Regulatory affairs manager
3 settimane fa
We're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You'll be working at the heart of a fast-paced, innovation-driven environment, driving dossier strategy, managing global submissions, and collaborating closely with cross-functional teams across markets. Responsibilities: Lead Regulatory Submissions: Oversee the planning, preparation, and timely submission of regulatory documentation (e.g., e CTD Modules 1–5) for product registrations, variations, renewals, and withdrawals, ensuring accuracy and compliance. Coordinate Stakeholder Engagement: Serve as the primary regulatory contact for designated product categories (e.g., analgesics), fostering effective communication with internal teams and external partners. Maintain Dossier Integrity: Manage the creation and upkeep of core product dossiers, ensuring alignment with current regulatory requirements and submission timelines. Ensure Documentation Readiness: Supervise the organisation and electronic archiving of regulatory records to support accessibility and inspection readiness. Collaborate Across Functions: Work cross-functionally with Regulatory Strategy, R& D, Pharmacovigilance, Quality, and Marketing to ensure regulatory alignment throughout the product lifecycle. Requirements: Degree in Pharmacy, Life Sciences, or a closely related field (Bachelor's or Master's level). At least 5 years of hands-on experience in regulatory affairs within the pharmaceutical or healthcare sector. Strong command of international regulatory guidelines (e.g., EMA, ICH, and national health authorities). Solid track record in preparing and submitting e CTD dossiers, including CMC M3 content development. Highly organised with excellent attention to detail and ability to manage multiple regulatory projects simultaneously.
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Regulatory Affairs Manager
4 settimane fa
Monza, Italia Scienta A tempo pienoWe're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You'll be...
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Regulatory Affairs Manager
3 settimane fa
Monza, Italia Scienta A tempo pienoWe're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You’ll be...
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Regulatory Affairs Manager
3 settimane fa
Monza, Italia Scienta A tempo pienoWe're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You'll be...
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Regulatory Affairs Manager
3 settimane fa
Monza, Italia Scienta A tempo pienoWe're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You'll be...
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Regulatory Affairs Manager
3 giorni fa
Monza, Italia Scienta A tempo pienoWe're currently partnering with a leadingglobal consumer health businessto find an experiencedGlobal Regulatory Operations Medicine Managerto join their dynamic Regulatory Affairs team.This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products.You'll be working at...
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Regulatory Affairs Lead: Central
3 giorni fa
Monza, Italia Jobbit A tempo pienoA pharmaceutical client in Florence is looking for a Regulatory Affairs Coordinator for Central and Latin America.The successful candidate will ensure compliance and support timely submissions across diverse markets.With at least 5 years of experience in Regulatory Affairs and a master's degree in a scientific field, you will work collaboratively with...
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Regulatory Affairs Lead: Central
3 settimane fa
Monza, Italia Jobbit A tempo pienoA pharmaceutical client in Florence is looking for a Regulatory Affairs Coordinator for Central and Latin America. The successful candidate will ensure compliance and support timely submissions across diverse markets. With at least 5 years of experience in Regulatory Affairs and a master's degree in a scientific field, you will work collaboratively with...
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Regulatory Affairs Lead – Central
2 giorni fa
Monza, Italia Menarini Group A tempo pienoA leading pharmaceutical company in Italy is seeking a Regulatory Affairs Central and Latin America Coordinator.This mid-senior level role requires a Master's degree in a scientific field and at least 5 years of experience in coordinating international regulatory affairs, with a focus on Central and South America.Responsibilities include planning regulatory...
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Regulatory Affairs Lead – Central
39 minuti fa
Monza, Italia Menarini Group A tempo pienoA leading pharmaceutical company in Italy is seeking a Regulatory Affairs Central and Latin America Coordinator.This mid-senior level role requires a Master's degree in a scientific field and at least 5 years of experience in coordinating international regulatory affairs, with a focus on Central and South America.Responsibilities include planning regulatory...
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Regulatory Affairs Lead – Central
15 ore fa
monza, Italia MENARINI Group A tempo pienoA leading pharmaceutical company in Italy is seeking a Regulatory Affairs Central and Latin America Coordinator. This mid-senior level role requires a Master's degree in a scientific field and at least 5 years of experience in coordinating international regulatory affairs, with a focus on Central and South America. Responsibilities include planning...
