Leben Life Sciences Hiring 2026 – AQA Jobs in Akola
Looking for experienced Quality Assurance jobs in the pharmaceutical industry?
Leben Life Sciences Pvt. Ltd. is hiring experienced professionals for its Quality Assurance (AQA) Department at its EU-GMP approved manufacturing facility in Akola, Maharashtra.
The current openings are focused on QC document review and are suitable for candidates with B.Pharm, M.Pharm or M.Sc qualifications and relevant pharmaceutical experience.
Two positions are available:
- Officer – AQA: 2–3 years of QC Documents Review experience
- Sr. Executive – AQA: 5–7 years of QC Documents Review experience
About Leben Life Sciences
Leben Life Sciences Pvt. Ltd. is a growing pharmaceutical company based in Akola, Maharashtra, focused on providing quality and affordable medicines.
The company operates an EU-GMP and WHO-GMP approved manufacturing facility for OSD formulations such as tablets and capsules, along with semi-solid formulations.
Its operations emphasize healthcare, quality excellence, regulatory compliance, ethical practices and continuous improvement.
Job Overview
| Details | Information |
|---|---|
| Company | Leben Life Sciences Pvt. Ltd. |
| Department | Quality Assurance – AQA |
| Positions | Officer / Sr. Executive |
| Experience | 2–7 Years, role dependent |
| Qualification | B.Pharm / M.Pharm / M.Sc |
| Location | Akola, Maharashtra |
| Work Type | On-site |
| Core Area | QC Documents Review |
Current AQA Job Openings
1. Officer – AQA
Department: Quality Assurance (AQA)
Experience: 2–3 years in QC Documents Review
Qualification:
- B.Pharm
- M.Pharm
- M.Sc
This role is suitable for professionals with experience in pharmaceutical QA and QC documentation review.
2. Sr. Executive – AQA
Department: Quality Assurance (AQA)
Experience: 5–7 years in QC Documents Review
Qualification:
- B.Pharm
- M.Pharm
- M.Sc
The senior-level position is suitable for experienced QA professionals with strong exposure to QC document review and GMP quality systems.
Eligibility Criteria
Candidates should have:
- B.Pharm, M.Pharm or M.Sc qualification
- Relevant experience in pharmaceutical Quality Assurance
- Hands-on experience in QC Documents Review
- Knowledge of documentation practices in a GMP environment
- Understanding of regulatory and quality-system requirements
- Strong attention to detail
- Ability to work effectively within a manufacturing quality team
The experience requirement varies by position, with 2–3 years for Officer – AQA and 5–7 years for Sr. Executive – AQA.
Skills Required
Candidates should have knowledge or experience in:
- QC document review
- Pharmaceutical Quality Assurance
- GMP documentation
- Quality systems
- Manufacturing records
- Compliance documentation
- Audit readiness
- Regulatory requirements
- Record accuracy and review
- Coordination with QC and related departments
Strong attention to detail is important because the roles involve reviewing pharmaceutical quality documentation.
Key Responsibilities
Selected candidates may be responsible for:
- Reviewing QC documents for accuracy and compliance
- Ensuring documentation meets GMP and quality standards
- Supporting AQA activities at the manufacturing facility
- Maintaining proper records and audit readiness
- Coordinating with QC and related teams
- Contributing to overall Quality Assurance activities
- Supporting documentation and quality-system requirements
Benefits & Career Opportunities
The available recruitment information highlights:
- Career growth within an EU-GMP approved facility
- Learning opportunities in quality systems and documentation
- Competitive salary package
- Professional quality-focused work environment
- Exposure to global-standard manufacturing practices
- Long-term career stability in the pharmaceutical industry
Job Location
Leben Life Sciences Pvt. Ltd.
Akola, Maharashtra
Both AQA positions are based at the company’s EU-GMP approved OSD and semi-solids manufacturing facility in Akola.
How to Apply
Interested candidates should send their updated CV to:
Email: career@lebenlifesciences.com
Applicants should clearly mention the position applied for in the application.
For inquiries:
Contact: 7498035480
Candidates can also visit the company’s official website for additional information.
Important Note
The supplied recruitment information states that the roles seek interested male candidates with relevant pharmaceutical QA experience.
Applicants should verify the latest eligibility requirements and vacancy status with the recruitment team before applying.
Why Consider Leben Life Sciences?
For experienced QA professionals, these positions offer an opportunity to work in a GMP-focused pharmaceutical manufacturing environment.
The roles can provide exposure to:
- QC document review
- Quality systems
- GMP documentation
- Manufacturing quality processes
- Audit readiness
- Regulatory compliance
- OSD and semi-solid manufacturing operations
This makes the opportunity relevant for professionals looking to strengthen their career in pharmaceutical Quality Assurance.
Frequently Asked Questions
1. Who is eligible for the Leben Life Sciences AQA positions?
Candidates with B.Pharm, M.Pharm or M.Sc qualifications and relevant QC Documents Review experience can apply.
2. What experience is required?
The Officer – AQA position requires 2–3 years of QC Documents Review experience, while the Sr. Executive – AQA position requires 5–7 years.
3. Where is the job located?
Both positions are based at the Leben Life Sciences facility in Akola, Maharashtra.
4. How can I apply?
Send your updated CV to career@lebenlifesciences.com and clearly mention the position you are applying for.
5. Is this a fresher opportunity?
No. The listed positions require relevant professional experience in QC Documents Review and pharmaceutical Quality Assurance.
6. What qualifications are accepted?
The advertised qualifications are B.Pharm, M.Pharm and M.Sc.
7. Are there career growth opportunities?
Yes. The recruitment information highlights learning opportunities in quality systems and documentation, career progression and exposure to global-standard manufacturing practices.
Final Words
The Leben Life Sciences AQA Recruitment 2026 is a relevant opportunity for experienced pharmaceutical professionals looking to advance their careers in Quality Assurance and QC document review.
With openings for Officer and Sr. Executive – AQA, candidates can apply according to their experience level and qualification.
📍 Location: Akola, Maharashtra
🧪 Department: Quality Assurance – AQA
🎓 Qualification: B.Pharm / M.Pharm / M.Sc
⏳ Experience: 2–7 Years, role dependent
📩 Apply: career@lebenlifesciences.com
📞 Contact: 7498035480
