Praca Regulatory Affairs Officer

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...

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...

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...

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...

Regulatory Affairs Manager page is loaded## Regulatory Affairs Managerlocations: Warsaw, Polandtime type: Full timeposted on: Posted Todayjob requisition id: R1521462IQVIA 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...

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...

About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise...

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...

The Banking Services (BBS) business unit at SIX is the competence center for operations, development, and innovation in Swiss payment transactions. The infrastructure for interbank payments, the connection to the Euro area (SEPA), as well as card-based and mobile payments are the main focus. In the Data Governance Office (part of Risk & Business Management), you will support the business as a...

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: 883084Regulatory Affairs Product Manager – General Products & Cosmetics – EMEA## Job...

Firma z branży Life Sciences poszukuje pracownika do nadzoru nad procedurami rejestracyjnymi produktów leczniczych w Warszawie. Poszukujemy osoby z wykształceniem farmaceutycznym oraz doświadczeniem w przygotowywaniu dokumentacji rejestracyjnej. Oferujemy hybrydowy model pracy oraz kompleksowy pakiet korzyści, w tym opiekę medyczną i program szkoleń. Jeśli masz wysokie umiejętności komunikacyjne...

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...

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...

The Banking Services (BBS) business unit at SIX is the competence center for operations, development, and innovation in Swiss payment transactions. The infrastructure for interbank payments, the connection to the Euro area (SEPA), as well as card-based and mobile payments are the main focus. In the Data Governance Office (part of Risk & Business Management), you will support the business as a...

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...

Lokalizacja: Warszawa – praca hybrydowa Typ: Pełny etat Twoje zadania - Nadzór nad procedurami rejestracji, re-rejestracji oraz zmian w dokumentacji produktów leczniczych w Polsce, Unii Europejskiej i Wielkiej Brytanii, aktywna komunikacja z Agencjami Rejestracyjnymi; - Sporządzanie części administracyjnej (moduł 1) oraz kompletowanie całości dokumentacji rejestracyjnej, rerejestracyjnej,...

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...

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...

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,...