Regulatory Affairs Data Specialist

Job DescriptionWe are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team in Warsaw, Poland.The successful candidate will be responsible for the preparation and submission of regulatory documents and applications to ensure compliance with applicable EU regulations and guidelines.This role will involve coordination of...

Company OverviewManpowerGroup Sp. z o.o. is a global firm with over 70 years of experience, operating in 82 countries. On the Polish market, we have been present since 2001 and currently have nearly 35 branches throughout the country. Our goal is to provide job seekers with new opportunities and assist them in finding employment matching their qualifications...

Social network you want to login/join with:Specialist, Regulatory Affairs (Poland), WarsawClient:InderoLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:0b22dd25b017Job Views:3Posted:21.03.2025Expiry Date:05.05.2025Job Description:Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In...

About the RoleAllegro is seeking a Senior Regulatory Affairs Specialist to join our team. In this role, you will play a critical part in shaping legislation related to postal, customs, logistics, and tax laws.You will monitor legislative proposals, develop analytical documents to facilitate engagement, and implement significant legal changes. Your primary...

About the RoleThe Regulatory Specialist will play a crucial role in supporting operational activities related to the maintenance of marketing authorizations across assigned markets and submission types in European Partnership Markets.This position requires close collaboration with country leads, global regulatory teams/centers, and local 3rd party service...

GSK is a global biopharma company dedicated to uniting science, technology, and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty and general medicines.As a Senior Regulatory Specialist, Product Variations, CD CMC, you will be responsible for managing CMC regulatory activities required during the lifecycle of our...

As a key member of our client's global CMC team, the Senior Regulatory Affairs Specialist will play a critical role in supporting regulatory strategies and documentation.About Our ClientOur client is one of the largest pharmaceutical companies in the world, committed to improving human health through innovative medicines and treatments.Key...

Job SummaryThe MDR, ISO 13485 Specialist plays a pivotal role in ensuring the company's software complies with Medical Device Regulation (MDR) and relevant standards. This position involves leading the preparation and submission of regulatory documentation, maintaining the quality management system, and ensuring ongoing compliance.Key Responsibilities:Lead...

manager regulatory affairs (established products), EMEAFor our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Manager EMEA, who will provide regulatory support to the Portfolio Leader for a portfolio of marketed oncology and internal medicine drug products which are supported by the Established Products...

ManpowerGroup Sp. z o.o., a global leader with over 70 years of experience, operates in 82 countries. In Poland, we have been present since 2001 and currently have almost 35 branches across the country. Our goal is to provide candidates with new opportunities and assist them in finding work that matches their qualifications and experience.We are searching...

Company OverviewGSK is a global biopharma company that unites science, technology and talent to get ahead of disease together. Our mission is to positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns.We are committed to making GSK a place where people can thrive. We want our employees to feel inspired,...

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Manager EMEA , who will provide regulatory support to the Portfolio Leader for a portfolio of marketed oncology and internal medicine drug products which are supported by the Established Products team.If you have relevant experience and would like...

About This RoleSyneos Health, Inc. is seeking an experienced Senior Clinical Operations Specialist to support our global operations. The successful candidate will have a strong background in clinical trials, with a focus on site activation and start-up processes.This role involves collaborating with cross-functional teams to ensure seamless execution of...

Job Description:Randstad is partnering with one of the largest pharmaceutical companies in the world to find a highly skilled Regulatory Affairs Specialist to join their CMC team. As a key member of the team, you will play a critical role in supporting global CMC regulatory strategies and documentation.About Our Client:Our client is a well-established...

We are committed to finding the right candidate for this challenging role as a Business Operations Specialist - Regulatory Affairs. In this position, you will be responsible for managing new business requests, implementing strategic initiatives, and proactively supporting clients.About the JobThe ideal candidate will have experience in financial services,...

Senior Global Regulatory Affairs SpecialistICON 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.We are currently seeking a Senior Global Regulatory...

Social network you want to login/join with:Manager Regulatory Affairs (Established Products), EMEA, WarsawClient:Location: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 96cb8c4b66c3Job Views: 4Posted: 10.02.2025Expiry Date: 27.03.2025Job Description:For our Client, one of the biggest Pharmaceutical Companies worldwide, we are...

Location field must contain 'city, state' or a zip code to perform a radius search (e.g., Denver, CO or 46122 ). City and state must be separated by a comma followed by a space (e.g., Houston, TX )J&J Family of Companies Manager Regulatory Affairs Process, Data, Compliance EMEA in Warsaw , PolandAt Johnson & Johnson, we believe health is everything. Our...

The Senior Quality and Regulatory Affairs Specialist role at Smith+Nephew offers a unique opportunity to work with a leading medical technology company that is passionate about improving patient outcomes. In this role, you will be responsible for ensuring the quality and regulatory compliance of our medical devices, working closely with cross-functional...

**About the Role**We are seeking a highly skilled Regulatory Affairs Professional to join our team at GlaxoSmithKline.The successful candidate will be responsible for managing multiple CMC variations and source transfers for Finished Products, Intermediates, and Active Pharmaceutical Ingredients for pharmaceutical, biopharmaceutical, and vaccine products....