QC Analyst II — GMP Biopharma Testing & Data Integrity

Genentech; Oceanside (CA); On-site; USD 45,000 - 84,000; Full time

Job summary

Genentech is seeking a Quality Control Analyst II in Oceanside to support biopharmaceutical product quality through routine testing, sample management, and lab maintenance. The role emphasizes data integrity, safety, and independent work in a fast-paced setting.

The position is a fixed duration for 2 years, with duties including routine testing, equipment maintenance, and adherence to GMP/GLP guidelines. A Bachelor’s degree in a relevant science and 0–2 years of experience are required.

Qualifications

• Bachelor’s degree in a related scientific discipline is required.
• 0–2 years of laboratory experience in a regulated environment.
• Strong organizational, time management, and problem-solving skills; able to work independently.
• Agile communicator with excellent interpersonal, written, and verbal skills.
• Working knowledge of laboratory safety protocols and software tools (LIMS, Microsoft Office, Google Workspace).

Responsibilities

• Perform routine compendial method testing (pH, osmolality, color) and chemical assays following SOPs and GMP guidelines.
• Conduct sample management, aliquoting, and reagent preparation to support routine testing operations.
• Oversee laboratory equipment through routine maintenance, calibration, and standardization.
• Execute basic troubleshooting of chemical assays and participate in special projects or protocol execution as needed.
• Maintain laboratory inventory, stock supplies, and keep the facility inspection-ready.
• Adhere to GMP, GLP, GDP, Data Integrity, and environmental safety guidelines.

Skills

Independent worker

Strong communication

Organizational skills

Problem-solving

Education

Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemistry, or related

Tools

LIMS

Microsoft Office

Google Workspace

Job description

Genentech is seeking a Quality Control Analyst II in Oceanside to support biopharmaceutical product quality through routine testing, sample management, and lab maintenance. The role emphasizes data integrity, safety, and independent work in a fast-paced setting.

The position is a fixed duration for 2 years, with duties including routine testing, equipment maintenance, and adherence to GMP/GLP guidelines. A Bachelor’s degree in a relevant science and 0–2 years of experience are required.