As a quality and compliance expert, you will be responsible for ensuring that GxP systems and processes adhere to the applicable regulatory requirements throughout the entire system lifecycle. Therefore, you stay up to date about evolving regulations from authorities such as the EMA and FDA and industry standards like GAMP and ISO. Depending on your role and expertise, you may be asked to provide Quality & Compliance support during audits and inspections, or to join a Sopra Steria validation service team.
Are you a technically skilled engineer with a passion for pharmaceutical processes? As a Project Engineer, you will contribute to various engineering projects. You’ll be responsible for the full project lifecycle of specific installations or equipment: from specification and procurement to installation, validation, and handover to operations. You’ll work in multidisciplinary teams, monitor planning and budget, and ensure safe, compliant, and efficient execution. You’ll also be part of creating technical solutions and be included in the technical follow-up with suppliers. You take ownership of your scope, communicate proactively with stakeholders, and contribute to continuous improvement.