Regulatory Affairs Associate

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines becauseGood Health Can't Wait.We started in 1984 with a modest investment, 20 employees and a bold...

Regulatory affairs of each country where our products will be sold, and cordination for documents, *Documentation for obtaining licensing and certificates for our medical Insitruments and kits. **Salary**: ₹22,000.00 - ₹30,000.00 per month Schedule: - Day shift Ability to commute/relocate: - Andheri west, Mumbai, Maharashtra: Reliably commute or...

Customer-oriented attitude with experience of around 08 -10 years - Excellent verbal and written communication skills - Liaising and negotiating with regulatory authorities. Filing of Govt Tenders as per deadline and adherence to Regulatory compliances. Coordinate with Clients. - keeping up to date with changes in regulatory legislation and guidelines -...

This role involves ensuring the preparation and review of regulatory documents to guarantee compliance with international guidelines and country-specific requirements.Key responsibilities include:Screening and analyzing documents for product registration requests according to country-specific guidelines.Preparing, compiling, and reviewing product dossiers in...

**Responsibilities**: Drug Approval, Drug related documentations,Product permission,Drug Control Visit,Making Dossier, Conduct of clinical studies, data collection, To give strategic and technical advice to R&D, production, QC department, etc right from the beginning of the development of the product, advise scientists and manufacturers on regulatory...

Requirement of Regulatory Affair- ManagerIndustry - Pharma/Healthcare(Only for Male)Address:-Diamond Heritage Building,BBD Bag, Kol-700001Job Role: Regulatory Affairs-Manager/Asst.ManagerSalary: Negotiable (No PF & ESI,only P-Tax deduction)Qualification: - · Bachelor's or Master's degree in Pharmacy, Life Sciences, Chemistry, or related discipline.Key...

Regulatory Affairs SpecialistWe are seeking a detail-oriented Regulatory Affairs specialist to support end-to-end submissions for global markets.The ideal candidate will have experience in managing Initial submissions, Variations, and full Lifecycle Management deliverables for the global markets. They must have hands-on experience with Veeva Vault RIM and...

JD's :Regulatory Strategy: ROW Market Expansion,CTD/eCTD Dossiers,Registrations,Renewals,Variations,CDSCOCompliance & Audits: Regulatory Audits,Inspections,Artwork Compliance,Promotional Materials,Risk MitigationMail-Annual bonus

**Responsibilities**: 1.Drug related Conduct of clinical studies, data collection, statistical analysis, report writing Keeping track of changing legislation in regions where the company distributes its products. collect, collate and evaluate scientific data from a range of sources. To give strategic and technical advice to R&D, production, QC department,...

Responsibilities: 1.Drug related Conduct of clinical studies, data collection, statistical analysis, report writing Keeping track of changing legislation in regions where the company distributes its products. collect, collate and evaluate scientific data from a range of sources. To give strategic and technical advice to R&D, production, QC department, etc...