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This hands on, on-site role delves into product validation, hardware development, pre-certification testing, and firmware development, along with PCB design and troubleshooting, knowledge of design software and extensive experience in embedded programming.
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The Equipment Validation Engineer supports the successful implementation of various process/lab. Job Title: Validation Engineer. most of resumes received has computer validation and CSV which manager does not want, not articulate in describing experience, needs good communication skills, someone experienced.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. Supports equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.b. Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.c. Completes all qualification and validation documentation with accuracy, completeness and compliance to standards.
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Completes all qualification and validation documentation with accuracy, completeness and. Develops validation/qualification deliverables such as Validation Plans, Requirements. Supports the execution of equipment qualifications and validation protocols.
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We are seeking a Validation Engineer to join our team and lead the implementation and maintenance of manufacturing and laboratory equipment and computerized systems. Job Title: Validation Engineer Location: 50% onsite Are you a meticulous engineer with a passion for validation and compliance in the pharmaceutical industry.
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Most Important Skills Needed: Computer Systems Validation, CFR Part , Laboratory Systems, LIMS, Scada Education Requirements: Degree. Client is looking for - years of Computer Systems Validation experience.
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Analysis of current business processes to translate development documents into user requirements and functional design specifications Establish validation standards, develop testing protocols, prepare equipment, document test results and maintain records for later analysis Documentation and remediation of deviations resulting from validations/qualifications.
ExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Completes all qualification and validation documentation with accuracy, completeness and compliance to Company standards. 5 years of experience in FDregulated industry, with 5 years experience in CSV.
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Manage validation documentation in automated systems, including document control and archiving. Expertise in validation documentation management and quality review processes. Perform quality reviews of IQ/OQ/PQ protocols, test scripts, and validation reports.
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Thorough knowledge of quality systems, Quality by Design, validation principles for product and engineering design and process control fundamentals. Job Title: Scientist/Engineer. Experience in Biologics/Vaccine Aseptic Drug Product Manufacturing and/or Technology Transfer.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We are looking for a dedicated Validation Engineer to join our talented team at our office located in Somerset, NJ. General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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We are seeking an experienced and detail-oriented Mid-Level Validation Specialist to join our team. The Validation Specialist will play a key role in ensuring that all processes, systems, and equipment within the client organization are commissioned, qualified, and validated in compliance with regulatory requirements and industry standards.
$50 an hourFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Assisting in development, review, and approval of cGMP documents including, but not limited to: Master Validation Plans, FAT/SAT documents, Turnover Packages, SOP’s, specifications, traceability matrices, thermal mapping documents, and design documentation.
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Perform end to end testing of all Transit Systems Software and Hardware (Ticket Vending Machine, Ticket Office Machine, Validation Systems, Web and Mobile) Experience with SharePoint, JIRA, JAMA, TFS, Oracle, SQL, UNIX, Angular services, Jasper Reports.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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We are looking for a Quality Validation Engineer for our client, a Global pharmaceutical Company. Functional responsibilities include ensuring accurate and timely maintenance of validation and qualification documents for all equipment and facility activities; investigations and evaluation of change control.
$64 an hourExpandApply NowActive JobUpdated 16 days ago
validation engineer jobs in South Plainfield, NJ
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