Product Supporter for Biopharm marketed products
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Gentofte
- Manufacturing
- Gentofte
Are you interested in working with Biopharm’s broad portfolio of products for treatment of haemophilia and growth hormone deficiency? Then you may be our new colleague. We are looking for an innovative and skilled professional, who has knowledge within pharmaceutical production and a keen eye for identifying opportunities for improvements.
About the department
You will become a part of the Biopharm Finished Product Manufacturing Development. As a department, we are responsible for the specifications of Biopharm’s liquid and lyophilised drug products, and for understanding how the manufacturing process can affect the product quality.
We are approximately 70 engaged and open-minded colleagues organised in 5 teams. It is our responsibility to handle product support for finished products in Biopharm and it is our job to support the productions in matters related to the process performance and product quality incl. stability. We maintain product specifications and regulatory documents, and we participate in transfer of products from Chemistry, Manufacturing and Control (CMC) to general production in Product Supply (PS) and between facilities.
The job
Your responsibility will be to create new documentation for our portfolio of products to ensure the required product quality is fulfilled and thereby, securing patient safety. You will write and review documentation defining specifications, stability, risk assessments, as well as regulatory submission documents to health authorities.
We have a lot of single-use in our production areas, so solid knowledge about materials and compatibility will be useful and tasks about compatibility will be part of the daily work.
All of this is conducted in cooperation with colleagues in our stability team, quality control (QC), quality assurance (QA), production, and regulatory affairs (RA).
An important part of the job is to identify opportunities for improvements in daily routines and general processes, where you will drive the improvement process and execute the implementation.
The position is temporary for two years, with the possibility of extension.
Qualifications
You are an experienced engineer, chemist or similar. You have a minimum of two years of experience from the pharmaceutical industry, and hence, you are used to work in accordance with GMP.
It is considered an advantage, if you have experience within the regulatory field. Knowledge with stability, aseptic production, compatibility, process validation and/or pharmacopeia requirements is preferable. You are professionally proficient in both written and spoken Danish and English.
As a person, you are responsible, dedicated and have open-minded approach and a solid quality mind-set. You have a positive approach to your job and thrive in a changing environment and with unexpected situations. You will work together with many different people, and therefore, it is important that you are able to motivate your colleagues and to at establishing good relationships.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambitions help us change lives for the better. In exchange, we offer unique possibilities for professional and scientific development in an informal working environment, and the chance to integrate into a dynamic team of highly qualified and enthusiastic colleagues.
We will interview candidates continually, as we receive the applications.
Contact
If you want to know more about the position, please contact
Anne-Mette Haahr +45 3079 8863 or Anders Malling Sørensen +45 3077 6524.
Deadline
8th Dec 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 "Kundeservicemedarbejder", og befinder sig i kategorien "Kontor, handel og service".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 21.11.2019, 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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