- Location: California, United States
- Type: Contract
- Job ID: 8315
- Work Setting: On-Site
- Posted: February 13, 2026
- Closing Date: February 15, 2027
- Tax Status: W2
QC Analyst
12-month Contract
Onsite in Novato, CA
Must be able to work on a W2
SUMMARY
The QC Analytical Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.
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
EXPERIENCE
• 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 preferred
• 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE) preferred
EQUIPMENT
• Waters HPLC, Waters UPLC, Dionex HPLC, Sciex PA800, ProteinSimple iCE3, UV/VIS Spectrophotometer, pH Meter
12-month Contract
Onsite in Novato, CA
Must be able to work on a W2
SUMMARY
The QC Analytical Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.
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
EXPERIENCE
• 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 preferred
• 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE) preferred
EQUIPMENT
• Waters HPLC, Waters UPLC, Dionex HPLC, Sciex PA800, ProteinSimple iCE3, UV/VIS Spectrophotometer, pH Meter