- Review analytical data, chromatograms, calculations, and laboratory records.
- Verify compliance of laboratory activities with GLP, GMP, and data integrity guidelines.
- Review analytical method validation, method transfer, cleaning validation, and stability study reports.
- Monitor control of laboratory instruments, calibration, qualification, and maintenance records.
- Review OOS/OOT investigations and ensure timely closure.
- Ensure adherence to ALCOA+ principles and regulatory expectations regarding data integrity.
Preferred Competencies
- Attention to detail and documentation excellence.
- Solid interpersonal and cross-functional coordination skills.
- Ability to work independently and manage multiple priorities.
- Effective investigation and root cause analysis skills.
- Commitment to continuous improvement and quality culture.
Job Snapshot
Updated Date
16-07-2026
Job ID
JOB10653
Division
CENTRAL QUALITY
Location
R&d; - Zrc|zyd.biologics-2, Ahmedabad, Gujarat, India
Experience
2 - 5 Years
Employee Type
C-C7-Confirmed-HO Staff
📌 Executive - AQA (India)
🏢 Zydus Group
📍 India
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