2027 Spring Intern - Analytical Method Validation and Tech Transfer

GenentechGenentechDaly City, California, United States
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Posted

9/24/2026

Employment

Full time, Internship

Range

$28 - $52/hr

Work style

On-site

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AI summary

Core responsibilities

The intern will support the characterization of new control lots for analytical method development and perform laboratory work including HPLC, IEC, and CE-SDS. They will also manage technical reports, data trending, and cross-functional database organization to support regulatory filings.

Requirements overview

Candidates must hold or be pursuing a degree in Biology, Chemistry, Biochemistry, or a related discipline. Proficiency in analytical chromatography techniques and experience with data trending or statistical analysis is preferred.

Key skills

Analytical method validationTech transferHPLCIECCE-SDSData trendingStatistical analysisTechnical reportingAI toolsData miningCharacterizationRegulatory filingsCommunicationCollaborationInterpersonal skills

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Education requirements

bachelor degreepostgraduate degree

About Genentech

Industry

Biotechnology Research

Employees

18,206

Type

Privately Held

Size

10,001+ employees

About Genentech We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal. Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers. Our patient resource center is dedicated to getting patients and caregivers to the right resources. You can reach them at 1 (877) GENENTECH (436-3683) Monday-Friday, 6am-5pm PST or patientinfo@gene.com. Community Guidelines: 1. We want to foster positive conversation around the issues we are passionate about. To that end, we remove profanity, content that contains threatening language, content that is aimed at private individuals, personal information, and repeated unwanted messages. 2. Don’t mention any medicines by name — ours or anyone else’s. Because of the fair balance rules governing our industry, we cannot post any comments that reference any pharmaceutical brand, product, or service. Please do not mention any specific medicines by name, or include any links to third party sites in your comments. 3. This isn’t the place to report or discuss side effects. This site is not intended as a forum for reporting side effects experienced while taking a Genentech product. Instead, you should report any side effects to Genentech Drug Safety at 1-888-835-2555. You can also report side effects of any prescription product directly to the FDA at 1-800-FDA-1088 or by visiting www.FDA.gov/medwatch. 4. Don’t pitch your product or service. Please don't use our page as a place to promote your product or pitch your services. Please also avoid posting links to external sites. We reserve the right to remove any posts that are deemed promotional.

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Job categories

Science & ResearchData & AnalyticsHealthcareEngineering

Description

The Position 2027 Spring Intern - Analytical Method Validation and Tech Transfer Department Summary 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. This internship position is located in South San Francisco, on-site. The Opportunity The primary goal is to support the characterization of new control lots utilized globally for analytical method development and system suitability. The intern will play a critical role in bridging clinical and commercial activities, ensuring consistent method performance across the global network. 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. Program Highlights Intensive 6 months, full-time (40 hours per week) paid internship. Program start dates are in January 2027 (Spring). A stipend, based on location, will be provided to help alleviate costs associated with the internship. Ownership of challenging and impactful business-critical projects. Work with some of the most talented people in the biotechnology industry. Who You Are (Required) Required Education: You meet one of the following criteria: 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. Required Majors: Biology, Chemistry, Biochemistry or related disciplines. Preferred Knowledge, Skills, and Qualifications 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. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California is $28.00-$52.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits. 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.

Requirements

  • •Analytical method validation
  • •Tech transfer
  • •HPLC
  • •IEC
  • •CE-SDS
  • •Data trending
  • •Statistical analysis
  • •Technical reporting
  • •AI tools
  • •Data mining
  • •Characterization
  • •Regulatory filings
  • •Communication
  • •Collaboration
  • •Interpersonal skills

Benefits

  • •Paid holiday time off
  • •Stipend

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