Regulatory Affairs Executive{0-3 Yrs}

We are seeking a Regulatory Affairs Executive Freshers To Work in the MNC For Hyderabad LocationThe ideal candidate should have hands-on experience in compiling and reviewing ACTD and CTD dossiers for various regulatory submissions. Required Candidate profileB.Pharm & M.Pharm With Knowledge of Regulatory Affairs CTD ECTD DMF and Regulatory Guidelines are...

Job Summary:","Regulatory Affairs Specialist: Artwork Management and Compliance"],

Looking for a full time Regulatory Affairs executive with 1-3 years experience in APIs (Active pharmaceutical ingredients). No freshers. **Job Types**: Full-time, Regular / Permanent **Salary**: ₹200,000.00 - ₹980,116.12 per year **Benefits**: - Paid time off - Provident Fund Schedule: - Day shift Supplemental pay types: - Yearly bonus Ability...

Regulatory Affairs AssociateExperience: 3-6 yearsEducation: Science GraduateLocation: HyderabadSkills: Regulatory Affairs, EU market, Formulation, RA, European market, Post and Pre approval

Regulatory Affairs Job OpportunityDesired Experience : 3- 9 yearsJob Location : Genome Valley, Shameerpet, HyderabadPreferred Industry : Vaccines / BiotechDesignation: Senior Executive/ ExecutiveQualification: M. Pharmacy/ M. Sc/ B. PharmacyJob Responsibilities:Responsible for Regulatory submission to Indian NRA, Emerging Markets, Regulated Markets and World...

Regulatory Affairs SpecialistThis is a unique opportunity to join our team as a Regulatory Affairs Specialist. The successful candidate will be responsible for the execution and coordination of global regulatory activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy...

Regulatory Affairs ExpertThe Regulatory Affairs Manager is responsible for leading the execution and coordination of global regulatory activities.Key Responsibilities:Develop and execute strategic plans for global and country-specific regulatory complianceProvide CMC regulatory strategy by defining filing requirements, submission strategies, and risk...

Job Title: Regulatory Affairs SpecialistAbout This RoleWe are seeking a detail-oriented professional to support end-to-end submissions for global markets, focusing on regulatory affairs - CMC (Chemical, Manufacturing and Controls) aspects.Key ResponsibilitiesPreparing Variation documentsEvaluating post-approval CMC changes in compliance with global...

Regulatory Affairs CMCExperience: 6-11 yearsEducation: Science GraduateLocation: HyderabadSkills: Regulatory Affairs, US market, CMC

**Job Summary**: **Key Responsibilities**: - Assist in the preparation and submission of regulatory documents for product registration and approvals (e.g., 510(k), CE Marking, CDSCO). - Support the creation and maintenance of Technical Files, Design Dossiers, and product master files. - Coordinate with internal teams (R&D, Quality, Manufacturing) to gather...