness Clinic About BFF BFF Medical Wellness Clinic is a membership-based, functional medicine and aesthetics practice focused on proactive health, body composition, and a concierge-level patient experience. We’re a young, growing clinic with high standards, a warm vibe, and real opportunities to grow with us. Role Snapshot This is the ultimate BFF Esthetician role—equal parts skin expert, patient educator, and calm clinic operator. You’ll deliver safe, effective treatments within California esthetician scope, guide patients through their wellness and aesthetics journey, and keep the front-to-back flow smooth and on time. You’ll confidently explain our membership model, help patients select the right plans and series, and support a consistent, brand-forward experience. What You’ll Lead * Patient Experience & Flow: Greet, consult, and prepare patients; maintain a reassuring, polished tone; keep visits on time and rooms turned efficiently. * Esthetic Services — Performed (within esthetician scope): * Customized facials and post-treatment skin care * Gentle chemical peels * Body contouring/cavitation/RF (per clinic protocols) * Lymphatic device massage * Treatment-room setup, sanitation, and device checklists * Light-Based Services — Educated & Coordinated (not performed by the Esthetician): * Laser Hair Removal — candidacy, expectations, pre/post care, membership/series options * IPL (Intense Pulsed Light) — goals, timelines, aftercare, and plan fit * DPL (Dynamic Pulsed Light) — benefits, process, and coordination steps In California, these light-based services are medical procedures performed by licensed medical professionals. Your role is to educate thoroughly and coordinate next steps per clinic protocols. * Education & Membership Guidance: Translate goals into treatment plans; clearly explain membership benefits, series, timelines, and home-care routines. * Detail-Driven Documentation: Accurate notes, photos (with consent), pre/post instructions, product recommendations, and follow-up scheduling. * Retail & Results: Curate home-care regimens aligned to treatment plans; track outcomes and patient satisfaction. * Safety & Standards: Impeccable sanitation, adherence to HIPAA and clinic policies; escalate concerns promptly. * Brand Presence: Support review invites, before/after galleries (consented), event days, and a beautiful, on-brand treatment environment. You’ll Thrive Here If You Are * Confident & Composed under pressure * An Exceptional Communicator with clear verbal ability and an encouraging bedside manner * Adaptable & Quick-Learning with new devices, protocols, and membership workflows * Detail-Obsessed Finisher who closes loops and keeps charts pristine * Curious & Growth-Oriented, seeking feedback and expanding scope as the clinic scales * Passionate About Wellness and whole-person skin health Qualifications (California) * Current California Esthetician License (Board of Barbering & Cosmetology) * Experience in med spa/clinic or high-touch aesthetics strongly preferred * Comfortable performing the services listed under “Performed” and educating/coordinating light-based services (LHR, IPL, DPL) with the medical team * Strong consultative skills (intake, goal-setting, plan building, home-care coaching) * Tech-comfortable: EMR/scheduling, online forms, digital payments, texting platforms * Bilingual (English/Spanish) is a plus Growth & Opportunity * Skill Building: Structured training on devices and treatment planning, plus membership education * Scope Expansion: Opportunities to own initiatives (events, reviews, before/after content, inventory cues, onboarding) * Career Pathing: Potential to advance into lead esthetician or treatment coordinator roles as we grow Success Metrics * On-time starts and efficient room turns * High patient satisfaction and sustained series/membership engagement * Accurate documentation and zero missed follow-ups * Visible skin-health progress with aligned home-care adherence Schedule & Compensation * Schedule: Full-time; one evening and occasional Saturdays preferred * Compensation: Competitive hourly, commensurate with experience * Perks: Training and mentorship, supportive team culture, staff rates on select services

