QC Analyst II
Department: Quality Control
Reports To: QC Analyst III/Team Lead
Job Location: 100 % Onsite – Los Angeles, CA
Position Summary
The QC Analyst II performs analytical testing on raw materials, in-process samples, and final products to ensure compliance with established quality specifications. This role supports method execution, troubleshooting, and documentation under moderate supervision and contributes to continuous improvement in lab practices.
Key Responsibilities
- Conduct analytical testing such as ELISA, PCR, gel electrophoresis, and microbiological assays
- Review and analyze test data for conformance with specifications
- Maintain laboratory equipment and participate in troubleshooting minor issues
- Draft and revise lab documentation, including SOPs and test records
- Prepare reagents and test solutions in accordance with protocols
- Support stability and validation studies
- Assist with investigations into deviations and non-conformances
- Follow and enforce laboratory safety protocols and cGMP requirements
- Collaborate cross-functionally with QA, production, and R&D teams
- Perform other duties as assigned
Required Qualifications
- Bachelor’s degree in Biochemistry, Microbiology, Biological Sciences, or a related field
- 2–4 years of experience in a GLP/GMP lab environment
- Hands-on experience with analytical instrumentation and biological assays
- Understanding of GLP, GMP, and data integrity principles
- Ability to interpret data, identify trends, and escalate issues
Preferred Qualifications
- Experience with DNA/RNA assays, chromatographic methods (HPLC/LC-MS), or spectroscopy
- Familiarity with laboratory systems such as LIMS
Work Environment & Physical Demands
- Full-time lab position with standing and moderate physical activity
- Required PPE and adherence to environmental safety standards
- Limited travel may be required
Salary Range: The salary range for this position is $72,000 to $87,000, 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