Principal Quality Engineer

Katalyst-Healthcares-; Richmond (VA); Vor Ort; USD 120.000 - 180.000; Vollzeit

Zusammenfassung

Creative Solutions Services, LLC is seeking an experienced Principal Quality Engineer to lead quality initiatives across manufacturing and product development. The role focuses on compliance, product quality, and continuous improvement, partnering with cross-functional teams to drive excellence.

The ideal candidate will oversee quality systems, risk management, validation, supplier quality, and regulatory compliance, while mentoring engineers and supporting audits and inspections.

Qualifikationen

• Bachelor's degree in Engineering or related field required.
• 8+ years of Quality Engineering in a regulated environment.
• FDA/ISO13485/cGMP knowledge required.
• Experience with Design Controls, CAPA, and risk management.

Aufgaben

• Lead quality engineering activities across product development and manufacturing.
• Develop and implement quality strategies compliant with FDA, ISO 13485, ISO 9001.
• Drive CAPA through structured problem-solving approaches (8D, 5 Whys, Fishbone).
• Lead risk management activities including DFMEA, PFMEA, risk assessments, mitigation plans.
• Review and approve ECOs, design documentation, validation protocols, and quality records.
• Support Design Controls including V&V, Design Reviews, and DHF.
• Analyze quality metrics and drive continuous improvement with Lean Six Sigma and statistics.
• Lead IQ/OQ/PQ and process capability studies; support audits and inspections.
• Collaborate with cross-functional teams to resolve quality issues.

Kenntnisse

Quality Engineering

Regulatory Compliance

Root Cause Analysis

CAPA

Process Validation

Risk Management

Lean Six Sigma

Statistical Analysis

Audits

Ausbildung

Bachelor's degree in Engineering

Master's degree (preferred)

Tools

Minitab

Jobbeschreibung

Job Description

We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product development processes. The ideal candidate will provide technical leadership in quality systems, risk management, validation, CAPA, supplier quality, and regulatory compliance while partnering with cross-functional teams to drive operational excellence.

Responsibilities

• Lead quality engineering activities supporting product development, manufacturing, and sustaining engineering.
• Develop and implement quality strategies that comply with FDA, ISO 13485, ISO 9001, and other applicable regulatory requirements.
• Drive root cause investigations and corrective and preventive actions (CAPA) using structured problem-solving methodologies.
• Lead risk management activities including DFMEA, PFMEA, risk assessments, and mitigation plans.
• Review and approve engineering change orders (ECOs), design documentation, validation protocols, and quality records.
• Support design control activities including Design Verification & Validation (V&V), Design Reviews, and Design History Files (DHF).
• Analyze quality metrics and implement continuous improvement initiatives using Lean Six Sigma and statistical tools.
• Lead process validation activities including IQ, OQ, PQ, and process capability studies.
• Collaborate with Manufacturing, R&D, Regulatory Affairs, Supply Chain, and Operations to resolve quality issues.
• Provide technical leadership during internal, customer, and regulatory audits.
• Mentor and coach Quality Engineers and cross-functional teams on quality best practices.
• Support supplier qualification, supplier audits, and supplier quality improvement initiatives.
• Ensure compliance with cGMP, FDA Quality System Regulation (21 CFR Part 820/QMSR), and applicable international standards.

Requirements

• Bachelor's degree in Engineering (Mechanical, Biomedical, Industrial, Manufacturing, Electrical, Chemical, or related discipline).
• 8+ years of Quality Engineering experience in a regulated manufacturing environment.
• Strong knowledge of FDA regulations, ISO 13485, ISO 9001, and cGMP requirements.
• Experience with Design Controls, Risk Management (ISO 14971), CAPA, Client, and change management.
• Hands-on experience with process validation (IQ/OQ/PQ), statistical analysis, SPC, MSA, and capability studies.
• Strong knowledge of Lean Manufacturing, Six Sigma, and continuous improvement methodologies.
• Excellent root cause analysis skills utilizing 8D, Fishbone, 5 Whys, and similar tools.
• Experience leading cross-functional projects and mentoring engineering teams.
• Strong written, verbal, and presentation skills.

Preferred Qualifications

• Master's degree in Engineering or related technical field.
• ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt or Black Belt.
• Experience in medical devices, pharmaceuticals, biotechnology, aerospace, automotive, or other highly regulated industries.
• Experience supporting FDA inspections and ISO certification audits.
• Knowledge of validation documentation, statistical software (Minitab), and quality management systems.