Contract Quality Engineer Jobs
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Quality Engineer Validation
Validation Engineer - Contract | Medical Device Manufacturer | North Carolina (Hybrid)A leading medical device manufacturer in North Carolina is seeking a Validation Engineer for a contract position to support product development, validation, and quality assurance initiatives.Position Summary:This role applies quality engineering principles across ...
Validation Engineer
This position is responsible for supporting the validation and quality engineering of various systems in a medical device manufacturing environment and assure the equipment/system and validation records are compliant with company standards and industry practices.Work requires originality and judgment in the independent evaluation, selection, and su...
Supplier Engineer
Essential Skills / ResponsibilitiesParticipate in the local cross-functional operational governance process that prioritizes projects across quality, delivery, and cost, assign cross-functional resources for execution, and provide updates on assigned projects against commitments.Lead or participate in a wide range of technical projects utilizing ap...
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PFAS Specialist Engineer
🌿 PFAS Specialist Engineer - Medical Devices📍 Switzerland | 💼 Hybrid | 🕒 6-Month ContractWe're recruiting on behalf of our clients for a PFAS Specialist Engineer to lead compliance and supplier engagement efforts related to PFAS (per- and polyfluoroalkyl substances). This role is critical in ensuring regulatory alignment (REACH, RoHS, MDR) and ...
Freelance Maximo Maintenance Engineer
Position: Maximo Planning EngineersLocation: East Coast, IrelandType: Contract RolesDescription: We are seeking experienced Maximo professionals to join our team at a major pharmaceutical site on the East Coast of Ireland. If you thrive in GMP environments, excel at planning and scheduling maintenance, and have a strong command of IBM Maximo, we wa...
Freelance Process Validation Engineer
Project Overview:Join a high-impact containment upgrade project focused on granulation suites within a solid oral dosage manufacturing facility. This is a key role within a multidisciplinary team, supporting critical validation activities from equipment qualification through to final documentation.Key Responsibilities:Develop and execute IQ, OQ, an...