Regulatory Affairs Manager Jobs in India

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...

Job SummaryManagement and oversight of a service delivery team handling the provision of corporate secretarial support to the Lux Fund CS & Cosec team (FCS) by providing guidance and leadership to the Indian CoSec TeamAs a supervisor the Cosec Manager leads organizes coordinates develops monitors th...

JOB DESCRIPTION:Critical Skills Required:Possess excellent interpersonal communication coordination and time-management skills.Ability to problem solve work in teams lead others toward defined objectives and present complex data clearly are also critical.Able to work independently and meticulously...

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...

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...

COMPANY DESCRIPTION:A career here is life-enhancing.At Syner-G we enable our people to build careers that impact positively on their quality of life. Through our expertise insight consulting and management skills we accelerate breakthrough science and delivery of life-enhancing therapies to more pat...

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...

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 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...

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...