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Salary
≈ $19k – $45k per year (Estimated)
Location
In office (Gurgaon)
Seniority
Middle · 3+ years exp

Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Oct 30, 2026.

Overview
Company
Impact
Profile match
Headquartered in Mumbai, India, Sun Pharmaceutical Industries Limited (Sun Pharma) is a global specialty generic pharmaceutical enterprise and the largest pharmaceutical company in India. The company manufactures and markets a broad portfolio of generic and branded generic pharmaceuticals, complex drug formulations, over-the-counter (OTC) products, and active pharmaceutical ingredients (APIs) across key therapeutic areas such as dermatology, ophthalmology, psychiatry, cardiology, and oncology. Supported by an extensive global manufacturing footprint and robust R&D capabilities, it delivers high-barrier-to-entry and affordable medicines to healthcare systems in more than 100 countries worldwide.

Job Title:

Manager - PSUR & Aggregate Reports

Business Unit:

GPV

Job Grade

G10

Location:

Gurgaon

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 Role:

  • Analyze individual case safety reports (ICSRs) within aggregate contexts, evaluating seriousness, expectedness, causality and integrate findings into cumulative safety profiles for New Chemical Entities (NCEs) or Innovator Products .
  • Risk Characterization
  • Review of published scientific literature for PSUR
  • Preparation of Summary tabulation for PSUR
  • Preparation of special situation cases write up for PSUR Interpret trends and emerging signals across datasets to assess and update the product’s benefit-risk balance
  • Work in Pharmacovigilance projects as assigned such as collation of response to assessment reports received from the agency
  • Perform Evaluation of Safety Notifications to qualify Emerging Safety Issues (ESIs) / Significant Safety Issues (SSIs)
  • Review Clinical Trial Protocols for NCEs or Innovator Products from PV point of view
  • Review Safety Management Plans.

Educational Qualification

  • MBBS or MD

Experience

  • Tenure: 3 to 5 years Proficient in causality assessment, MedDRA coding, and understanding regulatory document requirements, including DSUR, PSUR/PBRER, PADER, RMP, SMP, Clinical Study Protocols of New Chemical Entities (NCEs) or Innovator Products.

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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