Projektingenieur (m/w/d) Qualifizierung und Validierung Pharma

As a Project Engineer (m/w/d) Qualification and Validation of Pharmaceuticals, you will support our team in the Rhine-Main region in the qualification and validation of equipment and systems according to GMP regulations in the pharmaceutical industry. You will work on various projects in the GMP-regulated environment, creating self-responsible test documents, carrying out tests and measurement activities, and supporting project management and customers on site.

Requirements

• Bachelor's degree in chemistry, pharmaceutical technology, biotechnology, process engineering, or a comparable natural science subject
• Experience in the pharmaceutical / medical technology industry (ideally)
• Knowledge of the qualification of machines and equipment according to GMP regulations (ideally)
• Good German language skills on a native speaker level
• Safe handling of MS Office

Benefits

• Integrated compensation package with holiday pay, annual special payments, and employer contributions to occupational old-age provision
• Flexible working hours with a working time account
• 30 days of annual leave + December 24th and 31st paid leave
• Employee referral program with bonus payments up to €1000.00 per successful hiring
• Personal work clothing and protective equipment (including tools) provided and cleaned by the company
• Professional further education opportunities
• Discounts on various products and services (e.g. travel, leasing vehicles, or technology)
• Training at special conditions in fitness studios