At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an workplace 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 safe 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.
Review and approval of QA of QC and respectiv