Job Description
Specialist, Upstream ManufacturingApply locations Cruiserath - IE time type Full time posted on Posted Yesterday job requisition id R1586196Working with UsChallenging. 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 RoleBMS Cruiserath Biologics is seeking to 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 instructionsCreation and update of operating procedures & other relevant documentation for large scale manufacturingOperating production equipment within the assigned functional areaAdhering to Good Manufacturing Practices and Standard Operating ProceduresTaking part in investigations and optimisation of processes using scientific, engineering and lean principlesProficient use of process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP, Infinity, Maximo etc.)Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activitiesWorking with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation and operation of the MPCC manufacturing facilityEngaging in and supporting a culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and a safe working environmentQualifications, Knowledge and Skills Required:You 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)You have 3+ years’ working experience in a large-scale biopharmaceutical manufacturing facilityYou have experience with Delta V and MES or similar control and data acquisition systemsYou can demonstrate an ability to work independently and also as part of a team.You have a demonstrated problem-solving ability and the ability to adhere to scheduled timelinesYou have excellent communication skills and the ability to work in a cross-functional, collaborative and fast-paced environmentDue to the nature of the manufacturing role, shift work will be required as the site operates a 24/7 mode of operations.Why you should applyYou will help patients in their fight against serious diseasesYou 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-OnsiteIf 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 CareersWith 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