Position: Medical Technical Writer
Duration: 12+ months
Job Description:
The Medical Technical Writer is responsible for supporting Medicines Quality Organization (MQO) Quality Systems team to deliver high quality documents in the Safety and Efficacy Quality System. The Technical Writer will support a pharmacovigilance initiative where new process maps have been created and document changes include new documents, retirement, and revisions within the pharmacovigilance system around surveillance and case management processes. This role works closely with the business process owners and the Quality System Sr. Principal.
The Technical Writer is responsible for developing and maintaining accurate, clear, and concise procedures, required tools, and resource documents. The role is also responsible for quality checks of the quality system documents to ensure compliance with the client’s standards and procedures. The role manages workflows and metadata in the document control system using Veeva QualityDocs.
Job Responsibilities:
1. Quality Systems Document Management
2. Document Control:
General expectations:
Minimum Qualifications:
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