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 team-oriented spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Job
Job Summary:
• 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.
• To prepare narcotics & psychotropic substance related documents (If used).
• To prepare SOPs for laboratory equipment/i
📌 Executive _ Formulation Development Non-Orals (India)
🏢 Sun Pharmaceutical Industries
📍 India
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