A career is an ongoing journey of discovery: our 52,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
Your role: You ensure the full availability of process equipment to support API production with the required quality level. You guarantee that process equipment is operated and maintained within the given budget frame and by strictly following the technical norms, safety rules, company policies and cGMP regulations. You are responsible for the timely investigation of all non-conformities and that efficient CAPAs are put in place, including change control and risk analysis. You are the reference expert for the process equipment during audits (health authorities, ASIT and maintenance management system) and you support the technology transfers of new molecules with your department. You ensure the absence of critical spare part stock out and you drive continuous improvement projects (efficiency, quality and operating cost reduction).
Who you are
· Graduate degree in biotechnology engineering, mechanical engineering, chemical engineering (or equivalent)
· Proven and successful direct management experience
· Biotech or Pharma industry experience and cGMP knowledge
· Expertise in equipment construction / modification and CAMMS database management
· Fluent in French and English
What we offer: We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!