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 • ...
Apply for This Position
Ready to take the next step? Click the button below to submit your application.
Submit Application