• R&D Pilot Plant Technologist.

    Kerry (Beloit, WI)
    …world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier ... will collaborate across RD&A, Manufacturing, and Engineering teams to enhance process performance, support innovation, and ensure product quality. The ideal… more
    Kerry (11/11/25)
    - Related Jobs
  • Manufacturing Technician - NIGHTS (Sun-Tues)

    Novo Nordisk (West Lebanon, NH)
    … improvements/cost reduction program into manufacturing + Perform area equipment and process validations in accordance with validation procedures + Perform in- ... + 14 weeks Paid Parental Leave + Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and mentorship… more
    Novo Nordisk (11/05/25)
    - Related Jobs
  • Laboratory Equipment IT Engineer, Regeneron Cell…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …with automation systems and control system software + Support engineering and validation projects as well as provide support to manufacturing activities with ... process control and process monitoring equipment software...in a manufacturing/lab/IT setting. Must have experience in a pharmaceutical or biopharmaceutical manufacturing facility. Must have experience with… more
    Regeneron Pharmaceuticals (10/25/25)
    - Related Jobs
  • Manager, Value Stream Cryo Operations

    Bristol Myers Squibb (Summit, NJ)
    …for all processes associated with Cryopreservation and Sample Management, Frozen Process Material Retrieval, Movement, and Storage within CAR T clinical and ... and support team members' professional development. + Own the performance review process , provide continuous feedback, and recognize achievements. + Foster a culture… more
    Bristol Myers Squibb (01/19/26)
    - Related Jobs
  • Executive Director, Site Quality Lead

    Merck (Wilmington, DE)
    …to US and International Codes, Standards and Practices + Equipment and process validation + Drug substance/Conjugation processes + Sterile filling processes ... Quality Risk Management (QRM) shall: + Sponsor the QRM process and Site Quality Risk Management Committee (SQRMC) +...At least 15 years' experience in the biotechnology and/or pharmaceutical industry + Proven ability to lead a Quality… more
    Merck (01/17/26)
    - Related Jobs
  • Quality Control Analyst II/III-Analytical

    Actalent (Rockville, MD)
    …analytical testing programs to ensure compliance with cGMP standards including in- process , product release and stability testing. This individual will be required ... analytical testing programs to ensure compliance with cGMP standards including in- process , product release and stability testing. This individual will guide and… more
    Actalent (01/17/26)
    - Related Jobs
  • 3rd Shift Maintenance & Utilities Specialist…

    Merck (West Point, PA)
    …areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation . We ... maintenance, propose and develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations +… more
    Merck (01/09/26)
    - Related Jobs
  • Senior/Principal Manufacturing Asset Engineer, HTO

    Genentech (Hillsboro, OR)
    …objectives. You will: + Provide technical support and engineering solutions for process and equipment-related issues. + Understand the basis for the qualification of ... the qualified state of the equipment and provide maintenance oversight for process equipment. Ensure any changes are documented appropriately through the change… more
    Genentech (12/30/25)
    - Related Jobs
  • Senior Quality Engineer

    West Pharmaceutical Services (Rockford, IL)
    …to multiple concurrent product development programs to ensure product and process compliance to all applicable regulatory and cGMP requirements, including ensuring ... design manufacturing documentation (eg, product specifications, design verification and validation activities, FMEA risk documents, test methods, protocols, reports,… more
    West Pharmaceutical Services (12/17/25)
    - Related Jobs
  • Formulation Technician I

    PCI Pharma Services (Bedford, NH)
    …scheduled tasks/events are completed + Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, ... and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes + Complete executed Batch Records accurately… more
    PCI Pharma Services (12/12/25)
    - Related Jobs