Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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. 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 company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's 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 and 2021. BMS Cruiserath Biologics is seeking to recruit on a permanent contract an experienced Engineering professional to join the Drug Product maintenance team. Reporting to the Manager, Drug Product Maintenance, the Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply 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 start-up 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 is a 24/7 shift role. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA's. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA's in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team's performance and equipment reliability. Champion a safety culture within the 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. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelor's 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 experience in Sterile 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. You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. #J-18808-Ljbffr
Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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 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 company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's 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. The Role BMS Cruiserath Biologics is seeking to recruit on a permanent contract Senior Shift Technician, Sterile Drug Product Maintenance, reporting to Manager, Sterile Drug Product Maintenance. The Senior Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply of medicines for our patients. The Senior 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 start-up and commercialization of the facility, including GMP readiness and New Product Introductions. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA's. Be the point of contact for the self-managed technician shift team. Providing a clear line of communication to the Maintenance Manager through covering key areas of Safety/Quality/Downtime/Delivery & People. Liaise with Manufacturing Shift Leads and respective Senior Shift Technicians to pull together summary at the end of shift. This role requires the Senior Shift Technician to facilitate handovers. Operating to and maintaining dynamic schedules - management of any changes to work plan through prioritization and managing last minute unforeseen changes to the plan. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA's in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team's performance and equipment reliability. Champion a safety culture within the Maintenance team. Driving and promoting Good Manufacturing Practices, Good Documentation Practices, and adherence with Standard Operating Procedures across the 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. Drive and participate in reliability initiatives: Continuous Improvement (CI) projects, Support Toolbox Talks, Predictive Maintenance, Failure Codes, Surface Imperfection, gasket management, correct torquing, spare parts, etc. Training, coaching and development of other technicians on key tasks such as On-The-Job Training (OJT) on Lockout Tagout (LOTO) /Soft Parts Change Out (SPCO)/Calibrations and upskilling on complex work order execution activities. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelor's 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 experience in Sterile 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. You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. #J-18808-Ljbffr
Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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 Ireland Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. Ireland is home to External manufacturing's global headquarters, responsible for the management of manufacturing contract operations (CMO's) and ensuring reliable supply of product to patients across the Bristol Myers Squibb global network. In Ireland, External Manufacturing has two sites; Global Headquarters based in Dublin 15 and a distribution centre in Shannon, Co Clare. Position Summary The Supply Chain and Cell Therapy Data Enablement team within Business Insights and Technology (BI&T) partners with the Bristol Myers Squibb GPS organization to design, develop, and operationalize priority data products along with building AI/Gen AI and Decision Intelligence capabilities. This is a critical role for driving impactful data-driven solutions, enabling efficient decision-making, and ensuring seamless integration of advanced analytics and AI into operational workflows. Key Responsibilities Architectural Design and Technology Selection Drive the architectural design and implementation of foundational data products to address global challenges in Product Development, Manufacturing, and Supply Chain operations. Design and model new data enablement projects to enable data scientists to get insights from data. Architect scalable enterprise data lake and analytics solutions using AWS managed services. Gather business requirements and come up with design models for data products. Architect end-to-end frameworks to enable seamless integration and management of ML models and AI-powered solutions. Leverage data engineering expertise to design and implement robust data pipelines for ETL data from diverse sources into cloud environments. Implement serverless and distributed computing solutions to support data workflows and analytics requirements. Technical point of contact for AWS services and support technical teams to resolve issues. Optimize cloud resource utilization and costs while ensuring performance and scalability for data workloads. Review code built by technical team, provide feedback, and fix issues. Build Data Products using AWS cloud services. Own and maintain git repositories for code base. Translate business objectives into strategic architectural solutions. Develop and implement sustainable design patterns and best practices. Evaluate and select appropriate tools and technologies. Ensure consistent quality and timeliness in the delivery of data products. Collaboration and Stakeholder Engagement Work with BIT teams (US, EU, India) to develop, implement and enforce best practices. Contribute to implementing best practices relating to Software Engineering, DevOps, and DataOps. Engage a