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Senior Hardware Engineer

General Motors

Warren, Michigan, USA

Full-time

Job Description Job Description: Sr. Hardware Engineer: Connectivity Modules Hybrid: This role is categorized as hybrid. This means the successful candidate is expected to report to one of the following locations: Warren, MI three times (Tues., Wed., Thurs.) per week, at minimum. The Ideal Candidate: Connectivity plays a pivotal role in using and advancing technology to offer unparalleled customer experience and develop revenue generating streams while acting as a cornerstone to offer safety cr

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Colorado, USA

Full-time

Job Description: Process Validation Engineer with 5+ years of engineering experience. This role includes an in-depth training program, where the consultant will be paired with a team member to review training materials and receive hands-on floor training related to process validation and supplier quality activities. The engineer will work cross-functionally to assess manufacturing and supplier quality processes, identify improvement opportunities, and implement effective solutions. Strong c

Silicon Validation Engineer

Apple, Inc.

No location provided

Full-time

Imagine what you can do here. Apple is a place where extraordinary people gather to do their lives best work. Together we create products and experiences people once couldn't have imagined, and now, can't imagine living without. It's the diversity of those people and their ideas that inspires the innovation that runs through everything we do. Description APPLE INC has the following available in Cupertino, California and various unanticipated locations throughout the USA. Design application-speci

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

Facilities & Validation Engineer

BEPC Inc. - Business Excellence Professional Consulting

San Angelo, Texas, USA

Full-time

Job DescriptionJob Description: Facilities & Validation Engineer W2 6 month contract with potential for extension Pay rate $40-$45/hr Job Summary: The Facilities Engineer is responsible for overseeing the design, planning, and execution of building improvement projects. This role involves managing budgets, coordinating with contractors, ensuring compliance with safety regulations, and maintaining project schedules. Overall Responsibilities: Project Management: Plan, coordinate, and oversee const

C# .Net & Java Developer

APN Software Services, Inc

Lansing, Michigan, USA

Contract

Location: 608 West Allegan Street, Lansing, MI, 48933 Duration: 12+ months Hybrid: Will need to be onsite two days a week from start Top Skills & Years of Experience: 8+ years of Development Environment Support8+ years of .Net 4.8 with C#4+ years of JAVA8-11 + years of experience in the field or in a related area.Relies on experience, judgment and accomplish goals, independently performs a variety of complicated tasks, may lead, a wide degree of creativity and latitude is expected.Programmer An

Validation Engineer

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is looking for a Pharmaceutical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Los Angeles County area. Responsibilities for the Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Proficiency with cleaning validation as this is a multi-product production space Must be familiar and have experience with laboratory and manufacturing instrument selection, installation (IQ/OQ) and qua

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Colorado Springs, Colorado, USA

Full-time

Responsibilities: Lead and manage the Process Validation and Verification qualification at the plastic suppliers and other commodities across IGTD portfolio. Looking to hire somebody with Manufacturing Engineering and Design expertise to review the Specification of Product and Part requirement with R&D and design assurance against of part/product risk management file. Hands on driving and performing IQ, OQ, PQ and TMV at the suppliers. Strong Communicator to manage stakeholders and provide b

Validation Engineer

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities for the Validation Engineer Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.Coordinate validation efforts across shifts, pr

Quality/Validation Engineer

TEKsystems c/o Allegis Group

Scarborough, Maine, USA

Full-time

Description We are seeking a highly motivated and detail-oriented Validation/Quality Engineer to support our manufacturing operations. This role is critical in ensuring compliance with FDA regulations (21 CFR Part 820) and ISO 13485 standards. The ideal candidate will lead validation activities, maintain robust quality systems, and drive continuous improvement initiatives across manufacturing processes. Key Responsibilities: Validation & Qualification: Develop and execute validation protocols (I

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

Validation Engineer

Katalyst Healthcares and Lifesciences

Philadelphia, Pennsylvania, USA

Full-time

Job Summary The Validation Engineer is responsible for executing equipment and system validation activities within a regulated biopharmaceutical environment. This role involves implementing validation protocols, documenting results, and ensuring compliance with regulatory requirements. The position is based in West Philadelphia, Pennsylvania with a hybrid work arrangement. Responsibilities: Proficiency in Kaye AVS validation software. Experience with Valpro validation management systems. Compet

Sr. Process Validation Engineer

Katalyst Healthcares and Lifesciences

Grand Rapids, Michigan, USA

Full-time

Roles & Responsibilities: Minimum 7 years of CQV experience in a parenteral fill/finish environment. Lead process validation projects of broad scope. Responsible for project deliverables such as VMPs, pFMEAs, PPQ protocols and reports, change control assessments, technical transfer assessments, as well as other client deliverables as required. Provide technical support to Manufacturing - troubleshooting and resolving process related issues. Participate in investigations and provide documentation

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

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

Senior Platform Validation Engineer

BOTG LLC

Austin, Texas, USA

Contract

Job Description: Position: Senior Platform Validation Engineer Location: Austin, TX (Hybrid) Duration: 6+ months contract position Description: We need a Senior Platform Validation Engineer to work in the Infrastructure Line of Business with stakeholders from different groups including but limited to Solution Engineering, Central Engineering, Infrastructure LOB partners and support the growing demand for Neoverse CSS in the Cloud and Datacenter. You will be an individual contributor engaging and

Sr Process Validation Engineer

Katalyst Healthcares and Lifesciences

Grand Rapids, Michigan, USA

Full-time

Roles & Responsibilities: Lead process validation projects of broad scope. Collaborate with clients, Validation, and cross-functional team members to coordinate projects, resolve issues, and meet aggressive timelines. Represent Validation in customer interactions and communicate customer requirements to the broader Validation team as needed. Oversee execution of process validation (PPQ) protocols on the production floor on varying shifts as needed to ensure that protocol requirements are satisfi

Validation Engineer

Apex Systems

Lebanon, Indiana, USA

Full-time

Job#: 2078205 Job Description: Role: Equipment Validation Engineer Location: Indianapolis, IN (On-Site) Type: Long Term Contract Apex Systems, a global leader in Technology Services, is searching for an Equipment Validation Engineer in Indianapolis, IN for a large Life Sciences client. This is a long term contract with an immediate start date. This role requires on site support 5 days a week due to the nature of the role. See below for more details! Duties and Responsibilities: Supports the

Cyber Threat Hunting Program Lead

Tradeweb Markets LLC

Remote or Jersey City, New Jersey, USA

Full-time

Company Description: Tradeweb Markets is a world leader in the evolution of electronic trading. A fintech company serving approximately 2,500 clients ? including the world?s largest banks, asset managers, hedge funds, insurance companies, wealth managers and retail clients -- in more than 65 countries across the globe. Since our first trade in 1998, we have helped transform and electronify the fixed income markets. Tradeweb is a culture built on innovation, creativity and collaboration. Through

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Danvers, Massachusetts, USA

Full-time

Roles & Responsibilities: Process Validation (IQ/OQ/PQ). Product development experience. Process development. Process Layout, Modeling, and Documentation. Equipment and Tooling Development. Process Development and Characterization. Test Method Development and Validation. Developing / Updating MPIs. Supplier Development and Component Engineering. Manufacturing Engineering Support / Engineering Documentation. Update work instructions to match the practice on the floor to what's in the p