• cGMP Process Development

    University of Southern California (Los Angeles, CA)
    cGMP Process Development ( PD ) Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA ... cell and gene therapies and other biological products for internal/external users. The cGMP Process Development ( PD ) Specialized Lab Technician at the… more
    University of Southern California (06/11/25)
    - Related Jobs
  • cGMP Process Development

    University of Southern California (Los Angeles, CA)
    cGMP Process Development ( PD ) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - ... cell and gene therapies and other biological products for internal/external users. The Process Development ( PD ) Specialist is responsible for developing… more
    University of Southern California (06/09/25)
    - Related Jobs
  • Biologics Process Development

    University of Colorado (Aurora, CO)
    …and HPLC. + Draft and edit Batch Records, Bill of Materials, SOP, Forms for Process Development and cGMP manufacturing documentation. + Document Process ... edit Batch Records, Bill of Materials, SOP, Forms for Process Development and cGMP manufacturing...all cross functional activities including but not limited to Process Development ( PD ) and … more
    University of Colorado (07/24/25)
    - Related Jobs
  • Biologics Development & Manufacturing…

    University of Colorado (Aurora, CO)
    …chromatography and plate-based assays.o Chemical and Biological Engineering.o Biologics Process Development .o cGMP manufacturing.Applicants must meet ... Development & Manufacturing Supervisor - 37107 University Staff Supervise process development and manufacturing operations for biologics-based therapeutics.… more
    University of Colorado (07/29/25)
    - Related Jobs
  • Senior Manager, Upstream Process

    Catalent Pharma Solutions (Baltimore, MD)
    …different departments to make sure the process is successfully transferred from PD to cGMP manufacturing + Plan, develop, organize, and implement policies, ... **Job Title:** Sr. Manager Upstream Process Development **City:** Baltimore **State** :...: + Lead the client projects starting from the development and optimization toward cGMP manufacturing for… more
    Catalent Pharma Solutions (08/10/25)
    - Related Jobs
  • Director , Product Development

    Catalent Pharma Solutions (San Diego, CA)
    …leader to join us as Director , Product Development . The Director , Product Development ( PD ) is responsible for providing operational, scientific ... **Title: Director Product Development ** **About Catalent San...problem statements for small molecule and peptide therapeutics. The Director will lead the PD team and… more
    Catalent Pharma Solutions (06/13/25)
    - Related Jobs
  • Associate Manufacturing - Services - Days

    Amgen (Holly Springs, NC)
    …of a cross-functional team (ie, QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD ( Process Development ), Regulatory, etc.) in completing production ... a regulated industry such as biotechnology or pharmaceutical + Basic understanding and process experience in a cGMP manufacturing facility + Basic knowledge of… more
    Amgen (08/09/25)
    - Related Jobs
  • QC Manager, Bioanalytical

    ThermoFisher Scientific (Plainville, MA)
    …, a division of Thermo Fisher Scientific. At VVS, we deliver from process development through commercial supply, offering the expertise and resources vital ... manufacturing, and the transfer and validation of assay methods from clients and/or Assay Development & Analytics to the cGMP QC testing laboratory. The manager… more
    ThermoFisher Scientific (06/26/25)
    - Related Jobs
  • Manufacturing Senior Associate (12 Hour…

    Amgen (New Albany, OH)
    …and Validation. + Collaborate with Quality, Mfg Managers, Plant Engineering, Process Development and Regulatory Compliance staff in cross-functional teams. ... **Basic Qualifications:** High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience Or Associate's + 2 years… more
    Amgen (08/10/25)
    - Related Jobs
  • Associate - Parenteral Drug Product QA

    Lilly (Indianapolis, IN)
    …degree. Additional Skills/Preferences: + 2+ years' cumulative experience in commercial or development manufacturing in a cGMP environment, preferably in quality ... to make life better for people around the world. Responsibilities: The PD Drug Product QA Associate collaborates across functions to support the establishment… more
    Lilly (08/15/25)
    - Related Jobs