studies You witness development and validation studies You follow-up the sampling & testing plan with production and laboratories You evaluate study data results and write reports for the executed studies Execute process changes to APIs, excipients, primary packaging, and product contact materials and manage component specifications and qualifications of primary packaging components and product contact materials Assist the quality and production department in handling deviations, and executing the investigations and activities for problem solving and corrective and preventive actions Assist the Pharmaceutical Technical Operations (PTO) department in compliance driven activities such as the continued process verification program and annual product review Report into the PTO lead Requirements Master in scientific degree Relevant experience in pharmaceutical Formulation & Filling processes Knowledge of sterile drug product manufacturing technologies The ability to work on a project base and within team of technical experts Advanced knowledge of English (talking/writing/reading) Technical writing skills Problem solving skills Analytical mindset and project-minded Process and data driven Flexible/Committed Autonomous Team player/Collaborative On-the-floor approach STARGROUP
