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Senior Quality Control Analytical Lab Associate

Job in Carlsbad, San Diego County, California, 92002, USA
Listing for: Argonaut Manufacturing Services Inc.
Full Time position
Listed on 2026-01-29
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 41 - 45 USD Hourly USD 41.00 45.00 HOUR
Job Description & How to Apply Below

Corporate Overview

Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost‑effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables.

Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.

Benefits and Pay Range

At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well‑being and financial future. Eligible employees enjoy:

  • Medical, Dental, and Vision Insurance
  • Company‑Paid Life Insurance ("1x Annual Salary")
  • Voluntary Life Insurance Options
  • Short‑Term and Long‑Term Disability Insurance
  • Flexible Spending Account (FSA) & Health Savings Account (HSA)
  • 401(k) Retirement Plan with Company Matching
  • 14 Days of Paid Time Off (PTO)
  • 10 Paid Holidays Annually

The pay range for this position is $41.00 - $45.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.

Position Overview

The purpose of this position is to provide support services by means of executing the analysis of in‑process, finished product, and stability test samples. Further support services include Environmental Monitoring and Raw Material receipt activities. QC personnel are responsible for compliance with QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Supervisor, Quality Control.

This role is 100% on‑site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule.

Responsibilities and Duties
  • Primary responsibilities include: analysis of samples using a variety of analytical instrumentation and compendial methods, performing analytical method transfers and qualifications, and troubleshooting analytical method performance.
  • Assist in the expedition of test sample shipment to sponsors and 3rd party laboratories.
  • Manage deviation/OOS investigations and implement CAPAs and change controls per GMP requirements.
  • Directly contributes to daily laboratory operations for QC Chemistry and Microbiology, in full compliance with applicable SOPs and safety guidelines.
  • Manage incoming inspection of raw materials in accordance with company policy and procedures.
  • Analyzes on a routine basis in‑process, release, and stability test samples in accordance with established QC test methods and specifications.
  • Train QC personnel in appropriate laboratory and safety procedures.
  • Execute Installation and Operational Qualification of analytical instrumentation where applicable.
  • Author and revise QC related documents, study reports and batch records as required.
  • Interface with Sponsors on QC related inquiries.
Requirements and Qualifications
  • Undergraduate degree (B.A. or B.S.) in a Life Science discipline.
  • Analytical experience in the following methodologies:
    Buffer Characterization (pH, conductivity, osmolality), Concentration (UV/Vis and/or Fluorescence), Chromatography (HPLC, Electrophoresis).
  • High-level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction.
  • The ability to work effectively within cross functional teams comprised of Manufacturing, Tech Transfer, Quality Assurance, and Senior Management.
  • 5+ years' GMP experience in a Quality Control function within the medical device and/or biopharmaceutical fields.
  • The ability to perform daily tasks with keen attention to detail.
  • An affinity for precise and detailed documentation skills.
  • The ability to work effectively and contribute to a dynamic and fast‑paced work environment.
  • Well‑developed oral communication and listening skills.

Argonaut Manufacturing…

Position Requirements
10+ Years work experience
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