Quality Control Supervisor

New World Medical; Rancho Cucamonga (CA); On-site; USD 86,000 - 96,000; Full time

Job summary

A leading company in ophthalmic surgical devices is seeking a Quality Control Supervisor to oversee the Quality Inspection Team. This role involves ensuring compliance with quality standards, leading inspection protocols, and driving continuous improvement initiatives. The ideal candidate will have strong leadership skills, experience in manufacturing, and a background in quality control processes. Join a mission-driven organization focused on enhancing vision and improving patient care.

Qualifications

• At least 3 years of supervisory experience in manufacturing, preferably in medical devices.
• Experience with receiving inspections, ISO 13485, and 21CFR 820.

Responsibilities

• Supervise and coordinate activities of quality inspectors in the receiving inspection area.
• Lead quality improvement activities and support continuous improvement initiatives.
• Document inspection results and report quality issues to the Quality Manager.

Skills

Leadership

Communication

Organizational Skills

Flexibility

Education

Bachelor’s degree in a life science or engineering field

Tools

Microsoft Office

SAP

MiniTab

Job description

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About New World Medical
Founded in 1990, New World Medical is a mission-driven company focused on preserving and enhancing vision through innovative ophthalmic surgical devices, including the Ahmed Glaucoma Valve and Kahook Dual Blade. We partner closely with eye care professionals to deliver tools that improve clinical outcomes and patient care. Guided by our core values - Integrity, Accountability and Innovation, we strive to make a meaningful impact in eye health worldwide. In support of our global mission, we proudly donate surgical equipment to charitable organizations to expand access to quality eye care.

Job Type
Full-time

Description

The Quality Control Supervisor is responsible for providing leadership, training, and supervision to the Quality Inspection Team. This role oversees receiving inspection and testing of materials, parts, and products, ensuring compliance with quality standards. The supervisor leads inspection protocols, supports production and R&D teams, and drives continuous improvement within the department.

Essential Job Duties and Responsibilities

• Supervise and coordinate activities of quality inspectors in the receiving inspection area to ensure timely release of products.
• Plan work schedules, assignments, and inspection sequences supporting production and R&D goals.
• Coordinate with production and R&D to align operations.
• Inspect materials, products, or equipment for defects or malfunctions.
• Measure dimensions using appropriate instruments to verify specifications.
• Read blueprints, manuals, and other materials to determine inspection procedures.
• Lead quality improvement activities and support continuous improvement initiatives like Kaizen.
• Develop training materials, facilitate training, and troubleshoot quality issues.
• Approve incoming materials after inspection and testing; reject unacceptable items.
• Document inspection results, summarize re-work and waste, and input data into quality databases.
• Report quality issues to the Quality Manager and ensure corrective actions are taken.
• Initiate Non-Conformity Reports and follow up on their resolution.
• Coordinate with suppliers and internal teams to resolve quality issues.
• Maintain inspection records and review finished product documentation for release.
• Prepare work instructions and communicate procedures effectively.

Requirements

Knowledge, Skills, and Abilities

• Ability to work independently with minimal supervision.
• Leadership skills and ability to influence others.
• Flexibility and adaptability to change.
• Strong communication and organizational skills.
• Ability to interpret engineering drawings.
• Training capability on inspection concepts and procedures.
• Proficiency in Microsoft Office applications.

Education and Experience

• Bachelor’s degree in a life science or engineering field preferred.
• At least 3 years of supervisory experience in manufacturing, preferably in medical devices.
• Experience with receiving inspections, ISO 13485, and 21CFR 820.
• Experience with SAP, MiniTab, AQL sampling, and SOP writing.

Physical Requirements

• Ability to lift up to 50 pounds.
• Remain stationary for at least 50% of the time.
• Occasional movement within the office, including bending and walking.
• Operate a computer and related office equipment.
• Effective communication skills for listening and speaking.
• Ability to work long hours on a computer screen.

This description reflects management’s assignment of essential functions and does not restrict other tasks that may be assigned.

Salary Range: $86,000 - $96,000