Quality Control Technician

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

Salary: Up to €50,000

Cpl Life Sciences is collaborating with a growing Medical Device Organisation who are looking to recruit 4x QA Coordinators. These positions are on‑site roles, so you must be located close to the site.

Prior experience working for a medical device or diagnostic manufacturer is highly advantageous. You MUST also hold the full right to work; this employee does not offer job sponsorship.

This position will be integral in controlling the inspection of incoming materials to support development and manufacturing areas. Must be able to deal with changing priorities. Will inspect incoming and in‑process sub‑assemblies to quality documentation.

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.
• Monitor calibration contractors while testing equipment.
• Knowledge of basic shop math is essential.
• Experience with FDA and ISO inspections, documentation & standards.

Education and Experience

• High School degree
• Minimum of 2 years as a mechanical inspector in the Medical Device Industry

Preferred Skills and Competencies

• Effective verbal and written communication skills.
• Ability to communicate at multiple levels of an organization.
• Ability to organize and judge priorities.
• Ability to generate and maintain accurate records.
• Ability to lift up to 10 pounds.