Ref. 1336 \- and your Curriculum Vitae (CV) to **recrutamento@bluepharma.pt**. #### **Main Responsibilities** * Active participation in sterile drug manufacturing operations in classified areas, strictly complying with current Good Manufacturing Practices and safety procedures; * Prepare, assemble, and operate sterile equipment (e.g., filling systems, lyophilizers, isolators, autoclaves, etc.); * Support the transfer and execution of formulation processes, including compounding, aseptic filling, and process controls; * Record all activities, ensuring traceability and documentary compliance; * Contribute to process optimization by identifying opportunities for improving efficiency and robustness; * Collaborate with production, quality, and development teams. #### **Requirements** * Academic background in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Biotechnology, or related field; * Professional experience in the pharmaceutical industry, preferably in sterile injectable production (an asset); * Knowledge of aseptic techniques and manufacturing practices in classified areas; * Availability to work in shifts; * Proficiency in English (spoken and written); * Computer literacy; * Accuracy, attention to detail, and sense of responsibility; * Good communication skills and ability to work in a team.