PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Ad

Pharmacovigilance Openings | 1 – 12 Years

Published on

Orcapod Consulting Services / 2COMS

B.Pharm, M.Pharm

Mumbai, Pune, Hyderabad, Bengaluru

1–12 Years, depending on role

Verified Job

Online Application
Ad

Professionals looking for Pharmacovigilance jobs in India have new opportunities in ICSR safety case processing. Orcapod Consulting Services and 2COMS are hiring experienced Pharmacovigilance professionals for SPE, SME, Senior Associate and Team Leader roles across Mumbai, Pune, Hyderabad and Bengaluru.

These openings are particularly relevant for candidates with hands-on experience in ICSR case processing, Veeva Safety, Oracle Argus Safety, narrative writing, medical coding, quality review and case closure. Depending on the position, experience requirements range from approximately 1 year to 12 years.

Pharmacovigilance Hiring 2026 – Overview

ParticularDetails
Job AreaPharmacovigilance / Drug Safety
RolesPV Associate, Senior Associate, SPE, SME, Team Leader
Employers/RecruitersOrcapod Consulting Services / 2COMS
Experience1–12 Years, depending on role
LocationsMumbai, Pune, Hyderabad, Bengaluru
EmploymentFull-Time
Work ModeWork From Office for specified Orcapod roles
Key DatabasesVeeva Safety, Oracle Argus Safety
Core FunctionICSR Safety Case Processing
EducationPharmacy, Life Sciences, Medical Sciences or equivalent

Available Pharmacovigilance Roles

Pharmacovigilance Associate / SPE

Candidates with approximately 1–2 years of Pharmacovigilance safety case processing experience can be considered for associate or SPE-level opportunities.

Candidates should have practical knowledge of ICSR processing and preferably hands-on exposure to Veeva Safety or Argus Safety.

Senior Pharmacovigilance Associate / SME

Professionals with 2+ years of Pharmacovigilance experience can explore Senior Associate and SME positions.

The role requires stronger knowledge of safety case processing and may involve ICSR quality review, regulatory compliance checks and case-processing quality standards.

Pharmacovigilance Team Leader

Experienced candidates can also apply for ICSR Case Processing Team Leader opportunities.

The 2COMS listing specifies 7–12 years of Pharmacovigilance safety case processing experience, with two years of documented Team Leader experience indicated for the TL position.

Key Responsibilities

Selected Pharmacovigilance professionals may be responsible for:

  • ICSR book-in and initial case processing
  • Full safety case data entry
  • ICSR narrative writing
  • Medical and product coding
  • Performing self-quality checks using QC tools
  • Case assessment and processing according to applicable procedures
  • Unblinding cases when required
  • Safety case routing
  • Case lock and closure
  • USPI labeling assessment where applicable
  • Reviewing ICSRs for completeness and quality
  • Ensuring compliance with applicable Pharmacovigilance requirements
  • Maintaining accurate and timely safety documentation

Senior professionals and SMEs may additionally perform ICSR quality review and ensure cases meet internal quality and regulatory standards.

Qualifications & Eligibility

Candidates should generally have a Graduate, Postgraduate or Doctorate qualification in Pharmacy, Life Sciences, Medical Sciences or an equivalent relevant discipline.

Relevant degrees may include:

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • B.Sc / M.Sc in relevant Life Sciences disciplines
  • Medical Sciences qualifications
  • Other equivalent life-science qualifications, subject to employer requirements

Candidates should carefully verify their individual eligibility against the specific position before applying.

Skills Required

The most important skills for these Pharmacovigilance ICSR jobs include:

ICSR Case Processing: Understanding of end-to-end Individual Case Safety Report processing.

Veeva Safety / Argus Safety: Hands-on experience with at least one major Pharmacovigilance safety database is highly relevant.

Narrative Writing: Ability to prepare clear and accurate safety case narratives.

Medical Coding: Familiarity with medical terminology and safety coding workflows, including MedDRA-related activities where applicable.

Quality Review: Senior candidates should understand ICSR QC and quality-review processes.

Case Closure: Knowledge of routing, workflow management, case lock and closure.

Communication: Strong written and verbal English communication skills are required.

Experience Required

The current openings cover multiple experience bands:

PositionIndicative Experience
PV Associate1–2 Years
SPE / SME1+ Years depending on position
Senior PV Associate2+ Years
Team Leader7–12 Years
TL Experience2 Years on-paper TL experience specified in the listing

Candidates should apply to the role matching their actual Pharmacovigilance experience rather than applying solely based on the broad experience range displayed by the job portal.

Job Locations

The Pharmacovigilance openings mention opportunities across:

Mumbai | Pune | Hyderabad | Bengaluru

The Orcapod Consulting Services listing specifies work-from-office arrangements and indicates shifts including 7:00 AM–4:00 PM and 4:00 PM–1:00 AM. Candidates should confirm the final location, shift and work arrangement directly with the recruiter during the hiring process.

Estimated Salary

The employers have not disclosed an official salary package in the provided listings.

For structured-data purposes, an estimated market range of approximately ₹3.5 lakh to ₹18 lakh per annum may cover the broad Associate-to-Team-Leader experience spectrum represented by these vacancies. This is an estimate only and not an employer-disclosed salary.

Actual compensation can vary substantially according to experience, designation, current CTC, location, safety-database expertise and interview performance.

Why These Pharmacovigilance Roles May Be Relevant

These opportunities provide exposure to core operational Pharmacovigilance activities such as ICSR processing, Argus Safety, Veeva Safety, medical coding, narrative writing, quality review and safety case lifecycle management.

They may be particularly relevant for professionals already working in drug safety operations who want to progress from case-processing positions toward SPE, SME, Quality Reviewer or Team Leader roles.

How to Apply

Application Link For SPE-Pharmacovigilance Orcapod Consulting Services

Application Link For ICSR case processing TL 2coms

Application Link For ICSR case processing SPE/SME 2Coms

Ad

Share This Job

✅ Copied!