Job Description Community health is about more than just vaccines and checkups. It’s about giving people the resources they need to live their best lives. At Neighborhood, this is our vision: a community where everyone is healthy and happy. We’re with you every step of the way, with the care you need for each of life’s chapters. At Neighborhood, we are Better Together. As a private, non-profit 501(C) (3) community health organization, we serve over 500,000 medical, dental, and behavioral health visits from more than 100,000 people annually. We do this in pursuit of our mission to improve the health and happiness of the communities we serve by providing quality care to all, regardless of situation or circumstance. Since 1969, our employees have been making this mission a reality. Regardless of the role, our team focuses on being compassionate, having integrity, being professional, always collaborating, and consistently going above and beyond. If this sounds like an organization you would like to be a part of, we would love to meet you. The Speech Language Pathologist works to support the mission and vision of Neighborhood Healthcare by providing speech language pathology services for Participants. This role will design and develop Participant care plans based on speech language pathology assessments. Clinical supervision for this role is provided within the manager’s licensed scope of practice, while designated discipline-specific leads or clinical coordinators provide clinical oversight for services outside the manager’s licensed discipline. This position is part-time, 20 hours a week. Must be available to work between the hours of M-F, 9am-2pm. Schedule within these core hours is flexible. Responsibilities • Screens and evaluates participants for speech, language, cognitive-communication, voice, swallowing, and hearing needs according to the American Speech Language Hearing Association guidelines., • Develops and implements individualized plans of care to improve or restore communication, cognitive-linguistic function, and swallowing abilities; promotes independence; and support Participants in achieving their highest functional level., • Evaluates the effectiveness of treatment plans and modifies goals, as needed, • Communicate with staff regarding Participants’ needs in areas of communication strategies, dietary texture modifications, safe swallowing practices, and cognitive support, as needed., • Communicate with family members and caregivers to ensure that therapeutic recommendations—such as communication aids, diet modifications, and assistive technology—are clearly understood, feasible, and can be appropriately supported at home., • Makes recommendations and instructs Participants and caregivers on the use and maintenance of augmentative and alternative communication (AAC) devices and compensatory strategies to promote communication and safety., • Identifies malfunctioning AAC or adaptive equipment and takes appropriate action to repair or replace items., • Ensuring that device trials, education, and loan documentation are accurately recorded per department policy., • Collaborate, as indicated, with skilled nursing facility and assisted living staff regarding the communication, cognitive, and swallowing needs of Participants., • Provides speech language therapy targeting areas such as but not limited to expressive and receptive language, articulation, cognitive-linguistic skills, dysphagia management, and voice therapy., • Provides written home programs, visual support, and caregiver education to facilitate carryover of therapy goals outside of sessions., • Makes home and or community visits to perform evaluations and conduct educational sessions as needed and indicated in the plan of care; documents activities and Participant/caregiver responses in the Participant’s chart., • Delegates components of therapy or supportive tasks to SLP Assistants (if applicable), consistent with the California Speech-Language Pathology Practice Act and ASHA supervision standards., • Discusses plan of care with the multi-disciplinary team as needed to integrate services with overall plan of care for Participants., • Provides guidance to staff and team members that is consistent with state laws and company policies, • Documents all procedures performed in the Participant’s medical chart according to NHC policies and procedures; including but not limited to: Assessment, care plan, daily encounter notes, education, discharge summary., • Keeps abreast of all regulations and standards to ensure compliance with orders or directives issued by duly constituted government and regulatory agencies (PACE, CMS, DHCS), • Participates in training programs for staff and caregivers Education/Experience • Graduate of a Master of Speech Language Pathology program, accredited by the American Speech Language Hearing Association, required, • Valid CA Speech Language Pathology License, required, • Valid BLS certification from approved American Health Association provider required upon hire, • Excellent verbal and written communication skills, including superior composition, typing and proofreading skills, • Ability to interpret a variety of instructions in written, oral, diagram, or schedule form, • Knowledgeable about and experience with principles and methods for treatment and rehabilitation of functional impairments, • Ability to establish and maintain therapeutic relationships and to participate in a multi-cultural, multidisciplinary team, • Ability to successfully manage multiple tasks simultaneously, • Excellent planning and organizational ability, • Ability to work as part of a team as well as independently, • Ability to lift/carry 25 lbs./weight Compensation Disclosure: The posted salary range reflects the designated pay grade for this position. While this range represents the broader classification of the role, actual compensation will be based on several factors, including but not limited to: the candidate’s overall knowledge, skills, and experience, market data and industry benchmarks, internal equity within the organization, Budgetary considerations and organizational needs. As a result, placement within the range is not guaranteed, and the full pay grade range may not be utilized.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year, • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. Our location in Temecula, CA currently has an opportunity for a Manufacturing Engineer. The Opportunity This position works out of our Temecula, CA location in the Abbott Vascular Division. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. What You’ll Work On Provides support to the manufacturing organization by developing new processes and optimizing existing processes. Utilizes six sigma, lean, design control, and validation principles to create robust processes. This role requires completion of steps from process conception, design, validation, and implementation to manufacturing. Interfaces with Manufacturing, Quality and Research and Development organizations to integrate new processes into the existing manufacturing areas. WHAT YOU’LL DO Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Monitors performance of manufacturing lines, equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and other organizational functions to integrate new products or processes into the existing manufacturing area. Core Job Responsibilities Responsible for compliance with applicable Corporate and Divisional Policies and procedures. 1. Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate findings.;, 2. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.;, 3. Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized leader or authority in an area of specialization and applies this knowledge in leadership roles in the company.;, 4. Incorporates business policies and procedures into task completion. Understands the business needs of the company, and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends.;, 5. Cultivates internal and external network of resources to complete tasks. Serves has a resource in the selection orientation and training of new engineers and employees. May lead a project team, determining goals and objectives for the projects. Mentors employees by sharing technical expertise and providing feedback and guidance.;, 6. