Job Description
Elevate quality assurance with expertise as a Quality Engineer in the medical device industry. Embrace compliance, continuous improvement, and regulatory standards in your work environment.
This role requires a Quality Engineer with over three years in quality engineering within regulated spaces, particularly medical devices. Key skills include a strong grasp of FDA regulations and ISO standards, alongside experience in CAPA and process validation. You will play a crucial role in ensuring compliance and fostering improvements across various quality assurance activities in a regulated workplace.
Key Responsibilities:
• Support quality systems for compliance with standards
• Lead CAPA investigations and conduct root cause analysis
• Review and maintain quality documentation thoroughly
• Collaborate with teams to drive process improvements
• Assist in audits, ensuring timely closure of findings
Requirements:
• Minimum 3 years in Quality Engineering experience
This role requires a Quality Engineer with over three years in quality engineering within regulated spaces, particularly medical devices. Key skills include a strong grasp of FDA regulations and ISO standards, alongside experience in CAPA and process validation. You will play a crucial role in ensuring compliance and fostering improvements across various quality assurance activities in a regulated workplace.
Key Responsibilities:
• Support quality systems for compliance with standards
• Lead CAPA investigations and conduct root cause analysis
• Review and maintain quality documentation thoroughly
• Collaborate with teams to drive process improvements
• Assist in audits, ensuring timely closure of findings
Requirements:
• Minimum 3 years in Quality Engineering experience
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