Engineer for Validation of Equipment

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Engineer for Validation of Equipment

Do you want to help validate and implement equipment for purification of insulins and GLP-1s of the future? Would you like to help us upgrade our capacity within a growing portfolio of diabetes products? Are you an engineer with strong validation skills? If yes, then you could be our new Engineer for Validation of Equipment in CMC API Pilots!

About the department

In CMC API Pilots we are 67 employees in the department, divided into four teams, three facilities and two locations. Our task is to scale up processes and purify proteins for toxicological and clinical studies.

You will be a part of a team of academics and principal technicians, whose tasks are to ensure stable operation of production equipment as well as participate in the design, validation and commissioning of equipment. The team works closely with skilled project staff, chemists, process technicians and calibration technicians.

The Position

You will have the opportunity to influence the design process as well as the department's work with new technology, so understanding the processes is important. The job will give you a solid insight into workflows and procedures and you will succeed by being visible, proactive and independent.

Your main responsibilities will include:

  • Participation in the implementation of production equipment as well as changes to existing facilities for purification of proteins, where you will be responsible for implementation and validation.
  • Both practical and documentation tasks, including preparation of change requests, validation documents and instructions.
  • Opportunity to take part in cross-organizational tasks and problem solving, where you will be able to influence processes across different organizational areas.

We work actively with LEAN in our production. Therefore, you must be able to thrive in a work environment characterized by improvement projects and changes.

Qualifications

As our work is carried out and documented in accordance with GMP, a systematic approach and a strong quality mindset are expected.

To be successful in the role we expect you to have:

  • Science background, preferably a master and you will have a curiosity for technical solutions
  • Ideally, you have experience in operating plants and validation from the pharmaceutical or other regulated industry
  • Experience in working with change requests, requirement specifications, validation and test, as well as deviations
  • Large parts of our equipment are controlled and monitored via DeltaV or Sattline, so insight into operating systems or interest in IT is an advantage.
  • Good Danish language skills

You will work closely with different professional groups, so good collaboration and communication skills are highly valued. On a personal level you are result-oriented, good at planning and you take pride in driving tasks forward and meeting deadlines. We also emphasize that you are a team-player and that you can motivate others around you.

Contact

If you want to know more about the position, contact Anette Sikjær Jørgensen on +45 3079 5903.

Deadline

6th January 2020

Millions rely on us

To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

#LI-AMS


Information og data

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

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 12.11.2020, men kan have været deaktiveret og genaktiveret igen.

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