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A. American Made List
B. Approved manufacturer list
C. American medical laboratory
D. Association of Medical Laboratory Technologies
E. Authorized Manufacturer list
A. A parts bin with a specific part name
B. A list of all part numbers
C. A single part number
D. A master list
E. A single inventory bin
A. APQP
B. PMI
C. ISO
D. Six Sigma
A. ISO 9001:2008 quality management system certification
B. Six Sigma quality control
C. Statistical process control
D. APQP Advanced product quality planning
E. Six Sigma black belt methodology
A. All-Volksdorfer Damm
B. Aircraft Weight and Balance Laboratory
C. Air Vendor Data Link
D. Approved vendor list
E. Advanced vehicle diagnostics laboratory
A. Asset list
B. Approved vendor list
C. Vendor registration form
D. Vendor list
A. Component
B. Assembly
C. Subassemblies
D. Module
A. Subassemblies
B. Bill of materials
C. Parts
D. Packages
E. Parts list
A. Bottle of mineral water
B. Buffer inventory
C. Bottom-line expense
D. Beginning of the month
E. Bill of materials
A. System Level
B. BOM Level
C. Process Level
A. Package
B. BOM Type
C. Family
D. BOM Structure
E. BOM Level
A. Level
B. Component
C. Assembly
D. Package
A. Hewlett-Packard
B. Microsoft
C. Apple
D. Autodesk
A. PLM
B. CAD
C. Computer aided drafting
D. CNC
E. 3D printing
A. Corrective action/protective action
B. Committee on Accreditation of Professional Academic Programs
C. Carbon accounting/issue
D. Capacity evaluation and planning activity
E. Capital acquisition program administration
A. GMP
B. GMP/GLP
C. QMS
D. ISO
A. Six Sigma
B. ISO 9000
C. Just-in-time
D. CAPA
A. Cardiovascular exercise
B. Carbon dioxide removal
C. Corrective action request
D. Carbon Adsorption and Reduction
E. Canadian Automotive Research
A. Creating, reviewing and gaining formal approval for engineering change requests, change orders and change notifications
B. Coordinating with other business units to ensure compatibility of changes
C. Ensuring that all stakeholders are aware of the proposed changes and have an opportunity to provide feedback
D. Preparing the ground for change by creating a change management plan
E. Coordinating with team members and stakeholders to identify changes that need to be made and documenting those changes
A. EAN
B. ETC
C. ECT
D. ETP
E. ECN
A. Electronic Communications Network
B. Error correction code
C. Extended contract
D. Engineering change notice
E. Eurobond
A. SCAR
B. APR
C. CAP
D. CCP
E. CRAR
A. PLC
B. SWC
C. Request
D. FFR
E. Incident
A. An engine item
B. A fuel item
C. A motor
D. A required item
E. A child item
A. A screwdriver
B. A tool
C. A child
D. A screw
E. A drill
A. Its product
B. To inspect the product or part of the product
C. Its product or part of its product
D. To recommend changes to the product or part of the product
A. To provide consulting services to the company
B. Manufacture or assemble its product or part of its product
C. To oversee the day-to-day running of the business
D. Administer its business
E. Research and develop new products
A. Whether or not a product is safe
B. How much a company spends on researching and developing products
C. The company's stated policies
D. The customer's expectations
E. Government-imposed regulations or a company’s self-imposed standards
A. Financial regulations
B. Medical device regulations
C. Environmental regulations
D. Vehicle safety regulations
E. Food safety regulations
A. 21 CFR Part 820
B. 21 CFR Part 824
C. 21 CFR Part 820.3
A. A European Union requirement
B. A specific requirement
C. A general requirement
D. A U.S. requirement
E. A country of origin
A. Product or its packaging
B. Documents related to the product
C. Instructions for use
D. Regulation
E. Certifications or Approvals
A. DCR
B. Document Control Request
C. PRT
D. PMR
E. Document Change
A. Document change request
B. Data control request
C. Data change request
A. Standard Operating Procedure
B. Protocol
C. Procedure
D. SOP
E. Standard Operating Procedures
A. PHS
B. FMEA
C. DHF
D. CAD
E. GDS
A. Data history file
B. Hexadecimal blob
C. Design history file
D. Configuration history file
A. CAPA records
B. RTO reports
C. PIP records
D. Internal communication strategy
E. Incident response plan
A. Cargo Area Protection
B. Capacity Analysis and Planning Association
C. Carbonated Beverage Association
D. Committee on Audit
E. Corrective and Preventive Actions
A. ADR
B. DHR
C. DSR
D. CRM
E. DTR
A. CAPA records
B. PROCESS records
C. POLICY records
D. Incident Reports
E. Investigation Logs
A. The selection of a new production revision
B. All information required to correctly build the current production revision of the device
C. Information required to build all future revisions of the device
D. The date and time of the next scheduled update
A. Correctly export a manufacturing software project to a manufacturing line
B. Downgrade to an earlier software version
C. Modify the firmware of the device
D. Correctly build the next production revision of the device
E. Correctly build the current production revision of the device
A. Cleaning and sterilization requirements
B. Security requirements
C. Document management requirements
D. Storage requirements
A. BOM for a software product
B. BOM for a website
C. EBOM Engineering bill of materials
D. BOM for the product only
A. Service
B. Ticket
C. Sale
D. Physical product
A. SketchUp
B. Inkscape
C. AutoCAD
D. OrCAD
E. Inventor
A. ISO
B. TQM
C. Standards
D. Audits
E. ECN
A. Order entry
B. Execution
C. Error correction notice
D. Engineering change notice
E. Execution counter
A. Material authorization
B. Written proposal
C. Work authorization
D. Review and approval
E. Initiation of a change