At a Glance
- Tasks: Manage and assess veterinary pharmacovigilance cases while ensuring compliance and accuracy.
- Company: Leading multinational Animal Health client with a hybrid work model.
- Benefits: Gain valuable experience in Regulatory Affairs with a supportive team.
- Other info: Perfect for newly qualified graduates looking to grow in a collaborative environment.
- Why this job: Kickstart your career in a dynamic industry making a real difference for animal health.
- Qualifications: Degree in Veterinary Medicine and strong analytical skills required.
The predicted salary is between 25650 - 31350 £ per year.
PE Global is currently recruiting for a Regulatory Affairs for a 12 month contract role with a leading multinational Animal Health client based in Milton Keynes – hybrid.
This opportunity could be particularly suitable for newly qualified Veterinary Graduates looking to start their career in Regulatory Affairs within the Animal Health industry
Responsibilities
- Manage and enter Veterinary Pharmacovigilance (PV) cases into the relevant system (PV Works), ensuring accuracy and compliance with strict deadlines.
- Assess and evaluate pharmacovigilance cases, including VEDRA coding and causality assessment.
- Review and improve the technical quality, accuracy and consistency of pharmacovigilance case reports.
- Liaise with veterinary professionals, technical teams and external stakeholders to gather and validate relevant case information.
- Support the investigation and processing of Product Quality Complaints (PQC).
- Work closely with UK and Global Pharmacovigilance teams to ensure compliance with relevant regulatory requirements.
- Support the Pharmacovigilance Manager in maintaining and improving internal compliance procedures and processes.
- Provide technical guidance and support to internal teams, including Commercial and Technical Product Support.
Requirements
- Degree in Veterinary Medicine (BVet Med or equivalent).
- Good veterinary knowledge across different animal species.
- Strong analytical and decision-making skills, with the ability to assess technical information.
- Excellent attention to detail and high levels of accuracy.
- Ability to manage competing priorities and work effectively to tight deadlines.
- Strong written and verbal communication skills.
- Ability to work independently as well as part of a team.
- Ability to handle confidential information professionally.
- Previous experience or knowledge of Pharmacovigilance within the veterinary pharmaceutical or Animal Health industry.
- Familiarity with PV Works.
- Experience in Technical Support or Regulatory Affairs.
- Experience in project coordination or process improvement.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK
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Regulatory Affairs in Milton Keynes employer: PE Global
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