- Delivering right-first-time solutions with attention to detail and high quality
- Crucial for validation activities, change requests, deviations, documentation, etc.
- Ensuring readiness for audit situations
Qualifications
To excel in this position, you have:
- A bachelor, master's degree or PhD in a relevant field
- Extensive experience in industrial machinery, equipment, and validation
- Solid experience in GxP regulated environments in pharmaceuticals, with other regulated industries like aerospace, electronics, or plastics also valuable.
- Experience in equipment validation, GMP and deviation handling will be a plus
- Good communication skills in English
You have project management skills with technical expertise, and stakeholder management, both cross-functionally and with external suppliers.
As a professional, you are self-motivated, thrive on working independently, and enjoy driving projects, improvements, and initiatives across an organization. You possess a structured approach to challenges, utilizing problem-solving skills to establish standardized ways of working. Moreover, you are eager to influence process optimization and digitalization, focusing on innovation and intuitive solutions.
About the Department
The CMC Clinical Supplies Packaging & Shipping (CSPS) department, located in Måløv, comprises 110 employees divided into six teams. Our primary objective is to ensure the timely supply of clinical study products to patients. We collaborate closely with the Clinical Supply Chain at CMC to deliver high-quality products on time to patients worldwide. Continuously striving to optimize processes, reduce lead time, and efficiently utilize resources using various LEAN tools.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We're inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we're all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information about the position, please contact Associate Manager Daniel Bøjle at
Deadline
Apply before May, Please apply as soon as possible as interviews will take place on an ongoing basis.
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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Equipment Engineer - Måløv, Danmark - Novo Nordisk A/S - A1p
Beskrivelse
Are you seeking a new challenge where you can apply your extensive knowledge of equipment and qualification? Do you possess a strong passion for developing advanced machinery, managing deviations, and qualifications in a setup that supports business growth and ensures patient safety? Would you like to contribute to the growing Clinical Supply Packaging & Shipping (CSPS) division, where Novo Nordisk products for clinical trials are packaged and delivered worldwide?
If so, read on to learn more about our Qualification & Equipment Responsible opportunity in Clinical Supply Packaging & Shipping (CSPS) at Site Måløv.
The Position
As an Equipment Engineer you will oversee the current packaging lines, which includes upgrading/rebuilding and troubleshooting to maintain equipment in a validated state and enhance their performance. This entails project management and a commitment to driving LEAN processes for systematic problem-solving. Additionally, you will play a pivotal role in implementing new equipment to support the growth in clinical trials. Collaboration with stakeholders, both internal and external to the department, will be essential, with a focus on Design for Manufacturing (DfM) principles.
Your key responsibilities will include: