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 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 current received QC Instruments.
Travel Estimate
Job Requirements
Educational Qualification
M.Sc/B.pharma
Experience
Tenure: 8-10 Yrs
Your Success Matters to Us
At Sun Pharma, your success a
📌 Senior Executive (Jammu)
🏢 Sun Pharmaceutical Industries
📍 Jammu
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