Job Title:

Executive - Formulation Research Development Non Orals

Business Unit:

RD1 Regulatory Affairs

Job Grade

G12A

Location :

Baroda

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.

J ob 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

Travel Estimate

NA

Job Requirements

Educational Qualification

M. Pharm

Experience

*Tenure* : 0 - 4 yrs.

Y

📌 Executive - FRD Non Orals (Vadodara)
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