• Senior Regulatory Project Manager

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our ... etc.) within the business units to support the total product lifecycle. **Job Responsibilities:** _(Primary Duties, Roles, and/or Authorities)_ Responsibilities… more
    BD (Becton, Dickinson and Company) (09/13/25)
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  • Sr Packaging Engineer I

    Gilead Sciences, Inc. (Foster City, CA)
    …is essential for developing packaging solutions for combination products, device -integrated therapies, and temperature-sensitive and conventional dosage forms. The ... compliance, and cross-functional collaboration to ensure packaging systems meet product , patient, and global regulatory requirements. **Specific Job Requirements** +… more
    Gilead Sciences, Inc. (09/06/25)
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  • Medical Assembler/Cleanroom Assembler

    Aerotek (San Diego, CA)
    …years of previous assembly/packaging experience. + Experience in a regulated medical device manufacturing or pharmaceutical environment is strongly preferred. ... and meet unscheduled peaks in workload to ensure timely product release and avoid back orders. **Responsibilities** + Collaborate...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Aerotek (09/28/25)
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  • Medical Assembler

    Aerotek (Buffalo Grove, IL)
    **Now Hiring!** EKG Machine Assemblers - Medical Device Manufacturing **Location:** Buffalo Grove, IL **Shifts Available:** + Morning Shift: 5:45 AM - 2:00 PM ... + Conduct visual inspections to identify defects and ensure product quality + Operate basic hand and power tools...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Aerotek (09/19/25)
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  • Program Development Assoc Manager

    Zimmer Biomet (Indianapolis, IN)
    …4+ years experience of field support, engineering, or other customer facing function with a medical device company preferred OR + BS in Engineering with 5+ years ... a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer...support, engineering, or other customer facing function with a medical device company OR + A minimum… more
    Zimmer Biomet (09/12/25)
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  • Director of Validation

    Jabil (Hunt Valley, MD)
    …Director of Validation will lead all validation activities across pharmaceutical and medical device manufacturing operations with a strong focus on ... scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including validation of facilities,… more
    Jabil (09/11/25)
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  • Document Control Manager

    Fujifilm (Santa Ana, CA)
    …ISO 14971, Brazilian GMPs, Health Canada MDR, Australian Medical Device regulations and regulatory requirements for product registrations where products ... **A minimum of five (5) years of Quality Assurance and or Document Control in a medical device manufacturer or equivalent.** + **A minimum of four (4) years of… more
    Fujifilm (09/06/25)
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  • Sr. Principal Statistician

    Medtronic (Los Angeles, CA)
    …and high-quality work. + Understand the various regulations we operate under in the medical device industry and ensure that the statistical methods applied align ... this exciting role as Sr. Principal Statistician - Diabetes Product Innovation, you will have responsibility for supporting Diabetes...MS or PhD degree in Statistics or equivalent + Medical device domain knowledge Experience with Diabetes… more
    Medtronic (09/04/25)
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  • Director, Global Regulatory Affairs

    Candela Corporation (Marlborough, MA)
    …for both tactical and strategic initiatives. + Possess and exercise regulatory and medical device industry relationships to inform bold RA strategies and ... **Company Overview:** Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio...sciences/engineering/related field, plus 12 years of experience in the medical device industry with at least 10… more
    Candela Corporation (08/29/25)
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  • Sr. Software Design Assurance Engineer

    Philips (Colorado Springs, CO)
    …Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. + Serving as SME for Software Design Assurance and ... etc.) + 8+ years of experience in Software Quality and/or Software Development in medical device industry with hands on experience with SW Design verification… more
    Philips (08/27/25)
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