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.