Biologics Maintenance Engineer

Biologics Maintenance Engineer Team Horizon is seeking a Biologics Maintenance Engineer for a leading pharmaceutical company based in Athlone. The Biologics Maintenance Engineer is responsible for the managing the routine and non-routine maintenance activities carried out by the maintenance technicians. This includes all Upstream and Downstream production equipment and systems. This position is also responsible for the planning, co-ordination and scheduling of maintenance works performed by service vendors in a DS environment. The individual in this position is expected to represent the company interests, objectives and policies in a professional and responsible manner. This role will report into the Biologics Engineering Manager in the area and will offer scope for both personal and career development. Why you should apply: • Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work. • This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses. • Excellent contracting rates on offer. What you will be doing: • Proactively ensuring that all EHS responsibilities are carried out according to regulations and procedures including Risk Assessments, RAMS and safety GEMBAs. • Provide support to new equipment installations and product introductions. • Maintaining the Maintenance Quality System by adherence to all relevant SOP’s, policies and cGMP requirements. • Plan and coordinate scheduled and unscheduled maintenance tasks in accordance with site policies and procedures. • Maintaining spare parts, change parts and equipment both within the DS facility and in the Engineering Stores. • Ensure the Maintenance Management System is maintained correctly. • Utilising and maintaining IT systems as required, e.g. Computerized Calibration Systems and Computerized Maintenance Management Systems. • Leading shift-handovers and reporting issues using a Tier-meeting approach. • Provide support to Operations, Validation, Engineering and Quality where required. What you need to apply: • Associate Degree &/or certification in a mech, elec or related field is required. • 3-5 years experience in an appropiate cGMP commercial manufacturing environment, preferably with experience on upstream (cell culture) and downstream purification. • Prior hands-on experience with CMMS and Computerized Calibration Systems. • Prior experience with Quality Management Systems. High level of interpersonal, communication and technical problem-solving skills. • Demonstrable knowledgeable of cGMP for process equipment, instrumentats and calibration. Knowledge of Six Sigma and lean systems is an advantage. • Ability to make informed and timely decisions that take into account the facts, goals, constraints, and risks associated. • A team player with a can do, pro-active attitude and a passion for improvement