At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an setting 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 will 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 prepare the QC Master Documents like Specification and ATP [For Raw Materials, Working Standard, Finish, Stability and Packing Materials etc.] in LIMS.
- To Import/Export of LIMS documents from and to SUN locations.
- New Methods preparation and Formula preparation in LIMS as per Requirements.
- LIMS Software Verification [PQ] & Documentation.
- Preparation of Pharmacopoeial changes report based on Verification of Pharmacopoeial Methods raw data. Responsible for updation of Specification as per Pharmacopoeial changes Report.
- To initiate the change control for the revision and preparation of SOPs, Specifications, Standard Test Procedures etc. in TW software.
- To prepare and revise Quality Control SOP as per GQS & GSOP.
- Index preparation and updation of Specification.
- To prepare FP dispatch COA and regulatory submission COA.
- To provide Specification/ ATP for dossier filing and re-filing to regulatory.
- To provide Specification/ ATP to Commercial Department.
- To ensure LIMS User ID creation and deactivation of QA and QC department as per SOP.
- Responsible for initiation of change control for installation and Qualification of new received QC Instruments.
Travel Estimate
Job Requirements
Educational Qualification
M.Sc/B.pharma
Experience
Tenure: 8-10 Yrs
Your Success Matters to Us
At
📌 Senior Executive (India)
🏢 Sun Pharmaceutical
📍 India
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