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About the Role
This internship supports the characterization of new control lots for analytical method development and system suitability, bridging clinical and commercial activities to ensure consistent method performance globally.
Responsibilities
- Support data trending and statistical evaluation for new method control lots.
- Organize, source, and mine technical reports and manufacturing records to support future method control lot production and forecast future material demand.
- Perform analytical laboratory work (e.g., HPLC, IEC, CE-SDS) for comparability assessments and characterization of critical reagents.
- Map usage data across cross-functional departments to establish centralized databases and streamline material replenishment.
- Support design space characterization and data sourcing to aid regulatory filings and lifecycle method implementation.
Requirements
- Must have attained a Bachelor's Degree (not currently enrolled in a graduate program).
- Must have attained a Master's Degree.
- Must be pursuing a PhD (enrolled student).
- Must have attained a PhD.
- Majors: Biology, Chemistry, Biochemistry or related disciplines.
- Excellent communication, collaboration, and interpersonal skills.
- Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion.
- Experience and proficiency using AI tools to design presentations, organize data, draft documents, or model data variability.
- Practical experience or familiarity with analytical chromatography techniques (e.g., HPLC, IEC, CE-SDS).
- Background in data trending, statistical analysis, or managing technical record databases.
Skills
- HPLC
- IEC
- CE-SDS
- AI tools
- Data trending
- Statistical analysis
- Technical record databases
Location
- South San Francisco
Work Type
- On-site
- Full-time
- Internship
Experience Level
- Intern
Education Level
- Bachelor's Degree
- Master's Degree
- PhD
Salary/Compensations
- $28.00-$52.00 per hour
Benefits
- Stipend
- Paid holiday time off
About the Company
- The Analytical Method Validation and Tech Transfer team is a group of dedicated scientists, balancing technical validation expertise with cross-functional leadership, overseeing end-to-end project-based validation/transfer activities across the GNE and global Roche network.
Equal Opportunity
- Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
- If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.