Engineer - Degreed II

ManpowerGroup Global, Inc.; Austin (TX); On-site; USD 45,000 - 50,000; Full time

Job summary

ManpowerGroup Global, Inc. is seeking an Engineer - Degreed II for a Fortune 500 client in Austin, TX on a 9-month, 100% onsite contract.

You will support day-to-day Quality Operations in a medical device manufacturing setting and interface with the TPM for quality oversight. The ideal candidate holds a Bachelor's degree in engineering or a related field and has at least 3 years in quality engineering within medical device/pharma environments, including cleanroom and laboratory experience.

Qualifications

• Bachelor's degree in Engineering or related field; equivalent technical experience acceptable.
• 3+ years in Operations Quality or Quality Engineering in medical device/pharma manufacturing.
• Hands-on experience in cleanroom and laboratory environments.

Responsibilities

• Support day-to-day Quality Operations in a medical device manufacturing environment.
• Act as Customer Ops QA representative interfacing with Third-Party Manufacturer (TPM).
• Provide oversight of quality records: NCRs, CAPAs, change control, validations, supplier changes, DHRs.
• Review and ensure compliant resolution of nonconformances and CAPAs.
• Lead/support quality investigations and perform root cause analysis.
• Ensure adherence to GMP, FDA, ISO 13485, and QMS requirements.
• Review Device History Records (DHRs) and support product release activities.
• Partner with manufacturing and engineering to resolve defects and improve processes.
• Monitor and report quality KPIs and trends.
• Identify and drive continuous improvement initiatives.
• Ensure TPM maintains compliance with quality system requirements.
• Author/review quality documentation and investigation reports.

Education

Bachelor's degree in Engineering or closely related discipline

Job description

Title:Engineer - Degreed II
Location: Austin TX(100% Onsite)
Duration: 9Months
Shift Time: 8am to 4:00pm
Pay Range: $33/hr to $36/hr (On W2)
We are looking for a“Engineer - Degreed II“to join one of our Fortune 500 clients.

Job Responsibilites:

• Support day-to-day Quality Operations in a medical device manufacturing environment
• Act as Customer Ops QA representative interfacing with Third-Party Manufacturer (TPM)
• Provide oversight of quality records: NCRs, CAPAs, change control, validations, supplier changes, DHRs
• Review and ensure compliant resolution of nonconformances and CAPAs
• Lead/support quality investigations and perform root cause analysis
• Ensure adherence to GMP, FDA, ISO 13485, and QMS requirements
• Review Device History Records (DHRs) and support product release activities
• Partner with manufacturing and engineering to resolve defects and improve processes
• Monitor and report quality KPIs and trends
• Support deviations, validations, and supplier change activities
• Identify and drive continuous improvement initiatives
• Ensure TPM maintains compliance with quality system requirements
• Author/review quality documentation and investigation reports

Education:

• Bachelor's degree (preferably in Engineering, science or a closely related discipline is desired) or equivalent technical experience and demonstrated competence.
• Minimum 3+ years of work experience in an Operations Quality or Quality Engineering role supporting medical device or pharmaceutical manufacturing.
• Hands-on experience working in cleanroom and laboratory environments is preferred.

We are looking for the candidate who are eligible to work with any employers without sponsorship.