GMP Bioprocess Operator — Cleanroom Manufacturing

Emergent BioSolutions, Inc.

Canton (MA)

On-site

USD 58,000 - 70,000

Full time

2 days ago
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Job summary

Emergent BioSolutions is seeking a Bioprocess Associate to support GMP manufacturing across upstream, downstream or final formulation. You will operate aseptically with bioreactors and precision equipment, document batch records, and assist in GMP documentation revisions.

A strong foundation in GMP and scientific training is required to join a team focused on safety and quality. The role emphasizes collaboration with QA during audits, adherence to policy, and maintaining audit-ready cleanrooms

Qualifications

  • Bachelor’s degree in a Scientific, Engineering or Biotech field with 2+ years’ experience in biologic production under GMP.
  • Strong knowledge of GMP principles and documentation of batch records and forms.
  • Excellent documentation skills including batch records and SOPs.

Responsibilities

  • Operates pharmaceutical manufacturing equipment (autoclaves, incubators, bioreactors, centrifuges) in aseptic conditions.
  • Adheres to GMP standards, safety procedures and site policies.
  • Communicates status of daily production tasks with team and supervisors.
  • Documents logbooks, forms, solution prep and batch records per GMP requirements.
  • May assist in revising GMP documentation and ensuring audit readiness of cleanrooms.
  • Supports QA during audits and collaborates with cross-functional teams.

Skills

Biologic production
GMP compliance
Documentation

Education

Bachelor’s degree in a Scientific, Engineering or Biotech field

Job description

Emergent BioSolutions is seeking a Bioprocess Associate to support GMP manufacturing across upstream, downstream or final formulation. You will operate aseptically with bioreactors and precision equipment, document batch records, and assist in GMP documentation revisions.

A strong foundation in GMP and scientific training is required to join a team focused on safety and quality. The role emphasizes collaboration with QA during audits, adherence to policy, and maintaining audit-ready cleanrooms

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