Data Quality Manager jobs in San Jose, CA

Position Details :

Our client, a world-leading Pharmaceutical Company in Santa Clara, CA is currently looking for a Equipment Calibration Specialist to join their expanding team.

Job Title : Equipment Calibration Specialist / Medical Devices

Duration : 8 months contract, extendable up to 24 months

Location : Santa Clara, CA

Note :

The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance plan

Job Description :

Job Summary / Description

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.

Duties / 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.

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.

Last updated : 2024-04-24