Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there''s no magic formula for how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that''s the kind of work we want to be part of. The role:Join us as a Commissioning, Qualification and Validation (CQV) Technician, pivotal in ensuring flawless operations at our biopharmaceutical manufacturing plant in Slough, UK. Working as part of the CQV department, this role involves generating and executing commissioning and qualification lifecycle documentation in line with Good Manufacturing Practices (GMP), to commission and qualify equipment and utilities.You will be trained to execute commissioning and qualification activities for temperature-controlled equipment, automated manufacturing systems, sterilisation systems, and manual and automated cleaning methods in a biopharmaceutical manufacturing plant.This is an entry-level role for candidates who are keen to learn and grow into a CQV specialist field.Key responsibilities: Execution of commissioning and qualification lifecycle documentation in line with GMP, industry best practice and Lonza policy, for equipment and utilities that include: Temperature-controlled equipment Automated manufacturing systems SIP and CIP systems C