2027 Spring Intern - Quality Control

GenentechGenentechHillsboro, Oregon, United States
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Posted

10/5/2026

Employment

Full time, Internship

Range

$25 - $52/hr

Work style

On-site

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AI summary

Core responsibilities

The intern will support the Quality Control team by collecting and analyzing process data to drive continuous improvement initiatives. They will also participate in cross-functional meetings and assist in the implementation of Lean and 5S methodologies within the laboratory.

Requirements overview

Candidates must be currently pursuing or have recently attained a degree in Science, Engineering, Data Science, or a related field. Applicants should possess strong analytical skills, a systematic problem-solving mindset, and effective communication abilities.

Key skills

Process developmentQuality controlData analysisProblem solvingProject managementCommunicationLeanAgileLaboratory techniquesData visualizationProcess mappingTechnical servicesManufacturingBiotechnologyKPI tracking

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Education requirements

bachelor degreepostgraduate degree

About Genentech

Industry

Biotechnology Research

Employees

18,189

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 & ResearchEngineeringManufacturingData & AnalyticsHealthcare

Description

The Position 2027 Spring Intern - Quality Control Position Summary The intern will have the opportunity to join HTO’s Quality Control Team as a business analyst to support continuous improvement initiatives focused on delivering performance and increased efficiency. The role will be responsible for working with cross functional teams to assist in the collection and analysis of process data, brainstorming innovative solutions, and supporting the design and implementation of improvements. This internship position is located in Hillsboro, on-site. The Opportunity Actively participate in QC Improvement meetings and support Structured Problem Solving initiatives to help the team implement solutions that eliminate root cause contributing to performance challenges. Attend daily cross functional meetings to support Quality Control teams to deliver on daily plans related to product testing, environmental testing, maintenance, and validation of equipment and methods. Assist in the design, collection, and analysis of process data to enable improved understanding of QC capacity and performance. Support developing tools and dashboards to visualize key performance indicators (KPIs) and identify trends. Participate in mapping Quality Control processes and workflows to map processes, identify waste and improvement opportunities. Support 5S and Lean initiatives in the laboratory including improving tools leveraged at daily huddles, material flow, and simplified processes. Program Highlights Intensive 6 months, full-time (40 hours per week) paid internship. Program start dates are in January (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 be pursuing a Bachelor's Degree (enrolled student). Must have attained a Bachelor's Degree (recent graduates not currently enrolled in a graduate program). Must be pursuing a Master's Degree (enrolled student). Must have attained a Master's Degree. (recent graduates). Must be pursuing a PhD (enrolled student). Must have attained a PhD. (recent graduates). Required Majors: Science, Engineering, Data Science or related field. Required Skills Experience in Process Development, Quality Control, Engineering, Manufacturing, or Technical Services. Strong ability to collect, analyze and interpret data to identify trends and inefficiencies. Strong problem solving mindset and demonstrated capability to solve problems leveraging a systematic approach with data. Demonstrated understanding of project management skills. Excellent verbal and written communication skills to effectively document findings, present data, and collaborate with team members. 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. Understanding of Lean, Agile, or Toyota Production System is preferred. Knowledge of cGMPs or equivalent regulations in a laboratory environment is a plus. Experience in the pharmaceutical / biotech industry is a plus. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of Oregon is $25.00-$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

  • •Process development
  • •Quality control
  • •Data analysis
  • •Problem solving
  • •Project management
  • •Communication
  • •Lean
  • •Agile
  • •Laboratory techniques
  • •Data visualization
  • •Process mapping
  • •Technical services
  • •Manufacturing
  • •Biotechnology
  • •KPI tracking

Benefits

  • •Paid holiday time off
  • •Stipend

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