Project Engineer

Who are we? 

eyetec is an innovative and dynamic company based in Tielen, with both a national and international customer base and global operations. We are a recognized player in the field of pharmaceutical equipment and continue to expand our market share. 

At eyetec, we are a small but growing team of curious professionals who take pride in their work while valuing collaboration and team spirit. We work independently and flexibly, built on mutual trust. Because we believe that strong teams thrive on connection, we also make room for fun and a genuine sense of belonging. 

Are you passionate about pharmaceutical technology and eager to make an impact in a fast-growing company? Then you might be the person we are looking for. 

What will you do as a Project Engineer? 

As a Project Engineer, you will be involved in projects within the pharmaceutical industry. Your main responsibility is to ensure that projects and project activities such as machine testing are delivered on time, within budget and according to scope. 

You will work directly with pharmaceutical clients, your colleagues of the VI/CCIT (Visual Inspection/Container Closure Integrity Testing) consultancy team and you will be responsible for managing all deliverables related to your assigned projects. 

Your main tasks include: 

• Participating in projects involving both new and existing machines 
• Planning, coordinating and executing project activities from the tender phase through to production release 
• Preparing business cases 
• Drafting or reviewing user and system requirements 
• Developing risk analyses and test protocols 
• Reviewing designs, design documents and technical evaluations 
• Managing project budgets 
• Monitoring installation, engineering, qualification and validation activities 
• Qualifying systems within a GMP (Good Manufacturing Practice) environment 
• Collaborating with various stakeholders at client sites, including production, technical services, quality and engineering departments 

What we expect from you 

You hold a Professional Bachelor’s or Industrial Engineer or Master’s degree in electromechanics, electronics, chemistry, automation or equivalent experience. If you hold a different degree but believe you are a good fit, please explain your motivation in your cover letter. 

Ideally, you already have experience in project engineering within a GMP environment. However, if you are new to GMP or automatic visual inspection machines, you will receive comprehensive training in the relevant processes and technologies as well as pharmaceutical legislation such as Good Manufacturing Practice. 

Experience with GMP environments, troubleshooting and knowledge of vision systems, autoclaves, washing machines and measurement or control systems is a plus. 

You have strong communication skills and are fluent in English. Basic French is a plus. 

You are punctual, proactive, well-organized and structured in your work. 

You have excellent technical writing skills and a strong analytical mindset that allows you to identify and implement cost-effective technical solutions. 

Working in a regulated GMP environment suits you and you follow client procedures precisely and consistently. 

Above all, you are eager to grow with a rapidly expanding company and deepen your expertise in technology and project engineering. You bring a flexible and customer-oriented attitude and a passion for continuous improvement. 

What we offer 

• The opportunity to grow within a young and passionate company 
• A chance to develop your technical and project management skills in a high-tech environment 
• A flexible working model, with the option to work from home part of the time 
• Projects mainly with customers in Belgium, and occasionally in Germany, Italy and Switzerland 
• Collaboration with suppliers primarily based in Germany and Italy 
• An international scope, with approximately 20 percent of your time spent abroad 

Place of work 

Our office is located at Kemelbeekstraat 80D, 2460 Tielen (Belgium).