Senior Quality Technician IV – SAP & GMP

Medtronic; Memphis (TN); On-site; USD 64,400 - 96,600; Full time

Benefits offered by this job

Health, Dental and vision insurance

401(k) plan

Tuition assistance

Paid time off

Job summary

Medtronic in Memphis, TN is seeking a qualified professional to manage SAP Quality Module-based virtual inspections and on-site material verifications at the Memphis Manufacturing site.

You will perform inspections, data analysis, and documentation to ensure compliance with FDA, ISO 13485, and GMP standards while collaborating with cross-functional teams in a fast-paced manufacturing environment. The role requires 5+ years of relevant experience and a proactive approach to continuous improvement.

Qualifications

• Experience with Winshuttle, SAP QM, ASNs, and SQM for quality processes.
• Understanding of FDA, ISO 13485, GMP and documentation practices.
• Ability to read drawings, specs, tolerances.
• Experience in medical device or regulated industry is a plus.

Responsibilities

• Performs analyses, inspection, and tests of raw materials, packaging materials, quantitative assays on samples, and/or finished products from manufacturing, to ensure quality standards and compliance to customer and regulatory requirements, and tolerance specifications for the chemical or physical property.
• Performs a variety of qualitative tests or qualitative assays on samples, and to aid in maintenance and certification of test instruments and apparatus to ensure compliance.
• Performs required inspections, checks, analysis and documentation of studies.
• Prepares and monitors quality statistics and reports.
• Reviews production records for conformance to procedures.
• Conducts non-conformance tests of manufactured, packaged or tested product

Skills

Quality inspection

Data analysis

Cross-functional comms

Mentor others

Tools

Winshuttle

SAP Quality Module

Advanced Shipment Notice

Supplier Quality Module

Microsoft Office

Job description

Medtronic in Memphis, TN is seeking a qualified professional to manage SAP Quality Module-based virtual inspections and on-site material verifications at the Memphis Manufacturing site.

You will perform inspections, data analysis, and documentation to ensure compliance with FDA, ISO 13485, and GMP standards while collaborating with cross-functional teams in a fast-paced manufacturing environment. The role requires 5+ years of relevant experience and a proactive approach to continuous improvement.