Quality Control Chemist II-III
Listed on 2026-08-16
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager -
Science
QA Specialist - Analyst/Manager
Quality Control Chemist II-III
Kelly® Science & Clinical is seeking an experienced Quality Control Chemist II for a direct hire opportunity 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. Salary:
Quality Control Chemist II: $30-34 per hour Quality Control Chemist III: $30-38 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, st abilities, 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.
- 2-8 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.
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