Senior Internal Auditing Manager

The organisation

Our client is an international Medical Device company based in the Netherlands, and due to their expansion they are looking for a Senior Internal Auditing Manager. 

You will be part of an organisation that is growing fast due to organic growth and aquisition, which means immense opportunities for the people working there. Our client spends a lot of time and money on building a culture, which means that people tend to work for them for a very long period of time. They are very passionate about their products and what they can mean for patients; they expect no less from the people working for them.

Tasks & responsibilities

Your responsibility will be mainly to take ownership concerning their current auditing strategy & program, implement changes there where optimizing need to be done and strive for constant improvement. This will involve: 

• You plan, approve, manage and continually assess the quality audit program and the tactical execution carried out at the different manufacturing sites acrross the world.
• You ensure continuous quality compliance through quality audit program for the specific sites. 
• You enable standardised and consolidated internal audit planning & management activities, this by developing effective and efficient quality audit business process at the Regional Headquarters.
• You leverage greater efficiencies in the audit group by applying standardised methodologies to quality audit activity management and execution at the manufacturing sites.
• You ensure effective closure of audit findings.
• You create a formal audit reporting program which ensures the timely completion of audit reports, the associated corrective actions, the performance measurement of audit activities and the closure of actions from audit results. 
• You ensure the audit program adapts to changes to both internal and external quality requirements.
• You iIdentify areas of opportunity and you support continual improvement of Quality and you work with the relevant divisions on how these can be improved.
• You assist where needed with the co-ordination of external body audit activities at the manufacturing sites.
• You develop the team’s expertise and team dynamics through continuous coaching and by promoting development programmes.

Candidate profile

• You have a Bachelor’s degree in Science, Engineering or related subject
• You have minimum 8 years relevant quality experience in a (GMP) manufacturing environment.
• You have a good understanding of auditing – understand the process, operational terminology etc.
• You have experience in QMS.
• You are a "change manager"; your strength is in seeing what can be done better and start the chain of change. 
• You have highly developed problem solving skills. 
• You possess strong communication, project management & leadership skills as well you have the ability to manage multiple projects simultaneously. 

Interested?

If you’re interested in the above description, please apply with your CV and a letter of motivation by using the form below. For further information, please contact Daisy Tazelaar at +31 (0)20 20 44 502.