At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an setting where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
To monitor and ensure integrity, accuracy and adequacy of the analysis performed.
Review of analytical reports.
To ensure Lab Compliance (Lab instruments’ audit trail review, procedural compliance verification, Lab round and verification of online QC activities).
Review of Change Control request, Specification, Standard Test Procedure and SOP.
Periodic verification of application software on computer systems, associated with laboratory instruments with system administrator.
Review of lab instruments Calibration/Preventive maintenance data.
Review of OOS investigation report /Out of trend investigation report/ Out of Calibration report/ Laboratory Event /Deviation / CAPA / Action item.
To provide support in identification of Root cause analysis and CAPA.
To ensure implementation and check effectiveness of CAPA.
To prepare trend of OOS/OOT/Lab Event/QA of QC observation and evaluate the CAPA effectiveness for repetitive incidence and provide technical training to QC analyst.
Proactively assess quality issues and ensure compliance to the defined procedures and regulatory requirements in Quality Control laboratory.
Verify data associated with qualification of laboratory instrument.
Verify data associated with the sample destruction.
Issuance and retrieval / reconciliation of QC hard book, seq