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Intern Validation Engineer Ii Jobs (NOW HIRING)

LG Electronics

Validation Engineer II

Aliso Viejo, CA · On-site

$70K - $94K/yr

Validation Engineer II * Perform validation for infotainment/telematic products by utilizing test benches and vehicles * Responsible for executing basic Sanity, customer found issues, update ...

CYNET SYSTEMS

Validation Engineer 2

Austin, TX · On-site

$55 - $60/hr

Bachelor's in Electrical Engineering or Computer Engineering with 2+ years of related experience ... Writes comprehensive electrical & functional test plans for the processor interface validation of ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... * 2 - 5 years of experience in at least one of the following areas: equipment/utility ...

Magna

Intern - Validation Engineering

Auburn Hills, MI · On-site

$15.75 - $20.50/hr

Support EMC validation engineer on test data analysis and reporting * Support EMC validation engineering on test issue debug and tracking * Testing of electronic modules during development (ED), DV ...

Smith & Nephew

Software Validation Engineer 2

Austin, TX · On-site

$70K - $105K/yr

Software Validation Engineer 2 Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Software Validation Engineer will lead and support software ...

SMITH & NEPHEW SNATS INC

$70K - $105K/yr

Software Validation Engineer 2 Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Software Validation Engineer will lead and support software ...

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Intern Validation Engineer Ii information

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How much do intern validation engineer ii jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for intern validation engineer ii in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What is the difference between Intern Validation Engineer Ii vs Validation Engineer I?

AspectIntern Validation Engineer IiValidation Engineer I
CredentialsTypically pursuing or recently completed a relevant degree; internship experienceBachelor's degree in engineering, science, or related field; some entry-level experience
Work EnvironmentInternship setting, supervised, part-time or temporaryFull-time, professional engineering environment
ResponsibilitiesAssisting validation activities, learning procedures, supporting testingPerforming validation tests, analyzing data, supporting validation protocols

The main difference is that Intern Validation Engineer Ii is an entry-level, internship role focused on learning and supporting validation tasks, while Validation Engineer I is a full-time position with more independent responsibilities in validation processes.

What cities are hiring for Intern Validation Engineer Ii jobs? Cities with the most Intern Validation Engineer Ii job openings:
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:
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Intern Validation Engineer Ii jobs near you
Validation Engineer II

Validation Engineer II

ImmunityBio, Inc.

El Segundo, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.
Position Summary
The Validation Engineer II is responsible for generating and executing protocols, creating summary reports and executing validation activities in FDA regulated biopharmaceutical environments. Coordinates all validation activities by constant communication with affected departments and personnel. Will report to a manager or head of the department. The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and working under general supervision or mostly independently with minimal supervision.
Essential Functions
  • Collaborate with cross-functional departments to meet company expectations,
  • Perform validation activities for equipment, utility systems, facilities, processes, and automation systems in compliance with approved SOPs, cGMPs, and applicable regulatory requirements.
  • Generate, support and execute validation protocols (IQ/OQ/PQ/CV/PV) of all site equipment including laboratory equipment, production equipment, utilities (as applicable) and other related systems in an FDA regulated environment,
  • Author and review SOPs, protocols, reports, and validation master plans for GMP equipment, instruments, and computerized systems,
  • Generate and keep current inventory of GMP systems and requalification/periodic review schedules,
  • Perform and lead risk assessments for GMP systems as required,
  • Plan validation efforts according to risk,
  • Collaborate with clients, CMOs, and vendors to meet project and company objectives,
  • Assist with vendor communications,
  • Troubleshoots and resolve discrepancy reported during validation/qualification.
  • Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.

Basic Qualifications
  • Bachelor's degree in science or related discipline is required.
  • 3+ years of relevant validation or GMP-regulated industry experience is required.
  • Experience with facility commissioning and validation of equipment and facilities is required.

Preferred Qualifications
  • Strong technical document writing and reviewing with teams
  • Strong understanding and application of validation principles, concepts, practices, and industry standards.
  • Working knowledge of validation principles including commissioning, IQ/OQ/PQs related to equipment and facilities
  • Working knowledge of related quality systems such as change control; CAPA (including deviations/OOSs); training and document control is required.
  • Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment
  • Strong interpersonal skills and the ability to work well independently and in a team environment
  • Strong communication and organizational skills

Working Environment / Physical Environment
  • This position works on-site.
  • Exposure to onsite in-lab environment
  • Must be able to don and wear Personal Protective Equipment (PPE) as required
  • Lifting, standing, climbing, bending, grasping, sitting, pulling, pushing, stooping, stretching, and carrying are generally required to perform the functions of this position
  • Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
  • Must be able to lift frequently lift up to 35 pounds and occasionally lift/move 50 pounds

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.
$103,500 (entry-level qualifications) to $115,000 (highly experienced) annually
The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.
ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.
At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

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