Onsite QA Validation Engineer — ISO 13485 Medical Devices

PE Global (UK); Dún Laoghaire; On-site; EUR 50,000 - 70,000; Full time

Job summary

An international manufacturing company is seeking a QA Validation Engineer for a permanent onsite role in Co. Westmeath. The successful candidate will ensure Quality Assurance in compliance with ISO standards, participate in internal audits, and assist with new product development. Candidates should have a Bachelor's degree in a related field and a minimum of 3 years experience at a quality engineer level in an ISO 13485 regulated environment.

Qualifications

• Minimum 3 years experience working at quality engineer level in an ISO 13485 regulated environment.
• Internal Auditor qualified to ISO 13485.
• Experience with equipment validation.

Responsibilities

• Implement and maintain quality system to international standard.
• Carry out internal audits to ISO 13485 standard.
• Support new product development, production trials, and sampling.

Skills

Quality Assurance

Internal Auditing

Problem Solving

Statistical Analysis

Attention to Detail

Education

Bachelor’s Degree in Science, Engineering or a related field

Job description

An international manufacturing company is seeking a QA Validation Engineer for a permanent onsite role in Co. Westmeath. The successful candidate will ensure Quality Assurance in compliance with ISO standards, participate in internal audits, and assist with new product development. Candidates should have a Bachelor's degree in a related field and a minimum of 3 years experience at a quality engineer level in an ISO 13485 regulated environment.