Manager / Lead Associate Regulatory Affairs - Mississauga, ON, Canada

As a Regulatory Affairs Specialist you will support submission operations across all therapy areas within the Regulatory Affairs department. · ...

As a Regulatory Affairs Intern at Roche you will support the team in preparing regulatory submissions to Health Canada. · Bachelor's Degree in Science · Currently enrolled in a post-graduate certificate program in Regulatory Affairs · ...

Are you passionate about regulatory affairs and ensuring compliance in the pharmaceutical industry? · Do you have a strong strategic vision and leadership skills to drive in an unordinary way? If so, we invite you to join our team as Regulatory Affairs Manager at Novo Nordisk Can ...

Supports regulatory submissions to Health Canada · ...

We are seeking an experienced and detail-oriented Regulatory Affairs Specialist to join our team in Ontario. · ...

This entry-level opportunity is ideal for someone eager to begin their regulatory affairs career in a fast-paced, collaborative environment. As a Regulatory Affairs Intern, you will support BD's Canadian operations by contributing to regulatory submissions, market authorizations ...

The Regulatory Affairs Chapter is committed to ensuring patients have access to improved outcomes more quickly. · Supports the Regulatory Affairs team in the preparation of various regulatory submissions to Health Canada · ...

L'intitulé du poste Manager, Affaires réglementaires fiscales implique la gestion des demandes fiscales complexes et la conduite de l'analyse en matière d'impôts. · ...

Supports the Regulatory Affairs team in the preparation of various regulatory submissions to Health Canada and collaborates with external partners to shape regulatory policies. · ...

Develop and execute the regulatory strategy for SUN Innovative Medicines (IM) in-line and pipeline portfolios in Canada. Effectively represent GRA at national and international level across levels (from CEO to junior staff). Accountable/responsible for developing and implementing ...

The Regulatory Affairs Chapter is committed to ensuring patients have access to improved outcomes more quickly. Our strategic focus is on building, submitting, and obtaining approvals for clinical trial applications, new drug submissions, and new indications. · ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada. · Prepare review and submit CMC sections for regulatory filings ...

+You will lead regulatory CMC (Chemistry, Manufacturing and Controls) activities in Canada to support product development and lifecycle maintenance. You will work with cross-functional teams including R&D, Quality, Manufacturing and Commercial to build clear regulatory strategies ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance.You will work with cross-functional teams including R&D, Quality, Manufacturing and Commercial to build clear regulatory strategies and prepare submissions. · ...

The Regulatory Affairs Specialist, Intermediate role is a vital role at Synaptive Medical Inc. (SMI) where you will work with various regulatory authorities globally and other departments in the company. · You will lead the development of regulatory submissions in multiple jurisd ...

You will lead regulatory CMC (Chemistry, Manufacturing and Controls) activities in Canada to support product development and lifecycle maintenance. · Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada. · Prepare, review and su ...

We value people who are collaborative, curious, and focused on practical solutions. · Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada. · Prepare, review and submit CMC sections for regulatory filings, · ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · - Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada.<- Prepare review and submit CMC sections for regulatory filing ...

We are excited to announce the opening for the position of Quality Assurance and Regulatory Affairs. Working to support operations and to ensure compliance as related to pharmaceutical products and regulations, · The incumbent must have knowledge of Health Canada, DIN/NHP Guideli ...

The Regulatory Affairs Associate will prepare regulatory submissions for complex injectable products · Cordinates the assembly of documents to support submissions including complex generics and biosimilars per established business processes · Fulfills lifecycle management activ ...