Leben Life Sciences Pvt. Ltd. (LLS), a well-established pharmaceutical formulation company with more than four decades of industry presence, has announced new hiring opportunities for its EU-GMP approved OSD and Semi-Solids manufacturing facility located in Akola, Maharashtra. The company is inviting applications from experienced pharmaceutical professionals for the Quality Control department.
Candidates having expertise in HPLC analysis, GLP practices, IP/FP testing, and documentation activities can apply for this opportunity. This recruitment drive offers an excellent career opportunity for pharmacy and science graduates looking to work with a reputed pharmaceutical organization.
• Company Name: Leben Life Sciences Pvt. Ltd.
• Department: Quality Control
• Position: Officer
• Job Location: Akola, Maharashtra, India
• Experience Required: 2 to 4 Years
• Qualification: M.Sc / B.Pharm / M.Pharm
• Industry Type: Pharmaceutical Manufacturing
• Facility Type: EU-GMP Approved OSD & Semi-Solids Plant
Quality Control Officer
Leben Life Sciences is looking for skilled and experienced candidates for the Officer role in the Quality Control department.
Sections Involved
• HPLC
• GLP
• IP/FP
• Documentation
Candidates selected for the Quality Control Officer role will be responsible for:
• Performing HPLC analysis and laboratory testing
• Handling IP/FP sample analysis and documentation
• Maintaining GLP compliance within the laboratory
• Preparing and reviewing analytical reports
• Ensuring adherence to pharmaceutical quality standards
• Supporting quality systems and audit readiness
• Maintaining laboratory instruments and records
Applicants must possess any of the following qualifications:
• M.Sc
• B.Pharm
• M.Pharm
Candidates should also have 2 to 4 years of relevant experience in pharmaceutical Quality Control operations.
Leben Life Sciences is expected to offer an attractive salary package based on candidate experience and technical expertise.
Expected Salary Range
• ₹3.5 LPA to ₹6 LPA (Approx.)
Employee Benefits
• Opportunity to work in an EU-GMP approved facility
• Professional growth in Quality Control operations
• Exposure to regulatory pharmaceutical standards
• Stable and reputed pharmaceutical organization
• Learning opportunities in analytical and documentation systems
Interested and eligible candidates can send their updated resume to the official company email address mentioned below.
Email Address
Contact Number
7498035480
The position is based at the company’s pharmaceutical manufacturing facility in Akola, Maharashtra.