Meticulous Quality Manager for MARS Quality
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Søborg
- Quality
- Søborg
Can you lead and inspire a group of highly competent employees responsible for Quality Assurance (QA)? Do you like to work in an international environment with different stakeholders and feel motivated by challenges requiring a high level of professional competency and leadership experience? If your answer is yes, then we welcome you as our new Quality Manager within Medical Affairs, Regulatory and Safety (MARS) Quality.
About the department
MARS Quality is the QA department supporting our Medical Affairs, Regulatory Affairs and Global Safety departments. The department works with traditional QA tasks like SOPs, Deviations, Change Control. This specific team is comprised of about 10 Quality professionals and specialists all reporting directly to the manager.
The position
As our new Quality Manager, your main responsibilities include coaching/mentoring/training of direct reports, performance review and development employees, driving continuous improvements, contributing towards setting the direction for MARS Quality area, and ensuring dept. business and budget targets are met.
Furthermore, you will be involved in ensuring the establishment and maintenance of various systems used for QA activities in MARS thus have a strong collaboration with NN quality, Global Development and MARS departments along with providing QA support during audits/inspections.
In addition, you will be an active member of MARS quality management team and will be actively involved in contributing to set the direction and strategy for MARS quality. Moreover, it is required that you build and maintain good collaboration with stakeholders in order to achieve business results and timely raise and inform quality issues to the relevant parties.
Above all, driving projects and continuous improvement activities, including efficiency and customer satisfaction improvements thereby promoting a healthy and engaging work environment is an integral part of this position.
Qualifications
You hold a Master’s degree in Scientific, Medical or Biological education or have relevant professional experience within QA area or a similar position. Moreover, you have a minimum 3 years within pharmaceutical industry and 2 years managerial experience.
Furthermore, you have excellent proficiency in both written and spoken English and knowledge of GMP, GVP and GCP requirements including GxP documentation. Exposure in working internationally and with diverse professional groups is a nice to have for this position.
As a person, you are detail oriented with excellent analytical skills and a quality mindset. You have the ability to perform timely and effective performance management and have a strong sense of structure and timeliness. Moreover, you have a creative mind towards resolving issues and possess excellent communication skills.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Michael Sacco at +45 3079 6824.
Deadline
22. October 2019
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 chronical 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.
Information og data
Denne ledige stilling har jobtypen "Produktchef", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 30.9.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Produktchef
- Søborg
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