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:
• Ensure that batch production records are executed and reviewed in accordance with established SOPs and cGMP regulations.
• To release / reject the Batch after complete review of batch and related quality documentation.
• Conduct certification of BPR after completion of batch.
• Review and approve equipment qualification protocols and reports for accuracy, completeness,
and traceability as well as adherence to protocol / procedures.
• Review and approve Annual Product review reports for the products as per the schedule.
• Track to completion all deviation and investigations related to product release.
• Conduct thorough investigations into and complaints for products manufactured at the site and ensure on-time closure of complaints.
• Run reports in electronic systems to ensure that all requirements related to batch release are met.
• Work directly with planning, QC, other QA functions, and Regulatory Affairs to ensure batches are released to meet supply chain requirements.
• Participate in self-audits of facility and equipment in partnership with Manufacturing and Engineering to ensure readiness for operations.
• Identify continuous improvement opportunities to increase compliance, process clarity, and operational efficiency.
• Review and approve Master Formula (Manufacturing / Packing Inst
📌 Senior Manager (Baska)
🏢 Sun Pharmaceutical Industries
📍 Baska
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