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.”
Job
Key Responsibilities:
- Responsible for lifecycle management of development products with respect to knowledge management and lifecycle management as per ICH. Management of process changes in early phase development
- Review of clone development and cell banking documentation and ensuring regulatory compliance in plans and reports
- Review of product development documents such as process development reports, process descriptions, process control strategy documents etc.
- Review of analytical developments such as method development reports, method qualification/validation protocols and reports and ensure compliance as per latest quality and regulatory requirements
- Development, Implementation and continual improvement of Quality Management System at R&D; through SOPs, Manuals, training and audits and ensuring alignment with corporate QA and site QA.
- Verification of Laboratory data and its integrity, ensuring valuable documentation practices and data reporting as per ALCOA++
- Compilation and review of process and analytical documents for regulatory filing and CMC review
Travel Estimate
NA
Job Requirements
Educational Qualification
Qualification : M.Pharm /M.Sc
Experience
📌 Senior Executive (Tandalja)
🏢 Sun Pharmaceutical Industries
📍 Tandalja
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