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reference: 4973482

documentId: 4973482

connectionPointId: 7

lastModificationDate: 1554899430373

stillingsbetegnelse: Senior Analytical Professional

jobbeskrivelse:

In Oral Finished Products (OFP) we have set the ambitious target of being first to market with a tablet containing a new GLP-1 drug. 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 have invaluable importance for the lives of people living with diabetes.

 

About the department

In Oral Finished Products Quality Control (OFP QC) we count approximately 55 highly skilled and motivated colleagues. Our department delivers analytical support to oral protein products used for clinical phase 3 towards launch of the product. After launch, we will continuingly be supporting the production of oral finished products as well as prepare for new oral products, giving analytical support to manufacturing development. Our department has recently been established and therefore we are in an ongoing process of setting up and impacting working procedures.
 

The position

OFP QC is divided in 4 teams – you will be part of the team Specific Tablet Analysis, where you as an analytical scientist will approve 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 Malvern. Qualification of new equipment and validation of methods will also be a part of the job, as well as running projects on relevant matters. 

You will continuously ensure the optimal performance of the analyses and apply LEAN principles to trouble shoot and improve our working procedures. Furthermore, it will be a key task that you communicate and coordinate with stakeholders internally as well as externally within various subject areas.

 

Qualifications

You have a background as a pharmacist, cand. scient. or similar, and have a solid background (2 years as a minimum) from a Quality Control/Manufacturing Development laboratory working in a GMP regulated environment. You have experience in approval of analytical test results and standardisation of various tablet analyses. 

Competences within tasks such as method validation, preparing, updating and reviewing instructions (SOP’s), Non-Conformity (NC) reports and Change Requests (CR) will be considered as a plus. Experience with project management in a laboratory environment is considered as an advantage but not a demand. 

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 alike. You work in a structured manner with a non-compromised focus on quality. At the same time, you appreciate a casual working environment where you with your dedication, good mood and initiative contribute actively to solutions to various types of challenges. Finally, you use your LEAN skills to innovate our working procedures and you work in a systematic and analytical manner to be able to meet deadlines.

 

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 Pernille Hejner at +45 3079 8964. 
 

Deadline

29 April

 

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.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2421

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR