Sr. Executive-Analytical Quality Assurance (Lab QA)

Leben Life Sciences Pvt. Ltd.; Akola District; On-site; INR 600,000 - 800,000; Full time

Job summary

Leben Life Sciences Pvt. Ltd. in Akola, Maharashtra, is seeking a Sr. Executive AQA with 6+ years experience in AQA/QC Documentation to join the Quality Assurance Department at our EU-GMP approved facility.

The role focuses on ensuring compliance, data integrity, and documentation, with responsibility for review of specifications, calibration, audits, and lab incident handling. The ideal candidate holds B.Pharm/M.Pharm/M.Sc and is ready to contribute to our global standard operations.

Qualifications

• Must have 6+ years in AQA / QC Documentation.
• Experience in pharmaceutical Quality Assurance and documentation.
• Bachelor/Master in pharma or related field.

Responsibilities

• a. Verify cGMP, GDP, GLP and data integrity practices, compliance in Quality Control and microbiology laboratory.
• b. Review of Specification, Standard test procedures and test data sheet for adequacy and accuracy.
• c. Review Validation and calibrations of all Instruments.
• d. Review of AMV, AMT Protocols and reports.
• e. Handling of Lab incidents, Deviations, OOS, OOC, OOT etc.
• f. Handling of reserved sample of finished products and its visual inspection.
• g. Review of trend data of environmental monitoring, water analysis.
• h. Participation in audit the contract testing laboratory

Skills

AQA Documentation

Quality Assurance

Education

B.Pharm

M.Pharm

M.Sc.

Job description

Hiring..!!

Sr. Executive AQA

Leben Life Sciences Pvt. Ltd. is looking for an experienced Sr. Executive AQA to join our Quality Assurance Department at our EU-GMP Approved Global Standard OSD & Semi-Solids Formulation Manufacturing Facility in Akola, Maharashtra.Role & responsibilities

Position: Sr. Executive AQA
Department: Quality Assurance
Experience: 6+ years in AQA / QC Documentation
Qualification: B.Pharm / M.Pharm / M.Sc.
Location: Akola, Maharashtra

Who Were Looking For

We are looking for professionals with solid experience in pharmaceutical Quality Assurance and documentation. Candidates with relevant experience in AQA or QC Documentation are encouraged to apply.

Responsible for following activities:

a. Verify cGMP, GDP, GLP and data integrity practices, compliance in Quality Control and microbiology laboratory.

b. Review of Specification, Standard test procedures and test data sheet for adequacy and accuracy.

c. Review Validation and calibrations of all Instruments.

d. Review of AMV, AMT Protocols and reports.

e. Handling of Lab incidents, Deviations, OOS, OOC, OOT etc.

f. Handling of reserved sample of finished products and its visual inspection.

g. Review of trend data of environmental monitoring, water analysis.

h. Participation in audit the contract testing laboratory

Preferred candidate profile

ERP/ QMS/QC software system handling experience

Contact: 7498035480