Technical Writer
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.
- Locations
- Torrance, CA
Torrance, CA
Perks & Benefits
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Paid Holidays (13 Holidays)
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Paid Vacation Leave
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Paid Sick Leave
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Birthday Off
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Tuition Reimbursement Program
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Basic Life Policy & AD&D
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401K (6%Matching)
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Health Insurance (Medical, Dental, Vision)
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Student Debt Reduction Program
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Fresh Fruit Program
Our Values
INNOVATION
- We are curious and explore new ways.
- We are ambitious and find solutions.
EXCELLENCE
- We have a strong technical knowledge and we deliver results.
- We deliver quality in everything we do.
TRUST
- We believe in teamwork and collaboration.
- We lead by example and accept responsibility.
About PolyPeptide US
PolyPeptide is a specialized Contract Development & Manufacturing Organization (CDMO) for peptide and oligonucleotide-based active pharmaceutical ingredients (API). By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world.
PolyPeptide serves a fast-growing market, offering products and services from pre-clinical through to commercial stages. Its broad portfolio reflects the opportunities in drug therapies across areas and with a large exposure to metabolic diseases, including GLP-1.
Dating back to 1952, PolyPeptide today runs a global manufacturing network in Europe, the U.S. and India.
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