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Quality Control Chemist II at Kelly Science, Engineering, Technology & Telecom Quality Control Chemist II at Kelly Science, Engineering, Technology & Telecom in Costa Mesa, California Posted in about 5 hours ago.

Type:

full-time

Job Description:

Kelly® Science & Clinical is seeking a Quality Control Chemists II for direct hire opportunities with one of our clients, a leading small molecule CDMO at their Irvine, CA facility. 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.

Workplace:

Onsite in Irvine, CA.

Position Title:

Quality Control Chemist II Position Type:

Direct hire

Salary:

$30-34 per hour We are currently seeking a highly skilled and experienced Quality Control Chemist II to join our dynamic team in Irvine, CA. As a member of our Quality Control Department, you will play a pivotal role in ensuring the quality and integrity of our pharmaceutical products through meticulous analytical testing and method development. Responsibilities Perform method validation, verification, transfer, analytical testing for clinical submission materials, including raw materials, finished products, stabilities, and cleaning validation. Maintain and troubleshoot analytical instrumentation. Perform and document laboratory investigations, as necessary. Peer review data generated by other chemists and technicians. Develop, validate, and troubleshoot analytical methods. Conduct method transfers from other facilities and departments. Author standard operating procedures and analytical methods. Perform and/or assist with equipment calibrations and qualification. Assist laboratory management with laboratory employee training. Assist laboratory management in preparation for internal, customer and agency audits. Qualifications Bachelor's degree in chemistry or related discipline. 2-8 years' experience in a chemistry laboratory, or equivalent combination of education and experience. 2 years' experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus required. 2 years' experience in GLP or GMP (preferred) environment. Ability to follow standard operating procedures. Strong communication skills, both written and verbal. Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision. Strong attention to detail.

What happens next:

Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.