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Quality Engineer

Tyco Electronics / Medical Products is the world's leading producer of Electronic Interconnect Systems for medical OEM customers. Ours is a dynamic work environment where you can capture every bit of potential and possibility out of your career. We are known by our customers for exceptional quality, innovation and responsiveness. Our products demand density, flexibility and signal integrity previously thought impossible. If you enjoy working in a fast-moving environment that values customer interface at all levels and focuses on developing innovative solutions to customers' design needs, come join our company.

We have an open Quality Engineer position at our Harrisburg, PA facility.  Tyco Electronics / Medical Products offers a competitive compensation and benefits package. For more information about our products, please visit our web site at www.precisionint.com.  We are an EEO Employer Dedicated To Work Force Diversity.

Primary responsibilities include:

• Establish process metrics to evaluate process performance, define control points, and work with engineering, and manufacturing to ensure that minimum expectations are met.
• Support process validation studies for special processes and drive a reduction in TE's reliance on inspection as a quality assurance methodology.
• Resolve any special quality, test, and certification requirements in cooperation with engineering and assure overall agreement between TE and customer drawings and specifications.
• Be a resource for design of experiments (DOE) and capability studies.
• Support Product Development and Manufacturing Engineering as required in new product introduction.
• Create Quality Inspection Plans for components and assembly.
• Work to affect Cost of Quality improvement projects
• Support the new product develop processes to assure product meets customer requirements.
• Promote compliance to company procedures.
• Provide leadership to and be a capable resource for the development of and execution of statistical process control (and appropriate related methods).
• Support and manage the verification system at PI for new and existing products. This will involve the support of a 1st Article inspection program and/or process capability studies, and inspection audits to verify quality levels for problem P/Ns.
• Develop standard quality inspection procedures and methods.

Minimum qualifications include:

•  Five or more years quality engineering experience in order to plan, establish and coordinate test and inspection procedures, conduct process capability studies, prepare statistical quality control data and develop statistical designed experiments.
•  BS in science, engineering, manufacturing or technical discipline, CQE, or equivalent experience.
• Audit experience preferred.
• Maintains current knowledge of relevant new technologies, materials, equipment, and processes. Applies knowledge to continually enhance TE capabilities.
• Knowledge of FDA 21 CFR Part 820 and ISO 9001 or 13485.
• Knowledge of Six Sigma preferred.