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:
• Review and approval the QMS e.g OOS ,OOT, Lab event , deviations ,change control ,CAPA etc.
• Review /Approval the routine analytical raw data of finished products /API /IP/PV/Pkg etc.
• Assure all time readiness of site for regulatory agency inspectionsinternal audits and
appropriate implementation of corrective actions regarding observations made by the
agenciesinternal audit teams.
• Ensuring compliance to regulatory requirements on product, process and
release procedures. Ensure release of secure and effective drug products from site as per cGMP
Requirement and regulatory commitment.
• Facilitate internal and regulatory agency audits, ensuring that findings from site audits are
understood, assessed and addressed site wide in a comprehensive manner.
• Monitor industry trends/issues faced internally and identify scope for improving Site quality
assurance management and processes.
• Performs all work in support of our Corporate Values of Pride, Accountability, Integrity and
Diligence. Performs all work in accordance with all established regulatory and compliance and
safety requirements.
• To ensure the compliance on control and maintenance of Quality Control system this includes
daily round and observations.
• To be a team member in identification of RCA and CAPA.