Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:. Bristol Myers Squibb Ireland Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the companys first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the companys growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus. BMS Cruiserath has been awarded Biopharma Company of the Year 2019 in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022. The Role BMS Cruiserath Biologics is seeking an experienced Engineering professional to join the Drug Product maintenanceteam. Reporting to the Manager, Drug Product Maintenance,the Shift Technician will assist in delivering a safe working environment for our colleagues and areliableplant to ensure continuityofsupply of medicines for our patients. The Shift Technician will be tasked with initially supporting the facility during project phase, supporting equipment installation and commissioning - from initial specifications to final handover. Support will transition from project phase to operational phase to ensure a successful startup and commercialization of the facility, including GMP readiness and New Product Introductions. The Maintenance teams will also focus on complying with good engineering practices, company policies, regulations, and codes. The Shift Technician will also support their manager in ensuring that the Drug Product Maintenance teams objectives are aligned with the wider Engineering and Site Objectives. They will be part of a multi-functional team charged with commissioning of the significant capital investment and upon completion of the project, they will support the sustaining operation on site. This position will be initially on days but will move through various shift patterns as the project progresses to full commercial manufacture. Key Duties and Responsibilities: Work with the project & CQV team to facilitate delivery, validation, and safe operation of equipment associated with Vial/Syringe filling and inspection. Ensure any maintenance and calibration activities areexecuted in compliance with all Regulatory requirements including Quality (cGDP/GMPs), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/systemlayouts, wiringdiagrams,and specificationsinplanning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, andEHSfor deviation investigation, change controls, and CAPAs. ManageCMMS work requests/work orders, including generation, processing, tracking and follow-up. Ensuring all Work Orders are completed on time and in a safe and compliant manner, and asset management data is captured accurately. Assist in advanced troubleshooting, and repair of equipment and systems. Including, but not limited to, diagnosis and fault-finding of automation and controls. Respond promptly and appropriately to any equipment failures / issues thatmay arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibrationactivities. Understand and implement HSA and Safety requirements of Maintenance teams and how they apply in normal sustaining operations or major shutdown/overhaul situations. Collaborate with key stakeholders such as Manufacturing Operations, Manufacturing Planners and EHS. Work with Quality team ensuring the team supportalldeviations, change controls CAPAsinatimely manner. Workwith the EHS team to ensure Safety related Investigations and CAPAs are closed on time and with correct engineering rigor applied. Work with the Maintenance Manager to ensure the Production Planning schedule is cognizant of the maintenance requirements in the short, medium and long-term, ensuring major maintenance driven equipment outages are factored into thesite long range planning. Work to meet site metrics reflective of teams performance and equipment reliability. Championasafety culture withinthe Maintenance team. Assist the Maintenance Manager with any other maintenance work as per the business needs, including but not limited to development of training materials, vendor management, and other continuous improvement activities. Required Amulti-skilled individualwith craft qualificationin Electrical, Instrument or combined trades. Experience with a site start up and handover from CQV to Sustaining Operations, from a maintenance perspective. Experience in a regulated biopharmaceutical, pharmaceutical, medical device, facilities maintenance or FMCG facilityis required. Provenability to prioritize maintenance activities and resourcesto achieve a safeand reliable site. Experience of operating and faultfindingPLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and theability toworkas part of a multi-disciplined,cross functional team. High level ofattention to detailinfollowing procedures and must be flexible and open to change. Experience maintainingcomplex equipmentinfastpacedenvironment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelors degree in Engineering, Automation or equivalent experience in utilities or process controls, automation and/or information systems within manufacturing organizations in the Biotechnology or Pharmaceutical industries. Maintenance experienceinSterile Fill Finish. Why you should apply You will help patients in their fight against serious diseases You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. Youll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym Skills: Biotech or pharma manufacturing experience craft qualification in Electrical Instrument or combined trades