PPD Pharmacovigilance Quality Specialist Jobs

Exciting PPD Pharmacovigilance Quality Jobs 2026 | Remote PV Specialist

PPD, part of Thermo Fisher Scientific, is hiring a Quality and Training Specialist – Pharmacovigilance (PV) for a fully remote position in India. This opportunity is ideal for experienced pharmacovigilance professionals with expertise in PV quality systems, audits, inspections, GPV compliance, and training management.

Professionals with strong backgrounds in drug safety, quality assurance, pharmacovigilance operations, regulatory compliance, and quality management systems can take the next step in their careers with one of the world’s leading clinical research organizations.

About PPD – Thermo Fisher Scientific

PPD®, a Thermo Fisher Scientific company, is a leading global Contract Research Organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to patients worldwide.

The organization provides clinical development, pharmacovigilance, regulatory affairs, and clinical research services while maintaining the highest standards of quality, compliance, and patient safety.

Position Details

Job Title: Quality and Training Specialist – Pharmacovigilance (PV)

Job ID: R-01353358

Location: Remote, India

Job Type: Full-Time

Category: Clinical Research / Pharmacovigilance

Work Schedule: Monday to Friday

Work Model: Fully Remote

Key Responsibilities

As a Quality and Training Specialist, you will support pharmacovigilance quality oversight, compliance management, training programs, and process improvement initiatives.

Pharmacovigilance Quality Management

• Perform real-time quality review of PV deliverables.
• Conduct quality trend analysis and gap assessments.
• Support corrective and preventive action initiatives.
• Monitor adherence to Good Pharmacovigilance Practices (GPV).

Training & Development

• Design and deliver onboarding training programs.
• Conduct refresher and compliance training sessions.
• Develop project-specific training materials.
• Mentor and coach PV team members.

Audit & Inspection Support

• Prepare teams for internal and external audits.
• Support regulatory inspections and follow-up activities.
• Develop audit responses and remediation plans.
• Ensure continuous inspection readiness.

Documentation & Compliance

• Review and maintain SOPs and work instructions.
• Update project-specific guidelines and procedural documents.
• Develop compliance reports and quality metrics.
• Ensure documentation consistency and regulatory compliance.

Stakeholder Management

• Act as the primary contact for PV quality matters.
• Collaborate with cross-functional teams, vendors, and CRO partners.
• Present quality trends and recommendations to stakeholders.
• Lead process improvement initiatives across projects.

Eligibility Criteria

Educational Qualification

Candidates must possess:

• B.Pharm
• M.Pharm
• B.Sc Life Sciences
• M.Sc Life Sciences
• Pharm.D
• Biotechnology
• Microbiology
• Biochemistry
• Or related Life Sciences qualification

Experience Required

• Minimum 7 years of Pharmacovigilance experience.
• Minimum 5 years of PV Quality experience.
• Experience supporting audits and inspections.
• Experience with GPV compliance activities.
• Experience managing quality systems and process improvements.

Required Skills

Pharmacovigilance Expertise

• Pharmacovigilance Operations
• Drug Safety
• PV Compliance
• Case Processing Oversight
• Safety Reporting
• Risk Management

Regulatory Knowledge

• FDA Regulations
• ICH Guidelines
• EU GVP
• CDSCO-PvPI Regulations
• Good Pharmacovigilance Practice (GPV)
• PMDA Knowledge (Preferred)

Quality & Compliance Skills

• Quality Management Systems (QMS)
• CAPA Management
• Audit Readiness
• Inspection Management
• Process Improvement
• Compliance Monitoring

Technical Skills

• Learning Management Systems (LMS)
• Drug Safety Databases
• Documentation Management Systems
• Electronic Quality Systems

Why Join PPD?

• Fully remote work opportunity.
• Global exposure in pharmacovigilance quality operations.
• Opportunity to work with international clients and regulatory agencies.
• Career growth within Thermo Fisher Scientific.
• Exposure to audits, inspections, compliance governance, and training leadership.
• Collaborative and quality-focused work environment.

Salary Information

Based on current industry benchmarks, professionals with 7–12 years of PV quality experience may expect a competitive compensation package depending on experience, expertise, and project responsibilities.

How to Apply

Interested candidates can apply through the official Thermo Fisher Scientific careers portal:

https://jobs.thermofisher.com/global/en/job/R-01353358

Applicants should highlight pharmacovigilance quality experience, audit readiness activities, GPV compliance expertise, training management experience, and regulatory knowledge in their resumes.

Frequently Asked Questions (FAQs)

1. Is this a remote job?

Yes. This is a fully remote position based in India.

2. What experience is required?

Candidates should have at least 7 years of Pharmacovigilance experience and 5 years in PV quality roles.

3. Is audit experience mandatory?

Yes. Experience supporting audits, inspections, and GPV compliance activities is an important requirement.

4. Which qualifications are eligible?

B.Pharm, M.Pharm, Pharm.D, Biotechnology, Microbiology, Biochemistry, Life Sciences, and related disciplines.

5. Which regulatory guidelines should candidates know?

FDA, ICH, CDSCO-PvPI, EU GVP, and Good Pharmacovigilance Practices (GPV).

6. What are the primary responsibilities?

Quality oversight, training delivery, audit readiness, compliance management, SOP maintenance, and process improvement initiatives.

Job Overview

Category	Details
Company	PPD (Thermo Fisher Scientific)
Position	Quality and Training Specialist – Pharmacovigilance
Qualification	B.Pharm, M.Pharm, Pharm.D, Life Sciences
Experience	7+ Years PV Experience
Location	Remote, India
Job Type	Full-Time
Department	Pharmacovigilance Quality