Quality Validation Jobs

AbbVie is hiring an onsite Quality Validation Specialist in North Chicago to lead and approve validation activities, drive investigations/CAPAs, and maintain validated status for equipment, systems and processes.

Experienced QA leader sought to manage GMP quality systems, audits, and staff for a 3–6 month contract at a global CRDMO, with potential for full-time conversion.

Quality Manager sought to lead site QA and maintain regulatory and customer compliance for a regulated manufacturing operation in Mayfield, KY.

Experienced R&D Engineer II to design and execute verification/validation testing and develop new test methods for drug/device combination products at AbbVie's Irvine site.

Dandy is hiring a Senior Quality Engineer to lead ISO-driven quality systems, CAPA, and validation efforts for its manufacturing operations supporting dental prosthetics and medical-device-grade processes.

Remote Project Coordinator needed to organize documentation, track resources, and support AI training project roll-outs for a growing global studio.

A seasoned Quality Engineer role focused on leading design control, risk management, and verification/validation efforts for electromechanical and software-driven surgical systems at Intuitive Surgical.

Lead the Quality Engineering organization for Multiport Da Vinci instruments, driving NPI and sustaining quality, failure analysis, and continuous improvement to deliver safe, reliable medical devices.

Atomic Industries seeks a hands-on Manufacturing Engineer to design, commission, and scale automated injection-molding cells for a high-volume, high-mix production environment in Warren, MI.

Join UChicago Medicine's Clinical Chemistry Lab as an evening Medical Technologist performing high-complexity chemistry testing, instrument maintenance, and quality assurance in a 100% onsite Hyde Park role.

Lead and supervise multi-discipline clinical laboratory operations at Eurofins Lancaster, ensuring timely, accurate testing, staff development, and regulatory-quality systems adherence.

Lead the planning and execution of a new drug-delivery product line start-up at medmix's Flowery Branch facility, ensuring projects meet scope, schedule, quality, and budget targets.

Experienced Quality Manager needed to lead site compliance, GMP oversight, audits, and CAPA activities for Innovation Labs to ensure FDA and Health Canada regulatory adherence.

At Elanco's Winslow manufacturing site, the Quality Assurance Associate will ensure product and process quality by managing deviations, supporting batch disposition, and driving compliance across operations.

Intuitive seeks a Senior Quality Engineer in Peachtree Corners to lead sustaining manufacturing support, failure analysis, design control activities, and continuous quality improvements for the da Vinci Multiport service organization.

Experienced supplier-focused process engineer needed to qualify, develop, and scale electronic and electromechanical suppliers for high-volume medical device production at Intuitive.

Becton, Dickinson & Company seeks an experienced Associate Director of Plant Operations to lead manufacturing, quality and supply chain teams at its Sparks, MD facility to achieve safety, productivity and regulatory objectives.

A hands-on entry-level engineering role at AbbVie supporting small projects, compliance, testing, and process design within a collaborative pharmaceutical environment.

Experienced engineer with protein purification and strong technical writing skills needed to support validation and process improvement projects at a regulatory-focused services firm in Juncos, PR.

Lead cross-functional programs for battery cell development at GM by coordinating design, process readiness, validation, and stakeholder communications to deliver development and scaled batch builds.

Macmillan is hiring a QA Analyst to validate system and data changes for its Royalties program through manual and automated testing, defect management, and cross-team collaboration.

Osaro is hiring a Robotics Quality Engineer to lead validation, testing, and commissioning of complex robotic systems for production and customer sites.

Bristol Myers Squibb is hiring a Senior Engineer for IT Computer System Validation at the Devens Cell Therapy Facility to lead CSV lifecycle activities, act as a CSV SME, and ensure computerized systems meet GxP and regulatory standards.

Medtronic is hiring a Senior Hardware Quality Engineer to lead hardware quality assurance, design verification, and regulatory compliance efforts for medical devices at the North Haven site.

