Senior Process Improvement Engineer

Senior Process Improvement Engineer

Pharmaceutical Manufacturing & Global Supply Chain

About the Site

This site plays a critical role as a global pharmaceutical packaging and supply chain hub. Activities include labeling, secondary packaging, warehousing, and worldwide distribution of medicines. The location supports a diverse workforce across supply chain operations, manufacturing, and clinical research, operating within a highly regulated environment.

Role Summary

As a Senior Process Improvement Engineer, you will be part of the Operations Excellence organization, driving performance improvements across labeling and packaging operations. You will use data-driven insights to monitor process performance, identify inefficiencies, and lead continuous improvement initiatives across both shopfloor and supporting functions.

Key Responsibilities

• Analyze and interpret complex datasets from multiple sources to assess process performance and identify trends or deviations

• Continuously monitor operational KPIs and proactively identify improvement opportunities

• Ensure ongoing compliance with GMP, safety, quality, technical, and regulatory standards by evaluating process changes and risks

• Convert stakeholder needs into structured improvement initiatives using LEAN and Six Sigma methodologies

• Lead and deliver selected process improvement and engineering projects from concept through implementation

• Provide operational expertise and advanced analysis to support senior leadership decision-making, particularly for long-term or strategic initiatives

• Improve data collection, performance monitoring, analysis, and visualization practices

• Coach and support shopfloor change leaders and cross-functional teams in continuous improvement practices

Required Qualifications (Non-Negotiable)

• Bachelor’s or Master’s degree in Industrial Engineering, or equivalent experience

• Proven experience in process improvement, industrial engineering, operational excellence, or performance improvement within manufacturing or operations

• Demonstrated ability to work effectively in a highly regulated environment (GMP / GDP)

• Strong analytical thinking and problem-solving capabilities

• Fluent in English, both written and spoken

Essential Experience & Skills

• Experience optimizing internal value streams and end-to-end operational processes

• Proven track record of leading improvement or engineering projects

• Hands-on experience with structured problem-solving methodologies (e.g. Six Sigma, Root Cause Analysis)

• Strong stakeholder management skills with the ability to collaborate cross-functionally

• Advanced data analysis capabilities and experience using digital and analytical tools

Preferred Qualifications

• Background in pharmaceutical, biotech, or medical device manufacturing

• Six Sigma certification (Green Belt or higher)

• Experience contributing to strategic initiatives such as capacity expansion or new product introductions

Practical Details

• Location: Breda, The Netherlands

• Work Model: Hybrid (minimum 3 days on site per week)

• Start Date: ASAP