Supervisor QC Inspection

Meet the team:

A Supervisor QC Inspection manages in maintaining high-quality standards by supporting quality control processes, coordinating inspections, and managing documentation, contributing to the overall quality and compliance of products or services within an organization.

Where you come in:

As a member of the QA Receiving Inspection team, you play a vital role in ensuring the quality and compliance of incoming materials and components. Your work supports operational efficiency, sustainability, and adherence to regulatory and internal standards.

What makes you successful:

• You will perform supervisory and administrative duties associated with inspection personnel management.
• You will provide direct supervision to support individual contributors/matrix reports.
• You will coordinate the tasks and work plans of the Receiving Inspection area.
• You will observe and verify the accuracy and adequacy of the inspection activities and records.
• You will be responsible for material flow, storage of parts, and accurate inventory transactions within the MRP system.
• You will generate and maintain quality metrics and reports, as required, and implement appropriate preventive/corrective actions (as needed) to improve quality. Maintains component and supplier performance data and assists with supplier quality management.
• You will identify problems and propose solutions that are timely, cost-effective, and meet quality requirements.
• You will assist in development of visual and dimensional inspection/test procedures and material specifications.
• You will coordinate first article inspections and supplies data to engineering.
• You will work with Logistics and Distribution, Supplier Quality and Operations Engineering and other department personnel, as necessary, to support quality and business objectives. Assumes and performs other duties as assigned.
• You will plan, manage and prioritize tasks/projects, tracks progress toward overall goals, and provide periodic updates to management.

Travel Required:

• 0-20%

Experience and Education Requirements:

• Typically requires a Bachelor’s degree with 5-8 years of Medical Device or Manufacturing industry.
• Informal management/ team lead experience.
• Proficiency with inspection equipment such as Vision Measuring Machine (VMM), Vision System, and Digital Microscopes are a plus.
• Intermediate or advanced beginner with geometric dimensioning and tolerancing and the ability to read mechanical drawings is a plus.
• Proficiency with Microsoft Office Products.Previous direct involvement in the medical device industry or a regulated industry.
• Ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D and GMP manufacturing environment.
• Ability to deal with ambiguity/uncertainty and a willingness to try new/challenging things.
• Strong interpersonal and teamwork skills.Demonstrated written and verbal communication skills.
• Able to work in 12 hours shift pattern

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