Leben Life Sciences Hiring Quality Assurance

B.Pharm, M.Pharm, M.Sc QA Openings | Leben Life Sciences Akola
Apply now for Quality Assurance roles at Leben Life Sciences, Akola. B.Pharm, M.Pharm, M.Sc with 2–6+ years experience. EU-GMP approved facility.

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Build Your Career in Quality Assurance with Leben Life Sciences Pvt. Ltd.
Are you a qualified pharma professional eager to work with a globally recognized EU-GMP approved manufacturing company? Leben Life Sciences Pvt. Ltd. (LLS) is inviting applications for multiple openings in the Quality Assurance Department at its state-of-the-art OSD & Semi-Solids formulation facility in Akola, Maharashtra.

With over four decades of pharmaceutical excellence, Leben Life Sciences continues to deliver high-quality healthcare products to both domestic and international markets. This is your chance to join a forward-thinking organization that values integrity, innovation, and continuous improvement.

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Company Overview

Leben Life Sciences Pvt. Ltd. (LLS) is a well-established and trusted pharmaceutical formulation company with a legacy of more than 40 years. The company has evolved into a global name, offering a wide portfolio of oral solid dosage (OSD) and semi-solid formulations, catering to regulated and emerging markets.

Leben’s world-class manufacturing unit in Akola (M.S.) is EU-GMP approved and compliant with international standards, ensuring excellence in product quality, safety, and efficacy. With a strong focus on responsible healthcare, the company strives to create value for patients through innovation and continuous enhancement of manufacturing and quality processes.

For more details, visit their official website: 🌐 www.lebenlifesciences.com

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Job Role & Responsibilities

Department: Quality Assurance (AQA / QC Documentation)

Openings are available for experienced professionals who can uphold Leben’s high-quality standards and ensure regulatory compliance.

1. Officer – AQA (Analytical Quality Assurance)

Qualification: B.Pharm / M.Pharm / M.Sc
Experience: Minimum 2 years in AQA or QC Documentation
Key Responsibilities:

• Review and manage analytical documentation as per GMP guidelines.
• Ensure compliance with EU-GMP and other regulatory standards.
• Support in preparation and review of SOPs, protocols, and validation reports.
• Collaborate with Quality Control and Production teams for smooth documentation flow.
• Participate in internal audits and regulatory inspections.

2. Sr. Executive – AQA (Analytical Quality Assurance)

Qualification: B.Pharm / M.Pharm / M.Sc
Experience: Minimum 6 years in AQA or QC Documentation
Key Responsibilities:

• Lead AQA documentation and review processes.
• Manage change control, deviation, and CAPA documentation.
• Train junior QA staff and ensure continuous compliance improvement.
• Oversee preparation for regulatory audits and inspections.
• Coordinate with the manufacturing and regulatory affairs teams for document harmonization.

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Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, or M.Sc in Chemistry / Pharmaceutical Sciences.
• Experience: 2+ years for Officer and 6+ years for Sr. Executive in AQA or QC Documentation.
• Core Competencies:
  • Knowledge of Analytical Quality Assurance and documentation systems.
  • Understanding of GMP, GDP, and global regulatory standards (EU-GMP, WHO-GMP).
  • Excellent command of MS Office, documentation handling, and communication skills.
  • Attention to detail, accuracy, and process compliance.

Relevant Courses: Pharmaceutical Quality Assurance, Analytical Chemistry, Drug Regulatory Affairs, Pharmaceutical Technology, Quality Management Systems.

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Location & Salary

Location: Akola, Maharashtra, India.
Facility: EU-GMP approved, global standard OSD & Semi-solids manufacturing unit.
Salary: Market competitive based on experience and qualifications.
Job Type: Full-time (On-site)

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Application Process

Interested candidates are encouraged to email their updated resumes to the HR department at:
career@lebenlifesciences.com
Contact: 7498035480

Apply before November 8, 2025, to secure your chance to join one of India’s most trusted pharmaceutical companies.

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Why Join Leben Life Sciences?

• Work at a EU-GMP approved global standard facility.
• Collaborate with experienced pharma professionals in Quality and Compliance.
• Be part of a company with 40+ years of proven excellence.
• Strong focus on employee growth, training, and development.
• Contribute to delivering high-quality and responsible healthcare solutions worldwide.

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Frequently Asked Questions (FAQs)

Q1: Who can apply for these QA positions?
Candidates with B.Pharm, M.Pharm, or M.Sc and relevant experience in AQA or QC Documentation can apply.

Q2: What is the job location?
The position is based at Leben Life Sciences’ EU-GMP approved unit in Akola, Maharashtra.

Q3: Are these full-time or contractual roles?
These are full-time, permanent positions with career growth opportunities.

Q4: Is prior experience mandatory?
Yes. A minimum of 2 years (for Officer) and 6 years (for Sr. Executive) of relevant experience is required.

Q5: How can I apply?
Send your resume to career@lebenlifesciences.com or contact 7498035480 for more details.

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Category	Details
Company	Leben Life Sciences Pvt. Ltd.
Vacancies	Officer (AQA) & Sr. Executive (AQA)
Required Education	B.Pharm, M.Pharm, M.Sc
Experience	Officer: 2+ Years, Sr. Executive: 6+ Years
Location	Akola, Maharashtra
Contact Email	career@lebenlifesciences.com
Contact Number	7498035480