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Meddra Specialist | Senior Process Compliance Review & Analysis

Fortrea
0-2 years
INR 8-12 LPA
Pune, India
10 June 16, 2026
Job Description
Job Type: Full Time, Hybrid Education: None Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, Medical Billing

Role Summary

Responsible for ensuring the quality, compliance, and regulatory accuracy of pharmacovigilance activities across clinical and post-marketing safety programs.

The role focuses on:

  • Quality review of safety cases and regulatory documents

  • CAPA management

  • Quality metrics and trend analysis

  • Audit and inspection readiness

  • Pharmacovigilance process improvement

  • Safety data management oversight


Key Responsibilities

Quality Review & Compliance

  • Perform quality reviews of safety cases and pharmacovigilance deliverables.

  • Review adverse event reports for accuracy, completeness, and regulatory compliance.

  • Identify quality trends and areas for improvement.

  • Support periodic client quality reviews and audits.

  • Ensure compliance with global pharmacovigilance regulations.


Safety Case Review

  • Review expedited adverse event reports.

  • Review product quality complaints.

  • Review medical information cases.

  • Assess safety reports from medical, scientific, and documentation perspectives.

  • Ensure submissions meet client and regulatory timelines.


Regulatory & Safety Documentation

Review and quality check:

  • Annual Reports

  • IND Reports

  • PSURs (Periodic Safety Update Reports)

  • PADERs

  • Clinical Study Reports (CSRs)

  • Core Data Sheets (CDS)

  • US Package Inserts (USPI)

  • Summary of Product Characteristics (SPC)

  • Medication Guides


CAPA Management

  • Draft Corrective and Preventive Actions (CAPAs).

  • Track CAPA implementation and closure.

  • Maintain supporting documentation.

  • Coordinate with project teams and stakeholders.


Quality Metrics & Trend Analysis

  • Generate quality metrics and dashboards.

  • Conduct trend analysis.

  • Identify recurring quality issues.

  • Recommend process improvement initiatives.


Training & Knowledge Management

  • Develop training schedules.

  • Create training materials.

  • Support onboarding of new hires.

  • Conduct quality awareness sessions.

  • Share best practices across projects.


Audit & Inspection Support

  • Support client audits and inspections.

  • Assist in audit readiness activities.

  • Draft sections of Quality Management Plans.

  • Support regulatory inspections.


Process Excellence

  • Participate in process reviews.

  • Drive continuous improvement initiatives.

  • Apply Lean methodology concepts.

  • Recommend efficiency and quality enhancements.


Medical Information & Call Review

  • Review medical information queries received via:

    • Telephone

    • Email

    • Fax

  • Review call documentation.

  • Review follow-up activities.

  • Guide safety associates handling voice calls.


Required Qualifications

Education

Bachelor's, Master's, PharmD, MD, PhD, BAMS, BHMS, BDS, Nursing, Life Sciences, Pharmacy, Medical Sciences, or related discipline.


Required Experience

Overall Experience

  • Minimum 4+ years

Relevant Experience

  • Pharmacovigilance

  • Drug Safety

  • Safety Writing

  • Case Processing

  • Quality Review

  • Peer Review

Mandatory

  • At least 1 year of Quality Review / Peer Review experience


Technical Skills

Pharmacovigilance

  • ICSR Processing

  • Case Assessment

  • Safety Review

  • Signal Detection Awareness

  • Regulatory Reporting

Regulatory Knowledge

  • GVP Guidelines

  • EU Pharmacovigilance Regulations

  • FDA Regulations

  • Global Safety Reporting Requirements

Systems & Tools

  • Microsoft Office Suite

  • Safety Databases

  • Quality Tracking Systems

Preferred

  • MedDRA Certification

  • CAPA Management

  • Quality Metrics Reporting

  • Trend Analysis

  • Lean Methodology


Leadership & Functional Skills

  • Quality Oversight

  • Stakeholder Management

  • Problem Solving

  • Analytical Thinking

  • Audit Readiness

  • Communication Skills

  • Training & Mentoring

  • Process Improvement