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or manufacturing interpretations and advice on significant matters. Acts as a spokesperson to customers on business unit current and future capabilities., 7. Applies manufacturing concepts like LEAN manufacturing, push versus pull, 5S, etc. (Supervision Received) Work is monitored with autonomy. Follows specific, detailed instructions Position Accountability / Scope (Influence/Leadership) Begins developing a network of internal resources to facilitate completion of tasks. Individual influence is typically exerted at the peer level.; (Planning/Organization) Completes daily work to meet established schedule with guidance from supervisor on prioritization of tasks.; (Decision Making/Impact) May exercise authority within pre-established limits and approval. Failure to achieve results can normally be overcome without serious effect on schedules and programs. EDUCATION AND EXPERIENCE YOU’LL BRING Minimum Education: Bachelor's degree plus 2-5+ years of related work experience with a basic understanding of specified functional area, or an equivalent combination of education and work experience. Minimum Experience / Training Required: (Technical/Business Knowledge (Job Skills)) Basic technical knowledge of concepts, practices and procedures. Limited understanding of business unit/group function. Will perform this job in a quality system environment adhering to medical device standards. Failure to adequately perform tasks can result in noncompliance with governmental regulations.; (Cognitive Skills) Learns to use professional concepts and company policies and procedures to solve routine problems. Works on problems of various degrees scope/ complexity. Minimal independent decision making. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO, • An excellent retirement savings plan with a high employer contribution, • Tuition reimbursement, the ___ student debt program, and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our Temecula, CA location in the Abbott Vascular division. The Associate Manufacturing Engineer will serve as the primary manufacturing engineer supporting operations in Abbott Vascular Temecula. The individual performing this role will have to integrate with the team supporting the manufacturing line including but not limited to: the line supervisor, Quality Engineer and operators to address the opportunities found in their assigned manufacturing line. They will be accountable for quality, safety, product output and yield for their assigned manufacturing line. This person may also have a contributing role as a sustaining engineer for the department. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease. WHAT YOU'LL DO: • Responsible for the daily support to the manufacturing activities in order to meet established goals for safety, quality, cost, and production., • Maintains systems that support the monitoring of key performance indicators such as yield, nonconforming material or lead time. If indicators show an adverse trend, works with the functional team to plan and implement appropriate changes., • Works with line support team (QC Supervisor, Mfg Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance is present, determine initial bracketing and containment, and support generation of ER, if needed., • Prepares product and process reports by collecting, analyzing, and summarizing information and trends., • Responsible for product/process knowledge and understanding of basic cause and effect of line and process changes. Understands potential risk related to product nonconformance. Has knowledge and expertise on product requirements and specifications., • Stays current. Keeps aware of the changing technical and competitive environment as it relates to the business; establishes a means of keeping abreast with technology on own engineering area and sharing with co-workers, e.g., stays current in product/process innovations in areas of expertise., • Assures that production lines output meet the specifications of the product., • Has clear criteria of conforming/ non-conforming product and the on-line and reliability test methods used for verifying product conformance., • Maintains manufacturing documentation such as manufacturing process instructions, lot history records, bill of materials., • Investigates, conducts test or experiments, gathers data, performs preliminary analysis, and reports findings. Prepares and communicates recommendations and respective action plans., • Leads root cause analysis efforts for basic/simple manufacturing events, utilizing DMAIC model and A3s. Supports CAPA (Major) investigations with data gathering and analysis as needed., • Line support representative for related projects such as yield improvements, Cost Improvement Project “CIP's”, productivity, quality and safety. Responsible for providing the line with related Engineering solutions, such as tooling (TLTs) and Manufacturing Aids ( from idea definition to implementation). Responsible for simple continuous improvement projects development and execution. Evaluates ideas from the Localized Process Improvement “LPI” program for potential implementation. Reviews existing layouts and standards and creates a proposed design, e.g., uses appropriate tools to complete design drawing/layout; designs a simple piece of equipment or system; modifies an existing design to meet a new need., • Performs validation activities for new or existent production lines, meeting regulatory requirements. This includes equipment, process, product and test method validations., • Support maintenance technicians and supervisors in equipment availability issues. Review equipment work order completion and performs product impact analysis in order to release equipment for commercial manufacturing use., • Assists in the training of personnel required for the operation of equipment., • Responsible for working with Quality Assurance “QA” counterpart and determining quality impact of Out-of-Tolerance “OOT“ situations., • Responsible for execution of line-related change management (material, equipment and process changes). Responsible for change order “CO” and simple Change Request “CR” generation related to changes impacting the manufacturing line., • Complies with all regulations and standards for Quality, Environment, Health, Safety and Energy (EHS&E) Global Policies, Abbott Engineering Standards, and other governance areas as applicable., • Ability to travel approximately 5%, including internationally. Required Qualifications: • Bachelor's Degree, • 1 years related work experience, • Knowledge and proficiency in the application and principles of Manufacturing & Process Engineering. Ability to effectively communicate cross-functionally to assist in resolving Quality/Engineering issues., • Excellent written, verbal and interpersonal communication skills. Knowledge of common office applications: Word, PowerPoint, Excel. Ability to interact effectively with all employee job levels., • Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail., • Basic understanding of materials, product design, product testing., • Preferred: basic understanding and knowledge of statistics, GD&T, tolerance stack up analysis, Statistical Process Control “SPC”, fundamentals of Design of Experiments “DOE” and problem-solving methodologies Preferred Qualifications • Familiar with the use of various inspections tools including but not limited to: pin gauge, caliper, micrometer, snap gauge, drop gauge, block gauge, optical comparator, vision system, etc. Preferred: experience working in a medical device manufacturing environment such as: extrusion, injection