Junior validation lead jobs

Hybrid in Raritan, New Jersey

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2d ago

Role CSV Validation Lead Location -Raritan, NJ(Hybrid) Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation activities and 21 CFR remediation projects with knowledge of CSA, GAMP 5, 21 CFR Part 11, Annex 11, and audit/inspection readiness. Experience in the Pharmaceutical, biotechnology, or medical device industry. Experience in FDA and/or Global regulated environment with good understanding of GxP standa

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Contract

Depends on Experience

CSV Validation Lead

Hybrid in Raritan, New Jersey

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3d ago

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Contract

Depends on Experience

Validation Lead

Raritan, New Jersey

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4d ago

We are looking for Validation Lead - Hybrid for our client in Raritan, NJ. Job Title: Validation Lead Job Location: Raritan, NJ Job Type: Contract Job Overview: Pay Range: $50.00hr - $55.00hr Requirement/Must Have: 7-10 years of relevant experience in Infrastructure Qualifications and Business Systems Validations.Experience leading or advising junior and senior resources.Specific experience in the pharmaceutical, biotechnology, or medical device industry.Experience in FDA and/or global regulat

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Third Party, Contract

Depends on Experience

Computer System Validation (CSV) Quality Support Lead

Morristown, New Jersey

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Yesterday

A client of Innova Solutions is immediately hiring for a Computer System Validation (CSV) Quality Support Lead. Position type: Full-Time Contract (W2) Role: Computer System Validation (CSV) Quality Support Lead Duration: 4-6 Months Contract Location : Raritan NJ (Hybrid) Must be able to work from 3 days a week Job Description - CSV Lead Lead and execute validation deliverables across the lifecycle: risk assessment, validation planning, requirements traceability, test strategy, test execution

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Contract

Depends on Experience

Junior Validation Engineer with CSV / CQV

Cambridge, Massachusetts

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16d ago

Arthur Lawrence is looking for a Junior Validation Engineer with CSV / CQV one our clients in Cambridge MA. Please find the job description below and send us your updated resume if interested: Must-Have Skills: Experience performing validation and calibration activities for pharmaceutical manufacturing and sterile processing equipment in compliance with GMP and 21 CFR Part 11 requirements. Hands-on experience supporting Master Validation Plans (MVPs), SOPs, validation protocols, and Process Per

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Contract, Third Party

$30 - $39

Validation Lead - Raritan, NJ(Hybrid)

Raritan, New Jersey

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4d ago

We are looking for a Validation Lead to join our team. Please review the job description below, and let us know if you are interested and available. If this opportunity matches your experience and career goals, we would love to discuss it more. Additionally, feel free to share your updated resume for consideration Role - Validation LeadLocation Raritan, NJ(Hybrid) Duration: Long Term Contract Rate: $70/HR on C2C Max Must Have - Computer System Validation experience M&A related Data Migration

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Contract, Third Party

60 - 70

Validation Lead

Hybrid in Raritan, New Jersey

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5d ago

Role: Validation Lead Location: Raritan, NJ(Hybrid) Duration: 6+ Months Must Have - Computer System Validation Experience M&A related Data Migration and related infrastructure qualification in data Platform domain Job Description: Must be able to Independently support Business Separation activities for Large global & regional GxP Computerized systems. with minimal supervision.Recent experience with Acquisitions/Separations/Divestiture from J&J a huge plus.Strong CSV Expertise, especially withi

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Contract

Depends on Experience

Validation Lead

Hybrid in Raritan, New Jersey

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4d ago

Role - Validation Lead Location - Raritan, NJ (Hybrid) W2/C2C Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation activities and 21 CFR remediation projects with knowledge of CSA, GAMP 5, 21 CFR Part 11, Annex 11, and audit/inspection readiness. Experience in the Pharmaceutical, biotechnology, or medical device industry Experience in FDA and/or Global regulated environment with good understanding of GxP

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Contract, Third Party

55 - 60

Lead Computer Systems Validation Engineer I (Clinical & R&D)

Waltham, Massachusetts

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Today

Job Description This position provides leadership and accountability for Digital Quality across the organization's Quality, Regulatory, and R&D systems landscape, with responsibility for supporting computer system validation activities in alignment with applicable regulatory expectations, internal procedures, and data integrity requirements. The role is focused on ensuring GxP computerized systems are implemented, maintained, and governed in a compliant, risk-based, and inspection-ready manner

Full-time

USD 110,000.00 - 126,000.00 per year

NFC System Software Validation Engineer - Entry Level

San Diego, California

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Today

Enable possibilities with NFC: Near Field Communication (NFC) is a fast, intuitive technology that lets you interact securely with the world around you with a simple touch. NFC wireless proximity technology is available in billions of smartphones, tablets, consumer and industrial electronics-with new devices arriving almost daily. NXP Semiconductors Netherlands B.V. is seeking a talented and motivated NFC System Software Validation Engineer in San Diego location to contribute to the design, dev

