Aktuelle Jobs im Zusammenhang mit Regulatory Affairs Specialist - Frankfurt - IQVIA
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Regulatory Affairs Specialist
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitShape the future of regulatory excellence at IQVIAAt IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance and supporting successful product lifecycle management across Germany, Switzerland, and Austria. You'll collaborate...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt; London, Deutschland IFRS Foundation VollzeitLocation: Frankfurt or London. The IFRS Foundation operates under a multi-location operating model; morning and evening calls will occur occasionally. Duration: month contract Reports to: Director of Regulatory Implementation Job purpose: The Regulatory Affairs Manager plays a key role in the design, development and delivery of an effective...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland DEVATIS DE MEXICO S RL. DE C.V VollzeitPosition Title: Regulatory Affairs ManagerLocation: GermanyWorking Model: Remote from anywhere in GermanyReports to: HQ – Regulatory Affairs ManagerAbout Devatis GmbH:Devatis GmbH, founded in Lörrach in 2014, is the German subsidiary of DEVA Holding AŞ, a leading Turkish pharmaceutical company established in 1958 and exporting products to over 50...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland IFRS Foundation VollzeitLocation: Frankfurt or London. The IFRS Foundation operates under a multi-location operating model; morning and evening calls will occur occasionally. Duration: month contract Reports to: Director of Regulatory Implementation Job purpose: The Regulatory Affairs Manager plays a key role in the design, development and delivery of an effective...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitYOUR CONTRIBUTIONAs aRegulatory Affairs Manager (m/f/d), you will support regional regulatory strategies, approvals, and the life cycle management of medicinal products, ensuring compliance with regulatory and legal requirements. This position is currently limited to afixed term of 3 years. Your responsibilities will include the following tasks:Review...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland Merz Therapeutics VollzeitYOUR CONTRIBUTIONAs aRegulatory Affairs Manager (m/f/d) CMC, you will apply your knowledge of global regulatory quality requirements to support the approval and maintenance of medicinal products. Theposition is limited to 3 yearsand includes the following activities:Create, review, and update high-quality CMC documentation to obtain and maintain product...
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Emea Regulatory Affairs
vor 2 Wochen
Frankfurt am Main, Deutschland JPMorganChase VollzeitThe position will also be responsible for deepening relationships with EU based regulators including but not limited to the ECB, ESMA, EBA, and the European Systemic Risk Board. The position will be based in Frankfurt. The role would require regular travels, primarily to London and EU countries (approximately 25% of the time). As a Vice President within our...
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Regulatory Affairs Manager
vor 1 Tag
Frankfurt am Main, Hessen, Deutschland curasan AG VollzeitFür unseren Standort in Frankfurt am Main (vor Ort / hybrid) suchen wir zum nächstmöglichen Zeitpunkt eine/n:REGULATORY AFFAIRS MANAGER / TECHNICAL DOCUMENTATION (M/W/D)Ihre Aufgaben umfassen:Bearbeitung, Aufrechterhaltung und Koordination der technischen Dokumentation für nationale und internationale Medizinproduktezulassungen, gemäß der...
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Chemist (M/F/d) - Regulatory Affairs (Biocides)
vor 1 Woche
Frankfurt am Main, Deutschland Ramboll Vollzeit**Job Description** Welcome to SCC, part of the Ramboll Group,** one of Europe’s biggest consultancy companies in the regulation sphere, a respected partner of the chemical and pharmaceutical industry, and, for more than 160 experts from different countries, a professional home. Our passion: managing registration and approval procedures for agrochemicals...
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Frankfurt am Main, Hessen, Deutschland TRIGA Consulting GmbH & Co. KG - Internal VollzeitFür die Arzneimittelzulassung eines international tätigen biopharmazeutischen Unternehmens sucht TRIGA Verstärkung.Der Schwerpunkt des Unternehmens liegt auf der Entwicklung, Herstellung und Vermarktung biopharmazeutischer Humanarzneimittel mit Fokus auf Biosimilars.Der Arbeitgeber ist global organisiert und in zahlreichen internationalen Märkten aktiv....
Regulatory Affairs Specialist
vor 3 Wochen
Shape the future of regulatory excellence at IQVIAAt IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance and supporting successful product lifecycle management across Germany, Switzerland, and Austria. You’ll collaborate with leading global pharmaceutical companies and contribute to high‑quality regulatory outcomes that truly make a difference.What you will doManage country‑level regulatory activities for medicinal products, ensuring full compliance with local requirements.Prepare and coordinate regulatory submissions in partnership with internal and external stakeholders, including notifications, renewals, variations, new applications, and MAH transfers.Lead submission processes with local Health Authorities and follow up through approval.Prepare and translate product labelling into German (e.g., SmPC, PIL) for Germany, Switzerland, and Austria.Review and approve artwork and promotional materials in client systems.Support regulatory maintenance activities across multiple pharmaceutical products.Monitor local pharmaceutical legislation and ensure updates are applied appropriately.What you need to succeedBachelor’s degree in Life Sciences or equivalent professional background.3+ years of experience in EU regulatory affairs for medicinal products, including submission document preparation and coordination.Experience within a large regulatory organization, with both centralized and local activities, is an advantage.Knowledge of pharmaceutical legislation and regulatory requirements in Germany, Switzerland, and Austria is beneficial.Excellent organizational skills, attention to detail, and ability to meet timelines.Strong communication skills and a collaborative working style.Fluent written and verbal communication skills in German and English.Strong computer skills, including MS Office; experience with regulatory information systems and artwork tools is a plus.Why join IQVIAWhen you join IQVIA, you become part of a global team that is dedicated to driving smarter healthcare for everyone, everywhere. You will collaborate with industry experts, grow your regulatory career through continuous learning, and contribute to meaningful work that supports better patient outcomes. We foster a culture of innovation, teamwork, and shared purpose — and we’re excited to welcome passionate professionals like you.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
