Facility & Equipment Validation Scientist

Are you motivated by finding ways through the jungle of GMP (Current Good Manufacturing Practice), Validation/qualification projects & securing delivery of vital medicine to patients? Would you like to be part of an excellent team where “together” and “having fun” are key essentials? Then you are on the way to a unique job as Validation Scientist at AGC Biologics in Søborg, greater Copenhagen.

Key responsibilities:

• Responsible for performing validation plans and protocols, compiling data and completing validation reports for late stage/commercial manufacturing.
• Oversight the different validation activities from planning, execution to completion
• Updating and optimizing current procedures when needed
• Report on progress and milestones to stakeholders

The position offers interaction with different stakeholders both from the site in CPH but also from talented colleagues around the global AGC network. You will be introduced to global biopharmaceutical companies and be an active player in their projects.

The department that will be looking forward to have you on board

You will be a part of the Facility & Equipment validation department, where currently 14 highly qualified team members are waiting for you. We share a fun/relaxed tone while at the same time have high ambitions to deliver best in class validation/qualification activities across the entire organization, to benefit our global biopharmaceutical costumers.

• Degree in e.g science, engineering, or the like (BSc or M.Sc.)
• Experience from implementing new equipment from a GxP environment, validation/qualification activities
• Experience with process validation or late stage biopharmaceutical programs would be seen as a plus
• Make things happen in a context of high complexity
• Excellent English language skills both verbally and written
• Good team player, open minded and result-orientated.
• Ability to effectively communicate with a broad audience of stakeholders

We will process the applications in the order they arrive. Therefore, please submit your application and CV as soon as possible, When the right candidates are found, the add will close. For any further questions, are you welcome to contact Jeppe Palm Beckmann on Jpbeckmann@agcbio.com Please be aware that we only take applications into consideration that are send via our career page.

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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.