US-CA-SanDiego: Quality Engineer
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The Quality Engineer assists in determining, implementing and improving the evolution of the corporate quality control system, and its impact on both the strategic and daily product development and manufacturing operations. This individual is responsible for supporting the development and implementation of departmental policies and resources into the daily functions that will affect the long-term quality and manufacturing culture and business strategies within the organization. This individual must lead the efforts in resolving varying levels of quality and compliance issues independently and/or in unison within a cross functional team environment to efficiently and effectively eliminate the issue and its cause.
•Prefer a B.S. in Engineering/Chemistry/Biology/Technical Discipline or equivalent combination of certification and work experience. •5-10 years experience in Quality and Manufacturing Systems in Medical Device and high volume manufacturing environments •Quality Tools – Problem Solving •Computer skills – proficient in Microsoft Office, statistical software programs, operating systems, voice and email, etc. •Project management, multiple tasking and excellent prioritization skills. •Knowledge of quality systems and regulations for medical device industry. •The Quality Engineer should have a results oriented commitment to the continuing evolution of the quality control system within defined regulatory and corporate requirements. This requires a practical, common sense knowledge base and approach in developing, implementing and administrating the quality control system, especially as it relates to technical problem solving, implementation of corrective actions, development of statistical based inspection control plans and supplier management and direct material control.
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