Executive - MSTG

Sun Pharmaceutical Industries, Inc.; Dadra and Nagar Haveli; On-site; INR 600,000 - 900,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd is seeking a Senior Officer/Executive – MSTG Orals in the R&D1 Regulatory Affairs unit in Dadra. The role requires a Master of Pharmacy and 2–5 years of relevant experience.

You will coordinate with multiple departments for timely execution of projects, plan trial and scale-up batches, and prepare essential documents for launches and regulatory reviews. Ideal candidates will manage documentation, assess risk, and support regulatory evaluations while contributing

Qualifications

• Qualification: M.Pharm
• Experience: Tenure 2-5 years of relevant experience

Responsibilities

• To coordinate with different departments i.e. Formulation development (FDD), Analytical development (ADD), Packaging development (PDD), Production, Engineering, Quality control, Quality Assurance, Supply chain, Business development, Project management and any other department for timely execution of New projects
• To plan, monitor and support for execution of the trial batch, exhibit batch, scale up/characterization batch and process qualification batches
• To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc.
• To prepare and review approve new launch documents i.e. material requisition sheet, product history, trial/ characterization protocol and report, batch manufacturing record, process qualification protocol and reports etc
• To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc.

Education

M.Pharm

Job description

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Company: Sun Pharmaceutical Industries Ltd

Job Title

Senior Officer/Executive – MSTG Orals

Business Unit

R&D1 Regulatory Affairs

Job Grade

G11B/G12A

Location

Dadra

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.”

• To coordinate with different departments i.e. Formulation development (FDD), Analytical development (ADD), Packaging development (PDD), Production, Engineering, Quality control, Quality Assurance, Supply chain, Business development, Project management and any other department for timely execution of New projects
• To plan, monitor and support for execution of the trial batch, exhibit batch, scale up/characterization batch and process qualification batches
• To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc.
• To prepare and review approve new launch documents i.e. material requisition sheet, product history, trial/ characterization protocol and report, batch manufacturing record, process qualification protocol and reports etc
• To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc.

NA

Job Requirements

Educational Qualification

Qualification: M.Pharm

Experience

Tenure 2-5 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).