Would you like to a part of Quality Assurance for Biopharm Products?
Biopharm Quality Assurance is re-organising and is therefore looking for two new Associate Managers to lead the quality work in teams in Biopharm QA API and Biopharm QA FP. The two vacant positions are located in Kalundborg and Gentofte respectively.
As Associate Manager you will be reporting to the Directors in Biopharm Quality Assurance, and your key stakeholders will include Biopharm management groups and the Global Quality organisation. You will be part of the Biopharm Quality Assurance organisation which comprises a staff of nearly 120 dedicated and highly competent professionals.
Challenges
As Associate Manager in Biopharm Quality Assurance you will be responsible for driving and coordinating all quality related matters for your team. You will actively take part in the quality tasks in your team which means that you can and will work as a professional yourself.
The job tasks will include driving and coordinating releasing processes of produced batches, handling of non-conformities and change requests, Quality Audits, QAP process, development and standardisation of Quality Assurance SOPs, ISOtrain system management and training coordination.
In your work you will be exposed to different processes and organisational units in Biopharm operations, and you will build a strong cross-functional network. We expect you to be a leading part in the continuous development of the quality assurance processes in Biopharm to ensure highly value-adding quality activities.
We can offer you a job with a high level of contact with other people where you have a chance to take part in defining your own role in the new organisation. Beside that the job will give you good skills within Quality Assurance and will offer you the opportunity to develop a strong professional and management profile to prepare you for a job on next level.
Qualifications
We are looking for persons that hold a degree in pharmacy, science or engineering and possesses the following key competencies;
You have prior experience with quality assurance work in Novo Nordisk and your Quality Mindset is on a very high level. Furthermore you have the will to further enhance your professional quality competences to an expert level. Your professional competencies are a solid ground for you to assure a good cooperation with mutual respect to the production departments.
You have prior experience and good results in leading and motivating people. You know how to handle and get excellent result with highly educated and self-leading teams. You know when to step back and let the team find their own solutions to challenges and you also know when your management is needed in their daily work.
Good social skills and robustness are a must. You need to be the catalyst of an inspiring, friendly and efficient cooperation with the production departments and you need to know how to stand tall against the wind when it is needed.
On the personal level you are motivated by driving change and improvements involving several stakeholders at all organisational levels. You have a high level of drive, reliability and persistence and you are result-oriented. You have a flexible mind-set and you have the will and wish to define you own role in our new organisation.
Applications in both Danish and English are welcome.
Contact
For further information, please contact Karen Pilgaard at +45 3075 2237 or Rikke W. Jensen at +45 3075 1566
