Specialist, Downstream Manufacturing (Downstream Bioprocess Associate)

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. 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: careers.bms.com/working-with-us. The Role BMS Cruiserath Biologics is seeking to recruit a Specialist, Downstream Manufacturing (Downstream Bioprocess Associate) within the Manufacturing Operations group. Reporting to the Senior Manager, Downstream Manufacturing Shift Lead, the Specialist, Downstream Manufacturing will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for new product process’ and equipment where required. This is a 24/7 shift role. Key Duties and Responsibilities: * Working with the manufacturing operations group, QA teams, & the Automation reps to maintain high level and finite production schedules for the MPCC manufacturing facility. * Execution of commercial manufacturing processes according to established work instructions. * Adheres to Good Manufacturing Practices and Standard Operating Procedures. * Takes part in investigations and optimisations of processes using scientific, engineering and lean principles. * Operates all production equipment within the assigned functional areas. * Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise/ Veeva Vault, Maximo etc.). * Assists with real time reviewing of batch records for each manufacturing lot in conjunction with Quality representative and provide input to related investigations and QA audit activities. * Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment. Qualifications, Knowledge and Skills Required: * The successful candidate will ideally possess a 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) * Ideally possess 1-3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility * Experience with Delta V and MES would be considered an advantage. * The successful candidate must demonstrate an ability to work independently and also as part of a team. * The successful candidate must demonstrate problem solving ability and to adhere to scheduled timelines. * Excellent communication skills and the ability to work in a cross functional collaborative environment are required. Due to the nature of the manufacturing role, shift work will be required for 24/7 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. * You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, life assurance and on-site gym #LI-Onsite If you come across a role that intrigues you but doesn’t perfectly line up with your resume,...