Qc Analyst II

Title: QC Analyst II
Location: Thousand Oaks, CA
Pay: $50-58
Contract: 6+ months 

Summary

Are you ready to advance your pharmaceutical career with a global industry leader? We are seeking a detail-oriented QC Analyst II to support critical quality control operations in a cutting-edge cGMP manufacturing facility. This is a fantastic on-site opportunity to drive analytical excellence and ensure the safety of life-changing therapies.

Responsibilities

• Conduct biological, chemical, and physical analyses on raw materials, in-process samples, and final drug products.
• Execute analytical method transfers and drive the implementation of new laboratory methodologies.
• Support the investigation of nonconformances, troubleshoot unexpected results, and implement root-cause analyses.
• Perform rigorous review of test data ensuring compliance with Current Good Documentation Practices (cGDP).
• Draft and update Quality Control SOPs and support validation protocol deliverables.

Qualifications Required:

• Bachelor’s Degree in Chemistry, Microbiology, Biological Sciences, or a related scientific discipline.
• Minimum 2 years of related laboratory experience in a regulated environment.
• Proven experience within biotech, pharmaceutical, or similar GMP manufacturing quality operations.
• Strong working knowledge of FDA regulations, GLP, GMP, and cGDP.
• Hands-on experience with analytical equipment (e.g., HPLCs, plate readers) and wet/instrumental analysis.

Preferred:

• Experience utilizing LIMS or related computerized laboratory data systems.
• Demonstrated ability to write detailed laboratory investigation reports.