Quality Control Analyst II - 2-Year GMP Role

Roche

Oceanside (CA)

On-site

USD 45,000 - 84,000

Full time

7 days ago
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Benefits offered by this job

Discretionary annual bonus
Benefits package

Job summary

Genentech seeks a Quality Control Analyst II in Oceanside to support biopharmaceutical product quality through routine testing, sample management, and lab maintenance. The role works independently in a fast-paced environment while upholding data integrity and safety standards.

This is a fixed duration position for 2 years, with responsibilities including routine method testing, equipment maintenance, and strict adherence to GMP/GLP guidelines.

Qualifications

  • Bachelor’s degree in biology, microbiology, biochemistry, chemistry, or a related scientific discipline.
  • 0–2 years of related laboratory experience in a regulated environment.
  • Working knowledge of lab safety protocols and software tools such as LIMS, Microsoft Office, and 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 ensure the facility remains in an inspection-ready state.
  • Adhere strictly to GMP, GLP, GDP, Data Integrity, and environmental safety guidelines.

Skills

Organizational skills
Time management
Problem-solving
Communication skills
Interpersonal skills

Education

Bachelor's degree in Biology, Microbiology, Biochemistry, Chemistry, or related field

Tools

LIMS
Microsoft Office
Google Workspace

Job description

Genentech seeks a Quality Control Analyst II in Oceanside to support biopharmaceutical product quality through routine testing, sample management, and lab maintenance. The role works independently in a fast-paced environment while upholding data integrity and safety standards.

This is a fixed duration position for 2 years, with responsibilities including routine method testing, equipment maintenance, and strict adherence to GMP/GLP guidelines.

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