Black Swans Exist | Recruiting talents for life science companies 

You want… 

To put your validation engineering expertise to work in a high-impact role where your contribution directly helps in improving lives. You are excited by the challenge of shaping the next generation of medical mechanical equipment, using your meticulous attention to detail to drive quality and reliability. You thrive in environments that offer complex problem-solving opportunities and value your ability to improve systems through your knowledge of GMP. 

You will… 

Oversee validation activities in medical equipment, pharmaceutical, and biotechnological processes. Conduct risk assessments using methods such as FMEA, while ensuring regulatory compliance and preparing validation documentation. Monitor and supervise audits and inspections from regulatory authorities. Implement and work with equipment and process validation, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). 

You’ll join… 

A dynamic company at the forefront of innovation in medical technology. This company collaborates closely with partners to develop and validate the next generation of products and processes. They pride themselves on their innovative and reliable solutions that place strong emphasis on customer needs, dependability, and quality. Their unique drug candidate promises to revolutionize patient health and treatment economy, providing a solution that targets both active and latent infection cells. 

You have… 

• A Master’s or Bachelor’s degree in engineering or a similar field. 
• Over 5 years of experience in validation of production or process plants. 
• Proficiency in both Danish and English. 
• IT competence, specifically with Microsoft Office Suite and typical file exchange platforms. 
• Excellent analytical skills and attention to detail. 
• The ability to work both independently and as part of a team.