Medical Device QA Specialist – Implantables

Science Corp; Durham (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Science Corporation (Clinical-stage technology company) seeks a Quality Assurance Specialist to support QA activities for implantable medical devices. You will perform inspections, testing, and documentation, ensuring GMP-compliant manufacturing and product traceability.

The role requires 2+ years in quality control in a medical device or pharma setting, with English and French proficiency. Expect a dynamic production environment and opportunities to contribute to continuous improvement within

Qualifications

• 2+ year diploma/degree in quality, industrial processes, or related technical field, or equivalent experience.
• 2+ years of experience in quality control, preferably in medical device or pharmaceutical manufacturing.
• Proficiency in English and French (written and verbal).

Responsibilities

• Perform incoming, in-process, and final inspections of medical device components and finished products according to established procedures and specifications.
• Conduct dimensional, visual, and functional testing using appropriate measurement equipment and test methods.
• Document all inspection and test results accurately in the Quality Management System.
• Identify and report non-conforming products, initiating appropriate corrective actions.
• Maintenance of traceability of materials and products throughout the manufacturing process.
• Support CAPA investigations and participate in internal audits and regulatory inspections.

Skills

Quality inspections

GMP

QMS documentation

Root cause analysis

Documentation

Education

Diploma/degree in quality or related field

2+ years quality control experience

Job description

Science Corporation (Clinical-stage technology company) seeks a Quality Assurance Specialist to support QA activities for implantable medical devices. You will perform inspections, testing, and documentation, ensuring GMP-compliant manufacturing and product traceability.

The role requires 2+ years in quality control in a medical device or pharma setting, with English and French proficiency. Expect a dynamic production environment and opportunities to contribute to continuous improvement within