validation engineer Jobs in missouri

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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

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

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

Validation Engineer

Katalyst Healthcares and Lifesciences

St. Louis, Missouri, USA

Full-time

Responsibilities: The Validation Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. Our Engineers are responsible for protocol writing and execution (field verification), and development of summary reports. Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines. Ability to work independently. Support onsite and offsite activities, such as: FATs, SATs, IOQ

Sr. Computer system Validation Engineer

Katalyst Healthcares and Lifesciences

Saint Joseph, Missouri, USA

Full-time

Responsibilities: Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports). Experience in validating GMP Lab systems and Equipment. Responsible for assuring a system/application meets its requirements as outlined in system specification (URS/FRS) per process defined in the Validation Plan for the project. Identify and escalate, as necessary project risks and issues to the CSVC Manager. Enga

Process Validation Engineer

Katalyst Healthcares and Lifesciences

St. Louis, Missouri, USA

Full-time

Responsibilities: Provide technical support and routine process monitoring for commercial products manufactured at CMOs. Provides person-in-plant observations of manufacturing operations at CMOs and communicates observations to the product team. Reviews manufacturing processes, deviations, and/or development and production data. Reviews manufacturing batch records, protocols, and control strategies. Provide technical support and data analysis for investigations and deviation resolution. Recommen

Digital Platform Senior Validation Engineer

Merck KgaA

St. Louis, Missouri, USA

Full-time

Work Location: St. Louis, Missouri Shift: No Department: LS-QR-DV Validation Management Recruiter: Kathy Lewison This information is for internals only. Please do not share outside of the organization. Your Role: In this role, you will be the Digital Platform Senior Validation Engineer. This position is responsible for the guidance and direction of validation projects covering all the Life Science digital products, applications, and computerized systems. Your primary focus will be creating au

Validation Engineer III

Merck KgaA

St. Louis, Missouri, USA

Full-time

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious mind

CSV Engineer (Computer System Validation)

Katalyst Healthcares and Lifesciences

Kansas City, Missouri, USA

Full-time

Responsibilities: Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports) Experience in validating GMP Lab systems and Equipment. Responsible for assuring a system/application meets its requirements as outlined in system specification (URS/FRS) per process defined in the Validation Plan for the project. Identify and escalate, as necessary project risks and issues to the CSVC Manager. Engage

Sr. Systems Engineer

GDH

St. Louis, Missouri, USA

Contract

Job Description: Our client is seeking a highly skilled and experienced Sr. Systems Engineer to join their team. This role involves performing prototype bring-ups, tackling challenging system and board level issues, and running system tests. The successful candidate will work closely with architecture and design teams to ensure that products under development are functional, serviceable, manufacturable, and reliable. This position requires a deep understanding of x86/ARM architecture and acceler

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

Sr. Analyst, IT Validation Services

Hired by Matrix, Inc.

Remote or Stamford, Connecticut, USA

Contract

At-a-Glance:Are you ready to build your career by joining a pharmaceutical company? If so, our client is hiring a Sr. Analyst, IT Validation Services.Position Type: Contact Remote Required: BS/Equivalent Training/Certification and minimum of 5 years of relevant experience in computer systems validation, change management and systems development life cycle methodologies. Expertise in Computer System Validation (CSV), Systems Development Life Cycle (SDLC) methodologies and CSV regulations, stand

Senior IT Validation Analyst - Remote / Telecommute

Cynet Systems

Remote or Bentonville, Arkansas, USA

Contract

Job Description: Responsibilities: Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls: Validation Plans/Summary Reports. Risk Assessments. User Requirements. Specifications. Test Plans. Test Scripts: IQ, OQ, or PQ. Assess and implement the most effective validation stXXgy for each activity. Oversee test execution for cross-functional teams, including training, tracking, and reviews. Build strong relationships with business co

Sr. IT Validation Analyst

Radiant System, Inc

Remote

Contract

REMOTE ROLE Primary Responsibilities Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls:Validation Plans/Summary ReportsRisk AssessmentsUser RequirementsSpecificationsTest PlansTest Scripts: IQ, OQ or PQAssess and implement the most effective validation strategy for each activity.Oversee test execution for cross-functional teams, including training, tracking, and reviews.Build strong relationships with business counterparts t

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Validation Lead, SAP S4 HANA

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Responsibilities: Lead the validation team in a strategic, risk-based approach that optimizes legacy Computer System documentation, CSA strategies and strong SAP ECC->S/4 HANAconversion knowledge to successfully deliver a validated system meeting all project requirements. Review, approval, and processing of Computer System Lifecycle deliverables including: User Requirements, Specifications, Test Plans, IQ, OQ, PQ Test Scripts, User Guides. Fostering of effective relationships with implementati

Sr. Analyst, IT Validation Services

Russell, Tobin & Associates

Remote or Stamford, Connecticut, USA

Contract

Job Title: Sr. Analyst, IT Validation Services Location: Remote Duration: 12 Months Pay Range: $30/hr-$35/hr on W2 (DOE) Primary Responsibilities Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls: Validation Plans/Summary Reports Risk Assessments User Requirements Specifications Test Plans Test Scripts: IQ, OQ or PQ Assess and implement the most effective validation strategy for each activity. Oversee test execution for c

Contract Manufacturing Onsite Team Lead

GDH

St. Louis, Missouri, USA

Contract

Job Description: Our client is seeking a highly skilled and experienced Senior Validation Engineer to lead the testing and validation of semiconductor components, data center hardware, and GPUs. This role is critical in ensuring that all products meet the highest standards of quality, performance, and reliability. The successful candidate will be adept in system-level validation including both rack and tray level systems and will bring a strong background in Python scripting for test automation.