QC Analyst (Pharma)

QC Analyst (Pharma) Astrix Technology Group - 3.4 Ventura, CA Job Details Full-time | Contract $39 - $41 an hour 18 hours ago Qualifications Laboratory sample storage Data integrity assurance Biology Biotechnology Stability testing Biochemistry Laboratory inventory control Biological sample management Investigations regulatory compliance Quality records maintenance Laboratory equipment routine checks Stability studies in drug product development Shipping coordination Pharmaceutical laboratory environment Pharmaceutical regulatory compliance Labeling Good documentation practices (GDP) Mid-level Laboratory test results documentation Laboratory equipment calibration Bachelor's degree in biology Manufacturing standard operating procedures Laboratory quality control records management Bachelor's degree Quality assurance standard operating procedures Pharmaceutical company experience Pharmaceutical analysis Laboratory standard operating procedures Compliance documentation Bachelor's degree in pharmaceutical sciences Full Job Description Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst to join their team in Camarillo, CA!

Location:

Ventura County, CA Pay rate: $39- $41/hr.

Job type:

6-month contract (possibility of extension or conversion) Position Summary The QC Analyst is responsible for supporting routine laboratory testing, sample management, stability program activities, and quality system requirements within a cGMP-regulated environment. This role ensures accurate testing, documentation, and data integrity while collaborating cross-functionally to support product quality and operational timelines. Key Responsibilities Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT-IR for in-process, finished product, and stability samples. Support sample management activities including sample receipt, login, labeling, tracking, storage, inventory control, and shipment coordination. Assist with execution of the stability program, including sample pulls, submissions, inventory management, tracking, and documentation activities. Maintain accurate and complete documentation in compliance with cGMP, ALCOA+, data integrity requirements, and company procedures. Record and review laboratory data in notebooks, worksheets, logbooks, and electronic systems, ensuring records remain audit-ready at all times. Participate in laboratory investigations related to out-of-specification (OOS) results, deviations, invalid assays, and other quality events. Support laboratory maintenance activities including equipment calibration, routine housekeeping, inventory management, and inspection readiness. Collaborate with Quality Assurance (QA), Manufacturing, Stability, Microbiology, and external testing laboratories to ensure timely completion of testing and operational objectives. Follow approved Standard Operating Procedures (SOPs), test methods, and GMP laboratory procedures with minimal supervision. Qualifications Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline preferred. 1-3 years of experience working in a cGMP-regulated pharmaceutical, biotechnology, or life sciences laboratory environment preferred. Knowledge of laboratory analytical techniques, quality systems, data integrity principles, and regulatory requirements. Strong organizational skills with the ability to manage multiple priorities and meet deadlines. Excellent attention to detail, documentation practices, and problem-solving abilities. Effective communication and teamwork skills with the ability to work cross-functionally. Proficiency with laboratory documentation systems and Microsoft Office applications.

Note:

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-AH1