We are looking for an experienced Senior Manager, Quality Assurance - Machining & Production to lead and enhance manufacturing quality processes within our medical device operations. This role plays a pivotal part in ensuring product integrity from design transfer through full-scale production, driving quality excellence across machining, component inspection, and industrialization.
The ideal candidate will have a strategic mindset, a hands-on approach to solving complex quality challenges, and a track record of working collaboratively across manufacturing, supplier quality, and compliance teams. This position will also oversee quality-related integration efforts for acquisitions and ensure consistency in purchasing controls.
Key Responsibilities
- Establish and drive manufacturing quality strategy aligned with operational and business objectives.
- Oversee quality assurance processes throughout the product lifecycle, from design transfer to full-scale production.
- Lead machined part and component inspection, ensuring precision and compliance with quality standards.
- Proactively identify and resolve manufacturing quality issues, conducting thorough root cause analyses and implementing corrective / preventive actions.
- Develop strong relationships with manufacturing teams and suppliers to enhance process control and continuous improvement efforts.
- Conduct internal audits to assess compliance, identify gaps, and drive productivity enhancements.
- Utilize quality data analytics to monitor trends, identify potential risks, and implement meaningful improvements.
- Manage and develop a team of Quality Engineers and Inspectors, fostering a culture of accountability and excellence.
- Lead quality integration efforts for acquisitions, ensuring alignment with existing manufacturing and supplier controls.
- Oversee and optimize quality budgets, balancing cost efficiency with operational excellence.
Qualifications & Experience
Bachelor's degree in Engineering, Science, or a related field (MBA preferred).10+ years of experience in medical device, pharmaceutical, or regulated manufacturing, covering supplier quality, operations quality, or procurement quality.Strong knowledge of FDA regulations, ISO 13485, cGMP, and medical device directives.Expertise in root cause analysis, CAPA, statistical sampling, audit techniques, and supplier qualification.Ability to influence stakeholders at all levels, including senior leadership, through strong communication and persuasion skills.Proven ability to lead and develop high-performing quality teams.Skilled in writing and refining procedures, policies, and quality documentation.Strong budgeting and resource management experience.Why Join Us?
Be part of an innovative company shaping the future of medical device manufacturing.Lead impactful quality initiatives that directly improve patient safety and product reliability.Competitive compensation, benefits, and professional growth opportunities in a collaborative, high-performance environment.If you have a passion for quality excellence in machining and production, we encourage you to apply and make a lasting impact in the medical device industry!