• Associate Director External Quality Assurance

    Organon & Co. (Jersey City, NJ)
    …global GMP Quality Systems and regulatory requirements. + Experience in medical device Quality Systems is preferred, including familiarity with ISO13485, ... impact of products to Organon's revenue, number and complexity of in-markets, regulatory history, historical performance (production and compliance ), new product… more
    Organon & Co. (08/19/25)
    - Related Jobs
  • Quality Engineer ( Medical Devices)

    Astrix Technology (Rahway, NJ)
    …: $90-100K + 5% annual bonus eligibility Our client, a global leader in the medical device industry, is looking for a experienced Quality Engineer to join their ... **Quality Engineer ( Medical Devices)** Engineering Rahway, NJ, NONE Pay Rate...in the maintenance of the quality management system in compliance with appropriate regulatory requirements, customer requirements,… more
    Astrix Technology (08/28/25)
    - Related Jobs
  • Senior Counsel Life Sciences

    Fujifilm (Trenton, NJ)
    …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... new business ventures. + Keep abreast of legislative and regulatory changes that may affect HLUS and its subsidiary...and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. +… more
    Fujifilm (08/15/25)
    - Related Jobs
  • Sr. Design Quality Engineer I

    Integra LifeSciences (Princeton, NJ)
    …mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product ... processes are integrated into the overall product risk management process. ** Regulatory Compliance & Documentation:** + Ensure thorough documentation and… more
    Integra LifeSciences (06/11/25)
    - Related Jobs
  • Senior Legal Counsel, North America Commercial…

    embecta (Parsippany, NJ)
    …pragmatic solutions. The ideal candidate will have commercial legal experience in the medical device , pharma or healthcare industry supporting the US and/or ... to practice in at least one state. + 5+ years of experience, preferably within medical device , pharma or healthcare industries. + Thorough knowledge of the False… more
    embecta (08/28/25)
    - Related Jobs
  • Principal Field Clinical Engineer- North East

    Medtronic (Newark, NJ)
    …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...sales. + Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials. +… more
    Medtronic (08/22/25)
    - Related Jobs
  • Sales Manager

    System One (Jersey City, NJ)
    …revenue growth. + Strong understanding of the sales process, product knowledge and the medical device market. + Ability to lead, motivate and inspire a team ... 3 W-2's + 1099s. + Proven track record in sales preferably in the medical device /manufacturing and/or pharma industry. (ideally selling PRP to medi spas,… more
    System One (06/10/25)
    - Related Jobs
  • Associate Engineer, NPD

    J&J Family of Companies (Raritan, NJ)
    medical device products to other business functions such as Regulatory compliance activities and post-launch commercial activities. + Interact with ... (Design Of Experiments) and regression analysis. + Prior experience working in the Medical Device industry. + Knowledge of medical device regulations.… more
    J&J Family of Companies (08/27/25)
    - Related Jobs
  • Specialist, Quality Assurance - Individual…

    Robert Half Technology (Mahwah, NJ)
    …improvements to enhance the efficiency and effectiveness of documentation systems. * Support compliance with medical device regulations and quality assurance ... will play a crucial part in managing document-related changes while ensuring compliance with regulatory standards for medical devices. This is a long-term… more
    Robert Half Technology (08/11/25)
    - Related Jobs
  • Associate Director, Technical Solutions

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ... ISO frameworks, GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to align technical decisions… more
    BD (Becton, Dickinson and Company) (08/08/25)
    - Related Jobs