Process Engineer Summer Internship
Posted on 2/2/2024
INACTIVE
GRAIL

1,001-5,000 employees

Designs cancer screening tests
Company Overview
GRAIL's mission is to detect cancer early, when it can be cured. They are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care.
Data & Analytics

Company Stage

N/A

Total Funding

$11B

Founded

2016

Headquarters

Menlo Park, California

Growth & Insights
Headcount

6 month growth

4%

1 year growth

8%

2 year growth

22%
Locations
Durham, NC, USA
Experience Level
Intern
Requirements
  • Current enrollment in an engineering or science-related bachelor degree program
  • Strong problem-solving skills
  • Excellent communication skills
  • Excellent time management skills
  • Basic industrial, electrical, and mechanical knowledge
  • Familiarity of systems infrastructure
  • Strong writing and editing skills
  • Ability to work in a matrix organization
  • Good emotional intelligence
  • Experience working in a clinical laboratory regulated environment (preferred)
  • Knowledge of lean tools and root cause analysis methodologies (preferred)
  • Background in GMP manufacturing (preferred)
Responsibilities
  • Assist with the development and implementation of engineering documentation
  • Work closely with a cross functional team to address and resolve equipment documentation issues
  • Collaborate with validation engineers to draft, review and execute equipment qualification protocols
  • Recommend and implement changes to ensure ongoing high-quality and efficient engineering operations procedures
  • Support the planning and execution of qualification activities ensuring compliance with established procedures and guidelines
  • Participate and adhere to GRAIL’s policies and guidelines
  • Work closely with Compliance, Engineering, Quality and Regulatory to implement and follow the required policies and procedures for the lifecycle of equipments
Desired Qualifications
  • Experience working in a clinical laboratory regulated environment
  • Knowledge of lean tools and root cause analysis methodologies
  • Background in GMP manufacturing