Senior QA Specialist

• As a member of the quality assurance team, you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP) 
• Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP 
• Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results
• In addition, you will be the quality contact for our clients, and will present during their GMP audits 

My Qualifications

• A degree in Life Science (microbiology, biotechnology, chemistry)
• Relevant experience in the biopharmaceutical industry, ideally in GMP area 
• Strong communication skills, experience in working with stakeholders from different departments
• Experience with TrackWise, SAP, LIMS and DMS is a plus
• Fluency in English (writing and speaking) is required for stakeholder communication, German skills on B1 level are required to interact with colleagues on a daily bases

My Benefits

• A highly motivated team and an open way of communication
• A very renowned company

About Hays

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.