What are the responsibilities and job description for the Technical Writer position at PolyPeptide US?
Technical Writer – GMP Manufacturing Documentation
Location: Onsite - Torrance, CA | Employment Type: Full-Time
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.
What You’ll Do:
- 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.
What We’re Looking For:
- 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.
Why Join Us? Be part of a team that values precision, compliance, and collaboration in a fast-paced, regulated environment.
Salary: $75K - $90K
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Salary : $75,000 - $90,000