- Bachelor's or Master's degree in Science, Bio-Engineering, BioTechnology, Pharmacy or related field or equivalent experience required.
- A minimum of 3 years of operations experience within a cGMP or ATMP environment in the biotech/biopharma industry.
- A minimum of 3 years experience in aseptic techniques in clean rooms
- Prior experience in manufacturing, quality, or engineering is required
- Strong influence and relationship building skills with an emphasis on teamwork
- Highly developed organizational 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.
- Strong analytical, problem solving, pragmatic and positive critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability.
- Can do attitude, Right first time and Hands-on approach
- Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures. - Focus on quality, compliance and detail - Self-motivated, enthusiastic personality, team player, with a desire to learn new skills and train juniors - Flexible mindset capable to deal with ambiguity and to respond quickly, energetically, and enthusiastically to changes - Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook) is required. - Experience working in cGMP systems including PASx, eLIMs, Siemens, and SAP is preferred - Ability to accommodate unplanned overtime on little to no prior notice - Ability to accommodate changes in the schedule including working in other shifts, evenings and weekends as per operational needs is required. - Fluent in English and Dutch.