10 validation opportunities in Princeton updated today
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Cqv Consultant This is a full-time on-site role located in Princeton, NJ. The CQV Consultant will be responsible for day-to-day tasks related to system start up, commissioning, qualification, and validation. They will work towards ensuring compliance and quality standards for a biologics manufacturi
Csv Specialist The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders to validate new and existi
Job Title - Sr. Validation Engineer (CSV) Location - Princeton, NJ (Day 1 Onsite) Duration - Long term Job Description: Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. Should
CAIAre You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled per
Katalyst CROSummary The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders to validate new and existing syst
Katalyst CROA specialized pharmaceutical company in New Jersey is seeking a CSV Specialist to handle compliance validation activities for computer systems. You will collaborate with IT and Quality Assurance to ensure compliance with FDA regulations. The ideal candidate has a Bachelor's degree and 2+ years of ex
CAIA professional services company in New Jersey seeks a qualified individual to perform Commissioning, Qualification, and Validation (CQV) activities. The ideal candidate will have a background in Engineering or Life Sciences and 3+ years of experience in a GMP environment. Excellent communication ski
A consulting and technology firm is hiring a Validation Associate Consultant in Princeton, NJ. The role involves managing GxP-compliant validation processes and supporting clients across various projects. Candidates should have a relevant degree and experience in Computer System Validation. The posi
ZSZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you’ll work side-by-side
A data solutions company is seeking a Quality Manager for a contract position in Princeton, NJ. The successful candidate will lead validation of data pipelines and perform BI and Data Warehouse testing to ensure data accuracy. This role requires a Bachelor's degree and 8–10 years of experience in ET
Validation Engineer Location: Miami, FL (Onsite) Job Description & Skill Requirement: Walk through production lines, understand equipment and production processes. Understand the current state information from site leaders and functional managers. Understand current challenges and projects in place
Description Job purpose The Validation Engineer I is responsible to support company’s equipment and process validation activities. This position is responsible for developing and executing validation protocols and reports. The Validation Engineer I is also responsible for evaluating manufacturing pr
Description The Validation Engineering Intern will work with multi-discipline teams within Vivex Biologics, Inc. and assist the Validation Engineering Manager or designee with process and equipment validation activities, test method validation, and supporting quality systems documentation and regula
MooveAbout Moove AV At Moove AV, we are on a mission to make the world safer by enabling autonomy in transportation. Partnering with leading autonomous vehicle technology companies, we are redefining fleet management and accelerating the commercialization of self-driving vehicles. We are expanding global
MooveAbout Moove AV At Moove AV, we are on a mission to make the world safer by enabling autonomy in transportation. Partnering with leading autonomous vehicle technology companies, we are redefining fleet management and accelerating the commercialization of self-driving vehicles. We are expanding global
Description Job purpose The Senior Validation Specialist II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. This role mainly drives the preparation and execution of validation documentation, includin
Description The Quality Engineering Intern will work with multi-disciplinary teams within Vivex Biologics, Inc. and assist Quality Engineers with continuous improvement projects to ensure our products continue to meet all regulatory and internal quality standards. Projects include but are not limite
Description The Quality Assurance Engineer develops, applies, revises, and maintains quality metrics to support areas of operations at Vivex Biologics, Inc. The role assists in the planning, development, implementation, communication, and maintenance of Vivex’s quality management systems, polices, d
About Rivian Rivian is on a mission to keep the world adventurous forever. This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract. As a company, we constantly challenge what's possible, never simply accepting what has always been d
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Princeton. Actual salaries may vary depending on experience, company, and area.
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