Regulatory Affairs
Company: PE Global Agency
- Location: Milton Keynes, United Kingdom
- Work mode: Hybrid
- Seniority: Senior
- Employment type: Contract
- Posted: Yesterday
- Offer language: English
Job description
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 (BVetMed 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.
- Good IT skills, including Microsoft Office.
- Ability to work independently as well as part of a team.
- Ability to handle confidential information professionally.
Desirable
- 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.
Interested candidates should submit an updated CV.
*Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK*
