ZipRecruiter

Log In

1

Senior Computer System Validation Csv Jobs in Connecticut

W3Global Inc.

Senior Electrical Engineer

Windsor, CT · On-site

$100K - $150K/yr

Our client is seeking a Senior Electrical Engineer to drive the design and development of advanced ... Ensure adherence to NEC and applicable safety standards * Assist with system validation ...

Nihon Kohden

Validation Engineer

Guilford, CT · Hybrid

Develops and executes validation protocols based on system requirements and approved procedures and ... computer science) and 2+ years of relevant experience. * Previous experience in supporting ...

Defibtech, LLC

Validation Engineer

Guilford, CT · Hybrid

Develops and executes validation protocols based on system requirements and approved procedures and ... computer science) and 2+ years of relevant experience. * Previous experience in supporting ...

Nihon Kohden America

Validation Engineer

Guilford, CT · On-site

Develops and executes validation protocols based on system requirements and approved procedures and ... computer science) and 2+ years of relevant experience. * Previous experience in supporting ...

Nihon Kohden USA

Validation Engineer

Guilford, CT · Hybrid

Develops and executes validation protocols based on system requirements and approved procedures and ... computer science) and 2+ years of relevant experience. * Previous experience in supporting ...

Nihon Kohden

Validation Engineer

Guilford, CT · On-site

$65 - $90/hr

Develops and executes validation protocols based on system requirements and approved procedures and ... computer science) and 2+ years of relevant experience. * Previous experience in supporting ...

Cooper Companies

Senior Data Analyst

Trumbull, CT

$84K - $106K/yr

Proficiency in analyzing operational workflows and systems to support data analytics to make ... Analyze and convert datasets (CSV, JSON, XML, Excel) into Lua tables or scripts * Validate and test ...

CooperCompanies

Senior Data Analyst

Trumbull, CT · On-site

$84K - $106K/yr

Analyze and convert datasets (CSV, JSON, XML, Excel) into Lua tables or scripts * Validate and test ... Proficiency in analyzing operational workflows and systems to support data analytics to make ...

NYTP

Windchill Senior System Consultant

Stamford, CT · On-site +1

$60 - $68/hr

Windchill Senior System Consultant Location: *Now open to fully Remote* - Hybrid in Stamford, CT ... Experience in CAD worker setup for Windchill environments, including Creo, Office Worker, etc.

previous pagenext page

Showing results 21-40

All JobsComputer System Validation Csv JobsSenior Computer System Validation Csv JobsSenior Computer System Validation Csv Jobs in Connecticut

Senior Computer System Validation Csv information

What is a senior computer system validation (CSV) specialist?

A Senior Computer System Validation (CSV) specialist is an experienced professional responsible for ensuring that computer systems used in regulated industries—such as pharmaceuticals, biotechnology, or medical devices—meet compliance standards. This involves planning, executing, and documenting validation activities to demonstrate that systems consistently perform according to predefined specifications and regulatory requirements. Senior CSV specialists often lead validation projects, manage teams, and interact with regulatory auditors, making sure that systems are reliable, secure, and compliant with guidelines like FDA 21 CFR Part 11 and GxP. Their expertise helps organizations avoid compliance issues, data integrity problems, and costly system failures.

What are the key skills and qualifications needed to thrive as a senior computer system validation (CSV) professional?

To excel as a Senior Computer System Validation (CSV) professional, you need deep knowledge of regulatory compliance (such as FDA 21 CFR Part 11), validation lifecycle methodologies, and a background in computer science, engineering, or life sciences. Familiarity with validation management tools, risk assessment software, and quality management systems (QMS) is typically required, along with certifications like GAMP or Six Sigma being highly valued. Outstanding analytical skills, attention to detail, and strong communication abilities set high performers apart in this role. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support quality operations in regulated industries.

What are some common challenges senior computer system validation (CSV) professionals face when working on large-scale projects?

Senior CSV professionals often encounter challenges such as coordinating validation activities across multiple departments, managing evolving regulatory requirements, and ensuring thorough documentation throughout the project lifecycle. They also need to balance project timelines with the need for comprehensive testing and risk assessments. Effective communication and collaboration with IT, QA, and business stakeholders are essential to address issues proactively and ensure compliance in complex, regulated environments.

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

AspectSenior Computer System Validation CsvComputer System Validation Specialist
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentRegulated industries like pharma, biotech, medical devicesRegulated industries like pharma, biotech, medical devices
ResponsibilitiesLeading validation projects, ensuring compliance, mentoringExecuting validation activities, documentation, testing

While both roles require similar certifications and work in regulated environments, the Senior Computer System Validation Csv typically involves leading projects and overseeing compliance efforts, whereas the Computer System Validation Specialist focuses on executing validation tasks and documentation. The senior role often requires more experience and leadership responsibilities.

