Requirements: English
Company: MindCapture
Region: Antwerpen , Flanders
About the company Our client is a company with a mission to improve healthcare drastically. The company is a global biotechnology company dedicated to treating life-threatening diseases. They are focussing on advanced cell-based immunotherapies across a diverse array of technology platforms. They apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Job description As a Operations Supervisor, you are the lynchpin of our production. These are your responsibilities: Leadership and supervision: You will manage operational teams and supervise various operational units within the production process. Quality and compliance: You manage all aspects of quality and ensure strict compliance with cGMP standards. As a domain expert for Quality and Operations, you play a central role in GMP inspections. Collaboration: You are the first point of contact for production problems and work closely with other departments to find solutions. Documentation management: You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms. Batch record supervision: You oversee the release and review of batch records for quality control. Training: As a manager, you make sure that everyone on your team gets the training they need to perform at their best. Operational excellence: You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve. Required competences & skills Education: You have a bachelors or masters degree in science, bioengineering, pharmacy or a related field of study or you are equivalent through experience. Experience: You have at least 5 years of experience in a cGMP or ATMP environment, preferably in the biotech or pharmaceutical industry. You also have substantial experience with grade C aseptic GMP production. Languages: You speak and write fluent Dutch and English. Strengths: You have excellent communication and organizational skills. You are an empathetic people manager with strong leadership skills. You have a positive attitude and adapt easily to rapidly changing circumstances. You inspire others to do the same. You are good at problem solving, prioritizing and multitasking. You have an eye for detail and procedures. You are willing to accommodate a shift system where you work four days and have four days off. Expertise: You have a thorough knowledge of cGMP regulations and clean room operations. You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus. Interested? Want to share your ambitions? Let us get to know you and apply here!