Quality Manager

About the role

Molex is seeking a Quality Manager for our Hudson, WI site, a focused, fast-moving facility that serves the rapidly growing Optical Connectivity business through New Product Introduction (NPI) and volume production. This role will manage, lead, and coordinate the activities of the quality team with the goal of maximizing company profitability by providing products that meet customer expectations.

Create and implement quality systems/procedures that provide continuous improvement methodology supporting manufacturing, support groups, and ensure customer satisfaction is maintained. You will lead the quality department in a scaling manufacturing environment that produces high-quality optical connectivity products employing fiber termination, die cutting, surface mount electronics, and light assembly technologies.

Responsibilities

• Provide direction and leadership to the Quality department, including people management: personnel management, managing performance, team career development, fostering open communication in all directions, ensuring team is aligned with and accomplishing goals/objectives, applicable administrative processing, and fostering a team environment
• Serve as the Management Representative, whose primary responsibility is to ensure that the facility meets internal policies and requirements, customer requirements, and facility specific quality systems
• Devise and implement quality systems/procedures that provide continuous improvement methodology supporting manufacturing and operational consistency
• Ensure compliance with ISO 9001 quality system requirements
• Facilitate management review activity
• Identify and develop resources required to support customers’ product-specific needs and requirements
• Work with management to establish quality goals and objectives
• Develop procedures, processes, and provide leadership to Training Coordinators on each shift

Qualifications

The ideal candidate will have 5+ years directly related experience in quality or a regulated industry and 5+ years experience in a leadership role.

Skills

• Experience with FDA, international regulations, and/or ISO standards
• Experience navigating and leading customer or regulatory body audits
• Associates degree or higher
• Knowledge of current good manufacturing practice (cGMP)
• Knowledge of quality tools, such as SPC, design of experiment (DOE), root cause analysis

Benefits

Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance.