Regulatory Specialist for Global Product Variations

About VantiveVantive is a new company built on the legacy of Baxter, a leading player in the kidney care space. Our mission is to provide best-in-class care to patients worldwide by revolutionizing kidney care and other vital organ support.Job OverviewWe are seeking an experienced Regulatory Specialist to join our team in providing regulatory support for...

Regulatory Support Specialist Role OverviewBaxter is on a journey to separate our kidney care segment into a standalone company. Vantive will build on our legacy in acute therapies and home and in-center dialysis to provide best-in-class care to our patients.This role is responsible for providing regulatory support for on-market products. The Specialist will...

Improve Patient Lives with BaxterWe are on a journey to revolutionize kidney care and other vital organ support. Vantive, a new company built on our legacy, will provide best-in-class care to the people we serve.Key Responsibilities:Provide regulatory support for on-market products, including change assessment, variation planning, and submission...

Regulatory Affairs at Baxter: A Key Role in Delivering Innovative Healthcare SolutionsBaxter, a leading medical products company, is seeking a talented Regulatory Affairs Specialist to join its team. In this crucial role, you will play a key part in ensuring the company's products meet the highest regulatory standards, enabling us to deliver innovative...

Regulatory Role at BaxterBaxter is a leading company in the healthcare industry, and we are seeking a highly skilled Regulatory Affairs Specialist to join our team. In this role, you will be responsible for providing regulatory support for on-market products, ensuring compliance with regulatory requirements, and identifying opportunities for process...

Parexel seeks a dedicated Regulatory Affairs Specialist to support the life cycle management of biologic products in regulated and emerging markets.Key Responsibilities:8-9 years of experience in handling pre and post-approval life cycle management of biologic products in various markets (EU/US/Canada) and emerging markets.Good understanding of regulatory...

About this role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Parexel. As a key member of our Regulatory Affairs team, you will be responsible for handling the pre and post-approval life cycle management of drug products.Key Responsibilities:Contribute to the preparation and delivery of regulatory maintenance submissions...

About VantiveBaxter is on a transformative journey to separate its ~$5B Kidney Care segment into a standalone company, Vantive. This entity will build upon Baxter's nearly 70-year legacy in acute therapies and home and in-center dialysis, providing best-in-class care to patients worldwide. The creation of Vantive will not only solidify leadership in the...

Job Title: Global Biosimilars Regulatory Affairs SpecialistDescription:We are seeking a highly skilled Global Biosimilars Regulatory Affairs Specialist to join our team at Biocon Biologics.As a Global Biosimilars Regulatory Affairs Specialist, you will be accountable for the development and execution of CMC regulatory strategies, marketing applications, and...

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$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 believe Vantive will not only build our leadership in the kidney care...

As a Regulatory Affairs Consultant at Parexel, you will play a crucial role in ensuring the compliance of our medicinal products with regulatory frameworks across various markets.Key Responsibilities:8-9 years of experience in handling the pre and post-approval life cycle management of Biologic products in regulated and emerging markets.Profound...

About the RoleWe are seeking a highly skilled Global Regulatory Registrations Specialist to join our team at KPMG India.This is a unique opportunity to work with a purpose-led, values-driven organization that fosters a respectful, inclusive, and barrier-free workplace. As a specialist in regulatory registrations, you will play a critical role in helping our...

About ElancoAt Elanco, we're a global leader in animal health. Our mission is to advance the health of animals, people, and the planet.Job SummaryWe're seeking a Regulatory Affairs Specialist to work with our cross-functional teams to develop regulatory strategies, oversee submission preparation, and meet reporting requirements for new animal drugs with...

Job Title: Regulatory Affairs Specialist - Clinical EvidenceAbout the Role:We are looking for a highly experienced Regulatory Affairs Specialist to join our team in Stryker Global Technology Center Pvt Ltd. The successful candidate will be responsible for driving the establishment of a coherent Clinical Evidence strategy throughout the new product...

About the RoleWe are seeking a skilled professional to join our team as a Dimensional Variation Analyst. The ideal candidate will possess strong analytical skills and a deep understanding of engineering principles, specifically related to tolerance analysis and dimensional variation management.Your ResponsibilitiesSupport the design development of system and...

About the RoleParexel is seeking a skilled Regulatory Affairs Associate to join our team. As a key member, you will be responsible for handling pre and post-approval life cycle management of drug products, including small molecules and biologics.ResponsibilitiesYou will have around 4-8 years of relevant experience in handling regulatory submissions,...

About the RoleParexel is seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Consultant, you will be responsible for managing the pre- and post-approval life cycle of biologic products in various markets, including regulated (EU/US/Canada) and emerging markets.Key ResponsibilitiesDevelop and implement regulatory...

F335 Deutsche India Private Limited, Bangalore Branch is seeking a highly skilled Global Regulatory Compliance Specialist to join our team in Bangalore.About the RoleAs a Global Regulatory Compliance Specialist, you will be responsible for contributing to projects within the department and being accountable for the in-scope population assigned. You will...

We are seeking an experienced Global Regulatory Compliance Specialist to ensure our supplement products meet international regulatory standards. As a key member of our team, you will serve as the main point of contact between our factories and distributors for regulatory matters.Key Responsibilities:Liaison: Establish and maintain effective relationships...

Transforming Healthcare, One Document at a TimeBaxter is a global leader in medical innovations, and we're looking for a skilled Regulatory Affairs Specialist to join our team.As a Regulatory Affairs Specialist at Baxter, you'll play a critical role in ensuring the accuracy and compliance of regulatory documentation for our medical products.Responsibilities...