Responsibility for leading and executing qualification activities in projects and operational engineering
Preparation of qualification documentation in compliance with internal and regulatory requirements
Maintenance of established processes and presentation during audits
Active presentation of the work performed during inspections
Requirements
Degree (University/University of Applied Sciences) in a technical discipline
At least 5 years' practical experience in planning, commissioning or operation of production facilities in pharmaceutical, chemical or biotechnological environments
Familiarity with operational engineering and capital investment projects
Strong interpersonal skills, team player, and excellent communication and coordination abilities
Practical experience implementing technical GMP requirements of regulatory authorities