Flexible Hybrid Quality Engineer Jobs

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Quality Assurance Engineer III
BostonUS$90000 - US$110000 per year

Role: Quality Assurance Engineer III Location: USA, hybrid/remote Pay: $90,000 - $110,000 A client I'm working with is seeking a motivated and detail‑oriented Quality Assurance Engineer III to join their team in supporting the development, manufacture, and ongoing reliability of our medical device products. In this role, you will help ensure that ...

Quality Assurance Engineer III
BostonUS$90000 - US$110000 per year

Role: Quality Assurance Engineer III Location: Boston, MA (hybrid) Pay: $90,000 - $110,000 A client I'm working with is seeking a motivated and detail‑oriented Quality Assurance Engineer III to join their team in supporting the development, manufacture, and ongoing reliability of our medical device products. In this role, you will help ensure that ...

Quality Assurance Engineer III
BostonUS$90000 - US$110000 per year

Role: Quality Assurance Engineer IIILocation: Boston, MA (hybrid)Salary: $90,000 - $110,000EPM is partnered with an establish medical equipment manufacuturer which is already revenue-generating and bringing in over $1B+ annually. They are looking to bring on a Quality Assurance Engineer III to join and lead their QE team in supporting the developme...

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Selby Jennings Start Your Career In Recruitment
Design Quality Engineer II
BedfordNegotiable

Title: Design Assurance Engineer IILocation: Hybrid in Bedford, MA SummaryA growing medical technology organization is seeking a Design Assurance Engineer II to support product development, risk management, complaint investigation, and CAPA activities. This role partners closely with R&D from early concept through manufacturing transfer and helps e...

IT Compliance manager (CSV Manager)
LilleNegotiable

The IT Compliance Manager (CSV Manager) will be responsible for ensuring that computerized systems used in a pharmaceutical manufacturing environment are validated, compliant with regulatory requirements, and maintained in a validated state throughout their lifecycle. The successful candidate must have prior experience working within pharma manufac...

PAS-X Specialist Data Modelling Validation
ToulouseNegotiable

A leading biopharmaceutical manufacturing site in Toulouse is seeking an experienced PAS‑X Validation Specialist to support ongoing MES/EBR deployment and data‑modelling activities. The specialist will work within the digital manufacturing and QA/CSV teams to ensure compliant design, configuration, and validation of PAS‑X workflows, MBRs, and syste...