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Experience Level
Experience
Qualifications
Bachelor's Degree in Chemistry or a related field.Proven experience in developing Validation Plans, conducting Risk Assessments, and preparing IOQ, CSV IOQ, Traceability Matrices, and Validation Reports.Familiarity with validation processes for computer systems.Practical knowledge of 21 CFR Part 11 regulations.Strong understanding of Good Manufacturing Practices (GMP) regulations.Experience in technical writing.Specialized validation expertise in:- Sterilization- Kaye Validator & Data Loggers- Process Validation- Equipment Qualification- Re-qualification- Computer System Validation
About the job
Join our dynamic team as a Laboratory Equipment Validation Specialist, where you will play a crucial role in the development and execution of laboratory equipment validation processes. You will be responsible for creating comprehensive validation plans, conducting risk assessments, and executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Your expertise will also be essential in developing documentation packages that include original format documents, approved documents, and relevant drawings.
About Validation & Engineering Group, Inc.
Validation & Engineering Group, Inc. is a premier service provider delivering innovative solutions to the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries. We specialize in laboratory services, compliance, computer engineering, project management, validation, and manufacturing operations, ensuring our clients meet the highest standards of quality and efficiency.
Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.
Unlock Your Potential
Generate Job-Optimized Resume
One Click And Our AI Optimizes Your Resume to Match The Job Description.
Is Your Resume Optimized For This Role?
Find Out If You're Highlighting The Right Skills And Fix What's Missing
Experience Level
Experience
Qualifications
Bachelor's Degree in Chemistry or a related field.Proven experience in developing Validation Plans, conducting Risk Assessments, and preparing IOQ, CSV IOQ, Traceability Matrices, and Validation Reports.Familiarity with validation processes for computer systems.Practical knowledge of 21 CFR Part 11 regulations.Strong understanding of Good Manufacturing Practices (GMP) regulations.Experience in technical writing.Specialized validation expertise in:- Sterilization- Kaye Validator & Data Loggers- Process Validation- Equipment Qualification- Re-qualification- Computer System Validation
About the job
Join our dynamic team as a Laboratory Equipment Validation Specialist, where you will play a crucial role in the development and execution of laboratory equipment validation processes. You will be responsible for creating comprehensive validation plans, conducting risk assessments, and executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Your expertise will also be essential in developing documentation packages that include original format documents, approved documents, and relevant drawings.
About Validation & Engineering Group, Inc.
Validation & Engineering Group, Inc. is a premier service provider delivering innovative solutions to the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries. We specialize in laboratory services, compliance, computer engineering, project management, validation, and manufacturing operations, ensuring our clients meet the highest standards of quality and efficiency.