Job SummaryCoordinate and perform in house project Quality Assurance functions including, but not limited to quality audits, evaluations, reviews, and QA process improvements in accordance with ISO standards. Reviewing and maintaining QA processes, work instructions, quality records and source inspection instructions. Establish and maintain artifacts for established Quality Assurance processes. Review & inspect product on-site and at suppliers' facilities. Work with functional departments to coordinate quality assurance activities.
Essential Duties & Responsibilities- Quality Audits: Conduct and/or participate in internal, external and customer audits of products and processes to assure compliance to requirements in accordance with AS9100C. Formal Certification in performing quality audits (Internal Audits) is a plus.
- Corrective/Preventative Action System: Coordinate the investigation of nonconforming product (field returns, systemic internal nonconformance's, supplier issues, etc.) to determine root cause and corrective and/or preventative action plans necessary to avoid reoccurrence. Handling and follow-up of deviations.
- Process Improvement: Participate with Process Improvement Teams (PIT) in the continuous improvement of existing processes for CATS and suppliers.
- Manufacturing Support: Review the manufacturing processes to establish required inspection points. Help to prepare task specific inspection instructions for in process and final inspection. Assist manufacturing and inspection personnel in the interpretation of contractual and specification requirements. In conjunction with QA Manager and Manufacturing, assure the prompt disposition of questionable and/or non-conforming material. Serve as quality assurance representative on the Material Review Board (MRB), which includes writing and tracking MRB documentation, and assuring the required actions are complete prior to final approval to minimize impact of production flow. Request and verify Corrective Actions Requests (CAR's) and Non-Conformance Requests (NCR's) when issues are severe or systemic. Respond to customer requests for corrective action, as required. Review shipping documentation for compliance with contract and for customer sign-off.
- General day to day collaboration with Customer/Supplier representatives on company quality issues.
- Collects and analyzes data, and arrange data in reports for reporting to Management, compliance with ISO standards, and reporting to customer.
- Contributes to continual improvement in the work place from Quality perspective and in compliance with ISO standards.
- Supports quality audits, and document control. Perform internal AS9100 audits.
- Tracks procedures, change control, revisions, dates, signatures etc, within document control.
- May be required to support other activities to whatever extent their skills and knowledge may allow at managers discretion.
- Other duties: Attend program status reviews and respond to Quality issues. Prepare various company quality performance status reports both overall and project specific. Assist in the development and reporting of metrics on scrap, rework, supplier performance, FRACAS etc. to highlight opportunities for improvement.
Education/and or Experience- Bachelor's Degree in industrial management, Mechanical Engineer or equivalent
- No less than 5 year's QA Source /Final Inspection
- Experience in Contract Manufacturing CCA Inspection, in accordance with IPC-610, IPC-620 & J-STD-001 - Class 3 & knowledge of AS9100C processes required.
- Predominance in production and inspection processes in the following fields: Contract Assembly of Circuit Boards (PCB) and Electromechanical assemblies; Harnesses & Wiring; etc.
- Extensive experience in inspection or testing processes of electrical sub-assemblies, Mechanical parts and Build-To-Print (BTP) items.
- Proficient in the in-process /Final Inspection and evaluation of hardware and associated contract manufacturing processes and providing daily /weekly reports. Read and comprehend engineering drawings, specifications, technical documentation and contracts.
- Defense industry experience is a plus.
- Internal Auditor Certification is a plus.
- Quality Certifications /ASQ Member is a plus.
Basic Employment Requirements- Working knowledge of Microsoft Office applications software & databases and ERP system
- Ability to work with others as part of a team assisting in the resolution of product and process quality issues.
- Effectively communicate with system engineers, manufacturing, procurement, contract specialists, production workers, customer users and quality representatives in such a manner as to achieve their active support and cooperation.
- Ability to analyze problems and apply knowledge of quality and contract requirements, manufacturing processes, inspection concepts and AQL acceptance criteria.
- Ability to work with others as part of a team assisting in the resolution of product and process quality issues. Take a lead role in guiding the team.
- Ability to interpret various forms of assembly documentation.
- Must be focused and have high attention to detail.
- Must be authorized to work in the US and be eligible to obtain a passport and security clearance.
- Must pass Security background screening process.
- Willingness to work beyond regular work schedule to get the job done.
Work Environment/ Corporate Culture- The work environment is one of Production floor, subcontractors sites, customers and office.
- 25% desk work
- 75% walking and standing while interfacing with Manufacturing and others.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- 9/80 Work schedule or as assigned. Work schedule will fluctuate accordingly.
- Full benefits package including medical, dental, STD, LTD, GTL, 401K, Holidays, Vacation, paid time off to eligible employees.
