Quality Control Analyst

• Title : QC Analyst
• Location: Camarillo, CA
• Employment Type: Contract – W2
• Duration: Contract

• About the Role
• We are seeking a QC Analyst – Sample & Stability Management to support sample management, stability activities, and general laboratory operations within a GMP Quality Control environment.
• The ideal candidate will have experience working in a pharmaceutical, biotechnology, or GMP laboratory and strong organizational and documentation skills. The primary focus will be sample control, stability study coordination, laboratory organization, and maintaining accurate records, with hands-on wet-lab testing as needed.

• Key Responsibilities
• Coordinate sample receipt, tracking, storage, distribution, and disposition within the QC laboratory.
• Support stability studies, including sample pulls, scheduling, tracking, documentation, and testing coordination.
• Maintain accurate sample inventories, storage conditions, and chain-of-custody records.
• Coordinate testing schedules and ensure samples are tested within required timelines.
• Maintain laboratory records, logs, controlled documentation, and sample/stability tracking systems in accordance with GMP requirements.
• Support general QC laboratory management, organization, supplies, reagents, standards, and equipment documentation.
• Partner with QC analysts and laboratory leadership to track testing priorities, outstanding activities, and upcoming deadlines.
• Support investigations, deviations, OOS/OOT activities, and related documentation.
• Perform basic wet-lab and analytical testing according to approved procedures as needed.
• Assist with HPLC, compendial, or other routine analytical testing based on laboratory needs and prior experience.
• Collaborate with QC, QA, Manufacturing, and other cross-functional teams to support testing, stability, and product-release timelines.

• Required Qualifications
• Experience working in a pharmaceutical, biotechnology, or GMP laboratory environment.
• Strong organizational, documentation, and time-management skills.
• Ability to manage multiple samples, studies, priorities, and deadlines.
• Experience with sample management, sample control, stability studies, or QC laboratory coordination.
• Strong attention to detail and ability to maintain accurate and compliant laboratory records.
• Ability to work effectively in a regulated, cross-functional laboratory environment

Salary: The hourly rate for this position is $40 – $55 per hour.

Equal Opportunity Employer:

We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Background Check:

Background checks may be conducted in accordance with applicable law.

Work Authorization:

Applicants must be authorized to work in the United States.