Iq/oq/pq Jobs

Smith+Nephew Robotics is hiring an Advanced Manufacturing Engineer II to lead NPD design transfers, process validation, and tooling/fixture implementation at the Pittsburgh site.

Eurofins is hiring a technical Senior Sterilization Engineer / EO Facility Site Manager in San Jose to lead EO sterilization validation, operations, and regulatory compliance for our medical device testing facility.

Experienced CQV engineer needed to perform commissioning, qualification, and validation activities for Moderna's Norwood GMP manufacturing operations and support capital projects, audits, and continuous improvement.

Lead design verification strategy and execution for advanced drug-delivery and combination product systems within AbbVie's Device & Combination Product Development team.

Medtronic is hiring a Supplier Quality Engineering Manager in North Haven, CT to lead supplier quality programs, manage SCRs, and ensure uninterrupted medical device production.

AbbVie is hiring an Associate Validation Engineer in Worcester, MA to support validation activities, ensure regulatory compliance, and execute small engineering projects within pharmaceutical manufacturing.

Selution (partnered with Cordis) is hiring a Manufacturing Engineer II to lead process development, validation, and troubleshooting for Class IIb/III implantable devices in an onsite cleanroom manufacturing setting.

QRC Group is hiring a Senior Engineer to lead equipment commissioning, CIP/SIP cycle development, and qualification activities for pharmaceutical and biotech clients at their Juncos, PR site.

QRC Group is hiring a Validation Engineer to lead IQ/OQ/PQ, FAT/SAT, and cleanroom qualifications for a multi-dose preservative-free nozzle subsystem across the Southeast U.S.

Provide field-based installation, performance maintenance, and basic troubleshooting for Waters' LC instrumentation across an Eastern PA territory while ensuring regulatory compliance and high customer satisfaction.

Experienced manufacturing engineer needed to lead automation, controls, and technical transfer initiatives for GTI’s production facilities while supporting start-up sites and continuous improvement.

Experienced manufacturing engineer needed to perform failure analysis, improve manufacturing yields, and lead cross-functional reliability improvements for electromechanical surgical systems at a market-leading medical device company.

CRB is hiring a CQV Project Engineer III to lead commissioning, qualification, and validation activities across life sciences projects while providing technical leadership and field execution.

Join Donaldson's Life Sciences Operations as a Manufacturing Engineer II to drive process development, validation, and continuous improvement at the Bloomington, MN manufacturing site.

Medtronic is hiring a Quality Engineer I to develop and implement quality standards and testing protocols at the Grand Rapids manufacturing site to ensure product reliability and compliance.

Develop and maintain high-throughput laboratory automation systems and software integrations at insitro to accelerate ML-driven drug discovery.

Experienced Computer Systems Validation Engineer needed to author and execute validation artifacts, lead client requirements, and ensure compliant system deployment for pharmaceutical and device clients in a primarily remote contract role.

Experienced GxP IT Engineer needed to support and maintain compliant endpoints, lab instruments, and systems (MES, DeltaV, OSI PI) across Moderna’s Norwood site and global GxP environments.

Northwestern Medicine is hiring an onsite Cellular Therapy Scientist to manufacture and test cell and gene therapy products while supporting process/assay development and regulatory-compliant manufacturing.

Lead a production engineering value stream to drive safety, quality, delivery and continuous improvement for medical device manufacturing.

Becton, Dickinson and Company seeks an experienced R&D Staff Engineer – Product Sustaining in El Paso to lead material and design changes that ensure ongoing safety, performance, and regulatory compliance of medical products.

QRC Group is hiring Validation Engineers to lead IQ/OQ/PQ, FAT/SAT, cleanroom qualification, and traceability activities for a multi-dose preservative-free nozzle subsystem across the Southeastern U.S.