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Quality Engineer

Bradford

Job Title: Quality Engineer


Reports to: Quality Operations Manager

Job Function:

The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and works cross-functionally with Operations, Engineering, R&D, and Customer Service to ensure compliance with customer, regulatory (ISO, FDA, Organic, etc.), and internal requirements. The Quality Engineer plays a key role in audits, root cause analysis, and customer complaint management while driving continuous improvement across the site.

Essential Duties and Responsibilities:

Quality Systems and Compliance

  • Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and applicable customer requirements.
  • Lead internal audits, customer audits, and third-party audits; prepare documentation, support on-site activities, and ensure timely closure of audit findings.
  • Assist with document control, SOP updates, and change management activities.
  • Support risk assessments, control plans, and quality metrics reporting.
Root Cause Analysis & Corrective Actions
  • Lead and facilitate root cause analysis using structured problem-solving tools (e.g., 5 Whys, Fishbone, FMEA).
  • Develop, implement, and track corrective and preventive actions (CAPAs) to ensure effectiveness and sustainability.
  • Partner with Operations and Engineering to address quality issues, reduce defects, and improve process capability
Customer Complaint Management
  • Manage customer complaints from receipt through closure, including investigation, root cause analysis, corrective action development and implementation, and response preparation.
  • Coordinate cross-functional investigations to ensure timely, accurate, and professional customer responses.
  • Identify complaint trends and drive systemic improvements to prevent recurrence.
Manufacturing & Process Support
  • Provide quality support to manufacturing operations, including deviation investigations and nonconformance management.
  • Support sampling, documentation, and shipment of raw materials, batch, and finished product samples to outside labs for testing.
  • Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and subsequent process change control from a quality perspective.
  • Review batch records, inspection data, and quality documentation as needed.
Continuous Improvement
  • Analyze quality data to identify trends, risks, and improvement opportunities.
  • Participate in Lean, Six Sigma, or other continuous improvement initiatives.
  • Promote a culture of quality, compliance, and accountability throughout the organization.
Minimum Knowledge, Skills and Abilities:
  • Bachelor's degree in Engineering, Quality, Chemistry, or a related technical field.
  • 3+ years of quality engineering or quality assurance experience in a manufacturing environment.
  • Experience with audits, nonconformance investigations, customer complaint management, root cause analysis, CAPA development and implementation.
  • Working knowledge of GMP and quality management systems.
  • Strong analytical, organizational, and problem-solving skills.
  • Effective written and verbal communication skills.
  • Preference for Lean, Six Sigma or quality certification.
  • Familiarity with regulatory compliance requirements applicable to certifications such as organic, Halal, naturals etc... would be desirable.
Physical & Work Environment:
  • Manufacturing environment with regular presence on the production floor.
  • Ability to sit, stand, walk, and occasionally lift up to 25 lbs.
  • Occasional travel for customer or supplier audits may be required.
Vacancy posted 23 hours ago
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