Pharmacovigilance Analyst with French and Dutch

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

We are thrilled to announce an exciting opportunity for a Pharmacovigilance Analyst with French and Dutch to join our Belgium office, supporting pharmacovigilance activities within the France Benelux cluster.

Role Overview

As the Local Contact Person for Pharmacovigilance for Belgium, the Netherlands, and Luxembourg, you will collaborate closely with the Global Patient Safety team to maintain an efficient local Pharmacovigilance (PV) system. This system must align with European and national regulations, as well as Baxter procedures. This role presents an outstanding opportunity to contribute to a world-class team and make a significant impact on patient safety.

What you'll do :

• Management of Local PV Cases: Collect, document, and follow up on PV cases in accordance with established procedures to ensure efficient management and regulatory compliance.

• PV Quality Activities: Conduct reconciliations, quality control (QC), and deviation management/CAPA processes, supervise critical metrics, and participate in quality reviews to ensure the PV system's efficiency and maintain outstanding standards.

• Preparation and Participation in Audits/Inspections: Prepare for and participate in internal and external audits/inspections, ensuring all documentation and processes are audit-ready and aligned with regulatory standards, and collaborate with cross-functional teams to address findings and implement corrective actions.

• Participation in the implementation of SDEA/PV Agreements: Support the establishment, maintenance, and seamless integration of Safety Data Exchange Agreements (SDEAs) and Pharmacovigilance (PV) Agreements, ensuring compliance with regulatory standards.

• Support of France PV Team: Assist the France PV team with daily tasks and projects to ensure smooth operations and collaborative compliance throughout the France Benelux Cluster, fostering collaboration and knowledge sharing for flawless execution of PV activities.

What you'll bring :

• Degree or equivalent experience in Medicine or Pharmacy, or a Master's degree or equivalent experience in Sciences (biology) to provide a strong foundation in healthcare and scientific principles.

• Outstanding communication skills in English, Dutch, and French to ensure effective documentation and teamwork in a multilingual environment.

• Proven ability to manage PV cases strictly in compliance with regulatory requirements.

• Strong analytical skills for monitoring critical metrics and implementing effective quality control measures.

• Additional certifications or training in Pharmacovigilance or related fields are advantageous.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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