Technical writer

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Hjørring

Technical Writer Are you able to transform complex ideas and requirements into specifications and instructions in definite terms? Are you energised by interacting with many different stakeholders? Are you looking for an opportunity to use your skills as a communicator? Then you might be our new Technical Writer for our production site in Hjørring called Needle Manufacturing & Sourcing. The position At Novo Nordisk, we take the greatest care to deliver the same quality product to our patients every time and every day. To do so, we use standard operating procedures (SOP) for all our processes and thoroughly release test our products before they end up in the hands of the patients. To support the increasing demands of our products, we are launching a new project to transform the way we release test our products in our quality control (QC) laboratory. This involves specifying, procuring and validating new test equipment, new facilities and changing the very way we operate in our QC laboratory. As a Technical Writer, you will be a part of the project where your primary tasks will be to plan, manage and prepare a wide range of documents such as:
  • User requirement specifications
  • Risk analysis
  • Change requests
  • SOPS
  • Protocols and reports.
    • In the beginning of the project, you will participate in the conceptual and basic design of our new QC laboratory. You will be part of a project team covering metrology, automation, IT, process optimisation and change management. You will work together with the project team and other subject matter experts to collect and document requirements for the project. These requirements will eventually be the foundation for procurement of the new equipment and designing our new processes. When the project transition from the design phase to construction, so will your role in the project. Using the deep knowledge you have gained in the first part of the project, you will draft new SOPs describing how to perform the new processes. The procedures will be used by our operators, technicians and other experts every day and for training and onboarding new colleagues, so they need to be unambiguous and easy to understand. To ensure high quality in your work, you will plan and facilitate workshops to secure input from subject matter experts and validate the instructions by the people who will work according to them after implementation. As we are transforming our processes, you must have an eye for optimisation and simplification – and dare to ask critical questions. Only by doing so, we can build the foundation for our future QC. Organisationally, you will be part of a team of technical writers and training experts who will support you in your daily work. Qualifications You hold a degree in science, technology, medical science or communication and have experience as a technical writer in a production environment, preferably within the pharmaceutical industry. We also expect that:
  • You have great communication skills and the ability to explain complex matters in a simple and understandable way
  • You have a technical understanding
  • You are fluent and write effortless in both Danish and English to succeed in this role
  • You have experience within specification and design of new equipment or processes which will be a big advantage.
    • You have an eye for detail and logical structure, and you are used to working in complex situations with many stakeholders. As a person, you are a strong communicator and can build relations to your stakeholders. You have a curious mind and a can-do spirit. About the department You will be part of the Training & Development team and have 10 close colleagues. The team is part of Needle Manufacturing & Sourcing which is overall responsible for the global end-to-end supply chain of Novo Nordisk's pen needles including both internal and external production, quality assurance and manufacturing development. We are organised in eight departments and with app. 475 employees dedicated to ensuring the pen needle supply to Novo Nordisk. We are driven by a quality mindset and pride ourselves on being a workplace where our can-do spirit and high ambitions come together to create great results for the benefit of our patients. Working at Novo Nordisk At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in hemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact For further information, please contact Associate Manager, Bo Henrik Nielsen, on 30795671 or Project Manager, Christian Østergaard Gru, on 30775030. Deadline 10th December 2023 Please note that applications will be assessed on an ongoing basis and therefore the advert may close before the recruitment process is completed if we have proceeded with candidates to the screening or interview phase. 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. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your resume. 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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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hjørring.

    Jobbet er oprettet på vores service den 20.11.2023, men kan have været deaktiveret og genaktiveret igen.

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