Senior Regulatory Labeling Professional

Social network you want to login/join with:Regulatory Labeling Senior Manager, WarsawClient:ManpowerLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:9f311569cdfbJob Views:3Posted:21.03.2025Expiry Date:05.05.2025Job Description:Job Tasks:Lead the development, revision, review, agreement, and maintenance of primary labeling...

Job SummaryThis is a senior leadership position that oversees the development and maintenance of primary labeling for pharmaceutical products. The successful candidate will lead cross-functional teams and collaborate with external partners to ensure compliance with regulatory requirements.Key ResponsibilitiesLead the development and maintenance of primary...

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 looking for a Senior Manager, Global Labelling to be responsible for the labelling strategy for pharmaceutical products in international markets. The role requires close collaboration with global and regional teams and subject matter experts to ensure documentation is in line with regulatory requirements and business strategy.the incumbent will manage...

About the RoleWe are seeking an experienced Regulatory Labeling Senior Manager to join our team in Warsaw, Poland.The successful candidate will be responsible for leading the development and maintenance of primary labeling for assigned compounds. This includes making recommendations on labeling content, processes, timelines, and scientific integrity. The...

We are looking for an experienced Senior Regulatory Affairs Professional to support the implementation of regional regulatory strategies for pharmaceutical products at various stages of their lifecycle. This role involves close collaboration with global and regional teams to effectively execute regulatory submission plans, support product approvals, and...

We are seeking a skilled Senior Regulatory Expert 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 assigned markets.Your primary focus will be on assuring ingredients, formulas, labeling, and packaging...

We are pleased to offer a Regulatory Compliance Specialist position at Pfizer's Worldwide Safety department in Poland-Warsaw.The successful candidate will have a strong background in pharmacovigilance, regulatory compliance, or a related field, with excellent communication and analytical skills. As a Regulatory Compliance Specialist, you will be responsible...

For our Client, one of the biggest Pharmaceutical Companies worldwide we are looking for a Senior RA Professional EMEA, who will be responsible for supporting the Regulatory Liaison (RL) for a broad range of regulatory activities in the Established Products area in the Europe/Middle East/Africa (EMEA) region, providing regulatory input on submission...

Join our team at TN Poland as a Regulatory Affairs Associate, where you will have the opportunity to develop and implement effective secondary packaging and artwork strategies. As a key member of our team, you will work closely with cross-functional teams to ensure our clients' products meet regulatory requirements and market standards.About the JobYour...

Role OverviewThis senior manager position is responsible for overseeing the development and maintenance of primary labeling for pharmaceutical products. The successful candidate will lead cross-functional teams and collaborate with external partners to ensure compliance with regulatory requirements.Main ResponsibilitiesDevelop and maintain primary labeling,...

TN Poland is seeking a highly qualified Principal Regulatory Affairs Consultant to join their team in Warsaw. The successful candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of post-approval Chemistry, Manufacturing, and Controls (CMC) activities.This is a unique opportunity for a highly qualified...

For our Client, one of the largest Pharmaceutical Companies worldwide, we are looking for a Senior Manager, Regulatory Affairs Regional Strategy Implementation. This position resides within Global Regulatory Affairs and provides regional regulatory strategic implementation support for products in one or more therapeutic areas. The successful candidate will...

Join our Client's CMC team as a Senior Regulatory Affairs Specialist! We are seeking a highly motivated and experienced professional to support global CMC regulatory strategies and documentation.The ideal candidate will have a strong educational background in Life Sciences, Pharmacy, or a related discipline, and first-hand experience in CMC, regulatory...

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...

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...

**Role Overview**We are looking for a Regulatory Affairs Manager to join our team in Warsaw, Poland. In this role, you will be responsible for managing certification processes and ensuring compliance with all relevant regulations in Kazakhstan and Ukraine.The successful candidate will have extensive knowledge of applicable legislation, including technical...

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...

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Senior / Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD...

Job Title:Senior Specialist SRA Central Europe (f/m/x)About the Role:We are seeking a Senior Specialist in Scientific and Regulatory Affairs to join our team in Warsaw, Poland.Key Responsibilities:Ensure compliance with laws and regulations for ingredients, formulas, labeling, and packaging across assigned markets.Verify claims compliance with laws and...