QC Analyst I
Department: Quality Control
Reports To: QC Analyst III/Team Lead
Job Location: 100 % Onsite – Los Angeles, CA
Position Summary
The QC Analyst I supports laboratory operations by performing basic analytical testing and assisting with quality control activities under supervision. This entry-level position provides training and development in cGMP laboratory practices and routine QC assays essential to the production and release of biologics.
Key Responsibilities
- Perform basic lab tests (e.g., pH, conductivity, visual inspection) under supervision
- Assist with preparation and organization of reagents and materials
- Execute and document results in compliance with cGMP and GLP standards
- Support equipment calibration, maintenance logs, and lab cleanliness
- Log, label, and manage sample receipt and inventory
- Maintain complete, accurate, and legible records of testing activities
- Participate in lab safety and quality training sessions
- Assist in restocking laboratory consumables and supplies
- Escalate anomalies and deviations to senior team members
- Perform other duties as assigned
Required Qualifications
- Bachelor’s degree in Biological Sciences, Chemistry, or related field
- 0–1 year of experience in a laboratory or biopharmaceutical setting (internship or academic lab acceptable)
- Strong organizational and communication skills
- Familiarity with basic laboratory techniques and safety practices
- Ability to follow written procedures and protocols
Preferred Qualifications
- Knowledge of cGMP and GLP practices
- Experience with Microsoft Office and basic laboratory instrumentation
Work Environment & Physical Demands
- Laboratory-based role requiring use of personal protective equipment
- May involve standing for extended periods and lifting up to 20 lbs.
- Minimal travel required
Salary Range: The salary range for this position is $62,600 to $75,000, depending on experience and qualifications. Final compensation will be determined based on a variety of factors, including skills, background, and alignment with the role’s responsibilities. In addition to base pay, this position may be eligible for a discretionary annual bonus. Armata Pharmaceuticals offers a comprehensive benefits package that includes paid time off, paid holidays, company-sponsored medical, dental, vision, life insurance, short- and long-term disability insurance, and a 401(k) plan with employer matching.
Send cover letter and CV to: careers@armatapharma.com
About Armata Pharmaceuticals, Inc.:
Armata is a clinical-stage biotechnology company focused on the development of pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections using its proprietary bacteriophage-based technology. Armata is developing and advancing a broad pipeline of natural and synthetic phage candidates, including clinical candidates for Pseudomonas aeruginosa, Staphylococcus aureus, and other pathogens. Armata is committed to advancing phage with drug development expertise that spans bench to clinic including in-house phage specific cGMP manufacturing.
Armata is proud to be an Equal Opportunity and Affirmative Action Employer. We are committed to providing equal employment opportunities to all qualified applicants, regardless of race, color, religion, sex (including sexual orientation and gender identity), national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws.