Entry - level Quality Engineer at Celestica, responsible for quality standards in manufacturing processes. Engaging in ISO compliance, supply chain management, and process documentation.
About the role
- Quality Assurance Lead/Senior Consultant applying GMP knowledge in pharmaceutical consulting projects. Involves project management, compliance assessment, and client collaboration.
Responsibilities
- Establishing project plans that capture all aspects of the scope of work
- Prioritizing and managing compliance projects
- Completing critical assessments of data and documents to identify gaps compared to regulatory requirements
- Communicating project milestones on a monthly basis
- Completing client assigned tasks: deviation investigations, management of quality systems, review of documentation
- Developing documentation as required by the project: SOPs, protocols, reports, etc.
- Conducting audits both internal and external
- Releasing product to market
- Hosting Health Canada audits
Requirements
- Education - Bachelors' degree in Science required
- Experience in the following is an asset:
- Importation
- Change Management
- Deviation investigations
- Master manufacturing/batch record review and lot release
- Health Canada audit responses Annual Product Quality Reviews
- Stability review and assessment
Benefits
- Learn about what makes our company unique at www.qualityandcompliance.com.
- Q&C welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process
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