Validation Engineer III Jobs in New Jersey

Refine Results
1 - 20 of 33 Jobs

Validation Engineer III

Katalyst Healthcares and Lifesciences

Plainsboro Township, New Jersey, USA

Full-time

Job Description: Qualified candidates must be experienced in one or more of the following areas of validation: Equipment Qualification Process Qualification The candidate must utilize problem solving techniques to resolve issues and conflict in order to meet the high level goals set forth by the organization. The candidate must be well organized and technically sound in understanding scientific rationale and justifying criterion from a quantitative standpoint. The candidate must be familiar with

Engineer III, Validation

Thermo Fisher Scientific

Remote or Fair Lawn, New Jersey, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you're part of Thermo Fisher Scientific, you'll do meaningful work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the

Validation Engineer with Ciena Routing & Switching - Middletown, NJ (Remote is also fine)-Telecom Industry Prefer

GLOBAL IT CON LLC

Remote or Middletown Township, New Jersey, USA

Contract

Job Title: Validation Engineer Job Location: Middletown, NJ (Remote is also fine) Job Duration:12 months Job Description: This position allows you to assist customers in optimally crafting, deploying, operating, and continuously improving cost-effective solutions based on a Service-Aware Operating System (SAOS) based Routing & Switching portfolio (RSP) and its associated network management platform. This is an on-customer premise technical role with a focus on facilitating customers to understan

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles. Compliance Analysis, Validation Planning, Risk Assessments Test planning and strategy creation and execution of test protocols, scripts and reports. V

Sr. CSV Validation Engineer

Katalyst Healthcares and Lifesciences

New Brunswick, New Jersey, USA

Full-time

Responsibilities: Review computerized systems validation documents such as: Requirements Specification, Design Specification, CSV Risk Assessment, Test Plans, Test Summary Reports, Data Migration Plan, Pre/Post Executed Test Scripts, Traceability Matrix. Release to Production Statements Direct and review testing Provide guidance on quality issues that affect the integrity of the data, or the system Obtain and respond to QA review. Participate in establishing standard quality and validation pract

Sr. CSV Validation Engineer

Katalyst Healthcares and Lifesciences

Lawrence Township, New Jersey, USA

Full-time

Roles & Responsibilities: 8-10+ Years of Overall IT Experience Review computerized systems validation documents such as: Requirements Specification, Design Specification, CSV Risk Assessment, Test Plans, Test Summary Reports, Data Migration Plan, Pre/Post Executed Test Scripts, Traceability Matrix. Release to Production Statements Direct and review testing Provide guidance on quality issues that affect the integrity of the data, or the system Obtain and respond to QA review. Participate in

Validation Engineer

Katalyst Healthcares and Lifesciences

Summit, New Jersey, USA

Full-time

Position Overview: The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role, contributes to the completion of milestones associated with equipment qualification and systems validation. With minimum supervision and given general instructions, this individual carries out routine tasks, functions, and uses basi

RTL Validation Engineer

Millennium Global Technologies

Remote

Contract, Third Party

Position: RTL Validation Engineer Location: Dallas, TX ( Remote) Duration: 6 months Visa Preference: GC s, EAD s, L2 EAD s RTL Validation, working knowledge of PCIE/CXL protocols. Familiarity with simulation technologies.Exceptional analytical skills and problem solving skills.Experience in crafting testbenches, methodologies for large and complex chips.Deep understanding of verification concepts.Proficiency with at least one of these - C++, Object Oriented Programming, UVM, System Verilog.Fam

Validation Lead

Abhyanth Solutions

Remote

Contract

Hello, Greetings from Abhyanth Solutions ! Hope you are doing great ! This is Gaurav from Abhyanth Solutions. I have some urgent requirements with one of my clients. Please go through the Job Description and let me know your interest. Below is the job Details. Title: Validation Lead Location: Fully remote contract Duration: Long term contract Job Description Educational Qualification* BE, Comp Science, BCA, BSE computer science Job Description of Role* (RNR) (Mandatory - Minimum 500 words) Pr

Analytical Validation Engineer

Zachary Piper Solutions, LLC

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, NJ area. Responsibilities for the Analytical Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ) Experience supporting laboratory investigations from beginning to end, includ

Validation Engineer

Katalyst Healthcares and Lifesciences

Princeton, New Jersey, USA

Full-time

Roles & Responsibilities: Develop and execute validation protocols for computer systems. Ensure compliance with regulatory requirements and industry standards. Create detailed validation documentation including plans, reports, and scripts. Conduct risk assessments and impact analyses related to computer systems. Coordinate and supervise testing activities. Collaborate with cross-functional teams to maintain and improve system validation processes. Monitor and report on validation project

