manager regulatory affairs

What to Expect Line management, training of Regulatory Specialist Training of the direct reports in EMEA / FDA requirements Establish and manage regulatory submission timelines for both new and existing products across key global markets Engage with regulatory authorities and distribution partners to support product registrations Conduct global regulatory...

A leading life sciences recruitment agency is seeking an experienced Regulatory Affairs Manager in the Netherlands. You will manage regulatory submissions and ensure compliance with EMEA and FDA requirements. The ideal candidate will have over 8 years of regulatory affairs experience, with at least 4 years in a managerial role. Strong leadership and...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we’re not finished yet. Join Kite, as we make even...

Purpose of the Role The Manager, GRA Strategy is responsible for contributing to the development of, implementation of and advising upon global regulatory strategies for Pharming products in development as well as marketed. This individual will manage regulatory filings and submissions through all phases of development as well as post-approval across...

Purpose of the Role The Manager, GRA Strategy is responsible for contributing to the development of, implementation of and advising upon global regulatory strategies for Pharming products in development as well as marketed. This individual will manage regulatory filings and submissions through all phases of development as well as post-approval across...

Purpose of the Role The Manager, GRA Strategy is responsible for contributing to the development of, implementation of and advising upon global regulatory strategies for Pharming products in development as well as marketed. This individual will manage regulatory filings and submissions through all phases of development as well as post-approval across global...

Manager / Associate Director Regulatory Affairs Operations & Submissions Department Development ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic...

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters - it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in...

We believe that great healthcare is an essential safeguard of human dignity.At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.We support and empower our employees to grow their careers in...

Regulatory Affairs ManagerLONGDESCRIPTION (DO NOT USE)Dit ga jij doenWil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken. Als regulatory affairs manager sta je op het snijvlak van stakeholdermanagement en...

Dit ga jij doenWil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken.Als regulatory affairs manager sta je op het snijvlak van strategie, stakeholdermanagement en maatschappelijke verantwoordelijkheid. Je bent een...

Regulatory Affairs Manager BLONGDESCRIPTION (DO NOT USE)Dit ga jij doenWil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken. Als regulatory affairs manager sta je op het snijvlak van stakeholdermanagement en...

Regulatory Affairs Manager LONGDESCRIPTION (DO NOT USE) Dit ga jij doen Wil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken. Als regulatory affairs manager sta je op het snijvlak van strategie,...

Regulatory Affairs Manager LONGDESCRIPTION (DO NOT USE) Dit ga jij doen Wil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken. Als regulatory affairs manager sta je op het snijvlak van strategie,...

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

Dit ga jij doen Wil jij een sleutelrol spelen in de relatie tussen Tata Steel Nederland en haar belangrijkste toezichthouders én bijdragen aan de toekomst van duurzaam staal? Dan is dit je kans om impact te maken. Als regulatory affairs manager sta je op het snijvlak van stakeholdermanagement en maatschappelijke verantwoordelijkheid. Je bent een belangrijke...

ROLE OVERVIEWAn exciting opportunity for a Regulatory Affairs Project Manager to join our client, a leading organisation within the pharmaceutical, biotechnology and life sciences sector. This role will lead and coordinate regulatory projects across the product lifecycle, working closely with Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC),...