Quality Control Analyst I (Pharmaceutical)

TL;DR

Quality Control Analyst I (Pharmaceutical): Supporting routine laboratory testing and sample management for in-process and finished products with an accent on cGMP compliance and data integrity. Focus on performing analytical testing, maintaining audit-ready documentation, and collaborating cross-functionally to meet operational priorities.

Location: Must be based in Camarillo, CA

Salary: $82,500–$86,000

Company

hirify.global is a staffing and recruitment agency specializing in technical and scientific placements.

What you will do

• Perform routine QC laboratory testing using pH, Osmolality, and FT-IR for various sample types.
• Manage sample lifecycle activities including login, labeling, tracking, storage, and shipment.
• Execute stability program tasks such as sample pulls, inventory management, and tracking.
• Maintain laboratory records, notebooks, and logbooks in an audit-ready state following ALCOA+ standards.
• Assist with laboratory investigations, including OOS results and deviations.
• Collaborate with QA, Manufacturing, and Microbiology teams to support testing timelines.

Requirements

• Must be based in or able to work onsite in Camarillo, CA.
• Bachelor’s degree in a related scientific field.
• 1–2 years of laboratory experience, preferably in a GMP QC or pharmaceutical environment.
• Strong attention to detail and ability to follow SOPs and GMP procedures accurately.
• Ability to work independently and manage routine laboratory tasks with minimal supervision.
• Basic exposure to analytical laboratory equipment such as HPLC, analytical balances, or micropipettes.

Nice to have

• Familiarity with ICH, USP, and 21CFR Part 210/211 regulations.
• Previous experience in a fast-paced GMP QC laboratory.

Culture & Benefits

• Major medical, dental, and vision insurance coverage.
• 401k retirement plan participation.
• Statutory sick pay where required by law.
• Commitment to providing reasonable accommodations for individuals with disabilities.