About this role
Associate, Regulatory Affairs at Sun Pharmaceutical Industries Ltd. Location: Brampton, Ontario, Canada. Role: preparing submissions, reviewing documentation, maintaining records Requirements: B.Sc. in Chemistry/Pharmacy/Life Science with 3–5 years regulatory affairs experience (Canada and/or USA); knowledge of FDA/TPD guidelines, eCTD submissions, GMP/QA/QC; strong writing, communication and organizational skills. Category: Research and Development (R&D) Seniority: Mid Level Tools: eCTD, Adobe Acrobat, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Document Management Systems, eCTD Software Commitment: Full Time Workplace: Hybrid Languages: English