Quality Engineer

Your Job

Be part of a collaborative and professional workplace where you can make a meaningful impact on patient lives globally, contributing to audits, projects, and continuous improvement initiatives with a real influence on quality outcomes.

Our Team

As part of our Quality Team in Struer, you will work across projects and daily operations to ensure compliance, support manufacturing, and drive continuous improvement within a regulated medical device environment.

What You Will Do

• Support the setup, planning, and introduction of new products into production in collaboration with development teams
• Perform batch release activities in compliance with regulatory requirements and our Quality Management System
• Support manufacturing by ensuring effective in-process, incoming, and outgoing quality control
• Implement customer-specific quality requirements within production processes
• Identify and implement process improvements, including optimisation within SAP
• Drive deviations and CAPAs in collaboration with cross-functional teams
• Partner with customers to review quality agreements and participate in regular quality and project discussions
• Contribute to continuous improvement initiatives to enhance compliance, efficiency, and product quality outcomes

Who You Are (Basic Qualifications)

• Bachelor’s degree in engineering or a related field
• Understanding of product development processes and quality requirements
• Strong knowledge of quality documentation standards and compliance practices
• Ability to collaborate effectively across functions in a professional environment
• Proactive mindset with the ability to identify and drive improvement opportunities
• Strong communication skills in English
• Experience working with SAP and MS Office

What Will Put You Ahead

• Strong sense of ownership with a proven ability to deliver results
• Ability to balance compliance requirements with a pragmatic business mindset
• Recognition that quality is built into processes, products, and everyday actions
• Audit experience

What We Offer

A collaborative and professional workplace where you can make a meaningful impact on patients' lives globally. This role provides the opportunity to work across audits, projects, and continuous improvement initiatives with real influence on quality outcomes.

If you are passionate about quality, process excellence, and medical device compliance, and you thrive in an environment where no two days are the same, we would like to hear from you.

At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.

Who We Are

Phillips Medisize, a Molex company, collaborates with industry leaders to design and manufacture drug delivery systems, medical devices and diagnostic tools that save and improve the quality of life for millions of patients annually. With our dedicated team of 6,000+ employees in 29 locations around the world, we share our customers’ mindset that every product is critical to a healthcare provider and their patients somewhere in the world. Molex is a multi-sector global electronics brand owned by Koch, Inc., one of the world’s largest privately held companies. Discover your potential to make a difference.

At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.

Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.