regulatory affairs associate

This role requires a minimum of 40% on-site presence. Additional on-site work may be required based on business needs. On-site expectations are subject to change and may be adjusted on a temporary or permanent basis. Job posting ID: 9219 Employment status: Regular full-time Salary/Rate of pay:$86,400 - $101,700 Application requirements - Your up-to-date...

This role requires a minimum of 40% on-site presence. Additional on-site work may be required based on business needs. On-site expectations are subject to change and may be adjusted on a temporary or permanent basis.Job posting ID:9219Employment status:Regular full-time Salary/Rate of pay: $86,400 - $101,700Application requirementsYour up-to-date resume.We...

Join Jones Healthcare Group - Where Innovation Meets Purpose! Why this Role Matters This role helps ensure the safe and compliant delivery of products that customers and patients rely on every day. It protects the integrity of our operations by maintaining critical regulatory licenses, registrations, and submissions that keep our business moving forward....

Join Jones Healthcare Group - Where Innovation Meets Purpose!Why this Role MattersThis role helps ensure the safe and compliant delivery of products that customers and patients rely on every day. It protects the integrity of our operations by maintaining critical regulatory licenses, registrations, and submissions that keep our business moving forward. It...

Advance global regulatory efforts with Satellos as an Associate Director in Regulatory Affairs. This remote role focuses on crucial submissions, compliance, and strategy for DMD and FSHD pipelines.The Associate Director will report directly to the Chief Development Officer and Head of Regulatory Affairs. You will contribute to the success of our lead DMD...

Canadian Blood Services is seeking a Regular full-time Regulatory Affairs Associate to join our Regulatory Affairs team in our Quality and Regulatory Affairs division. This role focuses on ensuring biological products meet regulatory requirements throughout their lifecycle, collaborating with internal teams and regulators, and preparing submissions,...

Advance global regulatory efforts with Satellos as an Associate Director in Regulatory Affairs. This remote role focuses on crucial submissions, compliance, and strategy for DMD and FSHD pipelines. The Associate Director will report directly to the Chief Development Officer and Head of Regulatory Affairs. You will contribute to the success of our lead DMD...

Advance global regulatory efforts with Satellos as an Associate Director in Regulatory Affairs. This remote role focuses on crucial submissions, compliance, and strategy for DMD and FSHD pipelines. The Associate Director will report directly to the Chief Development Officer and Head of Regulatory Affairs. You will contribute to the success of our...

Canadian Blood Services is seeking a Regular full-time Regulatory Affairs Associate to join our Regulatory Affairs team in our Quality and Regulatory Affairs division. This role focuses on ensuring biological products meet regulatory requirements throughout their lifecycle, collaborating with internal teams and regulators, and preparing submissions,...

Jones Healthcare Group in Brampton, Canada is seeking a Regulatory Affairs Associate to manage regulatory compliance throughout the product lifecycle. You will lead license renewals, prepare submissions for Health Canada and FDA, and coordinate documentation with regulatory agencies and clients. The role emphasizes accuracy, cross-functional collaboration,...

Clear Destination Inc. in Oakville, Ontario, is seeking a Regulatory Affairs Specialist on a 9-month contract to manage international regulatory submissions and registration processes and ensure ongoing compliance across global markets. This hybrid role requires coordinating with cross-functional teams and maintaining thorough documentation. You will work...

Job description:About Us:CanPrev Natural Health is a dynamic and innovative company dedicated to providing exceptional products in the natural health industry. We grew out of the desire to make natural medicine safe, effective and accessible to everyone. And for close to two decades, we continue to believe and strive to help empower and inspire Canadians to...

Clear Destination Inc. in Oakville, Ontario, is seeking a Regulatory Affairs Specialist on a 9-month contract to manage international regulatory submissions and registration processes and ensure ongoing compliance across global markets. This hybrid role requires coordinating with cross-functional teams and maintaining thorough documentation. You will work...

Jones Healthcare Group in Brampton, Canada, is seeking a Regulatory Affairs Associate to manage regulatory compliance, licenses, and submissions for pharmaceutical products. You will coordinate documentation, maintain registrations, and support quality assurance initiatives with clients and regulatory agencies.The role requires a Pharmacy/Science degree and...

Clear Destination Inc. in Oakville, Ontario, is seeking a Regulatory Affairs Specialist on a 9-month contract to manage international regulatory submissions and registration processes and ensure ongoing compliance across global markets.This hybrid role requires coordinating with cross-functional teams and maintaining thorough documentation. You will work...

Ce poste offre une formule de travail hybride, permettant d’effectuer 50 % de ses tâches en télétravail. Cette approche favorise un équilibre entre performance et flexibilité, tout en maintenant une collaboration étroite avec les équipes. Le poste est basé dans notre bureau de Ville Saint-Laurent, à Montréal. À propos du poste Nous sommes à la...

Ce poste offre une formule de travail hybride, permettant d’effectuer 50 % de ses tâches en télétravail. Cette approche favorise un équilibre entre performance et flexibilité, tout en maintenant une collaboration étroite avec les équipes. Le poste est basé dans notre bureau de Ville Saint-Laurent, à Montréal.À propos du posteNous sommes à la...

Roche Holding AG au Canada propose le programme One PDR ET, une initiation de deux ans pour acquérir des connaissances réglementaires. Le parcours combine tâches pratiques et apprentissage sur mesure, idéal pour des débutants en réglementation.

Roche Holding AG au Canada propose le programme One PDR ET, une initiation de deux ans pour acquérir des connaissances réglementaires. Le parcours combine tâches pratiques et apprentissage sur mesure, idéal pour des débutants en réglementation.

Regulatory Affaris Associate Intern 12-Month Contract Assists with global/regional tactical submission plans on allocated projects/products that implement the agreed regulatory strategy to develop and maintain products. Fluent with submission compilation, publishing and approval information processes and tools. Seeks opportunities and develops 'rapport' with...