Job Description
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 isseekingto recruit a permanent Specialist,Upstream Manufacturing within the Manufacturing Operations group.Reporting to the Shift Lead, the Upstream Bioprocess Associate will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment.This is a 24/7 shift role. Key Duties and Responsibilities: Execution of commercial manufacturing processes according to established work instructions Creationand updateof operating procedures & other relevant documentation for large scale manufacturing Operating production equipment within the assigned functional area Adhering to Good Manufacturing Practices and Standard Operating Procedures Taking part in investigations andoptimisationof processes using scientific,engineeringand lean principles Proficient use of process automation systems (i.e.Delta V andSyncadeInteractions, OSI/Pi Historian) and some supporting business systems (i.e.SAP,Infinity, Maximo etc.) Assistingwith review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activities Working with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams tofacilitatethe implementation of the project design,validationand operation of the MPCC manufacturing facility Engaging in and supporting a?culture of continuous improvement and operational excellence through ownership of improvement for work processes,equipmentand a safe working environment Qualifications, Knowledge and Skills Required: Youpossessa minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g.cGMP, ISO or similar cleanroom industry experience strongly preferred) You have 3+ years working experience in a large-scale biopharmaceutical manufacturing facility You have experience with Delta V and MES or similar control and data acquisition systems You can demonstrate an ability to work independentlyand alsoas part of a team. You have a demonstrated problem-solving ability and the ability to adhere to scheduled timelines You have excellent communication skills and the ability to work in a cross-functional,collaborativeand fast-paced environment Due to the nature of the manufacturing role, shift work will berequiredas the siteoperatesa24/7 mode of operations. 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, life assurance and on-site gym Skills: 3+ years with large scale biopharmaceutical manufa Specialist Upstream Manufacturing