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Lead Auditor Specialist

Do you enjoy working in a complex, international and dynamic environment with many stakeholders? Are you ready to contribute to ensuring the high quality of Novo Nordisk Products? Are you a person who can set direction with a proactive attitude and with continuous improvement as one of your career objectives? Then you could be our new colleague in Supplier Audits.

 

About the department

Supplier Audits is a part of Novo Nordisk Quality and is responsible for conducting audits

of Novo Nordisk suppliers globally. Supplier Audits has 11 full time auditors who perform quality and responsible sourcing audits at Novo Nordisk suppliers together with some part time lead auditors.

 

Quality Audits comprises of 70 employees placed in Denmark, China and India. We conduct more than 700 audits annually and have process responsibility for the audits conducted globally within a variety of GMP expertise. Supplier Audits is one of four departments. Quality Audits has an engaging work environment, with collaboration across the organization and people with many different backgrounds.  


The position 
As Lead Auditor Specialist you will be safeguarding Product Quality and Compliance through audit coverage of Novo Nordisk supplier activities. You will be responsible for planning audits, conducting audits and reporting the audits including reporting of any critical compliance concerns to management. The audit can either be conducted at the supplier’s place or virtual via e.g. Teams. In addition, you will be responsible for presenting the audit process and audit reports at inspections from authorities.  

 

Furthermore, you will act as a role model and mentor for Auditor Trainees and share better practices and knowledge with colleagues, peers and stakeholders. You will be part of a team with highly skilled lead auditors who are passionate about working with safeguarding product quality and compliance.

 

Due to the global nature of the position you are expected to travel approx. 50 days a year.  


Qualifications
You hold a PhD or Master´s degree within science, pharmacy, biologist or similar. You have several years profound experience within compliance, processes and pharmaceutical business.

 

Moreover, you are expected to have relevant compliance knowledge with GMP, ISO and QMS and demonstrates subject matter expertise within own domain areas.

 

Naturally, you work independent and set direction in driving the compliance agenda and have strong stakeholder management capabilities. As a person you thrive in a setting with a high level of complexity and have solid analytical and problem-solving capabilities.

 

You have a natural personal integrity and a good situational understanding. Great communication skills are a must and you are expected to be fluent in English.

 

 
Contact 
For further information, please contact Susanne Poulsen at +45 3079 5831.

Deadline 
19. October 2020

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


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