Job Summary
A company is looking for a Technical Writer to support quality documentation efforts in a GxP-regulated environment.
Key Responsibilities
- Revise and update SOPs, Work Instructions, and labeling-related documentation in compliance with GxP requirements
- Collaborate with cross-functional teams to implement documentation updates and support Change Control processes
- Ensure documentation consistency, completeness, and compliance with internal quality standards
Required Qualifications
- 3+ years of experience in documentation or labeling support within a GxP-regulated pharmaceutical or biotech environment
- Prior experience with labeling documentation and Change Control processes
- Exposure to Business Continuity Planning (BCP) processes
- Familiarity with document management systems (e.g., Veeva, Documentum, SharePoint)
- Bachelor's degree in Life Sciences, Information Systems, or a related field
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