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Computer System Validation Jobs in Boston, MA (NOW HIRING)

Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...

... Computer System Validation experience Desired KNOWLEDGE, SKILLS AND EXPERIENCE In depth CSV experiences including as a Validation lead Essential The ability to communicate with employees of all ...

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Computer System Validation information

See Boston, MA salary details

$11

$59

$93

How much do computer system validation jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for computer system validation in Boston, MA is $59.00, according to ZipRecruiter salary data. Most workers in this role earn between $45.43 and $70.00 per hour, depending on experience, location, and employer.

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.

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 is the work of computer system validation?

Computer System Validation (CSV) is the process of ensuring that computer systems used in regulated environments function correctly and comply with industry standards. It involves documenting and testing software, hardware, and related processes to verify they meet specified requirements, often using validation protocols and tools. CSV is essential in industries like pharmaceuticals and healthcare to ensure data integrity and regulatory compliance.

What degree is best for cis jobs?

For Computer System Validation (CSV) roles, a bachelor's degree in computer science, information technology, life sciences, or engineering is typically preferred. Relevant certifications such as GxP or validation-specific training can enhance job prospects, and strong knowledge of regulatory requirements like FDA or EMA guidelines is beneficial.

What is the salary of SoC validation engineer?

The salary of a SoC validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Professionals in this role often have skills in hardware description languages and verification tools, which can influence compensation.
What are the most commonly searched types of Computer System Validation jobs in Boston, MA? The most popular types of Computer System Validation jobs in Boston, MA are:
What job categories do people searching Computer System Validation jobs in Boston, MA look for? The top searched job categories for Computer System Validation jobs in Boston, MA are:
What cities near Boston, MA are hiring for Computer System Validation jobs? Cities near Boston, MA with the most Computer System Validation job openings:
Computer System Validation Engineer

Computer System Validation Engineer

Barry-Wehmiller

Boston, MA • On-site

Full-time

Posted 6 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:

    • Computer Systems Validation Engineer

      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 Computer Systems Validation Engineer, 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.

      Interface with our clients and take responsibility for preparing and executing computer system validation documents for a variety of distributed control, process control, and stand-alone production systemsDevelop documents and execute computer system validation test scripts, including SFATs, HFATs, traceability matrices, IQs, and OQsParticipate in good documentation practices (cGMP and FDA CQV methods and systems)Read engineering documents, set priorities, and work on multiple projects simultaneouslyCommunicate verbally and via technical writingMake an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team

      What You'll Bring

      A minimum of four years of computer system validation experience in the pharmaceutical, biotech, medical device or other FDA regulated industriesCompetency with FDA Data Integrity requirements and exposure to data integrity risk and gap assessmentsA solid understanding of GAMP and 21 CFR Part 11 requirementsExperience in generating software development life cycle documentation such as FRSs, SDSs, HDSs and configuration specificationsHands-on experience with Emerson DeltaV, Syncade, Allen Bradley PLC, Wonderware, OSI PI, or Rockwell software platformAn understanding of laboratory systems and CSV for process control systems for clean utilities and bioprocess manufacturing equipmentA solid working knowledge of biologic unit operations, including fermentation and purification methods and equipmentA willingness to travel for project requirements including installation and start-up activities, client and company sponsored meetings, trainings, industry related seminars, forums, and conventionsA bachelor's degree in engineering, computer science, or related technical field

      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 Computer Systems Validation Engineer, 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 Computer Systems Validation Engineer 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. #LI-TH1

    • Additional Job Description

      Establishes validation standards, develops and executes validation protocols, reports on findings, and oversees resolution of compliance failures or deviationDevelops and maintains validation-related documentation, which may include specifications, SOPs, work instructions, or batch or testing recordsEnsures processes, products, equipment, or systems comply with all applicable external regulations or standardsMay assist with new equipment purchases or upgrades to existing equipmentOther duties as assigned

  • Additional Job Description
    • Maintains maps, detail design drawings, graphs, as-built drawings, structural detail drawings and other graphic engineering records.

    • Collects codes and posts data from prescribed sources for input to computer.

    • Corrects and updates existing records and prepares data for analysis.

    • Other duties as assigned


 

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