Quality Engineer, Medical Device Manufacturing (Onsite TN)

Actalent; Murfreesboro (TN); On-site; USD 80,000 - 85,000; Full time

Benefits offered by this job

Healthcare

401(k)

Paid time off

On-site amenities

Job summary

Actalent is seeking a Quality Engineer for a medical device manufacturing environment in Murfreesboro, TN. The role focuses on driving continuous improvement, maintaining robust quality systems, and ensuring regulatory compliance.

You will collaborate with manufacturing, engineering, and quality teams to optimize processes, improve product reliability, and support audits and inspections. The ideal candidate has extensive experience in regulated manufacturing, strong analytical skills, and

Qualifications

• Experience in regulated medical device manufacturing.
• Knowledge of FDA QSR and risk management principles.
• Proficiency with FMEA and SPC tools.
• Experience conducting internal audits in manufacturing/quality systems.
• Strong communication with clients and cross-functional teams.

Responsibilities

• Support quality manufacturing practices in FDA-compliant environment.
• Develop and improve quality systems, procedures, and documentation.
• Lead or support CAPA processes for nonconformances.
• Collaborate on process validation, risk management, and product development.
• Conduct internal quality audits and support regulatory inspections.
• Analyze quality data to identify improvement opportunities.
• Review manufacturing and quality documentation for approvals.
• Apply QEs tools to improve process capability and reduce variation.
• Support shop floor quality improvements with production teams.
• Manage quality projects and communicate deliverables to stakeholders.
• Interface with clients on quality matters, providing technical support.

Skills

FDA QSR knowledge

Root cause analysis

FMEA

SPC

Audits

Cross-functional teamwork

Education

Bachelor's degree in engineering

7+ years experience in lieu of degree

Tools

FMEA

PPAP

Job description

Actalent is seeking a Quality Engineer for a medical device manufacturing environment in Murfreesboro, TN. The role focuses on driving continuous improvement, maintaining robust quality systems, and ensuring regulatory compliance.

You will collaborate with manufacturing, engineering, and quality teams to optimize processes, improve product reliability, and support audits and inspections. The ideal candidate has extensive experience in regulated manufacturing, strong analytical skills, and