Technical Writer – GMP / Supply Chain Operations
About the role
We are seeking a Technical Writer to support GMP documentation activities in a biotech environment. This role will focus on creating, editing, and maintaining compliant documentation across supply chain, inventory management, manufacturing, and clinical supply operations. The Technical Writer will collaborate cross-functionally with Quality, Manufacturing, and Supply Chain teams to ensure accuracy and regulatory compliance.
Responsibilities
- Create, edit, and maintain compliant documentation across supply chain, inventory management, manufacturing, and clinical supply operations.
- Collaborate cross-functionally with Quality, Manufacturing, and Supply Chain teams to ensure accuracy and regulatory compliance.
- Work closely with ERP systems, MRP systems, EDMS, and clinical trial supply processes.
- Ensure adherence to GMP standards and regulations.
Requirements
- Bachelor’s degree or equivalent experience in Life Sciences, Supply Chain, or related field.
- 5+ years of technical writing experience in biotech, pharmaceutical, or regulated industry.
- Strong GMP documentation experience required.
- Familiarity with supply chain, warehouse, and clinical supply processes.
- Strong organizational, communication, and attention-to-detail skills.
Top Skills
- GMP
- Technical Writing
- Supply Chain
- SOP
- Forms
- Inventory
Additional Skills & Qualifications
Not specified.
Pay and Benefits
The pay range for this position is $35.00 - $55.00/hr.
Requirements
- Eligibility requirements apply to some benefits and may depend on your job classification and length of employment.
- Benefits are subject to change and may be subject to specific elections, plan, or program terms.
- If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in South San Francisco, CA.
Application Deadline
This position is anticipated to close on Jul 27, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
San Francisco Fair Chance Ordinance
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
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