Our client is a relatively young pharmaceutical company found in the US that focuses on treating oncology. It produces immunotherapy that serves as an alternative for the chemotherapy. We are looking for professionals to join the team in their European HQ that is located in Amsterdam area and provides treatment for the whole European market.
In this position you will join the Quality Assurance team with a focus of ensuring an efficient and timely documentation preparation process. Besides, you will be working closely with the Manufacturing Planning team to support you in the process.
-Arranging all necessary documentation for the manufacturing process and supporting audits
-Ensure accuracy and compliance with the GMP regulations
-Identify possible deviations and suggest ways to improve the processes
-Provide trainings on documentation procedures
-Bachelor degree in Chemistry, Pharmacy or another relevant discipline
-1+ years of experience working in a GMP-compliant QA environment
-Previous experience in documentation preparation
-Excellent communication skills in English
Are you interested in this or another role? Do not hesitate to contact me at email@example.com or by applying to this position.