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Biopharmaceutical Production Scientist

Job in Riverton, Salt Lake County, Utah, 84065, USA
Listing for: Placements24
Full Time position Listed on 2026-11-09
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing
  • Pharmaceutical
    Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 29000 - 44000 USD Yearly USD 29000.00 44000.00 YEAR

Job Description & How to Apply Below

About the Role

Our client, a cutting-edge biopharmaceutical company at the forefront of therapeutic innovation, is seeking a highly skilled Biopharmaceutical Production Scientist to join their team in
** Upington, Northern Cape**. This role is essential for the large-scale manufacturing of complex biological products, including monoclonal antibodies and recombinant proteins. You will be involved in upstream (cell culture) and/or downstream (purification) processes, ensuring adherence to strict GMP standards and regulatory requirements. The ideal candidate possesses a strong scientific background in cell biology, biochemistry, or bioprocess engineering, coupled with hands‑on experience in biopharmaceutical manufacturing.

This is a significant opportunity to contribute to the production of life‑changing biotherapeutics in a state‑of‑the‑art facility in
** Upington**.

Key Responsibilities
  • Execute and monitor mammalian cell culture processes (e.g., bioreactors, wave bags) for the production of biologics.
  • Perform downstream purification operations (e.g., chromatography, filtration) to isolate and purify target proteins.
  • Operate and maintain production equipment, ensuring proper calibration and functionality.
  • Follow Standard Operating Procedures (SOPs) and batch records meticulously to ensure product quality and consistency.
  • Perform in‑process testing and data analysis to monitor process performance.
  • Participate in process troubleshooting and optimization activities.
  • Ensure compliance with GMP, safety regulations, and environmental standards.
  • Maintain accurate and detailed production records and documentation.
  • Support process validation activities and technology
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