Regulatory Affairs Specialist Jobs in India

The Regulatory Specialist supports the Product Regulatory department with customer surveys regarding regulations internal queries regarding regulations and supportive measures to put new products on the market. Responsibilities: Author product SDSs that conform to global requirements Support...

This is whereyour work makes a difference.At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater...

We are seeking a detail-oriented and analytical Pharmaceutical Products Researcher / Regulatory Affairs professional to join our team in Mumbai this role you will be responsible for conducting research on pharmaceutical products and ensuring compliance with regulatory requirements throughout the dr...

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...

EOE/AA/Disabled/VeteransWhat are we looking forA Security 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:High school graduate or ab...

Associate Allied Chemicals (India) Pvt. Ltd. (AACIPL) is a leading distributor of aroma chemicals essential oils and specialty ingredients catering to the fragrance flavor personal care and home care industries.TasksPrepare review and maintain regulatory documents such as SDS CoAs TDS product declar...

About AstraZenecaAstraZeneca is a global science-led patient-focused biopharmaceutical company that focuses on the discovery development and commercialization of prescription medicines for some of the worlds most serious diseases. But were more than one of the worlds leading pharmaceutical companies...

Location: Hyderabad IndiaDepartment: Regulatory AffairsReporting to: MDExperience: 15–25 years in Regulatory Affairs (Injectables ROW markets; strong exposure to 505(b)(2) preferred)Role SummaryThe Regulatory Affairs Head – ROW Market will be responsible for leading and managing all regulatory submi...

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years our team has driven meaningful innovations in kidney care. As we build on our legacy we are deepening our commitment to elevating the dialysis experienc...

About AstraZenecaAstraZeneca is a global science-led patient-focused biopharmaceuticalcompany that focuses on the discovery development and commercialization of prescription medicines for some of the worlds most serious diseases. But were more than one of the worlds leading pharmaceutical companies....

About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable innovative medicines and health products for millions of people worldwide with a broad portfolio of generic biosimilar innovative branded pharmaceuticals and consumer health products. Headquar...

About Apotex Inc.Apotex Inc. is a Canadian-based global health company that produces high-quality affordable medicines for patients around the world. Apotex employs almost 7200 people worldwide in manufacturing R&D and commercial operations. Apotex medicines are accessible to patients in more than 7...

Responsibilities:Dossier Preparation:Compile review and prepare regulatory documentation ensuring accuracy and completeness.Collaborate with cross-functional teams to gather necessary information for dossier submissions.Maintain and update regulatory files and databases.DMF Management:Manage Drug Ma...

Team SummaryThe India & South Asia (INSA) cluster covers 6 markets divided into three sub-regions (India Bangladesh/Nepal/Bhutan and Sri Lanka/Maldives) with a total population of approximately 1.5 billion people.  Visa has ambitious business goals in this rapidly growing region and achieving these...

Regulatory Affairs Team Leader Authoring. Role detailed classificationRegulatory Affairs AuthoringJob Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Team Leader (TL) Authoring to join our LS Practice team. The successful candidate will be responsi...

Job Title: Regulatory Affairs Associate Authoring. Role detailed classificationRegulatory Affairs AuthoringJob Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate Authoring to join our LS Practice team. The successful candidate will be respon...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSupports the preparation of documentation and submissions under EUCTR guidance.Having good knowledge of RIMS documents managements.Coordinates and manages client deliverables supporting regulatory compliance.Liaises with int...

Ready to shape the future of workAt Genpact we dont just adapt to changewe drive it. AI and digital innovation are redefining industries and were leading the charge. Genpacts AI Gigafactory our industry-first accelerator is an example of how were scaling advanced technology solutions to help global...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionRCR Specialist (Admin) Regulatory Compliance Review Regulatory Affairs Perform global regulatory compliance review of essential documents supporting the customization of study-specific Essential Document Checklists Respond t...

Job description Job Title: Regulatory Affairs Specialist (Executive) on Randstad Payrolls Experience: 2 years CTC - 2 to 4 LPA Reports to: Manager- Regulatory Affairs (South Asia) Department: Regulatory Affairs Location: Noida -Sec 94 Education Graduate in Pharmacy (preferred) or Postgraduate in Sc...