Quality Document Control Associate

1 day ago

Windsor, Canada BioVectra Inc. Full time

BIOVECTRA Inc. is a leading bio-science business in Prince Edward Island and Nova Scotia, focused on contract manufacturing and product development of active pharmaceutical ingredients, pharmaceutical intermediates, and bioreagents.

**BIOVECTRA Inc.** has an opening for** Quality Document Control Associate. **This is a** permanent full-time position **located in** Windsor, NS.**
- Supporting the MasterControl Document Management System (Document control, Document Formatting, etc).
- Issuance and archival of Production Batch Records.
- Creation and issuance of Product Labels.
- Archival, retention and disposal of Quality Management Records.
- Participating in the internal audit program and supporting external audit requirements.
- Monitoring and enforcement of GMP requirements during day-to-day operations within the department.
- Prioritizing and timely completion of tasks to meet and exceed Key Performance Indicators.
- Timely escalation of problems and issues to their supervisor to prevent any delays and risk compliance.
- Preparing or assisting in the preparation of data and reports for KPIs.
- Participating in document lifecycle activities of SOPs, and QA review and approval of SOP changes.
- Adhering to BIOVECTRA’s Health and Safety Policy as outlined in CP0010 Occupational Health and Safety Policy, Statements of Principle, and Responsibilities.
- Additional duties assigned, based on business needs and the department supervisor’s request.
- Post-Secondary Education.
- One-year direct experience in a Quality Unit position.
- Working knowledge of MS office tools such as Word, Excel, Outlook
- Three years of work experience in a similar role in a food or drug manufacturing company is an asset.
- Strong written and oral communications skills are necessary, as this position requires interaction with various levels of management, as well as interaction with external technical support teams.

**Closing Date: October 3, 2024

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