- Bachelor¿s or Master¿s degree in Science, Bio-Engineering, Pharmacy or related field or equivalent experience required.
- Preferably 1,5 -3yrs years of operational experience within a GMP or ATMP environment in the biotech/(bio)pharma industry.
- At least 1 year experience in leading teams or Project management
- Knowledge of cGMP regulations and EMEA guidance related to logistics or manufacturing and cleanroom behaviors.
- Must exhibit Leadership skills and ability to effectively communicate and influence support operators and convey information to Technical Clean Room Leads, Supervisor and Manager.
- Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously.
- Strong developed organizational and logistic skills. Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members.
- Analytical, problem solving, pragmatic and positive critical thinking skills and the ability to act as a change agent to promote flexibility, creativity, and accountability.
- Can do attitude, Right first time and Hands-on approach
- Self-motivated, enthusiastic personality, team player
- Flexible mindset capable to deal with ambiguity and to respond quickly, energetically, and enthusiastically to changes
- Strong communication and organizational behaviors skills are required.
- Ability to accommodate shift work including evenings and weekends as required by the process.
- Ability to accommodate unplanned overtime on little to no prior notice
- Good knowledge of Dutch and English