broader community to help educate stakeholders on the use of data products. Support a culture of analytics and fact-based decision making. Understand and drive adherence to all BMS operating policies. The role could expand over time to include a wider range of applications. Qualifications & Experience Minimum Qualifications Minimum of 4-5 years of experience in information technology field in developing AWS cloud native data lakes. Bachelor's degree in computer science, information systems, computer engineering, or equivalent is preferred. Hands-on experience in building data products using AWS services. Experience with cloud-based environments (AWS, Azure, etc.) Significant experience with work information process tools and data-related tools. Hands-on expertise in Python and SQL. Expert with Github. Excellent communications and presentation skills. Ability to architect analytic and data science solutions. Experience in working in geographically dispersed teams. Experience Excellent interpersonal, collaborative, team building, and communication skills. Exceptional analytical skills with substantial knowledge of data engineering. Exceptional written and verbal communication skills. Ability to quickly gain and apply functional area specific knowledge. Ability to learn new tools and skills quickly. Experience in the pharmaceutical development, manufacturing or supply chain space. Experience interpreting analytical results and ascertaining implications to the business. Experience interacting with business stakeholders. Exceptional creative problem-solving skills. Ability to work with diverse teams across organizational lines. 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. You'll get a competitive salary and a great benefits package. #LI- Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This includes site-essential, site-by-design, field-based and remote-by-design jobs. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, direct your inquiries to adastaffingsupport@bms.com. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. #J-18808-Ljbffr
Location field must contain 'city, state' or a zip code to perform a radius search (e.g., Denver, CO or 46122 ). City and state must be separated by a comma followed by a space (e.g., Houston, TX ) Bristol Myers Squibb Shift Technician, Sterile Drug Product Maintenance in Cruiserath, Ireland Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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. 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, the 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 company's first European biologics manufacturing facility. This state-of-the-art facility will produce multiple therapies for the company's growing biologics portfolio. 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 and 2021. BMS Cruiserath Biologics is seeking to recruit on a permanent contract an experienced Engineering professional to join the Drug Product maintenance team. Reporting to the Manager, Drug Product Maintenance, the Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply 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 start-up 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. This is a 24/7 shift role. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA's. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA's in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team's performance and equipment reliability. Champion a safety culture within the 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. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Bachelor's 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 experience in Sterile 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. You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. Company: Bristol-Myers Squibb Updated: 2025-03-30 04:44:36.851 UTC Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr
Day Maintenance Technician, Sterile Drug Product Maintenance Day Maintenance Technician, Sterile Drug Product Maintenance Apply locations Cruiserath - IE time type Full time posted on Posted 3 Days Ago job requisition id R1590643 Working with Us Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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. The Role BMS Cruiserath Biologics is seeking an experienced Engineering professional to join the Drug Product maintenance team. Reporting to the Manager, Drug Product Maintenance, the Day Maintenance Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply of medicines for our patients. The Day Maintenance 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 start-up 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 Day Maintenance 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. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP’s), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA’s. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA’s in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team’s performance and equipment reliability. Champion a safety culture within the 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. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelor’s 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 experience in Sterile 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. You’ll get a competitive salary and a great benefits package including, but not limited to, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. BMSBL #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. #J-18808-Ljbffr
Location field must contain 'city, state' or a zip code to perform a radius search (e.g., Denver, CO or 46122 ). City and state must be separated by a comma followed by a space (e.g., Houston, TX ) Bristol Myers Squibb Senior Shift Technician, Sterile Drug Product Maintenance in Cruiserath, Ireland Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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. The Role BMS Cruiserath Biologics is seeking to recruit on a permanent contract Senior Shift Technician, Sterile Drug Product Maintenance, reporting to Manager, Sterile Drug Product Maintenance. The Senior Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply of medicines for our patients. The Senior 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 start-up 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 Senior 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. This is a 24/7 shift role. