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