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:
- Analysis of Process validation samples, finished product, Hold time samples and In Process samples.
- Analysis of Analytical method transfer, Analytical method validation, comparative dissolution profiling and Multimedia dissolution validation activity.
- Online documentation & Report Preparation.
- Overall upkeep of respective working bench as well as of the department.
- To follow the GLP's & GDP's and monitoring of running instrument as per work distribution.
- Analysis of samples of other sections and calibration of instruments as and when required based on departmental needs
- Responsible for participation and input for Out of Specification Investigations, Out of trend & lab Incidents happened in QC department.
