Regulatory Affairs Specialist IVD Jobs in India

What are we looking forA L&D Executive serving Hilton brands is always working on behalf of our Guests and working with other Team Members. To successfully fill this role you should maintain the attitude behaviours skills and values that follow:Previous experience in HR/trainingPositive attitudeGood...

DescriptionAbout your roleWe have vacancy for Global Regulatory Expert role in Regulatory Affairs team. We are looking for Assistant Manager . This individual will be based in Mumbai/ Hyderabad. The candidate has the possibility to utilize his/her own strengths with the support of the professionals....

Job OverviewIndividual contributor with advanced knowledge acquired from several years of experience in the professional discipline. Works independently under limited supervision.Essential Functions Acts as a Regulatory Team Leader on complex projects which may include technical writing and/or may a...

Job TitleRegulatory Affairs SpecialistJob DescriptionJob title: Regulatory Affairs Specialist Your role:Regulatory Affairs Specialist ISC will have an exciting opportunity to work with the ISC Commercial Regulatory Affairs Team and help business with product registration in the India Sub Continent...

Job TitleRegulatory Affairs SpecialistJob DescriptionJob title: Regulatory Affairs Specialist Your role:Regulatory Affairs Specialist ISC will have an exciting opportunity to work with the ISC Commercial Regulatory Affairs Team and help business with product registration in the India Sub Continent...

Job TitleRegulatory Affairs SpecialistJob DescriptionJob Title : Regulatory Affairs SpecialistJob Responsibilities: Monitors global regulatory changes interprets requirements and integrates findings into regulatory strategies ensuring timely communication with teams. Implements regulatory strategies...

Job Description: Max Bill Rate $11.95/hr. USDAssignment to last through 2026Location: Art Guild House Phoenix Market City Kurla (West) Mumbai Maharashtra IndiaWork Arrangement: Hybrid On-site 1 2 days/week for training and collaboration; remainder remoteWe are seeking a detail-oriented and col...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionWe are currently seeking a Regulatory Affairs Managerto join our global Regulatory Affairs department. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial settin...

Dear Candidates We have an opportunity with clinical trial development and CRO related assets and capabilities from an existing ACRO/SMO organization that is based in Chennai. We have over 10 years of experience running clinical trials as part of the global Group. Position Overview The Head of R...

Job TitleSr. Regulatory Affairs SpecialistJob DescriptionJob Title : Sr. Regulatory Affairs SpecialistJob Responsibilities:Implements global regulatory strategies and roadmaps by leveraging a comprehensive understanding of the competitive market landscape and product marketing strategy to ensure ali...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeDrive evidence-based medical affairs strategi...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeDrive evidence-based medical affairs strategi...

Line of ServiceInternal Firm ServicesIndustry/SectorNot ApplicableSpecialismOperationsManagement LevelAssociateJob Description & SummaryAt PwC our people in business application consulting specialise in consulting services for a variety of business applications helping clients optimise operational e...

Job TitleRegulatory Affairs Operations 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 Registration...