About The Position

DMS Vision, Inc. is seeking a temporary Quality Engineer to support the implementation of a new Manufacturing Execution System (MES). The role focuses on integrating quality operations with the new MES software, with particular emphasis on production support and the medical device industry. The position is onsite in Santa Clara, California, four days per week, and is listed as a 12+ month engagement. Applicants must be local.

Requirements

  • Bachelor's degree in Engineering, Quality Management, or a related field.
  • Several years of experience in Quality Engineering, preferably in Production Support within the medical device industry.
  • Proven experience with MES implementation, specifically Critical Manufacturing's MES software.
  • Strong understanding of quality management systems and regulatory requirements in the medical device industry.
  • Excellent documentation and communication skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Strong problem-solving skills and attention to detail.

Nice To Haves

  • Certification in Quality Engineering (CQE) or related certifications.
  • Experience with other MES software systems.
  • Familiarity with Lean Six Sigma methodologies.

Responsibilities

  • Collaborate with cross-functional teams to understand how MES implementation affects quality operations.
  • Assist in creating and updating documentation for quality operations affected by the MES transition.
  • Develop and route Document Change Orders (DCOs) to ensure compliance with regulatory and company standards.
  • Troubleshoot and resolve quality-related issues during MES implementation.
  • Train staff on new quality processes and procedures related to the MES.
  • Ensure quality documentation is accurate, up to date, and compliant with industry regulations.
  • Monitor and report on MES implementation progress and its impact on quality operations.
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