Amaris Clinical is seeking a dynamic individual to join our Bioanalytical Quality Control team and ensure compliance with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).
Bioanalytical QC
Key Responsibilities
Ensure Compliance
Monitor and enforce compliance with GDP, GLP and in-house SOPs in all bioanalytical activities.
Data Review & Verification
Review study concentration data, validation and analytical reports.
Verify data against raw data records.
QA Audit & Observations
Ensure data is transferred for QA audit after QC verification and monitor closure of QA observations within timeline.
Archival & Documentation
Coordinate with QA for archival and retrieval of bioanalytical documents and files.
Training
Provide training to QC associates and support their development.
Method Development & Validation
Ensure documents related to method development and validation comply with GDP and GLP standards.
Equipment Calibration
Verify equipment calibration documents to maintain accuracy and reliability.
In-process Verification
Conduct in-process verification of sample processing activities.
Verification of BAL Documents
Verify IQ, OQ, PQ documents related to BAL systems.
Additional Duties
Perform any other duties assigned by management
Experience : 7-10 Years (CRO Experience Required)
Qualification : B.Pharm / M.Pharm / M.Sc
Location : Chengalpattu, Tamil Nadu
Send your updated resume to hr@amarisclinical.com
Last Date : 31st August 2026
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