Technical Procedure Writer
Job Summary
Supporting the development and approval of Quality Documents, the full-time Technical Procedure Writer will manage the controlled document approval process and assist project teams with document updates, working remotely while collaborating with global teams.
Key responsibilities:
- Manage the controlled document approval process, including authoring, reviewing, and approving documents
- Assist project teams in updating global and local controlled documents while coordinating editing and review activities across multiple regions
- Edit draft procedural documents to ensure clarity and effectiveness for global users
Required qualifications:
- 3+ years of experience in technical writing, specializing in Standard Operating Procedures (SOPs) and Work Instructions for the Pharmaceutical industry
- Experience with the entire documentation development life cycle, including Change Requests and approval workflows
- AS or BS degree in a related field
- Proficiency in MS Office products and experience with electronic document management systems; Veeva experience is a plus
- Basic knowledge of GMP, GCP, and GPvP processes is a plus
Complete Job Description
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