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Leben Life Sciences Pvt. Ltd. (LLS), a trusted pharmaceutical formulation company with more than four decades of excellence, has announced new job openings at its EU-GMP approved, global-standard OSD and semi-solids manufacturing facility located in Akola, Maharashtra. Known for its strong quality culture and advanced production capabilities, LLS continues to expand its team by welcoming skilled professionals in the Quality Assurance domain.
Position: Sr. Officer – Quality Assurance
Department:
•Quality Assurance (QA)
Area of Work:
Documentation / Quality Management System (QMS)
Qualification Required:
M.Pharm
Experience:
2 to 4 years in a pharmaceutical QA documentation or QMS role.
The ideal candidate should possess strong knowledge of QA systems, documentation practices, and regulatory compliance for EU-GMP standards. Experience in handling SOPs, change controls, deviations, CAPA, and other QMS activities will be an added advantage.
Why Join Leben Life Sciences?
•Over 40 years of industry presence
•EU-GMP approved state-of-the-art facility
•Opportunity to grow within a reputed pharma organization
•Exposure to global quality standards
•Supportive workplace environment
How to Apply
Interested male candidates can share their updated resumes at:
📩 career@lebenlifesciences.com
📞 7498035480
Leben Life Sciences invites passionate and dedicated QA professionals to be part of its mission of delivering safe, effective, and responsible healthcare solutions.
