Regulatory Affairs

DDReg Pharma DDReg Pharma Full Time Gurgaon Posted 5 hours ago **Job Purpose**: DDReg is seeking a qualified Regulatory Affairs Specialist to join our team, responsible for ensuring compliance with regulatory requirements for India for a portfolio comprising of New Drugs, Generics, Biologicals, Cosmetics, Medical Devices & Nutraceuticals. **Key...

**Senior DRA Executive (Regulatory Affairs)** Ø Preparation and reviewing of administrative documents. Ø Preparation and Review of Dossier in CTD,ACTD and ECTD Format. Ø Preparing the SPC and SMPC as per country guidelines. Ø Preparation of Dossier for CIS, Africa countries, Gulf Countries, and south India countries. Ø Review and Making of...

Job Description This job is with Johnson & Johnson, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are...

**Title**:DGM/SM - Regulatory Affairs - CMC - Branded**: - Date: Sep 24, 2025 - Location: Gurgaon - R&D - Company: Sun Pharmaceutical Industries Ltd **Job Title**: Sr. Manager / DGM**Business Unit**: Sun Global Operations**Job Grade** G9A/G8**Location**: GurgaonAt Sun Pharma, we commit to helping you **“Create your own sunshine”**— by fostering an...

Regulatory Expertise: - Manage the regulatory process for Pharmaceutical Finished Formulations across CIS, LATAM, and Africa- Dossier Management: Compile and review ACTD and CTD dossiers to ensure accuracy and compliance. MOH Query Response: Address and respond to any Ministry of Health (MOH) queries for dossiers submitted in the relevant territories.-...

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...

DDReg Pharma DDReg Pharma Full Time Gurgaon Posted 5 hours ago **Job Purpose**: **Key Responsibilities**: **Compliance & Lifecycle Management**: Prepare variation and requalification dossiers. Manage regulatory product maintenance across EU, UK, WHO, and other emerging markets. **eCTD/CTD Sequence Review**: Perform Level-1 review of CTD/eCTD sequences for...

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 Life.Role Summary. The QARA Director for India will be responsible for leading a team supporting Quality...

Quality Systems Management: Develop, implement, and maintain quality systems and processes to ensure compliance with regulatory requirements, including Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). - Document Control: Manage document control processes, including document creation, review,...

Responsible for Medical Device and Drug registration in CDSCO State FDA office and other government office Lead negotiations with key health authority agencies during development registration and product lifecycle activities to resolve regulatory issues and or negotiate approvals establish and maintain proactive and professional communication relationship...