About this role
For an international pharmaceutical organization, we are looking for a QC Technician III. This full-time role is focused on performing laboratory testing, data review, and quality support activities within a GMP-regulated environment. What are you going to do? As a QC Technician III, you will perform sampling and testing activities for quality monitoring programs and support validation, development, stability, and cGMP projects. You will ensure accurate and timely results while maintaining compliance with quality and EH&S requirements. You will also support analytical data review and laboratory incident investigations. - Perform sampling and laboratory testing activities; - Execute QC testing for validation, development, and stability programs; - Review analytical data and laboratory documentation; - Support laboratory investigations and incident reporting; - Maintain protocols, logbooks, and reports; - Support equipment maintenance and calibration; - Contribute to continuous improvement of QC processes; - Ensure compliance with cGMP, quality, and EH&S standards. What do we offer? - Full-time position of 40 hours per week; - Contract for 6 months; - Start date: 9th of July; - Salary: €19.23 gross per hour, excluding weekend shift; - 25 vacation days and 8,33% holidays allowance on top; - Pension accrual from your first working day; - Travel expense reimbursement; - Access to the Adecco Academy with more than 150 online training courses and development programs; - Monday to Friday between 07:00–09:00 and 16:00–18:00 and weekend duty: Once every 4 weeks (Saturday and Sunday), followed by a shortened workweek (Tuesday–Friday) the following week. Where will you work? You will be working for an international pharmaceutical organization committed to delivering high-quality products that improve patients' lives worldwide. What do we ask? - MLO diploma or equivalent laboratory education; - Good command of English, both written and spoken; - Experience in a GMP-r