MicroVention is now Terumo Neuro

Supervisor I, Receiving & Release - CR

Position Overview

Responsible for providing necessary leadership, training, and day-to-day supervision to the Quality Inspection Team. Oversee and monitor the receiving inspection and testing of materials, parts, and final product release. Lead inspection protocols, first article inspections. Lead and initiate continuous improvements for the Quality Control department. Job duties:
  • Direct and coordinate Quality Control Incoming Inspection on the performance of raw materials and final product inspection.
  • Ensure department is adequately resourced and trained to perform jobs effectively.
  • Directly supervise Receiving Inspection Quality Control (RI QC) staff, including coaching and developing to enable maximum performance and individual employee growth and providing regular feedback.
  • Establish and adjust work priorities to meet department schedules.
  • Manage RI QC staff to ensure that inspection activities are compliant with documented procedures.
  • Review inspection procedures to ensure compliance with regulatory requirements.
  • 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.
  • Assist in the development of new inspections and test methods.
  • Provide feedback to Quality Assurance, Operations, and R&D on quality issues.
  • Assist Manufacturing Engineering and Quality Engineering team members in initiating document changes.
  • Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
  • Perform additional duties as assigned.

Job Details

Job ID 12848BR

Alajuela, Costa Rica

Apply for this job
    1. Currently studying at a university, working towards a university degree (over 50% of the career approved) in a related field of study.
    2. Minimum three (3) years of experience in quality control for medical device manufacturing.
    3. Minimum one (1) year of supervisory experience.
    4. Strong knowledge of inspection techniques; understanding of and ability to read technical documentation including mechanical drawings.
    5. Strong problem solving, decision making, and organizational skills.
    6. Ability to use inspection tools.
    7. Ability to perform inspection sampling plans.
    8. Strong written and verbal communication skills. Good interpersonal skills.
    9. Strong working knowledge of MS Word, Excel, PowerPoint, Teams, and Outlook and electronic inventory systems.
    10. Knowledge of GMP (QSR) and/or ISO regulations and requirements for inspection and testing.
    Desired Qualifications
    1. Ability to use video inspection equipment desirable.
    2. Ability to manage and prioritize multiple projects and deliverables while clearly communicating status and identifying obstacles.
    3. Able to investigate a product/process failure, determine the root cause, and take prompt corrective actions while minimizing product exposure and production downtime quickly and thoroughly.
    4. Ability to promote effective working relationships at all levels.
    5. Good cross-functional team collaborative skills.
    6. Knowledge of Quality Systems for medical device manufacturing and requirements for inspection and testing.