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Senior Manager, Process Compliance Review And Analysis

Fortrea
10+ years
INR 22 LPA – 32 LPA
Pune, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

Senior Manager, Process Compliance Review and Analysis

Location: Pune
Employment Type: Full Time


Job Overview

The Senior Manager, Process Compliance Review and Analysis is responsible for leading quality, compliance, and process excellence initiatives across Pharmacovigilance (PV) and Safety Writing engagements. The role focuses on driving quality culture, audit readiness, CAPA management, regulatory compliance, process standardization, and continuous improvement while supporting clients and internal stakeholders.


Summary of Responsibilities

Quality Leadership & Compliance Management

  • Establish and implement quality processes across assigned Pharmacovigilance and Safety Writing engagements.

  • Assume accountability for quality, compliance, and CAPA-related deliverables across assigned projects.

  • Drive a culture of quality and compliance across multiple client engagements.

  • Ensure implementation and adherence to Quality Management Plans (QMPs) and Quality Agreements.

  • Act as the primary quality and process expert for assigned clients and project teams.

  • Function as the key point of contact for regulatory updates, quality assurance concepts, applicable procedures, and best practices.

CAPA Management & Audit Readiness

  • Lead CAPA management activities across projects and ensure timely closure of quality findings.

  • Identify quality trends and implement corrective and preventive actions.

  • Establish feedback mechanisms and monitor implementation effectiveness.

  • Maintain organization-wide inspection and audit readiness.

  • Support internal audits, client audits, regulatory inspections, and system audits.

  • Ensure timely and accurate responses to audit findings and inspection requests.

Process Excellence & Continuous Improvement

  • Drive process improvement initiatives and implement best practices across projects.

  • Support process standardization and operational excellence initiatives within the practice.

  • Perform detailed analysis of quality metrics and operational data.

  • Identify opportunities for efficiency improvements and recommend strategic solutions.

  • Review trend analyses and drive implementation of process improvement actions.

  • Develop and enhance quality frameworks, methodologies, and governance models.

Quality Oversight & Project Support

  • Oversee all quality review activities, quality metrics, trend analysis, outcomes, and corrective actions.

  • Conduct and oversee process reviews to ensure compliance with regulatory and client requirements.

  • Work closely with Delivery Heads and Subject Matter Experts (SMEs) to develop:

    • Quality Management Plans

    • Quality Agreements

    • Training Plans

    • Quality Service Level Agreements (SLAs)

  • Monitor quality performance indicators across assigned projects.

  • Support Computer System Validation (CSV) activities where applicable.

Documentation & Regulatory Support

  • Develop and review:

    • Pharmacovigilance SOPs

    • Work Instructions (WIs)

    • Quality Procedures

    • Client-specific Process Documents

  • Assess client conventions and ensure alignment with regulatory requirements.

  • Support clients during regulatory inspections and audits.

  • Ensure compliance with:

    • Good Pharmacovigilance Practices (GVP)

    • FDA Guidelines

    • EU Regulatory Requirements

    • Industry Standards

Training & People Development

  • Identify training needs based on quality review findings and audit observations.

  • Support development and maintenance of training materials and training plans.

  • Conduct training sessions and knowledge-sharing initiatives.

  • Mentor project teams on quality and compliance requirements.

  • Promote awareness of quality standards and best practices across the organization.

Business Support & Strategic Initiatives

  • Support practice leadership in developing new service offerings and process frameworks.

  • Contribute to:

    • Request for Proposal (RFP) Responses

    • Client Proposals

    • Business Presentations

    • Client Meetings

  • Assist in developing customized solutions to meet client requirements.

  • Support strategic growth initiatives within the Pharmacovigilance practice.

  • Perform additional duties as assigned.


Qualifications (Minimum Required)

  • Bachelor's, Master's, or PhD Degree in:

    • Medicine

    • Alternative Medicine

    • Medical Sciences

    • Pharmaceutical Sciences

    • Nursing

    • Life Sciences

    • Related Healthcare Disciplines

  • Equivalent experience may be considered in lieu of formal educational qualifications.


Experience (Minimum Required)

  • Minimum 10 years of experience within:

    • Pharmaceutical Industry

    • Biotechnology Industry

    • CRO Industry

  • Significant experience in:

    • Pharmacovigilance

    • Safety Writing

    • Quality Management

    • Compliance Management

    • Process Excellence

  • Proven experience leading quality initiatives across multiple safety and pharmacovigilance projects.

  • Strong knowledge of:

    • Good Pharmacovigilance Practices (GVP)

    • FDA Regulations

    • EU Pharmacovigilance Guidelines

    • Global Drug Safety Regulations

  • In-depth understanding of:

    • Single Case Processing

    • Case Assessment

    • Safety Writing

    • Quality Management Systems

  • Knowledge of:

    • Lean Methodology

    • Six Sigma Concepts

    • Root Cause Analysis

    • Continuous Improvement Methodologies

  • Experience supporting:

    • Regulatory Inspections

    • Client Audits

    • Internal Audits

    • Inspection Readiness Programs

  • Technical proficiency in Microsoft Office applications.

  • Understanding of Computer System Validation (CSV).


Preferred Qualifications

  • Experience assessing safety reports from:

    • Medical Perspective

    • Scientific Perspective

    • Documentation Quality Perspective

  • Experience in:

    • Trend Analysis

    • Quality Metrics Development

    • Gap Assessments

    • Training Needs Analysis

  • Experience managing global Pharmacovigilance Quality programs.

  • Six Sigma Certification or Process Excellence Certification preferred.