QA Computer System Validation Contractor
il y a 4 semaines
A Freelance CSV specialist is needed to support the QA Engineering department in ensuring that all computer system validation (CSV) regulatory and procedural requirements are met throughout the full system lifecycle, including concept, project, operational, and retirement phases. The role will focus on manufacturing automation systems, providing expertise in reviewing and approving CSV documentation, advising on new or upgraded systems, addressing deviations, and ensuring compliance with cGMP standards and internal policies. Specific Services Review and approveCSV documentation and records, including: SOPs, User Requirements, Impact/Risk Analyses Test Plans, Test Scripts Change Controls, CAPAs Participate in engineering teams for the introduction of new or upgraded systems and processes. Provide advice and support for CSV activities, ensuring cGMP compliance. Address and follow up on deviations during CSV execution. Communicate status updates (quality, compliance, planning) to the QA Qualification team. Profile Requirements Knowledge & Experience Background in the chemical and/or pharmaceutical industry with focus on CSV for manufacturing automation systems. Strong knowledge of cGMP regulations and guidelines. Ability to translate technical information into clear, accessible language across all organizational levels. Skilled at assessing urgency, criticality, and impact of decisions. Proven ability to multi‐task across multiple projects. Capable of working independently and within cross‐functional teams. Strong communication skills. Fluent in English and Dutch (written and spoken). Specific System Know‐How Manufacturing automation systems (e.g., DeltaV) Problem report/change request systems (e.g., Comet) Document management systems (e.g., TruVault) Test tools (e.g., Kneat)
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QA Computer System Validation Contractor
il y a 4 semaines
Geel, Belgique EPM Scientific Temps pleinA Freelance CSV specialist is needed to support the QA Engineering department in ensuring that all computer system validation (CSV) regulatory and procedural requirements are met throughout the full system lifecycle, including concept, project, operational, and retirement phases. The role will focus on manufacturing automation systems, providing expertise in...
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Quality Engineer
il y a 4 semaines
Geel, Belgique Panda International Temps pleinJob Title: QA Computer System Validation (CSV) About the Role:We are looking for a QA Computer System Validation (CSV) Contractor to support the QA Engineering team in Geel, Belgium. This role ensures that all CSV-related regulatory and procedural requirements are met throughout the full system lifecycle — from concept and project phases to operational use...
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Quality Engineer
il y a 4 semaines
Geel, Belgique Panda International Temps pleinJob Title: QA Computer System Validation (CSV) About the Role: We are looking for a QA Computer System Validation (CSV) Contractor to support the QA Engineering team in Geel, Belgium. This role ensures that all CSV-related regulatory and procedural requirements are met throughout the full system lifecycle — from concept and project phases to operational...
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Senior Consultant
il y a 4 semaines
Geel, Belgique WhatJobs Temps pleinCSV & Data Integrity (DI) Squad Lead – Geel, Belgium Are you an experienced CSV professional with a strong background in industrial systems and a strategic mindset? We're seeking a CSV & DI Squad Leadto drive excellence in computer system validation and data integrity at a leading pharmaceutical manufacturing site in Geel. Location:Geel, Belgium 12 months...
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Quality Assurance Associate
il y a 1 semaine
Geel, Belgique Proclinical Staffing Temps pleinJoin a cutting-edge pharmaceutical team where your precision and passion for quality will help shape the future of life-saving medicines! Proclinical is seeking a Quality Assurance Associate specializing in Qualification and Validation to join a dynamic quality team. In this role, you will play a key part in ensuring equipment, systems, processes, and...
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QA Operational readiness Officer
il y a 2 jours
Geel, Belgique Arcadis Temps pleinDescription: The QA Operational Readiness Officer is responsible for ensuring quality readiness, operational excellence and compliance for the successful startup and commissioning of a new production facility. This critical role coordinates quality-related activities during the facility qualification phase, ensuring seamless transition from construction to...
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Validation engineer
il y a 3 semaines
Geel, Belgique Panda International Temps pleinCleaning Validation Engineer (MSAT Team) About the Role We are looking for an experienced Cleaning Validation Engineer to join our Manufacturing Science and Technology (MSAT) team. In this role, you will focus on cleaning validation within a GMP-regulated pharmaceutical environment, ensuring that all cleaning processes meet the highest quality and compliance...
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Validation engineer
il y a 4 semaines
Geel, Belgique Panda International Temps pleinCleaning Validation Engineer (MSAT Team)About the RoleWe are looking for an experienced Cleaning Validation Engineer to join our Manufacturing Science and Technology (MSAT) team.In this role, you will focus on cleaning validation within a GMP-regulated pharmaceutical environment, ensuring that all cleaning processes meet the highest quality and compliance...
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Cleaning Validation Specialist
il y a 3 semaines
Geel, Belgique Panda International Temps pleinAbout the Role: We are seeking an experienced Cleaning Validation Specialist to join our client's Manufacturing Science and Technology (MSAT) team. This role focuses on cleaning validation in pharmaceutical manufacturing, ensuring processes meet strict quality and regulatory standards. You will manage validation activities, documentation, audits, and support...
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Cleaning Validation Specialist
il y a 3 semaines
Geel, Belgique Panda International Temps pleinAbout the Role:We are seeking an experienced Cleaning Validation Specialist to join our client's Manufacturing Science and Technology (MSAT) team. This role focuses on cleaning validation in pharmaceutical manufacturing, ensuring processes meet strict quality and regulatory standards. You will manage validation activities, documentation, audits, and support...
