Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.
Location/Division Specific Information
The Groningen site is a multi-product and multi-client biopharmaceutical site with development and manufacturing facilities for pharmaceutical products for clinical trials (phase 1, 2 and 3) and commercial production.
How will you make an impact?
This is an exciting and important role within the site to ensure that the equipment we are using for manufacturing is reliable and that we are keeping up with the latest technology. You be working in, and leading, cross functional project teams to bring in new equipment and troubleshooting if any issues arise.
What will you do?
GMP and non-GMP change control, maintaining regulatory compliance
Equipment reliability practices & methodologies
Equipment specification, design, start-up, commissioning & qualification practice
Defining, communicating and maintaining design and operability envelope