QHSE Engineer [F/M/X]

TN Netherlands; Netherlands; On-site; EUR 45.000 - 75.000; Full time

Job summary

An innovative company is seeking enthusiastic QHSE Engineers passionate about quality and innovation. In this role, you will be the driving force behind ensuring top quality in processes, working on continuous product improvements while adhering to strict standards such as FDA regulations and ISO certifications. If you thrive on making an impact and striving for perfection in a dynamic international environment, this opportunity is perfect for you. You will collaborate with leading companies in the industry, contributing to strategic quality improvements and enhancing product development processes.

Benefits

Dynamic work environment

Opportunity for strategic improvements

Collaboration with leading companies

Qualifications

• 4-6 years of experience as a mid-level professional or 5+ years as a senior in a similar role.
• Excellent proficiency in English; Dutch is a plus.

Responsibilities

• Drive top quality in processes and continuously improve products.
• Ensure compliance with FDA regulations and quality standards.

Skills

Quality Management

Corrective and Preventive Actions (CAPA)

Quality Management Systems (QMS)

FDA Regulations

Good Manufacturing Practices (GMP)

ISO Standards (ISO 9001/13485:2016)

Statistical Process Control

5Why's

Ishikawa

Education

Bachelor's Degree

Master's Degree

Tools

5S + 1

Pareto Analysis

Root Cause Analysis

Job description

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We are looking for enthusiastic QHSE Engineers who have a passion for quality and innovation!

In this role, you will be the driving force behind ensuring top quality in our processes. You will work on continuously improving our products and ensuring that everything complies with the strictest standards, such as FDA regulations and other quality standards. Do you get energized by making an impact and want to strive for perfection together with us?

Requirements

• A Bachelor's degree or HBO diploma; a Master’s is a plus.
• 4-6 years of experience as a mid-level professional or 5+ years of experience as a senior in a similar role.
• Knowledge of:
• Corrective and Preventive Actions (CAPA)
• Quality management and Quality Management Systems (QMS)
• Experience with FDA regulations, Good Manufacturing Practices (GMP), and ISO standards (ISO 9001/13485:2016)
• Excellent proficiency in English (Dutch is a plus)
• Experience with improvement projects using methods such as 5Why's, Ishikawa, and statistical process control.

Nice-to-have skills

• Experience with Advanced Product Quality Planning (APQP).
• Experience with medical devices and product development processes.
• Knowledge of tools such as 5S + 1, Pareto analysis, and root cause analysis.

What do we offer?

• The opportunity to be part of strategic quality improvements in a dynamic and international environment.
• Work with leading companies in the industry.