• Quality Engineer II (Manufacturing)

    Teleflex (Chelmsford, MA)
    …10% **Requisition ID** :12403 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health ... growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients'...vendor audits if necessary. Support the Back Room during regulatory and notified body audits. * Production & Process… more
    Teleflex (07/16/25)
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  • Legal Counsel, Americas

    Danaher Corporation (Waltham, MA)
    …experience, ideally with a combination of law firm and in-house roles in the medical device , pharmaceutical, or life sciences sector. . Strong contract drafting ... guidance on a wide range of commercial, compliance, and regulatory matters, with a particular focus on Latin America....to eligible employees, including: * Paid time off * Medical , dental, and vision insurance * 401(k) retirement plan… more
    Danaher Corporation (07/03/25)
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  • Engineer: mechanical design engineer with plastics…

    Nanobiosym, Inc. (Cambridge, MA)
    …engineering grade resins a must More than 10 years experience Must have medical device experience, disposables preferred. familiar with ISO13485 and 14971 Must ... multiple "hats". -be ready to participate in quality systems, engineering, mfg, regulatory activities, etc. Individual would be a motivated, self-starter who handles… more
    Nanobiosym, Inc. (09/04/25)
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  • Senior Global Product Manager/Owner

    Philips (Cambridge, MA)
    …a plus. + You have 4+ years in a role associated with healthcare and/or medical device and software development in a regulated environment. + You have experience ... teams to prioritize claims based on market trends and regulatory requirements. Continuously optimize strategy through analysis of competitor activity,… more
    Philips (09/04/25)
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  • Director, Third Party Data Acquisition

    Takeda Pharmaceuticals (Boston, MA)
    …data, including laboratory data, pharmacokinetics (PK), ECG, biomarker, imaging, and wearable device data across global clinical trials. + Proven ability to define ... multiple third-party vendors, ensuring data integrity, compliance, and alignment with regulatory and business requirements. + Strong vendor management and business… more
    Takeda Pharmaceuticals (08/31/25)
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  • General Warehouse Worker- 2nd shift

    Lineage Logistics (Taunton, MA)
    …*Forklift preferred. Unwrap, sort, stack, and label products while following all regulatory and company safety standards, policies, and procedures. **KEY DUTIES AND ... unload product on and off pallets, skids, or lifting device + Wrap pallets using a wrap machine +...law. Benefits Lineage provides safe, stable, reliable work environments, medical , dental, and basic life and disability insurance benefits,… more
    Lineage Logistics (08/28/25)
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  • Principal Specialist, FP&A Operations

    NTT America, Inc. (Boston, MA)
    …with excellent judgment and ability to balance practical business needs with regulatory and legal requirements. + Effective at translating and explaining technical ... expenses associated with working remotely and use of a personal mobile device , if applicable._ NTT Global Data Centers Americas, Inc. offers competitive compensation… more
    NTT America, Inc. (08/28/25)
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  • Automation Engineer (DeltaV)

    Bristol Myers Squibb (Devens, MA)
    …with information technology to reduce down-time, elevate the level of regulatory compliance, and introduce efficiency gains through effective use of available ... of manufacturing equipment/devices to the Control System and troubleshooting device communication. + Understanding of engineering documentation such as P&IDs,… more
    Bristol Myers Squibb (08/26/25)
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  • Quality Control (QC) Inspection Technician…

    Consolidated Precision Products (Burlington, MA)
    …materials and escalate findings according to Standard Operating Procedures (SOPs) and regulatory or customer quality standards. + Perform visual inspections using a ... and execute experiments as requested. + Experience in pharma, bio, med device , defense, or aerospace manufacturing or related experience with highly detailed quality… more
    Consolidated Precision Products (08/24/25)
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  • Associate Scientist

    Kelly Services (Boston, MA)
    …maintenance and verification of lab equipment, and the preparation of device -related documentation (IQ/OQ, PQ and CSV documentation). + Contribute to laboratory ... with analytical method qualification, transfer, validation and general understanding of regulatory requirements for biotherapeutics development is a plus. As part of… more
    Kelly Services (08/23/25)
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