Analytical Professional

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Måløv

Qualification and Equipment Responsible for OFP QC

Do you want to be part of shaping the innovative journey in Oral Finished Product Quality Control (OFP QC)? Are you motivated by working with equipment within the laboratory field? Then join us as our new Equipment and Qualification responsible.

The position and responsibilities

As Equipment and Qualification responsible within OFP QC, you will be working in a cross-disciplinary team, consisting of a broad spectrum of competencies within laboratory equipment, automation, and PAT, where you will be helping bring our new laboratory standards (e.g. automation and PAT equipment) to a GMP level of readiness while taking responsibility of already uprunning laboratory equipment incl. UPLC/HPLC systems & dissolution. You will be a part of qualifying and maintaining laboratory equipment, PAT, new robotic solutions/ automation projects in a laboratory setting.

Qualifications and skills

Preferably, you have an educational background as a chemical, pharmaceutical, industrial, or mechanical engineering etc. You have sufficient insight to lead in the qualification and can facilitate verification and validation activities including test execution, documentation review and approval. Ideally, you have experience within laboratory equipment, or you have been responsible for similar equipments (e.g. Equipment within the Pharma Industry- production and packaging). Furthermore you have experience with delivery of complete validation packages, Requirement specifications, Installation/Operational/Performance Qualification Protocol/Report (xQP/R), Operation and Maintenance SOPs.

In addition, you have the following qualifications:

  • Detail-oriented mindset and quickly acquire new knowledge
  • Experience with maintenance of laboratory equipment incl. troubleshoot, test and documentation
  • Skills with qualification of complex equipment (automation/robots’ projects in regulated industries is an advantage)
  • Strong skills within troubleshoot and maintain equipment within the laboratory
  • Experience with life cycle documentation

We are looking for a team-player who is dedicated and enjoy to work independently and in a team. On a personal level, you are structured and skilled at knowledge sharing and you are not afraid to reach out to others for help or knowledge when relevant. You have a sincere interest in laboratory equipment and exploring innovative technologies and you enjoy being part of a team where it is important to have fun and where we work in a collaborative and trusting atmosphere.

The workplace is placed in Måløv, where the work language is Danish, and it is required that 3-4 days are on-site.

About OFP QC

Oral Finished Product (OFP) is organisationally located in Product Supply, which globally employs approx. 14.000 of Novo Nordisk more than 43.000 employees. In OFP, we are steadily growing and at present we are approximately 1100 committed colleagues in Måløv. We have great ambitions for the future, and we are working hard to get our new product successfully distributed to market.

The OFP QC area consist of approx. 165 dedicated colleagues newly divided in 3 departments, Market Release, New Product Entry and Analytical technology and Innovation.

Department Analytical Technology & Innovation is a newly established department, with the primary focus areas can be divided into the following areas:

  1. Daily operations maintaining the full responsibility of all equipment in OFP QC.
  2. Implement new technology and complex equipment in OFP QC (e.g. Qualification and Life Cycle Management of new equipment incl. training and maintenance)
  3. Automate existing laboratory processes and find new innovative solutions for the laboratories in OFP QC.

We are currently looking for 2 positions within bullet 1 & 2.

Working at Novo Nordisk
At Novo Nordisk, you will help millions of people who are living with diabetes and obesity. We expect high performance and the ambition to make your mark on our business. In exchange, we offer a wide range of opportunities for professionals and personal development.

Contact

For further information, please contact Anne Dorthe Vad Dockir +4530757037 or Iben Almar Meier at + 4530792662.

Deadline: 2nd of January 2023.

Applications can be written in Danish or English and will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.

To ensure an efficient and fair 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 recognise 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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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 25.10.2022, 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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