UlliLeading team of up to 10 pax within Production environment - GMP - Clean Room /liliSupervisor - state of the art Biotech Production - constant improvement /li /ulbrpOur client is a global market leader within bio pharmaceuticalb field /b specialising in the bdiscovery, development, manufacturing, and commercialisation of cell therapies. /b /ppIn order to sustain their constant growth, they are actively looking for a Production Supervisor - Biotech - Micro Biology. /p brulliLeadership and supervision: You will manage operational teams and supervise various operational units within the production process.br/liliQuality 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.br/liliCollaboration: You are the first point of contact for production problems and work closely with other departments to find solutions.br/liliDocumentation management: You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms.br/liliBatch record supervision: You oversee the release and review of batch records for quality control.br/liliTraining: As a manager, you make sure that everyone on your team gets the training they need to perform at their best.br/liliOperational excellence: You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve. /li /ulbrpbEducation /b /p ulliYou have a bachelor's or master's degree in science, bio-engineering, pharmacy or a related field of study or you are equivalent through experience. /li /ul pbExperience /b /p ulliYou have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry. /liliExperience with aseptic GMP production is nice to have. /li /ul pbExpertise /b /p ulliYou have a knowledge of cGMP regulations and clean room operations. /liliYou can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. /liliFamiliarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus. /li /ul pbLanguages /b /p ulliYou speak and write fluent English. /li /ul pbStrengths /b /p ulliYou have excellent communication and organisational skills. /liliYou are an empathetic people manager with strong leadership skills. /liliYou have a positive attitude and adapt easily to rapidly changing circumstances. You inspire others to do the same. /liliYou are good at problem solving, prioritising and multitasking. /liliYou have an eye for detail and procedures. /li /ulbrulliA meaningful job that contributes directly to the well-being of patients.br/liliAn excellent work-life balance. You work 4 days. Then you enjoy 4 days off.br/liliA supportive and innovative work environment. We value and encourage learning and personal development.br/liliThe opportunity to work with people from all over the world.br/liliA contract of indefinite duration and an attractive salary package complemented by many fringe benefits, such as additional statutory vacations, meal vouchers, group and hospitalisation insurance, double vacation pay, an end-of-year and performance bonus.br/liliMany fun and informal events. /li /ulbrWork Instructions, Expertise, Document management, Pharmaceuticals, Attention to detail, GMP, Quality Improvement, PowerPoint, Documentation, Communication, Science, Bioengineering, Production Issues, Clean room work, Transfer, Projects, ATMP, Inspection, Regulation, Production Area, Training, VOS, MS Outlook, Leadership, Problem Management, Strong Leadership, Empowering Others, cGMP, Multi Tasking, Cost Reduction, Production, MS Excel, Operations, Quality Control, Point of contact, Field Study, Adaptability, Biotechnology, MS Office Suite, Problem Management, Biotechnology, Batch Records, Pharmacy, Organization SkillsbrpJBRP1_BE /p