Global Regulatory Labeling Lead — Senior Consultant

Senior / Regulatory Affairs Consultant - Labeling Join to apply for the Senior / Regulatory Affairs Consultant - Labeling role at Parexel Direct message the job poster from Parexel Parexel is seeking an experienced Global Regulatory Labeling Manager to collaborate with a dedicated client team and oversee complex global labeling initiatives. In this role, you...

Parexel is seeking an experienced Global Regulatory Labeling Manager to collaborate with a dedicated client team and oversee complex global labeling initiatives. In this role, you will lead and coordinate labeling activities across foundational and non-foundational markets, ensuring compliance with global regulatory requirements and supporting product...

A leading global biopharmaceutical firm in Canada is seeking a Global Regulatory Labeling Manager to oversee complex global labeling initiatives. This pivotal role involves leading labeling activities across multiple markets, ensuring regulatory compliance, and supporting product lifecycle management. The ideal candidate will have a university degree in Life...

Job purposeThe goal of the Senior Regulatory Affairs Associate is to plan, coordinate, compile, submit, obtain approval, and maintain drug product registrations for the US, Canada, EU, UK & Australia as well as assist global drug product registrations.Duties and responsibilitiesPlan, coordinate, compile and file drug product submissions for Canada and the...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

A leading pharmaceutical company is seeking a Senior Manager for Global Regulatory Affairs - CMC. This remote role involves authoring regulatory documents and ensuring compliance with evolving CMC requirements. Candidates should have a strong background in the biopharmaceutical industry with over 9 years of CMC experience. The position offers competitive...

A global sustainability consultancy in Canada is seeking a Principal Consultant, Biologist/Regulatory Specialist to lead environmental permitting for energy projects. The role demands a strong background in regulatory compliance and mentoring capabilities. Ideal candidates will have over 6 years of consulting experience, deep knowledge of CEQA/NEPA...

Requisition ID: 245903Join a purpose driven winning team, committed to results, in an inclusive and high-performing culture.The role:Contributes to the overall success of the Global Finance, Regulatory Risk Governance group (1B) ensuring specific individual goals, plans, initiatives are executed / delivered in support of the team's mandate and overall...

Principal Consultant, Biologist/Regulatory Specialist, Power and Renewables Join to apply for the Principal Consultant, Biologist/Regulatory Specialist, Power and Renewables role at ERM . Why This Role Matters California’s energy and infrastructure projects are critical to meeting climate goals—but they require navigating complex regulatory landscapes...

VP Business Development @ Lorpon Labels | Packaging Expert About Lorpon Toronto label manufacturer in our 40th year, operating from our new facility at 100 Innovation Drive in Vaughan, Ontario. We run multiple HP Indigo digital presses and flexographic converting/finishing presses , with advanced capability in Expanded Content Labels (ECL) and shrink sleeves...