Leben Life Sciences Pvt. Ltd. is hiring for a Quality Control Officer position at its pharmaceutical formulation manufacturing facility in Akola, Maharashtra. The company is an established pharmaceutical formulation organization and has stated that its facility is EU-GMP approved for global standard OSD and semi-solids formulation manufacturing.
This opportunity is suitable for candidates with hands-on or relevant experience in Quality Control functions such as HPLC, GLP, stability studies and documentation. Candidates with M.Sc, B.Pharm or M.Pharm qualifications and 2 to 4 years of experience can apply by sending their resume through email.
Job Details
| Company | Leben Life Sciences Pvt. Ltd. (LLS) |
| Department | Quality Control |
| Designation | Officer |
| Section | HPLC / GLP / Stability / Documentation |
| Location | Akola, Maharashtra |
| Experience | 2 to 4 years |
| Qualification | M.Sc / B.Pharm / M.Pharm |
| Application Mode | Email Application |
Role Overview
The Quality Control Officer role is aligned with laboratory-based pharmaceutical quality functions. The selected candidate is expected to support QC activities related to analytical testing, GLP compliance, stability work and documentation requirements for a formulation manufacturing environment.
The position is part of the Quality Control department and is best suited for professionals who have prior experience in a regulated pharmaceutical setup, especially in OSD and semi-solid formulation-related operations.
Key Responsibilities
- Support Quality Control activities in the assigned section, including HPLC, GLP, stability and documentation-related work.
- Carry out analytical and documentation tasks as per Quality Control department requirements.
- Maintain records and documentation in line with laboratory and regulatory expectations.
- Contribute to quality compliance activities within the pharmaceutical formulation manufacturing facility.
- Work in coordination with QC team members to ensure timely completion of assigned laboratory and documentation tasks.
Required Qualifications
- M.Sc
- B.Pharm
- M.Pharm
Experience Required
- 2 to 4 years of relevant experience in Quality Control.
- Experience in HPLC, GLP, stability or documentation will be relevant for this role.
Required Knowledge and Skills
- Knowledge of Quality Control operations in a pharmaceutical manufacturing environment.
- Understanding of HPLC-related laboratory work.
- Awareness of GLP practices and quality documentation expectations.
- Ability to work with stability-related QC activities.
- Good documentation discipline for regulated pharmaceutical operations.
Why This Role Is a Good Opportunity
This role offers experienced QC professionals an opportunity to work with Leben Life Sciences Pvt. Ltd., an established pharmaceutical formulation company with an EU-GMP approved global standard OSD and semi-solids formulation manufacturing facility at Akola, Maharashtra.
How to Apply
Interested candidates can mail their resume to the email address below.
Contact Us: 7498035480
For more information, candidates may visit: www.lebenlifesciences.com