Process Validation Engineer

Katalyst Healthcares and Lifesciences

East Windsor, New Jersey, USA

Full-time

Responsibilities: Previous experience as a validation engineer in an aseptic pharmaceutical fill/finish environment. Prior experience executing validation protocols on a pharmaceutical fill/finish line. Specific line components include. Lyophilizers. Depyrogenation tunnels. Autocalves. Previous experience with the project management requirements of validation project in a GMP environment. Requirements: Managing validation schedule. Communication of delays and changes to timelines. Coor

Validation Engineer

Katalyst Healthcares and Lifesciences

Allendale, New Jersey, USA

Full-time

Responsibilities: Work under the direction of the Validation Lead and/or function as the validation lead for a project team. The Validation Engineer will be required to support multiple projects simultaneously. Develop and execute IQ, OQ, and PQ protocols for products, processes, facilities, software, and equipment within the facility. Experience authoring Validation Plan documents, User Requirements, Traceability Matrix, and Validation Summary Reports. Write reports summarizing results and s

Validation Engineer

Katalyst Healthcares and Lifesciences

Piscataway, New Jersey, USA

Full-time

Position Overview: Looking for an individual with experience in validations particularly with USP Water, chiller (utilities) and C&S. Responsibilities: Generation of qualification / validation documents, execution of qualification / validation documents, generation of reports, adhering to project timelines, ensure compliance with company and industry standards and participating in cross-functional teams. Required Skills: Experience with drafting and executing IQ / OQ / PQ. CAD proficiency to

Analytical Test Method Validation Engineer

Katalyst Healthcares and Lifesciences

South Plainfield, New Jersey, USA

Full-time

Develop, validate, and implement analytical test methods for combination products in compliance with regulatory standards and internal quality requirements. Collaborate cross-functionally with device engineers, laboratory teams, and quality departments to ensure alignment and successful execution of test method validation (TMV) activities. Provide expert guidance on analytical strategies for device-related products, ensuring robust and reproducible methods are established. Evaluate and optimize

Principal Process Controls & Validation Engineer

Regeneron Pharmaceutical

Remote or Rensselaer, New York, USA

Full-time

Regeneron is currently looking for a Principal/ Staff Process Controls & Validation Engineer for the Labeled Drug Product fill/finish manufacturing processes. This is Monday-Friday, 8am-4:30pm schedule. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering, and mathematical needs from the laboratory to the manufacturing floor. This role provides technical support to manufacturing, quality and CMC Regulatory for manufacturing processes f

CSV Lead Instrument Software Validation

NTT DATA Americas, Inc

Remote or Almont, Colorado, USA

Contract

CSV Lead Instrument Software Validation - 25-05061 100% Remote | CAD or USA 6+ Mths Duration W2/T4 or C2CNTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. NTT DATA's Client is currently seeking a CSV Lead Instrument Software Validation to join their team in Calgary, Ontario (CA-ON), Canada (CA).Job Description: Experience Level: 5-7 Years Job Descri

QA/QC Data Validation Consultant_Remote

Libsys, Inc.

Remote

Contract

Responsibilities Data Validation: Analyze and validate data for accuracy, completeness, and consistency.Quality Assurance: Develop and implement data quality standards and processes.Issue Resolution: Identify and resolve data quality issues, ensuring compliance with regulations.Collaboration: Work with IT and data management teams to design and implement data strategies.Reporting: Generate data reports and presentations for management. Skill Strong experience in data validation and data quality

Remote - Data Validation QA/QC Consultant

White Oak IT Solutions

Remote

Contract

Job Title: QA/QC Data Validation Consultant Location: Remote Duration: (6-12 Months ) Responsibilities Data Validation: Analyze and validate data for accuracy, completeness, and consistency.Quality Assurance: Develop and implement data quality standards and processes.Issue Resolution: Identify and resolve data quality issues, ensuring compliance with regulations.Collaboration: Work with IT and data management teams to design and implement data strategies.Reporting: Generate data reports and pres

QA/QC Data Validation Consultant - (Alteryx, Data Validation) (100% REMOTE)

American IT Systems

Remote

Third Party, Contract

Skills: QA/QC Data Validation Location: Remote Responsibilities Data Validation: Analyze and validate data for accuracy, completeness, and consistency.Quality Assurance: Develop and implement data quality standards and processes.Issue Resolution: Identify and resolve data quality issues, ensuring compliance with regulations.Collaboration: Work with IT and data management teams to design and implement data strategies.Reporting: Generate data reports and presentations for management. Alteryx: Prof