Description
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.