Regulatory Submission Lead

A global biopharma company in Mississauga is seeking a Regulatory Submission Lead to independently manage regulatory submission activities. The role involves overseeing complex registration requirements, preparing documents, and engaging with regulatory agencies while mentoring new team members. Ideal candidates should have at least 5 years of experience in...

Join to apply for the Regulatory Submission Lead - SDE LCM role at GSK. Site Name: Mississauga Milverton Drive Posted Date: Dec 18 2025 Working Model: GSK supports hybrid working through our Performance with Choice model. This position is based in-office 3 days per week at Mississauga, Ontario, with flexibility to work remotely the remaining days. Details...

**Site Name**: Poznan Grunwaldzka, Bangalore, Mississauga Milverton Drive **Posted Date**: Feb 27 2025 **SUBMISSON LEAD** works closely with the Global Regulatory Lead (GRL), Regulatory Matrix Team (RMT), global submission teams and Local Operating Company regulatory contacts to deliver e2esubmissions to agreed timelines and in compliance with Regulatory...

Site Name: Mississauga Milverton Drive Posted Date: Dec 18 2025 Only candidates with 5 years or more of experience with a strong understanding of industry, drug development, and R&D processes will be considered. Working Model GSK supports hybrid working through our Performance with Choice model. This position is based in-office 3 days per week at...

Site Name: Mississauga Milverton Drive Posted Date: Dec 18 2025 Only candidates with 5 years or more of experience with a strong understanding of industry, drug development, and R&D processes will be considered. Working Model GSK supports hybrid working through our Performance with Choice model. This position is based in-office 3 days per week at Mississauga...

Site Name: Bengaluru Luxor North Tower, Mississauga Milverton Drive, Poznan GrunwaldzkaPosted Date: Nov Job Title: Regulatory Global Submission ManagerKey ResponsibilitiesIn close collaboration with Regulatory Asset Oversight, GRL and RMT, provides project management support at submission level, drives execution of agreed plans and ensures timely and...

Join AstraZeneca, a place built on innovation and creativity. Where different views and perspectives are encouraged and valued. An environment that champions inclusion, and teams that reflect the diversity of the communities that we serve. We are looking for a **Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs Associate** to join us on a...

**At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation - ultimately providing employees with the opportunity to work across teams, functions and even the globe.**: **Recognizing the importance of individualized flexibility, our ways of working allow employees to balance...

A Canadian medical device company is seeking a Regulatory Affairs Specialist. This role requires proven experience in regulatory submissions, knowledge of FDA and Health Canada regulations, and a background in medical devices. The successful candidate will lead regulatory strategies and submissions while ensuring compliance with various jurisdictions. Strong...

A Canadian medical device company is seeking a Regulatory Affairs Specialist. This role requires proven experience in regulatory submissions, knowledge of FDA and Health Canada regulations, and a background in medical devices. The successful candidate will lead regulatory strategies and submissions while ensuring compliance with various jurisdictions. Strong...