Johnson & Johnson Family of Companies

Title: Equipment Calibration Specialist

Location: Santa Clara, CA

Duration: 8 months

Pay Rate: $31.08

Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits

Please note that this is a contract role providing services to the Johnson & Johnson Family of Companies through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be a member of the Johnson & Johnson Family of Companies.

Summary:

The Equipment Calibration Specialist is responsible to provide general support in the areas of equipment, inspection, document control and the overall maintenance of the equipment calibration and preventive maintenance program. This position supports R&D, Service and Manufacturing Operations through all phases of product lifecycle. The candidate will use digital tools such as CEERDAC to track assets and support the execution of the program as well as assist in compiling and trending metric data.

Responsibilities:

• Ensure maintenance and calibration are performed on time and that due dates are communicated well in advance to business partners.
• Reviews and enter documents related to Equipment calibration and maintenance.
• Notifies responsible personnel/user of upcoming calibration and maintenance due dates.
• Contact calibration and maintenance service providers and initiate purchase orders for the service.
• Ship equipment to service providers for calibration or maintenance.
• Review change orders related to calibration and maintenance.
• Maintain all controlled document files and test records in a timely and accurate manner.

Qualifications:

• Detail oriented with excellent organizational skills.
• 2 years in Equipment calibration and maintenance experience is preferred.
• Proficient in analytical, written, oral communication skills; and the ability to manage a variety of tasks simultaneously within cross-functional teams under minimal day-to-day supervision.
• Ability to work independently, prioritize activities and communicate well.
• Knowledge of a variety of testing equipment including Instron, pin gages, snap gages, micrometer, caliper, etc.
• Proficient technical writing skills and use of documentation programs (e.g., Office Windows, Excel, Access, Power Point, etc.) Preferred.
• Solid understanding of the FDA medical device Quality Systems Regulations and international quality system standards QSR/ISO 13485 and 21 CFR 820.