AddressAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job Overview
TE Connectivity's Quality Control and Reliability Teams ensure product and / or product components comply with specifications and quality standards. They test and inspect products against performance and integrity criteria to ensure product quality and reliability, and to determine the suitability of product release.
The Quality Control Manager - Manufacturing role is working for the Invitro Diagnostics (IVD) group of TE Medical's business unit within the Industrial Solutions sector. The Quality Control Manager will play an important role within the Manufacturing teams, and work with the NPI and NPD teams. The Quality Control Manager will guide their team to ensure that products and manufacturing processes are developed that meet customer needs, developed in accordance with local site development QMS (Quality Management System) expectations and are, in turn, aligned with regulatory requirements expected of a medical device manufacturing organization.
This position will be onsite at our Parker, CO location.
Responsibiites:
• Responsible for Quality Control activities related to the manufacturing of medical device components.
• Has the responsibility and independent authority to make decisions related to product quality, including the disposition of non-conforming product and deviations.
• Ensures all customer queries, concerns, and complaints are professionally addressed in a timely manner and escalates critical issues as appropriate, while delivering an extraordinary customer experience.
• Ensures compliance to the quality management systems in all activities performed.
• Participates in new product introductions to ensure quality is built into all products early in their life cycle.
• Reviews and consults on design & development projects, particularly, the development of the Design History File (DHF) for new products and ensures regulatory compliance.
• Leads and supports external audits from external sources including preparation activities in advance of such audits.
• Leads and demonstrates expertise in the areas of QSR and ISO standards within one’s own group, constantly promoting awareness of industry best practices and making appropriate decisions.
• Utilizing the best-in-class problem solving tools, drives robust and effective corrective and preventive actions through the CAPA system.
Building Effective Teams & Motivating Others
• Engages and manages an international, high-performance quality team including Quality Inspectors, Quality Engineers, and Supplier Quality Engineers.
• Demonstrates commitment to the Quality Policy (patient safety and product quality) through the daily execution of sound quality practices and the maintenance of an effective quality system.
• Ability to work with a cross-functional team to develop and deliver on the site strategic targets and objectives.
• Mentors and trains staff to perform effectively in their work and ensures the training is documented.
• Creates a strong team working environment with focus on customer needs, compliance, product quality, and risk mitigation.
• Develop talent by creating training/development plans with associated input into their career objectives
Strategy, Execution, Talent
• Work with leadership team to develop strategic plans for obtaining annual objectives and goals.
• Measures and monitors key process indicators to proactively evaluate the execution of the strategic plans developed.
• Develops and retains the staff that contribute to achieving the goals and objectives of the organization.
What your background should look like:
- Bachelor’s degree in related field of Engineering or Science
- 8+ years' total professional experience required; including 2+ years in a regulated, manufacturing environment
- 2+ years’ experience managing / supervising teams of Engineers / Technicians
- Previous medical device manufacturing experience, preferred
- Ability to apply a structured problem-solving approach
- Good people skills and the ability to work with different personnel skillsets within the Company. cross-functionally
- ASQ Certified Quality Engineer or MS degree, preferred
- Six Sigma Green/Black belt or other Continuous Improvement methodologies, preferred
Competencies
ABOUT TE CONNECTIVITY
TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive and connected future. Our broad range of connectivity and sensor solutions, proven in the harshest environments, enable advancements in transportation, industrial applications, medical technology, energy, data communications and the home. With more than 85,000 employees, including more than 7,500 engineers, working alongside customers in approximately 140 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at www.te.com and on LinkedIn, Facebook, WeChat and Twitter.
COMPENSATION
• Competitive base salary commensurate with experience: $$97,360 – $146,040 (subject to change dependent on physical location)
• Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity.
• Total Compensation = Base Salary + Incentive(s) + Benefits
BENEFITS
• A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits.
EOE, Including Disability/Vets
