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 Description
- To do Literature search & prepare summary report.
- To request/generate RM code, project code, product code.
- To apply for licenses for import of API/Innovator sample, for manufacturing license for examination, testing & analysis of drug products.
- To initiate procurement of raw material (API/Excipients), packing material & innovator samples in consultation with packing/purchase department.
- To prepare batches for pre-formulation, prototype, stability & method development & validation.
- To enter experimentation details in Log book/ELN.
- To prepare product development protocol for different development studies as per checklist, its execution & preparation of report.
- To prepare test request for analysis of raw material (API/Excipients) & drug product.
- To prepare stability protocol & submit samples to charge on stability.
- To prepare tech-transfer documents (e.g., Sheet II, MF, RA, FMEA, stability plan & SDS).
- To supervise scale up / exhibit / clinical batches at plant/CMO.
- To prepare documents required for regulatory submission for all markets & to prepare technical reports/scientific justification to respond regulatory queries.
- To propose in-process & finished product specification
