Your tasks

• Creation of GMP-compliant SOPs and risk analyses in German and English
• Participation in the qualification and documentation of pharmaceutical facilities and equipment
• Verification of facilities and processes for GMP compliance
• Coordination and organization of measures for maintenance, calibration and qualification
• Review of technical documentation for changes and deviations
• Support with change control and deviations

This is what you bring with you

• Degree in process engineering, pharmaceutical engineering, biotechnology, chemical engineering, life sciences engineering, mechanical engineering or a comparable engineering or natural science degree
• Basic knowledge of GMP or quality assurance is advantageous, but not necessary.
• Willingness to undertake longer customer assignments (Class B driving license required) and enjoyment of learning through practical experience
• Excellent German skills and good English skills

We offer this

• Entry into the GMP world with a comprehensive training concept
• Onboarding with top hardware and a mentoring program
• Modern and dynamic work environment with an informal, first-name basis culture from day one.
• Flexible working hours in a flexitime model, 30 days of vacation and a permanent employment contract on top of that.
• Social benefits such as company pension schemes, capital-forming benefits and supplementary health insurance
• Bike leasing, corporate events