Quality Assurance Manager
Dober
Job Description
About the Company
\nSince 1957, Dober Chemical has grown through innovation, strong partnerships, and a culture of Mutual Trust and Respect. We empower employees to make a difference, reward fresh ideas, and support both professional and personal growth.
\n \nOur Core Values foster a collaborative, people-first environment where your work truly matters. Join us and help shape the future with a company built on trust, creativity, and purpose.
\nWe offer a comprehensive benefits package that includes medical, dental, and vision coverage, short-term and long-term disability insurance, life insurance, paid time off (PTO), paid parental leave, volunteer time off, and the Calm app membership. Our expanding wellness program supports your overall health and work-life balance.
\n \nAbout the Job
\nPosition Summary
\nThe Quality Manager drives a proactive, data-driven quality culture by designing quality into processes - not inspecting it in after the fact. This role strengthens ISO compliance while advancing quality systems and built-in process controls, supplier integrity, and continuous improvement.
\n \nThe Quality Manager partners cross-functionally to ensure operational excellence through standardized work, statistical process control, structured audits, supplier quality management, and disciplined corrective action. This role champions accountability, real-time data visibility, and zero-error process design.
\n \n1. Quality Management System & Compliance
\n- \n
- Maintain and improve the ISO-compliant Quality Management System (QMS). \n
- Lead internal audits and customer audits; ensure timely closure and effectiveness verification of corrective actions. \n
- Understand minimum customer requirements in FDA regulated industries and ensure the QMS is built to bridge rigorous quality standards. \n
- Ensure documentation integrity, change control compliance, and standardized work across critical processes. \n
- Operate as an internal escalation point, providing guidance to other members of the Quality team. \n
2. Built-In Quality & Process Excellence
\n- \n
- Integrate quality at every stage using SPC, critical control points, in-line verification, and process validation techniques. \n
- Design and validate test methods (Gage R&R, correlation, progression studies). \n
- Analyze historical performance data to drive proactive specification improvements and reduce variability. \n
- Support mistake-proofing, digital verification, and structured process controls to prevent defects before they occur. \n
3. Data-Driven Problem Solving & Continuous Improvement
\n- \n
- Lead root cause investigations for internal failures and customer issues using structured problem-solving methodologies. \n
- Drive corrective and preventive actions with effectiveness monitoring. \n
- Build trend analysis, predictive insights, and performance dashboards to proactively identify risk. \n
- Lead quality improvement initiatives that reduce waste, variation, and cycle time while improving customer satisfaction. \n
- Support cross-functional Kaizen and process optimization initiatives. \n
4. Supplier & Material Quality
\n- \n
- Conduct supplier audits (paper and on-site) and manage supplier performance metrics. \n
- Ensure raw material verification, traceability, and supplier qualification standards. \n
- Partner with Supply Chain and Operations to prevent defects at the source. \n
5. Customer & Audit Readiness
\n- \n
- Support customer audits, quality agreements, and documentation requests. \n
- Maintain audit-ready documentation and performance metrics at all times. \n
- Ensure quality standards meet or exceed customer expectations. \n
6. Culture, Leadership & Accountability
\n- \n
- Champion a culture of ownership where quality is embedded in every role. \n
- Support training on quality systems, statistical tools, and standardized processes. \n
- Promote stop-work authority, proactive error prevention, and open reporting. \n
- Operate with structured project management discipline and data-backed decision making. \n
Success Profile (What “Great” Looks Like)
\n- \n
- Audit-ready at all times with zero major findings. \n
- Reduction in internal failures and customer complaints year-over-year. \n
- Strong supplier performance and measurable reduction in incoming defects. \n
- Quality metrics visible, understood, and owned by operations teams. \n
- Continuous improvement initiatives completed on time with measurable impact. \n
Required Experience
\n- \n
- Statistical Process Control (SPC) & data analysis \n
- Root Cause Analysis (5-Why, Fishbone, etc.) \n
- ISO 9001 \n
- Chemical experience/background \n
- Audit leadership (internal & external) \n
- Process validation & test method development \n
- Lean principles & waste elimination \n
- Cross-functional collaboration \n
- Strong documentation discipline \n
- Minitab experience \n
- Bachelor’s degree in chemistry or biology \n
This position requires 25% Travel domestically and internationally
\nBase Salary compensation to increase based upon applicable years of experience and leadership capabilities
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