Novo Nordisk A/S
Gladsaxe, 1 stilling
- Quality
- Denmark - Bagsværd
In Novo Nordisk we will manage quality to meet the expectations and needs of all stakeholders securing patient safety, product quality and compliance.
Internal Audits is looking for a new ambitious and international minded ISO/GMP Lead Auditor, so now you have the opportunity to fulfil your dream of a job as Lead Auditor with a high degree of flexibility, high level of responsibility, influence, and interaction with many different types of people at all levels of the organization.
About the department
The department “Internal Audits” is a corporate staff function and part of Corporate Quality situated in Bagsværd. The department is responsible for the internal ISO/GMP audits, Occupational Health & Safety (OH&S) and Environmental audits. We are 16 dedicated employees in the department with the ISO/GMP/OH&S audit team consisting of 13 Lead Auditors.
The job
In this position you will perform audits worldwide. You will have communication and interaction with management as well as all levels of employees both in Novo Nordisk and in other companies e.g. contract manufacturers. You will also have close collaboration with other auditors from Internal Audits and auditors from other auditor groups in Novo Nordisk. The impact of this position on quality related practices is strong and has bearings on existing and future business throughout the Novo Nordisk organisation.
As full-time Lead Auditor, you will assess the effectiveness and suitability of quality practices, with focus on systems, products and processes as well as verify compliance with current ISO 9001, GMP, requirements, and the Novo Nordisk Quality Management System.
You will be expected to participate actively in intensive audit-focused training and international conferences as well as develop your abilities of systematic fact-finding, which is the foundation for the audit function. The multidisciplinary experience you gain in this job will give you a personal and professional boost.
Qualifications
You are open-minded and have good written and oral communication skills in English, the ability to work independently and internationally, good co-operation skills, analytical skills, a high degree of flexibility, and a good sense of humour.
You have worked for a drug or device company for more than four years and have been involved in quality assurance activities for at least two years. You have a relevant scientific background within e.g. chemistry, biology, engineering, pharmacy, or equivalent at minimum bachelor level. You have an up-to-date and thorough knowledge of relevant GMP and ISO 9001 requirements, and an understanding of quality management systems, business objectives and perhaps have experience as manager/project manager. The preferred candidate has completed an ISO 9001 Lead Auditor course.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For additional information, please contact Inger Landtved on +45 3079 8772 or Lise-Lotte Guldmann on +45 30750 2315.
Deadline
27 October 2015.
