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Verification Expert Jobs (NOW HIRING)

ARM

Principal IP Verification Engineer

Chandler, AZ · Hybrid

$249K - $338K/yr

Our Solution Engineering division is seeking a skilled verification expert who is a lead-by-doing role to join our diverse team. This includes leading a team of verification engineers and developing ...

ARM

Principal IP Verification Engineer

Chandler, AZ · On-site

$249K - $338K/yr

Our Solution Engineering division is seeking a skilled verification expert who is a lead-by-doing role to join our diverse team. This includes leading a team of verification engineers and developing ...

Advanced Micro Devices

$150 - $200/hr

Expert in Verilog, System Verilog, Object Oriented programming * Expertise in developing UVM based verification frameworks and testbenches * Scripting and automation of verification processes and ...

Virtusa Corporation

Software Engineer

San Francisco, CA · On-site

PCIe Protocol IP Verification Expert: Consulting & Turnkey projects Virtusa Semiconductor BU is looking for seasoned professionals in the ASIC Verification domain. Virtusa is invested in AI/HPC [High ...

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How much do verification expert jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for verification expert in the United States is $20.70, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $21.88 per hour, depending on experience, location, and employer.

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Infographic showing various Verification Expert job openings in the United States as of August 2026, with employment types broken down into 82% Full Time, 14% Part Time, and 4% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $43,051 per year, or $20.7 per hour.

Scientist III - Continuous Process Verification

Saint Louis, MO • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

$132K/yr

Full-time

Re-posted 19 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 430 frontline employees who took The Breakroom Quiz

171st of 547 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information
Thermo Fisher Scientific's facility in St. Louis, MO, offers comprehensive services for developing and manufacturing biologic drugs. The 96,875-square-foot facility supports the entire process, from initial development to commercial production. It has extensive cell culture capabilities and can handle batch sizes from 100 grams to 20 kilograms using advanced single-use equipment.
The site is a leader in single-use technology, providing flexible options for scaling up production from 50 liters to 5,000 liters. The new 5,000-liter Dynadrive bioreactor, developed at the facility, showcases Thermo Fisher's expertise in biologics manufacturing and bioprocessing.
We are searching for a Continued Process Verification (CPV) Engineer III with education and experience in biopharmaceutical processing or a related field. This member of our team provides technological and statistical input in the validation and continued process verification of manufacturing processes. A CPV Engineer 3 routinely supports the Manufacturing Sciences and Technology team as a technical owner of commercial customer programs in a manufacturing environment and will assist in defining and shaping Thermo Fisher Scientific's continued process verification. expert in statistics and data analysis. This role will collaborate internally with Process Engineers, Quality Assurance, and Regulatory. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.
Responsibilities:
  • Perform all functions associated with process validation support, with a specific focus on CPV
  • Establish global CPV initiatives and standard practices
  • Act as the primary biostatistician in supporting Process Engineering and Process Development DoE studies
  • Manage the scope, schedule, and reporting of CPV program activities
  • Participate in Customer and Regulatory Audits
  • Draft, review, and approve CPV plans, CPV reports, and APQRs

Requirements:
  • Bachelor's degree in a scientific field, preferably an engineering field
  • 5+ years of experience in the GMP regulated Biologics/Pharma Industry or equivalent (or master's degree + 2 years' experience or Ph.D.)
  • Experience with process validation
  • Strong foundation in general scientific practices, principles, and concepts
  • Excellent written and verbal communication skills
  • Ability to work independently and collaboratively as part of a team
  • Proficiency in statistical analysis software programs such as JMP
  • Proficient in Microsoft Word and Excel

Must be able to pass a comprehensive background check, which includes a drug screening.

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