Senior Technical Engineer for Biopharmaceutical Production
Are you motivated by the pulse in a production department?
Do you want to be part of a strong team with high professionalism and challenging processes? And do you want to be the technical lead in projects aiming for better solutions in our production?
Then it could be you we are looking for.
About the department
BioFP GE NPE & Projects are responsible for introducing new products, as well as equipment and facility projects. You will be a part of a department of 50 employees consisting of technical and process specialists, project managers, IT specialists etc., who provide process and technical support to our aseptic filling departments. The biopharmaceutical production includes e.g. formulation, filling, freeze drying and inspection and is characterized by complex processes, supported by employees with high professionalism and commitment. As GMP requirements are tightened, it demands new and more innovative solutions to secure high quality products.
The position
You will be the technical lead in projects concerning design and implementation of new equipment and re-design of existing equipment in an innovative way with high quality in mind. The role is also to be the technical lead optimizing our end-to end production process and handle investments projects and suppliers. You will participate in designing, re-designing, prototyping and implementing equipment including all qualification activities e.g. URS, DQ, IQ, OQ PQ in accordance with GMP requirements.
Quality and documentation will be a part of the job, ex. writing documentation, protocol and report for qualification activities including URS, DQ, IQ, OQ and PQ etc. as well as participate in the qualification activities in important to secure delivery of high quality in a complex production set-up in according to GMP requirements.
Qualifications
You have a strong technical background, probably technical engineer, with minimum 5 years of experience and you have solid experience with technically complicated equipment. You have both practical and theoretical experience with designing and qualification of equipment, including documentation and testing according to GMP requirements. Experience with aseptic production will be considered an advantage as well as insights working according to GMP and documentation requirements. You master both hands-on and theoretical trouble shooting. English and Danish, both verbally and in writing, is a requirement.
As a person, you are social and positive by nature. You are proactive, solution-oriented and knowledge sharing is natural to you. You work systematically and are committed to your work and your colleagues. You are naturally good at collaborating and communicating, also across professional groups, and you can manage a high workload at times without losing sight.
Contact
For further information, please contact Associate Manager Kim Bech Poulsen at +45 3079 0613.
Deadline
12 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 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.
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