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Internship Computer System Validation Csv Jobs in Riverside, CA

Validation Manager

Corona, CA · On-site

$95K - $105K/yr

This position requires strong communication skills, computer skills, and experience in management ... The position reports to the Vice-President of Quality Systems. MAJOR FUNCTIONS & RESPONSIBILITIES:

This position requires strong communication skills, computer skills, and experience in management ... The position reports to the Vice-President of Quality Systems. MAJOR FUNCTIONS & RESPONSIBILITIES:

Quality Engineer Manager

Irvine, CA · On-site

$110K - $160K/yr

Computer System Validation * Cleaning validation and equipment qualification experience * Proficient in Change control process * Working independently to pull and trend data and write reports.

Quality Engineer Manager

Irvine, CA · On-site

$110K - $160K/yr

Computer System Validation * Cleaning validation and equipment qualification experience * Proficient in Change control process * Working independently to pull and trend data and write reports.

... and system validation needs across multiple teams. - Collaborate closely with RTL design ... What We're Looking For BS Computer Engineering, Electrical Engineering, or Computer Science with ...

... and system validation needs across multiple teams. - Collaborate closely with RTL design ... What We're Looking For BS Computer Engineering, Electrical Engineering, or Computer Science with ...

... system validation using presilicon hardware models. -Execute emulation test plans to support ... Requirements: - BS in Computer Engineering, Electrical Engineering, or Computer Science with 5-7 ...

... system validation using presilicon hardware models. -Execute emulation test plans to support ... Requirements: - BS in Computer Engineering, Electrical Engineering, or Computer Science with 5-7 ...

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Internship Computer System Validation Csv information

See Riverside, CA salary details

$30

$54

$78

How much do internship computer system validation csv jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for internship computer system validation csv in Riverside, CA is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $67.21 per hour, depending on experience, location, and employer.

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 to thrive as an Internship Computer System Validation (CSV) specialist, and why are they important?

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 some typical responsibilities for an intern in Computer System Validation (CSV), and how do they contribute to the overall validation process?

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 job categories do people searching Internship Computer System Validation Csv jobs in Riverside, CA look for? The top searched job categories for Internship Computer System Validation Csv jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Internship Computer System Validation Csv jobs? Cities near Riverside, CA with the most Internship Computer System Validation Csv job openings:
Sr. Validation Project Manager (Life Sciences)

Sr. Validation Project Manager (Life Sciences)

Paper Converting Machine

Santa Ana, CA

Full-time

Posted 17 days ago


Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Sr. Validation Project Manager

Who You'll Work With

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.

When you join Design Group as a Sr. Project Manager, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world's leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.

What You'll Do

You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.

  • Sr. Project Manager will interface with clients, lead teams of validation professionals, and provide subject matter expertise in the validation of a variety of utility, facility and process equipment.
  • The Sr. Project Manager will help lead business development efforts in the region as it relates to engaging with new clients in the life sciences sector, and expanding our engagements with existing clients
  • The Sr. Project Manager will be responsible for developing project scope statements, estimates and proposals.
  • Will work on multiple projects simultaneously
  • Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team

What You'll Bring

  • Minimum of 7 years' experience with increasing responsibility in validation/quality service and project management of life sciences, biotech or other FDA regulated projects.
  • This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on multiple projects simultaneously.
  • Strong understanding of EPCMV, Quality by Design and risk-and science-based approaches for compliance are desired.
  • Experience with system and process risk assessments; including FMEA, HAZOP and Fault Tree Analysis desired.
  • Experience with financial systems, project, and client administration and Requires strong leadership, verbal communication, technical writing, project management tools and word processing skills.
  • Diverse experience in leading project teams related to the commissioning and qualification of clean utilities, facility systems, process support systems, bioprocess manufacturing systems, packaging equipment, and process and cleaning validation is desirable.
  • Working knowledge of process automation and computer system validation concepts, GAMP methodologies, 21 CFR Part 11 compliance and latest industry expectations for data integrity.
  • Project Management experience in managing scope, cost, schedule, quality, and risk is required.
  • Experience in mentorship and multi-discipline collaboration
  • Displayed leadership in a consulting and service environment
  • Willing and able to travel as necessary for project requirements to include but not be limited to: project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc. BS Degree in Engineering or related technical degree.

Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Sr. Project Manager, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.

Feel like you're on the path to becoming a Sr. Project Manager but you're not quite there yet? We'd love to connect with you to see if we can take you from

where you are today and grow you into a Design Group Engineering Consultant.

The approximate pay range for this position is $120k-$160k. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position.

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At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group