molding, laser cutting, cleaning, passivation, electropolishing, assembly, bonding, packaging, testing, inspection methods, and others., • Experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment., • Experience use of statistical software (ex: Minitab, JMP), six sigma training and/or certification, use of Solidworks (or similar CAD software), MS project, Verification & Validation activities, basic understanding of FDA, Good Manufacturing Practice “GMP” and ISO guidelines. • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___, and on X @AbbottNews. The base pay for this position is $50,000.00 – $100,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Our location in Temecula, CA, currently has an opportunity for a Senior Plastics Engineer. WHAT YOU'LL DO: Responsible for implementing and maintaining the effectiveness of the quality system. The Senior Plastics Engineer is responsible for injection mold life cycle management and ongoing support of injection molded components that are used in Abbott Vascular products. Will serve as both a technical SME for injection molding as well as a project manager for molding projects, working regularly with molding suppliers, operations; supply chain; quality and R&D. Engagement in tactical and strategic activities to support ongoing business objectives, including cost improvement initiatives for molded components; supplier and resin changes; capital replacement strategy for end-of-life tooling. Troubleshoot molding and tooling issues in conjunction with supplier and lead/support internal investigations as needed to resolve. Work closely with molding suppliers to ensure reliable supply of parts. Perform capacity analysis for injection molds and press-side automation and make recommendations for future investment. Must have proven ability to participate in team atmosphere; exhibit and create a sense of urgency and maintain effective working relationships with peers; customers and vendors. Additional responsibilities include, but are not limited to the following: • Requirements gathering; process design and development; tooling design; procurement and qualification., • Concurrent management of multiple projects., • Development of cost estimates for capital and expense projects., • Create and maintain project schedules; oversee cross-functional team activities to achieve program objectives., • Transfer of molds to new suppliers; validation of injection mold tooling and process at new suppliers., • Regularly interact with molding suppliers to meet quality and cost objectives., • Participate on cross-functional teams to investigate and resolve molding issues., • Identify and evaluate potential cost improvement projects through up-cavitation of new molds, press-side automation to reduce labor, combining parts with insert/over molding/two shot molding and resin changes., • Write specifications; design verification/validation protocols and report., • Capacity analysis and long-range planning activities to ensure continuity of supply. Position is responsible for the reliable supply of molded commodities to all sites and customers. Must ensure that all molds are run in compliance with all quality standards and procedures. EDUCATION AND EXPERIENCE YOU’LL BRING: • Bachelors' Degree (Engineering or technical discipline desired) Required; or equivalent experience plus demonstrated competence., • 10+ years technical work experience with 5+ years of plastic injection molding, process engineering support and/or tooling experience, preferably in the medical device industry. At Abbott, you can have a good job that can grow into a great career. We offer: • A fast-paced work environment where your safety is our priority, • Training and career development, with onboarding programs for new employees and tuition assistance, • Financial security through competitive compensation, incentives and retirement plans, • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, • Paid time off, • 401(k) retirement savings with a generous company match Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with a high employer contribution, • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. Our location in TEMECULA, CA currently has an opportunity for a Senior Manufacturing Process Engineer. THIS IS AN ON-SITE DAILY ROLE. MAIN PURPOSE OF ROLE This role will provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to improve production efficiencies, manufacturing techniques and production yields for existing products. This position will design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality. MAIN RESPONSIBILITIES • Manage projects which include new production equipment, process improvements and cost reductions while supporting new product introductions., • Provide guidance to other engineers and technicians., • Additional responsibilities include:, • Provide technical mentorship to engineers and technicians. Conduct Process FMEAs and Process Validations. Improve product quality, labor efficiency, and throughput through the use of Lean manufacturing concepts. Coordinate the design, procurement, build and debug of tooling, machinery and test equipment. Work with Product Development to ensure Design for Manufacturability., • Draft, review or execute verification / validation protocols, identify validation risks and impacts., • Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors., • Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results., • Networks with key contacts outside own area of expertise., • Leads Continuous Improvement activities including Problem Solving Tools, Lean, Six Sigma, Management Operating Systems, Visual Factory, Suggestion Programs and Metric Tracking, • Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements., • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors., • Individual should: Be innovative, resourceful, and work with minimal direction. Have excellent organization, problem solving, communication, and team leadership skills. Work effectively with cross-functional teams. QUALIFICATIONS • Bachelors Degree (± 16 years), • Bachelor’s degree in mechanical, chemical or any engineering or technical field degree. Experience/Background • Minimum 5 years, • 5 years of experience, both overall and any industry-specific experience needed, • Strong analytical, problem solving and project management skills., • Experience in manufacturing engineering experience, medical device experience required., • International manufacturing experience preferred., • Demonstrated leadership capability in team settings., • Six Sigma certification preferred., • Experience working in a broader enterprise/cross-division business unit model preferred., • Ability to work in a highly matrixed and geographically diverse business environment., • Ability to work within a team and as an individual contributor in a fast-paced, changing environment., • Ability to leverage and/or engage others to accomplish projects., • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization., • Multitasks, prioritizes and meets deadlines in timely manner., • Strong organizational and follow-up skills, as well as attention to detail. WHAT WE OFFER : At Abbott, you can have a good job that can grow into a great career. We offer: • A fast-paced work environment where your safety is our priority, • Training and career development, with onboarding programs for new employees and tuition assistance, • Financial security through competitive compensation, incentives and retirement plans, • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, • Paid time off, • 401(k) retirement savings with a generous company match, • The stability of a company with a record of strong financial performance and history of being actively involved in local communities Learn more about our benefits that add real value to your life to help you live fully: ___ Learn more about our benefits that add real value to your life to help you live fully: Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.

