Senior QC Professional for Future QC Microbiology

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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, and consists of four teams. You will be joining the Microbiology and Stability team. As a Senior QC Professional with expertise in microbiology, your primary task will be to leverage your knowledge to define the necessary user requirements for designing the microbial laboratories. You will ensure that our Future QC is equipped to meet its intended use. Additionally, you will be responsible for implementing optimized processes and procedures for the future, qualifying the required equipment and classified areas, and maximizing automation to the highest possible level. Examples of your daily tasks are:
  • Prepare requirement and qualification documents, supervise design and construction, and execute the qualification process.
  • Optimize Microbial QC processes for Future QC, prepare necessary SOPs, and plan/facilitate workshops.
  • Participate in projects introducing automated equipment supporting microbial QC processes.
  • Support and ensure execution of all activities needed to relocate the departments into our new laboratory.
  • Validate microbiological analytical methods, prepare submission documents, and present data during audits/inspections.
  • 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:
  • A minimum of 3 years of experience in the pharmaceutical industry, preferably in QC or aseptic production, and a master’s degree in Microbiology, Engineering, or a related field.
  • Experience with cGMP, ICH guidelines, and pharmacopoeia requirements.
  • Experience with qualifying equipment and/or classified areas, as well as validating QC analytical methods.
  • 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 Site Hillerød and be the future workplace for 650 QC collages. Both 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 Jakob Hovalt Mathiassen on +45 30792404. Deadline 27 August 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. 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 27.7.2023, men kan have været deaktiveret og genaktiveret igen.

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