At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment 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, sequential log, register and forms.
- Follow the EHS policy, laboratory procedures and maintain the compliance to cGMP requirements.
