Senior Analytical Scientist

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Måløv

  • Quality
  • Måløv

Do you want to join us on a journey where you, as a true pioneer, will break new land?

You can look forward to a job where you will set direction for the future work in a recently established department and where your effort will be of invaluable importance for the lives of people living with diabetes.

About the department

Oral Finished Products Quality Control (OFP QC) employs approximately 60 highly skilled and motivated employees in four teams. The department delivers analytical support to oral protein products used for clinical phase 3 towards launch of the product. After launch, OFP QC will continuingly be supporting the production of oral finished products as well as prepare for new oral products, ensuring analytical support to manufacturing development. Working towards launch of the first oral protein product we are in process of standardisation and optimisation of our procedures.

The position

As an analytical scientist in OFP QC, you will ensure valid analytical results by approval of analytical test results and provide support to HPLC/UPLC based methods e.g. assay, dissolution, impurity, content uniformity and other methods such as Karl Fischer, UV, disintegration and particle size distribution. Maintenance, optimisation and validation of analytical methods will also be a part of the job, as well as leading projects on relevant issues when they arise. You will be working to continuously ensure optimal performance of the analyses and apply LEAN principles to trouble-shoot and improve our working procedures. You will communicate and coordinate with stakeholders internally as well as externally within various subject areas.

We are currently looking for two new colleaues, one for a permanent positon, and one for a temporary position for 12 months.

Qualifications

You have a background as a pharmacist, cand. scient. or similar, and you have a solid background from laboratory work in a GMP regulated environment. You have experience with approval of analytical test results, validation and standardisation of analyses. Competences within tasks such as method validation, preparing, updating and reviewing instructions, Non-Conformity reports and Change Requests will be considered as a plus.

As a person you thrive on a high level of flexibility – and with your ability to adapt you will enjoy a position where two days are not the same. You work in a structured manner with a non-compromised focus on quality. At the same time, you appreciate a good working environment where you with your dedication, good personality and initiative contribute actively to solutions to various types of challenges. Finally, you contribute to a healthy working climate and the continuous improvement of processes.

Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information please contact Maria Tonsgaard at +45 3075 1548.

Deadline

1 September 2019

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 chronical 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.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 9.8.2019, men kan have været deaktiveret og genaktiveret igen.

Rapportér
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • Måløv
  • Søndag den 01. september 2019
Rapportér

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