Sr. Quality Engineer

cardinalhealth

Greenwood (SC)

On-site

USD 60,000 - 85,000

Full time

6 days ago
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Benefits offered by this job

Medical, dental and vision coverage
Paid time off (PTO)
Health savings account (HSA)
401(k) savings plan
Early wage access (myFlexPay)
Flexible spending accounts (FSAs)
Short- and long-term disability
Work-Life resources
Paid parental leave
Healthy lifestyle programs

Job summary

Cardinal Health in Greenwood, SC, is seeking a Quality Engineer to plan, control and assure product and process quality across design, manufacturing and testing.

You will apply quality systems and statistical methods, perform FMEA, support audits, CAPAs and hold processes, and collaborate with R&D, Operations and suppliers to drive continuous improvement and regulatory compliance.

Qualifications

  • Bachelor's degree in related field or equivalent work experience.
  • 2+ years' experience in quality engineering or related field.
  • Green belt, white belt, or black belt certifications are a plus.

Responsibilities

  • Observe all safety precautions and report hazards.
  • Ensure tasks comply with Greenwood's Quality System.
  • Participate in Quality System Standards and Regulations, audits as required.
  • Provide GMP training for new hires and refresher training.
  • Support quality engineering in new product development.
  • Review designs for safety, testability, reliability, and manufacturability.
  • Perform FMEA and risk assessment.
  • Create verification/validation test plans and conduct prototype testing.
  • Perform statistical analysis of test results.
  • Conduct quality audits and develop preventive actions.
  • Support nonconforming product/material on hold systems and MRB processes.
  • Investigate customer complaints and determine disposition of nonconforming product.
  • Determine root cause and corrective/preventive actions for CAPAs and supplier actions.
  • Update product control plans and site documentation as needed.
  • Maintain and evaluate sampling plans.
  • Assist in process improvements related to quality and yields.
  • Develop specs and test methods with R&D/Operations to meet requirements.
  • Approve change notices (CNs).

Education

Bachelor's in related field
2+ years' experience in quality engineering or related field

Job description

What Quality Engineering contributes to Cardinal Health

Quality Engineering is responsible for product and service quality planning, evaluation and control. Works cross-functionally in the development and implementation of prevention based methodologies used in design, manufacturer, test, sustainability and correction of products and services.

Demonstrates understanding of quality philosophies, principles, systems, methods, tools, and standards.

Demonstrates understanding of the audit process including types of audits, planning, preparation, execution, reporting results and follow-up.

Develops and implements quality programs, including tracking, analyzing, reporting and problem solving.

Plans, controls, and assures product and process quality in accordance with quality principles, which include planning processes, design control, material control, acceptance sampling and measurement systems.

Demonstrates knowledge of reliability, maintainability, and risk management, including key terms and definitions, modeling, systems design, assessment tools and reporting.

Applies problem solving and quality improvement tools and techniques, including, preventative and corrective actions and how to overcome barriers to quality improvements.

Acquires and analyzes data using appropriate standard quantitative methods to facilitate process analysis and improvements.

Responsibilities
  • Observe all safety precautions and regulations at all times in all areas where duties are performed. Responsible for reporting all safety hazards and potential unsafe working conditions.
  • Responsible for seeing that all tasks are performed in a manner that complies with Greenwood's Quality System
  • Solid base knowledge of the Quality System Regulation (CFR 820)
  • Participate in applicable Quality System Standards and Regulations, FDA, supplier, customer and internal audits as required.
  • Conduct GMP training for all new hires as part of their orientation. Provide refresher training as needed for all employees.
  • Provide quality engineering support in new product development.
  • Review new and modified product designs for safety, testability, reliability, serviceability, and manufacturability.
  • Perform product risk assessment and failure mode effects analysis (FMEA).
  • Create verification and validation test plans and conduct prototype testing and analysis for reliability, standards compliance, and product requirements compliance.
  • Perform statistical analysis of test results.
  • Conduct quality audits and develop subsequent preventive action programs
  • Support the nonconforming product and material on hold systems, including placing product on electronic hold, reviewing and revising expiration dates as necessary and facilitating Material Review Boards to determine disposition of nonconforming products.
  • Investigate and respond to customer complaints, including facilitating Material Review Boards to determine disposition of nonconforming product.
  • Determine root cause/corrective and/or preventive action for material on hold, customer complaints, externally generated Supplier Corrective Actions (SCARs) and CAPAs.
  • Evaluate internally generated CAPAs for root cause and effective corrective actions.
  • Update/revise product plans of control and other site documentation where necessary.
  • Maintain and evaluate sampling plans.
  • Process Corporate Holds.
  • Assist in process improvements as related to improved quality and yields.
  • In conjunction with R&D, Operations, OPEX, and Sales and Marketing, develop specifications and test methods to meet customer, product and internal quality requirements. This may include writing procedures to carry out requirements.
  • Approve change notices (CNs).
Qualifications
  • Bachelors in related field, or equivalent work experience, preferred
  • 2+ years' experience in related field, preferred
  • Green belt, white belt, black belt certifications a plus
What is expected of you and others at this level
  • Applies working knowledge in the application of concepts, principles, and technical capabilities to perform varied tasks
  • Works on projects of moderate scope and complexity
  • Identifies possible solutions to a variety of technical problems and takes actions to resolve
  • Applies judgment within defined parameters
  • Receives general guidance may receive more detailed instruction on new projects
  • Work reviewed for sound reasoning and accuracy

Bonus eligible : No

Benefits : Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

  • Medical, dental and vision coverage
  • Paid time off plan
  • Health savings account (HSA)
  • 401k savings plan
  • Access to wages before pay day with myFlexPay
  • Flexible spending accounts (FSAs)
  • Short- and long-term disability coverage
  • Work-Life resources
  • Paid parental leave
  • Healthy lifestyle programs

Anticipated salary range : $59,600 - $85,100

Application window anticipated to close: 9/18/2026

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