Práce Regulatory affairs Praha

Regulatory Affairs Product Manager – General Products & Cosmetics – EMEA Job Description Regulatory Affairs Product Manager – General Products & Cosmetics (EMEA) Permanent, Full Time Location: UK, Poland, Czech Republic, Netherlands (other EU countries with a Kimberly-Clark office may be considered) Competitive Salary + Benefits You're not the person who will settle for just any role....

Dr. Max is the leading pharmacy chain in Central Europe. In every country where we are active, Dr. Max is dedicated to improving the level of health care available by guaranteeing access to a broad assortment of medicines and pharmacy services. Our pharmacies are currently present in 6 countries (Czech Republic, Slovakia, Poland, Romania, Serbia, Italy) with great expansion plans across Europe...

Are you passionate about ensuring regulatory compliance and patient safety? Do you have experience in Regulatory Affairs and Pharmacovigilance? If you are ready to make a difference in a dynamic and impactful role, we are looking for a new RA & PV Associate to join our team in Prague. The role is a substitute for a maternity and parental leave. Read on and apply today The position As an RA & PV...

Jsme Vilgain – rychle rostoucí lovebrand v oblasti výživy, potravin a zdravého životního stylu. Vyvíjíme produkty s čistým složením, jasným benefitem a vysokými nároky na kvalitu i compliance napříč trhy. S růstem portfolia i expanzí do zahraničí hledáme zkušeného Regulatory Affairs Officer, který nám pomůže řídit regulatorní komplexitu, minimalizovat rizika a nastavit jednotné, škálovatelné...

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint...

Job Description The role reports to the International Labeling Support (ILS) Associate Director and will partner cross-functionally within GRACS and cross divisionally where applicable to ensure all the Labeling and Artworks regulatory operational activities in scope of ILS are planned, managed, and executed timely, accurately and in a compliant way. The role includes any identification of...

Director, Regulatory Affairs ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Location: Remote – EU or UK Due to a number of exciting new projects being awarded to ICON, we are seeking...

When our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross-functional teams. The role can...

Job Description The Position Coordinating and supporting all regulatory activities to maintain registrations and to obtain new marketing authorisations for the company portfolio/pipeline subject to EU procedures (Centralised, Mutual Recognition, Decentralised, National authorised Procedures) across therapeutic areas. The position also requires strong project management skills to oversee...

Regulatory Affairs & Safety Associate City: Prague We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the highest quality hygiene, wellness, and...

Co budete dělat: - Spravovat portfolio léků registrovaných v EU i mimo EU. - Zajišťovat změny, obnovy a vyřazování registrací podle předpisů. - Připravovat a podávat registrační dokumentaci úřadům (např. SÚKL, EMA, MHRA). - Spolupracovat s interními týmy i externími partnery. - Sledujte legislativní změny a zajistěte, aby byly produkty v souladu s předpisy. Požadujeme: - Vysokoškolské vzdělání...

Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting...

Company Description Visa is a world leader in payments technology, facilitating transactions between consumers, merchants, financial institutions and government entities across more than 200 countries and territories, dedicated to uplifting everyone, everywhere by being the best way to pay and be paid. At Visa, you'll have the opportunity to create impact at scale — tackling meaningful...

Band Level 6 Job Description Summary #LI-Hybrid Location: Prague, Czech Republic This role is based in Prague, Czech Republic. Purpose of the role: The Medical Affairs Head leads the strategic design and execution of global medical programs, ensuring evidence generation, launch readiness, and scientific engagement that support patient, clinical, access and healthcare value needs. The role also...

Job Description Summary #LI-Hybrid Location: Prague, Czech Republic This role is based in Prague, Czech Republic. Purpose of the role: The Medical Affairs Head leads the strategic design and execution of global medical programs, ensuring evidence generation, launch readiness, and scientific engagement that support patient, clinical, access and healthcare value needs. The role also drives the...

Job Description Associate Director, Regulatory Submissions Archive Operations Location: San Jose, Costa Rica; Prague, Czech Republic (Hybrid role - onsite 3 days per week required) Functional Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions Archive Operations supports the...

When our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional specializing on in vitro diagnostics (IVD) and Companion Diagnostics (CDx) to join our Global Regulatory Affairs team. In this strategic role, you will provide expert guidance on regulatory pathways for IVD and CDx development, clinical trials, and...

When our values align, there's no limit to what we can achieve. We are seeking an experienced Senior Regulatory Affairs Associate Labelling to develop and execute artwork strategies for our global product portfolio. In this critical role, you will ensure comprehensive oversight throughout the product lifecycle while serving as the primary liaison between Regulatory Affairs and various...

Job Description Medical Affairs Manager - Cardiovascular/Metabolism Overview: Under the supervision of the Medical Director, the Medical Affairs Manager (MAM) oversees medical activities for one or more therapeutic areas, collaborating with marketing, market access, policy teams. Key Responsibilities: - Strategic Contribution: Optimize medical and clinical excellence throughout the product...

When our values align, there's no limit to what we can achieve. Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented Regulatory Affairs Consultant to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations. As the Regulatory Affairs Consultant you will...