Director, Regulatory Affairs - Brampton

Prepare and file drug product submissions to the US FDA · Prepare and/or review submissions to Health Canada and FDA for a variety of dosage forms. · ...

This position involves preparing and filing drug product submissions to regulatory agencies. The successful candidate will maintain approved product monographs and assist in global drug product registrations. · Prepare and file drug product submissions to regulatory agencies. · M ...

Develop and execute the regulatory strategy for SUN Innovative Medicines (IM) in-line and pipeline portfolios in Canada. · ...

Develops and executes regulatory strategy for SUN Innovative Medicines in-line and pipeline portfolios in Canada. · ...

Sun Pharmaceutical Industries Inc. is a global company with a diverse team and experience in developing and marketing pharmaceutical products. · ...

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. · ...

The Senior Regulatory Affairs Specialist is responsible for developing regulatory strategies and preparing Canada submissions. · Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company. · ...

The Senior Regulatory Affairs Specialist is responsible for developing regulatory strategies, preparing Canada submissions and maintaining approval for products. · ...

The Senior Regulatory Affairs Associate is responsible for planning, coordinating and filing drug product submissions in eCTD format to Canada & US.They will also support the preparation of regulatory filings to EU, UK & Australia. · Additional responsibilities include reporting ...

The Senior Regulatory Affairs Specialist is responsible for developing regulatory strategies, preparing Canada submissions and maintaining approval for products. · A Day in the Life · The Senior Regulatory Affairs Specialist is responsible for assessment of device changes for reg ...

This role oversees the daily operation of the Quality, Regulatory and Safety team who are involved in monitoring controlling improvement quality safety systems providing assistance marketing sales warehouse staff product regulatory matters managing corporate risk environmental he ...

Oversee daily operation of Quality Regulatory · Safety team monitoring controlling improvement quality safety systems providing assistance marketing sales warehouse staff product regulatory matters managing corporate risk environmental health safety regulatory. · ...

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 ...

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

Supports regulatory submissions to Health Canada · ...

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 · ...

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

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 ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

This position has a focus on the regulatory process accountable for providing high quality technical/administrative support as required in assessing product changes (RACs), managing and clearing GTS Blocks, supporting RFPs and Tenders, responding to regulatory queries, · and prom ...