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Senior Validation Engineer Jobs in Novi, MI (NOW HIRING)

Socket.dev

Senior Validation Engineer

Rochester, MI · On-site

$82.70 - $137.90/hr

  • Medical

  • Retirement

  • PTO

Overview The Rochester Senior Validation Engineer leads planning, scheduling, executing and guiding validation projects related to manufacturing processes, equipment, critical utilities, product ...

New

Stryker Corporation

Senior Validation Engineer

Rochester, MI · On-site

$83 - $138/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams.Support product transfers, new product development, regulatory ...

New

Pfizer

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams. * Support product transfers, new product development, regulatory ...

Pfizer, S.A. de C.V

Senior Validation Engineer

Rochester, MI · On-site

$83 - $138/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams. * Support product transfers, new product development, regulatory ...

New

Stellantis

Senior FOTA Validation Engineer

Auburn Hills, MI

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Stellantis is seeking an Electrical Systems Validation Engineer who will be responsible for validating the FOTA (Firmware Over The Air) validation the electrical system based on validation test plans ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI · On-site

$111K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... validation, as well as road load data collection. You will collaborate closely with cross ... Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI

$111K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... validation, as well as road load data collection. You will collaborate closely with cross ... Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI · On-site

$111K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... validation, as well as road load data collection. You will collaborate closely with cross ... Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ...

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All JobsValidation Engineer JobsSenior Validation Engineer JobsSenior Validation Engineer Jobs in Novi, MI

Senior Validation Engineer information

See Novi, MI salary details

$32

$60

$92

How much do senior validation engineer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for senior validation engineer in Novi, MI is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $48.51 and $68.99 per hour, depending on experience, location, and employer.

What does a senior validation engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

What are the key skills and qualifications needed to thrive as a senior validation engineer, and why are they important?

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What are some typical challenges faced by senior validation engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

What are the most commonly searched types of Validation Engineer jobs in Novi, MI?

The most popular types of Validation Engineer jobs in Novi, MI are:

What are popular job titles related to Senior Validation Engineer jobs in Novi, MI?

For Senior Validation Engineer jobs in Novi, MI, the most frequently searched job titles are:

What job categories do people searching Senior Validation Engineer jobs in Novi, MI look for?

The top searched job categories for Senior Validation Engineer jobs in Novi, MI are:

What cities near Novi, MI are hiring for Senior Validation Engineer jobs?

Cities near Novi, MI with the most Senior Validation Engineer job openings:

Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in Novi, MI as of July 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $126,399 per year, or $60.8 per hour.

Senior Validation Engineer

Socket.dev

Rochester, MI • On-site

$82.70 - $137.90/hr

Other

Medical, Retirement, PTO

Posted 2 days ago

New

Job description

Overview

The Rochester Senior Validation Engineer leads planning, scheduling, executing and guiding validation projects related to manufacturing processes, equipment, critical utilities, product, cleaning and sterilization. This role develops and authorizes project plans, protocols, test scripts and reports across the full lifecycle from initiation to ongoing monitoring. Collaboration with area owners and suppliers ensures validation/qualification requirements align with company policies, procedures and regulatory guidelines. The position may include troubleshooting, gap and risk assessments, regulatory inspection support and required training.

Responsibilities
  • Support validation/qualification of manufacturing equipment, facilities and critical utility systems.
  • Validate product, cleaning, shipping, aseptic processing (media fill) and sterilization (steam) cycles.
  • Validate laboratory equipment.
  • Develop and execute validation life-cycle documents (FRS, URS, FATs, SATs, DQ, IQ, OQ, PQ) and other relevant materials.
  • Develop/author validation master plans, SOPs, programs and policies; conduct system impact assessments, risk assessments and validation/qualification protocols (facility, equipment, process, product, change/modifications) and periodic requalification.
  • Coordinate cross-functionally with multiple departments to schedule and complete activities.
  • Support corrective actions, investigations and deviations as they relate to validation.
  • Provide technical training on processes and technologies as required by projects.
  • Assist in audit preparation and defend areas of Validation responsibility.
  • Carry out process capability analysis on commercial processes periodically and identify improvement opportunities where capability is unacceptable.
  • Prepare and review sections of the Annual Product Quality Reports (APQR).
  • Review site change controls to ensure validated state is not impacted by proposed changes.
  • Lead projects to reduce process risk and optimize plant and process productivity.
  • Where applicable, complete qualification in aseptic gowning and cleanroom techniques (Grade A through D).
Basic Requirements
  • Bachelor’s degree with at least 2 years of experience; or a Master’s degree with 0+ years; or an Associate’s degree with 6 years; or a high school diploma (or equivalent) with 8 years of relevant experience.
Preferred Requirements
  • Strong technical knowledge in validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems.
  • Experience with sterile products and medical devices.
  • Strong analytical, problem-solving, organizational and time management skills.
  • Ability to mentor and guide colleagues.
  • Experience in regulatory audits and compliance.
  • Experience using AI tools (e.g., ChatGPT, Microsoft Copilot) to support problem solving; demonstrated curiosity in responsible AI practices including risk management and ethical use.
Physical/Environmental Requirements

This is a penicillin manufacturing facility; candidates must not be allergic to penicillin and must be able to aseptically gown. Ability to lift 25–30 lbs.

Work Schedule and Travel

Non-standard work schedule may be required to support product release, including weekends, second shift, night shift, or on-call decisions. Minimal travel for training/seminars. Relocation assistance may be available.

Location and Compensation

Work Location: On Premise. Salary range: $82,700.00 to $137,900.00. Eligible for Pfizer Global Performance Plan with a target bonus of 10% of base salary. Benefits include 401(k) with company matching, retirement contributions, paid time off, caregiver/parental and medical leave, and comprehensive health benefits. Hiring is subject to location and eligibility requirements.

EEO, Compliance and Accessibility

Pfizer is an equal opportunity employer. We comply with applicable nondiscrimination laws and work authorization requirements. This posting complies with accessibility standards and provides accommodation on request via disabilityrecruitment@pfizer.com. Information on AI usage guidelines for recruitment is available on Pfizer Careers.

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