Quality Control Analyst II: Innovative Testing & Compliance

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

Job summary

Genentech in Oceanside, CA is seeking a QC Analyst II to ensure safety, quality, and regulatory compliance across manufacturing and products. You will conduct routine and non-routine analyses, calibrate equipment, and generate accurate reports within cGMP/GLP environments.

The role requires a Bachelor’s in Biology or related field with 1 year of experience (AA with 4 years or HS with 6 years). TSA STA clearance is required; you will work with cross‑functional teams and contribute to SOP

Qualifications

• Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry or related field with 1 year of relevant experience (AA with 4 years, or HS diploma with 6 years).
• Proficient in cGMP practices across laboratory assignments and environments.
• Strong teamwork and ability to share responsibilities to complete QC testing efficiently.
• Must be able to pass TSA Security Threat Assessment for warehouse access.

Responsibilities

• Conduct routine and non-routine analysis of the manufacturing environment and in-process products according to SOPs.
• Perform microbiological and chemical assays, basic troubleshooting, and instrument calibration.
• Represent QC and serve as a primary contact for manufacturing and other departments.
• Enter data into electronic systems and generate analytical reports.
• Initiate and perform laboratory investigations including document reviews and interviews.
• Assist with data trending, lab maintenance, and onboarding/training of new personnel.
• Develop, optimize, update SOPs and testing methods.
• Maintain compliance with cGMP, GLP and environmental safety guidelines.

Skills

cGMP practices

Teamwork

Communication

Education

Bachelor's degree in Biology/Microbiology/Biochemistry/Chemistry or related

AA with 4 years of related experience

Job description

Genentech in Oceanside, CA is seeking a QC Analyst II to ensure safety, quality, and regulatory compliance across manufacturing and products. You will conduct routine and non-routine analyses, calibrate equipment, and generate accurate reports within cGMP/GLP environments.

The role requires a Bachelor’s in Biology or related field with 1 year of experience (AA with 4 years or HS with 6 years). TSA STA clearance is required; you will work with cross‑functional teams and contribute to SOP