Arbejde Training & QC Professional Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Training & QC Professional

jobbeskrivelse:
- Pharmacovigilance - Denmark - Bagsværd Are you motivated by coordinating, developing and conducting training within pharmacovigilance? Do you thrive on working with a high level of responsibility, influence in pharmacovigilance training and interaction with colleagues across the global Novo Nordisk organisation? If you find such challenges exciting and inspiring, you may be our new Training & QC Professional, ensuring high-quality training in all areas of our work to provide the safest products to patients. About the department The job is in the Training & QC Department in the QPPV Office, an area within Global Safety. Global Safety is globally responsible for handling adverse events, monitoring product safety, customer complaints and potential recalls in Novo Nordisk. The primary responsibilities of the Training & Quality Control (QC) department are to ensure that Global Safety is providing pharmacovigilance training across headquarter and affiliate organisations, developing and maintaining the Global Safety intranet sites and performing quality control on safety case handling to ensure that we meet external and internal requirements. We are 14 colleagues with different professional backgrounds, ensuring support to the Qualified Person for Pharmacovigilance (QPPV) in Novo Nordisk. Since our unit is situated in both Bagsværd and India and also works with our affiliates across the globe, you will have the opportunity to work closely with many global colleagues. The job You will be responsible for coordinating and developing training material in relevant media and also performing training activities related to pharmacovigilance. Furthermore, you will be responsible for providing training, tools and techniques to ensure documented training efficacy. This also includes visits to NN affiliates and participation and presentation at NN regional meetings. You should expect up to 20 days of travel per year. You will be expected to ensure coherence in our training material with external regulatory requirements, and internal procedures and guidelines, as well as participating in cross-functional projects (e.g. the annual global conference). Other responsibilities include maintenance of all metrics related to these processes, trending and analysis of reports produced in the department, including writing executive summaries and conclusions based on your analysis. You will be expected to develop and maintain a professional and good collaboration and relation with our stakeholders, which range from staff throughout Global Safety to the clinical, regulatory areas and global affiliates. Qualifications You hold a Master’s degree within e.g. medical, biology, pharmacy or biomedical science and have documented experience within pharmacovigilance and training. You have excellent written and oral communication abilities in English. You are open-minded, enthusiastic and have the ability to work independently and globally, and drive your own job responsibilities. You have good cooperation skills, a high degree of flexibility and deliver according to targets. The role requires analytical skills and a strong quality orientation, including the ability to focus on details and adherence to standards. At Novo Nordisk we use our skills, dedication and drive to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment. Contact For further information, please contact Jakob Ellinshøj Larsen on +45 3075 9776. Deadline 11 June 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark

GÆLDER

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