QC Chemist I

QC Chemist I Location: Northridge, CA (100% Onsite) Pay Rate: $30.00/hour Assignment: 6-Month Contract with Potential for Extension or Conversion Schedule: Monday-Friday Position Overview We are seeking a QC Chemist I to join a Quality Control laboratory supporting pharmaceutical manufacturing operations. This is an excellent opportunity for recent science graduates or individuals with laboratory experience looking to build their career in a GMP-regulated environment. In this role, you will perform analytical testing on raw materials, packaging components, and finished products using a variety of laboratory instruments while ensuring compliance with quality standards and regulatory requirements. You'll work alongside an experienced team and receive hands-on training with industry-standard analytical techniques and instrumentation. Key Responsibilities Prepare samples, standards, reagents, and solutions for laboratory testing. Perform analytical testing using techniques such as HPLC, FTIR, UV-Vis Spectrophotometry, Gas Chromatography, Dissolution Testing, Instron, and Texture Analyzer. Analyze raw materials, packaging components, and finished pharmaceutical products according to USP, NF, EP, and approved testing methods. Accurately document laboratory results and maintain complete testing records. Meet testing timelines to support manufacturing and product release activities. Perform routine calibration and maintenance of laboratory equipment. Assist with laboratory investigations, non-conformances, and CAPA activities under guidance. Participate in training on laboratory procedures, analytical techniques, and new equipment. Follow GMP, GLP, safety, and quality procedures while maintaining a clean and organized laboratory. Support continuous improvement and laboratory safety initiatives. Qualifications Bachelor's degree in Chemistry or another scientific discipline from an accredited university preferred. Candidates with at least four years of analytical laboratory experience may be considered in lieu of a degree. Previous analytical testing experience is not required-entry-level candidates are encouraged to apply. Basic understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is preferred. Strong attention to detail, organization, and documentation skills. Ability to learn new laboratory techniques and work effectively in a team environment. Strong communication and problem-solving skills. Ideal Candidate This role is ideal for someone who is eager to launch or grow their career in pharmaceutical quality control. Successful candidates are detail-oriented, motivated to learn analytical instrumentation, and enjoy working in a collaborative laboratory environment while supporting the production of high-quality pharmaceutical products. TPS Group Company