Global Regulatory Affairs Specialist

ManpowerGroup Sp. z o.o., a global leader in the employment services industry, is seeking a highly skilled Regulatory Affairs Specialist to join our team. With over 70 years of experience and operations in 82 countries, we are committed to providing our clients with top-notch recruitment solutions.Job SummaryWe are looking for an experienced Regulatory...

Job Overview:Our client, a leading pharmaceutical company, is seeking a Regulatory Affairs Senior/Specialist in Submission Publishing. The successful candidate 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...

We are looking for a skilled Regulatory Affairs Specialist to join our team at Randstad. The successful candidate will be responsible for ensuring compliance with regulations and interpretations of regulatory agencies.Job Description:Operational submission managementDelivery of regulatory submissions required to support product development, registration, and...

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...

Regulatory Affairs Specialist Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Warsaw, Poland.Key Responsibilities:Prepare and submit regulatory documents, CTA packages, and submissions in assigned countries to ensure high quality standards.Coordinate regulatory timelines and deadlines for all assigned projects...

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: Regulatory Affairs ProfessionalWe are seeking an experienced Senior Regulatory Affairs Professional to support the implementation of regional regulatory strategies for pharmaceutical products at various stages of their lifecycle.Closely collaborate with global and regional teams to effectively execute regulatory submission plans, support product...

**Job Title:** Manager, Regulatory AffairsContribute to Global Development and Lifecycle ManagementYou will lead the development and execution of global CMC regulatory strategies, ensuring compliance with regulatory requirements and representing Global CMC Regulatory Affairs in cross-functional and external collaborations.About This Opportunity:This is an...

Medpace, a renowned full-service clinical contract research organization (CRO), is seeking a Global Medical Affairs Specialist to contribute to the success of our company. In this role, you will provide medical management and expertise for clinical trials, contribute medical expertise to study reports, regulatory documents, and manuscripts, and manage safety...

**About the Role:**We are seeking a highly skilled Regulatory Affairs Senior/Specialist to join our team at Randstad. As a key member of our team, you 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 format.The...

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...

At Randstad Polska Sp. z o.o., we are seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our global regulatory affairs function, you will play a pivotal role in shaping the development and lifecycle management of our groundbreaking pharmaceutical products.Your primary responsibilities will include leading the...

At Randstad Polska Sp. z o.o., we are seeking a highly skilled Regulatory CMC Manager to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products.About the RoleThis position will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and...

We are seeking a highly skilled Regulatory Affairs Manager to lead the development and maintenance of primary labeling for assigned compounds. This role requires strong leadership skills, as well as expertise in pharmaceutical regulatory guidelines.Key Responsibilities:Develop and maintain primary labeling documentsEnsure compliance with worldwide regulatory...

Job SummaryA highly skilled Regulatory CMC professional is sought to drive global regulatory strategies for innovative pharmaceutical products. This individual will lead the preparation of strategic regulatory plans, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development.Key...

Job SummaryA highly skilled Regulatory CMC Manager is sought to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products. This individual will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development.Key...

ManpowerGroup Sp. z o.o. is a global leader in the contingent workforce industry, operating in 82 countries and with over 70 years of experience. On the Polish market, we have been present since 2001 and currently have nearly 35 branches across the country.We are seeking a Regulatory Affairs Specialist in Submission Archiving for our client specializing in...

as Manager, Regulatory Affairs Established Products, you will be responsible for the regulatory support of a portfolio of established oncology and internal medicine products. Your objective will be to ensure compliance with regulatory requirements and to implement the global regulatory strategy for post-approval products.Regulatory Affairs Established...

We are seeking a highly skilled Regulatory CMC Manager to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products. In this position, you will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development. This...

GRC Regulatory Affairs ProfessionalThe Renewals CMC Team within the Global Regulatory Centres (GRC) is responsible for authoring, compiling, and checking regulatory submissions related to drug manufacturing and quality control. We are seeking a highly skilled Regulatory Specialist with expertise in Chemistry, Manufacturing, and Controls (CMC).Key...