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

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

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 ...

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

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 ...

Validation Engineer A123 Systems, LLC is a leading developer and manufacturer of lithium-ion batteries and battery systems for the transportation and commercial markets. A validation engineer is ...

... 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 ...

Validation Engineer A123 Systems, LLC is a leading developer and manufacturer of lithium-ion batteries and battery systems for the transportation and commercial markets. A validation engineer is ...

... 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 ...

... 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 ...

We are seeking a Senior AI Validation Engineer to design and implement testing strategies, frameworks, and automated pipelines that ensure the quality, safety, and reliability of deep learning and ...

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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 12, 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 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 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 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:
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

Pfizer, Inc.

Rochester, MI • On-site

$82K - $137K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago


Pfizer rating

8.2

Company rating: 8.2 out of 10

Based on 125 frontline employees who took The Breakroom Quiz

32nd of 86 rated pharmaceutical


Job description

Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.
What You Will Achieve
In this role, you will:
  • Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
  • Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.
  • Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.
  • Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.
  • Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.
  • Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations, and coordinate testing with functional groups.
  • 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 queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations.

Here Is What You Need (Minimum Requirements)
  • High school diploma (or equivalent) with 8+ years of experience or associate's degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
  • Proven expertise in Good Manufacturing Practices
  • Strong working knowledge of various quality systems and processes
  • Familiarity with information systems such as Global Document Management System, System Application & Products, and Quality Tracking System
  • Excellent verbal and written communication skills
  • Ability to work independently and in a team environment

Bonus Points If You Have (Preferred Requirements)
  • Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems
  • Experience with sterile products and medical devices
  • Strong analytical and problem-solving skills
  • Strong organizational and time management skills
  • Ability to mentor and guide other colleagues
  • Experience in regulatory audits and compliance
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

PHYSICAL/MENTAL REQUIREMENTS
  • This is a penicillin manufacturing facility. All candidates applying mist NOT be allergic to penicillin.
  • Must be able to aseptically gown.
  • Able to lift 25-30 lbs

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
  • Non- Standard work schedule at times maybe required to support product release, including weekend, second shift, night shift work / call for process decisions.
  • Minimal travel for training/seminars.

Work Location Assignment: On Premise
Last Date To Apply: August 14, 2026
The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
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About Pfizer

Sourced by ZipRecruiter

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Our Health and Science System Specialists Team provides leadership across patient care settings in the complex Hospital, Health System, and Key Medical Group environment to bring value to our customers and patients in this dynamic ecosystem.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US

Year founded

1849