Regulatory Affairs Specialist

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our international Regulatory Affairs Team. As a key member of the team, you will be responsible for coordinating lifecycle management procedures, ensuring timely submission of high-quality dossiers, and managing validation issues.Key Responsibilities:Coordinate...

Job Description:Novo Nordisk is seeking a highly skilled Regulatory Affairs Specialist to join our team in Poland. As a key member of our Regulatory and Pharmacovigilance Team, you will be responsible for handling Regulatory Affairs documentation related to Product Life Cycle Management (LCM) and/or New Drug Applications (NDA). Your main responsibilities...

Job DetailsWe are seeking a skilled Regulatory Affairs Specialist to join our international team at Randstad Polska.About the RoleThe ideal candidate will have experience in regulatory affairs data management within the pharmaceutical or cosmetics industry. Strong knowledge of English and Polish is essential, with a good understanding of pharmaceutical...

Job SummaryAs a Regulatory Affairs Specialist at Novo Nordisk, you will be responsible for handling Regulatory Affairs documentation related to Product Life Cycle Management (LCM) and/or New Drug Applications (NDA).Key Responsibilities:Preparing and submitting Regulatory documentation for New Drug Applications, post-marketing variations and renewal...

Are you looking for a challenging role in the pharmaceutical industry? We are seeking a highly skilled Regulatory Affairs Specialist to join our international Regulatory Affairs Team.Key responsibilities:Perform regulatory data entry activitiesTrack incoming data entry requests and follow up until completionEnter data in relevant systems based on information...

Key Responsibilities:We are seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have 2 years of experience in a similar role, with a strong understanding of EU and non-EU regulatory requirements.Responsibilities:Plan and prioritize product notification/registration for EU and non-EU countries.Prepare and submit...

{"text":"Job Title: Regulatory Affairs Specialist (Pharmaceutical Industry)Are you looking for a role that combines your passion for regulatory affairs with your experience in the pharmaceutical industry?We are currently seeking a Regulatory Affairs Specialist to join our team at Randstad Polska.Employment contract for 12 months with the possibility of...

Job DescriptionIntroductionRandstad Polska is seeking an experienced Regulatory Affairs Specialist to join their international Regulatory Affairs Team. The successful candidate will be responsible for coordinating lifecycle management procedures and ensuring timely submission of high-quality dossiers.Key ResponsibilitiesCoordinate lifecycle management...

Parexel is seeking a Regulatory Affairs Associate (Labelling) to support our team.The successful candidate will be responsible for managing and coordinating text and artwork changes, ensuring compliance with regulatory requirements and global labeling standards.Key Responsibilities:Track the status of ongoing changes to labelling/artwork projects, evaluating...

Regulatory Affairs Specialist RoleWe are seeking a highly motivated individual with a background in Polish and European regulatory law to support our team in delivering high-quality pharmaceutical products.Key Responsibilities:Ensure compliance with Polish and European regulations for pharmaceutical products.Liaise with internal departments and external...

Work with Us to Shape the Future of Clinical ResearchParexel, a leading Clinical Research Organization, is currently seeking a skilled and detail-oriented Regulatory Affairs Associate (Labelling) to join our team.As a Regulatory Affairs Associate, you will be responsible for managing and coordinating text and artwork changes, ensuring compliance with...

Key ResponsibilitiesAs a Senior Regulatory Affairs Specialist at Allegro sp. z o.o., you will play a crucial role in shaping critical legislation for our company and the CEE region. Your primary responsibilities will include monitoring legislative proposals, developing analytical documents to facilitate engagement, and implementing significant legal...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our international team at Randstad Polska. This role involves working closely with our clients in the pharmaceutical industry, providing expertise in regulatory affairs data management.Company OverviewOur client is an international company from the pharmaceutical industry,...

Job Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Boston Scientific. As a key member of our regulatory team, you will be responsible for planning and prioritizing product notification/registration for various countries, preparing and submitting regulatory applications, and maintaining active knowledge of product...

Regulatory Affairs ProfessionalManpower Group Sp. z o.o. is a global company with over 70 years of experience, operating in 82 countries. We have been present on the Polish market since 2001 and currently have almost 35 branches across the country. Our goal is to provide candidates with new opportunities, help them find a job that matches their...

Job Title: Regulatory Specialist We are seeking a highly skilled Regulatory Specialist to support our operational activities related to the maintenance of marketing authorizations (MAs) across assigned markets and/or submission types in European Partnership Markets.Key Responsibilities:Support country leads in activities related to MA maintenance for...

Unlock Your Potential in Medical ScienceBoston Scientific, a leader in medical science for over 40 years, offers an exciting opportunity for a Regulatory Affairs Specialist to join our team. With a deep commitment to advancing science for life, we're looking for a skilled professional to help us tackle the challenges that matter most.About the Role:This is...

Parexel is seeking a highly qualified Regulatory Affairs Expert to lead post-approval Chemistry, Manufacturing, and Controls (CMC) activities for small molecule projects.The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of CMC regulations. As a recognized professional in your field of...

Senior Regulatory Specialist, CTA/INDWe are seeking a highly skilled Senior Regulatory Specialist to join our Polish Hub. This role will be responsible for coordinating, developing, and refining the CTA/IND lifecycle strategy, ensuring timely content delivery and compliance with GSK policy and procedures.Key Responsibilities:Develop and implement the CTA/IND...

Unlocking the Potential of Regulatory Affairs ExpertsParexel, a leading Clinical Research Organization (CRO), is seeking an experienced Principal Regulatory Affairs Consultant (Associate Director level) to join our team. The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of post-approval...