Senior Automation Engineer (Delta V Engineer)

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS's continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.PURPOSE AND SCOPE OF POSITION:The incumbent will be responsible for the operational readiness of the process automation applications within the CTDO process scale-up facilities used in the manufacture of Cell Therapies for GMP and Non-GMP activities.Responsibilities will include:Troubleshooting, resolution and improvement of automation applications, including batch and continuous control as well as MS operating system and control system interfaces including Data Historian, Backups and Alarm PagingProviding automation expertise for assigned projects led by Engineering functionsMaintaining life cycle management of control system and documentation within applicable procedural documents and industry guidance.Lead use of new automated technologies into the clinical site, serve as SME for DeltaV process changes and OSI Pi process data monitoring dashboards.Build, troubleshoot and maintain recipes in accordance with local process and procedures.The incumbent is expected to communicate and partner with other groups such as, Project Engineering, ECQ, IT, Quality, & Manufacturing as well as interface with Site Engineering and outside contractors as needed.Incumbent is responsible for handling all activities with strict adherence to department procedural documents, current Good Manufacturing Practices and process safety programs.The individual must possess understanding of equipment, facilities, systems and unit operations used in the manufacturing of Cell Therapies and knowledge of computerized system life cycle development (SDLC)The successful candidate will be expected to multi-task numerous activities, as well as, be self-directed, lead and drive the completion of project deliverables. Proficiency in managing external resources is required.Ensure safe and compliant cGMP operations;Maintain permanent inspection readiness and actively support regulatory inspections.Interface with regulatory authorities as required to support Manufacturing Operations audits.Foster a culture of compliance and strong environmental, health, and safety performance.Design and execute test plans and other risk mitigation exercise as part of investigations (e.g. Root cause analysis and CAPAs)Support Clinical Production Activities;Support production related investigations, ensuring compliance with internal standards and regulatory requirements.Build, troubleshoot and maintain recipes. Review and revise the content of Delta V documentation (e.g. investigations, changes, SOPs and work practices)Continuously monitor, anticipate and permanently resolve issues that may arise during production.Interface with operators and serve as Delta V SME. Learn the procedures, analytics and document any known sensitivity.Work closely with Engineering /Maintenance on the design and implementation/upgrade utilizing Delta V related to production process needsInteract with other teams including Validation, Development, Operations, and QADisplay Leadership Qualities;Create an environment of teamwork, open communication, and a sense of urgencySupport the change agent in promoting flexibility, creativity, and accountabilitySupport organizational strategic goals and objectives that are linked to the overall company strategyDrive strong collaboration within the plant and across the networkBuild trust and effective relationships with peers and stakeholdersDeliver results through timely and quality decision making and advicePromote a mindset of continuous improvement, problem solving, and preventionREQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:Proficiency with Emerson DeltaV, OSI Pi, MS operating system, MS SQL, Excel, DCS, PLC, SCADA, HMI and Word is highly desired.Experience in a manufacturing environment, and expert knowledge of applicable cGMP, GAMP, OSHA requirements and multi-national biopharmaceutical/cell therapy regulations is required.Deep knowledge of facility/clean room design, process, equipment, automation, and validation is highly desirable.Excellent verbal and written communication skills and strong attention to detail is required.Education and Experience:BS in engineering or equal is required.Minimum 5-10 years' experience required. Level is commensurate with experience.WORKING CONDITIONS (US Only):This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.If you want to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients' lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.BMSCARTAround the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.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.Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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