Supervisor, Quality Control

Nordson Corporation; Allen (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Nordson Corporation is seeking a hands-on Quality Control Supervisor in Allen, TX, to lead daily quality inspection and testing activities within a regulated medical device manufacturing environment.

You will supervise Quality Control Technicians, support production priorities, and ensure inspection, calibration, and environmental monitoring comply with FDA requirements and ISO 13485. Strong leadership and problem-solving skills are essential.

Qualifications

• 5+ years quality experience in medical device manufacturing.
• Supervisory experience of a team.

Responsibilities

• Lead, train, schedule, and develop QC Technicians.
• Oversee incoming, in-process, and finished goods inspection and testing.
• Ensure inspection records and quality documentation are accurate and compliant.
• Coordinate with Quality, Operations, and Engineering to investigate nonconformances.
• Support calibration program and measurement-system improvements.
• Monitor environmental monitoring and data trend reporting.

Skills

Quality control

Supervisory

Medical devices

GMP

Education

BS/AS in science

Job description

Quality Control Supervisor

Location: Allen, TX

Department: Nordson Medical – Surgical Solutions, Quality

Position Type: Full-Time

Nordson Medical is seeking a hands‑on Quality Control Supervisor to lead daily quality inspection and testing activities within a regulated medical device manufacturing environment. This role supervises Quality Control Technicians, supports production priorities, and ensures inspection, documentation, calibration, and environmental monitoring activities comply with company procedures, FDA requirements, and ISO 13485.

Key Responsibilities

• Lead, train, schedule, and develop Quality Control and Calibration Technicians.
• Oversee incoming, in-process, and finished‑goods inspection and testing.
• Ensure inspection records and quality documentation are accurate, complete, and compliant.
• Partner with Quality, Operations, and Engineering to investigate and resolve nonconformances.
• Manage the calibration program and support measurement‑system improvements.
• Monitor environmental monitoring and particle‑count activities, including data review and trend reporting.
• Coordinate cycle counts, inventory reconciliation, quality holds, and related ERP transactions.
• Support new‑product introduction, process improvements, yield improvement, and manufacturability initiatives.
• Reinforce safety, attendance, and company policy expectations.
• Provide hands‑on inspection support when needed to meet business priorities.

Qualifications

• High school diploma required; associate or bachelor’s degree in a scientific or technical field preferred.
• At least five years of quality experience in medical device manufacturing, including cleanroom operations.
• At least three years of supervisory experience.
• Working knowledge of FDA Quality System requirements, ISO 13485, GMP practices, inspection methods, and calibration.
• Strong leadership, communication, organization, and problem‑solving skills.
• Ability to manage competing priorities and work effectively in a fast‑paced manufacturing environment.

Nordson Corporation is an equal opportunity employer. Employment offers are contingent upon successful completion of applicable pre‑employment screening requirements.