As a Validation Engineer, you will work in a pharmaceutical manufacturing environment with a focus on sterilisation validations, equipment qualification, and quality system compliance.

Responsibilities

• Steam-In-Place (SIP) process validations for Blow-Fill-Seal (BFS) machines and tanks
• Validation of heat sterilisation processes for polymer components
• Maintenance of production equipment and utility qualifications
• Small equipment qualifications
• Risk assessments and technical change management
• Participation in projects as the validation representative

Qualifications

• Bachelor’s or Master’s degree in Engineering
• Independent and proactive working style
• Experience in the pharmaceutical industry, validation and qualification activities
• Knowledge of quality systems and standards (ISO 9000, GMP)
• Customer-oriented mindset
• Fluent written ...