Support technical raw materials for regulatory submissions in the pharmaceutical sector. Collaborate with internal stakeholders and ensure compliance with local and international regulations.
Responsibilities
Collaborate with internal stakeholders in Regulatory Affairs and Research & Development
Provide technical support and documentation for Canadian and international regulatory submissions
Obtain, archive and distribute documents related to active pharmaceutical ingredients (APIs), excipients, or packaging materials
Communicate with the immediate supervisor, project managers and other colleagues on project progress
Requirements
Master's degree or higher in Chemistry or a related field
Minimum 2 years in the pharmaceutical industry
Proficiency in MS Office; experience with SAP and OpenText (DMS)
Benefits
Bilingual in French and English
Fluency in spoken and written English
Knowledge of local and international regulatory requirements
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