Company: Leben Life Sciences Pvt. Ltd.
Location: Akola, Maharashtra
Position: Regulatory Affairs Trainee
Qualification: M.Pharm (Freshers Eligible)
Interview Date: 7th May 2025 (Wednesday)
Reporting Time: 9:30 AM to 10:30 AM
About Leben Life Sciences Pvt. Ltd.
Leben Life Sciences (LLS) is a leading pharmaceutical formulation company with over four decades of expertise in the industry. The company operates a EU-GMP approved, global standard manufacturing facility in Akola, Maharashtra, ensuring high-quality pharmaceutical products for domestic and international markets.
LLS is known for its innovation, compliance, and excellence in the pharma sector, making it an ideal workplace for aspiring professionals in Regulatory Affairs.
Job Description: Regulatory Affairs Trainee
As a Regulatory Affairs Trainee, you will assist in ensuring compliance with global regulatory standards (including EU-GMP, USFDA, etc.). Key responsibilities include:
- Documentation & Submission: Assist in preparing and reviewing regulatory documents for drug approvals.
- Compliance Management: Ensure adherence to ICH, WHO, and other regulatory guidelines.
- Dossier Preparation: Support in compiling CTD, ACTD, and other regulatory filings.
- Regulatory Research: Stay updated with changing pharmaceutical regulations across different markets.
- Coordination: Work with cross-functional teams (QA, R&D, Production) for smooth regulatory processes.
Eligibility Criteria:
- M.Pharm (Pharmaceutics/Regulatory Affairs preferred)
- Freshers can apply (Prior internship in regulatory affairs is a plus)
- Strong knowledge of GMP, ICH, and regulatory guidelines
- Good communication & documentation skills
How to Apply?
Walk-In Interview Details:
- Date: 7th May 2025 (Wednesday)
- Time: 9:30 AM – 10:30 AM
- Venue:
Leben Life Sciences Pvt. Ltd.
Plot No. C-20/1 & C-21, Phase III, MIDC, Akola, Shivar, Maharashtra