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Computer Validation Jobs in Westborough, MA (NOW HIRING)

Sun Pharmaceutical Industries

Validation Engineer II

Billerica, MA · On-site

$104K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...

Sun Pharmaceutical Industries

Validation Engineer II

Billerica, MA · On-site

$104K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...

Actalent

Verification & Validation Engineer

Manville, RI

$62/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Verification & Validation (V&V) Engineer This role focuses on executing verification, validation ... Bachelor's degree in Electrical Engineering, Computer Engineering, or a related field, or ...

Alcami Corporation

Sr. Validation Engineer

Pepperell, MA · On-site

$43.27 - $53.49/hr

The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...

Alcami Corporation

Sr. Validation Engineer

Pepperell, MA

$43.27 - $53.49/hr

The Senior Validation Engineer will plan, schedule, coordinate, and track all facets of assigned ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...

Alcami Corporation

Sr. Validation Engineer

MA · On-site

$43.27 - $53.49/hr

The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA

$115K - $140K/yr

... 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 ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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 ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

... 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 ...

Deloitte

System Test and Validation Lead

Boston, MA · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Boston, MA · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Boston, MA · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

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Showing results 21-40

All JobsComputer Validation JobsComputer Validation Jobs in Westborough, MA

Computer Validation information

See Westborough, MA salary details

$10

$55

$88

How much do computer validation jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for computer validation in Westborough, MA is $55.96, according to ZipRecruiter salary data. Most workers in this role earn between $43.08 and $66.35 per hour, depending on experience, location, and employer.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment with opportunities for certification and skill development. The field is considered important in industries like pharmaceuticals and biotech, where system integrity and data accuracy are critical.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What are popular job titles related to Computer Validation jobs in Westborough, MA? For Computer Validation jobs in Westborough, MA, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Westborough, MA look for? The top searched job categories for Computer Validation jobs in Westborough, MA are:
What cities near Westborough, MA are hiring for Computer Validation jobs? Cities near Westborough, MA with the most Computer Validation job openings:
Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Westborough, MA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 75% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $116,396 per year, or $56 per hour.

Validation Engineer III

Barry-Wehmiller Companies

Boston, MA • On-site

Full-time

Re-posted 29 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:
Job Summary
The Validation Engineer III will serve as a key member of the validation team, providing expert-level support to ensure facility equipment, utilities, processes, instrumentation, and computerized systems are qualified and maintained in a validated state in compliance with applicable regulatory requirements. This role functions as a Validation Subject Matter Expert (SME) responsible for leading validation activities, authoring protocols and reports, and providing technical guidance to cross-functional teams. The Validation Engineer III will coordinate and execute qualification activities while collaborating with internal stakeholders and external vendors to support ongoing operations and capital projects.
Key Responsibilities
Validation Documentation & Execution
  • Author, review, and approve validation protocols, reports, and associated documentation including acceptance criteria development
  • Establish, revise, and maintain validation master plans, procedures, and lifecycle documentation for qualification of equipment, systems, and processes in accordance with cGMP requirements
  • Execute and oversee IQ/OQ/PQ protocols for equipment, utilities, and systems
  • Review and complete documentation in accordance with cGMP, ALCOA+ principles, and data integrity requirements
Project & Program Management
  • Lead and manage validation-related project activities including scheduling, resource coordination, protocol execution, and report review
  • Manage external vendors and contractors performing qualification activities
  • Serve as a key member of project teams for design, procurement, installation, and commissioning of new equipment and facility expansion projects
  • Develop and maintain validation project timelines and deliverables
Compliance & Change Control
  • Review proposed changes to validated systems and provide impact assessments
  • Identify validation requirements necessary to maintain systems in a validated state following change implementation
  • Manage periodic requalification activities to ensure equipment, utilities, and processes remain compliant
  • Support equipment and building monitoring systems compliance and updates
Technical Expertise
  • Serve as Subject Matter Expert (SME) in one or more of the following disciplines:
    • Process Mapping
    • Quality Management (Quality Risk Assessments; Change Controls; Deviations; CAPA; Documentation)
    • Equipment qualification (autoclaves, controlled temperature units, filling equipment)
    • Cleaning validation Aseptic process simulation (media fills)
    • Computer system validation (CSV)
    • Process validation Utility qualification (WFI, purified water, clean steam, HVAC)
    • Environmental monitoring systems
  • Provide technical guidance and troubleshooting support for equipment and system failures
  • Deliver training on validation program elements to junior validation personnel
Quality Systems Support
  • Author and support equipment and process-related deviation investigations and CAPA activities
  • Perform and support risk assessments (FMEA, etc.) and data integrity assessments
  • Support internal audits and regulatory agency inspections
  • Ensure all work is performed in accordance with SOPs, cGMPs, quality standards, and safety procedures
Qualifications
Education
  • Bachelor's degree in Engineering, Life Sciences, or related scientific discipline required
  • Master's degree (MS/MSc) preferred
Experience
  • Minimum 5+ years of professional experience in validation, engineering, or operations within a regulated environment
  • Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device manufacturing environment
  • Demonstrated expertise as a Subject Matter Expert (SME) in one or more validation disciplines
  • Experience with GMP utilities (WFI, purified water, clean steam, compressed gases, HVAC) and manufacturing equipment
  • Experience supporting regulatory inspections (FDA, EMA, or equivalent) preferred
  • Capital project experience including equipment design, selection, and commissioning preferred
Skills & Competencies
  • Strong technical writing skills with ability to author clear, compliant documentation
  • Solid working knowledge of cGMP regulations, FDA guidance documents, and industry standards (ISPE, PDA, GAMP)
  • Understanding of GDP requirements and ALCOA+ data integrity principles
  • Excellent communication and interpersonal skills with ability to interface across all organizational levels
  • Strong project management and organizational skills
  • Ability to work independently with minimal supervision while also functioning effectively in a team environment
  • Self-motivated with demonstrated initiative and problem-solving abilities
  • Proficiency in Microsoft Office Suite; experience with electronic validation systems a plus
Working Conditions
  • On-site presence required; may involve work in manufacturing, laboratory, and utility areas
  • Ability to gown into cleanroom environments as required
  • Occasional flexibility in schedule and travel may be needed to support project timelines or production schedules
    #LI-TH1

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

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