• Process Engineer

    Actalent (St. Paul, MN)
    …Author and execute test and validation protocols to comply with ISO and FDA medical device regulation requirements. + Verify documents are correctly filled out prior ... to set-up sign-off. + Provide training and coaching to peers and Process Technicians. + Maintain and promote a safe and clean working environment. + Follow all applicable safety procedures and guidelines as outlined in the company safety manual. + Perform… more
    Actalent (01/10/26)
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  • Principal Automation Engineer, BAS/Utilities (HIT)

    Genentech (Hillsboro, OR)
    …priorities in a fast-paced setting. + You possess in-depth knowledge of FDA regulations, cGMP standards, and compliance requirements specific to pharmaceutical and ... biotechnology production. + You are able to serve as a member of the 24/7 Rotational On Call Support Team. Preferred: + Cell/gene therapy industry experience. + Experience working in an environment utilizing change control and good documentation practices. +… more
    Genentech (01/10/26)
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  • Technician I, Sample Processing 2nd Shift

    Charles River Laboratories (Ashland, OH)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
    Charles River Laboratories (01/10/26)
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  • Operator - Solvent Recovery Operations

    Lilly (Lebanon, IN)
    …distillation unit operations or similar unit operations + Solid understanding of FDA guidelines and cGMP requirements. + Strong organizational skills and ability to ... handle and prioritize multiple requests. + Knowledge of lean manufacturing principles + Emergency Response Experience Industrial, military, volunteer, career firefighter + Indiana State or IFSAC Certification - Fire 1, Hazmat Technician **Additional… more
    Lilly (01/10/26)
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  • Sr. QA Technician

    Actalent (Maryland Heights, MO)
    …Maintain operational compliance with US and international regulatory agencies and guidelines, such as FDA , EU, HC, TGA, PIC/S, ISO, USP, NRC, and cGMP. PAY - $29 ... Responsibilities + Conduct thorough and efficient review and disposition of completed batch record documentation, ensuring adherence to Good Documentation Practices, cGMPs, and applicable local procedures. + Perform and oversee Quality Assurance On The Floor… more
    Actalent (01/10/26)
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  • Research Coordinator I - Orthopedics Clinical

    Houston Methodist (Houston, TX)
    …bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports clinical research protocols and extramurally ... This position ensures accurate data collection, documentation, organization and safety of research participants. **FLSA STATUS** Exempt **QUALIFICATIONS** **EDUCATION** + Bachelor's degree **EXPERIENCE** + Two years' research experience **LICENSES AND… more
    Houston Methodist (01/10/26)
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  • Research Associate II - Urology - Chan

    Houston Methodist (Houston, TX)
    …bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports clinical research protocols and extramurally ... This position provides advanced technical research skills and establishing test methods and procedures under the direction of Department Chairperson or Scientist (Faculty). The Research Associate II position evaluates results of (or response to) process;… more
    Houston Methodist (01/10/26)
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  • Associate Principal Scientist, Clinical Research

    Merck (Rahway, NJ)
    …policies and the procedures for interacting with health agencies (eg FDA ); understand key elements in pharmacovigilance, drug safety monitoring, signal detection ... and processing of adverse reports; (c) **Global Medical/Scientific Affairs:** Exposure to the management of a product asset prior to, during and after the launch phase (US and Global) including caveats on drug promotion. After a successful first year, the… more
    Merck (01/10/26)
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  • Equipment Tech

    UnityPoint Health (Moline, IL)
    …Child & Dependent Adult Abuse + Back Safety Training + Maintain requirements of FDA & DOT Regulations in applicable region + Mandatory annual equipment training and ... competencies. + Licensed driver in the State of Residence Other: + Use of usual and customary equipment used to perform essential functions of the position. Apply Today! + Ready to take the next step in your healthcare career? Apply now to join our team + make… more
    UnityPoint Health (01/10/26)
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  • Medical Administrative Officer (Title 32)

    Air National Guard Units (Scott AFB, IL)
    …Occupational Safety and Health Administration (OSHA), Food and Drug Administration ( FDA ), Environmental Protection Agency (EPA), Air Force Occupational Safety and ... Health (AFOSH), Federal Emergency Management Agency (FEMA), and Military Support to Civil Authorities (MSCA) that affect Air National Guard plans, directives and missions. Ensure medical capabilities support the federal mission of expeditionary medical… more
    Air National Guard Units (01/10/26)
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