Demo

Sr. Supervisor, Quality Control

MicroVention
Aliso Viejo, CA Full Time
POSTED ON 2/25/2025
AVAILABLE BEFORE 5/22/2025

Job Description

Direct, coordinate, and improve product inspection activities using knowledge of product technology, quality specifications and procedures. Job duties :

  • Responsible for planning and managing the Quality Control function including in-process inspections, and final assembly inspections.
  • Direct the workflow of the Quality Control group and report on the status and results of inspection and test activities.
  • Manage QC department and overall expectations pertaining to setting accurate schedules and allocating resources.
  • Ensure delivery against QC department goals and objectives, i.e. meeting commitments and coordinating overall inspection schedule.
  • Responsible for the execution, maintenance, and periodic review of inspection process and procedures.
  • Develop metrics to identify and prioritize activities pertinent to process control, risk reduction, and cost improvement.
  • Support the execution of improvement and cost saving projects and compliance remediation activities, ensuring proper leadership, interaction with cross-functional team, project management capability and accurate reporting.
  • Directly supervise QC staff including coaching and developing to enable maximum performance and individual associate growth, providing regular performance review and feedback.
  • Manage QC staff to ensure that inspection activities are compliant to documented procedures.
  • Support technical aspects of the inspection process, including method troubleshooting and statistics.
  • Ensure nonconforming and / or suspect material is appropriately documented, segregated, and reported to facilitate effective disposition.
  • Perform other duties as assigned.

Qualifications

  • Bachelor's degree or equivalent combination of education and experience in the medical device industry.
  • Minimum 4 years of quality control experience.
  • Minimum 1 year of recent supervisory experience for medical device manufacturing.
  • Hands-on experience with process improvement projects.
  • Technical expertise to drive troubleshooting and failure investigations.
  • Use of microscope and other hand measurement tools required to perform inspections.
  • Must have a desire for achieving excellence in customer satisfaction, process and product quality and reliability.
  • Desired Qualifications

  • Competent at inspection techniques; solid understanding of technical documentation including mechanical drawings.
  • Good written and verbal communications.
  • Ability to read technical documentation.
  • Experience working in controlled environments (clean rooms).
  • Good interpersonal skills.
  • Knowledge of Quality Systems for medical device manufacturing and requirements for inspection and testing i.e. FDA QSR and ISO 13485.
  • Ability to manage and prioritize multiple projects and deliverables while clearly communicating status and identifying obstacles.
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