Novo Nordisk
QA Specialist for Validation
Would you like to play an important role in ensuring the quality and safety of products for clinical trials, where you can use your solid QA and validation experience in a project context? Then we can offer you a unique position with a lot of responsibility and impact in a dynamic and highly professional environment, read more and apply now!
The position
Chemistry, Manufacturing and Control, Active Pharmaceutical Ingredients (CMC API) QA is looking for a QA Validation Specialist to be part of an optimization project that is already running at full speed. In the position you will refer to the QA Director.
CMC API Pilot facilities are expanding their production capacity for clinical trials phase 3. We are looking for a Validation specialist to be part of a team of 10 dedicated and highly skilled Project QA´s allocated for this project.
In this role, you will – together with our other QA Validation Specialist - be responsible for:
Setting the quality direction for the capacity expansion project
Deliver best-in-class quality for qualification of equipment/facilities and IT-systems
Handle larger and complex quality issues
Ensure a LEAN culture and drive improvement activities across areas
Represent CMC QA in cross organisational groups in Novo Nordisk
Moreover, you will be leveraging knowledge of quality assurance to strengthen the QA competences in the department through training and sparring within own area of expertise.
Qualifications
In this dynamic team, a high level of innovation to deal with new situations is expected, which will help you with solving complex problems and take a new perspective using existing solutions.
To succeed in this role, you:
Hold a Master in Pharmacy, Engineering, Biology, Biotechnology, Chemistry or similar
Have at least 7 years of experience in QA roles in the pharmaceutical industry
Ideally have experience within validation of GMP facilities and equipment
Have a flair for IT
Are fully proficient in English
On a personal level, you show excellent interpersonal skills, with the ability to clearly and precisely communicate complex matters to stakeholders; this will help you when providing professional direction with scientific sparring partner to management.
You think above and beyond own area and improve our processes based on value chain understanding, leading the way and take co-responsibility for employee development by knowledge sharing and valuable feed-back.
Finally, you are self-driven and independent with a high sense of responsibility and initiative, and you thrive in a dynamic environment, where teamwork is on the top of the agenda and you like working with many different stakeholders.
About the department
CMC API QA is a department which employ + 40 skilled and motivated colleagues divided in 4 teams all based in Site Bagsværd. We work with assuring quality and compliance of the CMC API facilities & equipment and release of raw materials, cell banks and API for clinical trials. We participate as QA for smaller or bigger investment projects to make our API Pilot facilities prepared for the future.
Our department values teamwork, diversity, and humour and we will make sure that you, as our new employee, feel welcome and included. A thorough individual training plan will be made for you together with your mentor.
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