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA's. Be the point of contact for the self-managed technician shift team. Providing a clear line of communication to the Maintenance Manager through covering key areas of Safety/Quality/Downtime/Delivery & People. Liaise with Manufacturing Shift Leads and respective Senior Shift Technicians to pull together summary at the end of shift. This role requires the Senior Shift Technician to facilitate handovers. Operating to and maintaining dynamic schedules - management of any changes to work plan through prioritization and managing last minute unforeseen changes to the plan. Manage CMMS 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 diagnosis and fault-finding of automation and controls. Respond promptly and appropriately to any equipment failures/issues that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA's in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team's performance and equipment reliability. Champion a safety culture within the Maintenance team. Driving and promoting Good Manufacturing Practices, Good Documentation Practices, and adherence with Standard Operating Procedures across the 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. Drive and participate in reliability initiatives: Continuous Improvement (CI) projects, Support Toolbox Talks, Predictive Maintenance, Failure Codes, Surface Imperfection, gasket management, correct torquing, spare parts, etc. Training, coaching and development of other technicians on key tasks such as On-The-Job Training (OJT) on Lockout Tagout (LOTO) /Soft Parts Change Out (SPCO)/Calibrations and upskilling on complex work order execution activities. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Bachelor's 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 experience in Sterile 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. You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. Company: Bristol-Myers Squibb Updated: 2025-03-30 04:44:36.850 UTC Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr
Bristol Myers Squibb Day Maintenance Technician, Sterile Drug Product Maintenance in Cruiserath, Ireland Working with Us Challenging. Meaningful. Life-changing. Those aren't 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. You'll 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. The Role BMS Cruiserath Biologics is seeking an experienced Engineering professional to join the Drug Product maintenance team. Reporting to the Manager, Drug Product Maintenance, the Day Maintenance Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply of medicines for our patients. The Day Maintenance 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 start-up 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 Day Maintenance 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. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA's. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA's in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team's performance and equipment reliability. Champion a safety culture within the 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. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Bachelor's 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 experience in Sterile 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. You'll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. Company: Bristol-Myers Squibb Updated: 2025-03-30 04:44:36.850 UTC Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr
Shift Technician, Sterile Drug Product Maintenance Shift Technician, Sterile Drug Product Maintenance Apply locations Cruiserath - IE time type Full time posted on Posted 3 Days Ago job requisition id R1590642 Working with Us Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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. 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 company’s first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. 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 and 2021. BMS Cruiserath Biologics is seeking to recruit on a permanent contract an experienced Engineering professional to join the Drug Product maintenance team. Reporting to the Manager, Drug Product Maintenance, the Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply 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 start-up 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 is a 24/7 shift role. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP’s), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA’s. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA’s in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team’s performance and equipment reliability. Champion a safety culture within the 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. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelor’s 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 experience in Sterile 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. You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. BMSBL #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference. #J-18808-Ljbffr
Senior Shift Technician, Sterile Drug Product Maintenance Senior Shift Technician, Sterile Drug Product Maintenance Apply locations Cruiserath - IE time type Full time posted on Posted 3 Days Ago job requisition id R1590640 Working with Us Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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. The Role BMS Cruiserath Biologics is seeking to recruit on a permanent contract Senior Shift Technician, Sterile Drug Product Maintenance, reporting to Manager, Sterile Drug Product Maintenance. The Senior Shift Technician will assist in delivering a safe working environment for our colleagues and a reliable plant to ensure continuity of supply of medicines for our patients. The Senior 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 start-up 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 Senior 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 is a 24/7 shift role. 