QA Specialist – Batch Record Review (m/f/d)

Für unseren Kunden in Ludwigshafen suchen wir zum nächstmöglichen Zeitpunkt QA Specialist – Batch Record Review (m/f/d) Job Responsibilities: - GMP-compliant and timely review of batch records and manufacturing documentation - Quality review of production, packaging and QC documents to support batch release decisions by the Qualified Person - Documentation review for finished medicinal products, semi-finished goods, bulk products and intermediates - Processing of inspection lots, data maintenance and research in SAP and other quality management systems - Preparation, uploading and archiving of certificates and batch documentation - Support in reviewing and updating SOPs, forms and templates Requirements: - Bachelor's degree in natural sciences or completed vocational training in a comparable technical, pharmaceutical or scientific field - At least 2 years of relevant professional experience, preferably in the pharmaceutical industry - Very good GMP knowledge and a strong understanding of regulatory documentation requirements - Proficiency in MS Office; knowledge of SAP and quality management systems is an advantage - Fluent German and good English communication skills, both written and spoken - Structured, accurate and independent working style with a strong sense of quality, teamwork and resilience Our Benefits: - Remuneration in accordance with the GVP collective bargaining agreement - Assignment-related allowances may apply - Holiday and Christmas bonuses - Optional working time account, with hours recorded from the 41st working - hour per week - Long-term assignments – no day-to-day placements - Subsidy for the Deutschlandticket (German public transport pass) - Opportunity for permanent employment with our clients - Dedicated support and career development guidance