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Computer System Validation Csv Remote Jobs in Boston, MA

Emvia, Inc.

Automation Validation Lead

Andover, MA · On-site +1

Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... computer system software and hardware: Windows operating systems Windows Terminal Services/Remote ...

Valspec

QA Consultant

Boston, MA · Remote

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... Computer Science, or related field preferred * 3+ years of experience in Automation QA, CSV, CQV ...

BioNTech SE

Business Capability Specialist

Cambridge, MA · Remote

$113K - $181K/yr

Support GxP Computer System Validation activities by creating key documentation such as Validation Plans, User Requirements Specifications (URS), Testing Protocols (IQ/OQ/PQ/UAT), Traceability ...

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All JobsComputer System Validation Csv Remote JobsComputer System Validation Csv Remote Jobs in Boston, MA

Computer System Validation Csv Remote information

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$11

$59

$93

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

As of Jun 10, 2026, the average hourly pay for computer system validation csv remote in Boston, MA is $59.01, 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 is a Computer System Validation (CSV) specialist and what do they do remotely?

A Computer System Validation (CSV) specialist is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards and function as intended. When working remotely, CSV specialists perform tasks like developing validation protocols, reviewing documentation, executing test scripts, and liaising with teams via digital tools to ensure systems adhere to regulatory guidelines. Their work helps guarantee data integrity, product quality, and regulatory compliance in industries where strict standards are critical.

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

AspectComputer System Validation Csv RemoteComputer Validation Specialist
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentRemote, regulated industries like pharma and biotechOn-site or hybrid in regulated industries
Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, biotech, medical devices
Job FocusValidating computer systems and software complianceValidating computer systems and software compliance

Both roles require similar certifications and work in regulated industries like pharma and biotech. The main difference is that Computer System Validation Csv Remote typically involves remote work, focusing on validating computer systems remotely, while Computer Validation Specialist may work on-site or in hybrid settings. Both roles aim to ensure compliance with industry standards and regulations.

What are some common challenges faced by Computer System Validation (CSV) professionals working remotely, and how can they be addressed?

Remote CSV professionals often encounter challenges such as coordinating validation activities across different teams, ensuring secure access to validation environments, and maintaining clear documentation. Effective communication is key—using project management tools and regular virtual meetings helps keep everyone aligned. It's also important to implement robust cybersecurity measures and standardized documentation practices to ensure compliance. Proactively addressing these challenges fosters a smooth validation process and supports regulatory requirements.

What are the key skills and qualifications needed to thrive as a Computer System Validation (CSV) specialist in a remote role, and why are they important?

To excel as a Computer System Validation (CSV) specialist, you need a solid background in computer science or life sciences, experience with GxP regulations, and knowledge of validation documentation standards. Familiarity with validation management tools, electronic quality management systems (eQMS), and understanding regulatory frameworks like FDA 21 CFR Part 11 or EU Annex 11 is crucial. Strong attention to detail, problem-solving skills, and effective remote communication set top performers apart. These competencies ensure validated systems meet compliance requirements, maintain data integrity, and support regulatory audits in remote environments.
What are popular job titles related to Computer System Validation Csv Remote jobs in Boston, MA? For Computer System Validation Csv Remote jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Csv Remote jobs in Boston, MA look for? The top searched job categories for Computer System Validation Csv Remote jobs in Boston, MA are:
What cities near Boston, MA are hiring for Computer System Validation Csv Remote jobs? Cities near Boston, MA with the most Computer System Validation Csv Remote job openings:
Computer System Validation Csv Remote jobs near you
Infographic showing various Computer System Validation Csv Remote job openings in Boston, MA as of June 2026, with employment types broken down into 100% Contract. Highlights an 100% Remote job distribution, with an average salary of $122,744 per year, or $59 per hour.
Manager, Quality Computerized System Validation (CSV)

Manager, Quality Computerized System Validation (CSV)

Nuvalent, Inc.

Cambridge, MA • Remote

Other

Posted 22 days ago

Job description

The Role:

Reporting to the Director, Quality Systems, the Manager, Quality Computerized System Validation (CSV) is responsible for maintaining the validation lifecycle of GxP-regulated computerized systems across the organization in a remote pharmaceutical operating model. The ideal candidate is a strategic thinker with strong hands-on validation experience, excellent cross-functional communication skills, and understanding of compliance in a cloud-based and SaaS environment.

Responsibilities:

  • Partner with IT, Quality, Regulatory, Clinical, TechOps, Pharmacovigilance, and vendors to support GxP system implementations, enhancements, and upgrades.
  • Develop, maintain, and continuously improve CSV policies, SOPs, and forms aligned with regulatory expectations and industry best practices.
  • Ensure application of risk-based validation approaches and data integrity principles (ALCOA++).
  • Act as CSV subject during internal audits, vendor audits, and regulatory inspections.
  • Review and approve GxP system validation deliverables, change controls, deviation investigations, and periodic reviews.
  • Assess inspection trends and proactively update validation practices accordingly.
  • Evaluate vendor documentation for GxP system validation and SDLC for suitability and leverage where appropriate.

 Competencies:

  • Risk-based decision making
  • Strategic thinking with practical execution
  • Strong written and verbal communication
  • Attention to detail with business mindset

 Qualifications:

  • Bachelor's degree or related experience
  • 3-5 years' experience in GxP computerized system validation within the pharmaceutical, biotech, or medical device industry.
  • Veeva QualityDocs experience required.
  • Deep knowledge of CSV, SDLC, Part 11, Annex 11, ICH E6(R3) Data Governance, and data integrity principles.
  • Experience validating cloud-based and SaaS systems.
  • Strong understanding of change management and system lifecycle management.
  • Ability to work Eastern Time Zone and across time zones as needed 

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