for the Quality Control department to ensure strict compliance with
Good Laboratory Practices
(GLP) and industry standards. The ideal candidate will play a critical role in maintaining laboratory integrity, data accuracy, and regulatory compliance in all
QC activities
.
Key Responsibilities:
Ensure GLP compliance in all laboratory practices, documentation, and operations.
Maintain and monitor lab protocols, SOPs, and equipment calibration records.
Conduct routine testing, sampling, and documentation of raw materials, in-process, and finished pharmaceutical products.
Perform and review analytical reports, ensuring accuracy, traceability, and integrity.
Participate in internal audits, regulatory inspections, and CAPA implementations.
Train QC personnel on GLP and laboratory best practices.
Maintain proper documentation in line with WHO-GMP, ICH, and regulatory guidelines.
Coordinate with QA and R&D teams for cross-functional documentation and compliance activities.
Key Requirements:
B.Pharm / M.Pharm / M.Sc in Chemistry, Pharmaceutical Sciences, or a related field.
Minimum 3-5 years of experience in a GLP-compliant pharmaceutical QC environment.
Strong understanding of analytical techniques like HPLC, UV, Dissolution, and Titration.
Familiarity with regulatory guidelines (GLP, GMP, ICH, FDA, etc.).
Excellent documentation and communication skills.
Proficiency in MS Office and laboratory software systems.
Why Join Us?
Opportunity to work with a leading WHO-GMP certified pharmaceutical manufacturing company.
Growth-oriented and compliance-driven work culture.
Exposure to state-of-the-art laboratories and best-in-class industry practices.
Job Type: Full-time
Pay: ?25,000.00 - ?50,000.00 per month
Supplemental Pay:
Performance bonus
Yearly bonus
Work Location: In person
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