St. Luke's Health System seeks a Data Registry Coordinator to abstract, validate, and submit cardiovascular procedure data to national registries to support program performance and quality initiatives.

Lead a New Orleans food testing lab team at Eurofins, overseeing analytical testing, QC, method development and staff training in a fast-paced regulated environment.

Experienced Manufacturing Technician needed to support process development, equipment setup, validation, and continuous improvement in an onsite production environment.

Experienced process development scientist needed to support protein formulation, filling processes, technology transfer and process validation for regulated pharmaceutical environments.

Experienced Systems Engineer needed to support sensor imaging systems, product quality requirements, system integration, and testing within a mission-focused engineering team at TGC.

Clinigen seeks an experienced Quality Operations Manager to lead on-site Quality Assurance operations and QMS implementation at CSM USA, ensuring regulatory compliance and operational excellence.

UChicago Medicine is hiring a Technical Lead in Clinical Chemistry to drive method implementation, ensure high-quality testing, and lead technical staff at its Hyde Park laboratory.

Eurofins Scientific is hiring a Pharmaceutical QA Senior Specialist - Group Leader to lead QA oversight for QC operations, ensuring cGMP compliance and robust release-ready documentation at the Sanford site.

QRC Group is hiring a bilingual Quality Systems Documentation Specialist to manage and maintain regulatory documentation and support validation activities at its Vega Baja, PR location.

Oura is looking for a Medical Device Quality Assurance Engineer to drive compliance, risk management, and verification for SaMD across development and lifecycle activities.

QRC Group is hiring a bilingual Technical Writer in Gurabo to produce and maintain GMP- and regulatory-compliant documentation supporting pharmaceutical development, manufacturing, and inspections.

Lumafield is hiring a Regulatory Affairs Specialist to define and execute regulatory strategy and compliance processes for its industrial CT hardware-software products.

Eli Lilly is hiring an experienced QA leader in Indianapolis to oversee external parenteral drug product manufacturing quality and manage QA operations for contract manufacturers and alliance partners.

Lead a large QC laboratory organization at AbbVie's Waco facility, directing lab operations, compliance, and technical projects to support manufacturing and product quality.

An experienced engineer to design, test, and lead mid-size projects at AbbVie's North Chicago site, contributing to product/process development and continuous improvement.

Lead Penumbra's quality engineering team in Alameda to maintain regulatory compliance and drive product and process quality improvements for catheter products.

SQA Services is hiring a Process Quality Engineer to support an aerospace client in Duluth, MN with production line validation, troubleshooting, and supplier quality resolution on a six-month on-site contract.

Experienced program management leader needed to oversee global device and combination product industrialization programs and ensure timely, compliant transfers into manufacturing at AbbVie.

AbbVie is hiring an Associate Director of Program Management to lead global device and combination-product industrialization programs, coordinating cross-functional teams to deliver manufacturing transfers and launches.

VahatiCor seeks a Process Development Engineer to lead catheter process development, transfer, and validation in its onsite Santa Clara manufacturing environment.

CVS Health's Caremark LLC is hiring a Senior Quality Engineer to lead testing, data validation and QA automation across cloud-based healthcare systems.

QRC Group is hiring a Specialist QA in Juncos, Puerto Rico to lead validation, commissioning/qualifications and quality system activities for manufacturing operations.

Truist is hiring a Data Assessment Analyst to design and execute regulatory data conformance tests using SQL and SAS and to document audit-ready findings for key bank reports.

Lead Eurofins' Richmond aerosol extraction team to deliver ISO 17025‑compliant sample preparation and high-quality analytical data for diverse clients.

Eli Lilly is hiring an Associate Director to lead analytical project management and technical transfers supporting manufacturing and laboratory governance.

Flex is hiring a Validation Associate Engineer in Austin to drive validation activities, maintain quality programs, and support regulatory-compliant product development in a medical device manufacturing environment.