Competitive salary with numerous lifestyle, family, and leisure benefits.
What you will do: Participation in qualification and validation of pharmaceutical production lines and processes (fill&finish lines) in a cleanroom Adherence to the relevant SOPs, EHS and GMP regulations Independent operation of the assigned parts of the fill&finish equipment and devices, including their pre- and post-processing Execution of microbiological environmental monitoring, in-process controls and sampling Identification and reporting of potential issues, as well as active support in continuous improvement processes Timely and GMP-compliant documentation of all activities (e.g. in computer systems such as MES or in logbooks) Inspection of equipment, ensuring that it is cleaned and correctly stored
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.
