• Regulatory Coordinator - Days - 8:00am to 5:00pm

    LSI Solutions (Victor, NY)
    …1-2 years of experience working as a Regulatory Coordinator at a medical device company operating within a Quality Management System (QMS) certified to ISO ... working as a Regulatory Coordinator at a medical device company operating within a Quality Management System (QMS) certified to ISO 13485, said experience… more
    LSI Solutions (11/28/25)
    - Related Jobs
  • Sr. Quality Engineer

    Tecomet (Lansing, MI)
    …Preferred:** + ASQ CQE or CMQ/QE preferred + 4 years' experience in quality within medical device manufacturing industry preferred + ISO ... Full-time **Salaried/Hourly** Salaried **Travel Requirements** No **Job Description** **Sr. Quality Engineer** **Position Summary** The Sr. Quality Engineer… more
    Tecomet (11/19/25)
    - Related Jobs
  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Juneau, AK)
    …field or equivalent work experience, preferred + 2+ years' experience in Medical Device Regulatory Affairs/ Quality experience preferred + Certification ... affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function… more
    Cardinal Health (12/13/25)
    - Related Jobs
  • Software Engineer - AI Development

    GE HealthCare (Waukesha, WI)
    …for the Software Development Life Cycle (SDLC) within the Medical Device industry. + **Agile Methodologies & Software Quality Systems** : Familiarity ... and Machine Learning techniques. + Hands-on experience integrating AI Models into medical device products + Experience in developing AI inference pipelines… more
    GE HealthCare (12/06/25)
    - Related Jobs
  • Quality Engineer

    Actalent (Watertown, CT)
    …Essential Skills + Quality engineering + Quality assurance + Audit + Medical device expertise + CMM programming + GD&T + Statistical analysis + Root ... Job Title: Quality Engineer For immediate consideration, please email resume...all testing processes and product developments comply with relevant medical device regulations such as FDA (21… more
    Actalent (12/04/25)
    - Related Jobs
  • Software Engineering Technical Lead

    Lilly (Indianapolis, IN)
    …Agile delivery of software components of Lilly's platform + Obtain and use knowledge of medical device delivery models and quality system to ensure solutions ... and align technology that enables the platform architecture all while meeting medical device regulatory expectations. Additionally, the organization will look to… more
    Lilly (11/14/25)
    - Related Jobs
  • Principal Regulatory Compliance

    J&J Family of Companies (Danvers, MA)
    …equivalent is required, with 8-10 years of proven experience in medical Device . + Current certification of quality system auditor or lead auditor ... https://www.jnj.com **Job Function:** Supply Chain Engineering **Job Sub** **Function:** Quality Engineering **Job Category:** Scientific/Technology **All Job Posting Locations:**… more
    J&J Family of Companies (12/04/25)
    - Related Jobs
  • R&D Sustaining Engineer

    Caldera Medical (Westlake Village, CA)
    …is Caldera Medical ? Caldera Medical is a growth stage medical device company dedicated to improving the quality of life for women. In 2018, Caldera ... role is not eligible for work visa sponsorship) Caldera Medical 's Mission - To Improve the Quality ...the ongoing reliability, compliance, and cost-effectiveness of our existing medical device products. This role is crucial… more
    Caldera Medical (12/13/25)
    - Related Jobs
  • Manufacturing Quality Incoming Inspectio

    West Pharmaceutical Services (Salome, AZ)
    …+ Education- Technical/ Practical Eng. + At least 2 years of relevant experience in Quality in the Medical Device /pharma industry + Courses related to ... Experience** + At least 2 years of relevant experience in Quality in the Medical Device /pharma industry **Preferred Knowledge, Skills and Abilities** +… more
    West Pharmaceutical Services (12/13/25)
    - Related Jobs
  • Staff Design & Reliability Assurance…

    Integra LifeSciences (Mansfield, MA)
    …industry with knowledge of Risk Management (ISO 14971 2019), MDD ( Medical Device Directive), IEC 62366, ISO 13485 ( Quality Management Systems), FDA QSR and ... knowledge of DFSS techniques * 8 years of experience in a Quality Assurance role for medical device or pharmaceutical product development * Fluent in French… more
    Integra LifeSciences (11/12/25)
    - Related Jobs