Are you passionate about optimizing processes, procedures and equipment in pharmaceutical aseptic production? Are you ready to establish new standards and simplify our processes to ensure the right quality and at the same time drive exciting new initiatives to transform how we work with filtration and formulation? Are you creative and able to think out of the box? Can you set the pace and create the road ahead in a complex and highly regulated environment where prioritisations can change quickly? Then, come join us and utilize your knowledge and skills in an exciting organization, where you will get challenged, grow and expand your capabilities to the fullest. The position We are looking for a specialist within Formulation and Filtration in FP Manufacturing Development with a specialized understanding of formulation and filtration processes and principles and with a creative flair for continuous improvement. As our new Specialist your primary responsibility will be implementation of new technologies and approaches, supporting production in problem solving, supporting audits and regulatory inspections. Area of expertise further include filter knowledge, filter validation, integrity testing (PUPSIT), filtration set-ups etc. You will be joining a team of 12 highly dedicated and qualified colleagues in an informal and dynamic work environment and will be working across the organisation:

Ensuring implementation of new processes as well as ongoing support of existing facilities and products.

Being involved in establishing of new sites as SME within Filtration and Formulation.

We have a strong focus on innovation and optimization of the processes in our production facilities in Biotech and Rare Disease (BRD) area and utilise our test laboratory to further increase focus on science and implementation of new technology. We strive at making a difference in close collaboration with the production sites by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations. You can expect a position with a high degree of independence where your specialist skills combined with good communication skills are a must, including the ability to target your communication to a broad set of stakeholders at all organisational levels ensuring clear argumentation to ease decision making for senior management. Qualifications To succeed in this role, we expect that you to have:

A master’s degree in Engineering, Pharmacy, Biology or other relevant education.

Specialized knowledge within the field of formulation and filtration from pharmaceutical production as well as experience in managing projects in a GMP regulated environment.

Relevant experience from the pharmaceutical industry as well as experience such as process or product support, transfer or process validation, process optimisation, aseptic production processes and implementing new technologies.

A high level of Business understanding is appreciated.

Full proficiency in oral and written English.

On a personal level you have an innovative mindset, a personal drive and enjoy working in a dynamic environment where teamwork is on top of the agenda, so the ability to manage multiple tasks and define the steps needed to achieve goals is part of your natural skills. You are inspiring and motivating, a strong innovator, that strives for continuous improvement and likes to challenge existing processes. As you have a structured approach to your work you can navigate in uncertainty and constant change while keeping an overview of the big picture and when needed paying attention to the small, but crucial details. Besides, you are a fast learner who enjoys new challenges and have a pragmatic approach and a hands-on can-do attitude.. About the department BRD Manufacturing Development & Quality Control has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible. Additionally, we have a strong focus on innovation and optimization of the processes in BRD’s facilities and utilise our test laboratory to further increase focus on science and implementation of new technology.
Working in BRD, Novo Nordisk Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2650 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact If you have any questions about the job or just want to get a feeling of the department and our exciting road ahead, please do not hesitate to call Camilla Aasholm Bradley +45 3077 6243 Deadline 23 July 2023. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. In addition, please avoid the use of photos in your CV. This provides a better and more fair process. Applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates are identified. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.