Lavori attuali relativi a Regulatory Affairs Manager - Monza - Scienta
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Regulatory Affairs Manager
3 giorni fa
Monza, Italia Randstad Italia A tempo pienoFor a multinational company in the pharmaceutical field we are looking for a Regulatory Affairs Manager. The Regulatory Affairs Manager is responsible for managing regulatory activities for an assigned product portfolio. The goal is to secure and maintain marketing authorizations, ensure compliance with local and EU regulations, review promotional materials,...
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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
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
7 giorni 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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Ehs Regulatory
1 giorno fa
Monza, Italia Trace One A tempo pienoOverviewDescrizione dell’offerta di lavoroContext: Within the Regulatory & Scientific Affairs team and in an international and multicultural environment, as Junior Specialist of EHS Regulatory & Scientific Affairs you will ensure full regulatory compliance of products by monitoring requirements, updating technical databases, and executing assigned...
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Ehs Regulatory
2 giorni fa
Monza, Italia Trace One A tempo pienoOverview Descrizione dell’offerta di lavoro Context: Within the Regulatory & Scientific Affairs team and in an international and multicultural environment, as Junior Specialist of EHS Regulatory & Scientific Affairs you will ensure full regulatory compliance of products by monitoring requirements, updating technical databases, and executing assigned...
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Regulatory Affairs Lead: Central
1 settimana 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
4 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 settimane 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
3 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 Affairs Manager
7 giorni fa
We'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 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., eCTD 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 eCTD dossiers, including CMC M3 content development.Highly organised with excellent attention to detail and ability to manage multiple regulatory projects simultaneously.
