Quality Assurance Job at Glenmark | Excellent Opportunity for Pharma Candidates
Looking for a Quality Assurance Job with one of India’s leading pharmaceutical companies? Glenmark Careers brings an excellent opportunity for experienced B.Pharm, M.Pharm professionals to join as Senior Officer – Analytical QA at Dindori, Nashik. If you have expertise in analytical data review, GMP compliance, HPLC, GC, and laboratory quality systems, this Quality Assurance Job through Glenmark Careers could be the perfect next step in your pharmaceutical career.
- Job Title: Quality Assurance – Analytical QA
- Location: Dindori, India
About the Company
Glenmark Healthcare Limited is a global leader in the development and commercialization of high-quality generic medicines. Established in 2023 as a subsidiary of Glenmark Pharmaceuticals, the company launched its first product in March 2024 and has rapidly emerged as one of India’s leading pharmaceutical organizations. Glenmark is committed to improving healthcare by delivering high-quality medicines while reducing healthcare costs worldwide.
Job Descriptionquality-assurance-job-glenmark-careers
Glenmark Healthcare Limited is inviting applications for the Senior Officer – Analytical QA position under the Quality Assurance Job function. The selected candidate will be responsible for Quality Assurance, Analytical Data Review, and ensuring compliance with cGMP, GLP, and ICH guidelines.
Key Responsibilities
- Review QC lab data, including chromatographic data and notebooks, for compliance with cGMP, GLP, and ICH guidelines.
- Audit sample login, analytical worksheets, instrument logbooks, and Certificate of Analysis (COA) for accuracy.
- Investigate Out of Specification (OOS) results, deviations, and laboratory inconsistencies.
- Ensure laboratory analysts follow approved Standard Operating Procedures (SOPs) and validated test methods.
- Coordinate with QC analysts to address data discrepancies, audit findings, and inspection queries.
- Prepare, review, and revise SOPs, Specifications, and Analytical Method Validation (AMV) protocols.
Qualifications
- B.Pharm/ M.Pharm
Experience
- 3–5 years in the Pharmaceutical Industry.
- Experience in Analytical Data Review.
Preferred Skills
- Analytical data review experience.
- GMP compliance.
- Analytical techniques.
- Knowledge of HPLC, GC, UV Spectrophotometer, and Auto Titrator.
- Familiar with Quality Control department processes.
- Sterile operations experience preferred.
- Knowledge of CFR.
- SAP or other ERP systems.
- Excellent written and verbal communication skills.
- Professional approach and strong interpersonal skills.
- Team player with influencing and negotiation capabilities.
- Fluent in English.
Key Performance Indicators
- Analytical Development and Validation activity.
- Analytical Data Review experience.
Required Competencies
- Knowledge of operating sophisticated instruments like HPLC, GC, UV Spectrophotometer, and Auto Titrator.
- Review of analytical data.
- Familiarity with pharmaceutical Quality Control processes.
