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Computer System Validation Jobs in Michigan (NOW HIRING)

Lancesoft

Manufacturing Engineer II - Exempt

Dexter, MI · On-site

$45 - $50/hr

Computer System Validation (CSV) * Manufacturing, Packaging, and Laboratory Equipment * Technical experience (Troubleshooting) or any similar experience or background * Quality / Process Control ...

formeldusa

Validation Engineer

Troy, MI

Experience working with Control Modules or ADAS systems. Computer literacy with strong knowledge of the MS Office Suite. Validation experience with knowledge of test and validation methods. Strong ...

Formel D USA

Validation Engineer

Troy, MI · On-site

Experience working with Control Modules or ADAS systems. Computer literacy with strong knowledge of the MS Office Suite. Validation experience with knowledge of test and validation methods. Strong ...

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How much do computer system validation jobs pay per hour?

As of May 31, 2026, the average hourly pay for computer system validation in Michigan is $47.34, according to ZipRecruiter salary data. Most workers in this role earn between $36.44 and $56.15 per hour, depending on experience, location, and employer.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
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Computer System Validation jobs near you
Validation Engineer III

Validation Engineer III

Thermo Fisher Scientific

Detroit, MI • On-site

Full-time

Posted 8 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 388 frontline employees who took The Breakroom Quiz

186th of 512 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.)
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.
DESCRIPTION:
Join our validation engineering team, where you'll ensure product quality and regulatory compliance across pharmaceutical manufacturing operations. As a Validation Engineer III, you'll lead complex validation projects for equipment, processes, utilities, and computer systems while collaborating with cross-functional teams to maintain GMP standards. You'll contribute to continuous improvement initiatives, support team members, and provide technical expertise during client and regulatory audits. This role offers professional growth opportunities as you help enable life-changing therapies through robust validation strategies and execution.
REQUIREMENTS:
• Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in validation in pharmaceutical/biotech manufacturing or comparable regulated industry
• Preferred Fields of Study: Engineering, Life Sciences, Chemistry or related technical field
• Strong knowledge of cGMP regulations, including FDA, EMA and ISO requirements
• Experience writing and executing validation protocols, including IQ/OQ/PQ documentation
• Expertise in risk assessment methodologies and statistical analysis
• Proficiency with validation of manufacturing equipment, utilities, cleaning processes and computer systems
• Experience leading complex validation projects and coordinating cross-functional teams
• Strong technical writing and documentation skills
• Advanced problem-solving abilities and root cause analysis experience
• Excellent verbal/written communication and interpersonal skills
• Proficiency with relevant software tools (MS Office, statistical packages, validation systems)
• Experience with regulatory inspections and client audits preferred
• Knowledge of lean manufacturing and continuous improvement methodologies
• Ability to work in cleanroom environments when required
• Flexibility to work extended hours or alternate shifts based on project needs
• May require up to 25% travel

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