Develop and maintain a GMP state of the art laboratories for Chemical & Biochemical analytics
Ensuring test and results in the area of : Analytics for utilities monitoring, Raw material analytics and Drug substance / Intermediate release
Supporting QC Head for budgeting
Ensuring that the laboratories are audit ready at all times
Consistent and timely investigation of OOE / OOS-results and laboratories deviations
Proper management of procedural documents
Any steps from the requirement of new equipment to calibration and monitoring
Collaboration in resolution of technical problems or questions
Support internal QC / QM projects and other QC departments
Procurement and control of reference and control material
Recruitment of employees on the basis of an accurate analysis of skills
Promotes and executes a KPI driven management approach
Masters Degree or higher in Chemistry or Life Sciences (Chemistry, Biochemistry, Biology etc.)
Minimum 7 years experience in pharmaceutical quality control and more than 10 in GMP regulated industry
Experience in people management as a team leader or in a deputy team leader role, so you would be able to strengthen and develop your team while maintaining an external and strategic focus
Proven experience and knowledge in analytical QC methods, method development, validation and analytical issue management, as well as experience in technology and qualification of analytical instruments
Good knowledge of German and business fluent English are required
A very reputable company
About Hays With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential.
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