Medical Device QA Coordinator - Inspection & Testing

Cpl Life Sciences; Waalwijk; On-site; EUR 45,000 - 55,000; Full time

Job summary

Cpl Life Sciences is seeking 4 QA Coordinators for a Medical Device Organisation located in Waalwijk, Netherlands. These on-site roles require prior experience in the medical device industry and full eligibility to work. The role involves inspecting incoming materials and supporting manufacturing areas.

Candidates should have at least a High School degree and a minimum of 2 years of mechanical inspection experience. Skills in communication and the ability to manage priorities are essential.

Qualifications

• Minimum of 2 years as a mechanical inspector in the Medical Device Industry.
• Experience with FDA and ISO inspections, documentation & standards.

Responsibilities

• Perform functional testing of devices as it pertains to lot qualification.
• Perform package integrity testing of devices as procedurally required.
• Mechanical inspection of incoming components and materials.
• Maintain and file inspection records and reports.
• Data input into the computer system.
• Assist Quality Engineers in the development of test methods and device investigations.
• Conduct internal quality audits, as required.

Skills

Effective verbal and written communication skills

Ability to organize and judge priorities

Knowledge of basic shop math

Education

High School degree

Job description

Cpl Life Sciences is seeking 4 QA Coordinators for a Medical Device Organisation located in Waalwijk, Netherlands. These on-site roles require prior experience in the medical device industry and full eligibility to work. The role involves inspecting incoming materials and supporting manufacturing areas.

Candidates should have at least a High School degree and a minimum of 2 years of mechanical inspection experience. Skills in communication and the ability to manage priorities are essential.