Quality Manager

PSG is the global pump, metering and dispensing-solution expert, enabling the safe and efficient transfer of critical and valuable fluids that require optimal performance and reliability in applications where it matters most. Additionally, PSG is a leading provider of flow meters designed to reduce waste and downtime while accurately measuring, monitoring and controlling the distribution of fluids. Headquartered in Downers Grove, IL, USA, PSG is comprised of several world‑class brands, including Abaque, All‑Flo, Almatec, Blackmer, Ebsray, em‑tec, Griswold, Hydro, Malema, Mouvex, Neptune, PSG Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents - North America, Europe, and Asia - in state‑of‑the‑art facilities that practice lean manufacturing and are ISO-certified. PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional information on PSG, please visitpsgdover.com. We thrive on winning and being number one; and are always looking to add the best and brightest to our talented team of professionals. PSG offers a unique combination of the both small company atmosphere: with an ownership mindset that allows you to make close‑to‑the‑customer decisions; an innovative approach in seeing beyond what is possible today and entrepreneurial spirit in the pursuit of new opportunities; combined with benefits of a large company's scale, tools, expertise, and financial strength with Dover. Join PSG, a growing global company where your curiosity, hard work and ambition is rewarded with exceptional career opportunities in a friendly & fast paced environment. PSG is part of the Pumps and Process Solutions segment of the Dover Corporation (NYSE: DOV). Dover is a diversified global manufacturer and solutions provider with annual revenue of over $7 billion. We deliver innovative equipment and components, consumable supplies, aftermarket parts, software and digital solutions, and support services through five operating segments. Recognized for our entrepreneurial approach for over 65 years, our team of over 24,000 employees takes an ownership mindset, collaborating with customers to redefine what's possible.

POSITION SUMMARY:

The Quality Manager leads the PSG Hydro Cincinnati quality function with ownership for manufacturing quality, customer quality, supplier quality, and the site Quality Management System. This role is accountable for building a proactive, data‑driven quality culture that prevents defects, improves product reliability, reduces cost of poor quality, and ensures products and services meet customer expectations.

PRIMARY RESPONSIBILITIES/DUTIES:

Lead the Cincinnati Quality team and provide clear direction, coaching, prioritization, and accountability across customer quality, manufacturing quality, supplier quality, inspection, QMS, and corrective‑action processes. Own and continually improve the site Quality Management System, including quality procedures, document control for QMS records, internal audits, management reviews, calibration, corrective and preventive actions, quality alerts, and audit readiness. Drive measurable improvement in quality performance using data from customer complaints, RMAs, audit failures, rework, incoming inspection, supplier performance, and cost of poor quality. Lead customer quality processes, including complaint investigations, CAR/CAPA responses, customer audits and surveys, quality communications, containment actions, and cross‑functional problem solving for key accounts. Support Operations by preventing and resolving manufacturing quality issues, improving inspection methods, strengthening production quality audits, supporting work instruction effectiveness, and ensuring appropriate quality controls are in place before product reaches the customer. Lead supplier quality in partnership with Supply Chain, including supplier qualification, incoming inspection strategy, supplier performance reviews, SCARs, vendor corrective actions, supplier visits, and risk‑based controls for critical components. Partner with Engineering and NPD teams to embed quality planning into product development, design reviews, validation planning, ECO/change control, PFMEA, control plans, first article/first‑off approvals, and product reliability improvements. Support Engineering‑led Regulatory Affairs by ensuring supplier changes, component changes, product changes, and corrective actions are properly documented, risk assessed, and traceable to QMS requirements. Escalate any changes that may affect product certification, listing status, customer requirements, or regulatory commitments. Facilitate recurring quality reviews that turn data into action, including Pareto analysis, root‑cause review, aging corrective actions, supplier quality trends, floor audit trends, customer complaint trends, and progress against quality improvement priorities. Build cross‑functional discipline around root cause and corrective action using structured problem‑solving methods such as 8D, 5 Why, fishbone, PDCA, DMAIC, and mistake‑proofing. Develop Quality team capability through standard work, training, career development, performance management, and clear expectations for ownership and urgency. Perform other duties as assigned.

INUMUM REQUIRMENTS:

Bachelor's degree in Engineering or other related technical field. 7+ years of Quality, Manufacturing Quality, Supplier Quality, or Quality Systems experience, with 2+ years leading people or cross‑functional quality programs. Demonstrated experience leading a manufacturing quality function in a technical, industrial, assembled‑product, electronics, plastics, fluid‑handling, equipment, or similar manufacturing environment. Hands‑on experience with core quality tools including PFMEA, control plans, APQP/PPAP or equivalent quality planning methods, capability studies, root cause analysis, 8D, 5 Why, SPC, and corrective action management. Experience working with supplier quality, incoming inspection, supplier corrective actions, supplier qualification, and vendor performance improvement. Strong written and verbal communication skills, with the ability to influence at all levels of the organization and translate quality data into clear business actions. Proven record of hands‑on project leadership, follow‑through, accountability, and driving sustained process improvement.

PREFERRED REQUIRMENTS:

Experience with plastic components, machined parts, electronics, electro‑mechanical assemblies, fluid‑handling equipment, dispensing systems, or similar products. ASQ certification such as CQE, CQA, or CMQ/OE; Lean Six Sigma Green Belt or Black Belt preferred. Systems experience with Microsoft Office, Power BI, Oracle ERP, MES, quality databases, and structured issue‑tracking systems is strongly preferred. Work Arrangement :Onsite Pay Range: $118,151.00 - $148,924.00annually. Bonus Eligible: This position is eligible to earn a discretionary bonus based on performance metrics and other criteria outlined in our applicable bonus plan. a 401(k) savings plan with employer contributions medical, dental and vision insurance wellness programs health savings account, health care and dependent care flexible spending accounts company paid short‑term disability and long‑term disability company paid employee basic life and AD&D insurance supplemental employee and dependent life insurance optional accident, hospital indemnity and critical illness insurance adoption, surrogacy, and fertility benefits and assistance commuter benefits parental, military, jury duty, and bereavement leaves of absence paid time off, including 11 paid holidays per calendar year, paid vacation days beginning at 120 hours annually, 40 paid sick leave hours annually or as provided under state and local paid sick leave laws, business travel services employee discounts and an employee assistance program that includes company paid counseling sessions and legal services. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law. Attention Applicants: If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please let us know. Likewise, if you are limited in the ability to access or use this online application process and need an alternative method for applying, we will determine an alternate way for you to apply. Please View email address on click.appcast.io assistance with an accommodation. Kindly specify Job Requisition Number / Job Title and Location in response. Job Function : Other; Engineering; Manufacturing & Operations; Quality & Continous Improvement

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