Process engineer

Blue Medical Devices B.V. a Translumina Company; Helmond; On-site; EUR 60,000 - 80,000; Full time

Benefits offered by this job

Salary €60,000–€80,000 per year

28 vacation days

Pension scheme

Education budget & training

Relocation allowance

Canteen

Job summary

Blue Medical Devices is seeking an experienced Mid-Level / Senior Process Engineer to analyse, improve and future-proof production processes within a highly regulated medical-device manufacturing environment. You will improve process performance, product quality, reliability and efficiency, translating production data, deviations and technical challenges into robust, validated processes.

You will work closely with Production, Engineering, R&D, QA/RA, QC and international colleagues within our

Qualifications

• 8+ years of relevant experience as Process/Manufacturing Engineer or similar
• Senior level: 6+ years on complex projects
• Experience with process development, optimization and validation
• Experience with CAPA, FMEA, risk management and change control
• Knowledge of ISO 13485, MDR or similar standards
• Willingness to work on-site in Helmond and on full-time basis
• Strong analytical mindset and structured approach

Responsibilities

• Analyse and improve production processes, yield, OEE and KPIs
• Identify bottlenecks, risks and deviations and implement solutions
• Perform root cause analyses, impact assessments, CAPAs and risk analyses
• Develop, optimise and embed production processes
• Prepare validation protocols, reports and work instructions
• Manage change controls and assess changes to processes, tooling and materials
• Contribute to risk assessments and verification of risk-control measures
• Support transfer of new or modified processes and technologies
• Plan and lead improvement projects and subprojects
• Perform statistical analyses and translate data into actions
• Provide technical advice to Production, Quality and other stakeholders
• Document and transfer knowledge through training

Skills

Process improvement

Root cause analysis

Statistical methods

Quality Management System

English proficiency

Dutch learning willingness

Education

Bachelor’s or Master’s degree in a technical discipline

Tools

Minitab

Job description

Blue Medical Devices is looking for an experienced Mid-Level / Senior Process Engineer who can analyse, improve and future-proof production processes within a highly regulated medical-device manufacturing environment.

You will improve process performance, product quality, reliability and efficiency. You translate production data, deviations and technical challenges into structural improvements and robust, validated processes.

You will work closely with Production, Engineering, R&D, QA/RA, QC and international colleagues within our parent company.

Your responsibilities

• Analyse and improve production processes, yield, OEE, KPIs and process data.
• Identify bottlenecks, risks and process deviations and implement structural solutions.
• Perform root cause analyses, impact assessments, CAPAs and risk analyses.
• Develop, optimise and embed new and existing production processes.
• Prepare, execute and maintain process validations.
• Prepare validation protocols, reports, work instructions and other technical documentation.
• Manage change controls and assess and implement changes to processes, tooling and materials.
• Contribute to process risk assessments and the verification of risk-control measures.
• Support the transfer of new or modified processes and technologies into Operations.
• Plan and execute improvement projects and subprojects and, depending on experience, lead them independently.
• Perform statistical analyses and translate process data into practical improvement actions.
• Provide solicited and unsolicited technical advice to Production, Quality and other stakeholders.
• Document, share and transfer knowledge through training and coaching.

What we are looking for

• At least 8 years of relevant experience as a Process Engineer, Manufacturing Engineer or in a comparable technical position.
• For the senior level, typically more than six years of relevant experience and demonstrable experience with complex projects.
• A completed bachelor’s or master’s degree in a technical discipline.
• Experience with process development, process optimisation and problem-solving within a manufacturing environment.
• Experience with process validation and preparing validation protocols and reports.
• Knowledge of root cause analysis, CAPA, FMEA, risk management and change control.
• Experience analysing process data, applying statistical methods and translating results into improvements.
• Experience working within a Quality Management System and according to controlled procedures.
• The ability to set priorities independently, take ownership and implement improvements successfully.
• Good command of English, both written and spoken.
• Good command of Dutch, or a genuine willingness to learn the language.
• Full-time availability and the willingness to work on-site in Helmond.

Preferred:

• Experience within medical devices, pharmaceuticals, hightech or another highly regulated manufacturing environment.
• Knowledge of ISO 13485, MDR, GMP or comparable quality standards.
• Experience with IQ, OQ, PQ, PPQ, cleanroom validation or sterilisation processes.
• Experience with Minitab or comparable statistical software.
• Lean Six Sigma Green Belt or Black Belt certification.
• Experience with Design Transfer, material qualification or test-method validation.
• Experience leading multidisciplinary improvement or validation projects.
• For senior candidates: experience with stakeholder management, coaching and knowledge transfer.

What makes you successful?

You are analytical, quality-conscious and practically minded. You understand that a process improvement must not only work technically, but must also be controlled, validated and properly documented. You work in a structured manner, take ownership and communicate clearly. You are successful when processes become more stable and efficient, deviations are resolved structurally and projects demonstrably contribute to quality, output and reliability.

What we offer

• A gross annual salary between €60,000 and €80,000, depending on your experience and the position level.
• A one-year employment contract followed by a permanent contract, or an immediate permanent contract depending on your experience.
• 28 vacation days, in addition to all official Dutch public holidays.
• A pension scheme starting on 1 January 2027.
• Fully funded job-related education, professional training and courses.
• A travel allowance of €0.25 per kilometre without a maximum distance, or full reimbursement of public-transport costs.
• A relocation allowance of up to €5,000 when your current commute exceeds 60 minutes.
• Regular working hours from 07:30 to 16:00, with flexibility where needed.
• A one-hour break each day, of which 30 minutes are paid by the employer.
• Full salary continuation during the first year of sickness and 70% during the second year.
• A €30 net monthly contribution towards health-insurance costs.
• An allowance of €200 for glasses or contact lenses every two years.
• A well-funded company canteen, with a monthly budget of more than €400.
• Fresh fruit at the office.
• An annual employee-activities budget of €6,600.
• An annual year-end celebration budget of €10,000.
• Collaboration with international Process Engineering, Engineering and R&D colleagues within our parent company.