Duration: 1 year (extension is possible)
Start date: 15-11-2022
Our client is a biopharmaceutical company engaged in the development of cancer immunotherapies with the aim to provide long term response and eliminate this chronic disease.
About the role
As a Manufacturing Engineer you will be responsible for the process validations, change control, technical reports and assessments in order to provide product expertise for GMP manufacturing.
-Perform root-cause investigations and deviations
-Monitor process performance through data-based trending
-Write and review SOPs and batch records
-Collaborate with technical operational stakeholders
-Understanding of process development and validation
-Degree in Engineering, Biotechnology, Life Sciences or related discipline
-Minimum of 3 years in a manufacturing environment (GMP)
Ready for the next step in your career? Do not hesitate to contact me!