Abbott Pharmacovigilance Hiring PV Specialist

Abbott Hiring PV Compliance Specialist – Pharmacovigilance & Drug Safety Job in Mumbai

Abbott is currently hiring for the position of PV Compliance Specialist in the Research & Development division. The role is based in Mumbai, India and offers an excellent opportunity for professionals interested in pharmacovigilance, drug safety compliance, and regulatory monitoring within the pharmaceutical industry.

This role supports the global pharmacovigilance (PV) compliance monitoring system and focuses on tracking safety metrics, managing corrective and preventive actions (CAPA), and ensuring adherence to global drug safety regulations. Professionals working in this position contribute directly to patient safety by ensuring that pharmacovigilance systems operate according to regulatory requirements and international safety standards.

The PV Compliance Specialist works closely with global pharmacovigilance teams, regulatory professionals, and quality management groups to monitor compliance indicators, analyze safety reporting metrics, and ensure that pharmacovigilance processes align with industry regulations.

For candidates seeking careers in drug safety, pharmacovigilance operations, compliance monitoring, or pharmaceutical quality systems, this opportunity provides strong exposure to global safety surveillance systems and regulatory frameworks.

Company Overview

Abbott is a globally recognized healthcare company focused on developing innovative medicines, diagnostic technologies, nutrition products, and medical devices. With a presence in more than 160 countries, Abbott plays a major role in advancing healthcare through research, technology, and scientific innovation.

The company’s research and development teams work continuously to improve patient outcomes through the development of safe and effective healthcare solutions. Abbott’s pharmacovigilance and drug safety programs are designed to ensure that medicines and medical devices meet strict regulatory standards and maintain the highest levels of patient safety.

Abbott invests heavily in regulatory science, clinical development, safety monitoring, and compliance management. Employees working in pharmacovigilance and regulatory roles contribute to global healthcare safety systems that monitor adverse events, evaluate risk signals, and support regulatory reporting requirements.

Professionals joining Abbott gain exposure to international pharmaceutical regulations, safety surveillance systems, and global quality standards used in modern drug development and post‑marketing safety monitoring.

Job Role and Responsibilities

The PV Compliance Specialist will support the pharmacovigilance compliance monitoring framework and ensure that safety processes meet internal quality standards and regulatory requirements.

Key responsibilities include:

• Collecting compliance data from global pharmacovigilance teams and medical device vigilance systems within agreed timelines
• Maintaining and enhancing pharmacovigilance compliance tracking systems and databases
• Supporting development of monitoring tools with assistance from internal IT teams
• Compiling key pharmacovigilance metrics and preparing compliance monitoring reports
• Drafting Key Performance Indicator (KPI) reports and pharmacovigilance compliance summaries
• Requesting non‑compliance details and corrective actions from responsible teams when required
• Reviewing corrective and preventive action (CAPA) records and ensuring timely follow‑up on quality issues
• Monitoring trends related to compliance deviations and identifying root causes of recurring issues
• Initiating investigations into pharmacovigilance compliance deviations and documenting findings
• Proposing corrective solutions according to established pharmacovigilance processes
• Coordinating with relevant stakeholders to ensure PV compliance indicators are monitored effectively
• Supporting training programs for staff on pharmacovigilance compliance processes and CAPA management systems
• Escalating significant compliance issues to the Head of PV System & Compliance or Qualified Person for Pharmacovigilance (QPPV) when required

This role plays an important part in maintaining regulatory compliance within pharmacovigilance systems and ensuring that drug safety monitoring activities remain consistent with global healthcare regulations.

Eligibility and Qualifications

Candidates applying for this pharmacovigilance and drug safety role should meet the following educational and professional requirements.

Required Education

A bachelor’s or master’s degree in life sciences, pharmacy, or healthcare-related disciplines.

Relevant courses include:

Pharmacy, Pharmacology, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Toxicology, Public Health

Experience

Experience in pharmacovigilance operations, drug safety monitoring, regulatory compliance, or quality management systems is preferred.

Candidates with exposure to pharmacovigilance compliance systems, CAPA processes, or safety reporting frameworks will have an advantage.

Required Skills

• Knowledge of pharmacovigilance systems and drug safety regulations
• Understanding of CAPA processes and compliance monitoring frameworks
• Ability to analyze safety metrics and regulatory compliance data
• Strong attention to detail and documentation accuracy
• Ability to manage compliance tracking databases and reporting tools
• Effective communication and collaboration skills
• Ability to work with cross‑functional regulatory and safety teams

Professionals with experience in pharmacovigilance auditing, safety surveillance systems, and regulatory reporting environments are well suited for this role.

Location and Salary

Job Location: Mumbai, India

The position operates within Abbott’s Research & Development and pharmacovigilance compliance environment.

Salary details for this position have not been publicly disclosed by the company. Compensation typically varies depending on candidate experience in pharmacovigilance operations, regulatory compliance management, and pharmaceutical safety monitoring.

Application Process

Candidates interested in this pharmacovigilance job opportunity can apply through the official Abbott careers portal.

Apply here:

https://www.jobs.abbott/us/en/job/ABLAUS31141459ENUSEXTERNAL/PV-Compliance-Specialist

Applicants should apply only through the official company website to ensure authenticity and avoid recruitment scams.

Frequently Asked Questions

What does a PV Compliance Specialist do?

A PV Compliance Specialist monitors pharmacovigilance compliance systems, tracks safety reporting metrics, reviews CAPA processes, and ensures drug safety activities follow regulatory guidelines.

What qualifications are required for this role?

Candidates typically require a degree in life sciences, pharmacy, pharmacology, biotechnology, or related healthcare fields.

Is pharmacovigilance experience required?

Experience in pharmacovigilance operations, drug safety monitoring, or compliance management is generally preferred for this role.

What skills are important for pharmacovigilance compliance roles?

Key skills include regulatory knowledge, compliance monitoring, CAPA management, data analysis, documentation accuracy, and collaboration with safety and regulatory teams.

How can I apply for this job?

Candidates can apply through the official Abbott careers website using the application link provided above.

Job Summary

Company	Abbott
Vacancies	PV Compliance Specialist
Required Education	Pharmacy, Pharmacology, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Toxicology, Public Health
Experience	Pharmacovigilance, drug safety, or regulatory compliance experience preferred

Tagged as: Pharma Jobs in Mumbai