Technical Writer

PolyPeptide LaboratoriesTorrance, CA
38dOnsite

About The Position

Are you detail-oriented and passionate about clear, compliant documentation? Join us as a Technical Writer and play a key role in supporting GMP manufacturing operations by creating and maintaining accurate SOPs, batch records, and controlled documents.

Requirements

  • Bachelor's degree in a science-related field.
  • 2+ years in GMP manufacturing, technical writing, or regulated operations.
  • Strong writing, editing, and proofreading skills.
  • Familiarity with GMP documentation practices and electronic document systems.

Responsibilities

  • Draft and revise SOPs, Master Batch Records, and work instructions.
  • Collaborate with manufacturing and QA teams to ensure accuracy and compliance.
  • Manage document control, versioning, and change requests.
  • Support training materials and communicate updates across departments.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Chemical Manufacturing

Number of Employees

1,001-5,000 employees

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