Regulatory Affairs Jobs in Bengaluru

Job Title: International CMC Regulatory Affairs Associate Director IGlobal Career Level:E1Introduction to roleThis role leads and manages complex iCMC projects and product ranges across the portfolioto meet the needs of both AstraZeneca and patients. It combines strong project management with tactic...

Department : Regulatory AffairsLocation : Novo Nordisk Global Business Services (GBS) India BangaloreJob Level : 7Shape regulatory strategies that bring life-changing therapies to patients with Obesity & Cardiometabolic Health worldwide.Your new roleAs a Senior Regulatory Professional youll be the...

Job TitleSr Regulatory Operation SpecialistJob DescriptionJob Responsibilities:International RegistrationsUpload Verify and Validate the data with new Regulatory Information to the RIM databaseMaintain Registration &Licensing InformationCreate Submission Packages for International RegistrationsIniti...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

Job TitleR&D CAPA ManagerJob DescriptionJob title:R&D CAPA ManagerYour role:1. CAPA Execution & OwnershipOwn end-to-end execution of assigned R&D CAPAs (intake investigation action definition implementation verification of effectiveness).Ensure CAPAs are completed on time within scope and meet quali...

Job TitleSr Product Manager IGT Fixed systemsJob DescriptionSr Product Manager IGT Fixed SystemsAs Sr. Product Manager you will own the lifecycle of the IW platform and iApps across launched Image Guided Therapy products. You will drive MLD updates manage compatibility and obsolescence and ensure al...

Lead end-to-end manufacturing/technology transfer projects for medical device products across global manufacturing sites.Coordinate with R&D Quality Regulatory Affairs Supply Chain and Manufacturing teams to ensure successful transfer and production readiness.Manage regulatory submissions and countr...

Department - Regulatory Affairs Organization Novo Nordisk India Pvt Ltd Are you passionate about helping bring life-changing medicines and clinical trials to patients by securing timely regulatory approvals Join Novo Nordisk as a Regulatory Affairs Professional and play a key role in supporting su...

Job TitleRegulatory Affairs Global Regulations SpecialistJob DescriptionJob Title: Regulatory Affairs Global Regulations SpecialistJob Responsibilities: Stays updated on global regulatory requirements by monitoring regulatory bodies industry publications and relevant sources ensuring preparedness fo...

Introduction to role:Are you ready to turn breakthrough science into approved medicines faster Do you thrive at the intersection of CMC excellence regulatory strategy and real-world impact for patients with few optionsIn this role you will effectively manage the production of Chemistry Manufacturing...

Introduction to role:Are you ready to turn breakthrough science into approved medicines faster Do you thrive at the intersection of CMC excellence regulatory strategy and real-world impact for patients with few optionsIn this role you will effectively manage the production of Chemistry Manufacturing...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

Job Title: Lit FTA (Full Text Article) Review AdvisorCareer Level: CIntroduction to role:Are you ready to turn complex literature and safety data into timely compliant regulatory submissions that protect patients and strengthen trust In this role you will be a key partner enabling our teams to move...

At Moodys we unite the brightest minds to turn todays risks into tomorrows opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they arewith the freedom to exchange ideas think innovatively and listen to each other and customers in meaningfu...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...