Equipment Responsible

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Do you thrive in a position that offers the opportunity to take on a serious responsibility? Would you like to grow personally and professionally? Are you passionate about equipment-related projects and are seeking to establish a career in a challenging and dynamic environment? If so, you are our new Equipment Responsible for Retrofit Project Team. Read more and apply today!
The Position As an Equipment Responsible, you will be responsible for purchasing and validating new equipment in tablet production. Our project team works closely with other department and team. Your main focus will be on:
• Driving equipment projects from idea to implementation.
• Establishing the validated state for new tablet productions equipment.
• Preparing the equipment for GMP production.
• Validating new or modified equipment.
• Being responsible for driving continuous improvement projects. Qualifications To be a competitive candidate, you should have:
• A minimum of bachelor's degree in natural science, pharmaceutical science, mechanical engineering or similar.
• Knowledge or experience from a GMP production environment
• Ability to independently drive equipment-related projects from idea to implementation.
• Experience working in a fast-paced environment and adapting to daily changes.
• Fluency in English, Danish is a plus. On a personal level, you are result-oriented, good at planning, and take pride in and meeting deadlines. You foster a strong quality mindset and an open-minded approach to problem-solving. Being a team-player, with ability to motivate colleagues and influence the direction for future projects in tablet production are abilities we like to build the foundations on for this team’s success. About the department Oral Product Development (OPDev) Clinical Operations is located in Måløv. The area is responsible of producing tablets as well as new products. You will be a part of the campaign support team in ET OPDev Clinical Operations. In the department we optimize production making the processes ready for GMP in large scale production. We transfer processes from R&D to commercial production. 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, please contact Morten Verdoner at +45 3079 3506. Deadline 2 April 2024. 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.


Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 14.3.2024, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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