Chemist

Kelly

Irvine (CA)

On-site

USD 62,000 - 78,000

Full time

4 days ago
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Job summary

Kelly® Science & Clinical in Irvine, CA is seeking a Chemist II/III for a full-time, direct position. The role focuses on analytical testing of raw materials, in-process samples, and finished products using a wide range of advanced laboratory instrumentation.

You will contribute to method development and validation, equipment qualification, and support laboratory management through training, audits, and the authoring of standard operating procedures.

Qualifications

  • Perform analytical testing of raw materials, in-process samples, and finished products.
  • Support method development and validation in cGMP environment.

Responsibilities

  • Perform analytical testing of raw materials, in-process samples, and finished products.
  • Assist with method development and validation, equipment qualification, and training.
  • Support laboratory management through audits and SOP authoring.

Skills

Analytical testing
Method thinking

Tools

Laboratory instrumentation

Job description

Description

Chemist II/III

Kelly® Science & Clinical is seeking a Chemist II/III for a full-time, direct position at a cutting-edge client in Irvine, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay:
II : $30-34/hour
III:$34.00 - $38.00/hour

Overview
Our client is an industry-leading company at the forefront of analytical and pharmaceutical sciences, driving innovation in raw material testing, method development, and quality compliance within a cGMP-regulated environment.
In this role, you will perform and assist with analytical testing of raw materials, in-process samples, and finished products, while utilizing a wide range of advanced laboratory instrumentation. You'll play a key role in method development and validation, equipment qualification, and supporting laboratory management through training, audits, and the authoring of standard operating procedures.

Schedule: Full-Time

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