• Project Manager - Global Supply Chain

    Hologic (Marlborough, MA)
    …highly motivated, detail-oriented, and dynamic **Project Manager** to join our team in the ** medical device industry** . This role offers a unique opportunity to ... strong relationships with internal teams across engineering, supply chain, regulatory , and quality functions. + Drive alignment...3-5 years of project management experience, preferably in the ** medical device or regulated industry** . +… more
    Hologic (08/02/25)
    - Related Jobs
  • Manager, Analytics & Data Engineering, Onsite

    AbbVie (Worcester, MA)
    …systems and laboratory information management. + Must also be familiar with cGMP, Quality Systems, ALCOA+ principles, and other global regulatory requirements of ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Data Integrity to lead site analytics web and data quality initiatives within our pharmaceutical operation reporting into Digital… more
    AbbVie (07/12/25)
    - Related Jobs
  • Sr Account Director/Executive Account Director,…

    ThermoFisher Scientific (Boston, MA)
    …organizational expertise, and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a proven track record ... business development and key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in global sales with diverse… more
    ThermoFisher Scientific (06/22/25)
    - Related Jobs
  • Senior Specialist Product Performance

    Abbott (Burlington, MA)
    …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...position of SENIOR SPECIALIST, PRODUCT PERFORMANCE works within our Quality Team supporting all parts of Abbott Heart Failure.… more
    Abbott (07/12/25)
    - Related Jobs
  • QA Lead Technical Operations

    System One (Harvard, MA)
    …+ Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical testing is highly desirable. + Extensive knowledge ... Actions. + Decision making of non-conformance through a deep understanding of Quality Systems Regulatory expectations + Reviews and approves Quality more
    System One (08/03/25)
    - Related Jobs
  • R&D Project Manager - Transducer Hardware…

    Philips (Cambridge, MA)
    …of professional experience with leading complex new product development projects in medical device regulated environment and proven track record of delivering ... achieving project scope and objectives while balancing schedule, cost, quality to meet product requirements. **Your role:** + Leading... and reliability metrics, risk management, and FMEA in medical device regulated environment. + You have… more
    Philips (07/04/25)
    - Related Jobs
  • Engineering Maintenance Technician II…

    Integra LifeSciences (Braintree, MA)
    …with building management systems (BMS) and automated environmental controls. + Knowledge of regulatory requirements in the medical device or pharmaceutical ... Minimum of 3 years of experience in refrigeration maintenance, preferably in a medical device or regulated manufacturing environment. + Strong knowledge of… more
    Integra LifeSciences (06/18/25)
    - Related Jobs
  • Director, Business Development, Acquisition…

    Olympus Corporation of the Americas (Westborough, MA)
    …of the typical functional roles and responsibilities in medical device organizations. + Practical understanding of global regulatory / quality ... 7 years of experience in a cross-functional project leadership role in the medical device industry, preferably leading due diligence and post-merger integration… more
    Olympus Corporation of the Americas (06/12/25)
    - Related Jobs
  • Sr Clinical Consultant, MI I

    Fujifilm (Boston, MA)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/11/25)
    - Related Jobs
  • Senior Clinical Consultant II, International

    Fujifilm (Boston, MA)
    …I. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The resource will assist with the development...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/08/25)
    - Related Jobs