Pharmaceutical Consulting role focusing on applying GMP knowledge and experience to various projects. Prioritizing and managing compliance projects in a hybrid work environment from Mississauga, Ontario.
Responsibilities
This Pharmaceutical Consulting role focuses on applying your GMP knowledge and experience to various projects
Consultants work independently within a team environment to ensure activities are undertaken in a timely manner
Support projects assigned to you, meeting the client’s needs
Prioritize, plan, organize and execute projects related to quality and compliance
May involve coordinating/working with client personnel to meet project goals
Responsible for 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, review of importer documentation
Developing documentation as required by the project: SOPs, protocols, reports, APQRs etc.
Releasing product to market
Assisting with hosting Health Canada audits, corporate audits, and self-inspections
Requirements
Education - Bachelors' degree in Science required
1 – 3 years industry experience in the following is an asset:
Change/CAPA management
Deviation investigations
Master manufacturing/batch record review and lot release
Annual Product Quality Reviews
Stability review and assessment
APQR review and assessment
Exposure to Health Canada audits, corporate audits and self-inspections
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 selections process.
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