Leben Life Sciences Hiring 2026 – Quality Control Officer Job in Akola
Leben Life Sciences Pvt. Ltd. is inviting applications for a Quality Control Officer position at its pharmaceutical manufacturing facility in Akola, Maharashtra.
The opening is intended for professionals with 2–4 years of relevant Quality Control experience. Candidates with M.Sc, B.Pharm or M.Pharm qualifications can apply.
The position covers important QC activities such as HPLC analysis, GLP compliance, stability testing and laboratory documentation.
About Leben Life Sciences
Leben Life Sciences Pvt. Ltd. (LLS) is an established pharmaceutical formulation company with more than four decades of experience.
The company operates an EU-GMP approved manufacturing facility in Akola, Maharashtra, producing Oral Solid Dosage (OSD) and semi-solid formulations.
The facility operates within a regulated pharmaceutical manufacturing environment, with a focus on quality systems, compliance and pharmaceutical manufacturing standards.
Job Overview
| Details | Information |
|---|---|
| Company | Leben Life Sciences Pvt. Ltd. |
| Position | Quality Control Officer |
| Department | Quality Control |
| Experience | 2–4 Years |
| Qualification | M.Sc / B.Pharm / M.Pharm |
| Location | Akola, Maharashtra |
| Work Type | Full-Time, On-site |
| Industry | Pharmaceutical Formulation |
Quality Control Officer – Job Description
The selected candidate will work within the Quality Control department at Leben Life Sciences’ formulation manufacturing facility.
The role covers laboratory and quality activities involving:
- HPLC analysis
- GLP compliance
- Stability studies
- Quality Control documentation
- Laboratory testing
- SOP and regulatory compliance
Candidates should be comfortable working in a regulated pharmaceutical laboratory environment where accuracy and proper documentation are important.
Eligibility Criteria
Candidates applying for the position should have:
Educational Qualification
- M.Sc
- B.Pharm
- M.Pharm
Experience
- 2–4 years of relevant Quality Control experience
Relevant experience in pharmaceutical QC and laboratory operations will be useful for this position.
Skills Required
Candidates should have knowledge or experience in:
- HPLC analysis
- Pharmaceutical laboratory techniques
- Good Laboratory Practices (GLP)
- Stability testing
- QC documentation
- SOP compliance
- EU-GMP or other regulated manufacturing standards
- Laboratory data accuracy
- Quality and regulatory compliance
Strong attention to detail is important because the position involves analytical testing and quality documentation.
Key Responsibilities
As a Quality Control Officer, the selected candidate may be responsible for:
HPLC Analysis
- Perform HPLC analysis according to approved methods
- Follow laboratory procedures and testing requirements
- Record and review analytical results accurately
GLP Compliance
- Support GLP-compliant laboratory operations
- Follow approved laboratory procedures and SOPs
- Maintain proper testing records
Stability Studies
- Handle stability sample testing
- Perform analysis according to approved protocols
- Maintain stability-related documentation
Documentation & Quality Records
- Maintain QC records and reports
- Ensure laboratory documentation is accurate and complete
- Follow applicable regulatory and internal requirements
Quality Compliance
- Support QC activities within the formulation facility
- Follow GMP and laboratory procedures
- Contribute to maintaining quality standards across QC operations
Work Environment
The position is based at Leben Life Sciences’ EU-GMP approved facility in Akola, Maharashtra.
The facility covers pharmaceutical formulation manufacturing, including OSD and semi-solid products.
The role provides exposure to a regulated Quality Control environment involving analytical testing, stability studies, documentation and laboratory compliance.
Career Opportunities at Leben Life Sciences
This position can provide practical experience in several areas of pharmaceutical Quality Control, including:
- HPLC analysis
- GLP practices
- Stability testing
- QC documentation
- Pharmaceutical laboratory operations
- GMP and regulatory compliance
- Formulation manufacturing quality systems
Such experience can help professionals build their technical profile within the pharmaceutical Quality Control and quality-compliance functions.
Benefits & Professional Exposure
The position offers exposure to:
- EU-GMP manufacturing standards
- Pharmaceutical formulation QC
- OSD and semi-solid products
- HPLC and analytical laboratory work
- Stability testing
- GLP practices
- Quality documentation
- Regulated pharmaceutical operations
Job Location
Leben Life Sciences Pvt. Ltd.
Akola, Maharashtra, India
The role is full-time and on-site.
How to Apply
Interested candidates who meet the required qualification and experience can send their updated resume to:
📧 Email: career@lebenlifesciences.com
📞 Contact: 7498035480
Candidates should mention the Quality Control Officer position in their application and provide relevant details of their QC experience.
Company website:
Leben Life Sciences
Important Note for Applicants
Before applying, candidates should confirm the latest vacancy status, eligibility requirements and recruitment process with the company.
Applicants should also ensure that their CV clearly highlights relevant experience in HPLC, GLP, stability testing and pharmaceutical QC where applicable.
Frequently Asked Questions
1. What position is Leben Life Sciences hiring for?
Leben Life Sciences is hiring for a Quality Control Officer position.
2. Where is the job located?
The position is based in Akola, Maharashtra.
3. What qualifications are required?
Candidates with M.Sc, B.Pharm or M.Pharm qualifications can apply.
4. How much experience is required?
The listed requirement is 2–4 years of relevant Quality Control experience.
5. What skills are required?
Important skills include HPLC analysis, GLP, stability testing, documentation and pharmaceutical laboratory practices.
6. Is the job on-site?
Yes. The position is a full-time, on-site role at the Akola facility.
7. How can I apply?
Candidates can send their updated CV to career@lebenlifesciences.com or contact 7498035480 for more information.
8. What type of facility will the candidate work in?
The role is based at Leben Life Sciences’ EU-GMP approved OSD and semi-solid formulation facility in Akola.
