Explore quality control jobs at Leben Life Sciences with Officer/Sr. Officer roles in GLP. Boost your pharmaceutical careers in India at an EU-GMP certified facility focused on innovation and compliance.
Contents
About the Company
Leben Life Sciences Pvt. Ltd. (LLS), with roots tracing back over four decades to 1980, has evolved into a dynamic pharmaceutical formulation powerhouse in Akola, Maharashtra. Specializing in Oral Solid Dosage (OSD) and semi-solids, the company operates a state-of-the-art EU-GMP approved manufacturing facility adhering to global standards for quality and efficacy.
Committed to “Responsible Healthcare,” LLS delivers affordable, high-quality medicines to masses worldwide, emphasizing regulatory compliance, innovation, and sustainability.
As one of India’s fastest-growing pharma entities, it invests in advanced R&D to expand its portfolio across therapeutic areas, fostering a credible legacy of excellence and employee-centric growth in pharmaceutical careers.
Job Details
- Company Name: Leben Life Sciences Pvt. Ltd.
- Experience: 2-4 years
- Qualification: M.Sc./B.Pharm/M.Pharm
- Location: Akola, Maharashtra
- Work Type: On-site
Job Description
Leben Life Sciences is seeking dedicated professionals to strengthen its Quality Control team at the EU-GMP certified facility in Akola. This Officer/Sr. Officer role in the GLP section ensures rigorous laboratory standards for OSD and semi-solids formulations. Join a compliant environment driving safe, effective medicines through precise testing and documentation.
Officer/Sr. Officer – Quality Control (GLP)
- Department: Quality Control
- Section: GLP
- Location: Akola, Maharashtra
- Role: Officer/Sr. Officer
- Experience: 2-4 years
- Education/Qualification: M.Sc./B.Pharm/M.Pharm
Skills/Qualifications
- Strong foundation in Good Laboratory Practices (GLP) and analytical methodologies
- Proficiency in QC testing for pharmaceutical formulations like OSD and semi-solids
- Knowledge of EU-GMP regulations and quality management systems
- Hands-on experience with lab instruments and documentation protocols
- Excellent attention to detail and problem-solving in controlled environments
- Effective communication for team collaboration and compliance reporting
- Commitment to ethical, patient-focused healthcare standards
Key Responsibilities
- Execute GLP-compliant testing on raw materials and finished products
- Maintain accurate lab records and documentation per EU-GMP standards
- Perform analytical assays for OSD and semi-solids quality assurance
- Support method validation and stability studies efficiently
- Ensure adherence to SOPs and regulatory guidelines daily
- Collaborate on continuous improvement in QC processes
Benefits/Perks
- Clear career progression with training in global pharma standards
- Opportunities for skill enhancement in EU-GMP environments
- Competitive salary aligned with industry benchmarks
- Positive work culture promoting work-life balance and innovation
- Exposure to international formulation projects and R&D
How to Apply
Email your updated resume, highlighting relevant QC-GLP experience, to career@lebenlifesciences.com. Include your contact details and a brief cover note.
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For comprehensive pharma job listings, visit Pharma Recruiter. Applications are reviewed ongoing—apply now to join Leben’s legacy of responsible healthcare!
Why You Should Join
At Leben Life Sciences, embrace a culture rooted in over 40 years of excellence, where EU-GMP compliance fuels innovation in affordable medicines. Gain long-term stability in a fast-growing Indian pharma leader, with tailored growth via hands-on GLP training and cross-functional roles.
Thrive in an environment valuing quality, sustainability, and employee empowerment, advancing your pharmaceutical careers in India toward global impact.
FAQs
What qualifications are required for QC Officer jobs at Leben Life Sciences?
M.Sc., B.Pharm, or M.Pharm degrees, coupled with 2-4 years in GLP or related QC roles, are essential for eligibility.
How do I apply for the Akola-based pharma positions?
Simply email your resume to career@lebenlifesciences.com with key experience details—no formal application form needed.
What does the GLP section role entail in quality control?
Focus on compliant lab testing, documentation, and assays for OSD/semi-solids, ensuring EU-GMP adherence.
What growth prospects exist in these pharmaceutical careers?
Leben offers advancement through R&D exposure, regulatory training, and stable progression in a compliant, innovative setup.
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