- Company's 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 for facilitating management review meetings and report on the performance of the quality system and its' metrics.
- 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.
- Bachelor's degree.
- 5 years' experience in Quality Control/Assurance in a tightly tolerance industry with an automotive and/or 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 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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Description
RESPONSIBILITIES
QUALIFICATIONS