Job Title: Medical Device Assembler.Shift: 05:00 to 06 : 00AM To 01:30 to 02:30 PM.This position is responsible for the production of high quality medical devices within a manufacturing cell.Working under close supervision, may perform a combination of assembly, repair, and test operations on pacema

Medical, Dental, and Vision / PTO / 401k Match - As a Device Support Specialist at Modivcare, you will: Troubleshoot and resolve technical issues for customers using Modivcare devices; Provide excellent customer service by assisting with inquiries and concerns related to device usage; Educate custom

Aerotek - JobID: JP-005588335 [Production Operator / Assembly Line Worker] As an Assembler at Aerotek, you'll: Perform assembling, loading, and unloading of parts; Be involved in a fast-paced environment and many overtime opportunities; Perform other duties as assigned.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Job Title Supplier Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career of which you dream., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity We are seeking a Supplier Quality Engineer to work at our Temecula, CA location in our Vascular division. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. Our location in Temecula, CA currently has an opportunity for a Supplier Quality Engineer. The Supplier Quality Engineer is responsible for conducting supplier audits, qualifying new suppliers, and monitoring the performance of current suppliers. Must be able to handle supplier audit situations and interactions in a tactful, professional and effective manner. WHAT YOU’LL DO • Supplier Audits Develop and execute to a supplier audit schedule per current requirements., • Develop audit plans and associated supplier communications., • Approve and monitor Supplier CAPA plans and activities to closure including objective evidence of effectiveness., • ISO lead auditor certification or equivalent is preferred., • Qualify and then monitor supplier performance Per current requirements perform activities that will qualify new suppliers and monitor current supplier base to ensure the status of the suppliers is correct., • Work with suppliers as needed to ensure their performance is acceptable per site requirements., • Work with Design and Development, Manufacturing, Purchasing and IQA when qualifying and monitoring supplier performance., • CAPA Through the supplier audits and internal issues with supplier product, issue SCARs for supplier corrective/preventive action activities., • Analyze Supplier information and present supplier metrics to appropriate CAPA boards., • Demonstrated writing and communication skills are required for this position., • A thorough understanding of the ISO/QSRs and the ability to apply that knowledge with an understanding of business operations to achieve regulatory compliance is needed., • Must be able to explain audit results and influence other's understandings of audit observations in a tactful and professional manner., • Knowledge of regulations and standards affecting in vitro diagnostic's device manufacturing. EDUCATION AND EXPERIENCE YOU’LL BRING Required Experience • Associates Degree, • Minimum 1 year related experience in technical or other QA related positions in a regulated industry is preferred. Preferred Experience • 5 years experience Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution., • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity The Sr, Quality Engineer position works onsite of our Temecula, CA location in the Abbott Vascular Division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. • Lead on-time completion of Design Control Deliverables, • Create and ensure on-time execution of Quality Plans for internal development, OEM-based, Clinical Product Development (CPDP), and design change projects, • Accountable for Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation & resolution activities, • Lead Risk Management activities from product Concept through Commercialization, • Lead design test and inspection method development, and lead method validation activities, • Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps, • Support manufacturing process development & qualification for new product commercialization and product changes What You’ll Work On • Support/lead and ensure internal & external audit responses, • Support/lead and ensure on time product re-certifications, • Support and ensure the establishment of objective, measurable, discrete, and verifiable customer and product requirements, • Support and ensure objective component specification definitions, supplied component sampling plan development, and vendor qualifications, • Accountable for development, execution and analysis of biocompatibility and sterilization qualifications, • Complete Document Change Request Reviews in a timely and objective manner, • Develop and lead other team members., • Perform other duties and responsibilities as assigned by management., • Support/lead all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements., • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors., • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Required Qualifications • Bachelors Degree in Engineering or Technical Field ☒ an equivalent combination of education and work experience, • Minimum 5 years Previous Quality engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, and ISO 13485, • Solid communication and interpersonal skills. Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner., • Advanced computer skills, including statistical/data analysis and report writing skills. Preferred Qualifications • Masters Degree Preferred, • Prior medical device experience preferred. ASQ CQE certification preferred. Design for, • Six Sigma and Critical to Quality training and experience preferred., • Experience working in a broader enterprise/cross-division business unit model preferred., • Ability to work in a highly matrixed and geographically diverse business environment., • Ability to work within a team and as an individual contributor in a fast-paced, changing, • Ability to travel approximately 10%, including internationally. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews. The base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with a high employer contribution, • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. Our site in Temecula, CA is currently looking for a Quality Engineer. THIS POSITION IS ON-SITE DAILY REQUIRED. NO RELOCATION ASSISTANCE IS AVAILABLE FOR THIS POSITION. WHAT YOU'LL DO: Perform Abbott Vascular quality engineering activities by developing and maintaining data integrity and cybersecurity policy, standards, applications, systems, etc. Work closely with R&D, Equipment Engineering, Quality Engineering and IT on risk identification and mitigation activities. Facilitate cross functional team collaboration to achieve data management goals. MAIN RESPONSIBILITIES • Support project planning and perform assessments and mitigations with cross functional teams. Develop and manage training programs including training material and training audience. Track and report metrics., • Provide support to internal and external audits. Manage relevant audit findings and CAPAs., • Continuously improve processes to align with current and emerging regulatory and customer requirements and best industry practices. Collaborate with AV key stakeholders, Abbott corporate functional groups and other Abbott business units., • Responsible for compliance with applicable Corporate and Divisional Policies and procedures., • Independently, or lead a project team to, identify, plan and conduct medium-size assigned projects requiring a combination of conventional and custom risk-managed execution plans and investigations. manages multiple often concurrent projects., • Lead technical projects with inter-coordinating elements where problem resolution may involve the application of new methods and/or approaches and may require consideration of impact with other system components and/or users., • Lead and/or participate on cross-functional teams to support organizational goals., • Responsible for completing documentation in a timely manner and in accordance with business standards., • Serve as a subject matter expert (SME) on a subset or select subsets of a project's technical matters. may interface with external firms or agencies., • Responsible for implementing the effectiveness and maintaining compliance of the Quality System. (e.g. compliance with internal procedures and FDA, BSI regulations etc)., • Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures., • Interprets and executes policies that affect work processes and personnel within the assigned organizational unit., • Contributes to the development of operational policies and procedures that affect personnel within the assigned organizational unit., • Assists with evaluating project costs., • Identifies, develops and implements processes to improve department performance., • Implements improvements to Quality Systems and tools by directing personnel to gather data on existing quality tools, identify weaknesses, and research/select new tools based on findings., • Ensures sustaining support of Quality System