What are the responsibilities and job description for the Sr. Supervisor, Quality Control position at Terumo Neuro?
Job Description
Direct, coordinate, and improve product inspection activities using knowledge of product technology, quality specifications and procedures. Job duties:
US - United States
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.
- 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.
- 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.
US - United States
