Junior validation lead jobs

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

CSV Validation Lead

Hybrid in Raritan, New Jersey

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3d 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

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

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

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

Delaware City, Delaware

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6d 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

Lead Validation Engineer II

Wilmington, Ohio

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Today

Responsibilities Job Description: Serve as a subject matter expert in and lead equipment, facility, and utility qualification for clinical and commercial pharmaceutical manufacturing and laboratory systems. Serve as technical lead for maintenance of GMP compliance through monitoring, review, assessment and qualification of activities. Ensure Validation systems (policies, procedures, reviews, VMPs) effectively meet current/changing industry demands. Oversee maintenance of validation systems and

Full-time

USD 135,000.00 - 150,000.00 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

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

Junior Validation Engineer with CSV / CQV

Cambridge, Massachusetts

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10d 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

Artificial Intelligence / Machine Learning Lead Verification and Validation Engineer

Reston, Virginia

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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 168,000.00 - 318,840.00 per year

Artificial Intelligence / Machine Learning Lead Verification and Validation Engineer

State College, Pennsylvania

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Today

Full-time

USD 140,004.00 - 265,704.00 per year

Contract role: Pharma Validation Lead at Raritan, NJ (Onsite Hybrid Model)

Hybrid in New Jersey

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Today

Validation Lead Raritan, NJ (Onsite Hybrid Model) Long Term Contract 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 understandin

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Third Party, Contract

Validation Associate-IT

Chicago, Illinois

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Today

Validation Associate-IT This position will have primary responsibility for supporting system owners with the generation and management of IT related documents for instrument qualification and computerized system validation process to ensure compliance with the associated regulations. These activities will focus on IT related functions involved with laboratory Analytical Instruments utilized in the engineering, chemistry, and information technology areas for Baxter R&D. All activities must be pe

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Contract, Third Party

Depends on Experience

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

Junior Analyst

Miramar, Florida

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Today

RESPONSIBILITIES: Kforce has a client seeking a Junior Analyst in Miami, FL (Florida). Duties: * Assist with project and operational coordination activities across multiple teams * Track tasks, action items, and project updates to ensure deadlines are met * Maintain and update records, documentation, and status reports * Perform data entry, data validation, and data clean-up activities to support business operations * Prepare presentations, summaries, and meeting materials as needed * Support s

Contract

$21.25 - $28.75 hourly

Validation Lead

Hybrid in Raritan, New Jersey

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6d 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

Easy Apply

Contract, Third Party

55 - 60

Senior Validation Engineer / Project Lead (Medical Devices)

Salt Lake City, Utah

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Today

Summary: We are seeking a highly skilled R&D/Validation Engineer with mandatory experience in the Medical Devices domain. The ideal candidate will be responsible for planning, leading, and coordinating project execution and validation activities in strict alignment with ISO 13485 and ISO 14971 standards. This role requires a hands-on leader who can manage equipment, process, and product transfers while liaising with global teams and customers to ensure on-time delivery. Roles & Responsibilities

Full-time

Graduate - Validation Engineer

San Jose, California

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Today

#WeAreIn for driving decarbonizationand digitalization. As a global leaderin semiconductor solutions in power systems and IoT, Infineon enablesgame-changing solutions for green and efficient energy, clean and safemobility, as well as smart and secure IoT. Together, we drive innovation andcustomer success, while caring for our people and empowering them to reachambitious goals. Be a part of making life easier, safer and greener. Are you in? Your role Key responsibilities in your new role Vali

Full-time

USD 92,000.00 - 102,000.00 per year