Chef principal de la conformité et de la validation/Sr. Manager Compliance & Validation
Listed on 2025-12-02
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Location: Montreal
Jubilant Hollister Stier, a subsidiary of Jubilant Pharma Holdings Inc., is currently recruiting a Sr. Manager Compliance and Validation to join our team in Kirkland, Quebec, or Spokane, Washington.
What We OfferA culture that values growth and professional development, a highly competitive base salary, comprehensive health, dental and disability insurance programs, a group retirement plan, and wellness programs. Jubilant Hollister Stier is a rapidly growing company with offices in Kirkland and Spokane. As a fully integrated contract manufacturing organization, we manufacture sterile injectable formulations as well as solid and semi‑solid dosage forms.
Our four facilities in North America and India provide specialized manufacturing services for the pharmaceutical and biopharmaceutical sectors. For more information, visit
The Sr. Manager of Validation and Compliance is responsible for ensuring that all manufacturing equipment, processes, and documentation meet regulatory standards and demonstrate suitability.
Responsibilities- Oversee validation of manufacturing processes, equipment and systems to ensure regulatory and quality standards.
- Maintain compliance oversight of all qualification, maintenance, metrology and other records, including FDA, GMP and other relevant standards.
- Prepare, review and maintain detailed validation and compliance documentation, including CAPAs, change controls, protocols, deviations and reports.
- Support internal and external audits and inspections to ensure compliance with regulatory standards.
- Design and implement training programs for staff on validation and compliance procedures.
- Identify areas for improvement in validation and compliance processes and implement corrective actions.
- Manage validation and compliance projects, including scheduling, resource allocation and milestone tracking.
External:
- Regulatory Inspectors
- Client Auditors
Internal:
- Engineering Management
- Maintenance Management
- QA Compliance
- Bachelor’s of Science
- 10+ years of pharmaceutical experience
- FDA regulated industry experience
- 3–5 years of managerial experience
- Experience with Trackwise Quality Management System
Functional Skills:
- Office (Word, PowerPoint, Excel, Teams)
- Working knowledge of U.S. and E.U. GMPs
Behavioral Skills:
- Works autonomously with high ownership, without regular direction
- Supervises salaried and hourly staff
- Creative problem solving
- Manages conflicts, collaborates and leads teams to solutions
If qualified individuals with a disability need assistance in applying for this position, please contact Human Resources at MTL‑ with the nature of your request and your contact information.
Senior LevelDirector
Employment TypeFull‑time
Job FunctionFinance and Sales
IndustriesPharmaceutical Manufacturing
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