Quality Engineer

Danaher • Timonium, MD

39d • $75,000 - $100,000 • Onsite

About The Position

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Pall Corporation, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper—everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation. Learn about the Danaher Business System which makes everything possible. The Quality Engineer is responsible for Quality Assurance & Quality Control activities supporting quality, production, and process requirements for Pall Corporation Timonium. This includes product and process support starting from review of customer requirements, insuring flow down into drawings, routers, and purchase orders, to final shipment of product to customer and aftermarket support. This position reports to the Quality Manager and is part of the Quality Assurance department located in Timonium, Maryland. This is an on-site role.

Requirements

• Bachelor’s degree in engineering or quality with 5+ years of Quality experience, or 15+ years of equivalent experience in Quality within a manufacturing environment in regulated industries such as medical devices or microelectronics.
• Demonstrated success working under a formal QMS with strong discipline in documentation, change control, training records, and compliance to applicable frameworks such as CAPA expectations, ISO management-system requirements, and customer specific requirements.
• Ability to investigate customer complaints fast, drive containment, lead structured root-cause analysis, implement corrective actions, and verify effectiveness with objective evidence.
• Hands-on experience with process controls (SPC/capability basics), inspection strategy, measurement system readiness (MSA/Gage R&R, Calibration Protocols), and qualification/validation activities to ensure processes consistently meet CTQ requirements.
• Proven ability to support customer/regulatory audits, write clear technical reports, and coordinate actions across Manufacturing, Engineering, Supply Chain/Logistics, and Supplier Quality, ensuring containment is communicated plant-wide and supply continuity is protected.

Nice To Haves

• SmartSolve, Minitab, Microsoft Power Apps, M365, and Power BI software
• Knowledge of Kosher and Halal certification requirements
• Related professional certifications such as ASQ CQE, CQA, and Six Sigma

Responsibilities

• Lead and coordinate customer quality complaint investigations, partnering closely with the manufacturing plant to perform structured root‑cause analysis (e.g., 8D, Fishbone diagram, FMEA, Pareto Analysis) and drive effective and on-time delivery CAPA resolution.
• Drive daily management and problem‑solving activities within the manufacturing environment, to address process deviations, defects, and improvement opportunities by providing Statistical Process Control data to support your investigation.
• Administer and maintain document-controlled databases to assist in Standard Operating Procedures, CAPA traceability and SPC data collection.
• Apply expertise in ISO 9001:2015 and be familiar with upcoming ISO9001:2026 and internal Quality Management System (QMS) procedures, maintaining and generating quality documentation such as inspection reports, First Article Inspection records (FAI), APQP, PPAP, Submissions.

Benefits

• We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
• Check out our benefits at danaherbenefitsinfo.com

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level