Práce Regulatory affairs manager

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...

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....

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...

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...

Popis pracovní pozice 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...

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...

Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of...

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 title: Principal Regulatory Affairs Specialist Department: Regulatory Affairs Location: Poland / Czech Republic / Hungary or UK GLS: P04 A brighter future awaits you CooperVision is one of the world’s leading manufacturers of soft contact lenses with a presence in over 100 countries. Being part of CooperVision means helping improve the way people see each day. It’s more than making...

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...

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...

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 lead our medical devices and combination products clinical trial regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and serve as the key regulatory representative for our global...

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. 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...

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...