Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA. Accuprec provides all type of Pharmaceutical testing solutions to its domestic and MNC clients.
Hiring for Regulatory Affairs Department
Experience : 03-05 Years
Qualification : M.Pharm (Regulatory Affairs)
Job Description
• Prepare, compile, review, and submit product registration dossiers in CTD I eCTD format as per country-specific requirements and EAEU Unified Registration Procedure.
• Support preparation of Site Master File (SMF) and documentation for GMP inspections related to CIS approvals.
• Perform gap analysis of existing CTD dossiers against EAEU unified requirements.
• Track and monitor updates in CIS/EAEU pharmaceutical regulations pharmacopoeial changes, and submission guidelines.
Accuprec Research Labs Pvt. Ltd.
Head Office: Opp. Pharmez, Changodar - Bavla Highway,
Nr. Matoda Patia, Post, Matoda, Ahmedabad - 382213, Gujarat, India
Last Date : 28th February 2026
Send your Resume to : career@accuprec.in
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