Johnson & Johnson Careers
Quality Inspector 3
Requisition ID: 1805680503W
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1. Overall responsibilities
Responsible for ensuring company products are in compliance with internal and external
specifications by performing a variety of routine and non-routine inspections and
evaluations. This includes activities related to Inspection and Testing, Batch Release and
Records Management, First Article Inspection, 3D CMM, and Calibration.
2. Position duties and responsibilities
Inspection and Testing
Performs varied product inspections, generally of finished goods, components, incoming
materials, materials prior to be sent to external service suppliers, or new products, by
observing, measuring and recording data.
Compares inspection results to defined requirements or specifications and documents
differences found. Compiles and inputs data into router, log book and/or computer
databases and documents findings.
Provides external service suppliers with appropriate gages.
Accepts, rejects items or reroutes for rework based on established guidelines.
Reports rework/reject to proper department.
Confers with other departments regarding quality standards.
Identifies workmanship defects and recommends corrective action.
Ensures proper disposition of defective products.
Acts as the Subject Matter Expert (SME) for programming, release, usage and
troubleshooting of standing-wave ratio meter.
Acts as the SME for usage and troubleshooting of Coordinate Measurement Machines
Batch Release and Records Management
Audits batch records to ensure compliance with policies, procedures and regulations.
Identifies, records and reports on batch nonconformances.
Stores and maintains batch files both physically and electronically based on established
First Article Inspection
Performs (moderately) complex tests and analyses to assure that products comply with
Carries out (difficult) calculations and prepares documentation that shows the results of
Compiles data and prepares reports (FAI and FIR).
Acts as the SME for GD+T.
Acts as the SME for programming and release (PLM, ERP and CAD) of 3D CMM.
Orders test equipment and GMD from approved suppliers.
Administers test equipment and GMD physically and electronically within local GMD
Conducts scheduled calibration and maintenance on test equipment and GMD.
Establishes maintenance and calibration schedule for test equipment (including 3 D
CMM) and GMD based on manufacturers recommendations and maintains equipment
Acts as the SME for Gage R+R.
Applies principles of Good Documentation Practices.
Provides training on test equipment and (special) GMD.
Provides assistance for the performance of validation activities including application of
Implements revisions, corrections and changes to test equipment, procedures and
Issues and executes NCR within the software application.
Acts as owner of actions assigned from Quality Systems (NCR, CAPA, Audit
High School/Secondary Education or Equivalent.
Other education and professional experience:
Generally requires (6-8) years related experience
Interpersonal skills / characteristics:
Synthes Produktions GmbH (7117)