Job Description
**ob Title:**
Senior Executive / Executive FRD Non-Orals
**Business Unit:**
R&D1 Regulatory Affairs
**Job Grade**
G11B / 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, youll 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 others journeys.
**Job Description**
1. To prepare & execute metered dose inhaler (MDI) formulation development experiments
2. To design pre-formulation and prototype experiments and to monitor batches prepared for stability studies, method development & validation.
3. To prepare documents for import of API/Innovator sample and for manufacturing license for examination, testing & analysis of drug products.
4. To ensure procurement of raw material (API/Excipients), packing material & innovator samples in consultation with packing/Purchase department.
5. To evaluate Innovator pack details and review Innovator procurement quantity with justification.
6. To prepare product development protocol & report for different development studies.
8. To prepare test request for analysis of raw material (API/Excipients) & drug product.
9. To prepare stability protocol & report.
10. To prepare tech-transfer documents (e.g.sheet II, MF, RA, FMEA, stability plan, scale up report and SDS)
11. To support in execution of scale up /exhibit /clinical batches at plant/CMO
12. To prepare documents required for regulatory submission for all markets & to prepare/review technical reports/scientific justification to respond regulatory queries.
13. To prepare/review SOPs for laboratory equipment/instrument.
14. To prepare troubleshooting/investigational reports for failures/OOS/OOT.
15. To ensure compliance of internal quality system.
**Travel Estimate**
NA
**Job Requirements**
**Educational Qualification**
M.Pharm
**Experience**
_Tenure_ : minimum - 6 years
**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. Lets create a brighter future togethe_
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Senior Executive / Executive FRD Non-Orals
**Business Unit:**
R&D1 Regulatory Affairs
**Job Grade**
G11B / 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, youll 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 others journeys.
**Job Description**
1. To prepare & execute metered dose inhaler (MDI) formulation development experiments
2. To design pre-formulation and prototype experiments and to monitor batches prepared for stability studies, method development & validation.
3. To prepare documents for import of API/Innovator sample and for manufacturing license for examination, testing & analysis of drug products.
4. To ensure procurement of raw material (API/Excipients), packing material & innovator samples in consultation with packing/Purchase department.
5. To evaluate Innovator pack details and review Innovator procurement quantity with justification.
6. To prepare product development protocol & report for different development studies.
8. To prepare test request for analysis of raw material (API/Excipients) & drug product.
9. To prepare stability protocol & report.
10. To prepare tech-transfer documents (e.g.sheet II, MF, RA, FMEA, stability plan, scale up report and SDS)
11. To support in execution of scale up /exhibit /clinical batches at plant/CMO
12. To prepare documents required for regulatory submission for all markets & to prepare/review technical reports/scientific justification to respond regulatory queries.
13. To prepare/review SOPs for laboratory equipment/instrument.
14. To prepare troubleshooting/investigational reports for failures/OOS/OOT.
15. To ensure compliance of internal quality system.
**Travel Estimate**
NA
**Job Requirements**
**Educational Qualification**
M.Pharm
**Experience**
_Tenure_ : minimum - 6 years
**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. Lets create a brighter future togethe_
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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