Upstream Bioprocess Associate – 3rd Shift

System One

Pennington (NJ)

Presencial

USD 30 000 - 34 000

Tempo integral

Há 2 dias
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Resumo da oferta

System One seeks a Manufacturing Associate I, Upstream Processing, for a 3rd shift in Pennington, NJ. The role involves supporting day-to-day upstream bioprocessing in a cGMP environment, including media prep, seed train expansion, bioreactor operations, harvests, and aseptic processing.

Candidates with biology/biotech backgrounds and familiarity with SOPs and GMP documentation will thrive in a collaborative, quality-driven team.

Qualificações

  • Experience or academic exposure to cell culture, bioprocessing, or biological manufacturing.
  • Experience with cell culture operations, shake flasks, bioreactors, media and buffer preparation, or aseptic processing.
  • Strong attention to detail and documentation practices.
  • Ability to follow SOPs and work effectively in a team; cGMP knowledge preferred.

Responsabilidades

  • Prepare media and buffers following batch records and SOPs.
  • Support cell culture operations, including seed train expansion, bioreactor processes, and harvest activities.
  • Perform equipment setup, cleaning, sanitization, and basic maintenance.
  • Execute manufacturing activities in a cGMP cleanroom using aseptic techniques.
  • Complete batch records and GMP documentation accurately.
  • Report deviations, equipment issues, and operational concerns.
  • Participate in training and continuous improvement initiatives.

Conhecimentos

Cell culture operations
Shake flask cultivation
Bioreactor systems
Media and buffer preparation
Aseptic processing
SOP adherence

Formação académica

Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or related field
High School Diploma/GED with 4+ years biopharmaceutical manufacturing

Descrição da oferta de emprego

System One seeks a Manufacturing Associate I, Upstream Processing, for a 3rd shift in Pennington, NJ. The role involves supporting day-to-day upstream bioprocessing in a cGMP environment, including media prep, seed train expansion, bioreactor operations, harvests, and aseptic processing.

Candidates with biology/biotech backgrounds and familiarity with SOPs and GMP documentation will thrive in a collaborative, quality-driven team.

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