Our client is a game-changer with a unique goal which is contributing to better care, such as the development of innovative therapies. Our client focuses mainly on patients with conditions for which few or no treatment options don’t exist, through the development of high-quality medicines.
As a Manufacturing Process Technician you will be responsible, to support the primary production process in process and system (MES). You will drive continuous improvement of the primary production process following SOP’s, performance reviews, deviations, CAPA’s, electronic Batch Record.
-Work within full GMP compliance
-Assist in training of staff on new or updated processes and procedures
-Actively participate in continuous improvement initiatives
-Assist in CAPA’s, and other investigational records
-Develop, revise, and maintain production related (GMP) documentation
-Create proposals and implement initiatives to further develop and train staff on MES
-Bachelor degree in Automation Processes or Process Design
-At least 3 years of experience in an industrial environment (Pharma)
-Strong experience working within GMP environment
-Experience in writing procedures and/or records proven experience with Lean principles
-Experience with transactional data systems (SAP / PAS|X)
-Excellent communication skills in English and Dutch
Our client is seeking to highly motivated talents for different positions, do you want to join them and be part of an exciting journey in the development of innovative cancer immunotherapies. If you are interested or know someone who is, contact me via the apply button. I would be happy to discuss this opportunity with you.