Executive Job at Sun Pharma Careers | FRD Non-Orals R&D Opportunity
Looking to grow your career with an Executive Job at a leading pharmaceutical company? Sun Pharmaceutical Industries Ltd is inviting applications under Sun Pharma Careers for the role of Executive – FRD Non-Orals in its R&D1 Regulatory Affairs division. This Executive Job opportunity through Sun Pharma Careers is ideal for candidates seeking professional growth in formulation research and development within a globally recognized pharma organization.
Job Details
- Job Title: Executive – FRD Non-Orals
- Location: Baroda (Tandalja – R&D)
About the Company
Sun Pharmaceutical Industries Ltd is a leading global pharmaceutical company committed to helping employees “Create your own sunshine” by fostering an environment where individuals grow at every step, take charge of their journey, and thrive in a supportive community. As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress, ‘Take charge’ with confidence, and ‘Thrive together’ with collaborative teamwork through Sun Pharma Careers.
Job Description
The Executive – FRD Non-Orals position at Sun Pharmaceutical Industries Ltd under R&D1 Regulatory Affairs involves formulation research and development activities with a strong focus on injectable and non-oral dosage forms. This Executive Job requires involvement in product development, regulatory documentation, laboratory experiments, technology transfer documentation, and cross-functional coordination while complying with internal quality systems as part of Sun Pharma Careers.
Key Responsibilities
- Experience in Formulation R&D product development with experience in injectable product development in Novel drug delivery systems/Lyophilized product/Solution product.
- To do a literature search relevant to projects requirement and understanding of Regulatory guidance.
- To procure raw materials (API/excipients), packaging materials, and Reference product in consultation with the packaging/purchase department.
- To prepare request application for Testing/analysis license for new product/Reference product.
- To design, conduct pre-formulation and formulation developmental experiments with the QbD approach, and to enter the details about drug product manufacturing experiments inthe Lab Notebook.
- To prepare TR/IOM for the respective API/Excipients/product sample analysis.
- To prepare product development/stability study protocols and reports, prepare SOPs for related laboratory equipment/instrument and maintain critical data records for regulatory audits.
- To prepare document for Technology Transfer like sheet II, Master Formula, Risk assessment based upon CPP & CQA, FMEA and SDS.
- Group work for lab management, handling instruments, common group activities, and coordination with cross-functional teams for handling project issues.
- To support cross-functional activities at the plant for Scale- up/ Exhibit batches/commercial batches and new assignments.
- Preparation of Product development report (PDR), Risk assessment reports, and compilation of project issues.
- To comply with the internal quality system while performing any activity.
Qualifications
Educational Qualification:
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Graduate: M.Pharm
Experience:
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Tenure: 2–4 years