Full-time

USD 83,800.00 - 115,200.00 per year

Entry Level Validation Engineer

Columbus, Ohio

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Today

Are 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 performance at the highest standard-through our rigorous approach, field-tested processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted solution for our clients

Full-time

USD 60,000.00 - 70,000.00 per year

Pharma IT Testing & Validation Delivery Lead

Boston, Massachusetts

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Today

Job Summary: leading organization is seeking an experienced Pharma IT Testing & Validation Delivery Lead to manage global testing and validation services across multiple Life Sciences programs. Roles & Responsibilities: Own end-to-end testing and validation delivery across multiple pharmaceutical IT projects. Lead onsite and offshore QA teams across the United States, United Kingdom, and India. Define testing strategy, governance, KPIs, delivery standards, and quality metrics. Oversee functional

Full-time

Senior Lead Engineer, Systems/Applications Validation

Austin, Texas

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Today

Req ID: 139551 Region: Americas Country: USA State/Province: Texas City: Austin General Overview Summary The Senior Lead Engineer, Systems/Applications designs, integrates, and manages complex systems over their life cycles. They are engineering leads engaged in issues such as requirements engineering, reliability, logistics, coordination of different teams, testing and evaluation, maintainability and many other disciplines necessary for successful system design, development, implementation

Full-time

Senior Lead Engineer, Systems/Applications Validation

Austin, Texas

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Today

Req ID: 139550 Region: Americas Country: USA State/Province: Texas City: Austin General Overview Summary The Senior Lead Engineer, Systems/Applications designs, integrates, and manages complex systems over their life cycles. They are engineering leads engaged in issues such as requirements engineering, reliability, logistics, coordination of different teams, testing and evaluation, maintainability and many other disciplines necessary for successful system design, development, implementation

Full-time

Artificial Intelligence / Machine Learning Lead Verification and Validation Engineer

State College, Pennsylvania

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Today

APPLICATION INSTRUCTIONS: CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday.CURRENT PENN STATE STUDENT (not employed previously at the university) and seeking employment with Penn State, please login to Workday to complete the student application process. Please do not apply here, apply internally through Workday.If you are NOT a current empl

Full-time

USD 140,004.00 - 265,704.00 per year

Artificial Intelligence / Machine Learning Lead Verification and Validation Engineer

Reston, Virginia

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Today

Full-time

USD 168,000.00 - 318,840.00 per year

Data Validation Risk - Senior Associate

New York, New York

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Today

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Senior Associate Job Description & Summary The Opportunity As a Data Validation Risk - Senior Associate, you will play a pivotal role in transforming raw data into actionable insights, enabling informed decision-making and driving business growth. Within our Risk & Regulatory practice, you will focus on designing and building data infrastructure and systems to enable efficient data processing and analysis. You w

Full-time

USD 77,000.00 per year

Senior Project Validation Lead

Austin, Texas

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Today

Job Title: Senior Project Validation Lead Location: Austin, TX (Hybrid: Mon/Wed/Thurs onsite - No remote) Hours: 8:00am-5:00pm (some flexibility) Regulatory Requirement: W2 only. Must be able to obtain CFIUS clearance About the Role Our client is seeking a highly experienced IVVQM (Integration, Verification, Validation, and Qualification Manager) / Senior Project Validation Lead to join their Austin-based team. You'll be critical to delivering tailored solutions for state and local governme

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Contract

Lead Validation Engineer

New Jersey

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Today

Job Description: The Lead Validation Engineer leads GMP equipment installation, commissioning, and qualification projects supporting large-molecule biologics manufacturing. This role supports upstream and downstream processes and ensures projects are executed safely, on schedule, and in compliance with regulatory and quality requirements. Responsibilities: Lead end-to-end CQV execution for GMP equipment projects, managing activities from installation through IQ, OQ, and PQ for biologics manufact

Full-time

Senior Test Method Validation (TMV) Subject Matter Expert (SME) / Lead

Delaware City, Delaware

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13d ago

Less of a LEAD and MORE of an SME Hands On Senior Level Subject Matter Expert ONSITE Title: TMV Engineer SME Daily duties of the contractor: TMV Engineer/specialist Key Requirement and experience: Develop and validate test methods for complex electromechanical medical device systems to verify essential clinical and system performance requirements. Demonstrate expertise in converting design and clinical requirements into repeatable, reproducible, and validation-ready test methods, including de

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Contract

$50 - $55