Leben Life Sciences Hiring QC Officer
- Company Overview
- Job Role & Responsibilities
- Quality Control Officer – HPLC Section
- Eligibility / Qualifications
- Educational Requirements
- Experience Criteria
- Location & Salary
- Application Process
- SEO-Optimized Job Title Variations
- Why Join Leben Life Sciences
- FAQs
- Who can apply for this role?
- Is HPLC experience mandatory?
- Is this an EU-GMP facility?
- Are freshers eligible?
- How can I apply?
M.Sc B.Pharm QC HPLC Jobs | Leben Akola
Leben Life Sciences hiring QC Officer (HPLC) in Akola. M.Sc, B.Pharm, M.Pharm eligible. EU-GMP facility.
Leben Life Sciences Pvt. Ltd. is hiring qualified Quality Control professionals to support analytical operations at its EU-GMP approved formulation manufacturing facility located in Akola, Maharashtra. This opportunity is ideal for candidates with hands-on HPLC experience who want to build long-term careers in a globally compliant pharmaceutical manufacturing environment.
With more than four decades of presence in the pharmaceutical industry, Leben Life Sciences continues to strengthen its quality systems to meet international regulatory expectations. The current opening focuses on analytical quality control activities that directly ensure product safety, efficacy, and regulatory compliance.
Company Overview
Leben Life Sciences Pvt. Ltd. is a well-established pharmaceutical formulation company with over 40 years of industry experience. The company operates a global-standard manufacturing facility approved by EU-GMP, specializing in oral solid dosage forms and semi-solid formulations.
Leben Life Sciences follows stringent quality management systems and global regulatory standards, supplying pharmaceutical products to domestic and international markets. Its Akola facility plays a critical role in maintaining analytical excellence and regulatory readiness across multiple dosage forms.
Job Role & Responsibilities
Quality Control Officer – HPLC Section
The Quality Control Officer will be responsible for analytical testing and compliance activities within the QC laboratory.
Key responsibilities include:
- Performing routine analysis using HPLC as per approved specifications
- Executing method verification and system suitability testing
- Ensuring compliance with GLP and GMP requirements
- Handling raw material, in-process, and finished product analysis
- Maintaining accurate analytical documentation and records
- Supporting stability studies and audit readiness activities
- Assisting in investigation of OOS and analytical deviations
This role requires strong analytical discipline and familiarity with regulated QC laboratory operations.
Eligibility / Qualifications
Educational Requirements
- M.Sc
- B.Pharm
- M.Pharm
Relevant courses include: Pharmaceutical Analysis, Analytical Chemistry, Pharmaceutics, Industrial Pharmacy, Quality Assurance, Chemistry
Experience Criteria
- 2 to 4 years of relevant Quality Control experience
- Mandatory hands-on exposure to HPLC analysis
- Working knowledge of GLP documentation practices
Location & Salary
Job location: Akola, Maharashtra.
Salary will be offered as per industry standards and will depend on experience, technical competency, and interview performance. Compensation is competitive for EU-GMP regulated QC laboratory roles.
Application Process
Interested and eligible candidates can apply by sharing their updated resume via email or contacting HR directly:
- Email: career@lebenlifesciences.com
- Contact Number: 7498035480
Candidates should clearly mention “QC Officer – HPLC” in the email subject line.
SEO-Optimized Job Title Variations
- Leben Life Sciences QC HPLC Jobs in Akola
- Pharma Quality Control Officer Jobs – Leben Life Sciences
- EU-GMP QC Analyst Careers in Maharashtra
- HPLC Analyst Jobs in Pharmaceutical Manufacturing
Why Join Leben Life Sciences
Working at Leben Life Sciences offers exposure to EU-GMP compliant manufacturing systems, robust analytical laboratories, and quality-driven pharmaceutical operations. Quality Control professionals at Leben directly contribute to responsible healthcare by ensuring that every batch meets global safety and regulatory standards.
FAQs
Who can apply for this role?
Candidates with M.Sc, B.Pharm, or M.Pharm qualifications and 2–4 years of QC experience can apply.
Is HPLC experience mandatory?
Yes. Hands-on HPLC experience is mandatory for this role.
Is this an EU-GMP facility?
Yes. The Akola facility is EU-GMP approved.
Are freshers eligible?
No. Prior QC laboratory experience is required.
How can I apply?
You can apply by emailing your resume or contacting the provided HR number.
| Company | Leben Life Sciences Pvt. Ltd. |
|---|---|
| Vacancies | Quality Control Officer – HPLC |
| Required Education | M.Sc, B.Pharm, M.Pharm |
| Experience | 2–4 years |
To apply for this job email your details to career@lebenlifesciences.com
