Glp Executive

**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.

Pay: ₹25,000.00 - ₹50,000.00 per month

Supplemental Pay:

- Performance bonus
- Yearly bonus

Work Location: In person