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 are executed in compliance with all Regulatory requirements including Quality (cGDP/GMP’s), EHS, Global Engineering procedures, as well as all Local Regulatory requirements. Understand and interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs. Use your knowledge of sterile fill/finish process equipment to support Manufacturing, Quality, Automation, Validation, and EHS for deviation investigation, change controls, and CAPA’s. Be the point of contact for the self-managed technician shift team. Providing a clear line of communication to the Maintenance Manager through covering key areas of Safety/Quality/Downtime/Delivery & People. Liaise with Manufacturing Shift Leads and respective Senior Shift Technicians to pull together summary at the end of shift. This role requires the Senior Shift Technician to facilitate handovers. Operating to and maintaining dynamic schedules - management of any changes to work plan through prioritization and managing last minute unforeseen changes to the plan. Manage CMMS 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 that may arise and provide guidance and solutions for preventative action where required. Execute planned maintenance routines including predictive, preventative and calibration activities. 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 support all deviations, change controls CAPA’s in a timely manner. Work with 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 the site long range planning. Work to meet site metrics reflective of team’s performance and equipment reliability. Champion a safety culture within the Maintenance team. Driving and promoting Good Manufacturing Practices, Good Documentation Practices, and adherence with Standard Operating Procedures across the 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. Drive and participate in reliability initiatives: Continuous Improvement (CI) projects, Support Toolbox Talks, Predictive Maintenance, Failure Codes, Surface Imperfection, gasket management, correct torquing, spare parts, etc. Training, coaching and development of other technicians on key tasks such as On-The-Job Training (OJT) on Lockout Tagout (LOTO) /Soft Parts Change Out (SPCO)/Calibrations and upskilling on complex work order execution activities. Qualifications, Knowledge and Skills: Required A multi-skilled individual with craft qualification in 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 facility is required. Proven ability to prioritize maintenance activities and resources to achieve a safe and reliable site. Experience of operating and faultfinding PLC based control systems. Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufacture. Excellent communication skills and the ability to work as part of a multi-disciplined, cross functional team. High level of attention to detail in following procedures and must be flexible and open to change. Experience maintaining complex equipment in fast paced environment. Demonstrated experience and ability to effectively manage stakeholders. Desired Bachelor’s 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 experience in Sterile 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. You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. BMSBL #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. #J-18808-Ljbffr
Specialist, Site Support & Logistics Planning Apply locations Shannon - IE time type Full time posted on Posted 5 Days Ago job requisition id R1587552 Working with Us Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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. The Role BMS External Manufacturing is looking to recruit a Specialist, Site Support & Logistics Planning to be based in Shannon. This is a 12-month fixed term contract role. Key Duties and Responsibilities: Logistics Planning Manages the planning of Transportation Movements with BMS approved transportation companies and storage facilities, on behalf of ExM from all sites (CMOs, DCs, Intercompany etc) for EMEA/APAC. Manages, resolves issues, implements improvements and ultimately fosters relations between CMO’s and BMS approved transportation companies. Manages transportation redeployments to markets and returns to manufacturing sites. Assist with the Investigation, and successful resolution, of Transportation & Distribution incidents on behalf of ExM in Infinity. Utilises the LIR Tool to facilitate the investigation of Transportation and Distribution Incidents. Ensures that Logistics are managed in the most efficient and cost effective manner by utilising OPEX tools to drive Continuous Improvement to meet, and exceed customer expectations. Assists with reviewing, analysing and authorising Vendor Logistics Invoices. Site Support Support Facility Management Company and create online requests for Shannon facility. Support Site Leader by organising Site repairs and maintenance with vendors. Support the Procurement Group by obtaining quotes from suppliers within the Shannon Facility. Raise electronic requisitions which in turn converts into a Purchase Order/Service Order. Follow up on Invoice queries and pricing issues relating to these PO/SO’s. Update training file for all contractor training completed. Process small parcel shipments and Provide details to requestors. Ensuring all SOP’s are adhered to at all times. Update Electronic Visual Display from HR Connect each Week. Perform receptionist duties including first point of contact for visitors to the site. Qualifications, Knowledge and Skills Required: Creates and maintains strong working relationships within the BMS organisation and externally with customers, BMS approved transportation companies & CMOs. Self-driven with a strong customer focus and possess skillset to work on own initiative within a team environment to drive issues to resolution. Ability to translate technical issues into business impact and relevant solutions. Appreciation of performance metrics and their value in influencing Supply Chain results. Must have knowledge of and model the BMS core behaviours. Proactive and positive attitude. Working Knowledge of SAP, Ariba, Microsoft Packages, Outlook, & Web based Applications. Ability to work in a diverse, cross functional team. Ability to prioritise, organize and manage multiple tasks to tight deadlines. Interact with key stakeholders both Internal & External. Enhance the ability to work and manage in a complex matrix organization. Excellent interpersonal, communication, negotiation, analytical & presentation skills. Proven ability to prioritise, organise and manage multiple tasks to tight deadlines. Knowledge of GMP & GDP. Qualification in Logistics, Supply Chain or similar would be advantageous. 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. You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days of annual leave and life assurance. #LI-Onsite If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science,” every BMS employee plays an integral role in work that goes far beyond ordinary. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. #J-18808-Ljbffr
