QA Operations Specialist (GMP Review & Compliance)

• Renowned pharmaceutical company • Start immediately // 2 year contract // Hybrid in Schachen (60=on site/40=remote) About Our Client ## Renowned pharmaceutical company Job Description ## • Review and evaluation of GMP-relevant documents, records, and quality systems • Support in the release or blocking of GMP materials and components • Participation in quality-relevant projects and compliance initiatives • Ensuring compliance with GMP guidelines and internal quality standards • Support in the further development of quality processes and quality systems • Participation in the creation, review, and maintenance of SOPs and quality documentation • Analysis and processing of quality-relevant issues in the operational environment • Close cooperation with interdisciplinary teams within production, quality, and supply chain • Ensuring high data integrity as well as correct GMP documentation The Successful Applicant ## • Completed studies (Bachelor or higher) in pharmacy, biology, chemistry, biotechnology, life sciences, or a comparable field • Language requirements: German and English business fluent • Alternatively, a technical or scientific education with relevant professional experience in a GMP environment • Initial professional experience in the area of Quality Assurance, Quality Operations, or GMP documentation review • Experience in a regulated environment of pharma or biotech • Good knowledge of GMP guidelines and quality standards • Experience with electronic quality systems (e.g., SAP, TrackWise, Veeva, MES, or comparable systems) is an advantage • High affinity for document review, compliance, and quality processes What's on Offer ## Interested in the next career step? I look forward to your application. Quote job ref JN-082026-7088256 Job Function Engineering & Manufacturing Specialisation Quality Industry Healthcare / Pharmaceutical Where Lucerne Contract Type Interim Job Reference JN-082026-7088256