Ajanta Pharma is a specialty pharmaceutical company providing quality medicines across 30+ countries in the world
Post : LAB QA - Deputy Manager
Qualification : M.Pharma / B.Pharma / MSc
Experience : 14 to 18 Years
Job Responsibilities :
• Responsible for ensuring cGMP compliance in the QC laboratory, reviewing analytical documentation, and approving Certificates of Analysis for all materials and products.
• Accountable for investigating quality issues (OOS, deviations, incidents) and implementing CAPAs. Oversee data integrity through review of chromatographic / non-chromatographic data and LIMS audit trails for OSD sites.
• Review and approve QC documents, stability protocols, study reports, and raw material storage conditions. Manage manufacturer details and GRN approvals in BLPS software to ensure compliance and traceability.
Technical & Functional Skills:
• Regulatory requirements (ICH, WHO, USFDA, EU guidelines) exposure
• Quality Systems Knowledge
• Analytical Techniques-Chromatographic(HPLC,GC) and non-chromatographic methods.
• Data Integrity &AuditTrail Review-Expertise in Empower, LIMS, and electronic systems compliance.
• Documentation Control-Reviewinganalytical documents, CoAs, protocols, and reports.
Analytical & Investigative Skills:
• Root Cause Analysis-For OOS, deviations, and incidents.
• Risk Assessment-ldentifying and mitigating compliance risks.
Soft Skills :
• Attention to Detail-For document review and data integrity checks.
• Communication & Collaboration-Working with QC, QA, and cross-functional teams.
• Problem-Solving-Handling complex investigations and implementing CAPAs.
• Time Management-Managing multiple reviews and approvals efficiently.
Location : Guwahati, Assam
Share your updated CV at sahil.sinha@ajantapharma.
Mention the current CTC and notice period
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