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At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via

  • Access – Providing high quality trusted medicines regardless of geography or circumstance;
  • Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
  • Partnership – Leveraging our collective expertise to connect people to products and services.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.

What you'll be doing

  • Assist in the retrospective quality review of adverse drug reaction reports stored in the global drug safety database to ensure quality, accuracy, and consistency with the Viatris standard operating procedures (SOPs) and conventions.
  • Assist with the development and updates of global Pharmacovigilance Operations (PV Ops) standard operating procedures (SOPs), work instructions and training materials.
  • Review changes to legislation concerning pharmacovigilance, clinical and medical devices.
  • Participate in PV Ops projects as required.
  • Monitoring the UK PV OPs mailbox and responding to queries relating to the management of adverse reaction reports in the global safety database.

About your skills and experience

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills, and experiences:

  • Life Science/Medical degree/ Pharmacist or relevant experience
  • Good understanding of post marketing and drug development, including knowledge of applicable post-marketing safety regulations.
  • Good knowledge of common data processing software (EXCEL, PowerPoint, Microsoft Word)
  • Strong organizational skills, including the ability to prioritize independently with minimal supervision.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Benefits at Viatris

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:

  • Top Employer Accreditation, demonstrating that we provide excellent people policies and practices
  • Competitive compensation package inclusive of annual discretionary bonus and stock options
  • Focus on career progression with growth and development opportunities
  • Emphasis on Health & Wellness programmes
  • 100% paid medical insurance and Employee Assistance Programme
  • Life cover
  • Hybrid working
  • Excellent employer-matched pension scheme with Viatris contributing up to 11%
  • 2 paid volunteer days per year