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Internship Computer System Validation Csv Jobs in Michigan

Corium Innovations

Validation Engineer

Grand Rapids, MI

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... computer systems.  This includes successfully working with other departments, contract resources, and customers/vendors (as applicable) to plan, develop, maintain and execute validation and ...

Stellantis

AI Validation Engineer

Auburn Hills, MI · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We are seeking a Senior AI Validation Engineer to design and implement testing strategies ... system integration disciplines. Basic Qualifications: * Bachelor's degree in computer science ...

Agile Global Solutions, Inc

CAD Designer

Detroit, MI · On-site

$24.75 - $34/hr

Light Gauge Steel (CFS) framing systems * Structural detailing and shop drawings * Building ... Generate fabrication data, Bills of Materials (BOMs), and CSV files for automated roll-forming ...

Torc Robotics

Software Integration Engineer

Ann Arbor, MI · On-site

$101K - $137K/yr

Through Hardware-in-the-Loop systems, on-truck development, automation frameworks, validation ... computer science, robotics, or related field. * 1-3 years of relevant experience (internships ...

CompTech Computer Technologies

Computer Operator

Battle Creek, MI

$42K - $50K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Windows Operation System Security (WOSS) by Day 1 * Must have the following: valid state driver's license, personal vehicle and proof of insurance Overview We are seeking a Computer Operator to join ...

Polaris, Inc.

Sr. Cybersecurity Validation Engineer

Novi, MI · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Work with control systems engineers to plan test script development and software validation ... Requires a Bachelor's degree in Electrical Engineering, Computer Science, Software Engineering ...

Polaris, Inc.

Sr. Cybersecurity Validation Engineer

Novi, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Work with control systems engineers to plan test script development and software validation ... Requires a Bachelor's degree in Electrical Engineering, Computer Science, Software Engineering ...

Stellantis

Senior FOTA Validation Engineer

Auburn Hills, MI · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Stellantis is seeking an Electrical Systems Validation Engineer who will be responsible for ... Bachelor of Science in Electrical Engineering, Computer Engineering, Software Engineering or ...

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Internship Computer System Validation Csv information

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What is the difference between Internship Computer System Validation Csv vs Computer System Validation Specialist?

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.

What are the most commonly searched types of Computer System Validation Csv jobs in Michigan?

The most popular types of Computer System Validation Csv jobs in Michigan are:

What are popular job titles related to Internship Computer System Validation Csv jobs in Michigan?

For Internship Computer System Validation Csv jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Internship Computer System Validation Csv jobs in Michigan look for?

The top searched job categories for Internship Computer System Validation Csv jobs in Michigan are:

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Cities in Michigan with the most Internship Computer System Validation Csv job openings:

Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Validation Engineer

Corium Innovations

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Job description

Corium Innovations is seeking a Validation Engineer II/Sr. Validation Engineer who will be responsible for the maintenance and execution of the site validation programs including equipment, facilities, utilities, lab instrumentation and computer systems.  This includes successfully working with other departments, contract resources, and customers/vendors (as applicable) to plan, develop, maintain and execute validation and qualification activities.  This position will also be involved with site audit activities, investigations, change management evaluation and qualified utility ownership. The Sr. Validation Engineer is responsible for performing appropriate validation/qualification activities (IQ/OQ/PQ) and other system support activities to meet department, site and corporate objectives. This position involves the review and reporting of data, annual review and routine qualification/verification activities required for all systems.
Your most Innovative career move is here!
At Corium Innovations, we’ve led the way in innovating drug delivery technologies for millions of patients whose GI systems just can’t tolerate pills, who can’t remember to take their meds as directed, or who have needle-phobia. This is only the beginning! There’s so much more to deliver, and we need YOU to do it!
Our Purpose is to create, develop and manufacture innovative healthcare products for partners that deliver superior value to patients.
Our Goal is to be the best-in-class specialty CDMO through the use of innovative technologies and superior execution.
Our Company Values are core to our positive and people-centric culture which inspires all of us to come to work every day on behalf of our people, our partners, our customers, and our patients. Through our four core values, we put people first and create opportunities to make each day better than the last.
  • Celebrate Individuals: We’re looking for talent who will celebrate the uniqueness of each of our team members by encouraging everyone to bring their authentic self to work.
  • Successful Together: We believe we’re better together, so we prioritize teamwork as we work to achieve our shared vision knowing each one of us has an important role to play.
  • Embrace Innovation: We embrace new challenges and opportunities while encouraging creative thinking and innovative solutions to best meet the needs of our people and our partners.
  • Pride in Ownership: We take pride in owning our progress and successes, feeling empowered to pursue our growth to reach our full potential. And we hope you will too!
Responsibilities:
  • Development of validation or qualification deliverables, performing testing, verification, calibration, and routine maintenance of equipment, facilities, utilities, lab instruments and computer systems.
  • Develop and maintain procedures for qualification utilizing known industry best practices.
  • Utility and functional area reporting.
  • Quality system interaction (investigation, CAPA, change control)
  • Asset Management System ownership and maintenance
  • Continuous Improvement and other special projects in the Engineering Services functional area.
Qualifications:
  • Bachelor’s degree in a STEM field.
  • 5+ Years’ experience in the pharmaceutical industry.
  • Strong knowledge of FDA/cGMP/ISO requirements.
  • Knowledge of GMP Quality Systems and working knowledge of regulatory requirements.
  • Previous hands-on experience with equipment, facilities, utilities, lab instruments and computer system qualification (IQ/OQ/PQ), requirements documents, impact assessments, and summary reports preferred.
  • Previous hands-on experience with lab instrumentation and calibration, including but not limited to HPLC/UHPLC, GC, Dissolution Baths.
  • Cleanroom and qualified utility monitoring and qualification experience preferred.
  • Demonstrated analytical skill/problem solving skills. 
  • Must have good organizational skills, able to multi-task, and be capable of adjusting to changing priorities.
  • Self-starter
  • Excellent interpersonal and communication skills, both written and verbal.
Benefits:
  • Highly competitive benefits program including medical, dental, vision, flexible spending accounts, life insurance, disability insurance, and employee assistance program.
  • 401(k) retirement savings account with a company match and immediate vesting.
  • 12 paid holidays.
  • Competitive paid vacation plan plus ~1 additional week of paid time off for our annual holiday shutdown.

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