Quality Engineer

g2 Recruitment; Zeeland; On-site; EUR 52,000 - 75,000; Full time

Job summary

Goes Zeeland-based market leader seeks a Quality Engineer on a permanent basis to drive quality across R&D through to manufacturing.

You will partner with engineering and manufacturing teams, uphold GMP and ISO 13485, lead CAPAs and root-cause analyses, and ensure robust documentation. Fluent Dutch is essential for collaboration and compliance in this role.

Qualifications

• Bachelor's degree in an engineering or scientific discipline.
• Experience working on Quality, GMP, CAPAs and GLP.
• Background in Medical Manufacturing with ISO 13485 preferred.
• MDR knowledge and ability to work independently.

Responsibilities

• Lead quality responsibilities and ensure adherence to relevant standards.
• Collaborate closely with engineering and manufacturing teams.
• Focus on GMP, root cause analyses and CAPAs.
• Coordinate multiple processes independently and efficiently.

Skills

Quality

GMP

CAPAs

Root cause analysis

Documentation

GLP

Education

Bachelor's degree in engineering or scientific discipline

Job description

G2 are partnering with a market leader based near to Goes, Zeeland, who are looking for a Quality Engineer to join their team on a permanent basis.

The client specialises in the medical device manufacturing sector, with a primary focus on hardware, from R&D/NPI through to product manufacturing and validation phases.

You will be working on Quality responsibilities and playing a lead role within the team, working closely with the engineering and manufacturing teams, ensuring relevant standards are adhered to, with a specific focus on GMP, root cause analyses and CAPAs. The client ideally wants people who have experience with MedTech, specifically ISO 13485.

Permanent Opportunity – Quality Engineer - Zeeland

Contract type: Permanent

• Bachelor's degree in an engineering or scientific discipline


• Background as Quality Officer, Specialist, Quality Engineer, or similar


• Experience working on Quality, documentation, GMP, CAPAs and GLP


• Working history in the Medical Manufacturing sector strongly preferred, pharmaceuticals can also be considered


• Experience working with ISO 13485 essential


• MDR Knowledge


• Ability to work independently, coordinating multiple processes simultaneously


• Fluent Dutch is essential