Senior QC Professional for Future QC Support & Facility

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Are you ready to be part of an exciting journey to design, build and relocate to our new QC Laboratory facility, which will secure the needed QC capacity for the future? Then this is a unique opportunity to join a project of highly competent laboratory technicians, academics and specialists impacting the future QC setup. The position
We are looking for a Senior QC Professional to join our newly established department, QC Processes, which is part of the Future QC project organization. The department oversees all QC activities related to chemistry, microbiology, stability, and support functions. You will be joining the Support, LEAN & Flow team. As a Senior QC Professional with expertise in QC support, your primary task will be to apply your skills and experience, to ensure that we build the optimal common processes across all future QC departments etc. all flows of samples and material. You will also have the task of giving input for ensuring the right design of common facility & Utilities in the building. You will also have the task of finding/implementing the future equipment’s for the cross-cutting processes, as well as support a wide range of GMP activities needed to relocate the common processes into our new shared facilities. This includes implementation SOPs and qualification of supporting equipment. You will be working closely together with stakeholders both locally in the project and from Line of business. Examples of your daily tasks are:
  • Prepare requirement and qualification documents and supervise facility design e.g., Sample receiving area, Warehouse and laboratory utensil washing area.
  • Qualification of equipment’s. Relevant experience in validation (FAT, SAT, IQ, and OQ). Experience with science and risk-based validation approach is preferred.
  • Optimize the processes for joined facilities in Future QC, prepare necessary SOPs, and plan/facilitate workshops.
  • Coordinate/Support and ensure execution of all activities needed to build the joined facilities and relocate the existing processes into our new laboratory facility.
  • Participate in a highly important project of introducing new fully automated process and equipment where needed.
  • Responsible for creating a set-up and governance that ensures maintaining the established processes/equipment after implementation.
  • Moreover, you will be expected to identify challenges and secure the necessary agreements/clarifications with stakeholders such as consulting engineers, end users, QA, regulatory and IT. This also entails being curious about how other teams and departments work, both within and outside Novo Nordisk. Qualifications The ideal candidate for this Senior QC Professional role should possess the following qualifications:
  • You hold a MSc in Natural Sciences, Engineering or similar, preferably with 3+ years of experience from a QC function in the pharmaceutical industry.
  • Experience with qualifying equipment and/or facility areas/processes.
  • A strong Lean-methodology toolbox, combined with a natural passion for doing things smarter.
  • A project management toolbox to enable a structured approach.
  • Strong communication skills in both written and spoken English, with a natural ability to establish new relationships across teams and departments.
  • On a personal level you possess strong collaboration skills, and the ability to set direction and motivate less experienced colleagues. You have the right quality mindset, dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. About the project The project will build multi-functional QC laboratory at Novo Nordisk located on Zealand and be the future workplace for many QC collages. Both shared facilities, chemistry and microbial QC-laboratories will be established, as well as development laboratories within these areas. When functional the laboratory will deliver analytical support to production units across Novo Nordisk covering products for treatment of diabetes, obesity, rare blood and endocrine disorders. The laboratories will be ready for our ambitious goals for QC Automation & Digitalisation. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you want to hear more about the position, contact Heidi Ardal Larsen on +45 30758469. Deadline 10 December 2023 We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 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.


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    Jobbet er oprettet på vores service den 17.11.2023, men kan have været deaktiveret og genaktiveret igen.

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