Leben Life Sciences Pvt. Ltd. (LLS), an established pharmaceutical formulation company with more than four decades of experience, has openings in its Quality Assurance Department at its EU-GMP Approved Global Standard OSD & Semi-solids Formulation manufacturing facility in Akola, Maharashtra.
The company is hiring candidates for AQA positions with experience in QC Documents Review.
Job Details
| Details | Information |
|---|---|
| Company | Leben Life Sciences Pvt. Ltd. (LLS) |
| Department | Quality Assurance |
| Location | Akola, Maharashtra |
| Facility | EU-GMP Approved Global Standard OSD & Semi-solids Formulation manufacturing facility |
| Industry | Pharmaceutical Formulations |
Positions and Eligibility
1. Officer – AQA
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: c in QC Documents Review
2. Sr. Executive
- Experience: 5 to 7 years in QC Documents Review
Responsibilities
The provided job details specify experience in QC Documents Review for the available positions.
Eligibility / Qualifications
Candidates applying for the Officer – AQA position should have:
- B.Pharm
- M.Pharm
- M.Sc
- 2 to 3 years of experience in QC Documents Review
For the Sr. Executive position, candidates should have 5 to 7 years of experience in QC Documents Review.
Required Skills
- QC Documents Review experience
Application Details
Interested candidates can send their resume to:
Email: career@lebenlifesciences.com
