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.
- Review and approval of QA
📌 Executive - QC (Halol)
🏢 SUN PHARMA
📍 Halol
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