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Contract Quality Engineer
Contract Quality EngineerMonica Burt & Associates • Memphis, TN, United States
Contract Quality Engineer

Contract Quality Engineer

Monica Burt & Associates • Memphis, TN, United States
1 day ago
Job type
  • Full-time
Job description

Job Description

MB&A, a recruiting and consulting firm specializing in the medical device manufacturing industry, is seeking a qualified Contract Quality Engineer to join our team in Memphis, TN. This position is designed for a skilled professional who is dedicated to ensuring the highest standards of quality in the production of medical devices. The successful candidate will work on a contract basis, contributing their expertise to support quality assurance initiatives.

Key Responsibilities :

  • Quality Assurance : Implement and maintain quality assurance processes to ensure compliance with industry standards and regulations in the medical device manufacturing sector.
  • Risk Management : Collaborate with cross-functional teams to identify, assess, and mitigate risks associated with manufacturing processes and product quality.
  • Documentation : Create and review quality documentation, including standard operating procedures, work instructions, and quality records, ensuring accuracy and compliance.
  • Audits and Inspections : Conduct internal audits and support external audits to verify compliance with quality management systems and regulatory requirements.
  • Continuous Improvement : Participate in continuous improvement initiatives to enhance product quality, operational efficiency, and overall effectiveness of the quality management system.
  • Root Cause Analysis : Investigate and address non-conformities and customer complaints, conducting thorough root cause analyses and implementing corrective and preventive actions.
  • Collaboration : Work closely with cross-functional teams, including manufacturing, engineering, and regulatory affairs, to ensure seamless integration of quality processes.

Requirements

  • Bachelor's degree in Engineering or a related field.
  • Proven experience in quality engineering within the medical device manufacturing industry.
  • Knowledge of relevant regulations, such as ISO 13485 and FDA requirements.
  • Strong analytical and problem-solving skills, with the ability to conduct thorough root cause analyses.
  • Excellent communication and interpersonal skills to collaborate with diverse teams effectively.
  • Detail-oriented with a commitment to maintaining high standards of quality.
  • Ability to work independently and efficiently in a contract capacity (20-30 hours per week).
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