Pharmacovigilance Inspection Readiness Principal

*Pharmacovigilance Inspection Readiness Principal – Global Pharma –contract – Macclesfield*
My client is a Global Pharmaceutical company and they have a position available for a Pharmacovigilance Inspection Readiness Principal to join their team initially until the end of the year and then for a further 12-month

Within this role you will be taking responsibility for the management of assigned projects and partnerships including: continuous improvement; process updates; communication; quality and compliance. You will be accountable to develop relationships across Chief Medical Office and other relevant functions, to execute the delivery of the QPPV & PV Excellence strategy and priorities.
In order to apply for the Pharmacovigilance Inspection Readiness Principal contract, you should possess a scientific degree and have experience of working in the Pharmaceutical Industry with previous experience and knowledge of Pharmacovigilance processes and regulatory requirements. You will possess experience of supporting major (FDA/MHRA/EMA) regulatory inspections in GVP and / or GCP area and have experience of working in the CAPA management process. Proven good communication skills and the ability to work in cross functional teams is a must.

Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.

To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on 0203 465 0045.

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Job type:
Working Pattern
Drug Safety and Pharmacovigilance
Circa £450 p/d
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Talk to Roberta Atkins, the specialist consultant managing this position, located in London-City

4th Floor, 107 Cheapside

Telephone: 0203 465 0045

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