Our client is a professional Pharmaceutical organisation, based in Netherlands. This company has a particular focus in commercial manufacturing within an cGMP environment.
There are facilities available such as inhouse QA and QC
You will be responsible for making sure that every operation of and every decision made regarding the QA department is in line with all regulations within the Netherlands, the relevant authorities and EMA.
Furthermore it it your responsibility to maintain the the good image of the company towards our customers and authorities, thereby maintaining the companies cGMP compliance.
Maintain and manage the resources within the QA group.
Responsible for hiring within your particular departments
Arrange that objectives related tot site manages are in line with the objectives of your team
Discuss and initiates career development and training of QA staff.
Responsible for setting up structures in terms of roles, responsibilities and competency profiles for QA staff
Setting up projects together with the project manager, thereby making full use of attributes and resources available.
Setting KPI's and follow up every three months with the QA Team
Reports regularly to Site Manager on all relevant matters.
Minimum 15 years’ experience working in biological or pharmaceutical industry
Minimum 10 years’ experience managing / leading a Quality / Manufacturing team / unit
Preferable certification as qualified person .
Thorough understanding of pharmaceutical industry
Knowledgeable in the manufacturing science and monoclonal antibodies
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.