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Supplier Compliance Specialist – Temporary
PharmascienceSpécialiste en conformité qualité gérant les ententes entre Pharmascience et ses partenaires. Nécessitant une expérience en réglementation et en production dans l'industrie pharmaceutique.
About the role
Key responsibilities & impact- Manage quality agreements: draft and negotiate quality clauses with partners and obtain approval of quality agreements.
- Maintain quality agreements with the relevant partners.
- Coordinate activities with Health Canada and foreign sites to obtain the documentation required to add or retain sites on the designated licence.
- Support product launches and business initiatives such as audits and inspections.
- Participate in continuous improvement projects.
Requirements
What you’ll need- Three (3) to five (5) years of experience in the pharmaceutical industry in an equivalent role.
- Excellent knowledge of Good Manufacturing Practices (GMP).
- Knowledge of local and international regulatory requirements, standards, and Quality Management Systems.
- Good knowledge of dosage forms (solids, semi-solids, liquid dosages) and manufacturing and packaging processes.
- Bilingual French/English.
Benefits
Comp & perks- No benefits mentioned
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Good Manufacturing PracticesQuality Management Systemsdosage formsmanufacturing processespackaging processes
Soft Skills
negotiationcoordinationcontinuous improvement