Pq Jobs

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

LanceDB is hiring a Senior Software Engineer to design and implement high-performance, GPU-accelerated vector indexing and search systems for its open-source data lake.

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.

Moderna is hiring a Supply Chain Logistics Engineering Co-Op in Norwood, MA to support cold chain operations, shipping validation, and logistics process improvements.

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.

Nemera seeks a Quality Validation Engineer to lead validation projects, supplier quality activities and investigations to maintain regulatory and ISO compliance at its Buffalo Grove medical device manufacturing site.

Dandy is looking for a Senior Quality Engineer to lead ISO 13485 quality systems, CAPA activities, and statistical quality programs at its Carrollton manufacturing facility.

Experienced analytical science SME needed to lead development, validation, and network implementation of rapid microbiology safety methods for Vertex’s biologics and cell & gene therapy commercial programs on a 24-month part-time contract.