Regulatory Affairs Executive

Job PurposeWe are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and dossier preparation, particularly for EU and emerging markets.Key...

About the Role:We are seeking an experienced and strategic Medical Affairs Lead. The ideal candidate will be a post-graduate (MD) in Pharmacology with a strong background in medical affairs, medico-marketing, and clinical research within the Nutrition, Pharmaceutical or Consumer Healthcare industries. This role requires a professional with a proven track...

Area Of ResponsibilityTo review quality and manufacturing end data for various in-house developed APIs for regulatory adequacy for compilation of Drug Master Files/Registration Dossiers, Amendments/Variations, Technical Data Package/Open Parts of DMFs for In-House developed APIs and their updation to meet current regulatory requirements.To review outsourced...

DDReg PharmaDDReg PharmaFull TimeGurgaonPosted 14 minutes agoJob Purpose:We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and dossier...

JOB PURPOSE:We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support globalregulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and dossier preparation, particularly for EU and emerging markets.Key...

**Internal Title**:Regulatory Affairs Professional **External Title**:Deputy General Manager **Position Summary** This position is primarily responsible to ensure pre market & post market compliance to Medical Device Rules(MDR) 2017 governed by Central Drug Standard Control Organization (CDSCO) & state FDA for SHPL's IVD devices & medical devices to be...

JOB DESCRIPTION Position Manager Senior Manager Job Location Gurgaon Education M Pharm Department Global Regulatory Affairs Job Responsibilities Serve as a Regulatory CMC Product Lead and provide CMC Regulatory leadership within Regulatory and on cross-functional teams for the assigned branded being developed for US and other advanced markets like EU Canada...

Company: Sam Global Biocare Pvt. Ltd.Location: Gurgaon (Gurugram), Sector 67, HaryanaJob Description:Sam Global Biocare Pvt. Ltd. is looking for a skilled Drug Regulatory Affairs Specialist with a strong understanding of international regulatory guidelines. Our focus is on exporting to the Middle East and expanding into African markets, so familiarity...

Roles and Responsibilities (5 days working)Manage regulatory dossiers for solid oral products, including CTD and ACTD preparation and submission to global markets.Handle team responsibilities related to dossier compilation, review, and approval.Ensure compliance with GMP regulations and provide guidance on regulatory affairs matters within the...

Position: Sr. Manager / AGM Regulatory AffairsQualification: M.Sc. / Ph.D. (Life Sciences, Biotechnology, or related 13 to 16 years in Regulatory Affairs The role is responsible for global product registrations (LatAm, Africa, GCC etc.), WHO Prequalification, Product lifecycle management, and regulatory compliance/audit support. The role ensures accurate...