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Minimum of 10 years of experience in quality assurance in the pharmaceutical industry in quality operations and validation. JOB OBJECTIVES<br>Ensure that activities carried out as part of the transfer of production from the OM1 line to OM2 meet quality and GMP compliance requirements. Review b

In depth knowledge of Canadian regulations, processes and issues for hospital generic drugs and biologics development and registration including detail knowledge of ICH, Health Canada guidelines, GMPs and offer relevant guidelines focus in area of specialization. The Head of Quality – CMO and Supp

Join a reputable not-for-profit human services Association with a mission to make a positive difference in our communities and the province of Saskatchewan!. Full-time, fixed term 1 year funded in April of each year, with a good possibility of extension. In this newly created role, you will provide

In depth knowledge of Canadian regulations, processes and issues for hospital generic drugs and biologics development and registration including detail knowledge of ICH, Health Canada guidelines, GMPs and offer relevant guidelines focus in area of specialization. The Head of Quality – CMO and Supp

In depth knowledge of Canadian regulations, processes and issues for hospital generic drugs and biologics development and registration including detail knowledge of ICH, Health Canada guidelines, GMPs and offer relevant guidelines focus in area of specialization. The Head of Quality – CMO and Supp

Une gamme d’avantages sociaux, incluant des assurances complètes, un fonds de pension;. Développement professionnel et opportunités d’avancement de carrière;. Il ne nous est malheureusement pas possible d'offrir de parrainage international pour ce poste.

This position is deemed Safety Sensitive for purposes of United Rentals’ policies and procedures. As an Equipment Associate at United Rentals, you will perform a variety of manual tasks to ensure smooth branch operation. En tant qu'associé à l'équipement à United Rentals, vous devrez effectuer

Ensure that activities carried out as part of the transfer of production from the OM1 line to OM2 meet quality and GMP compliance requirements. Review batch records (including analysis results and related documents) concerning the acceptance (or rejection) of transferred batches that will be markete

Review batch records (including analysis results and related documents) concerning the acceptance (or rejection) of transferred batches that will be marketed. Minimum of 10 years of experience in quality assurance in the pharmaceutical industry in quality operations and validation. Ensure that activ

Based out of Montreal, you’ll have the opportunity to work as part of multi-disciplinary project teams to contribute directly to all phases of government and privately-owned infrastructure projects. Head of Sustainability -- Montreal Canada. Drive the integration of environmental, social, and gove