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Senior Manager, Process Compliance Review And Analysis

Fortrea
10+ years
INR 25-40 LPA
Pune, India
10 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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, MedDRA Coding, Medical Billing

Key Responsibilities

Quality Management & Compliance

  • Design and implement quality processes across assigned PV and Safety Writing projects.

  • Ensure compliance with client requirements, regulatory guidelines, and internal SOPs.

  • Maintain Quality Management Plans and Quality Agreements.

  • Monitor project quality metrics and compliance indicators.


CAPA Management

  • Lead Corrective and Preventive Action (CAPA) activities.

  • Track CAPA effectiveness and closure.

  • Analyze recurring quality issues and implement preventive actions.

  • Drive root cause analysis and risk mitigation initiatives.


Audit & Inspection Readiness

  • Maintain continuous audit and inspection readiness.

  • Support sponsor audits, internal audits, and regulatory inspections.

  • Manage responses to audit findings and observations.

  • Ensure timely completion of inspection requests. 


Process Excellence & Continuous Improvement

  • Lead process improvement initiatives across projects.

  • Implement Lean and Six Sigma methodologies.

  • Conduct quality trend analysis and performance reviews.

  • Recommend operational improvements and efficiency enhancements.


Safety Writing Quality Oversight

  • Review quality aspects of aggregate safety reports.

  • Ensure consistency with global regulatory requirements.

  • Support development and quality review of:

    • PSUR/PBRER

    • DSUR

    • RMP

    • Signal Reports

    • Safety Narratives

    • Clinical Safety Summaries


Regulatory Compliance

  • Provide guidance on:

    • Good Pharmacovigilance Practices (GVP)

    • FDA Regulations

    • EMA Requirements

    • ICH Guidelines

    • Global Safety Reporting Standards

  • Monitor regulatory updates and communicate impacts to project teams.


Training & Capability Development

  • Identify training needs based on quality review findings.

  • Develop and review training materials.

  • Conduct quality and compliance training sessions.

  • Mentor project teams on quality standards and best practices.


Client & Stakeholder Management

  • Act as Quality SME for clients.

  • Support client meetings, audits, and inspections.

  • Provide quality governance oversight.

  • Participate in quality review boards and governance meetings.


Business Support

  • Contribute to:

    • RFP Responses

    • Client Proposals

    • Business Development Initiatives

    • Process Framework Development

    • New Service Offerings


Technical Skills Required

Pharmacovigilance Expertise

  • Single Case Processing

  • Medical Review

  • Aggregate Reporting

  • Signal Detection

  • Risk Management Plans (RMP)

  • Safety Writing

  • Benefit-Risk Evaluation


Quality & Compliance

  • CAPA Management

  • Root Cause Analysis

  • Audit Management

  • Inspection Readiness

  • Quality Metrics

  • Quality Risk Management


Regulatory Knowledge

  • ICH Guidelines

  • EU GVP Modules

  • FDA Pharmacovigilance Requirements

  • EMA Regulations

  • Global Safety Reporting Requirements


Systems Knowledge

  • Argus Safety

  • ARISg

  • Veeva Vault

  • TrackWise

  • Quality Management Systems (QMS)

  • Computer System Validation (CSV)


Core Competencies

  • Pharmacovigilance Quality Management

  • Regulatory Compliance

  • Audit & Inspection Management

  • CAPA Leadership

  • Risk Assessment

  • Stakeholder Management

  • Client Relationship Management

  • Process Excellence

  • Lean Six Sigma

  • Strategic Thinking

  • Leadership & Mentoring


Preferred Candidate Profile

Candidates currently working as:

  • PV Quality Manager

  • Senior PV Manager

  • Drug Safety Manager

  • PV Compliance Lead

  • Safety Writing Lead

  • Quality Assurance Manager (PV)

  • PV Operations Lead

  • Associate Director Pharmacovigilance

would be strong fits for this role.