Description

In this role, you will engage in hands-on laboratory work, executing and reporting on pharmaceutical process development studies. Your day-to-day responsibilities will involve planning experiments, documenting results, and ensuring compliance with quality and safety standards.

Requirements

• •Science or engineering degree (MSc) in a relevant discipline, or training as lab technician, or equivalent
• •Knowledge in fill and finish process for parenteral pharmaceutical products, ideally experience in process development lab
• •Very good knowledge of reporting, interpretation and documentation of scientific results
• •Good communication skills
• •Excellent communication skills with excellent command of English, written and spoken

Tasks

• •Execute small scale pharmaceutical process development studies in the laboratory
• •Report on mixing hold time, VHP stress, filtration, filling behavior, and lyophilization studies
• •Support the installation, qualification, and maintenance of equipment and lab for pharmaceutical development
• •Plan and perform pharmaceutical development studies for liquid and lyophilized parenteral drug products
• •Document data according to lab procedures and data integrity standards
• •Evaluate results and summarize findings in short reports
• •Implement and execute analytical tests for pharmaceutical development
• •Manufacture non-GMP drug product samples for stability studies and preclinical use
• •Apply aseptic working techniques during manufacturing processes
• •Ensure compliance with GMP qualifications, documentation, and material handling
• •Adhere to health and safety standards

Benefits