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Validation Engineer Jobs in Bridgeport, CT (NOW HIRING)

Deloitte

System Test and Validation Lead

Stamford, 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

Stamford, 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

Stamford, 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 ...

Herzog

Locomotive Engineers

New Haven, CT · On-site

$51.01/hr

Must maintain a valid Engineer Certification under 49 CFR Part 240. * Three years of safe, increasingly responsible railroad experience as a certified locomotive engineer; passenger rail operations ...

Herzog

Locomotive Engineers

New Haven, CT · On-site

$51.01/hr

Must maintain a valid Engineer Certification under 49 CFR Part 240. * Three years of safe, increasingly responsible railroad experience as a certified locomotive engineer; passenger rail operations ...

Maxxima

Electrical Engineer

Hauppauge, NY · On-site

$65K - $75K/yr

Hands-on electrical engineering role focused on hardware, testing, and product validation * Exposure to full product development lifecycle in LED lighting and automotive electrical systems

Maxxima

Electrical Engineer

Hauppauge, NY

$65K - $75K/yr

Hands-on electrical engineering role focused on hardware, testing, and product validation * Exposure to full product development lifecycle in LED lighting and automotive electrical systems

Hia Li

Electrical Engineer

Hauppauge, NY · On-site

$85 - $120/hr

Hands-on electrical engineering role focused on hardware, testing, and product validation * Exposure to full product development lifecycle in LED lighting and automotive electrical systems

Maxxima

Electrical Engineer

Hauppauge, NY · On-site

$65K - $75K/yr

Hands-on electrical engineering role focused on hardware, testing, and product validation * Exposure to full product development lifecycle in LED lighting and automotive electrical systems

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Validation Engineer information

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How much do validation engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for validation engineer in Bridgeport, CT is $52.87, according to ZipRecruiter salary data. Most workers in this role earn between $40.10 and $64.28 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Bridgeport, CT as of August 2026, with employment types broken down into 90% Full Time, 7% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $109,966 per year, or $52.9 per hour.

Validation Engineer

North Haven, CT • On-site

Katalyst Healthcares & Life Sciences
Scientific Research and Development Services • 51 - 200 employees
Learn more about Katalyst Healthcares & Life Sciencesexternal

Contractor

Re-posted 10 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • As a Validation Engineer within the Mold & Capital Tooling Organization, you'll play a pivotal role on a global enterprise team, collaborating with various sites around the world. In this role, you'll facilitate or perform critical validation & qualification activities, ensuring the seamless release of high-quality injection molded components that drive our mission forward.
  • Ensure proper qualification and validation of suppliers and their processes, ensuring supplier meets the requirements for producing high-quality, reliable products.
  • Developing and executing validation plans, conducting audits, and managing the overall PPAP process to ensure compliance with ISO 13485/ Medical standards.
  • Write, review and approve validation change controls and validation protocols IQ OQ PQ PV standard operating procedures, standard calibration methods, standard test methods, specifications CAPAs and exception reports.
  • Strong documentation skills - Accurately recording and managing validation processes in compliance with internal SOPs and external regulations.
  • Review test results and measurements to identify discrepancies.
    SPC (Statistical Process Control).
  • Knowledge on ISO 13485, FDA GMP, ISO 14971, FDA CFR 820.
  • Clean Room experience and medical prod mfg exp (added advantage).
  • Communicates with stakeholders, obtains stakeholder engagement to ensure the end products or processes will solve the business problems.

Requirements:

  • Bachelor's degree with a minimum of 5-7 years of experience in a regulated environment, OR an advanced degree with a minimum of 3 years of experience.
  • Minimum of 5 years of professional experience in a relevant field.
  • Experience with Agile PLM and SAP or BPCS ERP systems.
  • Experience with CAD model with use of Solid works or AutoCAD.
  • Experience with NPI and design transfers deliverables for injection moulded components.
  • Experience within highly regulated industry.
  • Hands on experience within production and enterprise environment.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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