QC Analyst
Novato, CA
Experience: 0
Category: Scientific & Clinical
Contractor Work Model: Onsite
Brand: Joulé
Compensation Range: 35.00 - 40.00 Per Hour
Job ID: 346318
Date Posted: 02/13/2026
Shortcut: http://jobs.systemone.com/lox0Z9
Job Title: QC Analyst
Location: Novato, CA
Type: Contract
Compensation: $35 - $40 hourly
Contractor Work Model: Onsite
Hours: Monday-Friday 9am to 5pm
Overview
The QC Analytical Analyst works with minimal supervision to perform lot release, stability, and non-routine testing of pharmaceutical drug substances and products in compliance with cGMP standards. The role includes independently executing and documenting assays, identifying deviations, and ensuring accurate record keeping. The Analyst is expected to demonstrate strong regulatory knowledge, support inspections as a subject matter expert, and contribute to the training and development of team members.
Responsibilities:
- Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines.
- General cGMP lab experience at the Analyst level.
- Works independently on assays they have mastered
- Develops and maintains proficiency in a broad range of test methods
- Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations
- Evaluates data against defined criteria/specifications
- Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices
- Identifies key issues in complex situations, analyzes problems, and makes sound decisions
- Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned
- Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise
- Holds self and others accountable for adherence to department and company policies and practices
- Maintains a safety and quality focused culture
- B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry).
- 1-2 + years of experience in a cGMP/GLP laboratory
- 1-2+ years hands-on experience in separation sciences (HPLC, UPLC, CE)
- Ability to follow written instructions and to perform tasks with direct or minimal supervision
- Strong leadership skills demonstrated through past work history
- Use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel
- Good written and verbal communication skills
- Attention to detail and strong documentation skills
- Ability to contribute effectively in team environments and independently
- 1-2+ years of Quality Control laboratory experience
- 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE)
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Ref: #558-Scientific
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