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Pv System Specialist

Abbott
Abbott
5-12 years
₹12 LPA – ₹22 LPA
Mumbai, India
10 March 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

PV System Specialist

Location: Mumbai, India
Category: Research & Development / Pharmacovigilance
Experience: 5 – 8 Years
Qualification: Bachelor’s or Master’s Degree in Life Sciences, Pharmacy, or related field
Approx Salary: ₹12 LPA – ₹22 LPA (depending on PV systems and compliance experience)


Job Overview

The PV System Specialist is responsible for ensuring the compliant rollout and management of pharmacovigilance (PV) training programs across global, regional, and local PV teams. The role focuses on maintaining PV training matrices, supporting documentation systems, and ensuring compliance with Good Pharmacovigilance Practices (GVP) and regulatory requirements. The specialist will work closely with cross-functional teams to maintain PV systems, training records, and documentation in electronic platforms.


Key Responsibilities

1. PV Training Management

  • Maintain and update PV training matrices for headquarters and affiliate PV staff.

  • Ensure PV training is effectively rolled out to all relevant employees across global and regional teams.

  • Assign training modules and track completion using the ISOtrain Learning Management System.

  • Communicate PV training requirements to non-PV employees across departments.

2. Documentation & System Administration

  • Establish and maintain PV procedures in the electronic Document Management System (eDMS).

  • Act as a Business Administrator for eDMS and support system users.

  • Assist with document authoring, editing, review, approval, and version control.

  • Manage document lifecycle processes including periodic reviews and archiving.

3. Pharmacovigilance Compliance

  • Ensure PV system processes align with Good Pharmacovigilance Practice (GVP) Module II requirements.

  • Support maintenance of the Pharmacovigilance System Master File (PSMF).

  • Review procedural changes and assess potential impact on PV processes.

4. Audit & Inspection Support

  • Assist in internal audits, third-party audits, and regulatory health authority inspections.

  • Track key performance indicators (KPIs) related to PV system compliance.

  • Prepare compliance reports for PV Compliance teams.

5. Collaboration & Projects

  • Coordinate with departments such as Clinical, Medical Affairs, and Regulatory Affairs.

  • Act as PV representative within the EPD Training Community.

  • Participate in PV system improvement projects and global training initiatives.

  • Manage GPV SharePoint coordination and documentation oversight.


Required Skills

Technical Skills

  • Pharmacovigilance systems and regulatory compliance

  • Good Pharmacovigilance Practices (GVP) knowledge

  • Learning Management Systems (ISOtrain)

  • Electronic Document Management Systems (eDMS)

  • PSMF maintenance and regulatory documentation

Soft Skills

  • Strong coordination and stakeholder management

  • Attention to detail and compliance focus

  • Effective communication and documentation skills

  • Ability to manage multiple processes and deadlines


Role Impact

This role plays a critical part in maintaining the pharmacovigilance system integrity and compliance, ensuring training, documentation, and PV processes align with international regulatory standards and support patient safety initiatives.