Cleaning Validation Specialist
il y a 2 semaines
About 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 the introduction of new products and equipment, contributing to compliance and operational excellence.Key Responsibilities:Prepare and update cleaning validation documentation, including protocols, reports, and studies.Gatekeep proposed changes and prioritize cleaning validation projects.Support audits and ensure timely responses to findings.Facilitate the introduction of New Product Introductions (NPI) and new equipment in the validation program.Report incidents, deviations, and propose solutions to improve compliance.Collaborate with cross-functional teams, including manufacturing, quality, and engineering.Key Competencies:Strong expertise in API manufacturing processes and cleaning validation.Solid understanding of validation principles and statistical methods.Knowledge of Quality & Compliance/regulatory requirements (GMP) in cleaning validation.Project management, planning, organization, and coordination skills.Ability to manage complexity, deadlines, and competing priorities.Excellent communication and interpersonal skills, able to interact at different organizational levels.Familiarity with systems such as eLIMS, truVAULT, COMET, PRX, CRB, SAP, PASx, Minitab, CPV Automation (preferred).Requirements:2–4 years of relevant work experience in pharmaceutical manufacturing or validation.Practical's:Location: Geel, BelgiumDuration: 12+ monthsStart Date: ASAPWork Model: Full-time, On-site
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Cleaning Validation Specialist
il y a 2 semaines
2440 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 Specialist
il y a 2 semaines
Geel, Belgique Actalent Temps pleinAn exciting QA Cleaning Validation Contractor opportunity in Geel. This role focuses on supporting the QA Engineering department to ensure compliance with cleaning validation requirements.Involves:Reviewing and approving cleaning validation activities (SOPs, trend reports, protocols, and reports).Participating in change controls and projects related to...
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Cleaning Specialist
il y a 2 semaines
Geel, Belgique Actalent Temps pleinAn exciting QA Cleaning Validation Contractor opportunity in Geel. This role focuses on supporting the QA Engineering department to ensure compliance with cleaning validation requirements. Involves: Reviewing and approving cleaning validation activities (SOPs, trend reports, protocols, and reports). Participating in change controls and projects related to...
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Cleaning Specialist
il y a 2 semaines
2440 Geel, Belgique Actalent Temps pleinAn exciting QA Cleaning Validation Contractor opportunity in Geel. This role focuses on supporting the QA Engineering department to ensure compliance with cleaning validation requirements. Involves: Reviewing and approving cleaning validation activities (SOPs, trend reports, protocols, and reports). Participating in change controls and projects related to...
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Cleaning Validation Engineer
il y a 5 jours
Geel, Belgique Arcadis Temps pleinTasks:Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this.Perform validation of systems in scope for which there...
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Cleaning Validation Engineer
il y a 5 jours
Geel, Belgique Arcadis Temps pleinTasks:Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this.Perform validation of systems in scope for which there...
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Cleaning Validation Engineer
il y a 5 jours
Geel, Belgique Arcadis Temps pleinTasks: Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this. Perform validation of systems in scope for which...
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Cleaning Validation Engineer
il y a 5 jours
2440 Geel, Belgique Arcadis Temps pleinTasks: Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this. Perform validation of systems in scope for which...
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Student Development Specialist
il y a 2 semaines
2440 Geel, Belgique Actalent Temps pleinAn exciting QA Cleaning Validation Contractor opportunity in Geel . This role focuses on supporting the QA Engineering department to ensure compliance with cleaning validation requirements. Reviewing and approving cleaning validation activities (SOPs, trend reports, protocols, and reports). Participating in change controls and projects related to...
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Quality Assurance Associate
il y a 3 semaines
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...
