Specialist collaborating on technical support for regulatory submissions in pharmaceutical industry. Working closely with regulatory affairs and R&D teams for Canadian and international markets.
Responsibilities
Provide necessary support to Regulatory Affairs
Provide technical support to the Compliance group
Collaborate with Regulatory Affairs and internal teams
Obtain, archive and distribute documents related to active pharmaceutical ingredients (APIs)
Requirements
Bilingual in French and English
Proficient in written and spoken English
Ability to interpret technical and scientific documentation
Proficient in MS Office
Proficient in SAP and OpenText (DMS)
2 years' experience in the pharmaceutical industry
Benefits
Hybrid work model
Technical support and documentation for regulatory submissions
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