Quality Engineering Supervisor — Compliance & Process

cardinalhealth; El Paso (TX); On-site; USD 71,000 - 102,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off

401k savings plan

Access to wages before pay day

Flexible spending accounts

Short- and long-term disability

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Job summary

Cardinal Health seeks a Quality Engineer to contribute to the development and implementation of quality policies, procedures, and processes ensuring products and services meet regulatory standards. The role collaborates across functions to drive prevention-based methodologies in design, manufacturing, testing, and corrective actions.

The ideal candidate has 4–8 years of experience, a related bachelor's degree, and knowledge of ISO 13485 and FDA regulations.

Qualifications

• 4-8 years of experience preferred.
• Bachelor's degree in related field preferred or equivalent work experience.
• Knowledge with ISO 13485 and FDA regulations preferred.
• Experience in Internal Audits preferred.
• Experience with CAPA systems preferred.
• Knowledge of document control preferred.

Responsibilities

• Develop and implement quality policies, procedures, and processes to ensure regulatory compliance.
• Manage quality planning, evaluation, and process control across products and services.
• Supervise staff to achieve quality goals and regulatory compliance.
• Work with multiple QMS systems for data and record management.

Skills

Quality management

Regulatory compliance

CAPA

Document control

Internal audits

Cross-functional collaboration

Education

Bachelor's degree or equivalent

Job description

Cardinal Health seeks a Quality Engineer to contribute to the development and implementation of quality policies, procedures, and processes ensuring products and services meet regulatory standards. The role collaborates across functions to drive prevention-based methodologies in design, manufacturing, testing, and corrective actions.

The ideal candidate has 4–8 years of experience, a related bachelor's degree, and knowledge of ISO 13485 and FDA regulations.