• Principal Process Engineer, Packaging

    Genentech (Hillsboro, OR)
    …tactical business processes and procedures. + You will participate in process validation activities, including protocol development, execution, and report ... activities from development to commercial manufacturing, ensuring successful scale-up and process validation . + You will support regulatory inspections and… more
    Genentech (09/06/25)
    - Related Jobs
  • Quality Specialist Investigator

    Kelly Services (Parsippany, NJ)
    …various validation and qualification documentation, including but not limited to, Process Validation , Cleaning Validation , Computer Validation , ... (5) years of hands-on experience in executing and reviewing documentation related to Process Validation , Cleaning Validation , Computer Validation ,… more
    Kelly Services (08/13/25)
    - Related Jobs
  • Lead Engineer, CSV

    Bristol Myers Squibb (Summit, NJ)
    …qualification and support requests. + Provides technical support and guidance on Validation , Quality Process , and equipment qualification issues. + Interfaces ... at BMS with our Cell Therapy team. The **Lead Computer System Validation (CSV) Engineer** supports the successful implementation of manufacturing and laboratory… more
    Bristol Myers Squibb (09/07/25)
    - Related Jobs
  • Process Development Engineer

    Amgen (Thousand Oaks, CA)
    …team in the Drug Product Technologies organization. Working with the Principal Engineer Process Validation Manager of Amgen Thousand Oaks (ATO) Process ... products to patients through demonstrated excellence in aseptic processing, technology transfer, process characterization, process validation and continuous … more
    Amgen (09/13/25)
    - Related Jobs
  • Associate Process Engineer

    Hovione (East Windsor, NJ)
    …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... life. You will be responsible to: Enables the efficient manufacture of pharmaceutical products, including highly potent compounds, in compliance with applicable cGMP… more
    Hovione (08/20/25)
    - Related Jobs
  • Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …manufacturing. This role requires deep technical expertise in injection molding and process validation within a regulated, high-precision environment. The ideal ... molding techniques to ensure high-quality, repeatable manufacturing outcomes. + Oversee process validation activities (IQ/OQ/PQ) in compliance with ISO 13485… more
    West Pharmaceutical Services (07/18/25)
    - Related Jobs
  • Manager, CQV Portfolio Delivery

    Bristol Myers Squibb (Warren, NJ)
    …The incumbent's focus is support of small to medium size validation projects, such as new product introduction, facilities/utilities upgrade and modification, ... manufacturing and laboratory systems upgrade and modification, including validation delivery and decommissioning/retirement. The incumbent in this role may supervise… more
    Bristol Myers Squibb (09/11/25)
    - Related Jobs
  • CQV Specialist - Upstream Process Equipment…

    Mentor Technical Group (Juncos, PR)
    validation tools (eg, AutoCAD, TrackWise, Veeva). Preferred Skills: + CQV, Process Validation , or Project Management certifications. + Experience with ... related field. + Minimum 3-5 years of experience in commissioning, qualification, and validation of biotech process equipment (both upstream and downstream). +… more
    Mentor Technical Group (09/07/25)
    - Related Jobs
  • Process Engineer II

    PCI Pharma Services (Philadelphia, PA)
    …+ Work with staff on development of new equipment performance requirements. + Assist Validation with OQ and PQ (Operational and Process Qualifications) of new ... to pioneer and shape the future of PCI. The Process Engineer II role is focused on floor operations...Tests). + Responsible for determining OQ parameters to start validation . + Approves validation protocols and MPI's.… more
    PCI Pharma Services (08/30/25)
    - Related Jobs
  • Director, Engineering Assembly and Packaging…

    Merck (Rahway, NJ)
    …components, process , and equipment, as well as qualification and validation , medical device design controls and device risk management, and design verification/ ... transfers across the network inclusive of aligning the control and validation strategies. **Minimum Education Requirements and Experience:** + Bachelor of Science… more
    Merck (08/12/25)
    - Related Jobs