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Validation Engineer Entry Level Jobs in California

Position Summary The Validation Engineer I is responsible for generating and executing protocols ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

Position Summary The Validation Engineer I is responsible for generating and executing protocols ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

Position Summary The Validation Engineer I is responsible for generating and executing protocols ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

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Validation Engineer Entry Level information

What engineer makes $500,000 a year?

While most entry-level validation engineers earn significantly less, highly experienced engineers in specialized fields such as aerospace, petroleum, or software engineering with advanced skills and certifications can reach or exceed $500,000 annually. These roles often require extensive experience, leadership responsibilities, or working in high-paying industries and may include bonuses or stock options.

What engineers make $300,000 a year?

Highly experienced engineers in specialized fields such as petroleum engineering, software engineering, or aerospace engineering can earn $300,000 or more annually, often with advanced skills, certifications, and leadership roles. Salaries at this level typically require many years of experience, working in high-demand industries, or holding executive or senior management positions.

What is a Validation Engineer Entry Level job?

An Entry-Level Validation Engineer is responsible for testing and verifying that products, systems, or processes meet required standards and specifications. They work in industries like pharmaceuticals, manufacturing, and software, ensuring compliance with regulations and quality standards. Their tasks may include writing test protocols, analyzing data, and troubleshooting issues. This role requires attention to detail, problem-solving skills, and knowledge of engineering principles. Typically, they work under supervision but gain experience to take on more complex validation tasks over time.

Are validation engineers in demand?

Validation engineers are in demand across industries such as pharmaceuticals, biotechnology, and manufacturing, where ensuring compliance and quality standards is critical. The role often requires knowledge of regulatory requirements, validation protocols, and tools like GxP and SOPs, making skilled professionals valuable in regulated environments.

How to get into validation engineering?

To enter validation engineering, candidates typically need a bachelor's degree in engineering, science, or a related field. Gaining experience with quality systems, validation protocols, and tools like GMP or ISO standards is important, along with developing skills in documentation and troubleshooting. Certifications such as CQE or CSQE can enhance job prospects in this field.

What are the key skills and qualifications needed to thrive in the Validation Engineer Entry Level position, and why are they important?

To thrive as a Validation Engineer Entry Level, you need a solid background in engineering or the life sciences, attention to detail, and a basic understanding of validation protocols and regulatory standards. Familiarity with technical tools such as data logging software, validation documentation, and quality management systems like ISO or GMP is highly valuable. Strong analytical thinking, problem-solving, and effective communication are crucial soft skills for collaborating with multidisciplinary teams and presenting findings. These abilities ensure accuracy, compliance, and effective teamwork in delivering reliable processes and products in regulated industries.

What are the typical daily responsibilities of an Entry Level Validation Engineer?

As an Entry Level Validation Engineer, your daily tasks often include executing validation protocols, documenting test results, and assisting with equipment or process qualification under supervision. You'll collaborate closely with senior engineers, quality assurance teams, and production staff to ensure systems meet regulatory and company standards. Troubleshooting, process improvement, and maintaining accurate records are also common parts of the role. This position is a great opportunity to develop technical expertise and gain practical experience in a regulated industry, setting the foundation for future career advancement.

What are the most commonly searched types of Validation Engineer jobs in California? The most popular types of Validation Engineer jobs in California are:
What are popular job titles related to Validation Engineer Entry Level jobs in California? For Validation Engineer Entry Level jobs in California, the most frequently searched job titles are:
What job categories do people searching Validation Engineer Entry Level jobs in California look for? The top searched job categories for Validation Engineer Entry Level jobs in California are:
What cities in California are hiring for Validation Engineer Entry Level jobs? Cities in California with the most Validation Engineer Entry Level job openings:
Validation Engineer I

Validation Engineer I

ImmunityBio

El Segundo, CA

$98K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 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 I is responsible for generating and executing protocols, creating summary reports and executing validation activities in FDA regulated biopharmaceutical environments. The role coordinates all validation activities by constant communication with affected departments and personnel. The Validation Engineer I works on projects and matters of minimal complexity in a support role and works closely with senior staff.

Essential Functions

  • Support collaboration with cross-functional departments, clients, CMOs, and vendors to meet project and company expectations and objectives.
  • Assist in 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,
  • Generate and keep current inventory of GMP systems and requalification/periodic reviews schedules.,
  • Perform risk assessments for GMP systems as required.
  • Plan validation efforts according to risk.
  • Troubleshoot discrepancies reported during validation/qualification and assist senior engineers with resolutions.
  • Support the Validation team purchasing acquisitions and oversee the supplies and equipment inventory as needed.
  • Adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates.
  • 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 a science or related discipline is required.
  • 1+ years of relevant validation or GMPregulated industry experience is required.
  • Experience with facility commissioning and validation of equipment and facilities is required.

Preferred Qualifications

  • Good technical document writing and reviewing with teams
  • Good 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
  • Good interpersonal skills and the ability to work well independently and in a team environment
  • Good 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.

$88,200 (entry-level qualifications) to $98,000 (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.