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Quality And Training Specialist-Pharmacovigilance (Pv)

Thermo Fisher Scientific
7+ years
INR 14 LPA – 24 LPA
Remote, India, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. 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

Quality and Training Specialist – Pharmacovigilance (PV)

Location: Remote, India
Job ID: R-01353358
Job Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote

About the Role

The Quality and Training Specialist (QTS) plays a critical role in ensuring Pharmacovigilance (PV) project teams are equipped with the necessary skills, training, and quality oversight to maintain high performance and regulatory compliance standards. This role focuses on training delivery, quality review, audit readiness, procedural document management, and continuous process improvement across PV operations.

Key Responsibilities

Training & Development

  • Design and deliver training programs for PV project teams, including onboarding and refresher training.

  • Assess training effectiveness and identify areas for continuous improvement.

  • Mentor and coach team members on PV processes, compliance requirements, and best practices.

Quality Management

  • Conduct real-time quality reviews of PV deliverables.

  • Perform trend analysis, gap assessments, and identify areas requiring corrective actions.

  • Implement corrective and preventive actions (CAPA) through targeted training and process enhancements.

Compliance & Documentation

  • Develop, maintain, review, and update:

    • Standard Operating Procedures (SOPs)

    • Work Instructions (WIs)

    • Project-specific guidelines

    • Client procedural documents

    • Training plans and compliance materials

  • Ensure consistency and adherence to regulatory and company requirements.

Audit & Inspection Support

  • Ensure ongoing readiness for internal and external audits and inspections.

  • Support audit preparation, inspection management, and follow-up activities.

  • Assist in developing responses to audit findings and regulatory observations.

PV Compliance & Metrics

  • Support the development and reporting of Pharmacovigilance compliance metrics.

  • Monitor compliance with Good Pharmacovigilance Practices (GPV).

  • Identify compliance risks and recommend mitigation strategies.

Process Improvement

  • Lead quality-related escalations and process improvement initiatives.

  • Collaborate with cross-functional teams, CROs, and vendors to improve operational efficiency.

  • Incorporate industry best practices into PV quality and training frameworks.

Stakeholder Management

  • Serve as the primary point of contact for PV quality assurance matters.

  • Present quality trends, compliance issues, and recommendations to internal stakeholders and clients.

  • Build strong partnerships across project teams and external collaborators.

Required Qualifications

Education

  • Bachelor’s or Master’s Degree in Pharmacy, Life Sciences, or a related field.

Experience

  • Minimum 7+ years of Pharmacovigilance (PV) experience.

  • Minimum 5+ years of experience in PV Quality roles supporting:

    • Audits and inspections

    • GPV compliance activities

    • Quality management systems

  • Experience developing quality systems and implementing process improvements.

  • Experience managing risk-based Pharmacovigilance audit programs.

Knowledge, Skills & Abilities

Regulatory Knowledge

  • Strong understanding of global Pharmacovigilance regulations and guidelines, including:

    • FDA

    • ICH

    • CDSCO-PvPI

    • EU GVP

    • PMDA (preferred)

Quality & Compliance Expertise

  • Expertise in audit and inspection management.

  • Advanced knowledge of:

    • Quality Management Systems (QMS)

    • Quality governance frameworks

    • Process improvement methodologies

Technical & Functional Skills

  • Experience with electronic systems used in regulated environments, including:

    • Drug Safety Systems

    • Learning Management Systems (LMS)

    • Documentation Management Systems

Professional Skills

  • Strong communication and presentation skills.

  • Excellent stakeholder and client management abilities.

  • Ability to manage multiple projects and training initiatives simultaneously.

  • Strong analytical and problem-solving skills.