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Upstream Manufacturing Associate

Job in Passaic, Passaic County, New Jersey, 07055, USA
Listing for: Global Life Science Hub
Full Time position
Listed on 2026-06-02
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

We are supporting a commercial-stage biologics manufacturer in New Jersey that has successfully transitioned into full-scale GMP production following multiple FDA approvals.

As part of continued expansion, they are hiring Upstream Manufacturing Associates with prior industry experience to support large-scale biologics manufacturing operations.

This role is suited to candidates with 2+ years of hands-on upstream manufacturing experience within a GMP environment.

Key Responsibilities
  • Execute upstream manufacturing processes including cell culture, seed train, bioreactor operations and harvest
  • Operate and monitor single-use and/or stainless-steel bioreactors
  • Prepare media and buffers in accordance with GMP procedures
  • Perform in-process sampling and monitoring activities
  • Complete batch records and ensure accurate GMP documentation
  • Support troubleshooting and manufacturing execution on the production floor
  • Collaborate with QA, QC and MSAT teams
Requirements
  • Bachelor’s degree in Biology, Biotechnology, Biochemistry or related field
  • 2+ years of upstream manufacturing experience within a GMP environment
  • Hands‑on experience with mammalian cell culture and bioreactor operations
  • Understanding of GMP documentation and batch execution
  • Ability to work on‑site in New Jersey
Nice to Have
  • Experience with CHO cell culture processes
  • Exposure to large-scale biologics or biosimilars manufacturing
  • Experience supporting process scale-up or tech transfer activities
  • Familiarity with single-use bioreactor systems
Why Apply
  • Opportunity to join a commercial biologics manufacturing site with approved products
  • Exposure to large-scale GMP production and advanced upstream operations
  • Clear progression into senior manufacturing or technical roles
  • Growing organisation with continued investment and expansion
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Position Requirements
10+ Years work experience
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