ppFor one of our clients, we are currently looking for a bQuality Auditor (m/w/d) /b to join the Global Development Quality Operations (GDQ OPS) team. /ppThis Specialist-level position plays a key role in supporting quality and compliance activities at the Schachen site. As part of the Global Development Quality Operations team, you will contribute to maintaining and improving GMP compliance by supporting cross-functional projects, quality system enhancements, compliance monitoring, SOP management, and quality initiatives. You will work closely with manufacturing and quality stakeholders to ensure that products, processes, and documentation meet the highest regulatory and quality standards. /ph3Your Responsibilities /h3ulliSupport the release or rejection of GMP materials and components through batch release activities and participation in critical quality-related investigations and programs. /liliPerform reviews of GMP documentation, electronic systems, batch records, and other quality-related records in accordance with Quality Operations requirements. /liliEnsure all activities are conducted in compliance with cGMP regulations, internal procedures, and quality standards. /liliSupport quality system processes, compliance monitoring activities, and continuous improvement initiatives. /liliCollaborate with cross-functional teams to maintain inspection readiness and support quality-related projects. /li /ulh3Your Profile: /h3ulliBachelor's or Master's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, Engineering, Quality Management, or a related field. /liliInitial experience in Quality Assurance, Quality Operations, or a GMP-regulated environment (pharmaceutical, biotech, or medical device industry). /liliBasic understanding of cGMP requirements, quality systems, and manufacturing processes. /liliExperience reviewing GMP documentation, batch records, deviations, or change controls is an advantage. /liliStrong organizational skills, attention to detail, and the ability to manage multiple priorities. /liliProactive and collaborative approach to problem-solving and continuous improvement. /liliFluent German and English language skills (minimum C1 level, written and spoken). /li /ulh3What We Offer /h3ulliAn opportunity to work in a highly regulated and innovative biopharmaceutical environment. /liliExposure to global quality processes and cross-functional collaboration. /liliA dynamic team culture with opportunities for professional growth and development. /liliHybrid work model. The candidate is expecting to be at minimum 3 days per week on site and might increase depending on business needs. /liliLocation: Schachen /liliContract duration: This is a 12-month contract position, planned to start in September, with the possibility of extension. /liliType of employment: Temporary staffing /liliLatest start entry date that can be considered is 01 October 2026 /li /ul /p #J-18808-Ljbffr
Quality Auditor (m/w/d)
