Regulatory Affairs Executive

This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications**: Regulatory Documentation, Regulatory Requirements, and...

Regulatory Executive (Medical Devices & IVDs)Experience:1–3 years inregulatory affairs for medical devices and/or IVDs under Indian MDR 2017Location:Noida (On-site)CTC :INR 3-6 LPAAbout SR Strategy Services LLP:SR Strategy Services LLP is a leading consulting firm specializing in strategic government affairs, regulatory advisory, market access solutions,...

**Role Description** This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications** - Regulatory Documentation,...

Job Description:We are looking for a Regulatory Affairs Sales Executive (Fresher) who will be responsible for driving sales in the regulatory compliance sector. This role is ideal for candidates from pharmaceutical and biotech backgrounds who want to explore a career in sales and client handling within the regulatory domain.Key Responsibilities:Understand...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**Job Summary**: The Regulatory Affairs Executive is responsible for ensuring compliance with regulatory requirements for pharmaceutical products. This role involves preparing and submitting regulatory documentation, coordinating with internal teams, and maintaining up-to-date knowledge of industry regulations. **Roles and Responsibilities**: - Prepare and...

**Description** Drug Regulatory Affairs - Job description - Prepare CTD, ACTD Dossiers and file regulatory submissions. - Perform assessments of new or revised products. - Manage complaint documentation (including investigation and closure). - Respond to inquiries from regulatory bodies. - Should be technically well versed with requirements for medicines...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**Key Responsibilities**: - Understand regulatory services offered by the company (BIS, CDSCO, etc.) - Identify and approach potential clients in pharmaceutical, biotech, and related industries - Build and maintain strong client relationships to ensure repeat business - Provide accurate information to clients regarding regulatory approvals and...

Job Position: Cosmetics Regulatory Affairs SpecialistWorking Days: Monday to FridayShift Time- 12 PM IST- 9 PM ISTOn-Site RoleWe are looking for a detail-oriented and knowledgeable Cosmetics Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong understanding of regulatory policies, documentation, and compliance requirements...