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Executive _ Formulation Development Non-Orals

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Job Description - Executive _ Formulation Development Non-Orals



















































Job Title:



Executive – Formulation Development (Non-Orals)



Business Unit:



R&D1 Regulatory Affairs



Job Grade



G12A



Location :



Vadodara



 



 



 



 



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   


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/instrument.


• To be a part of equipment / instrument qualification activity in case of procurement of any


new equipment / instrument and prepare/ review qualification documents.


• To use different applications introduced by management as a part of IT enablement.


• To participate in different management initiatives like PACE, Kaizen & process excellence.



 


 


 



Travel Estimate



NA



Job Requirements



Educational Qualification



Qualification: M.Pharm



Experience



Tenure 1-4 years of relevant experience



Your Success Matters to Us


At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!


 



Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).




 


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About the Company

Sun Pharmaceutical Industries

Sun Pharma is the fourth largest global specialty generic pharmaceutical company with a presence in more than 100 countries.

Read more about the company

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