Quality Assurance Manager

1 week ago

East Hanover, United States Weiss-Aug Group Full time

Weiss-Aug Group is an internationally recognized leader in precision metal stamping, injection molding, value-added assembly solutions and tooling.At our Corporate Headquarters we have served the medical device industry, automotive industry, and industrial sector for over 50 years. Our vision as a company is to create an exciting environment that will attract and retain the finest people committed to manufacturing creative and innovative components and products.Join our team where every day we push the boundaries of manufacturing technology.Our highly respected precision metal stamping company is seeking a highly skilled and motivated Quality Assurance Engineer to oversees all aspects of the organization's quality system and improvement efforts, such as developing, implementing, and administrating the program, training and coaching employees and facilitating needed changes in the organization. Responsible for establishing policies and procedures at all levels to ensure quality improvement efforts will meet or exceed internal and external customer needs and expectations. Ensures the promotion of awareness of customer requirements throughout the company. Responsible for dealing with customers and suppliers on quality or performance issues. Responsible for safety/environmental engineering. Responsible for Safety related to products and manufacturing processes reference IATF Standard.RESPONSIBILITIESIs the company Management Representative responsible for implementing, establishing and maintaining the company quality system in accordance with ISO 9001/ ISOTS 16949 Automotive, ISO 13485 Medical and other specifications as required. Ensures the company meets any other additional customer specific requirements. Represents the company as the liaison with external parties regarding the company quality system and its' capabilities.Responsible to facilitate management review meetings and report on the performance of the quality system and its' metrics. Is a certified Lead Auditor responsible for the company internal audit program in compliance with ISO 9001, ISO/TS 16949 Automotive, ISO 13485 Medical and other specifications as required. Conducts QMS, Process and Final Product Audits. Manage internal corrective actions (ICAR) database: issue ICARS, assist in corrective actions and verify effectiveness of corrective actions through auditing. Interfaces with customers, sales, manufacturing, and engineering to resolve quality and contractual issues. Manages the customer corrective action process and database, including facilitating and leading corrective action teams, maintains dialogue and correspondence with customers and suppliers, controls records regarding corrective actions. Facilitates company quality system related training programs, gives on the job instruction and presentations as needed. Coordinates diverse training needs with outside consultants. Obtains outside funding for training (NJ customized training) as needed. Provides guidance and training to quality, manufacturing, or engineering groups in the use of automotive core tools: APQP; FMEA, control plans, MSA, statistical techniques and PPAP and other related iso 13485 medical, ISO TS 16949 automotive and other requirements. Maintains and is responsible for the company's document control system. Responsible for the maintenance of the master databases on the company network used to control company documents. Maintains and controls the company ISO/TS training records for all company team members. Responsible for the maintenance of master training databases on the company network. Manages the company motivation and empowerment program including maintenance of database. Interpret blueprints and specifications related to geometric tolerancing, gauging, statistical requirements, and related specifications. Provide interpretation and guidance within the quality group and to manufacturing and engineering departments. Requirements Four-year college degree. 5 years' experience in Quality Control/Assurance in a tightly tolerance industry with an automotive and medical customer base. Requires verbal and written communication skills and the ability to communicate technical information to people of various degrees of ability. Must be organized and detail oriented. Needs a thorough understanding of automotive and medical industry quality requirements (APQP, FMEA, Process Flows, Control Plans, Measurement System Analysis). Requires training in and thorough understanding of ISO 9000 ISO TS 167949 Automotive, ISO 13485 Medical. Must have general knowledge and training in the principles related to metals or resins. Individual must be proficient in blueprint interpretation, geometric tolerancing and statistics. Must be computer literate in MS Office (Word, Excel, PowerPoint). Requires understanding of the capabilities and practical uses of various types of measuring equipment: basic mechanical instruments, complex programmable vision systems and computerized data collection systems.

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