(Senior) Analytical Coordinator
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Looking for an exciting opportunity to lead analytical method implementation for new products in a QC department? Novo Nordisk Pharmatech A/S in Køge has something for you! As a (Senior) Analytical Coordinator, you'll be responsible for setting direction, ensuring quality control of high-quality products, and coordinating with internal and external labs. If you have a strong foundation in planning and coordinating smaller projects and a passion for Quality Control processes, we want you to join our team!
Don't miss out on the chance to develop your skills while driving deliverables to success! Apply today for a life-changing opportunity! The position
As our new Analytical Coordinator, you will have the unique opportunity to play a major role in setting direction for our way of implementing analysis and analytical equipment on new products and existing products.
Your primary tasks will include: Participation in cross-functional projects as our representative for QC Securing that the impact on QC is identified in collaboration with your colleagues and management in QC Preparing project plans and coordinating with stakeholders across the organization Being responsible for securing effective transfer and implementation of analytical methods developed in our Manufacturing Development department to us in QC Securing implementation of analytical methods at external laboratories with regards to contracts and quality agreements This will give you a variety of challenges, and therefore, strong cross-functional collaboration with your colleagues will be essential. Qualifications
We are open to candidates with extensive experience, as well as to more junior ones. To be successful in this role, you should: Hold an academic degree in Chemistry, Pharmacy, Engineering, or another relevant field within the natural science. Have strong skills in communication and ability to motivate your colleagues with a positive, diplomatic, and forthcoming attitude Have demonstrated proficiency in defining scope, planning and coordinating smaller projects Knowledge within validation of analytical methods and qualification of analytical equipment is an advantage Be fluent in Danish (or another Scandinavian language) and English – oral and written As a person, you enjoy working in project groups and have a high level of energy to drive yourself and your colleagues forward to deliver on milestones. You work in a structured manner and find solutions that are robust and will ensure the correct quality level. About the department
We are 30 employees in the Quality Control unit organised in three teams, consisting of a Specialist, Professionals and Laboratory Technicians. It is a chemical QC laboratory with high complexity as we have many different analytical techniques such as HPLC, GC, LABX, ÄKTA, UV, Platereader, etc.
The laboratory is moving towards paperless documentation, and we are in the process of replacing our current LIMS solution. Working at Novo Nordisk Pharmatech A/S Novo Nordisk Pharmatech A/S (NNPR) is located in Køge, Denmark, and is 100% owned by Novo Nordisk. The company has close to 400 employees and the core task of the business is to enable better medicines through biopharmaceutical manufacturing for Novo Nordisk as well as for the global industry. NNPR is in the coming years expanding an already wide product portfolio within Enzymes, Synthetic Molecules, and Resins. The company has the full value chain with both R&D laboratories, production facilities, and a commercial organisation, plus a wide range of support departments on top. Contact
For further information please contact Manager Jeanette Eva Lylloff +45 31 97 00 34 or Senior Manager Lise Skjødt Pedersen +45 31 99 59 67. Deadline
11 March 2024.
Please, note that applications will be reviewed, and interviews scheduled on an ongoing basis, so we advise you to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
Don't miss out on the chance to develop your skills while driving deliverables to success! Apply today for a life-changing opportunity! The position
As our new Analytical Coordinator, you will have the unique opportunity to play a major role in setting direction for our way of implementing analysis and analytical equipment on new products and existing products.
Your primary tasks will include:
We are open to candidates with extensive experience, as well as to more junior ones. To be successful in this role, you should:
We are 30 employees in the Quality Control unit organised in three teams, consisting of a Specialist, Professionals and Laboratory Technicians. It is a chemical QC laboratory with high complexity as we have many different analytical techniques such as HPLC, GC, LABX, ÄKTA, UV, Platereader, etc.
The laboratory is moving towards paperless documentation, and we are in the process of replacing our current LIMS solution. Working at Novo Nordisk Pharmatech A/S Novo Nordisk Pharmatech A/S (NNPR) is located in Køge, Denmark, and is 100% owned by Novo Nordisk. The company has close to 400 employees and the core task of the business is to enable better medicines through biopharmaceutical manufacturing for Novo Nordisk as well as for the global industry. NNPR is in the coming years expanding an already wide product portfolio within Enzymes, Synthetic Molecules, and Resins. The company has the full value chain with both R&D laboratories, production facilities, and a commercial organisation, plus a wide range of support departments on top. Contact
For further information please contact Manager Jeanette Eva Lylloff +45 31 97 00 34 or Senior Manager Lise Skjødt Pedersen +45 31 99 59 67. Deadline
11 March 2024.
Please, note that applications will be reviewed, and interviews scheduled on an ongoing basis, so we advise you to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Køge.
Jobbet er oprettet på vores service den 9.1.2024, 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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- Køge
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