Jobs in Sun Pharma: Hiring a Senior Officer – MSTG Orals at its Dadra plant | Apply Now
Are you currently looking for Jobs in Sun Pharma? Sun Pharmaceutical Industries Ltd, a global leader in the pharmaceutical sector, is hiring a Senior Officer – MSTG Orals at its Dadra plant. This role offers an exciting opportunity to coordinate cross-functional teams, support trial and scale-up batches, and contribute to new product development while fostering innovation and continuous improvement in regulatory and R&D processes.
About Sun Pharma:
Sun Pharmaceutical Industries Ltd, commonly known as Sun Pharma, is a leading global pharmaceutical company committed to improving healthcare and patient outcomes worldwide. Founded with a vision to deliver affordable and high-quality medicines, Sun Pharma has grown into one of the largest specialty generic pharmaceutical companies, with a strong presence in over 100 countries. The company focuses on innovation, research, and development across a wide range of therapeutic areas, including cardiology, psychiatry, neurology, diabetology, and oncology, among others. With a robust pipeline, state-of-the-art manufacturing facilities, and a strong R&D network, Sun Pharma emphasizes quality, compliance, and operational excellence. Sun Pharma’s culture encourages employees to “Create your own sunshine”, fostering continuous learning, leadership, collaboration, and personal growth while making a meaningful impact on patients’ lives globally.
Job Details:
- Job Title: Senior Officer / Executive – MSTG Orals
- Location: Dadra Plant, India
- Business Unit: R&D1 Regulatory Affairs
- Job Grade: G12B/G12A
Job Description
The Senior Officer – MSTG Orals will:
- Coordinate with departments including Formulation Development (FDD), Analytical Development (ADD), Packaging Development (PDD), Production, Engineering, QA/QC, Supply Chain, Business Development, and Project Management for timely execution of new projects.
- Plan, monitor, and support trial batches, exhibit batches, scale-up/characterization batches, and process qualification batches.
- Prepare and review new product documents including material requirement sheets, master formula cards, bills of material, risk assessment reports, scale-up protocols and reports, trial/exhibit batch manufacturing records, and protocols.
- Initiate gate passes for sample transfer across Sun Pharma sites.
- Prepare and review launch documents, including product history, trial/characterization protocols, batch manufacturing records, and process qualification reports.
- Share process knowledge with cross-functional teams through presentations to ensure smooth technology transfer.
- Review product history and process parameters for technical remediation and improvement of product robustness.
- Prepare and review investigation reports, justification reports, additional activity protocols, and regulatory evaluations.
Educational Qualification:
M.Pharm
Experience:
2–5 years in relevant pharmaceutical R&D or regulatory roles
