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Csv Engineer Jobs in Boston, MA (NOW HIRING)

Astrix Inc

CSV Specialist

Lexington, MA · On-site

$45 - $52/hr

Hyrbrid - 3 days a week in person (Lexington, MA) Pay: $45-52/hr 6month contract The CSV Engineer is responsible for validating GxP computer systems and ensuring compliance with global procedures ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

... in Engineering, Computer Science or related discipline Desired ON-THE-JOB EXPERIENCE 7+ years of Computer System Validation experience Desired KNOWLEDGE, SKILLS AND EXPERIENCE In depth CSV ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

... in Engineering, Computer Science or related discipline Desired ON-THE-JOB EXPERIENCE 7+ years of Computer System Validation experience Desired KNOWLEDGE, SKILLS AND EXPERIENCE In depth CSV ...

Genezen

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

... in Engineering, Computer Science or related discipline Desired ON-THE-JOB EXPERIENCE 7+ years of Computer System Validation experience Desired KNOWLEDGE, SKILLS AND EXPERIENCE In depth CSV ...

Deegit Inc

CSV Validation

Lexington, MA · On-site

Company Description CSV Validation with Application Testing Qualifications Additional Information All your information will be kept confidential according to EEO guidelines.

Moderna, Inc.

Sr. Engineer I, Automation

Marlborough, MA · On-site

$107K - $141K/yr

The engineer will collaborate with cross-functional teams to deliver scalable, compliant, and ... Background in CSV and regulatory compliance (21 CFR Part 11, Annex 11) * Experience developing ...

Corning

Division Quality Engineer I

Tewksbury, MA

$77K - $100K/yr

Author, review, execute, and approve CSV lifecycle documentation, including: * Ensure computerized ... Partner with IT, Automation, Quality, Engineering, and system owners to support implementation ...

Slope

Senior Software Engineer, Deepview

Boston, MA · On-site

$166 - $220/hr

Deepview ingests protobuf, image, video, and CSV data streams--rendering them in a time ... Our team's mission is to give engineers and operators the deepest possible visibility into what ...

Syner-G

Validation Engineer

Waltham, MA · On-site +1

The Validation Engineer will play a key role in supporting operational readiness, tech transfer ... Demonstrated experience writing IQ, OQ, PQ, and CSV reports. Knowledge, Skills, and Abilities

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Csv Engineer information

See Boston, MA salary details

$39.6K

$109.3K

$151.2K

How much do csv engineer jobs pay per year?

As of Aug 26, 2026, the average yearly pay for csv engineer in Boston, MA is $109,307.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,700.00 and $128,100.00 per year, depending on experience, location, and employer.

What is a CSV engineer?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What are the key skills and qualifications needed to thrive as a CSV engineer?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

What are the common challenges faced by a CSV engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.

How much do CSV engineers make?

CSV engineers typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and industry. They often work with data processing tools and scripting languages like Python or SQL to manage and analyze CSV data efficiently.

How to become a CSV engineer?

To become a CSV engineer, you should develop strong skills in data management, scripting languages like Python or SQL, and familiarity with CSV file formats. Earning relevant certifications or degrees in data science, computer science, or related fields can also enhance your qualifications, along with experience working with data processing tools and environments.

What are the most commonly searched types of Csv Engineer jobs in Boston, MA?

The most popular types of Csv Engineer jobs in Boston, MA are:

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For Csv Engineer jobs in Boston, MA, the most frequently searched job titles are:

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Csv Engineer jobs near you
Infographic showing various Csv Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $109,307 per year, or $52.6 per hour.

CSV Engineer

Woburn, MA • On-site

Katalyst Healthcares and Lifesciences
See more jobs at Katalyst Healthcares and Lifesciencesexternal

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This job post has expired 6 days ago. Applications are no longer accepted.

Job description

Job Summary:
  • We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment.
  • The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance.

Roles & Responsibilities:
  • Develop, execute, and maintain Computer System Validation (CSV) documentation and validation protocols for QC laboratory systems and manufacturing systems.
  • Support the complete validation lifecycle, including preparation, execution, review, and approval of User Requirements Specifications (URS), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Risk Assessments, and Validation Reports.
  • Perform risk assessments to identify and mitigate validation and compliance risks.
  • Ensure compliance with GAMP 5, 21 CFR Part 11, GMP, and internal quality standards.
  • Review validation documentation to ensure accuracy, completeness, and regulatory compliance.
  • Collaborate with Quality Assurance (QA), Manufacturing, Engineering, and IT teams to support validation activities and system implementations.
  • Provide validation support for QC laboratory systems and manufacturing equipment throughout their lifecycle.
  • Assist with change control, deviation investigations, and periodic reviews related to validated systems.
  • Maintain accurate validation records and ensure documentation is audit ready.
  • Support internal and external regulatory inspections by providing validation documentation and technical expertise.

Requirements / Qualifications:
  • Bachelor's degree in engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or a related field.
  • Experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment.
  • Strong knowledge of GAMP 5, 21 CFR Part 11, and GMP regulations.
  • Hands-on experience supporting QC laboratory systems and/or manufacturing equipment validation.
  • Experience developing and reviewing validation lifecycle documentation, including URS, IQ, OQ, PQ, Risk Assessments, and Validation Reports.
  • Experience working collaboratively with Quality Assurance (QA), Manufacturing, Engineering, and IT teams.
  • Strong understanding of the CSV lifecycle, risk-based validation, and documentation best practices.
  • Excellent technical writing, documentation, communication, and problem-solving skills.
  • Ability to manage multiple validation activities while maintaining compliance with regulatory and quality requirements.

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