Job Description & How to Apply Below
At Sun Pharma, you will be responsible for leading investigations into deviations and ensuring regulatory compliance. Your work will involve close collaboration with various stakeholders, performing impact analyses, and preparing detailed reports that drive corrective actions. The role emphasizes a commitment to improving healthcare through innovative problem-solving and efficient processes.
Key Responsibilities:
• Write and manage Deviations investigation reports
• Facilitate detailed analysis meetings with SMEs
• Monitor ongoing investigations and timelines
• Prepare training on Root Cause Analysis and CAPA
• Participate actively in the internal audit program
Requirements:
•
B.Sc. in Chemistry or related field required
• Minimum three years of investigation experience
• In-depth knowledge of cGMP and FDA guidelines
• Strong communication and technical report writing skills
• Ability to prioritize in a fast-paced environment
Contribute to the high standards of quality management that Sun Pharma embodies in improving patient outcomes.
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