Regulatory Affairs Specialist for Global CMC

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...

We are searching for a skilled Global CMC Regulatory Strategist to support our CMC team. As a key member of our team, you will be responsible for developing and implementing global CMC regulatory strategies and documentation.Your first-hand experience in CMC or other regulatory affairs areas and university degree in Life Sciences or a related field will be...

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...

**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...

Parexel, a leading Clinical Research Organization (CRO), is seeking an experienced Principal Regulatory Affairs Consultant to join their team in Warsaw. The ideal 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...

We are seeking a highly skilled and experienced Regulatory Affairs Professional to join our team at TN Poland. In this role, you will have the opportunity to leverage your expertise in CMC, exceptional communication skills, and strong writing experience to contribute to the success of our clients in the pharmaceutical industry.This position offers a wide...

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...

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...

We are looking for a talented CMC Regulatory Expert with strong strategic thinking and problem-solving skills. As a key member of our CMC team, you will be responsible for supporting global CMC regulatory strategies and documentation.If you have a background in the pharmaceutical industry and are passionate about regulatory affairs, we encourage you to...

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...

About the RoleThe Regulatory Affairs Director will play a pivotal role in shaping the future of global regulatory strategies for pharmaceutical products.This is an exciting opportunity to lead high-performing teams, drive strategic initiatives, and collaborate with global leaders to ensure compliance, innovation, and excellence throughout the product...

Join one of the largest pharmaceutical companies worldwide as a Regulatory Affairs Director (CMC) and play a pivotal role in shaping the future of global regulatory strategies for pharmaceutical products. This is an exciting opportunity to lead high-performing teams, drive strategic initiatives, and collaborate with global leaders to ensure compliance,...

We are seeking a seasoned CMC Regulatory Expert to join our global regulatory affairs function at Randstad Polska Sp. z o.o. As a key member of our team, you will contribute to the development and lifecycle management of our groundbreaking pharmaceutical products by providing regulatory expertise and input to team recommendations.Your primary...

TN Poland is seeking a talented and experienced CMC Regulatory Affairs Professional to join our team. In this role, you will have the opportunity to utilize your expertise in CMC, exceptional communication skills, and strong writing experience, contributing to our clients' success in the pharmaceutical industry.This position offers exposure to novel...

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

We are seeking a seasoned Global Regulatory Affairs Specialist to join our team at Randstad. In this role, you will be responsible for managing the operational delivery of regulatory documents for product registration and compliance. Your expertise will help us ensure that all regulatory requirements are met, and our products reach the market...

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...

TN Poland is seeking an experienced Senior Regulatory Specialist to join our team. As a key member of our CMC team, you will be responsible for supporting global CMC regulatory strategies and documentation.We are looking for someone with first-hand experience in CMC or other regulatory affairs areas and a university degree in Life Sciences or a related...

Are you looking for a challenging role that combines technical expertise with business acumen? TN Poland is seeking a highly qualified Principal Regulatory Affairs Consultant to lead their regulatory affairs efforts in Warsaw.The successful candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of...

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...