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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

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

Electrical Validation Engineer on W2 Only

Sovereign Technologies

Mossville, Illinois, USA

Contract

Title : Electrical Validation EngineerLocation : Mossville, ILDuration : 6 MonthsRate : $OpenVisa Status : Any work Status On W2 OnlyRelevant Experience: 5+ Years Job Duties/Responsibilities may include, but are not limited to: Work with machine systems teams to establish converter requirements for e-powertrainPerform analysis and evaluation needed to select best supplier option.Collaborate with suppliers and system s teams to develop production components from requirements definition to validat

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

Mechanical Methods and Validation Engineer

System One

Bellevue, Washington, USA

Contract

Job Title: Mechanical Methods and Validation Engineer Type: Contract Compensation: $84 - $90 hourly Contractor Work Model: hybrid (local to Bellevue, WA), or fully remote System One is seeking to contract with a senior or principal level engineer for a hybrid (local to Bellevue, WA), or fully remote role to support development and validation of mechanical analysis methods. The position is broad in scope and may include supporting mechanical validation test design and conducting pretest predict

Senior Validation Engineer

General Motors

Warren, Michigan, USA

Full-time

Job Description Work Arrangement Onsite - This role requires the employee to be onsite full time. The primary work location will be the General Motors Global Technical Center in Warren, MI. The Role The Autonomous Robotics Center (ARC) team is seeking a detail-oriented and highly motivated Validation Engineer to join our team. In this role, you will be responsible for developing and executing validation protocols to ensure systems, equipment, and processes meet regulatory standards and inter

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

Lab Equipment Validation Engineer

Katalyst Healthcares and Lifesciences

Philadelphia, Pennsylvania, USA

Full-time

Responsibilities: Our client is looking for a lab equipment validation engineer to come on-site for a 6 months project. This work will be fully on-site in PA. They are moving buildings, so all of the Laboratory equipment will be decommissioned and then put in the new building. They need this Consultant to come in and requalify, revalidate, and commission the Laboratory Equipment. They will also be getting some new Laboratory Equipment in as well - HPLC, Cell Counters.Requirements: This Consultan

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 II

Katalyst Healthcares and Lifesciences

Athens, Georgia, USA

Full-time

Responsibilities: Perform Smoke studies and assist in semiannual Media fill qualifications as a SME Perform requalification/periodic review of autoclaves, depyrogenation tunnels, cold rooms, freezers, and warehouse areas. Has worked with Ellabs data loggers and software. Write and execute protocols and complete final reports. Understanding of cleaning validation concepts and principles. Understands pharma grade utilities (water HVAC, gases). Requirements: Support Maintenance, Engineering

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

Validation Engineer

Katalyst Healthcares and Lifesciences

Springfield, Illinois, USA

Full-time

Job summary: Seeking a Facilities Validation Specialist who will be responsible for working across two state-of-the-art medical device facilities. They will have a long-term contract position with significant project ownership an opportunity to work with advanced cleanroom environments and warehouse facilities. Responsibilities: Lead facility commissioning activities across multiple sites. Conduct temperature and humidity mapping studies. Perform cleanroom validation for Class 6, 7, and 8 envi

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Swiftwater, Pennsylvania, USA

Full-time

Roles & Responsibilities: Bachelor's degree in science or engineering (MS accepted, PhD is overqualified). Minimum 2+ years in Process Validation within the biotech/pharma industry. Writing and executing process validation documents. Strong Process Performance Qualification (PPQ) experience. Hands-on experience collecting process samples. Must have on-the-floor manufacturing experience. Familiarity with GMP best practices. Proficient in MS Office (Word, Excel, PowerPoint). Strong w

Lead Post-Silicon Validation Engineer

NVIDIA Corporation

Santa Clara, California, USA

Full-time

We are seeking Lead Post-Silicon Validation Engineer within the GPU Engineering Team to help drive development of future GPUs be used in 3D graphics, deep learning, HPC and automotive markets. Make the choice to join our dynamic team today! NVIDIA has continuously reinvented itself over two decades. Our invention of the GPU in 1999 fueled the growth of the PC gaming market, redefined modern computer graphics, and revolutionized parallel computing. More recently, GPU deep learning ignited modern

Process Validation Engineer

Katalyst Healthcares and Lifesciences

Albany, Georgia, USA

Full-time

Responsibilities: Spearhead qualification protocols for next-generation manufacturing processes. Drive manufacturing investigations and implement innovative solutions. Design validation strategies for new product launches and technology transfers. Lead comprehensive IQ/OQ/PQ validation activities across multiple projects. Create robust standard operating procedures for manufacturing excellence. Ensure continuous process verification for robust manufacturing operations. Coordinate cross-fu

System Validation Software Engineer

Apple, Inc.

No location provided

Full-time

The Product Integrity group is seeking a System Validation Software Engineer to help validate and debug future products. As part of the OS Diagnostics team, you will be responsible for crafting and maintaining software applied for characterizing, calibrating, and testing novel hardware. Your duties will also include debugging software and hardware independently and multi-functionally, and working with numerous other teams within Apple and with various contract manufacturers. Your proficiency in

Validation Engineer

Flextronics

Libertyville, Illinois, USA

Full-time

Job Posting Start Date 05-15-2025 Job Posting End Date 07-28-2025 Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraord

Validation Engineer

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Responsibilities: NPD, NPI, Process & product development. Process and Equipment Validation. Process Characterization. good manufacturing practices and documentation. Process Improvement. Requirements: GMP (Good Manufacturing Practices) & ISO (International Organization for Standardization) 13485 and regulatory affairs. Knowledge in Experiment design and SPC. Management of statistical procedures. Strong creative, analytical and problem-solving skills. Comprehension of standard costs and

Verification & Validation Engineer

PeopleNTech

Branford, Connecticut, USA

Contract, Third Party

Role: Verification & Validation Engineer Location: Northford CT (complete onsite) Experience: 8+ Years What candidate will Be Doing: Product validation activities both Manual and Automation testingExtending the internally developed custom test framework (involves robotics, computer vision, distributed computing and sensor simulation) and utilizing the framework to perform testsExtending the framework hardware test fixtureDefining and developing automated test plans, test cases, and proceduresDe