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Quality System Manager Jobs
Company | Hays |
Address | Langley, British Columbia, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Medical Equipment Manufacturing,Food and Beverage Services,Pharmaceutical Manufacturing |
Expires | 2023-09-28 |
Posted at | 8 months ago |
HAYS Manufacturing has partner again with an amazing client in the pharmaceuticals industry, who is growing their Quality Team. Looking for a challenging and rewarding role in Quality Control and Regulatory Affairs? We are currently looking for their next Quality Systems Manager to join their team.
Your Role
As the Quality Systems Manager, you will be overseeing quality control and assurance processes in manufacturing. The responsibilities include executing action plans and projects, monitoring product quality testing, reviewing change control documents, attending management meetings, training staff, identifying manufacturing process issues, and providing data for monthly reports. The candidate should have knowledge of GMP standards.
You will work closely with employees, Health Canada, and suppliers to develop product requirements and ensure partner, customer, internal, and regulatory requirements are met.
The QSM will be looking after CQI development and implementing quality systems to comply with various industry certifications and regulatory requirements. The candidate will also be responsible for training employees on quality principles, recruiting resources, managing vendor quality systems, and ensuring the completion of corrective actions. They will be in charge of managing documentation, selecting and managing third-party testing labs and quality consultants, and overseeing self-inspection programs. Additionally, they will act as a point person for customer and third-party audits and follow up on non-conformances.
Role Requirements
- University degree in science or a related field,
- Quality Control certification, and experience with ISO9001.
- HACCP
- Experience in Food, Pharmaceutical, Medical Devices, or highly regulated environments.
- You must be proficient with the operations of GPP/GAP/GMP
- Minimum 7 years' of experience leading Quality Control, Quality Assurance, and Regulatory Affairs teams.
What you'll get in return?
Salary 85k – 95k + Benefits + 3 weeks of vacation.
Career development to Senior Manager.
The shifts are onsite Monday – Friday 8:00 am – 5:00 pm, with the ability to work an irregular work schedule depending on the needs of the business (no late nights/no weekends). Travel is not required on a regular basis.
NEXT Steps ->
If you are interested in this exciting opportunity, please apply today! or please share your resume to [email protected] your career to the next level.
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