Experienced Chemist within API production and with EM knowledge - Professional

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Gentofte

  • Manufacturing
  • Gentofte

Are you looking for an opportunity to work in Biopharm Manufacturing Development? and do you have a desire to use your API production knowledge and project management skills and are you eager to develop your competences within aseptics and environmental monitoring (EM) even further? If so, we offer you the opportunity to be MDev EM API Process responsible in Biopharm. You will become part of a high performing team in Novo Nordisk Biopharm Manufacturing Development working with manufacturing development, implementing new technologies and providing support to Biopharm’s Production sites in Gentofte, Hillerød, Måløv, Kalundborg and New Hampshire.

About the department

The department Biopharm Finished Product Manufacturing Development employs approximately 70 engaged and open-minded colleagues organised in 5 teams. The team you will be a part of consists of 12 people. Our focus is the optimization of our supporting processes (EM, cleaning, sterilisation, utility, HVAC and metrology) and providing of excellent support to Biopharm’s Production departments (AP, FP, API). Members of the team are PGR’s or PGR-leads across PS, PM’s and specialist or chemist within their main processes. In our team responsibility, challenges and development goes hand in hand.

The position
As an Environmental chemist within the API area your core competences are within the API manufacturing process and environmental monitoring. You will be MDev process responsible for EM API and you will be responsible for hosting PG meetings and providing general support. You will therefore be in close dialog and coordination with lead-PGR for environmental monitoring in PS who is part of the team. On a daily basis you will be involved in taking crucial decisions within the EM area across API productions in Biopharm and you need to have the ability to solve complex issues in the production. To a very large extent, your success depends on your ability to collaborate, to communicate in a transparent way and to teach your colleges. You will also be involved in aspects of project management within the EM area including handling of compliance signals. Knowledge within the compliance signals process and GxP experience related to writing different kinds of documents and SOP’s will be needed. You will have a broad range of contacts, e.g. with Biopharm’s API production departments, QA, QC and process responsible across PS.

Your tasks will include the following: MDev Process responsible for EM API in Biopharm, hosting EM API process group meetings in Biopharm, handling of compliance signals in Biopharm across PS, support and troubleshoot at our API production sites and ensure that better practices are identified and shared across the sites and updating/writing corporate documents and SOPs

Qualifications
You hold a MSc in Microbiology/Chemical/Pharmacy/Engineer or similar. You have at least 2-3 years of professional experience from working in an API production facility preferable in Biopharm. You have knowledge related to the environmental monitoring requirements and guidelines related to the API production. Your hands-on experience has sharpened your already good communication and project management skills. You have knowledge within handling of compliance signals and great GxP experience related to writing different kind of documents and SOPs.

You are highly skilled at communicating at all organisational levels - with operators, managers and specialists - verbally as well as in writing. Finally, you are fluent in both Danish and English.

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 Merete Ørting at +45 30752305 or Anja Bagger +45 30758044.

Please send your application as soon possible. We will be reading applications and conducting job interviews continuously. Deadline 30 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 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 "Laborant", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Gentofte.

Jobbet er oprettet på vores service den 12.12.2019, 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.
  • Laborant
  • Gentofte
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