Oq Jobs

Smith+Nephew is hiring a Laboratory Validation Specialist to lead lab method validations, equipment qualifications, and computer system validation activities in a GMP-regulated laboratory at the Fort Worth facility.

As a Validation Engineer 2 at Illumina's San Diego site, you will lead validation strategy, execute IQ/OQ/PQ and testing activities, and ensure compliance with regulatory and quality standards for manufacturing processes and systems.

Moderna is hiring a Senior Automation Engineer I to design, implement, and harden GMP-capable automated workflows for cell-based bioassays at its Norwood manufacturing campus.

Lead the engineering transformation at Alcon's Houston manufacturing site by delivering automation, Industry 4.0, CI-driven savings, and an energy transition while building a high-performing engineering organization in a regulated environment.

Contribute manufacturing and equipment design expertise to develop and qualify production lines and tooling for minimally invasive robotic surgical instruments at a leading medical robotics company.

Kincell Bio seeks a hands-on Senior Equipment Engineer to lead GMP equipment onboarding, validation, and lifecycle management at its Durham manufacturing site.

Stryker seeks a Senior Quality Assurance Engineer to lead validation, quality improvement, and risk-reduction activities at its Irvine manufacturing site.

Experienced C&Q leader needed to define and lead a global, partner-centric commissioning and qualification strategy for major capital projects at CSL Behring.

Smith+Nephew is hiring an Advanced Manufacturing Engineer II to lead process development and design transfer activities for new medical device products at the Memphis manufacturing site.

Intuitive seeks a Manufacturing Mechanical Engineer to design and implement assembly and test processes and equipment for the da Vinci multi-port surgical system, improving manufacturability, quality, and throughput.

Senior Electrical Manufacturing Engineer to own and lead PCBA, cable/harness, controller, and battery manufacturing and validation in an FDA-regulated Class III medical device environment at BiVACOR in Huntington Beach, CA.

Computer Software Validation Specialist to lead validation, testing, and compliance for GxP-regulated software implementations at Syner-G's San Diego operations.

QRC Group is hiring a QA Specialist to deliver cGMP quality oversight, validation support, and quality systems leadership for drug substance operations in Juncos, Puerto Rico.

BD is hiring a Quality Engineer II to lead validation and quality assurance activities at its Sumter, SC medical device manufacturing site, ensuring regulatory compliance and process improvement.

Join iota Biosciences as a Mechanical Engineer II to design fixtures, build and test prototypes, author verification protocols, and support transition of implantable and external systems from development into production.

Lead a multidisciplinary manufacturing engineering team at GE HealthCare's State College facility to improve process stability, equipment uptime, and product quality on 2nd shift.