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Pharmacovigilance Specialist - 1 year FTC

Req # JR - 176378 Location Reading, England, United Kingdom Job Category Patient Safety Date posted 06/16/2025
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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.

The Pharmacovigilance Specialist for the UK and Ireland, Malta is responsible for: in collaboration with the Pharmacovigilance Manager, to maintain an efficient local Pharmacovigilance system in the UK and Ireland meeting the European and national regulations and in compliance with the Baxter Pharmacovigilance procedures. To ensure appropriate contacts with the other organisations not limited to country Regulatory Affairs, Country Quality Assurance, Quality Assurance, Business Units and with HCP and Competent authorities (HPRA and MHRA).

To work closely with the PV Nordic colleagues based in Nordic according to the cluster model and provide back-up activities as needed.

This is a one year fixed term contract to be office based 3 days per week in Reading, Berkshire.

Essential Duties and Responsibilities:

The PV Specialist is accountable and responsible for the following activities:

  • Local PV system
  • ADR Reporting
  • Clinical trials activities
  • Agreements with third parties
  • Training
  • PSP/MRPs
  • Regulatory intelligence
  • Audits and inspections
  • Compliance
  • Other local PV activities
  • Activities related to associated countries in the cluster

Qualifications:

  • Knowledge or skills gained through a combination of academic study, job experience is required, e.g.: ability to communicate efficiently verbally and in writing in English
  • Structured and organised approach to work
  • Ability to write and discuss medical documentation.
  • Ability to use computerised applications and systems and especially Global PV Database.
  • Ability to liaise with the different functions i.e., Global Pharmacovigilance, Regulatory Affairs, Country Quality Assurance, businesses, Legal Affairs.

What are some of the benefits of working at Baxter?

  • Competitive total compensation package
  • Professional development opportunities
  • High importance placed on work life balance
  • Commitment to growing and developing an inclusive and diverse workforce

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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.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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Address

Explore this location Spur A - 2nd Floor, Reading International Business Park
Basingstoke Road
Reading
West Berkshire
RG2 6DH
United Kingdom
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