Position Title: MCS Associate Quality Control
Work Location: Thousand Oaks, CA 91320
Assignment Duration: 12 Months
Work Schedule: Monday–Friday, 8:00 AM–5:00 PM
Work Arrangement: 100% on-site
 
Position Summary: Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory operations.
 
Key Responsibilities:

• Perform routine laboratory procedures and analytical testing in a regulated QC environment
• Document, calculate, compile, interpret, and enter laboratory data accurately and in a timely manner
• Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required.
• Maintain laboratory reagents and maintain an inspection ready area
• Maintain complete and compliant laboratory documentation, including logbooks, worksheets, and electronic records
• Follow all applicable safety guidelines, cGMPs, and CFR requirements
• Maintain training records and comply with written procedures and laboratory systems
• Support controlled document updates and change implementation activities
• Identify and escalate compliance, safety, or data integrity issues as appropriate
• May recommend and implement improvements related to routine job functions

 
Qualifications & Experience:

• Recent graduates or early-career professionals with a Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific field
• Candidates with hands-on QC GMP laboratory experience, even if a degree is not held
• Highly trainable and enthusiastic about learning analytical testing techniques
• Team-oriented professionals with strong time management, reliability, and organizational skills
• Candidates comfortable working with basic computer systems and laboratory documentation
• Familiarity with GMP principles is preferred but not required
• Ability to follow regulatory requirements, written procedures, and safety guidelines
• Ability to review and evaluate data and documentation in accordance with company and regulatory standards
• Strong organizational skills with the ability to manage multiple priorities and meet deadlines
• Excellent attention to detail
• Strong written and verbal communication skills
• Flexibility and adaptability in a fast-paced, regulated environment
• Understanding of when and how to appropriately escalate issues
• Ability to identify, recommend, and implement improvements related to routine job functions
• Commitment to continuous learning and compliance with cGMP and safety requirements

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 23.00/hr.