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Quality Engineer | Quality Engineer in Quality Assurance Job in Tempe AZ | 5196137859

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Quality Engineer

Tempe, AZ

Position description Experience a more rewarding quality career with Viant. This is your chance to immediately impact an industry innovator and be recognized for your accomplishments. Viant, a leading medical device manufacturer, is looking for a Quality Engineer to join their highly skilled team in Tempe, AZ. Reporting to the RA/QA Director, the successful applicant will provide technical ability on a broad range of issues related to medical device production where quality is extremely critical. Peoples lives depend on the precision of the products. Emphasis is placed in this position on providing vision to internal and external customers on sound principles of product design, process development/validation/improvement, quality assurance methods, and quality system management. This is a unique career opportunity where you will not be stuck in your office or in this role throughout your tenure with Viant. You will visit offsite and interface with customers, vendors and third party assessors. You will not be pigeonholed at Viant as they are a large organization that offers room for professional advancement and hire/promote heavily from within. As a valued team player of Viant, you will receive: :Above average compensation:Benefits package that includes: medical, dental, vision and 401(k):Greater stability : Viantrecently doubled in size and is investing heavily in their facilitiesIf you have a Bachelors degree (BA/BS) from accredited four:year college or university and min 3yrs of track record, Viant definitely wants to hear from you Experience should include medical device industry experience in engineering, preferably in quality assurance role. Previous supervisory experience wanted. Please click Apply or email your details to: Responsibilities: :Lead Quality Assurance Departments participation in maintenance and development of quality system documentation.:Serve as a Quality Assurance resource to internal and external customers for new product design, design changes, and process development/improvement/validation.:Interface with supplier and customer quality representatives on quality issues and assure that effective corrective action is implemented.:Promote and implement quality standards and associated quality assurance methods, including inspection processes, test methods, quality plans, documents and reports.:Develop verification and validation protocols for product designs and manufacturing processes.:Develop, execute and analyze data from quality:reporting measures.:Report to management on quality issues and trends.:Lead and participate in internal and external quality audits.:Manage complaint handling, CAPA, and discrepancy report systems.:Author and deliver training material on quality standards and activities.:Assure compliance with FDA qualifications and ISO standards in association with above activities.:Requires some overnight travel (up to approx 20).About the company: With over 35 yrs of medical device molding experience, Viant, formerly known as MedPlast, has become a comprehensive solutions provider for single use medical devices. Services range from concept and design of components to assembly of finished products. They are headquartered in Foxborough, MA and operate seventeen manufacturing facilities in the US, with additional locations in China, Mexico, Costa Rica, Puerto Rico, France, Germany and the UK. All candidates who are qualified will receive consideration for employment without regard to the individuals race, color, sex, national origin, religion, age, disability, genetic details, status as a military veteran or any other characteristic protected by applicable law.Company DescriptionViant, formerly known as MedPlast, has rebranded to repesent their new direction and even stronger commitment to become a complete solutions provider for their customers. With three acquisitions in just over a year, Viant has doubled in siz
February 20 on Tip Top Job
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