Quality Inspector II (2nd Shift)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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About MedTech

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for Quality Inspector II.

Purpose:

The Quality Inspector II will perform inspections checks tests review of quality documents such as a device history report and sampling procedures of incoming materials parts/components partially assembled or finished medical devices. Provide support as needed to the Operations group.

You will be responsible for:

Perform inspections on multiple and varied purchased parts subassemblies or finished product according to well-defined criteria using standard visual physical mechanical and/or electrical measurements

Perform visual inspection on large lots size under a microscope.

Perform mechanical inspection using advanced inspection systems including using a vision and or touch probe system

Perform electrical and optical cable and sensor testing

Crossed trained in all inspection steps for purchased components and finished product

Accurately document the results of inspections and testing

Maintain all controlled document files and test records in a timely and accurate manner

Perform data entry into associated data systems.

Monitor critical equipment and instrumentation to ensure proper operation and calibration

Identify problems and make initial recommendations for possible corrective action to the supervisor

Qualifications / Requirements:

Prior experience in quality inspection/control or Medical Device preferred

Ability to read critical dimensions on component drawings and technical data sheets

Knowledge in Geometric Dimensioning & Tolerance preferred

Knowledge in IPC 610 preferred

Ability to use all standard inspection gages electrical test equipment and microscope

Knowledge in ISO and FDA 21 CFR QSR and ISO 13485 preferred

Attention to detail with the ability to follow SOPs inspection procedures

Ability to perform complex component inspection

Strong verbal and written English communication skills

Ability to execute tasks in a timely manner under general supervision

Strong computer literacy required. Working knowledge of Microsoft Office Suite MRP system; SAP knowledge desired

Receiving/logistics knowledge preferred

Ability to work in a cleanroom environment

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