Quality Control Supervisor

Nuclein • Austin, TX

5d

About The Position

The Quality Control Supervisor trains personnel and plans, facilitates, and executes quality control activities to inspect and test Nuclein’s diagnostic medical devices, subassemblies, and components. The role ensures product quality and adherence to specifications through rigorous, technically informed daily operations and collaboration with team members on investigations. The supervisor is expected to understand QC methods, criteria, and strategy and to train and develop QC Technicians.

Requirements

• Associate’s degree or higher in a technical discipline, or equivalent work experience.
• At least 4 years of QC work experience.
• At least 2 years of experience in the medical device industry or another regulated industry.
• Strong computer skills and experience with laboratory equipment.
• Strong attention to detail and problem-solving skills.
• Proficiency reviewing records for completeness and accuracy.
• Strong organizational and time-management skills.
• Ability to meet the stated physical requirements, including repetitive motion, lifting less than 50 lbs, sitting and standing, and speaking and communicating.
• Local candidates only; sponsorship is not offered at this time.

Nice To Haves

• Previous supervisory experience.
• Quality certification, such as ASQ CQI, CQT, or ASME GD&T.

Responsibilities

• Supervise, train, and mentor QC personnel.
• Coordinate and deploy QC resources efficiently to meet production schedules.
• Perform QC testing and inspection of materials for release to production and of finished products, including reviewing records for compliance.
• Maintain work areas and equipment to GMP standards; perform equipment maintenance and metrology; and order and receive supplies.
• Analyze data, record and approve results, and archive quality records.
• Understand the Quality Control strategy.
• Promptly and accurately recognize and report deviations, non-conformances, and out-of-specification events, and quarantine materials.
• Initiate Nonconformance (NC) records with appropriate information, assist with investigations, and resolve assigned NCs.
• Review quality records for completeness, accuracy, and compliance, and resolve discrepancies.
• Lead creation and revision of work instructions; support test method development and continuous improvement as assigned.
• Participate in validation activities as needed.
• Support quality audits as needed.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: Associate degree