Quality Control Analyst I (GMP)

Location: Camarillo, California 93012, United States

Salary: $82,500 per year

Company

hirify.global provides staffing and employment opportunities for technical and laboratory roles.

What you will do

• Perform routine QC laboratory testing using pH, osmolality, and FT-IR for in-process, finished-product, and stability samples.
• Manage sample login, labeling, tracking, storage, shipment coordination, and stability-program activities.
• Record and review data in accordance with cGMP, ALCOA+, and data-integrity requirements.
• Maintain laboratory notebooks, worksheets, logbooks, and electronic records in an audit-ready condition.
• Assist with OOS results, deviations, invalid assays, laboratory maintenance, calibration, and audit-readiness activities.
• Coordinate with QA, Manufacturing, Stability, Microbiology, and external laboratories to meet testing timelines.

Requirements

• Bachelor’s degree in a related field.
• At least 1–2 years of laboratory experience; GMP QC laboratory or pharmaceutical industry experience is preferred.
• Strong attention to detail, organization, time management, and ability to manage multiple priorities.
• Ability to follow SOPs, test methods, and GMP procedures accurately with minimal supervision.
• Basic exposure to HPLC, pH, density, osmolality, FT-IR, analytical balances, micropipettes, or analytical laboratory testing is preferred.
• Familiarity with ICH, USP, 21 CFR Part 210, and Part 211 is preferred.

Culture & Benefits

• Work in a fast-paced GMP QC laboratory environment with routine and changing testing priorities.
• For temporary assignments lasting 13 weeks or longer, benefits may include medical, dental, vision, 401(k), and statutory sick pay where required.
• Reasonable accommodations are available during the employment process.