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Engineer - Degreed II

ManpowerGroup

Austin, TXJob$33–36/hrSeen 2w agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$33–36/hr
Location
Austin, TX
Work Authorization
Not specified

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Job overview

ManpowerGroup seeks an Engineer - Degreed II to support day-to-day quality operations in a medical device manufacturing environment, acting as a Customer Ops QA representative, overseeing quality records, ensuring compliance with GMP, FDA, ISO 13485, and driving continuous improvement.

Skills & qualifications

RequiredNice to have

Skills

Quality OperationsCustomer Ops QANCR ManagementCAPA ManagementChange ControlValidationSupplier Change ManagementRoot Cause AnalysisGMP ComplianceFDA ComplianceISO 13485 KnowledgeQMS KnowledgeQuality KPI MonitoringContinuous ImprovementCleanroom ExperienceLaboratory Experience

Qualifications

Bachelor's Degree in Engineering or Related Field3+ Years Operations Quality or Quality Engineering Experience

Full job description

Title: Engineer - Degreed II

Location: Austin TX (100% Onsite)

Duration: 9 Months

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 .

If you’re interested, please click “Apply” button

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

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