Staff Validation Engineer (West Hills, CA)

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Cold Room / Freezers -22°F / -6°C, Laboratory Setting, Loud Noises (Equipment / Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous / toxic materials

Job Description

When you're part of Thermo Fisher Scientific, you'll do exciting work and be part of a team that values performance, quality, and innovation. As part of a successful, growing global organization, you will be encouraged to perform at your best. Thermo Fisher provides our people the resources and opportunities to make significant contributions to the world.

In Validation, every day is different, and with varied day-to-day responsibilities, there is always the opportunity to learn something new, develop your skills in a new area, and meet different people.

How you will make an impact

As the Staff Validation Engineer at the West Hills site, you will oversee continuous improvements in our validation processes, improving efficiency and quality. You will be leading the preparation and execution of validation documentation, including User Requirements Specifications, Installation and Operational Qualification Protocols and Reports, Performance Qualification Protocols and Reports, and Validation Protocols and Reports. We cover validation of equipment, computer systems validation, and process validation, working closely with the site to produce a complete validation package.

The Staff Validation Engineer also provides guidance and mentorship to system owners with impact risk assessments to identify the qualification and validation requirements, carrying out validation activities on equipment and processes before returning or handing over to the system owner, and assist in arranging external services when required.

Location : West Hills, CA. Relocation assistance is NOT provided.

What you will do

• Training and advising staff on validation guidelines.
• Leading multi-functional teams in operations, external contractors, internal multi-functional teams to assist us in completing our validation protocols and reports.
• Maintaining all documentation (electronic and hardcopy) in line with our quality management system.
• Ensuring compliance with safety, health, and environment (OSHA) legislation.
• Developing a compliant and efficient validation strategy for equipment (IOPQs) and process validations for temperature-controlled storage, diagnostic instruments, and production lines.
• Connecting and communicating with all individuals across the business, relaying information about our benchmarks and ongoing projects.

Qualifications

We are looking to engage someone who has the ability to adapt to rapid changes in project priorities and meet challenging deadlines!

At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner, and safer.

Compensation and Benefits

The salary range estimated for this position based in California is $103,100.00–$154,700.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and / or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes :

For more information on our benefits, please visit : https : / / jobs.thermofisher.com / global / en / total-rewards.

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