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 workplace 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 (India)
🏢 SUN PHARMA
📍 India