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You will be updated with latest job alerts via emailThe 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.
The PV Compliance coordinator will play a key role in maintaining documentation ensuring data integrity and supporting cross-functional collaboration.
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 teams 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.
Academic degree in sciences;pharmacy or nursing preferred
Some experiencein Pharmacovigilance Quality or Regulatory activities within thePharma/Life Sciences industry
Fluent inEnglish(written and spoken); proficiency in other languages is an asset
Proficient inMicrosoft Office withstrong Excel skills
Self-motivated with the ability toprioritize schedule and organizedaily activities
Excellent communication skills: ability to communicate across organization levels and to connect with different audiences in a multicultural environment
Ability toset priorities and pivotas needed in a dynamic environment
Demonstratesreliability flexibility and willingness totravel occasionally
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 youd expect from an organization with global strength and scale and youll be surrounded by career opportunities in a culture that fosters care collaboration and support.
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Relocation Assistance Provided: No
Required Experience:
IC
Full-Time