Quality Manager - Medical Device - Litchfield, CT
: Job Details :


Quality Manager - Medical Device - Litchfield, CT

Michael Page

Location: Litchfield,CT, USA

Date: 2024-12-22T00:14:45Z

Job Description:
My client is seeking an experienced and dynamic Quality Manager to join our team in Litchfield, CT. This is a fantastic opportunity to drive quality excellence and make a significant impact on a growing company. They work with some of the major suppliers of Medical Device Nationwide and project excellent from their Connecticut facility.Client DetailsMy client is global manufacturer and leading provider of assembly for medical devices. They are backed by over 60+ years of excellence and have over 10 locations worldwide. Three of those locations are located in New England with the site in Litchfield anticipating excellent growth over the coming year.DescriptionThe Key Responsibilities of the Quality Manager are:
  • Quality Assurance Leadership: Develop, implement, and manage the company's quality assurance strategies, policies, and programs to ensure product and process excellence.
  • Compliance and Standards: Ensure compliance with applicable quality standards (e.g., ISO 13485, FDA, industry-specific regulations).
  • Process Improvement: Lead continuous improvement initiatives using methodologies such as Six Sigma, Lean, and root cause analysis to enhance product quality and operational efficiency.
  • Team Management: Supervise, mentor, and develop a quality team, fostering a culture of accountability and innovation.
  • Customer Focus: Collaborate with customers to address quality concerns and proactively meet their expectations.
  • Audits and Inspections: Oversee internal and external quality audits, ensuring readiness for inspections by regulatory bodies or certification organizations.
  • Documentation and Reporting: Maintain accurate quality documentation and prepare reports on quality metrics, identifying trends and areas for improvement.ProfileThe successful Quality Manager will have the following:Required:
    • Heavy experience with Inspection Processes
    • Experience with ISO 13485 Standards
    • Strong Business Sense and great communicator to employees and customersHighly Desirable:
      • Metrology experience- Ideally with Calypso (Zeiss CMM software)
      • Minitab experience
      • Injection molding exposureJob OfferThe client can offer the following:
        • Competitive Base Salary
        • Bonus Potential
        • Terrific Benefits
        • Opportunity to lead Quality Department for Growing ManufacturerApply today! All relevant applicants will receive follow up within 72 hours of submission.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
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