Process Engineer

Are you motivated to contribute in a global multidisciplinary engineering environment that fosters continuous professional growth? Help build our new division at a dedicated site a completely new end‑to‑end facility for powder filling and packaging, compliant with EU‑GMP and FDA regulations. Join us at our Boxmeer Animal Health Manufacturing site as a Process Engineer.

About the Role
In this dynamic position you are responsible for challenging technology projects to support manufacturing of Boxmeer Small molecule products as well as supporting and leading global (strategic) projects and activities. The majority of these projects will concentrate around sterile suspended pharmaceuticals. The first years, this role will be focused on the technology transfer(s).

You will be challenged to (further) develop as a Subject Matter Expert in the area of pharmaceutical production processes. In this position you will gain knowledge of powder filling, (sterile) manufacturing and the associated requirements including raw material, equipment and process changes and analytics. As Process Engineer you will lead root cause investigations of major manufacturing or quality issues, projects for continuous improvement and technology transfer.

You will have to connect to suppliers, contract manufacturers and external laboratories, including occasional external visits across Europe.

Primary Responsibilities

Managing and contributing to end‑to‑end technical projects at the Boxmeer site, including API, packaging and process‑related changes, and leading / contributing to cross‑functional teams for the submission, approval and implementation of these efforts.

Collaborate with Manufacturing (sites), Quality, Engineering, Supply Chain, Regulatory Affairs, Pharma R&D, Procurement and Contract Manufacturing Organizations.

Serve as a troubleshooter for technical issues and challenges in the manufacturing environment.

Lead and contribute to the introduction of new technology platforms.

Provide in‑line product support and implement productivity initiatives through scientific rigor and appropriate technical expertise.

Support regulatory inspections for PTS‑owned GMP systems.

Engage in knowledge management, communities of practice, virtual technical networks and best practice sharing.

Your profile

Master or Ph.D. degree in Science (Bio) process technology or Pharmaceutical technology.

3–7 years of experience in a technology or manufacturing position.

Experienced as a project manager, connecting multidisciplinary teams and supporting individual activities and interactions.

Experience with GMP, powder handling and filling, Lean Six Sigma and statistics are assets.

Ability to go deep in a project but also handle multiple projects at the same time.

Excellent communication skills in English and Dutch are required.

What We Offer

A competitive salary, depending on your knowledge and experience.

A 3 % year‑end allowance and an annual bonus based on individual and company performance.

A minimum of 35.5 days of paid leave.

Travel expense reimbursement and a solid pension plan.

A high‑quality company restaurant offering fresh and healthy options daily.

Excellent accessibility; the train station is located directly at the main entrance and ample parking is available.

A beautiful private park on site, ideal for walking, taking a break or relaxing.

Mental wellbeing support via Lyra Health for you and your family members.

Access to a dedicated prayer/meditation room.

Extensive career development opportunities thanks to the size of the site and the presence of many disciplines and global departments represented in Boxmeer.

A workplace within an organization that continues to grow and evolve.

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