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:
- Responsible for Qualification of Plant Equipment (Protocol preparation, Review and Execution)
- Responsible for review and to coordinate for all type of third party calibration in the plant.
- Responsible for review of process validation protocol.
- Responsible for preparation and data compilation of process validation report.
- Preparation of protocol and reports for HVAC and Water System.
- Responsible for risk assessment of product as well as equipment.
- Responsible for sampling and collection of validation sample.
- Execution and preparation of hold time study protocol and sample collection
- Preparation and annual product review.
- Responsible for initiate and evaluate of change control, CAPA and risk assessment of product as well as equipment.
- Responsible for handling cleaning validation activities.
