Accuprec Research Labs Pvt. Ltd. has announced a new hiring drive for its Regulatory Affairs department as part of a new venture. The company is looking for experienced M.Pharm (Regulatory Affairs) candidates with 3–5 years of experience in pharmaceutical regulatory submissions and dossier preparation.
This opportunity is ideal for professionals experienced in CTD/eCTD submissions, CIS/EAEU regulatory requirements, and GMP documentation who want to advance their career in the pharmaceutical regulatory domain.
With a reputation for regulatory expertise and global compliance support, Accuprec Research Labs offers a collaborative work culture, career growth opportunities, and exposure to international pharmaceutical regulations.
Job Details
- Position: Regulatory Affairs Executive / Officer
- Company: Accuprec Research Labs Pvt. Ltd.
- Department: Regulatory Affairs
- Experience Required: 3–5 Years
- Qualification: M.Pharm (Regulatory Affairs)
- Job Location: Ahmedabad, Gujarat, India
Professionals searching for Regulatory Affairs jobs in Gujarat, M.Pharm Regulatory Affairs jobs in India, or pharma regulatory dossier preparation jobs may find this role highly relevant.
Key Responsibilities
The selected candidate will work closely with the regulatory team and handle international dossier preparation and compliance tasks.
Major responsibilities include:
- Prepare, compile, review, and submit product registration dossiers in CTD / eCTD format according to country-specific regulatory requirements.
- Support submissions under the EAEU Unified Registration Procedure.
- Assist in preparation of Site Master File (SMF) and documentation required for GMP inspections related to CIS approvals.
- Conduct gap analysis of existing CTD dossiers against EAEU unified requirements.
- Track and monitor updates in CIS/EAEU pharmaceutical regulations and submission guidelines.
- Monitor updates related to pharmacopoeial changes and regulatory compliance.
These responsibilities provide strong exposure to global regulatory submissions, making the role valuable for professionals aiming to build expertise in international pharmaceutical regulatory affairs.
Required Qualifications
Candidates applying for this Regulatory Affairs job in the pharmaceutical industry must meet the following criteria:
- Educational Qualification: M.Pharm in Regulatory Affairs
- Experience: 3–5 years in pharmaceutical regulatory affairs
- Hands-on experience with CTD/eCTD dossier preparation
- Understanding of CIS/EAEU regulatory requirements
- Familiarity with GMP inspection documentation
- Strong regulatory documentation and compliance skills
Professionals with experience in international regulatory submissions will have an added advantage.
Why Join Accuprec Research Labs?
Accuprec Research Labs is known for providing regulatory and analytical solutions to the pharmaceutical industry. Employees benefit from an environment that encourages professional development and technical expertise.
Benefits include:
- Professional growth opportunities
- Collaborative and research-driven work environment
- Exposure to global regulatory submissions
- Comprehensive employee benefits package
- Opportunities to work on international regulatory projects
This makes the position attractive for candidates looking to grow in pharmaceutical regulatory affairs careers.
How to Apply
Interested candidates can apply by sending their updated resume through the following contact details:
📧 Email: career@accuprec.in
Company Address:
Accuprec Research Labs Pvt. Ltd.
Opp. Pharmez, Changodar–Bavla Highway,
Near Matoda Patia, Post: Matoda,
Ahmedabad – 382213, Gujarat, India
