Job Summary
A company is looking for a QA Technical Writer contractor who is engaged and collaborative.
Key Responsibilities
- Write GMP procedures, work instructions, and policies for the QA team
- Facilitate the review and approval of SOPs and ensure consistency with internal style guidelines
- Engage with cross-functional teams to establish implementation plans for document revisions and change requests
Required Qualifications
- B.S. Degree in a relevant field is required
- Technical knowledge of drug product/drug substance manufacturing
- Experience with vendor management and risk evaluation
- Familiarity with Veeva QualityDocs system
- Ability to manage work independently while collaborating with cross-functional teams
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