Quality Systems and Compliance Manager

Be visionary Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. ​ We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.

Summary The Quality Systems and Compliance Manager is responsible for developing, implementing, maintaining, and continually improving the Quality Management System (QMS) in accordance with ISO 9001:2015, ISO 13485:2016, applicable regulatory requirements, and EU Medical Device Regulation (MDR) 2017/745. This position provides leadership and oversight for quality assurance, regulatory compliance, risk management, supplier quality management, internal audits, corrective and preventive actions, complaint handling, post-market surveillance activities, and management review processes. The Quality Assurance Manager ensures products and processes consistently meet customer, statutory, regulatory, and organizational requirements while promoting a culture of quality, continuous improvement, and risk-based decision making. Assignments are complex and strategic in nature, requiring independent judgment, technical expertise, and leadership across cross-functional teams. Essential Duties and Responsibilities include the following, but not limited to: Quality Management System Leadership Establish, implement, maintain, and continuously improve the organization's QMS in compliance with ISO 9001, ISO 13485, EU MDR, applicable national regulations, and company requirements. Serve as management representative or designated quality leader to ensure QMS processes are effectively established, implemented, maintained, and reported to executive management. Monitor QMS performance through quality objectives, KPIs, trend analysis, and management review reporting. Ensure appropriate process interactions, documented information, and quality records are maintained and controlled. Regulatory Compliance and MDR Ensure compliance with applicable medical device regulations including EU MDR 2017/745, FDA Quality System Regulation (as applicable), and other global regulatory requirements. Support regulatory inspections, notified body audits, customer audits, certification audits, and governmental inspections. Ensure quality system procedures support technical documentation, device lifecycle controls, vigilance reporting, and post-market surveillance requirements. Support regulatory submissions and product registrations through quality system compliance activities. Risk Management Promote application of risk-based thinking throughout the organization. Ensure quality activities incorporate risk management principles in accordance with ISO 14971 where applicable. Review and monitor quality risks related to products, processes, suppliers, complaints, nonconformities, and field performance. Ensure risk controls remain effective and are periodically evaluated. Product and Process Quality Establish and maintain quality plans, inspection strategies, acceptance criteria, validation activities, and process controls. Ensure appropriate verification, validation, qualification, and monitoring activities are performed and documented. Review manufacturing, inspection, testing, and service processes to ensure compliance with established requirements. Support design and development activities by participating in design reviews, verification, validation, and design transfer activities. Supplier Quality Management Establish and maintain supplier qualification, monitoring, re-evaluation, and approval programs. Conduct supplier audits and assessments using risk-based methodologies. Ensure supplier quality