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Cipla Hiring Senior Team Member PV Operations

Cipla Hiring Senior Team Member PV Operations in Vikhroli for MBBS pharmacovigilance professionals. Apply online for drug safety career growth.

Cipla Ltd. has announced a new opening for the role of Senior Team Member – PV Operations at its Vikhroli location in Maharashtra. This opportunity is ideal for MBBS professionals with prior experience in pharmacovigilance and drug safety operations. Candidates with expertise in medical review, case processing, and signal detection will find this role highly relevant for career growth in global pharmacovigilance.

The position offers hands-on involvement in regulatory safety processes, aggregate report evaluation, and global pharmacovigilance compliance, making it suitable for medical professionals aiming to build long-term careers in drug safety. Cipla Hiring Senior Team Member PV Operations


Company Overview

Cipla Ltd. is one of India’s leading pharmaceutical companies with a strong global presence across regulated and emerging markets. Known for its commitment to affordable and high-quality medicines, Cipla has established robust pharmacovigilance systems to ensure patient safety worldwide. The company’s drug safety division plays a critical role in maintaining regulatory compliance and monitoring product safety across therapeutic areas.

Working with Cipla offers exposure to global pharmacovigilance frameworks and collaboration with international regulatory bodies. Cipla Hiring Senior Team Member PV Operations


Job Location & Employment Type

  • Location: Vikhroli, Maharashtra, India
  • Job Type: Full-Time
  • Application Mode: Online Application

Open Position Details

  • Job Title: Senior Team Member – PV Operations
  • Company: Cipla Ltd.
  • Experience Level: 2–3 Years
  • Domain: Pharmacovigilance / Drug Safety

This role is designed for experienced medical reviewers involved in global pharmacovigilance processes. Cipla Hiring Senior Team Member PV Operations

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Key Roles & Responsibilities

Case Processing & Medical Review

  • Perform medical review of Individual Case Safety Reports (ICSRs)
  • Evaluate seriousness and listedness for case triage
  • Provide medical input aligned with global regulatory requirements
  • Conduct post-processing quality checks within SOP timelines
  • Offer guidance on MedDRA coding practices
  • Serve as a point of contact for pharmacovigilance queries

Aggregate Reports & Safety Surveillance

  • Conduct medical review of key pharmacovigilance documents such as:
    • PSUR
    • PBRER
    • PADER
    • Risk Management Plans (RMP)
    • Safety Summary Reports
  • Ensure clinical consistency across aggregate safety reports
  • Support regulatory inspections and audit readiness

Signal Detection & Regulatory Intelligence

  • Participate in signal detection and validation activities
  • Review safety signals and trend analyses
  • Contribute to Drug Safety Review Committee discussions
  • Evaluate responses prepared for health authority queries
  • Monitor regulatory intelligence updates impacting safety operations

Cipla Hiring Senior Team Member PV Operations


Health Hazard Evaluation

  • Perform medical assessment of product quality complaints
  • Conduct patient safety risk evaluations
  • Support internal safety risk management processes

Cipla Hiring Senior Team Member PV Operations


Training & QPPV Support

  • Deliver pharmacovigilance training to internal teams and partners
  • Provide updates and training on MedDRA changes
  • Assist in QPPV-related responsibilities for assigned regions
  • Coordinate with cross-functional stakeholders including safety, labeling, and medical writing teams

Eligibility Criteria

Education

  • Mandatory Qualification: MBBS

Due to the medical nature of the role, only qualified medical graduates are eligible.


Experience

  • 2–3 years of experience as a Medical Reviewer in pharmacovigilance
  • Hands-on exposure to drug safety case processing required

Preferred Experience:

  • Aggregate report review (PSUR, PBRER, RMP)
  • Signal detection and safety surveillance
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Skills Required

Candidates should demonstrate:

  • Strong understanding of pharmacovigilance workflows
  • Experience in medical review and safety evaluation
  • Knowledge of MedDRA coding and safety databases
  • Familiarity with global PV regulations
  • Ability to perform causality assessment and signal evaluation
  • Strong documentation and analytical skills
  • Excellent stakeholder communication abilities

Salary & Benefits

  • Salary: As per company norms
  • Exposure to global pharmacovigilance compliance systems
  • Opportunity to work on regulatory audits and inspections
  • Involvement in signal detection and safety strategy
  • Strong career growth in drug safety and medical affairs

Cipla Hiring Senior Team Member PV Operations


Selection Process

The hiring process typically includes:

  1. Resume shortlisting based on pharmacovigilance experience
  2. Technical interview focusing on medical review expertise
  3. Final interaction with pharmacovigilance leadership

The process may vary depending on internal recruitment policies.


How to Apply

Interested candidates should apply through Cipla’s official careers portal using the online application link available on the job listing.

Before applying, ensure your resume clearly highlights:

  • MBBS qualification
  • Pharmacovigilance experience
  • Case processing exposure
  • Aggregate report involvement (if applicable)
  • Signal detection experience

A well-structured PV-focused resume will improve your chances of shortlisting.

Apply Here


Important Dates

Candidates are encouraged to apply early due to strong demand for pharmacovigilance roles at leading pharma companies.


Why Apply for This Pharma Job?

Pharmacovigilance continues to be one of the fastest-growing domains in the pharmaceutical industry due to increasing regulatory scrutiny and focus on patient safety. A role at Cipla offers exposure to large-scale global safety systems and real-world regulatory challenges.

This position provides a unique opportunity to work on end-to-end drug safety activities including case review, signal detection, and aggregate safety reporting. Exposure to regulatory inspections and global safety frameworks can significantly strengthen long-term career prospects in pharmacovigilance leadership, risk management, and regulatory safety strategy.

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Additionally, working with an established organization like Cipla enhances professional credibility and opens doors to future roles in multinational pharmaceutical environments. Cipla Hiring Senior Team Member PV Operations


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform that publishes verified pharmaceutical and healthcare job updates for informational purposes only. We are not affiliated with Cipla Ltd. and do not participate in the hiring process. Applicants should verify all details through official company sources before applying. Cipla Hiring Senior Team Member PV Operations


Final Words

If you are an MBBS professional with pharmacovigilance experience and looking to advance in global drug safety operations, this Cipla opportunity is worth considering. The role offers strong exposure to medical review, regulatory compliance, and signal detection activities within a reputed pharmaceutical organization.

Eligible candidates should prepare a detailed pharmacovigilance resume and apply online at the earliest to secure their chance. Cipla Hiring Senior Team Member PV Operations


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