Contract Bioanalytical Chemist Development & CRO Oversight

Genentech Inc.

South San Francisco (CA)

On-site

USD 90,000 - 130,000

Full time

4 days ago
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Job summary

Genentech Inc. is seeking a Bioanalytical Scientist Contractor to support the Development Bioanalysis team.

This role focuses on hands-on bioanalysis, including assay development, troubleshooting, non-GLP sample analysis, and scientific oversight of external bioanalytical activities across preclinical and clinical programs. Under supervision, you will contribute to project coordination and coordinate with CROs and partner departments, ensuring GLP/GCP compliance and high-quality data to advance

Qualifications

  • Bachelor's degree in Analytical Chemistry, Biochemistry, or related field.
  • Hands-on quantitative bioanalysis experience.
  • Experience developing, validating, and troubleshooting bioanalytical assays.
  • Strong communication and organizational abilities.
  • Agile mindset for quick prioritization.

Responsibilities

  • Support development bioanalytical group with in-house sample analysis.
  • Troubleshoot complex assays as needed.
  • Oversee CRO bioanalytical activities for GLP/GCP compliance.
  • Provide technical oversight during method development and validation.
  • Review method and study reports and documentation.
  • Participate in CRO evaluations and SOP reviews.
  • Evaluate emerging analytics technologies to enhance capabilities.
  • Maintain study information, timelines, and status in tracking tools.
  • Support ongoing operational activities within Development Bioanalysis.
  • Contribute to a culture of scientific excellence and collaboration.

Skills

Quantitative bioanalysis
Bioanalytical assay development
Bioanalytical method validation
Troubleshooting
Communication skills
Organizational skills
Agile mindset

Education

Bachelor's degree in Analytical Chemistry or Biochemistry

Job description

Genentech Inc. is seeking a Bioanalytical Scientist Contractor to support the Development Bioanalysis team.

This role focuses on hands-on bioanalysis, including assay development, troubleshooting, non-GLP sample analysis, and scientific oversight of external bioanalytical activities across preclinical and clinical programs. Under supervision, you will contribute to project coordination and coordinate with CROs and partner departments, ensuring GLP/GCP compliance and high-quality data to advance

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