Medical Affairs Team Member

Social network you want to login/join with:Medical and Scientific Affairs Senior Scientist (Poland, Ukraine, CIS), WarsawClient: HaleonLocation: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference:0fd1617ff101Job Views:6Posted:22.03.2025Expiry Date:06.05.2025Job Description:Hello. We're Haleon. A new world-leading consumer health...

Regulatory Affairs SpecialistThis role involves handling Regulatory Affairs documentation related to Product Life Cycle Management (LCM) and/or New Drug Applications (NDA). It requires ensuring Regulatory Affairs compliance according to local legislation and Standard Operating Procedures (SOPs).Main Responsibilities:Prepare and submit Regulatory...

Our Client, a leading pharmaceutical company, is seeking a talented and motivated Senior Regulatory Affairs Specialist to join their CMC team. As a key member of the team, you will be responsible for supporting global CMC regulatory strategies and documentation.The ideal candidate will have first-hand experience in CMC, regulatory affairs, or a related...

Medical Partnership OpportunitiesWe are seeking an experienced Global Medical Partner to join our team. As a key member of our Clinical Research department, you will play a crucial role in identifying unmet medical needs and implementing innovative solutions in collaboration with healthcare professionals and external partners.Your primary responsibility will...

At TN Poland, we are seeking a seasoned Regulatory Affairs Specialist to join our team. As a key member of our regulatory department, you will play a critical role in ensuring compliance with complex regulatory issues and projects.Responsibilities:Provide consulting and advisory services for regulatory matters.Author and maintain documentation to sustain...

Indero, a contract research organization specialized in dermatology and rheumatology, is seeking a highly skilled Regulatory Affairs Specialist. As a key member of our team, you will be responsible for ensuring the quality and compliance of regulatory documents and submissions. This role requires strong knowledge of EU regional regulatory guidelines and...

About the RoleWe are seeking a highly skilled Medical Liaison Expert to join our team. As a key member of our Clinical Research department, you will play a crucial role in shaping medical strategy and driving innovative solutions in collaboration with healthcare professionals and external partners.Your primary responsibility will be to identify unmet medical...

At Neusoft Medical, we are seeking a highly skilled Medical Equipment Installation Specialist to join our team.About the RoleThis is a unique opportunity to work with cutting-edge medical devices, providing installation, maintenance, and technical support services to our customers.The ideal candidate will have a strong background in biomedical engineering,...

**About the Role:**We are seeking a highly skilled Regulatory Affairs Expert to join our team. As a key member of our regulatory department, you will play a crucial role in ensuring compliance with all applicable regulations and guidelines.In this position, you will be responsible for the preparation and submission of clinical trial applications (CTAs)...

Tasks:- Team Leadership and Development:- Team Leader for CHC Regulatory Advisors, acting as a key coordinator of overall CHC activities and point of contact with CHC Product Development Head and Regulatory Affairs function leadership- Recommending and cascading goals consistent with the directions of the business development strategy- Preparation of budget...

Regulatory Affairs Manager/Senior Manager in Global LabelingWe are seeking a highly skilled Regulatory Affairs Manager/Senior Manager to join our team at {company}. This individual will be responsible for ensuring the quality of primary and derived labeling documents, providing support for these documents, and contributing to the global labeling strategy.Key...

We are seeking an experienced Senior Quality and Regulatory Affairs Manager to join our team in Warsaw, Poland. This role will be primarily located at Smith+Nephew's Warsaw office, with occasional travel to 3PL locations.As a Senior Quality and Regulatory Affairs Manager, you will lead a team of quality professionals and be responsible for developing,...

Job Description:GSK is a global biopharma company that unites science, technology, and talent to get ahead of disease together. Our ambition is to positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns.We are looking for a skilled Regulatory Affairs Specialist to join our team in Poland. As a key member...

We are driven by a passion for innovation and a commitment to improving patient outcomes. As a Scientific Affairs Manager, you will play a key role in developing and executing medical-marketing initiatives, such as conference planning and support, medical education content development, and faculty speaker training.You will be responsible for identifying...

We are looking for a highly skilled Central Europe Affairs Specialist to join our team at TN Poland. As a key member of our Scientific and Regulatory Affairs department, you will be responsible for ensuring that our products comply with all relevant laws and regulations in Central Europe.Your primary focus will be on assuring ingredients, formulas, labeling,...

About Us:Moderna Therapeutics is a leading biotechnology company that is revolutionizing medicine through mRNA technology. We are committed to advancing the technological frontier of mRNA medicines and making a significant impact on patients' lives worldwide.Job Description:We are seeking a highly skilled Commercial and Medical Affairs Procurement...

Step into a pivotal role as Manager, Regulatory Affairs and contribute to the global development and lifecycle management of groundbreaking pharmaceutical products. As a key member of team, you will lead the development and execution of global CMC regulatory strategies, ensure compliance with regulatory requirements, and represent Global CMC Regulatory...

We are seeking a highly skilled Safety Scientist to join our team at ICON plc. As a Safety Scientist, you'll play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Your primary responsibilities will include conducting safety surveillance...

Are you passionate about regulatory affairs and project management in the pharmaceutical industry?About UsTN Poland is a leading provider of pharmaceutical services, and we are seeking a dynamic Regulatory Affairs Associate to join our Labelling & Artwork team.About the Role: As a Regulatory Affairs Associate focusing on Secondary Packaging & Artwork, you...

TN Poland is a global leader in clinical research services, and we are looking for a highly qualified Regulatory Affairs Manager to join our team. As a Senior Quality Assurance Auditor, you will be responsible for conducting audits that impact business operations, processes, and systems.The Regulatory Affairs Manager will have extensive experience in quality...