Technical Writer / Procedure Document Specialist IV
JMD Technologies Inc.Plainsboro, NJ, US3 days ago
Job type
- Full-time
Job descriptionBachelor's degree required; advanced degree preferred. 7+ years of experience in pharmaceutical documentation, SOP writing, and process development Strong background in GxP (Good Practice) environments Pharmacovigilance (PV) experience is a major plus. Excellent project management and multitasking skills (PMP certification a plus). Skilled in Visio for process mapping and MS Office / SharePoint / Teams Proven ability to work under pressure while maintaining accuracy and detail orientation.
Key Responsibilities :
- Develop, revise, and maintain GxP procedural documentation , SOPs, and process maps.
- Collaborate with subject matter experts, business process owners, and stakeholders to ensure documentation aligns with compliance and operational needs.
- Create clear and engaging training materials, job aids, and process workflows that support operational excellence.
- Ensure all documents meet global regulatory and inspection-readiness standards
- Evaluate existing documentation to identify gaps and recommend continuous improvement opportunities.
- Contribute to audit readiness and compliance initiatives.
Qualifications :
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Document Specialist • Plainsboro, NJ, US