Onsite QC Chemist & Microbiology Analyst (6-Month)

Spectraforce Technologies, Inc.; Carlsbad (CA); On-site; USD 70,000 - 95,000; Part time

Job summary

Spectraforce Technologies, Inc. is seeking a QC Expert in Carlsbad, CA to apply chemistry lab skills, perform analytical testing, and ensure SOPs and compendia compliance.

The role emphasizes data integrity and regulatory compliance within a GMP environment. The position requires hands-on microbiological QC, HPLC/UPLC operation, and collaboration with cross-functional teams to support site qualification, validation activities, and timely issue resolution.

Qualifications

• 3–5 years of experience in a GMP testing laboratory environment.
• Good Manufacturing Practices (cGMP) experience.
• Quality Control
• Quality Management Systems
• Technological Expertise
• Quality Control Microbiology
• Laboratory Excellence
• Documentation Management
• Quality Compliance

Responsibilities

• Ensure all activities comply with cGxP, including data integrity review and approval of analytical data/tests (analytical release).
• Review and approval of analytical tests (analytical release).
• Perform HPLC/UPLC analyses (Empower software experience preferred).
• Conduct microbiological QC: testing of materials, utilities, environmental and personnel monitoring; support site qualification and validation activities.
• Support sample planning and sampling execution.
• Report technical complaints/adverse events/special cases within 24 hours of receipt.
• Maintain a good general understanding of chemistry and microbiological lab concepts.
• Monitor KPIs: timely training, GMP-compliant analysis & documentation, and low OOS rates.

Skills

Problem Solving

Communication

Data Integrity

Education

B.S. in Life Sciences

Tools

HPLC

UPLC

Empower

Job description

Spectraforce Technologies, Inc. is seeking a QC Expert in Carlsbad, CA to apply chemistry lab skills, perform analytical testing, and ensure SOPs and compendia compliance.

The role emphasizes data integrity and regulatory compliance within a GMP environment. The position requires hands-on microbiological QC, HPLC/UPLC operation, and collaboration with cross-functional teams to support site qualification, validation activities, and timely issue resolution.