Engineer

Study of Octapharma's production processes (internship at other Octapharma production sites); Support of project activities related to the department's operations according to the project schedule: approval of project documentation (User Requirement Specifications (URS), layouts, P&ID, technical and functional specifications), proposing ideas for optimization and improvement; Support of equipment acceptance and qualification processes: participation in FAT, SAT, IQ, OQ, and PQ, approval of protocols and reports; Continuous deepening of knowledge and expertise in fractionation processes and equipment; Implementation of Octapharma production processes at the new plant in full compliance with GMP requirements; Development and maintenance of up-to-date technological documentation; Support in conducting technology transfer for Octapharma products; Development and approval of SOPs, work instructions, and completed forms related to the department's activities; Training of production personnel on equipment operation and production methods in accordance with GMP requirements; Monitoring of production operations for compliance with technological instructions, production recipes, safety instructions, SOPs, and GMP requirements.

Requirements

Higher education in natural sciences, preferably in chemistry, biology, pharmacy, biotechnology, pharmaceutical, or chemical technology. At least 2 years of experience in GMP and production (preferably in the pharmaceutical industry). Experience with tank equipment, pressure vessels, and industrial chromatography will be an advantage. Special requirements for the candidate: Intermediate level of English (B1 level and above). Knowledge of EU and EAEU GMP requirements and guidelines.

Higher education — Bachelor's degree; Experience: 2 years