Save Job Back to Search Job Description Summary Similar Jobs Added 24/02/2026Ghent based - State of the art manufacturing siteQuality & Operations - Shifts model (6 am - 2 am)About Our ClientOur client is a global market leader within bio pharmaceutical field specialising in the discovery, development, manufacturing, and commercialisation of cell therapies. In order to sustain their constant growth, they are actively looking for a Production Supervisor - Biotech - Micro Biology. Job DescriptionLeadership 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.The Successful ApplicantEducationYou 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.ExperienceYou have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry.Experience with aseptic GMP production is nice to have.ExpertiseYou have a 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.LanguagesYou speak and write fluent English.StrengthsYou have excellent communication and organisational 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, prioritising and multitasking.You have an eye for detail and procedures.What's on OfferA meaningful job that contributes directly to the well-being of patients.An excellent work-life balance. You work 4 days. Then you enjoy 4 days off.A supportive and innovative work environment. We value and encourage learning and personal development.The opportunity to work with people from all over the world.A 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.Many fun and informal events.ContactCharles JeanQuote job refJN-022026-6953147Job summarySectorLife SciencesSub SectorResearch & DevelopmentIndustryHealthcare / PharmaceuticalLocationGhentContract TypePermanentConsultant nameCharles JeanJob ReferenceJN-022026-6953147
