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.”
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Job Profile:
- Perform QC review of departmental operations to ensure compliance to SOPs, study protocol, Good Laboratory Practice (GLP), Positive Clinical Practice (GCP), quality standards and regulatory requirements.
- Perform Project-based, Process-based and Facility-based reviews of BA/BE study operations (including Bioanalytical, Pharmacokinetic and statistical).
- Perform In-process reviews of Lab activities.
- Review of method validation Raw data and BA/BE study raw data for accuracy, integrity, compliance and completeness.
- Review of method validation reports and BA/BE study reports to ensure that they accurately reflect the raw data and BA/BE study conduct.
- Review of Pharmacokinetic and Statistical data for compliance to SOPs, study protocol and regulatory requirements.
- Provide appropriate CAPA (Corrective Action and Preventive Action) to Quality Assurance audit reports.
- Prepare, review and revise departmental SOPs in accordance with regulatory requirements, GSOP and GQS.
- Document control of all raw data forms, paper laboratory notebooks and logbooks in the department.
- Perform the role of Department Training Coordinator. Conduct and coordinate induction training for new joiners and ongoing training sessions in the department and maintain training records for department personnel.
- Review contract service provider assessmen
📌 Sr.Executive-QC for Bioanalytical Lab (India)
🏢 Sun Pharmaceutical Industries
📍 India
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