Manager Global Regulatory Affairs

Job Title: Manager Global Regulatory AffairsAt Biocon Biologics, we are seeking a highly skilled and experienced Manager Global Regulatory Affairs to join our team.Key Responsibilities:Develop and execute global regulatory strategies for biosimilar products, ensuring compliance with regulatory requirements and industry standards.Collaborate with...

Job Title: Manager Global Regulatory AffairsAt Biocon Biologics, we are seeking a highly skilled and experienced Manager Global Regulatory Affairs to join our team.Key Responsibilities:Develop and execute global regulatory strategies for biosimilar products, ensuring compliance with regulatory requirements and approved filing plans.Collaborate with...

Assistant ManagerGlobal Regulatory AffairsBangalore, IndiaJob Description:Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products for emerging markets.Biosimilars or injectables experience is mandatory for this role.Responsible for:Development and Implementation of...

Assistant Manager Global Regulatory Affairs Bangalore, India Job Description: Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products for emerging markets. Biosimilars or injectables experience is mandatory for this role . Responsible for : Development and...

Assistant ManagerGlobal Regulatory AffairsBangalore, IndiaJob Description:Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products for emerging markets.Biosimilars or injectables experience is mandatory for this role.Responsible for:Development and Implementation of...

Regulatory Affairs Manager Bangalore, India Job Description: Hands on experience on drug substance manufacturing process, designing and executing process characterization studies (upstream, downstream, formulation) as well as process comparability for biologics (monoclonal antibodies/growth factors/hormones) Accountable for development and execution of CMC...

Regulatory Affairs ManagerBangalore, IndiaJob Description:Hands on experience on drug substance manufacturing process, designing and executing process characterization studies (upstream, downstream, formulation) as well as process comparability for biologics (monoclonal antibodies/growth factors/hormones)Accountable for development and execution of CMC...

Job SummaryWe are seeking a highly experienced Regulatory Affairs Manager to lead our global biosimilar regulatory strategy and ensure compliance with regulatory requirements.The successful candidate will have a strong background in drug substance manufacturing, process characterization, and regulatory strategy development.Develop and execute global...

Job Title: Sr. Regulatory Affairs SpecialistYou will be an integral member of our Clinical Informatics Regulatory Affairs team, influencing and shaping the regulatory capabilities for future success of Philips.Your Key Responsibilities:Ensure safe and effective products/solutions are brought to market on time and sustained throughout their lifecycle via...

Job Description:Unlock Your Potential in Regulatory AffairsParexel is seeking a highly skilled Regulatory Affairs Consultant to join our team. As a key member of our regulatory team, you will play a critical role in ensuring compliance with regulatory requirements for biologic products in various markets.Key Responsibilities:Develop and implement regulatory...

Transforming Healthcare through Regulatory ExcellenceBaxter is a leading global healthcare company that has been pioneering medical innovations for over 85 years. Our mission is to save and sustain lives, and we're looking for talented individuals to join our team in Regulatory Affairs.As a Regulatory Affairs Specialist, you will play a critical role in...

Parexel's Regulatory Affairs Team: A Hub for ExpertiseWe're seeking a skilled Regulatory Affairs Manager to join our dynamic team, bringing experience in clinical trial regulatory submissions, managing studies, and playing regulatory leads for global trials.Regulatory Experience: Over 10 years of experience in clinical trial regulatory submissions, with a...

Regulatory Affairs SpecialistBaxter is a leading healthcare company that is on a journey to separate its ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve.We are seeking a highly skilled Regulatory Affairs...

Job Title: Regulatory Affairs Manager ICareer Level - DIntroduction to role:The Regulatory Affairs Manager I is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, including delivery as an individual contributor, if required. The Regulatory Affairs...

Regulatory Affairs ManagerAt Parexel, we're committed to delivering exceptional results for our clients. As a Regulatory Affairs Manager, you'll play a critical role in ensuring the success of our clinical trials.Key Responsibilities:Regulatory Submissions: Lead the preparation and submission of regulatory documents for clinical trials, ensuring compliance...

Job Title: Regulatory Affairs AssociateAbout the Role:Parexel is seeking a highly skilled Regulatory Affairs Associate to join our team. As a key member of our regulatory team, you will be responsible for handling the pre and post-approval life cycle management of Biologic products in various markets, including Regulated (EU/US/Canada) and Emerging...

Job Title: Principal Regulatory Affairs SpecialistJob Summary:We are seeking a highly experienced Principal Regulatory Affairs Specialist to join our team at Philips. The successful candidate will be responsible for developing and executing the regulatory strategy for new product development, design changes, and field safety corrections for US, EU, and...

Regulatory Affairs SpecialistAt Parexel, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for managing the regulatory life cycle of drug products, from pre-approval to post-approval. Your expertise will be essential in ensuring compliance with regional regulatory...

Job Title: Principal Regulatory Affairs SpecialistJob Description:Key Responsibilities:Develop and execute regulatory strategies for new product development, design changes, and field safety corrections for US, EU, and RoW.Author 510k submissions, lead pre-sub meetings, create EU MDR Technical Documentation, Health Canada license applications, and lead...

Transforming Healthcare through Regulatory ExcellenceBaxter is a leading global healthcare company that has pioneered significant medical innovations for over 85 years. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the compliance and quality of our products and therapies.Your key responsibilities will include:Creating and...