Capa Jobs

Medtronic is hiring a Quality Systems Business Analyst in Northridge to support and optimize eQMS processes and quality metrics for the Diabetes business, ensuring regulatory compliance and continuous improvement.

Red Wing Shoe Company is hiring a Quality Systems Manager to own ISO certification, internal auditing, and enterprise quality systems across its manufacturing and supplier network.

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

Lead regional Quality Operations at Plexus to ensure compliance, drive APQP/FAI/PFMEA execution, reduce CoPQ and mentor teams for continuous improvement across multiple manufacturing sites.

As a Lead Systems and Security Representative at GE HealthCare, you will architect and lead secure, scalable system designs while driving security compliance and technical project delivery.

Experienced QA professional needed to lead GMP quality oversight, batch disposition, and investigations for drug product operations at a client site supporting clinical and commercial manufacturing.

Eliquent Life Sciences seeks a Vendor Quality Management Specialist to coordinate vendor management activities, maintain AVL and vendor records, and ensure vendor compliance with GMP/GDP requirements.

Haleon is hiring a Quality Systems Co-Op at its Oak Hill (East Durham), NY manufacturing site to support quality systems, CAPA, audits and supplier/complaint tracking while learning GMP-driven quality operations.

Lead a supplier engineering organization at Intuitive to drive supplier selection, development, performance and risk mitigation for high-volume medical device components.

Alcon is hiring an Associate II, Quality Control Labs in Houston to manage metrology and microbiology equipment validation, create inspection programs, and support batch release to ensure product quality and compliance.

Lead the Indianapolis engineering and facilities team at Novartis to ensure reliable RLT manufacturing through maintenance, calibration, validation and continuous improvement.

Lead production and program delivery for enterprise localization accounts at LILT, optimizing workflows and ensuring SLAs and KPIs are met across cross-functional teams.

Experienced QA and regulatory leader needed to build and run quality systems and compliance strategies for EVERSANA’s regulated healthcare services in Memphis.

Experienced biochemistry or molecular biology professional needed to perform PCR/ELISA/HPLC workflows, maintain data integrity, and support GMP/GLP quality processes at Eurofins' Indianapolis laboratory.

Eurofins is hiring a Scientist in Santa Monica to perform raw materials release testing and support GMP analytical operations for Global Reference Standards.

Everly Health is hiring a Lab Quality Manager to own CLIA/CAP/NYS compliance, internal auditing, and quality systems for its Hoffman Estates moderate-complexity diagnostic laboratory.

Coca‑Cola is hiring a Quality System Analyst in Cidra, PR to lead CAPA and risk/opportunity programs, perform root cause analysis, and support plant food-safety and quality systems.

Sanofi is hiring a Manager, Quality Operations - Vaccine to lead operational QA, CDMO oversight, and quality system harmonization at its Waltham site.

ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.

Lead clinical and companion diagnostic compliance efforts at Grail by driving inspection readiness, audits, CAPA management, and cross-functional quality improvements to support clinical studies and CDx development.

GeneFab is hiring a hands-on QA Operations Specialist to provide frontline GMP support and drive quality initiatives at our Alameda cell therapy manufacturing site.

Dymax is hiring a Senior Quality Manager to lead multi-site quality operations, regulatory readiness, and continuous improvement across its Torrington, CT manufacturing locations.

DeepHealth seeks a hands-on QA/RA Project Manager to drive quality, regulatory readiness, and cross-functional delivery for medical device software and digital health products in a fully remote role.

Eliquent Life Sciences seeks a Facilities Engineer to produce and maintain GMP-compliant facilities documentation and support commissioning/qualification of critical utility and facility systems onsite in Rensselaer, IN.

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Lead the development and execution of the end-to-end quality program for Hims & Hers' CLIA-certified diagnostic testing operations to ensure regulatory compliance, patient safety, and operational excellence.

AbbVie is hiring a QA Validation Engineer to lead validation planning, execute validation tasks, and support quality and regulatory compliance at its North Chicago manufacturing facility.

