Production Quality Engineer

Job Description: Quality Systems & Regulatory Compliance (Primary Responsibility)Develop, implement, and maintain quality system processes aligned with: ISO 13485:2016FDA QMSR / 21 CFR Part 820 Author and maintain quality documentation, including: SOPsWork instructions Forms and records Support and maintain compliance of a predominantly electronic (paperless) QMSEnsure adherence to good documentation practices (GDP) and 21 CFR Part 11 (as applicable)Support annual FDA establishment registration and device listing activities; assist with preparation, maintenance, and coordination of regulatory submissions, including 510(k) support, technical file/design dossier support, and submission documentation coordination with Regulatory Affairs, as applicable Support internal audits and external audits (FDA, ISO certification, MDSAP readiness)Investigate nonconforming product and process deviations Lead and support CAPA activities, including: Root cause analysis (RCA)Corrective and preventive actions Effectiveness verification Support complaint investigations and ensure feedback into manufacturing and process control Drive timely and complete resolution of quality events Production Quality &Hands‑On Problem Solving Work directly with production and technicians to: Investigate product and process issues Identify sources of variation and failure modes Implement corrective actions Ensure production processes meet defined quality requirements Support real‑time decision‑making on product disposition and quality concerns Identify and elevate risks to product quality or regulatory compliance This role requires a "get your hands dirty" mindset, including active engagement in troubleshooting and issue resolution on the production floor. Process Validation & Control Develop, execute, and maintain: IQ/OQ/PQ validation activities Support process changes and assess validation impact Ensure processes remain in a validated state Support development and maintenance of control plans and process monitoring methods Support risk management activities aligned with ISO 14971 Process FMEA (PFMEA)Risk assessment for manufacturing and process changes Ensure risk‑based decision making in quality and production activities Supplier Quality (Supporting Role)Support incoming inspection processes and acceptance criteria Assist in supplier issue investigations and corrective actions Collaborate with supply chain and engineering to ensure material quality Cross‑Functional Collaboration Partner with: Manufacturing Engineering Supply Chain Regulatory / Quality teams Provide quality input on: Design changes Manufacturing processes Product performance issues Support design transfer and production readiness as needed Supplier Quality & Material Control Support supplier selection, qualification, and evaluation Oversee incoming inspection and acceptance criteria Participate in supplier audits and drive supplier corrective actions as needed Ensure material quality supports consistent production outcomes Training & Workforce Development Train and support technicians performing assembly, testing, and inspection Develop training materials and ensure competency and training effectiveness Promote best practices in documentation, quality, and process adherence Benefits and Salary We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, and tuition reimbursement. Voluntary Self-Identification As set forth in Black Canyon Consulting's Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.