Quality Manufacturing Engineer

3 weeks ago


Torrington, Connecticut, United States Michael Page Full time
About Our Client

Our client is a global manufacturer and leading provider of assembly for medical devices. With over 60+ years of excellence and 10 locations worldwide, they are a trusted partner in the industry.

Job Description

The Lead Quality Engineer will be responsible for developing and implementing quality assurance strategies and processes for injected molded medical device components. This role will collaborate closely with production teams to ensure adherence to quality standards and regulatory requirements (FDA, ISO, etc.).

The successful candidate will conduct root cause analysis and implement corrective and preventive actions (CAPA) to address non-conformances and quality issues. They will also perform process validation and qualification activities for new and existing manufacturing processes.

Key responsibilities include:

  • Developing and implementing quality assurance strategies and processes
  • Collaborating with production teams to ensure quality standards and regulatory requirements
  • Conducting root cause analysis and implementing CAPA
  • Performing process validation and qualification activities
  • Driving continuous improvement initiatives
Requirements

The successful Lead Quality Engineer will have prior experience with validation protocols (IQ, OQ, PQ) and root cause analysis. Independent time management and communication skills are highly desirable.

What's on Offer

The client can offer a competitive base salary, bonus potential, terrific benefits, and growth opportunities for advancement within the organization.



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