Category: Reg Affairs & Safety Pharmacovigilance
Location:
Gatwick, South East, GB
Pharmacovigilance Specialist
Location: Gatwick, United Kingdom
Your work will directly safeguard patients by ensuring the safety of medicines that millions of people depend on every day. In this role, you will be at the intersection of science, regulation and patient care – playing a critical part in how Novo Nordisk monitors, evaluates and acts on safety data across our growing portfolio.
Your new role
As a Pharmacovigilance Specialist based in the UK, you will be responsible for ensuring that safety information about Novo Nordisk products is collected, assessed and reported in compliance with local and global regulatory requirements, supporting and overseeing our case processing vendor. You will work in a dynamic environment where the portfolio is expanding rapidly, and your expertise directly protects patients.
Your key responsibilities will include:
Providing the UK Affiliate with pharmacovigilance (PV) and product quality complaints (PQC) process Ensuring compliance with UK and EU PV requirements
Monitoring of Safety Mailboxes
Ensuring oversight and Compliance monitoring of the external PV Case Processing Vendor and Customer Engagement Programme Vendors
Participation in safety related and product quality complaint related projects
As a person, you thrive in diverse environments where collaboration is key to success. You are adaptable and able to manage complex tasks in a changing environment while maintaining patient focus and the highest level of integrity.
Your new department
The UK Patient Safety & Medical Information team plays a vital role in safeguarding patients through rigorous pharmacovigilance processes. You will join a collaborative team that works cross-functionally with regulatory, commercial and global patient safety colleagues to ensure safety remains at the heart of everything we do.
Your skills & qualifications
To be successful in this role, you should have the following:
Graduate degree in Life Science (essential)
Proven track record of relevant industry experience specifically within pharmacovigilance (minimum 3 years, essential)
In-depth knowledge of UK and EU pharmacovigilance and regulatory systems, government guidelines, and the ability to understand and interpret new legislation to assess business impact
Sound understanding and experience of Pharmacovigilance Agreement lifecycles
High level of computer literacy, including MS Office
Good attention to detail and problem-solving ability
Demonstrable proficiency in written and oral English
Excellent communication skills and ability to engage effectively with all levels within the organisation; strong collaborator with proven customer and stakeholder management skills
Ability to independently prioritise and manage workload to meet deadlines
Ability to work as part of a team as well as autonomously
Ability to manage operational PV tasks while contributing to the business strategy
Ability to review and simplify operational activities to find efficiencies
Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.
What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.
Salary: Details available on application. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.
Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.
Learn more about our Reward Philosophy here.
Deadline
Apply before 4 September. Applications are reviewed on an ongoing basis. To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line managers before applying.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
