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Validation Analyst Jobs in Michigan (NOW HIRING)

Pfizer

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

Carryout process capability analysis on all commercial processes on a periodic basis. Identify ... Review site change controls to ensure the validated state of a process is not impacted by a ...

Expleo

Automotive Test & Validation Engineer

Troy, MI · On-site

Review and analyze test service requests and customer specifications in collaboration with the Product Project Team Member and Quality PTM, challenging requirements and defining the final validation ...

Gentex

Laboratory Validation Engineer II

Zeeland, MI · On-site

Analyze and interpret test data against pass/fail criteria, providing technical consultation to the ... in validation practices. * Other duties as assigned. HOW YOU'LL DO IT * Attention to detail ...

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Validation Analyst information

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How much do validation analyst jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for validation analyst in Michigan is $27.48, according to ZipRecruiter salary data. Most workers in this role earn between $22.02 and $31.20 per hour, depending on experience, location, and employer.

How does a validation analyst typically collaborate with cross-functional teams during a project?

As a Validation Analyst, you will regularly work with cross-functional teams, including Quality Assurance, Regulatory Affairs, Manufacturing, and IT. Your role involves gathering requirements, designing validation protocols, and ensuring compliance with industry standards by facilitating communication between these groups. Effective collaboration is key to resolving issues quickly and ensuring that validation deliverables meet both technical and regulatory expectations. This teamwork not only enhances project success but also provides valuable learning opportunities from experts in related fields.

How much does a validation analyst make?

A validation analyst's average salary in the United States ranges from $60,000 to $85,000 per year, depending on experience, location, and industry. Entry-level roles may start around $50,000, while experienced professionals with certifications can earn over $100,000 annually. The role often requires knowledge of validation processes, regulatory standards, and proficiency with tools like GxP or validation software.

What is the difference between Validation Analyst vs Quality Assurance Analyst?

AspectValidation AnalystQuality Assurance Analyst
Required CredentialsBachelor's in Life Sciences, certifications like CQE or CSQEBachelor's in related fields, certifications like CQE or Six Sigma
Work EnvironmentRegulatory, pharmaceutical, or biotech industriesManufacturing, software, or product development sectors
Employer & Industry UsageUsed in regulated industries for complianceUsed across various industries for process improvement
Common Search & ComparisonOften compared for compliance rolesCompared for quality process roles

The main difference is that Validation Analysts focus on ensuring that processes, equipment, and systems meet regulatory standards, especially in pharma and biotech. Quality Assurance Analysts oversee overall quality processes, including testing and process improvements across industries. Both roles require similar certifications but serve different aspects of quality management.

What is a validation analyst?

Validation Analysts are professionals responsible for ensuring that systems, processes, or products meet specific regulatory, industry, and company standards. They develop and execute validation protocols, analyze test results, and document compliance with quality and safety requirements. Validation Analysts often work in industries such as pharmaceuticals, biotechnology, and manufacturing, where strict validation of processes is required. Their role is critical in maintaining product integrity and regulatory compliance.

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

To thrive as a Validation Analyst, you need a strong background in quality assurance, process validation, and regulatory compliance, often supported by a degree in life sciences, engineering, or a related field. Familiarity with validation protocols, data analysis tools, and industry-specific guidelines like FDA or GAMP is typically required. Attention to detail, critical thinking, and strong written and verbal communication skills set outstanding candidates apart. These skills ensure that products and processes consistently meet quality standards and regulatory requirements, minimizing risks and ensuring compliance.
What are the most commonly searched types of Validation Analyst jobs in Michigan? The most popular types of Validation Analyst jobs in Michigan are:
What are popular job titles related to Validation Analyst jobs in Michigan? For Validation Analyst jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Validation Analyst jobs in Michigan look for? The top searched job categories for Validation Analyst jobs in Michigan are:
Validation Analyst jobs near you
Infographic showing various Validation Analyst job openings in Michigan as of August 2026, with employment types broken down into 85% Full Time, 7% Part Time, 1% Temporary, and 7% Contract. Highlights an 81% Physical, 7% Hybrid, and 12% Remote job distribution, with an average salary of $57,167 per year, or $27.5 per hour.

Qualification Validation Engineer

TOWER LABORATORIES LTD.

Montague, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Join a team where your expertise can spark real innovation by shaping a future of wellness. We’re seeking a skilled chemist ready to transform ideas into impactful solutions.

Tower Laboratories is a leading effervescent product manufacturer in the U.S. We develop and manufacture over-the-counter medications, prescription pharmaceuticals, nutritional supplements, soft drink tablets and other consumer products on a contract basis. We are continually expanding our effervescent product base and currently have several new and interesting products in the research and development phase right now. We are a family owned company and have been in business for over 40 years.

Tower Labs' production environment is clean and temperature and humidity controlled. Uniforms provided free of charge.

We are not offering relocation assistance for this position.

www.towerlabs.com

POSITION SUMMARY:

This position is responsible for initiating, conducting and implementing engineering evaluations, new equipment or processes installations (in coordination with Staff Engineer and Facilities Manager), design and general improvements associated with the manufacturing processes at Tower Laboratories. These activities support operational requirements to maximize operating effectiveness as well as fulfilling the need to document manufacturing systems and satisfy regulatory requirements.

ESSENTIAL FUNCTIONS:

    • Write and perform qualifications and validations for products and processes
    • Write and execute IQ, OQ and PQ on manufacturing equipment
    • Prepare annual reports to assess product trends, submit recommendations to management by summarizing and analyzing the processes, develops action plan to correct the issues highlighted in the evaluations
    • Writes specifications and procedures
    • Interfaces with R&D in new product development by working with department on scale-ups and new product development
    • Conducts internal as well as external audits as needed
    • Reviews existing manufacturing processes and leads a team of representatives from a number of departments in improving the processes
    • Interfaces with customers on the transfer and implementation of manufacturing process
    • Conducts related training when needed
    • Performs evaluations, conducts research and initiates compatibility studies on alternate materials
    • Assists in the writing and reviewing of new Batch Records
    • Interfaces on technical issues between the Manufacturing and Technical Departments
    • Performs all work in accordance with established Safety, cGMP and company procedures
    • Other related responsibilities as assigned other duties as requested

ESSENTIAL SKILLS and EXPERIENCE:

  • Minimum 2 years experience in chemical engineering
  • Computer literate with spreadsheet, databases and CAD
  • Familiarity with SPC & IE analysis techniques
  • Strong problem analysis and problem resolution at both a strategic and a functional level
  • Strong verbal and written communication skills
  • Ability to organize and manage multiple projects
  • Ability to communicate effectively with team members and other plant personnel

EDUCATION:

Technical engineering degree required; Bachelor’s degree in an engineering discipline preferred

BENEFITS:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Health insurance
  • Life insurance
  • Paid time off
  • Tuition reimbursement
  • Vision insurance
  • Prescription safety lens reimbursement
  • ANSI - approved safety shoe reimbursement

SCHEDULE:

  • Monday to Friday
  • Overtime
  • Full time
  • On Site

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.