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Biopharma Validation Specialist (GMP/QA)
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Biopharma Validation Specialist (GMP/QA)
Job summary
A biopharmaceutical company in Toronto seeks a Validation Associate to implement validation strategies and ensure project milestones are met. You will be responsible for commissioning production equipment, optimizing validation procedures, and assisting in regulatory compliance. This role requires 2-3 years of GMP-related experience and a degree in Science or Engineering. Join a dedicated team and grow your career in a fast-paced, quality-driven environment.
Benefits
Qualifications
- 2 to 3 years of GMP-related experience in biopharmaceutical or pharmaceutical manufacturing facilities.
- Strong knowledge of cGMP/GDP principles and international regulatory requirements.
Responsibilities
- Perform commissioning and qualification of new and existing production equipment.
- Participate in optimization of existing process validation procedures.
- Assist in the development of a process validation program.
- Draft, review, execute and approve protocols and reports.
- Evaluate and update the Validation Master Plan.
- Contribute to regulatory audits and corrective actions.
Skills
Education
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.