and regulatory compliance by individually working quality system issues and by delegating project work for maintaining quality system capability. QUALIFICATIONS Experience/Background Minimum Education Bachelor's degree (Engineering/Life Sciences) AND 2-5+ years of related work experience with a strong understanding of specified functional area, or an equivalent combination of education and work experience. Experience Minimum 2-5+ years. Requires 2-5+ years of quality experience to develop the competence to meet the skills and responsibilities of the position. • Strong technical knowledge and application of concepts, practices and procedures., • Ability or aptitude to work on problems that are complex in scope where analysis of situations or data involves multiple competing factors., • Ability to form and develop interpersonal, professional relationships., • Display socially and professionally appropriate behavior., • Ability to work independently and in groups., • Ability to work cross-functionally., • Demonstrated initiative and problem-solving skills., • Critical-thinking skills., • Ability and aptitude to use various types of databases and other computer software., • Ability to prioritize., • Strong organizational and project management skills., • Demonstrated competency with financial systems and in fiscal controls., • Ability to quickly gain knowledge, understanding or skills and is willing to learn. WHAT WE OFFER : At Abbott, you can have a good job that can grow into a great career. We offer: • A fast-paced work environment where your safety is our priority, • Training and career development, with onboarding programs for new employees and tuition assistance, • Financial security through competitive compensation, incentives and retirement plans, • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, • Paid time off, • 401(k) retirement savings with a generous company match, • The stability of a company with a record of strong financial performance and history of being actively involved in local communities Learn more about our benefits that add real value to your life to help you live fully: ___ Learn more about our benefits that add real value to your life to help you live fully: Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Job Title ECHO Administrator Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career of which you dream., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity We are seeking an ECHO Administrator to work at our Temecula, CA or St. Paul, MN location in our Vascular division. The ECHO Administrator will support the ECHO complaint handling system used by Abbott Vascular and Structural Heart, including automation. Maintain user access and training requirements for the system. Maintain internal data to the system. Support business with troubleshooting and tool creation in collaboration with the run team. Supporting changes to the system in collaboration with BTS. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. WHAT YOU’LL DO • Maintain user access and training requirements for the system., • Maintain business data in the system (contacts, accounts, part/lot, drug lot, GUIDID information, Device and patient codes, reporting details), • Creating / supporting refreshable queries that are used as business tools and for automation, • Support business with troubleshooting in collaboration with the run team., • Work with business to identify low impact changes and implement with the run team., • Supporting changes and upgrades (driven by regulatory requirements, platform upgrades, business needs) to the system in collaboration with BTS., • Work with PPG teams to understand ideas for improvement and translate these needs into User Requirements and Functional Requirements and draft / execute UAT, • Work with business to identify business deliverables and implementation timing associated with system changes and coordinate training and execution, • Cultivates a wide range of internal networks and begins to develop an external network of resources to facilitate completion of tasks., • May demonstrate basic project management skills by acting as a project lead on small, well-defined projects., • Provides guidance to less experienced staff., • Influence exerted at peer level and occasionally at first levels of management., • Plans, organizes, and prioritizes own daily work routine to meet established schedule., • Exercises authority and judgment within defined limits to determine appropriate action., • Failure to achieve results or erroneous decisions or recommendations may cause delays and may result in the allocation of additional resources., • Will perform this job in a quality system environment., • Failure to adequately perform tasks can result in noncompliance with governmental regulations., • Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors., • Exercises judgment within defined procedures and practices to determine appropriate action., • Has a general knowledge of technical alternatives and an understanding of their impact on the systems environment. EDUCATION AND EXPERIENCE YOU’LL BRING Required Experience • Bachelor’s Degree in a related study or an equivalent combination of education and work experience., • Minimum 2-5 years of related work experience with a good understanding of specified functional area., • Working knowledge and application of business concepts, procedures and practices. Preferred Experience • Familiar with Excel for use in data transformation, v-lookup and pivot tables., • Coding experience e.g. Python or C++, • Complaint handling process experience, • Experience in a highly regulated environment Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Job Title Quality Assurance Manager Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career of which you dream., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with high employer contribution, • Tuition reimbursement, the ___ student debt program and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position will work out of our Temecula, CA location in our Vascular Division. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease. THIS IS AN ONSITE DAILY REQUIRED POSITION. Manages experienced QA professionals who exercise latitude and independence in their assignments. Often heads one or more sections/functions or a small quality department. Interprets policies , processes and procedures that may affect sections and subordinate work units. Assignments are defined in terms of activities and objectives. Work is reviewed for adequacy in meeting objectives. MAIN RESPONSIBILITIES • Interacts frequently with internal personnel and outside representatives at various levels., • Routinely operates as a liasion with customers and suppliers., • Participates and presents at meetings with internal and externals representatives., • Interaction typically concerns resolution of operational and scheduling issues., • Responsible for managing one or more quality system elements/functions as defined in the site Quality Manual., • Implements the quality plan in accordance with the quality objectives/goals and maintains the effectiveness of the quality system., • Recommends staffing and other necessary resource requirements needed to achieve business goals and compliance requirements., • Resolves project team issues with minimal oversight., • Responsible for ensuring that functional areas of responsibility have adequate training programs for adhering to all safety requirements and business EHS goals., • Manage the development and implementation of quality goals., • Emerging leader that demonstrates strong leadership competencies., • Decision making that has impact on work processes and outcomes, that could cause serious delays and considerable expenditure of a additional time, human recourses and funds., • May define and implement critical parameter for design control and related systems throughout the product lines., • May maintain effective Quality Metrics and define and execute activities to resolve decreases in performance., • May support NPD at all stages of development process and ensure its compliance to FDA and other agencies. EDUCATION AND EXPERIENCE YOU’LL BRING: Required Qualifications • Bachelors Degree in a scientific or technical discipline or an equivalent combination of education and work experience, • Masters Degree Preferred, • Minimum 5 years, • 5-7 years of experience in function or related field. 2 years of direct supervisor experience., • Medical Device Experience, • Must have demonstrated solid knowledge and experience in discipline., • Demonstrated leadership competencies., • Considered a Subject Matter Expert., • Demonstrated ability to lead cross-functional projects., • Flexibility, strong problem solving skills, excellent written and oral communication skills, solid organizational ability , negotiations skills with ability to drive cross functional teams., • Emerging leader that demonstrates strong leadership competencies. Preferred Qualifications • Understanding of R&D and Product Development, a plus, • Regulatory Compliance, a plus Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $97,300.00 – $194,700.00. In specific locations, the pay range may vary from the range posted.

