Looking for QA jobs and pharmaceutical careers in India? Join Leben Life Sciences’ EU-GMP facility in Akola for Quality Assurance roles focused on QC documents review.
About the Company
Leben Life Sciences Pvt. Ltd. is a growing pharmaceutical company based in Akola, Maharashtra, with a legacy of providing quality, affordable medicines. The company operates an EU-GMP and WHO-GMP approved global-standard manufacturing facility for OSD (tablets and capsules) and semi-solids formulations.
Driven by a mission of responsible healthcare, Leben focuses on accessible medicines for patients across India and export markets. Its state-of-the-art plant, DSIR-approved R&D centre, and commitment to regulatory compliance support continuous innovation and growth. The organization emphasizes ethical practices, quality excellence, and expanding reach to serve more patients worldwide.
Job Details
- Company Name: Leben Life Sciences Pvt. Ltd.
- Experience: 2–7 years (varies by role)
- Qualification: B.Pharm / M.Pharm / M.Sc.
- Location: Akola, Maharashtra
- Work Type: On-site
Job Description
Leben Life Sciences is hiring experienced professionals for its Quality Assurance Department (AQA Section) at the EU-GMP approved OSD and semi-solids manufacturing facility in Akola. These roles focus on QC documents review and support the company’s commitment to high-quality pharmaceutical production and regulatory compliance.
Officer – AQA
- Department: Quality Assurance (AQA)
- Experience: 2 to 3 years in QC Documents Review
- Education/Qualification: B.Pharm / M.Pharm / M.Sc.
Sr. Executive – AQA
- Department: Quality Assurance (AQA)
- Experience: 5 to 7 years in QC Documents Review
- Education/Qualification: B.Pharm / M.Pharm / M.Sc.
Skills/Qualifications
- B.Pharm, M.Pharm, or M.Sc. degree
- Proven experience in pharmaceutical Quality Assurance and QC Documents Review
- Strong knowledge of documentation practices in a GMP environment
- Attention to detail and accuracy in record review
- Understanding of regulatory and quality system requirements
- Ability to work effectively in a manufacturing quality team
Key Responsibilities
- Review QC documents for accuracy and compliance
- Ensure documentation meets GMP and quality standards
- Support AQA activities in the manufacturing facility
- Maintain proper records and audit readiness
- Coordinate with QC and related teams on documentation
- Contribute to overall quality assurance processes
Benefits/Perks
- Career growth in an EU-GMP approved facility
- Learning opportunities in quality systems and documentation
- Competitive salary package
- Professional work culture focused on quality and compliance
- Exposure to global-standard manufacturing practices
- Long-term stability in the pharmaceutical industry
How to Apply
Verified Post
Verification: shared by HR.
Interested candidates should share their updated CV at [email protected].
Clearly mention the position applied for in your application.
For inquiries, contact: 7498035480.
Visit the company website at www.lebenlifesciences.com.
Apply now and advance your career in pharmaceutical Quality Assurance. Discover more opportunities on Pharma Recruiter.
Why You Should Join
Leben Life Sciences offers a professional environment at its EU-GMP certified manufacturing facility, where quality and patient-focused values drive daily operations. Employees benefit from a culture of continuous improvement, regulatory excellence, and team collaboration.
The company provides opportunities for skill development, career progression, and contribution to accessible healthcare solutions, ensuring long-term stability in India’s growing pharmaceutical sector.
FAQs
Who is eligible for these AQA positions?
Candidates with B.Pharm / M.Pharm / M.Sc. and relevant experience in QC Documents Review (2–3 years for Officer or 5–7 years for Sr. Executive) are eligible. The roles seek interested male candidates with solid pharmaceutical QA experience.
How do I apply?
Email your updated CV to [email protected], mentioning the specific position (Officer – AQA or Sr. Executive – AQA).
What is the work location?
Both positions are based at the EU-GMP approved facility in Akola, Maharashtra.
Are there growth opportunities?
Yes. Leben Life Sciences supports career growth through learning in quality systems, documentation excellence, and progression within a expanding pharmaceutical manufacturing organization.
