Job Description Summary

We are seeking a detail-oriented and proactive Pharmacovigilance Coordinator to support the operational and compliance activities of our Pharmacovigilance Quality Team (PV-QA).
The PV/QA team serves as a strategic bridge between the Quality Assurance (QA) and Global Pharmacovigilance (PV) organizations, fostering a culture of compliance and continuous improvement. PV-QA are accountable for ensuring PV compliance with regulatory obligations and the GEHC PDx Quality Management System across the global PV network, through the following activities:
• Maintain and continually improve a suite of lean PV operating procedures that can be consistently applied across the organisation
• Design and implement supporting PV training and awareness initiatives
• Continuous monitoring of the effectiveness of the QMS through deviation management, audit outcome, KPI reporting, management review, and authority inspection support to drive strategic improvement.

Job Description

GE Healthcare is a leading global medical technology and digital solutions innovator with over 100 years of healthcare industry experience and around 50,000 employees globally.

We enable clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by our Edison intelligence platform. We operate at the center of an ecosystem working toward precision health -digitizing healthcare, helping drive productivity and improving outcomes for patients, providers, health systems and researchers around the world.

The PV Compliance coordinator will play a key role in maintaining documentation, ensuring data integrity, and supporting cross-functional collaboration.

This entry-level position offers a great foundation for individuals seeking to build a career in the pharmaceutical or life sciences industry, particularly in the areas of drug safety, quality assurance, and regulatory compliance. As part of a global team, the coordinator will gain hands-on experience with pharmacovigilance systems and global PV operations and will have access to a structured environment to develop core competencies in Good Vigilance Practices (GvP) and Quality Management Systems.

Key Responsibilities:

• PV Network Support: Assist in the onboarding and offboarding of PV Local Safety Units (LSUs). Maintain accurate and up-to-date records of contact details, regulatory requirements, and training documentation in the PV network database.
• Data Reconciliation: Perform regular reconciliation of safety information tracking logs to ensure timely and compliant submissions to the Central Safety Unit (CSU) and regulatory authorities.
• Cross-Functional Coordination: Collaborate with stakeholders across departments (e.g., Commercial, Medical Affairs) to reconcile data related to product complaints, medical inquiries, and other safety-relevant communications.
• Mailbox Management: Monitor and triage the team’s shared mailbox. Respond independently to routine queries and escalate complex issues to appropriate team members.
• Third-Party Compliance: Support adherence to PV obligations outlined in agreements with distributors, contractors, and collaborative partners.
• Compliance Monitoring: Identify instances of noncompliance and contribute to investigations and implementation of corrective and preventive action plans (CAPAs).
• Audit and Inspection Readiness: Provide administrative and logistical support during internal audits and external regulatory inspections.

Desired Characteristics:

• Self-motivated with the ability to prioritize, schedule, and organize daily activities
• Excellent communication skills: ability to communicate across organization levels and to connect with different audiences in a multicultural environment
• Ability to set priorities and pivot as needed in a dynamic environment
• Demonstrates reliability, flexibility, and willingness to travel occasionally

Required Qualifications:

• Academic degree in sciences; pharmacy or nursing preferred
• Minimum 1 year of experience in Pharmacovigilance, Quality, or Regulatory activities within the Pharma/Life Sciences industry
• Fluent in English (written and spoken); proficiency in other languages is an asset
• Proficient in Microsoft Office, with strong Excel skills

GE Healthcare  is an Equal Opportunity  Employer  where inclusion matters.  Employment  decisions  are  made  without regard  to race,  color, religion,  national or ethnic  origin, sex, sexual  orientation,  gender  identity  or expression,  age, disability,  protected  veteran  status  or other  characteristics protected  by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

#LI-AG1

Additional Information