Job Description Medical Device Assemblers – Temecula, CA | $19.25–$20.75/hr. | 1st Shift • Join a leading healthcare company and help build life-saving cardiovascular devices!, • Assemble medical devices in a cleanroom environment, • Use microscopes, hand tools, syringes, and bonding techniques, • Perform inspections, tests, and packaging, • 6+ months of manufacturing experience, • High School Diploma or GED, • 1st Shift: 5am/6am–1:30pm/2:30pm (Monday–Friday+ Overtime on Saturdays), • Operator I: $19.25/hr., • Operator II: $20.00/hr., • Be part of a respected healthcare brand, • Work on impactful projects in a professional, cleanroom setting Pay and Benefits The pay range for this position is $19.25 - $22.83/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Temecula,CA. Application Deadline This position is anticipated to close on Oct 12, 2025. About Aerotek: We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Verification & Validation Engineer in a fast-growing medical device company, ideally focused on specialty medical practices. The focus will be mechanical / medical device testing and V&V protocols through simulated use studies in partnership with surgeons. Solid understanding of how different areas

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A small, high-growth medical device company is adding a strategic marketing role to their team. Youll work in cross-functional teams with marketing, sales, medical affairs, regulatory and other departments. Experience working with surgical med devices is a must, spine, orthopedic or trauma product e

