Position: Medical Technical Writer
Location: Onsite in Indianapolis, 2–3 days per week
Duration: 5 months
Job Description
The Medical Technical Writer will support the Medicines Quality Organization (MQO) Quality Systems team by delivering high-quality documents within the Safety and Efficacy Quality System. This role is part of a pharmacovigilance initiative, which includes managing new process maps and overseeing documentation changes such as creation, revision, and retirement related to surveillance and case management.
This position collaborates closely with business process owners and the Quality System Sr. Principal to ensure clear, compliant, and well-maintained documentation. Responsibilities include overseeing workflows and metadata in the document control system, using Veeva QualityDocs.
Key Responsibilities
Quality Systems Document Management
Document Control
General Expectations
Minimum Qualifications
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