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.