Pharmacovigilance professional for Global Safety Compliance in [xxxxx]

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  • Clinical Development and Medical
  • Bagsværd

Are you an experienced pharmacoviligance professional looking for a dynamic role where you can combine your project management skills and natural drive for improvement? Do you want to be part of an organisation where passion and engagement are met with opportunities for professional development?

About the department

You will be working within Global Safety Compliance, which is part of the QPPV Office under Global Safety, located in our headquarters. Global Safety is globally responsible for handling adverse events, monitoring product safety and customer complaints, and potential recalls in Novo Nordisk. The primary responsibilities of the Global Safety Compliance department are ICSR Compliance Tracking, Safety Data Exchange Agreements, Pharmacovigilance System Master File, Regulatory Surveillance, coordination of PV Audits and Inspections. Furthermore, we provide support to HQ functions and affiliates, including compliance advice and support regarding handling of safety in Patient Support Programmes, Market Research Programmes and Digital Health initiatives.

You get the opportunity to join a high-performing team of 10 employees with different professional backgrounds. We use our differences to create novel ideas and high-quality solutions to ensure support and continuous improvement to the Qualified Person for Pharmacovigilance in Novo Nordisk, Global Safety and affiliates worldwide.

The position

As Pharmacovigilance Compliance Professional, your key responsibilities will be:

  • Managing the Pharmacovigilance System Master File
  • Participating in maintenance of our pharmacovigilance processes by providing advice and support, contribute to improvement efforts and initiatives, and participate in audits and inspections.
  • You will be expected to keep an eye on any quality or compliance concerns that require escalation to management
  • Providing training to internal employees on procedural matters
  • Ensure coherence between requirements and internal operating procedures and guidelines in collaboration with other colleagues in the department

You will also play a key role in contributing with ideas for improvement and participating in optimization projects within the department, which requires strong project management skills to lead and execute the development projects. Besides your main responsibilities, you will also be able to form the role and assignments based on your professional experience and interest.

Qualifications

  • Master’s Degree in biomedical sciences
  • A minimum of 3 years of experience within pharmacovigilance, preferably from a similar position within the pharmaceutical industry
  • Solid knowledge of the Pharmacovigilance System Master File and EU regulations
  • Experience with complex project management involving multiple stakeholders
  • High attention to detail and quality while at the same time being able to see the bigger picture
  • Fluency in both written and spoken English and good communication skills are required
  • IT know-how and analytical skills are highly desirable

As a person, you are open-minded with a high degree of flexibility. You are truly passionate and enthusiastic about working in a highly regulated compliance department with complex projects. You have excellent collaboration skills and can easily navigate on all levels in the organisation. Furthermore, we expect you to work independently and drive a variety of tasks with responsibility for delivering according to targets. Last, but not least, you have a natural drive to always find ways of improvement, without compromising on quality.

Working at Novo Nordisk

At Novo Nordisk, we have been changing diabetes since 1923. If you are ready to help us

strengthen our position as an innovative pioneer and respected industry leader, we encourage you to join us and make the most of your talent.

Contact

For further information, please contact Eirik Quamme Bergan at +4530793513

Deadline

November 15th 2020

Please note that applications will be assessed on an ongoing basis and therefore the advert may close before the recruitment process is completed if we have proceeded with candidates to the screening or interview phase.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Kemiker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 12.11.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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