junior validation lead Jobs

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Validation Engineer

Katalyst Healthcares and Lifesciences

Waltham, Massachusetts, USA

Full-time

Responsibilities: Independently perform validation activities including installation qualification, operational qualification, performance qualification for Base Camp projects related to facility, utilities, equipment and instrument. Generate protocols for tests, verification, and qualification for GxP assets, as well as reports to document execution. Ensure deliverables meet the overall facility milestones. Perform and support periodic assessment review and revalidation activities. Ensure deliv

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

Validation Engineer

Katalyst Healthcares and Lifesciences

Mossville, Illinois, USA

Full-time

Responsibilities: ssess and plan work to mitigate risk in NTI and NPI programs. Work with design leads to establish an initial first-pass test plan early in a program (pick list review to document leverage opportunity, VPD and potential test load). Participate in or Plan and Host Simulation and Test Collaboration Workshops (STCW) early in programs, pre-DFMEA to create high-level Validation Plan. Communicate progress in Gateway Reviews including System Readiness Summaries. Quality approval of FME

Validation Engineer

Katalyst Healthcares and Lifesciences

Los Angeles, California, USA

Full-time

Responsibilities: Coordinate sample builds and maintain traceability documentation. Prepare process validation protocols (IQ/OQ/PQ) and generate accompanying test plans/reports. Route and track all protocol documents for proper approvals. Characterize new process equipment. Document experiments and results in engineering reports. Create and present summary presentations to management. Collaborate and coordinate with outside vendors. Provide technical support to engineering and provide li

Validation Engineer

Katalyst Healthcares and Lifesciences

South Carolina, USA

Full-time

Responsibilities: Provide technical input to validation activities. Represent process validation during equipment installations. Support process validation Quality Systems. Identify opportunities for personal and professional development, continuous improvements, and help deploy best practices. Participate in regulatory agency inspections for Process Validation. Serve as one of the main points of contact in communication to customers whose equipment and processes are being validate. Responsible

Validation Engineer

Katalyst Healthcares and Lifesciences

Norwood, Massachusetts, USA

Full-time

Responsibilities: Support team to investigate and resolve issues related to equipment failures, system deficiencies, deviations, and equipment troubleshooting. Support authoring quality systems records such as deviations, change controls, and CAPAs as required Monitor and communicate method lifecycle (acquisition, qualification/validation, implementation) timelines using project management tools. Ordering supplies and maintaining inventory for equipment consumables/accessories. CTU alarm respon

Validation Engineer

Katalyst Healthcares and Lifesciences

Thousand Oaks, California, USA

Full-time

Responsibilities: Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment. Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equi

Validation Engineer

Katalyst Healthcares and Lifesciences

San Jose, California, USA

Full-time

Responsibilities: Process and equipment qualification (IQ/OQ/PQ). Development of test methods for Design V&V, Process Validation, and Production. Validation of test methods. Execution of Engineering Builds, Gauge R&R Studies, Attribute Analysis Studies, and other validation work. Authoring/releasing of new test methods and editing/redlining of old test methods. Experience working in a regulated and/or medical device environment. To define equipment requirements. To draft equipment specification

Validation Engineer

Katalyst Healthcares and Lifesciences

Charlotte, North Carolina, USA

Full-time

Roles & Responsibilities: t least a bachelor's degree (or equivalent experience) in Computer Science, Software/Electronics Engineering, Information Systems, or closely related field is required. Develop and execute validation plans, protocols, and test scripts for equipment, processes, and systems. Collaborate with cross-functional teams to establish validation strategies. Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Conduct testing

Validation Engineer

Katalyst Healthcares and Lifesciences

Hillsboro, Oregon, USA

Full-time

Responsibilities: Develop proficiency for the client standard implementation of the Pharma Suite platform to enable better understanding for how to validate a multi-environment implementation, and some support for actual system configuration. Develop proficiency in interfaces to the Pharma Suite platform, including warehouse management through the eWM module of SAP, SAP manufacturing, MuleSoft middleware layers, and communication to DeltaV, PI, and other manufacturing automation systems using i

