Computerized System Validation jobs

CSV Consultant(Computer System Validation ? GenAI, Agentic , SAP

Raritan, New Jersey

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Today

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Contract

USD45.0/HOURLY - USD52.0/HOURLY

Senior Desktop Support

Saint Joseph, Missouri

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4d ago

We are looking for Senior Desktop Support -for our client in St Joseph, MO Job Title: Senior Desktop Support Job Location: St Joseph, MO Job Type: Contract Job Overview: Pay Range: $25.22hr - $30.22hr Requirement/Must Have: Experience with GxP computerized systems.Experience with SQL.Well-organized; ability to prioritize assigned tasks.Experience working within a team environment.Experience with customer service.IT or Business Degree (Associate or Bachelors).Preferred: Experience with global sys

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Contract, Third Party

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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Contract, Third Party

Depends on Experience

Computer System validation Engineer

Wilmington, Delaware

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Today

Hi, Title:Computer System validation Engineer Compute System Validation(CSV) with R&D Knowledge Qualification: Bachelor of Science OR Bachelor of Technology OR Bachelor's in Pharmacy Experience: Over 8+ years of overall experience with at least 5 years of experience in Computer System validation for GxP system Knowledge, Experience and Skills: { CORE CSV 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic r

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Full-time, Part-time, Third Party, Contract

Data Engineer

Toronto, Ontario

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4d ago

We are looking for Data Engineer for our client in Toronto, ON Job Title: Data Engineer Job Location: Toronto, ON Job Type: Contract Job Overview: Requirement/Must Have: 6 8+ years of experience in supporting and managing data pipelines in production (L1/L2 support).Experience in Data Collection flows using CDC tools (e.g., Debezium) and file-based ingestion (CSV).Hands-on experience with Google Cloud Platform services including Pub/Sub, Dataflow (Apache Beam), and Datastream.Experience working

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Contract, Third Party

Depends on Experience

DeltaV Batch Engineer

Muskegon, Michigan

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2d ago

ole:DeltaV Batch Engineer Location:Muskegon, MI Employment Type:Contract W2 Job Description: Role requires a senior level automation engineer comfortable operating independently while supporting others.No CSV authorship responsibility: CSV activities are supported indirectly through automation execution and issue resolution.DeltaV DCS automation experience in pharmaceutical / biopharma manufacturing (DeltaV Batch experience is a must, not Continuous DeltaV)Strong troubleshooting and problem sol

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Contract

Depends on Experience

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

SAP PP Consultant

Remote or Hybrid in Fort Worth, Texas

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12d ago

SAP PP Consultant Location: Dallas-Fort Worth, TX (Hybrid) Role/Responsibilities: Strong hands-on experience with SAP PP (Production Planning). Working knowledge of SAP MM and WM to support cross-functional processes. Supporting the Operational Qualification (OQ) phase of a regulated SAP programme, including Computer System Validation (CSV) activities. Assisting with complex testing scenarios and execution of OQ scripts. Supporting the transition into dry-run scenarios ahead of a planned m

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Contract

Depends on Experience

Computer System Validation Engineer

Phoenix, Arizona

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Today

Job Description: In this role, you will collaborate with cross-functional teams to ensure systems meet quality standards and regulatory requirements through a risk-based approach. This position focuses on maintaining data integrity and system lifecycle management while contributing to operational efficiency. Responsibilities: pply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures, and training. Ensure system validation aligns with Data

Full-time

Computer System Validation Engineer

Princeton, New Jersey

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Today

Full-time

Computer System Validation Engineer

Wilmington, Delaware

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Today

Roles & Responsibilities : 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic reviews, access roster and audit trail reviews, Deviation/CAPA management, SOP/policy compliance processes uthoring of URS/FS, protocols, final reports, validation plan/report High-level understanding of Veeva Vault suits Risk-based testing aligned to CSA fundamentals High-level understanding of Biostatistics, Clinical, Discovery, Med

Full-time

Computer System Validation Engineer

Bothell, Washington

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Today

Job Summary: We are seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will work cross-functionally to lead and execute validation activities for GxP electronic systems and applications. The CSV Engineer will partner with Business Owners, Technical Owners, and Quality teams to create and manage validation deliverables throughout the validation lifecycle. The primary responsibility is to ensure that validation activities supporting Manufacturing Exec

Full-time

Computer System Validation Engineer

Raleigh, North Carolina

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Today

Job Description: We are seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will work cross-functionally to lead and execute validation activities for GxP electronic systems and applications. The CSV Engineer will partner with Business Owners, Technical Owners, and Quality teams to create and manage validation deliverables throughout the validation lifecycle. The primary responsibility is to ensure that validation activities supporting Manufacturing

Full-time

CSV Engineer

Boston, Massachusetts

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Today

Job Description: Seeking experienced CSV Engineers to provide onsite validation support within a regulated biopharmaceutical manufacturing environment. The primary focus of the position will be Computer System Validation, while also supporting equipment qualification and broader CQV activities as project priorities require. Consultants will support validation documentation and execution activities, assess computerized systems against GMP requirements, execute approved validation protocols, do

Full-time

Software Developer (Full Stack Developer)

Chantilly, Virginia

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Today

Analyzing client/business requirements and designing appropriate cloud-based systems and architectures // Developing, testing, and debugging cloud-native applications using programming languages like Python, Java, REACT, JNode and JavaScript // Developing, testing, and debugging cloud serverless functions // Developing, testing, and debugging web-based UI pages to ingest data and generate JSON, CSV, and TXT files

Full-time

Senior Validation Engineer

Fishers, Indiana

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Today

Description INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter expertise and practical experience in qualification and va

Full-time

Automation SME

Gaithersburg, Maryland

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19d ago

Catalyx is seeking an Automation Subject Matter Expert (SME) provides technical leadership for the design, implementation, validation, and lifecycle support of automation systems supporting biologics manufacturing operations. This role ensures automation solutions are reliable, compliant, secure, and aligned with industry standards while supporting upstream and downstream process performance. The SME works closely with engineering, manufacturing, quality, validation, and system integration teams

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Contract

140,000 - 170,000

System Engineer 5

Annapolis, Maryland

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Today

Required Skills: Ability to form good relationships with customers and mission partners Reach out to external customers for requirements and understanding of the data and the data needs of the users Ability to critically think through complex data flow problems, break down effort into manageable tasks, and create/maintain scope out of sometimes vague customer requirements. Good working skills with Atlassian products such as Confluence and Jira Good understanding of data processing capabilities U

Full-time

Fire Alarm System Programmer

Rocky Hill, Connecticut

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Today

Johnson Controls, a global leader in thermal management, mission-critical building systems, energy efficiency, and decarbonization, helps customers use energy more productively, reduce carbon emissions, and operate with the precision and resilience required in rapidly expanding industries such as data centers, healthcare, pharmaceuticals, advanced manufacturing, and higher education. For more than 140 years, Johnson Controls has delivered performance where it really matters. Backed by advanced

Full-time

Validation Engineer

Portsmouth, New Hampshire

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Today

Job Description: The CSV Specialist Level 4 provides team leadership and training to assess new and changing computer systems to ensure compliance with company policies, procedures and industry guidance. The CSV Specialist Level 4 will risk assess systems, review change requests and test scripts, draft protocols and initiate and review GMP documentation revisions. Specialist will be involved as the QA CSV representative during small and large-scale projects. Responsibilities: Perform all aspect

Full-time