Role: GMP Senior Quality Auditor Location: Hybrid, Saxony-Anhalt, Germany Company: Global Life Sciences Company As a GMP Senior Quality Auditor in our newly formed Quality Auditing team, you will lead the supplier qualification process and manage initiatives to complete requirements audits, including on-site supplier audits. Core responsibilities will include the following activities: Performing and processing supplier quality requirements audits and supplier reassessments in collaboration with the QA department Developing audit evaluation strategies and logistics, identifying weaknesses, ineffective procedures, policy exceptions and discrepancies, and recommending appropriate corrective actions Evaluate supplier responses to corrective and preventive actions related to audit findings Assist in the review of supplier requirements by obtaining quality requirements and obtaining solutions for areas identified as compliance issues Collaborate with the purchasing and quality control teams to ensure supplier requirements are met Subject matter expert during customer audits, internal audits and/or regulatory inspections Conduct training for other team members as needed Qualifications: Degree in science or engineering with several years of professional experience in quality, manufacturing or engineering GMP Auditing experience Experience in the pharmaceutical, medical device, combination product and/or biologics industry desirable Experience in auditing production facilities and laboratories IT skills in Microsoft Office and eQMS software (TrackWise, JDE, Veeva, etc.) ASQ, ISO and/or RAB auditor certification desirable Knowledge of pharmaceutical regulations and international standards for aseptic manufacturing as well as project management skills Ability to work in a team, strong interpersonal skills and excellent communication skills in German and English