Site Validation Engineer

Katalyst Healthcares and Lifesciences

Holdrege, Nebraska, USA

Full-time

Responsibilities: Support the plant on assigned new and existing product initiatives with technical expertise and determine associated resource needs to accomplish project goals. Develop and maintain the Validation Master Plan and validation tracking schedule. Provide visibility related to all validation activities through tracking and reporting plant metrics. Support and influence change management within the plant: liaison between the core team, program managers, and Global quality. Conduct tr

Validation Engineer

Katalyst Healthcares and Lifesciences

San Diego, California, USA

Full-time

Responsibilities: Experience performing equipment and process validation studies such as writing and/or reviewing protocol, report, data analysis and deviations for new, existing and site relocation activities. Have a working knowledge of medical device or biological equipment maintenance from Quality standpoint such as Preventive Maintenance, Calibration and Out Of Tolerance activity support to the site and equipment owners. Author and execute installation, operational, and performance quali

System Verification and Validation Engineer

Jacobs

Houston, Texas, USA

Full-time

Are you passionate about human space exploration, understanding the origins of the universe, and working with a passionate and diverse team to make a difference? If you are, we need you! We need your talent, teamwork, and energy to help us achieve great things that inspire people all over the globe. We need you to bring creative ideas and diverse backgrounds to help us envision, shape, and deliver systems that will enable the exploration of space while benefiting people here on Earth. We are exc

Validation Engineer II

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is seeking an experienced Validation Engineer II to support a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities: Responsible for risk analysis, packaging validation, cleaning validation, and equipment qualification required for new products, processes, and equipment and any changes to existing products, processes, and equipment. Provide recommendations for product disposition or other actions related to product and equipment performance issue

Validation Engineer

Quest Global Services-NA Inc.

San Jose, California, USA

Contract

Hi,Greetings from Quest Global. We have a requirement for which we are actively sourcing. If you feel that your experience and skill set might be suitable for this requirement, please send us your most recently updated resume along with your contact information, best times when we can contact you. Would appreciate if you could refer your friends or colleagues. You may please forward my email to them.Title: Silicon Validation EngineerLocation: San Jose, CAJob DescriptionSilicon Validation experie

Senior Validation Engineer

Katalyst Healthcares and Lifesciences

Jacksonville, Florida, USA

Full-time

Responsibilities: Designing validation plans. Conducting and documenting impact and risk assessments with a full understanding of equipment/system/software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes. Maintaining (and ensuring the team maintains) clear, detailed records of qualification and validation, and change control activities for future compliance audits. Designing and executing engineering studies for critical process p

Admin/Data Validation & Entry

Sunrise Systems, Inc.

Concord, New Hampshire, USA

Contract

Job Title: Admin/Data Validation & Entry Job ID: 25-07946 Location: Concord, NH Duration: 18 Months of Contract IMPORTANT NOTES - PLEASE READ:This is a FULLY ONSITE position. Only submit LOCAL candidates who are willing to work fully onsite, 40 hours/week in these roles.Candidates must be willing and able to go to the client location for an ONSITE, IN-PERSON interview if selected for interview.In addition to the experience/skills required, candidates must have the physical ability to lift full

Silicon Validation Software Engineer

Apple, Inc.

No location provided

Full-time

The Product Integrity group is seeking a Systems Software Engineer to chip in to the development of 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 writ

Admin/Data Validation & Entry

Caresoft

Concord, New Hampshire, USA

Contract

Title: Admin/Data Validation & Entry Location: Concord, NH (Onsite) Durartion: Long Term Skills: Professional experience reviewing various data and document sources for accuracy and completing data entry once accuracy is confirmed Experience compiling, coding, categorizing, calculating, tabulating, auditing, or verifying information or data. Experience proactively communicating information to supervisors, co-workers, and vendors by telephone, in written form, e-mail, or in person. Experien

Validation Engineer 4

Katalyst Healthcares and Lifesciences

Littleton, Colorado, USA

Full-time

Job Description: We are seeking a detail-oriented and experienced LabVantage Business Analyst to support the implementation, optimization, and ongoing support of LabVantage LIMS (Laboratory Information Management System). The ideal candidate will work closely with business stakeholders, scientists, QA teams, and IT to gather requirements, analyze workflows, and ensure that LabVantage solutions align with organizational needs. Responsibilities: ct as the liaison between scientific/business teams