Senior QA Validation Lead — GMP

For a global customer in Limburg, we are searching for x3 QA Validation Officers. The purpose of this position is to establish and maintain the validation of systems, processes, facilities, and equipment at the required standard within the organisation. This must be carried out in accordance with legal requirements, particularly pharmaceutical regulations...

This position can be filled by freelance or employee consultancy via a payroll partner.For a customer in Limburg, we are searching for a CSV Specialist to ensure that all IT systems that have an impact on GMP are maintained in a validated state.ResponsibilitiesMaintain an overview of all IT systems and the extent to which they have undergone CSV; manage and...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements. This is a part‑time role...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements.Key...

Location State/Province: Limburg Job Description As a QC Analyst, you play a key role in ensuring the quality, consistency and compliance of our manufacturing processes and Investigational Medicinal Products (IMPs). You perform analytical testing, support GMP activities, investigate deviations, and collaborate closely with colleagues across QC, QA,...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements.Key...

For a global customer in Limburg, we are searching for x3 QA Validation Officers. The purpose of this position is to establish and maintain the validation of systems, processes, facilities, and equipment at the required standard within the organisation. This must be carried out in accordance with legal requirements, particularly pharmaceutical regulations...

This position can be filled by freelance or employee consultancy via a payroll partner.For a customer in Limburg, we are searching for a CSV Specialist to ensure that all IT systems that have an impact on GMP are maintained in a validated state.ResponsibilitiesMaintain an overview of all IT systems and the extent to which they have undergone CSV; manage and...

This position can be filled by freelance or employee consultancy via a payroll partner.For a customer in Limburg, we are searching for a CSV Specialist to ensure that all IT systems that have an impact on GMP are maintained in a validated state.ResponsibilitiesMaintain an overview of all IT systems and the extent to which they have undergone CSV; manage and...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements.This is a part-time role for...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements.Key...

For a global customer in Limburg, we are searching for x3 QA Validation Officers. The purpose of this position is to establish and maintain the validation of systems, processes, facilities, and equipment at the required standard within the organisation. This must be carried out in accordance with legal requirements, particularly pharmaceutical regulations...

This position can be filled by freelance or employee consultancy via a payroll partner.For a customer in Limburg, we are searching for a CSV Specialist to ensure that all IT systems that have an impact on GMP are maintained in a validated state.ResponsibilitiesMaintain an overview of all IT systems and the extent to which they have undergone CSV; manage and...

This position can be filled by freelance or employee consultancy via a payroll partner.For a customer in Limburg, we are searching for a CSV Specialist to ensure that all IT systems that have an impact on GMP are maintained in a validated state.ResponsibilitiesMaintain an overview of all IT systems and the extent to which they have undergone CSV; manage and...

For a customer in Limburg, we are searching for QA Specialist with a scientific profile who can apply all elements of the Quality Management System (QMS) support the Lead Qualified Person (QP) in ensuring that every batch is manufactured and tested in compliance with applicable legislation and Marketing Authorization requirements.This is a part-time role for...