Senior Qualified Person – Sterile Products & Batch Release Purpose of the Role The Senior Qualified Person (QP) is legally responsible for certifying batches of medicinal products before release to market (human and veterinary). The role is responsible for
Quality Assurance Specialist | QA Specialist | Medical Devices | ISO 13485 | 32-40 uur Voor een internationale organisatie binnen de medical devices / medische technologie ben ik op zoek naar een Quality Assurance Specialist. De
QA Operations Specialist Job Purpose Support GMP-related quality activities with a focus on the timely release of batches and materials, ensuring compliance with regulatory requirements and the local Quality Management System. Key Responsibilities Review and approve batch release documentation.
ROLE OVERVIEW A leading organisation in the pharmaceutical industry is seeking a Senior Qualified Person to join their team in the Voorschoten area. As the Senior Qualified Person, you will play a pivotal role in ensuring
The Senior Qualified Person is legally responsible for certifying batches of medicinal products before release to market (human and veterinary). Responsible for managing assigned commercial and strategic projects with a focus on batch release compliance, ensuring all quality, regulatory,
We are looking for a new colleague with thorough knowledge on QA processes, with a first experience in a GMP environment, preferably within the pharmaceutical industry. Experience in a commercial GMP manufacturing setting and ATMP’s are
ROLE OVERVIEW A leading organisation in the pharmaceutical industry is seeking a Senior Qualified Person to join their team in the Hague. As the Senior Qualified Person, you will play a pivotal role in ensuring the