Regulatory Affairs Specialist

Regulatory Affairs Specialist / Associate Manager Warszawa, mazowieckie Regulatory Affairs Specialist / Associate Manager Warszawa Warszawa, Mazowieckie, Polska Regulatory Affairs Specialist / Associate Manager Warszawa Warszawa, Mazowieckie, Polska For our client, a global FMCG company, we are looking for a Regulatory Affairs Specialist / Associate...

Senior Regulatory Affairs Specialist/Manager Warsaw, Masovian Voivodeship Job Responsibilities: 1. Stay up-to-date with evolving regulatory requirements in Europe, particularly for medical devices. 2. Offer expert regulatory advice for strategic decision-making, ensuring effective execution of regulatory strategies. 3. Manage maintenance activities and...

Valued Team member: We are glad you are exploring new opportunities within Zimmer BiometWhat You Can ExpectAs a Regulatory Affairs Specialist for systems team, you provide support for the maintenance and implementation of RA systems, with a particular focus on Regulatory Information Management System (RIMS) and Regulatory Distribution Controls through SAP...

We are seeking a highly motivated and experienced Regulatory Affairs Consultant (MAAs) to join our team. As a Regulatory Affairs Consultant, you will provide operational regulatory support for assigned programs and activities. This role can be office or home based in various European locaitons.Job Responsibilities: Coordinate with other groups within...

Regulatory Affairs Manager CEEWarsawCoty is a leading beauty company globally, showcasing a portfolio of renowned brands in fragrance, cosmetics, and skincare. With products distributed in over 150 countries, Coty is dedicated to various social causes and environmental sustainability.ROLE AND DEPARTMENTWe are seeking a Regulatory Affairs Manager to join our...

We are looking for a Consultant Regulatory Affairs for Labeling. This is a client dedicated role. The role can be based in multiple locations in UK and EU (home or office based).In this role you will partner with Label Strategist to:Conduct international labeling operations activities to support global new product and supplemental applications to product...

Galderma is a leading company in dermatology, present in around 90 countries, delivering innovative products and services for the skin.We are seeking individuals who are committed to achieving results, love learning, and radiate positive energy. Our ideal candidates show initiative, teamwork, and a passion for making a meaningful difference for consumers and...

What You Can ExpectCreate and maintain regulatory affairs registrations and licenses in RIMS/GTS distribution control systems in support of regulatory controls for global product distribution.Generate and communicate distribution control reports in a timely fashion.Maintain records (objective evidence) per established procedures.Perform and support User...

Dla Naszego Klienta – międzynarodowej firmy z branży farmaceutycznej poszukujemy osoby na stanowisko:Regulatory Affairs / Pharmacovigilance SpecialistLokalizacja: Warszawa Śródmieście (praca hybrydowa)Zakres obowiązków:Działania związane z utrzymaniem pozwoleń na dopuszczenie do obrotu (MA), odpowiedziami na pytania i zobowiązania regulacyjne,...

Are you looking for a career opportunity at a renowned company where you can engage in diverse projects and collaborate across various functions? Joining Stryker's Regulatory Affairs/Quality Assurance (RAQA) team offers you continuous learning prospects and ample room for professional growth. If you seek to be a part of a globally recognized workplace, take...

Intern, Regulatory Affairs Assistant to Regulatory and Registration Manager Location: Warsaw Overview The purpose of an internship is to provide real-world experience that enables the intern to put everything he/she learned into action. An internship can help the candidate gain skills that can be applied to future jobs. As an Intern, Regulatory...

DescriptionKey ResponsibilitiesTake the lead in developing and executing regulatory strategies for CIS and non-EU CEE countries, ensuring timely submissions of high quality.Oversee the entire registration process, including approvals for new products, manufacturing and import permits, and product amendments.Assist distributors in engaging and negotiating...

Job DescriptionAs a Regulatory Submission Specialist, in this role, you will be tasked with delving into medical documents, pinpointing the correct references for pharmaceutical marketing materials, uploading content onto the Veeva Vault platform, and overseeing internal processes and project management. This position is ideal for individuals with top-notch...

Hobson Prior is seeking a Senior Manager for Regulatory Operations. This role will be the primary contact for Regulatory Affairs in business projects that involve or impact data, systems, and processes. The successful candidate will ensure data compliance, accuracy, and usability, and will also provide support and training for the relevant community. This...

Job DescriptionAs a Regulatory Submission Specialist, you will be responsible for researching medical documents, identifying correct references for pharmaceutical marketing assets, submitting content into the Veeva Vault platform and maintaining internal processes and project management. This role is ideal if you possess strong organizational and...

Warsaw, Poland Category: Research and Development, Internship, Supply Chain Job ID: 26872 Assistant to Regulatory and Registration ManagerLocation: WarsawOverviewThe purpose of an internship is to provide real-world experience that enables the intern to put everything he/she learned into action. An internship can help the candidate gain skills that can be...

Site Name: Poznan Grunwaldzka, WarsawPosted Date: Jun 7 2024Regulatory Specialist supports operational activities related to maintenance of marketing authorisations (MAs) across assigned markets and/or submission types in European Partnership Markets, working in close collaboration with country leads, as well as global regulatory teams/centers and local 3rd...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

Are you a visionary professional with a strong interest in enhancing scientific communication and fostering connections within the medical field? Are you prepared to take charge and oversee medical initiatives and ventures? If so, an exciting opportunity awaits you to become a Medical Affairs Director at Novo Nordisk. Keep reading for a chance to embark on a...

Description Overview Within the Consumer Self-Care International business unit (main focus on Europe), lead the growing and evolving Regulatory Affairs Operations team responsible for centralised Regulatory systems & processes and Regulatory data management & compliance. Scope of the Role The main objectives of the job are To be the main...