Job Detail

Your Assignment

•  Manage and maintain all Quality Systems consistent with regulatory requirements and industry best practices (GMP/GLP/GCP/ISO 17025)


• Responsibility for CAPA Management as well as for Deviation/Change/OOS Management


• Preparation, execution and follow-up of self-inspections, customer audits and inspections by health authorities (e.g. Swissmedic, US FDA)


• Review and approval of analytical data and reports


• Training of employees and daily support


• Work on complex problems that involve staff outside of QA as well as clients


• Performance of Computer System Validations


• Represent QA function in global company setting

Your Profile

•  PhD in natural science e.g. biochemistry, biology, pharmacy, etc.


• Direct Experience leading GMP and/or GLP/GCP Quality Systems including development, implementation, and continuous improvement (at least 5 years)


• Previous responsibility as Qualified Person is an Advantage


• Analytical knowledge in drug development of pharmaceuticals and biologics


• Strong leadership, open minded and professional communication skills


• Management experience, including the ability to effectively manage staff and multiple tasks utilizing organization and prioritization skills and driven to meet timelines


• Good knowledge in computer literacy and proficiency in German and English

We offer

•  A versatile and ambitious spectrum of fascinating tasks


• A motivated and dynamic team in a professional working atmosphere


• A rewarding, dynamic and challenging work experience


• 40 hours week and 5 weeks of vacation


• Participation in qualification and on-the-job training


• State-of-the-art Technologies

Your Contact
For further information, please contact: Tel. +41 58 400 1900 or www.synlab.com.

We are happy to receive your complete application with photo and reference No. 1633 to: SYNLAB Analytics & Services Switzerland AG, Personalabteilung, Sternenfeldstrasse 14, CH-4127 Birsfelden (BL) or via e-mail to as.birsfelden.info@synlab.com