Verification & Validation Engineer in a fast-growing medical device company, ideally focused on specialty medical practices. The focus will be mechanical / medical device testing and V&V protocols through simulated use studies in partnership with surgeons. Solid understanding of how different areas

A small, high-growth medical device company is adding a strategic marketing role to their team. You’ll work in cross-functional teams with marketing, sales, medical affairs, regulatory and other departments. Experience working with surgical med devices is a must, spine, orthopedic or trauma produc

Director, Product Management (Medical Device). Marketing experience in start-up medical device company preferred. Product Management, Manufacturing, Medical Device, Orthopedics, Neuro or Spine Surgery, People Management, Marketing, Global.

A small, high-growth medical device company is adding a strategic marketing role to their team. Youll work in cross-functional teams with marketing, sales, medical affairs, regulatory and other departments. Experience working with surgical med devices is a must, spine, orthopedic or trauma product e

Director, Product Management (Medical Device). Marketing experience in start-up medical device company preferred. Product Management, Manufacturing, Medical Device, Orthopedics, Neuro or Spine Surgery, People Management, Marketing, Global.

Verification & Validation Engineer in a fast-growing medical device company, ideally focused on specialty medical practices. The focus will be mechanical / medical device testing and V&V protocols through simulated use studies in partnership with surgeons. Solid understanding of how different areas

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Description Medical Device Sales - Paid Internship Looking for a rewarding and lucrative career in the medical sales industry? Our paid Internship may be the right path for you! Here are just some of the reasons a career in Orthopaedic Surgical Sales is fulfilling: Average entry level income of over

We’re looking for enthusiastic, self-driven, individuals to assist existing and prospective clients within our organization.This position will work with multiple clients throughout the day providing outstanding service and product knowledge.Distributes all benefit enrollment materials and

Description Medical Device Sales - Paid Internship Looking for a rewarding and lucrative career in the medical sales industry? Our paid Internship may be the right path for you! Here are just some of the reasons a career in Orthopaedic Surgical Sales is fulfilling: Average entry level income of over

We’re looking for enthusiastic, self-driven, individuals to assist existing and prospective clients within our organization.This position will work with multiple clients throughout the day providing outstanding service and product knowledge.Distributes all benefit enrollment materials and

Description Medical Device Sales - Paid Internship Looking for a rewarding and lucrative career in the medical sales industry? Our paid Internship may be the right path for you! Here are just some of the reasons a career in Orthopaedic Surgical Sales is fulfilling: Average entry level income of over

We’re looking for enthusiastic, self-driven, individuals to assist existing and prospective clients within our organization.This position will work with multiple clients throughout the day providing outstanding service and product knowledge.Distributes all benefit enrollment materials and

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We’re looking for enthusiastic, self-driven, individuals to assist existing and prospective clients within our organization.This position will work with multiple clients throughout the day providing outstanding service and product knowledge.Distributes all benefit enrollment materials and

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We Don't Follow Trends, We Create Them.For over 75 years, Ashley Furniture has been the largest home furnishings manufacturer, transforming homes worldwide.With our customer base continuously growing, we are expanding our reach by opening more stores to meet the increasing demand.Our dedication to q

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We Don't Follow Trends, We Create Them.For over 75 years, Ashley Furniture has been the largest home furnishings manufacturer, transforming homes worldwide.With our customer base continuously growing, we are expanding our reach by opening more stores to meet the increasing demand.Our dedication to q