Validierungs-Spezialist (m/w/d) CSV

We are a subsidiary of Syntegon Technology GmbH offering services for the GMP environment to manufacturers of innovative therapies. We are looking for a Validation Specialist (m/w/d) to work on computerized system validation (CSV) projects.

Requirements

• Completed university degree in engineering sciences or natural sciences
• At least 2 years of experience in the pharmaceutical industry in CSV and IT validation
• In-depth knowledge of GMP requirements and EU GMP Guide
• Very good knowledge of MS Office
• Fundamental and negotiation-secure English skills
• Very good German skills (C1 or better)
• Good team skills, analytical approach, high communication skills, willingness to travel

Benefits

• Market-average remuneration
• Performance-related bonus model
• Flexibility of a small company and stability of a large parent company
• Own design scope and network care
• Opportunities for profile and further development