Praca Regulatory Affairs Coordinator Polska

Main Responsibilities: Oversee the remediation of regulatory orders, ensuring all requirements are addressed promptly and thoroughly. Diligently follow up on outstanding regulatory actions to drive timely completion and compliance. Maintain comprehensive oversight of all regulatory orders to ensure ongoing compliance and resolution. Monitor changes in regulation and implement necessary updates...

Overview At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and...

Currently we are looking for a person for the position: Regulatory Affairs Manager Place of work: Warsaw Contract type: Fixed-term contract (18 months) Tasks and responsibilities - Lead of the local Regulatory Affairs team. - Manage registration activities in Poland (NP, DCP and CP procedures). - Manage allocated products, processes and databases. - Execute strategy for new submissions in the...

Senior Regulatory Intelligence Consultant Senior Regulatory Intelligence Consultant Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to...

Regulatory Affairs & Market Access Manager Join to apply for the Regulatory Affairs & Market Access Manager role at Convatec 5 days ago – Be among the first 25 applicants About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading...

A global consumer products company is seeking a Regulatory Affairs Product Manager to ensure compliance for their general products and cosmetics across the EU and UK. The ideal candidate will have a Bachelor’s degree in a scientific field and over 5 years of experience in Regulatory Affairs. Key responsibilities include leading regulatory implementations, managing documentation, and engaging with...

Regulatory Affairs Manager page is loaded## Regulatory Affairs Managerlocations: Warsaw, Polandtime type: Full timeposted on: Posted Todayjob requisition id: R IQVIA is The Human Data Science Company. We use data, technology, analytics and human ingenuity to help healthcare clients deliver better solutions for patients and drive healthcare forward.Join our Regulatory Affairs and Drug Development...

Overview Stanowisko To Podlega Lead Counsel W ABB pomagamy przemysłowi wyprzedzać konkurencję - działać sprawniej i ekologicznie. U nas postęp to standard – dla Ciebie, Twojego zespołu i całego świata. Jako globalny lider dajemy Ci to, czego potrzebujesz, by to osiągnąć. Nie zawsze będzie łatwo, rozwój wymaga determinacji. Ale w ABB nigdy nie będziesz działać sam. Zarządzaj tym, co porusza...

A global healthcare data solutions provider is seeking a Regulatory Affairs Manager in Warsaw to lead global regulatory strategies and submissions for human medicinal products. The role demands extensive experience in Regulatory Affairs, including interactions with EMA and FDA. The ideal candidate will have strong communication skills in English and be able to operate independently in a dynamic...

Opis stanowiska Do zadań osoby na tym stanowisku należeć będą w szczególności: - Realizacja kompleksowych projektów wdrożeniowych oraz doradczych w obszarze systemu zarządzania jakością wg ISO 13485 oraz wymagań rozporządzenia MDR (UE 2017/745); - Opracowywanie i weryfikacja dokumentacji technicznej wyrobów medycznych; - Wsparcie klientów w procesach rejestracji wyrobów i podmiotów (EUDAMED,...

Qualifications - Wykształcenie wyższe (mile widziane kierunkowe m.in.: inżynieria biomedyczna, jakość, prawo, medycyna, farmacja, biologia); - Praktyczna znajomość wymagań normy EN ISO 13485 oraz umiejętność ich interpretacji w środowisku produkcyjnym i dystrybucyjnym; - Ogólna znajomość wymagań norm zharmonizowanych dla wyrobów medycznych i wytycznych MDCG; - Doświadczenie we wdrażaniu,...

New banking structure in PL Compliance, KYC & AML area Compliance , który dołączy do zespołu nowo powstającego banku. Osoba na tym stanowisku będzie odpowiedzialna za zapewnienie zgodności działalności banku z obowiązującymi przepisami prawa, regulacjami nadzorczymi oraz wewnętrznymi politykami. Monitorowanie zgodności działalności banku z przepisami prawa, regulacjami KNF, EBA, AMLD i innymi...

Join Natek as a Regulatory Process Coordinator and work for a top global pharmaceutical company ! This roles supports Process Directors and Associate Directors in managing key processes and projects. The role focuses on activities related to process implementation, communication, compliance, performance tracking, and inspection readiness. You will collaborate closely with teams across Regulatory...

CSE MCO Corporate Affairs Launch Lead page is loaded## CSE MCO Corporate Affairs Launch Leadlocations: Warsawtime type: Vollzeitposted on: Heute ausgeschriebentime left to apply: Enddatum: 6. Januar 2026 (Noch 17 Tage Zeit für Bewerbung)job requisition id: R Location: Poland## About the jobJoin our cross-functional team driving strategic launches across multiple therapeutic areas and business...

Regulatory Affairs Product Manager – General Products & Cosmetics – EMEA page is loaded## Regulatory Affairs Product Manager – General Products & Cosmetics – EMEAlocations: Walton Oaks: Netherlands- Ede: Poland-Krakow: Czech Republic -Praguetime type: Full timeposted on: Posted Todayjob requisition id: Regulatory Affairs Product Manager – General Products & Cosmetics – EMEA## Job...

IQVIA is The Human Data Science Company. We use data, technology, analytics and human ingenuity to help healthcare clients deliver better solutions for patients and drive healthcare forward. Why this role, why IQVIA? Join our Regulatory Affairs and Drug Development Solutions organization, where technology enabled regulatory services reduce time, cost, and risk across the product lifecycle, from...

Main Responsibilities: Oversee the remediation of regulatory orders, ensuring all requirements are addressed promptly and thoroughly. Diligently follow up on outstanding regulatory actions to drive timely completion and compliance. Maintain comprehensive oversight of all regulatory orders to ensure ongoing compliance and resolution. Monitor changes in regulation and implement necessary updates...

A leading healthcare analytics firm in Warsaw is seeking a Regulatory Affairs Manager to lead global regulatory strategies and submissions for human medicinal products. This involves collaborating with cross-functional teams and managing health authority interactions. The ideal candidate has over eight years of regulatory affairs experience, including significant involvement with EMA and FDA...

A global medical solutions provider is seeking a Regulatory Affairs & Market Access Manager in Poland. This role involves ensuring regulatory compliance for products in the CEE market and supporting reimbursement processes. Candidates should have extensive experience in regulatory affairs within the medical devices or pharma industries, fluency in English and Polish, and excellent communication...

Wiodąca firma doradcza w Polsce poszukuje specjalisty do realizacji projektów doradczych w obszarze jakości. Osoba na tym stanowisku będzie odpowiedzialna za opracowywanie dokumentacji technicznej oraz współpracę z klientami w zakresie regulacji ISO 13485 oraz MDR. Oferujemy elastyczne formy współpracy, w tym możliwość pracy hybrydowej lub zdalnej, a także szerokie możliwości rozwoju kompetencji...