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Leben Life Sciences Pvt. Ltd. is hiring experienced pharmaceutical professionals for its Quality Assurance Department at its EU-GMP Approved Global Standard OSD & Semi-Solids Formulation Manufacturing Facility in Akola, Maharashtra.
The company is looking for candidates with strong experience in AQA/QC Documentation for the position of Sr. Executive – AQA.
Job Details
Company: Leben Life Sciences Pvt. Ltd.
Position: Sr. Executive – AQA
Department: Quality Assurance
Section: AQA
Location: Akola, Maharashtra
Experience: 6+ years
Qualification: B.Pharm / M.Pharm / M.Sc.
Industry: Pharmaceutical Manufacturing
Facility: EU-GMP Approved OSD & Semi-Solids Formulation Facility
Key Requirement
Candidates should have 6+ years of relevant experience in AQA, Quality Assurance, or QC Documentation within the pharmaceutical industry.
Professionals with hands-on experience in pharmaceutical documentation and QA processes are encouraged to apply.
Eligibility
- B.Pharm / M.Pharm / M.Sc. qualification
- Minimum 6+ years of relevant pharmaceutical experience
- Experience in AQA / QC Documentation
- Strong understanding of pharmaceutical Quality Assurance documentation
- Candidates with relevant experience in formulation manufacturing will be preferred
How to Apply
Interested candidates can share their updated CV through the details provided in the recruitment announcement:
📧 Email: career@lebenlifesciences.com
📞 Contact: 7498035480
If you are an experienced AQA/QC Documentation professional looking for your next opportunity in the pharmaceutical industry, this could be a suitable career opportunity with Leben Life Sciences.
