Job for Senior Associate in Quality Control at Novo Nordisk
Graduation and/or post-graduation in life sciences.
Preferably 3 years and above experience in PV.
Good knowledge of medicinal terminology and clinical pharmacology
Solid knowledge of Pharmacovigilance principles and international regulatory requirements regarding drug safety
A good knowledge of computers and databases. Fluency in English, written and spoken, is a must.
Strong ability to coordinate and prioritise tasks for ensuring department’s time and quality compliance concerning QC activities.
Good ability to guide and instruct other employees on quality procedures
Ability to efficiently collaborate and communicate with stakeholders from the global NN organisation.
Continuous contact and interaction with relevant stakeholders with very diverse professional and/or cultural background.
Understand and respect GS stakeholders expectations and concerns.
Proactively contribute to solving GS customer’s needs.
Education: life sciences
Industry Type: Pharma
Functional Area: Pharmacovigilance
Job ID: 46414BR
End Date: 10th May 2017
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