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Steri-Tek
Fremont, CA | Temporary
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QA Associate (Temporary)
Steri-Tek Fremont, CA
$102k-128k (estimate)
Temporary 2 Weeks Ago
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Steri-Tek is Hiring a QA Associate (Temporary) Near Fremont, CA

The QA Associate provides vital support to the Quality department, contributing to the maintenance and enhancement of Steri-Tek’s quality management system. In this role, the QA Associate will be responsible for scanning and uploading various documents, ensuring accuracy and attention to detail in all aspects of work (i.e. folder Quality checks), and archiving documents. This position requires a meticulous approach to document management, including the verification of document versions, proper labeling, and adherence to regulatory compliance standards.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Scan and upload a variety of quality-related documents into Steri-Tek’s digital system.
  • Ensure accuracy and attention to detail in the scanning process, verifying that all pages are clear, legible, and properly indexed.
  • Organize and maintain electronic files in an orderly and accessible manner for easy retrieval.
  • Collaborate closely with the Quality team (and other cross functional teams) to gather and compile necessary documents for scanning and uploading.
  • Review information of outputs from various departments (i.e. customer information and dosimetry data).
  • Other duties as assigned by Quality Manager.

ADDITIONAL INFORMATION:

This QA Associate role is a temporary position (through August 2024). It is an on-site position in Fremont, CA. Working days are Monday - Friday, regular business hours.

Job Summary

JOB TYPE

Temporary

SALARY

$102k-128k (estimate)

POST DATE

06/07/2024

EXPIRATION DATE

08/05/2024

WEBSITE

steri-tek.com

HEADQUARTERS

FREMONT, CA

SIZE

25 - 50

FOUNDED

2015

CEO

LARRY NICHOLS

REVENUE

$5M - $10M

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About Steri-Tek

SteriTek is a high-volume E-beam/X-ray contract sterilizer and R&D innovation center serving the medical device, biotech, pharmaceutical and other industries. Steri-Tek is ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as State of California Medical Device and Drug Manufacturing licensed facility. The facility boasts two state-of-the-art 10 MeV, 20 KW linear accelerators, opposite each other along the conveyor to provide uniform dose to the product without having to rotate the customers boxes. This dual-beam configuration significantly increases efficiencies, expands... product options, and serves as an effective back-up for the accelerators. The facility provides the most 10 MeV sterilization capacity, the most comprehensive product options, and the highest uptime availability than any other facility in North America. SteriTek offers a seamless dose map validation of customers product from any other contract irradiator. Our staff of validation engineers provide expert consultation for setting up any products to be dose mapped. We also offer turnkey sterilization validations for any new products to be introduced into the market at some of the most competitive rates. Call 510.933.9700 today to learn more about how SteriTek can help you with your medical devices, pharmaceuticals, material modification, and food safety. More
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