About Leben Life Sciences Pvt. Ltd.
Leben Life Sciences Pvt. Ltd. (LLS) is a well-established 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 production. LLS is known for its commitment to innovation, compliance, and excellence in the healthcare sector.
Job Description: QA Documentation Trainee
As a Trainee in Quality Assurance (Documentation), your responsibilities will include:
- Assisting in the preparation, review, and maintenance of GMP documentation.
- Ensuring compliance with EU-GMP and other regulatory standards.
- Managing SOPs (Standard Operating Procedures), batch records, and quality reports.
- Supporting the QA team in audits and regulatory submissions.
- Maintaining accurate documentation for manufacturing and quality control processes.
Eligibility Criteria:
- Qualification: M.Pharm (2024/2025 pass-outs preferred).
- Experience: Freshers are eligible (prior internship experience in pharma documentation is a plus).
- Skills Required: Strong documentation skills, attention to detail, knowledge of GMP/GLP.
- Gender Preference: Male candidates (as per company policy).
Walk-In Interview Details
- Date: 10th May 2025 (Saturday)
- Time: 9:30 AM to 10:30 AM
- Venue:
Leben Life Sciences Pvt. Ltd.
Plot No. C-20/1 & C-21, Phase III,
MIDC, Akola, Maharashtra
Documents Required:
- Updated Resume (Hard Copy)
- Passport-size color photograph
- Educational Certificates (Photocopies)
How to Apply?
- Walk-In Directly on the scheduled date with your documents.
- No prior registration required.
- For more details, visit: www.lebenlifesciences.com
Why Join Leben Life Sciences?
✅ EU-GMP Approved Manufacturing Facility
✅ Career Growth in Pharmaceutical Quality Assurance
✅ Hands-on Experience in Regulatory Documentation
✅ Opportunity to Work in a Reputed Pharma Company