Work as a QC Analyst at a fast-growing biopharma in New Jersey performing GMP analytical and microbiological testing, with relocation support for qualified U.S. citizens.

GRAIL is hiring a Staff Quality Systems Specialist in Durham, NC to manage and improve eQMS-driven document control, records management, and training programs (Veeva experience highly preferred).

Work on master data, MRP oversight, and cross-functional supply chain projects at Novartis' Indianapolis RLT operations to ensure accurate data and timely production support.

Datavant seeks a proactive Senior Compliance Analyst to support enterprise-wide compliance programs, audits, and policy governance in a remote, fast-moving healthcare data company.

Lead Synthego's GMP quality programs as a hands-on Quality Assurance Manager overseeing eQMS, CAPA, deviation management, audits, and team development to ensure product and process compliance.

Lead the plant QA function at J&J Snack Foods in Rock Island, overseeing food safety, quality systems, lab operations and a small team to ensure product compliance with HACCP, GMP and customer specifications.

Take ownership of manufacturing process improvements and compliance as a 2nd Shift Senior Manufacturing Engineer supporting life-saving cardiovascular devices.

Plexus is hiring a Supplier Quality Engineer II to lead supplier qualification, audits, and continuous improvement initiatives that ensure incoming material quality at the Nampa, ID manufacturing site.

Edwards Lifesciences seeks a Supplier Quality Engineer II to lead supplier quality investigations, audits, and change-control activities at its Draper, Utah manufacturing site.

Kincell Bio seeks a detail-oriented Manufacturing Specialist to support on-site cGMP cell therapy production, operate automated and manual equipment, and manage GMP documentation and corrective actions.

Experienced QA Specialist needed to perform cGMP document reviews, batch and lab data release, audits, and investigations for Lonza's Tampa manufacturing site on the 3–11 PM shift.

Eliquent Life Sciences is hiring a Supplier Quality Consultant to lead supplier qualification, audits, and compliance activities for pharmaceutical and biopharmaceutical clients.

Orca Bio is hiring a 2nd-shift QA Technician to perform real-time documentation review and on-floor quality oversight for cGMP cell therapy manufacturing in Sacramento.

Lead BD’s failure analysis function in Irvine to drive root-cause investigations, corrective actions, and continuous quality improvements for medical device products.

Lead the Raw Materials & Incoming Materials QC laboratory at AbbVie's Barceloneta site, driving compliance, investigations, and team performance for a high-volume biologics manufacturing environment.

Lead controls engineering and automation initiatives at Baxter’s Marion manufacturing site, applying deep PLC, robotics, and validation expertise to ensure safe, compliant, and efficient production.

VahatiCor is hiring a hands-on Quality Engineer with direct catheter device experience and ISO 13485 expertise to lead quality activities for catheter manufacturing and validation.

Provide technical leadership for upstream tech transfer, troubleshooting, and process validation to support large-scale monoclonal antibody manufacturing at the Holly Springs site.

Pfizer is hiring a Quality Risk Management Manager in Kalamazoo to lead QRM programs, maintain QRM tools and libraries, and provide guidance to site teams to ensure compliant, risk-based quality practices.

FUJIFILM Biotechnologies is hiring an Associate Director to lead Cleaning Validation and CQV strategy at its Holly Springs biologics facility, ensuring compliant, risk-based validation for multi-product manufacturing.

Amentum seeks a proactive EHS Compliance Manager to oversee high-hazard safety, compliance programs, training, and incident response at its La Jolla pharmaceutical R&D site.

Alphatec Spine is looking for a Mechanical Quality Engineer II to lead mechanical quality activities across new product development, supplier qualification, and production validation for implantable devices.

Senior Manager to lead the Raw Materials & Incoming Quality Control laboratory at AbbVie's Barceloneta biologics site, ensuring regulatory compliance, robust testing programs, and effective team leadership.

Abbott is hiring a Supplier Quality Engineer II in Westfield, IN to lead supplier audits, qualify vendors, and drive CAPA closure to maintain ISO/QSR compliance for Structural Heart products.