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Director Computer System Validation Csv Jobs in Bloomfield, CT

Deloitte

System Test and Validation Lead

Hartford, CT · 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

Hartford, CT · 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

Hartford, CT · 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 ...

Cadence Inc

Validation Engineer II

Suffield, CT · On-site

$83K - $105K/yr

Monitor system performance and lead requalification activities. * Qualify suppliers and vendors ... Requires clear communication, computer use, and occasional physical movement around facility.

SCA Pharma

Validation Engineer

Windsor, CT

Represent validation in teams assembled to procure, install, troubleshoot systems, equipment, and ... Bachelor's degree in life sciences, engineering, or related discipline. * 5+ years of direct ...

Socket.dev

Validation Engineer

Windsor, CT · On-site

$95 - $140/hr

Represent validation in teams assembled to procure, install, troubleshoot systems, equipment, and ... Bachelor's degree in life sciences, engineering, or related discipline. * 5+ years of direct ...

SCA Pharma

Validation Engineer

Windsor, CT · On-site

Represent validation in teams assembled to procure, install, troubleshoot systems, equipment, and ... Bachelor's degree in life sciences, engineering, or related discipline. * 5+ years of direct ...

AVS Bio

AVS Bio Senior QA Scientist

Storrs, CT · On-site

$46/hr

... and executing validation protocols (process, method, equipment, CSV/computer systems ... Direct hire with long-term career stability * 401(k) with company match * Up to 3 weeks paid ...

AVS Bio

AVS Bio Senior QA Scientist

Storrs, CT · On-site

$76.50 - $93.50/hr

Proven experience designing and executing validation protocols (process, method, equipment, CSV/computer systems). * Demonstrated experience leading or supporting regulatory inspections (FDA, EMA ...

HallKeen Management

Executive Director

Chicopee, MA · On-site

$125K/yr

... knowledge of computer systems, particularly Microsoft Excel and Word. • Licensed as an ... Valid driver's license. Physical Demands: • Physically able to move at least 20 lbs. without ...

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

As of Aug 22, 2026, the average hourly pay for director computer system validation csv in Bloomfield, CT is $51.77, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $64.38 per hour, depending on experience, location, and employer.

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Infographic showing various Director Computer System Validation Csv job openings in Bloomfield, CT as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $107,674 per year, or $51.8 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Springfield, MA • On-site

Contractor

Re-posted 28 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Validation Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Validation Engineer
Location: Massachusetts
Duration: Long Term

Position Overview

We are seeking an experienced Validation Engineer to support qualification and validation activities within a pharmaceutical manufacturing environment. This role will focus on equipment qualification, process validation, cleaning validation, computerized system validation, documentation review, and compliance with FDA and cGMP requirements. The ideal candidate will work closely with Manufacturing, Engineering, Quality Assurance, and Regulatory teams to ensure validated systems remain compliant and inspection-ready.

Key Responsibilities

• Develop, execute, and review validation protocols and reports, including IQ, OQ, PQ, and requalification activities.
• Support equipment, utility, facility, process, and cleaning validation programs.
• Prepare and maintain validation documentation in accordance with cGMP and regulatory requirements.
• Coordinate validation activities with Manufacturing, Engineering, Quality Assurance, and project teams.
• Perform risk assessments and gap analyses to identify validation and compliance requirements.
• Investigate validation deviations, implement corrective actions, and support CAPA activities.
• Ensure validation lifecycle activities comply with FDA regulations, 21 CFR Part 210/211, and industry standards.
• Support commissioning and qualification activities for new equipment, facilities, and manufacturing processes.
• Participate in audits, inspections, and validation-related regulatory submissions.
• Contribute to continuous improvement initiatives to enhance validation processes and compliance.

Required Qualifications

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Chemistry, Life Sciences, or a related technical discipline.
• 3–7+ years of Validation Engineering experience within pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Strong experience with equipment qualification (IQ/OQ/PQ), process validation, and validation lifecycle management.
• Knowledge of cGMP regulations, FDA requirements, data integrity principles, and validation industry standards.
• Experience supporting cleaning validation, computerized system validation (CSV), or utility validation is preferred.
• Familiarity with risk assessments, deviation investigations, CAPA, and change control processes.
• Strong technical writing, documentation, analytical, and problem-solving skills.
• Ability to manage multiple validation projects and work effectively in a cross-functional environment.
• Experience supporting regulatory inspections and audit readiness activities is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/