Job Description & How to Apply Below
Lead regulatory strategy in Canada with Teva Pharmaceuticals as a Regulatory Affairs Manager in Scarborough, Ontario. Focus on submissions, product launches, and compliance within a hybrid work environment. Teva Pharmaceuticals is seeking a Regulatory Affairs Manager to spearhead Canadian regulatory planning for various medicinal products.
In this hybrid role, you will navigate the intricacies of Abbreviated New Drug Submissions, oversee labelling updates, and manage deficiency responses with precision. Collaborating with global teams, your expertise in health regulations will ensure timely product launches while adhering to evolving guidelines.
Key Responsibilities:
Lead the preparation and submission of ANDSs and sANDSs
Update product labelling materials for compliance
Manage deficiencies and submission timelines
Participate in essential regulatory meetings
Act as Canadian regulatory lead in project teams
Requirements:
Bachelor’s degree in a science‑related field
5+ years in pharmaceutical industry
Robust regulatory strategy background
Experience with complex generics and biosimilars
Knowledge of Health Canada regulations
Bring your leadership and regulatory expertise to Teva Pharmaceuticals in Scarborough.
#J-18808-Ljbffr
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×