*Director, QC Chemistry

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Are you passionate about serving a range of customers and help supply life changing medicines...? and do you want to be part of building a brand new factory with state of the art laboratories? Then join a dynamic and international company that produces new biological medicines and where everyone is responsible for delivering right on time as one team.

We are looking for a skilled Director to lead our Chemistry department within Quality Control.

About the department

With reference to the head of QC you will join an area consisting of 5 departments and 160 dedicated colleagues. The departments are QC Chemistry ,QC Microbiology, QC Bioassay, QC Support and QC Planning & Systems. We are responsible for method validations for early and late stage products, release analysis of clinical batches as well as commercial and not least analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.

The job

To succeed in the job, you thrive in a fast-paced environment. You have a strong desire to motivate employees and ensure that your department is continuously improving while cooperate widely across the organization. You naturally create a positive and inspiring environment around you and lead by being the good example.

You will lead managers for scientists and technicians and your working day is characterized by ongoing collaborations with stakeholders such as customers, project managers, business development, QC departments and analytical development.

The main responsibilities are

Along with your department you will manage the QC chemical aspect of customer projects, identify, and manage the analytical packages needed for the projects. You will use your expertise to motivate, challenge and guide your employees to be a high performing quality control team and together with the other QC leaders ensuring overview of the work to come. You will play a large part in the quality control of our existing production lines and establishment of a new production facility and labs. In relation to this, your responsibilities involve:

  • Ensuring cGMP compliance with relevant guidelines (EU, FDA)
  • Managing analytical validation projects in close cooperation with Analytical Development, PM, QC colleagues and customers
  • Ensure timely deliveries on release and stability testing
  • Continuously improve QC systems and processes
  • Provide leadership and guidance to the QC chemistry team during customer audits and regulatory inspections

Proactive leader
To be successful, it is important that you have the necessary management skills to drive a first-class QC department. You approach your tasks with an open mind and enjoy problem solving along with many different stakeholders, and you are flexible in regards to working hours to meet business objectives.

More specifically, you have:

  • An academic degree or PhD (preferably in life science)
  • 5+ years of relevant experience in the pharmaceutical or biopharmaceutical industry
  • 7+ years of management experience
  • Sound knowledge of chromatographic methods and cGMP
  • The ability to communicate clearly in English – both in speech and writing
  • Demonstrated experience in driving continuous improvement and/or productivity programs

AGC offers
AGC Biologics offers a dynamic working place and an excellent opportunity for working and growing with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a biologics contract development and manufacturing organization interact in order to achieve success. AGC Biologics offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC employees have a flexible attitude and we help each other to reach deadlines together as one team, in accordance with our slogan - Right. On Time.

Application
Submit your application as soon as possible. We treat the applications as we receive then, and conduct interviews with qualified candidates. When the right candidates are found, the add will close.

For further information regarding the position, please contact Martin Faxoe, Senior Director QC, at +45 5387 9153.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

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

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 22.12.2022, 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
  • København
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