GMP Biotech Manufacturing Associate

Precigen, Inc

Germantown (MD)

On-site

USD 70,000 - 85,000

Full time

3 days ago
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Job summary

Precigen, Inc. in Germantown, MD is seeking a GMP Manufacturing Associate I/II to join a dynamic team focused on clinical and commercial adenovector product manufacturing. The role requires GMP experience, attention to detail, and proactive process improvement.

The position involves assembling materials, executing Master Batch Records, and supporting deviations, SOPs, and technology transfer in a fast-paced cGMP environment. Weekend/shift work may be required.

Qualifications

  • Bachelor’s or Master’s degree in biology, biomedical science or life sciences is required.
  • Minimum 1–3 years in a GMP environment for Associate 1, 3+ years for Associate 2.
  • Aseptic technique experience is required.
  • Knowledge of current Good Manufacturing Practices (cGMPs) is required.
  • Prior cell culture and/or purification experience in GMP facility is preferred.

Responsibilities

  • Perform manufacturing in GMP setting for clinical and commercial materials.
  • Assemble raw materials and execute Master Batch Records (MBR).
  • Follow SOPs, MBRs, deviations and prepare summary reports.
  • Support deviations initiation and closure; assist in changeover procedures.
  • Participate in technology transfer and work in cross-functional teams.
  • Adhere to safety and regulatory requirements; occasional weekend/shift work.

Skills

Aseptic technique
cGMP knowledge
Team collaboration
Attention to detail

Education

Bachelor’s or Master’s in biology or life sciences

Tools

GMP equipment operation
MBR documentation

Job description

Precigen, Inc. in Germantown, MD is seeking a GMP Manufacturing Associate I/II to join a dynamic team focused on clinical and commercial adenovector product manufacturing. The role requires GMP experience, attention to detail, and proactive process improvement.

The position involves assembling materials, executing Master Batch Records, and supporting deviations, SOPs, and technology transfer in a fast-paced cGMP environment. Weekend/shift work may be required.

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