regulatory manager

[Please note this is a Direct Search led by Bacardi, Applications from agencies will not be accepted nor will fees be paid for unsolicited CVs.] WHAT DOES A TECHNICAL REGULATORY MANAGER DO? Ensures global packaging compliance by assessing regulatory requirements, identifying gaps and driving corrective actions across projects, markets and...

Sonova Group is seeking a dedicated Clinical Affairs Manager to support clinical evaluation of hearing instrument systems and market access alignment in a regulated environment.The role requires a master’s or PhD in health sciences or related field, experience with clinical studies, and strong analytical skills. Fluent English is required; German is a...

Sonova Group is seeking a dedicated Clinical Affairs Manager to support clinical evaluation of hearing instrument systems and market access alignment in a regulated environment.The role requires a master’s or PhD in health sciences or related field, experience with clinical studies, and strong analytical skills. Fluent English is required; German is a...

WHAT DOES A TECHNICAL REGULATORY MANAGER & SUSTAINABILITY LEAD DO? Ensures global packaging compliance by assessing regulatory requirements, identifying gaps and driving corrective actions across projects, markets and suppliers. Standardizes technical documentation for regulatory reporting, customer requests, compliance checks and sustainability data...

ppWir bei SIGA streben nach einer Welt, in der Gebäude keine Energie verschwenden. SIGA produziert eine rundum dichte, energieeffiziente Gebäudehülle aus hochwertigen Membranen, Dichtbändern und Dichtstoffen, welche weltweit vertrieben werden. Heute arbeiten mehr als 650 Mitarbeitende in 23 Ländern an der Realisierung dieser Vision. /ppUm...

**Il contributo che puoi dare**: - Assumere la responsabilità técnica per l'autorizzazione delle specialità farmaceutiche della farmacia dell'esercito, redigere i dossier di autorizzazione (CMC) in lingua tedesca in collaborazione con la responsabile Regulatory Affairs e i reparti GMP, nonché gestire le autorizzazioni esistenti per l'intero ciclo di...

Steinfels Swiss sucht Verstärkung für das Produktionsteam, um regulatorische Anforderungen über das gesamte Produktportfolio sicherzustellen und Compliance zu gewährleisten. Sie gestalten Organisationsstrukturen mit, koordinieren Zertifizierungsprozesse und unterstützen Vertrieb, Marketing sowie Projektmanagement in regulatorischen Belangen.Sie bringen...

ppAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan...

ph3Innovative Produkte hautnah - Region Basel /h3pUnser Kunde ist ein pharmazeutisches Familienunternehmen in der Health Care Branche im Grossraum Basel. Der Hauptsitz und Standort in der Schweiz forscht, entwickelt und produziert ein hochwertiges Produkteportfolio. Davon zählen einige Präparate in der Schweiz zu den Marktführern. Die Produkte werden...

**Ihr Aufgabengebiet**: - Sicherstellung der Einhaltung von regulatorischen Anforderungen für die Entwicklung, Herstellung und Markteinführung von Medizinprodukten - Pflege und Aktualisierung regulatorischer Dokumentationen zur Sicherstellung der Compliance - Ansprechpartner für Behörden/Agenturen für die Produktezulassung - Fachliche Unterstützung...

Our company is a leading provider of innovative medical technology solutions. With our advanced technologies and services, we improve the quality of life of patients worldwide. To strengthen our team at the Burgdorf site in Regulatory Affairs, we are looking for an experienced person as **Regulatory Affairs Manager |**80 - 100%**: Ref. No....

Role OverviewThe EMENA Regulatory Affairs Manager oversees regulatory compliance and affairs for the business group across Europe, the Middle East, and North Africa. This position acts as the primary expert on EU frameworks, driving product compliance strategies while aligning with business growth initiatives. The role balances high‑level strategic...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

pul liSIGA /li liRuswil /li liSchachen LU /li liBerufserfahrung /li liQualitätsmanagement, Qualitätssicherung /li /ul pWir bei SIGA streben nach einer Welt, in der Gebäude keine Energie verschwenden. SIGA produziert eine rundum dichte, energieeffiziente Gebäudehülle aus hochwertigen Membranen, Dichtbändern und Dichtstoffen, welche weltweit vertrieben...

Qualität & Regularien treffen auf Unternehmergeist und Produktmanagement Die Axanova AG ist ein erfolgreiches Schweizer Unternehmen in Uetliburg, am oberen Zürichsee, welches ein innovatives Sortiment an Gesundheitsprodukten und Nahrungsergänzungsmitteln führt und in der Schweiz vertreibt. Im Rahmen einer Nachbesetzung suchen wir per sofort oder nach...

**About the Department**: Research and Development Department (R&D) **About the Office**: **Location and contract** **Overview**: The Drugs for Neglected Diseases initiative (DNDi) and Medicines for Malaria Venture (MMV), two successful mission-driven non-for-profit Product Development Partnership organizations (PDP), have joined forces to create an...

Research and Development Department (R&D)Location and contractThis function can either be situated in Geneva, under Swiss employment contract and with a hybrid working requirement of 3 days per week on site at DNDI offices. Alternatively, the successful candidate could be located in Africa or in the EU, under a home-based working set up and with a local...

What to Expect Line management, training of Regulatory Specialist Training of 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...

Ein pharmazeutisches Familienunternehmen in der Region Basel sucht einen Experten für die Erstellung von Swissmedic Zulassungsanträgen. Die Rolle erfordert eine langjährige Erfahrung in der Arzneimittelzulassung sowie einen naturwissenschaftlichen Abschluss. Favorisiert werden Kenntnisse im Bereich Dermokosmetika. Deutsch als Muttersprache und...

Line of ServiceTaxIndustry/SectorNot ApplicableSpecialismBanking & FinanceManagement LevelSenior AssociateJob Description & SummaryAt PwC, our people in legal services offer comprehensive legal solutions and advice to internal stakeholders and clients, maintaining compliance with regulations and minimising legal risks. These individuals provide strategic...