Production Quality Engineering Manager

Title: Production Quality Engineering Manager Location: On-site, Lakewood, CO Schedule: M-F 9:00am- 5:00pm Pay: $120-$150k, 10% bonus (bonus, excellent healthcare benefits, unlimited PTO Type: Direct/Permanent Start date: Immediate Overview: Our client a global medical device company, is currently seeking qualified candidates for the position a global leader to be the Production Quality Engineering Manager oversee and provide leadership for the Production Quality Engineering, Validation, and In-process testing teams.

This role is integral in driving quality improvements in manufacturing, maintaining compliance to standards and regulations, and ensuring product testing is completed in timely and consistent manner.

Responsibilities: Provides leadership and direction to the quality team, ensuring alignment with business and corporate objectives Identifies and implements initiatives to reduce defects, enhance product quality, and improve quality system efficiency Manages the Nonconformance process, ensuring timely investigations, thorough root cause analysis, and reduction of recurring issues Collaborates with Production, Engineering, R&D, and external partners to ensure proper handling of changes and quality events Participates in annual budget planning and ensures operations remain within financial targets Develops, tracks, and reports key performance indicators (KPIs) for quality metrics Analyzes quality data to identify trends and provides actionable insights to the management team Requirements: Bachelor’s degree required; B.S.

in Engineering strongly preferred Equivalent combination of education and experience may be considered Strong leadership skills with experience guiding, coaching, and developing teams Proven project management and problem-solving abilities Skilled in mentoring and training staff in an organizational setting Experienced in cross-functional collaboration with engineering, production, and quality teams Effective communicator with strong verbal and written skills Demonstrated ability to lead technical teams and influence decision-making across departments Serves as primary technical contact on complex projects involving multiple stakeholders Ability to build consensus and promote open, constructive communication Deep knowledge of ISO 13485 and 21 CFR Part 820 quality system requirements Experience working with regulatory agencies and supporting audits Familiarity with cleanroom environments, sterilization processes, and product testing protocols Able to clearly present complex technical data and respond to technical inquiries Proficient in PC software applications and tools relevant to quality and engineering work #M3 #LI-GS1 Ref: #558-Scientific

Full Time