Technical Specialist, Qualification and Validation (GMP Compliance) | Technischer Mitarbeiter (m/w/d) Qualifizierung und Validierung, GMP-Compliance

Job Summary

As a Technical Specialist in Qualification and Validation, you will play a vital role in ensuring the highest quality standards within a pharmaceutical production environment. Your day-to-day responsibilities include performing qualification tasks for production equipment, cleanrooms, and computer systems, as well as executing process validations for sterilization, cleaning, and manufacturing processes. You will also participate in trial manufacturing and filling activities, draft technical documentation in compliance with GMP regulations, and contribute to process optimization. The ideal candidate possesses a technical or scientific background, such as a Pharmaceutical Technician, and brings practical experience in GMP-regulated manufacturing. This role is perfect for a detail-oriented professional who thrives in a collaborative, team-based environment. You will benefit from a secure position in a growing family-owned company, a structured onboarding process, and long-term career development opportunities within the pharmaceutical industry.