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’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:
- Initiation, review and QA approval of change controls related to process, equipment and facility in TrackWise system for all the modules/Dept. to fulfill the production requirement at Toansa site.
- Preparation of draft MPRs/BRCs along with necessary data as per the production requirement of modules at Toansa site.
- Uploading of draft MPRs/BRCs in BPR Printing Module for implementation and release.
- Preparation, review and QA approval of validation/qualification protocols, reports, PPV, SPR, temperature mapping, product manuals, plant development reports, Cleaning matrix, CPDR, Equipment suitability, HAZOP, Investigations (OOS/OOT/UPD) as per current SOPs for all the production modules at Toansa site.
- To coordinate with Production modules effectively for collection of supporting data / documents for CCR / Validation / Qualification related activities to complete the record as per the requirement.
- Tracking the completion of the activities as per the actions items for closure of CCRs/Protocols as per the dues dates. Wherever applicable, provide suitable justification for extension of records in TrackWise.
- To prioritize CCRs/Validation/Qualification related work to align with the production commitments.
- To harmonize documentation practices related to CCRs, Validation & Qualification activities at site.
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📌 Senior Officer (India)
🏢 Sun Pharmaceutical
📍 India
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