What are the most commonly searched types of Computer System Validation Csv jobs in Connecticut?

The most popular types of Computer System Validation Csv jobs in Connecticut are:

What are popular job titles related to Senior Computer System Validation Csv jobs in Connecticut?

For Senior Computer System Validation Csv jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Senior Computer System Validation Csv jobs in Connecticut look for?

The top searched job categories for Senior Computer System Validation Csv jobs in Connecticut are:

What cities in Connecticut are hiring for Senior Computer System Validation Csv jobs?

Cities in Connecticut with the most Senior Computer System Validation Csv job openings:

Senior Computer System Validation Csv jobs near you
Infographic showing various Senior Computer System Validation Csv job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Quality System Manager - Remote

The Jackson Laboratory

Farmington, CT • Remote

$85.99 - $130K/hr

Full-time

Re-posted 5 days ago

Key responsibilities

  • Develop and implement strategies to enhance process efficiency, risk mitigation, and quality improvements across all locations.

  • Oversee key quality functions including audits, deviation reviews, CAPA facilitation, document control, and change management.

  • Lead and train the Quality team in industry best practices and promote a quality culture across the organization.

The Jackson Laboratory rating

8.6

Company rating: 8.6 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

22nd of 121 rated laboratories

Job description

This position will direct efforts to harmonize practices across all JAX locations, both domestic and international where applicable, drive organizational change and implement quality improvements. This position will develop and execute JAX-wide strategies to enhance process efficiency, improve risk mitigation, and oversee key quality functions, including internal and external audits, deviation reviews, CAPA facilitation, document control, and change management. Position will be responsible for training and leading the Quality team in industry best practices, and will be responsible for reshaping quality culture across the global organization.

The salary range is $85.987 - $130,000. Salary will be determined based on qualifications and experience.

This role is remote with occasional travel to JAX locations. The ideal candidates will be located on the east coast.

Key Responsibilities (What you contribute):

  • Develop a long-term process development and improvement strategy, focused on assuring quality, and in collaboration with others in the global organization
  • Proactively identify, analyze and leverage quality data to identify trends and risks, manage risk-based assessments and support the implementation of risk mitigation strategies
  • Develop and implement continuous quality improvements in systems to reduce complexity, improve effectiveness, efficiencies and productivity and ensure sustainability and globalization
  • Develop and ensure a high-quality process development and improvement policy is propagated, understood, and implemented organization-wide; provide strategic leadership in a policy setting
  • Determine and implement the quality assurance/quality system subset strategy for global team
  • Co-lead the implementation of quality and regulatory compliance software systems
  • Direct quality personnel by coaching, counseling, and leading employees
  • Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies
  • Other duties as assigned

Minimum Qualifications:

  • Bachelor's degree and 7 years of relevant quality experience
  • Minimum of 2 years supervisory experience.
  • Expertise in risk management tools including Design FMEA, Process FMEA (pFMEA).
  • Proficiency in Root Cause Analysis (RCA), statistical analysis and data-driven decision-making.
  • Experience with MSA/Gauge R&R, quality metrics and performance monitoring.
  • Experience with and knowledge of ISO 9,001 standards.
  • Computer System Validation requirements.
  • Strong knowledge of Quality by Design (QbD) principles and stage-gate product development.
  • Lean/Six Sigma Certification preferred. Quality certifications (CQA, CQM/OE, etc.) a plus.
  • Functional management/leadership experience in a pharmaceutical or biotechnology operation.
  • Research regulatory compliance experience preferred.
  • Grows relationships with key organizational influencers and customers by building credibility and trust.
  • Experience with change management in multi-site, complex environment.
  • Advanced interpersonal skills sufficient for developing complex, dynamic relationships with a diverse variety of individuals representing a broad cross-section of cultures, disciplines, and levels of sophistication.
  • Advanced verbal and written skills sufficient to communicate with the senior leaders in a variety of partner institutions.
  • Ability to formulate, analyze and evaluate complex plans and programs.
  • Ability to keep current on industry practices, regulatory requirements and industry changes.
  • Champion of Lean and continuous improvement .
  • Ability to travel, 10%.

#CA-DS5

About JAX:

The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California),Japan andChina. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health.

Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visitwww.jax.org.

EEO Statement:

The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

What The Jackson Laboratory employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply