At SIMABS, we are redefining bioprocessing. We are a growing biotechnology company developing innovative and sustainable biomanufacturing solutions for biologics and advanced therapies. Combining scientific excellence with a hands-on, entrepreneurial mindset, we help biopharmaceutical innovators accelerate development and GMP manufacturing. At SIMABS, you will join a small, passionate team where your ideas matter, your impact is visible, and innovation, ownership and collaboration are part of everyday work. Our values guide everything we do: • Keep It Simple & Smart • Innovate the Process • Enjoy the Flow The Role As a GMP Production Operator (with R&D Support), you are an essential part of our manufacturing team. You perform production activities in a GMP cleanroom environment, ensuring that our processes and products meet the highest quality standards. Depending on production planning, you will also support R&D activities, contributing to process development and the implementation of new technologies. You enjoy hands-on laboratory work, but also like to think along about how processes can be improved. Because SIMABS is a growing startup, no two days are exactly the same. You are comfortable working across different projects, adapting to changing priorities, and supporting the team wherever needed. Key Responsibilities GMP Manufacturing • Execute manufacturing activities according to GMP procedures and batch records. • Perform upstream and downstream production operations in a cleanroom environment. • Prepare materials, equipment and production areas for manufacturing activities. • Carry out cleaning, assembly and sterilization activities where required. Documentation & Compliance • Complete GMP documentation accurately and in a timely manner. • Ensure compliance with GMP guidelines, SOPs and safety procedures. • Report observations and contribute to maintaining a high-quality manufacturing environment. Teamwork & Continuous Improvement • Collaborate closely with colleagues from Production, QC, QA and R&D. • Support R&D activities and process development projects, depending on production planning. • Support technology transfers and the implementation of new manufacturing processes. • Contribute ideas to improve workflows, efficiency and operational excellence. • Embrace the flexibility and ownership that come with working in a startup environment. Vereisten Education & Experience • Bachelor's degree in Chemistry, Biochemistry, Biomedical Laboratory Technology, Biotechnology, Pharmaceutical Sciences or equivalent through relevant experience. • Experience in a GMP production or cleanroom environment is a strong asset. • Recent graduates with the right mindset and motivation are also encouraged to apply. Technical Skills • Familiar with GMP principles and aseptic working techniques. • Experience working in a controlled cleanroom environment is an advantage. • Comfortable following procedures while maintaining a critical and quality-focused mindset. • Accurate in documentation and record keeping. Personal Skills • A true team player who enjoys working towards shared goals. • Flexible and comfortable working across different projects and priorities. • Hands-on, proactive and eager to learn. • Thinks along, takes ownership and contributes ideas for improvement. • Quality-minded, accurate and well organised. • Enjoys the energy, variety and ownership that come with a startup environment.