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 our team, you will be responsible for providing Regulatory Affairs support, ensuring compliance with regulatory requirements, and maintaining accurate records.Key Responsibilities:Provide Regulatory...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Novo Nordisk. As a key member of our Regulatory Affairs 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).Main...

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...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our international team. As a key member of our Regulatory Affairs Team, you will be responsible for ensuring compliance with regulatory requirements and ensuring the quality of our data.Key Responsibilities:Enter regulatory data into relevant systemsTrack and...

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...

Regulatory Affairs SpecialistWe are seeking a highly motivated Regulatory Affairs Specialist to join our team at RICG Poland Sp. z o.o. in a dynamic pharmaceutical company.Key Responsibilities:Ensure compliance with Polish and European regulations for pharmaceutical products, including the preparation and review of labeling, promotional materials, and other...

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...

We are seeking a highly skilled Regulatory Affairs Specialist to join our international team at Randstad Polska. The ideal candidate will have experience in a similar position in the pharmaceutical or cosmetics industry and a higher education degree.Key Responsibilities:Regulatory Affairs data entry activitiesTrack incoming data entry requests and follow up...

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...

Regulatory Affairs Support OpportunityWe are seeking a highly skilled Regulatory Affairs Support professional to join our international Regulatory Affairs Team at an international pharmaceutical company.Key Responsibilities:Provide Regulatory Affairs support with the assembly, transmission, storage, and handling of regulatory information.Enter document...

{"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...

Role OverviewAllegro sp. z o.o. is seeking a dedicated Regulatory Affairs Specialist to monitor, analyze, and engage with EU and Polish legislation related to product safety, sustainability, and consumer empowerment for the green transition.Key ResponsibilitiesAnalyze legislation in the area of sustainability and product safety to share insights with...

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...

Parexel's Expertise in Regulatory AffairsWe are seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for biological products and/or vaccines.The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth...

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...