GLP Executive

Medella Softgel Pvt. Ltd. is seeking a dedicated and detail-oriented GLP Executive 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