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Regulatory affairs associate Jobs in Old toronto, ON
- Promoted
Senior Associate Regulatory Affairs 15 Month Contract
BiogenToronto, Ontario, Canada- Promoted
Administrative Assistant – Regulatory Affairs
Quantum Management Services Ltd.Toronto, ON, CanadaAssociate, Regulatory Affairs - Packaging Compliance & EPR
DeciemToronto, ONManager of Environment & Regulatory Affairs
CSG TalentThunder Bay District, OntarioManager, Regulatory Affairs (Temporary Full Time)
CB CanadaOntario, Canada- Promoted
Associate Vice President, CISO, Regulatory Execution
TDOld Toronto, ON, Canada- Promoted
Associate Director Regulatory Affairs
Apotex Inc.North York, ON, Canada- Promoted
Senior Regulatory Affairs Specialist
FGF BrandsToronto, ON, CanadaAssociate / Director of Regulatory Affairs (remote US or Canada)
ParexelRemote, Ontario, CanadaManager, Regulatory Affairs
Innomar StrategiesRemote, ONAdministrative Assistant - Regulatory Affairs
Services de Gestion Quantum LtéeToronto, Ontario, CanadaLegal Counsel, Regulatory Affairs
TSX Inc.Adelaide St W,Torontoregulatory affairs officer
Freyr Life Science CorpScarborough, ON, CA- Promoted
Documentation Specialist
BrunelOntario, CanadaSenior Associate Regulatory Affairs
AttaineoDowntown, Toronto, n / a, CanadaRegulatory Reporting Associate
International Financial GroupToronto, OntarioManager Scientific and Regulatory Affairs Compliance and Innovation
Coca ColaOntario,ON,CanadaSenior Manager, Regulatory & Public Affairs
GS1 CanadaToronto, Ontario, CAVP, Regulatory & Scientific Affairs
EVERSANAToronto, ON, CASenior Manager, Government and Regulatory Affairs
Questrade Financial Group5700 Yonge St, North York, ON M2M 4K2, CanadaSenior Associate Regulatory Affairs 15 Month Contract
BiogenToronto, Ontario, Canada- Full-time
- Temporary
Job Purpose :
Reporting to Head of Regulatory Affairs Canada. As a senior associate in Regulatory Affairs you will lead the development and implementation of Canadian regional preclinical clinical and CMC regulatory strategy for products in development and / or post NDS approval in alignment with the Canadian business strategy.
Responsibilities :
- Leading the planning coordination and preparation of regulatory submissions and label development with the support of the Senior Manager for products in development and / or post MAA approval.
- Identify and assess regulatory risks associated with assigned projects.
- Provide input on project teams and subcommittees and represent regulatory on project teams for assigned projects.
- Participate in the preparation for regulatory agency meetings and can be the contact with the authorities on specific projects.
- Review published and promotional / advertising material to support compliance with regulatory requirements.
- Perform company business in compliance with relevant regulations company policies and procedures.
- All other duties required.
Qualifications : Education
Experience including # of years
Language(s)
Skills
Additional Information :
Why Biogen
We are a global team with a commitment to excellence and a pioneering spirit. As a midsized biotechnology company we provide the stability and resources of a wellestablished business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning growth and expanding their skills. Above all we work together to deliver lifechanging medicines with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds cultures and perspectives make us a stronger and more innovative company and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
Remote Work : Employment Type :
Fulltime