Manufacturing Associate I
Department: Manufacturing
Reports To: Manufacturing Supervisor
Job Location: 100 % Onsite – Los Angeles, CA
Position Summary:
The Manufacturing Associate I supports the execution of biologics manufacturing processes in a clinical-stage, cGMP-compliant environment. This entry-level role is responsible for preparing media and buffers, supporting upstream and downstream operations, and assisting with sterile fill/finish activities. The Associate I contributes to cleanroom operations, documentation, and compliance efforts as the company advances toward commercial readiness.
Key Responsibilities:
- Prepare media and buffer solutions using calibrated equipment
- Perform upstream operations including fermentation
- Perform downstream purification activities
- Perform sterile fill/finish operations
- Perform visual inspection of final Drug Product
- Execute tasks according to batch records and SOPs in classified cleanroom environments
- Accurately document data in logbooks and batch records in real time
- Perform equipment and area cleaning, sanitization, and material staging
- Perform all required cleanroom procedures per cGMP requirements
- Report deviations and support investigations under supervision
- Participate in ongoing training and maintain qualifications for assigned tasks
- Support deviations, CAPAs, and documentation improvements
- Support revisions to SOPs, logbooks, and job aids for assigned tasks
- Coordinate with other departments as needed to ensure production readiness
- Perform other duties as assigned
Required Qualifications
- High School Diploma or GED required, associate or bachelor’s degree in life sciences or engineering preferred
- 0–2 years in cGMP manufacturing, bioprocessing, or laboratory environment
Key Skills
- Basic knowledge of bioprocessing and aseptic techniques
- Strong attention to detail and adherence to procedures
- Ability to follow written instructions and maintain accurate records
- Familiarity with aseptic techniques and cleanroom behavior standards
- Understanding of cGMP, and GDP practices
- Ability to accurately document activities
- Effective verbal and written communication skills
- Ability to follow SOPs and collaborate in a team-oriented environment
- Basic proficiency with Microsoft Office (Excel, Word, Outlook)
Preferred Qualifications
- Experience working in cleanrooms, preparing sterile solutions, or supporting sterile filling
- Familiarity with single-use systems and small-scale bioreactors
- Awareness of GMP documentation standards and safety procedures
Work Environment & Physical Demands
- Work in ISO-classified cleanrooms with full gowning
- Standing, lifting (up to 50 lbs.), and repetitive motions required
- May require shift work, weekends, and holiday availability
Salary Range: $20 – $25
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.