Senior Manager, Manufacturing Shift Lead, Downstream ManufacturingWorking 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.
Position Summary BMS Cruiserath Biologics is seeking to recruit a permanent Downstream Shift Lead within the Manufacturing Operations group. Reporting to the Associate Director, the role will support the ongoing manufacturing operations within the facility, as well as qualification activities for new processes and equipment.
This is a 24/7 shift role. Key Responsibilities Manage, develop and mentor the Upstream shift team.Engage the shift team to deliver manufacturing schedule requirements while maintaining a culture of compliance, safety and innovation.Provide critical communications upwards and downwards within the organization.Work with manufacturing teams to develop and generate Standard Operating Procedures and Training documentation required to enable Upstream Manufacturing start-up operations and complete training on same.Act as an Upstream manufacturing SME for all technical issues on the process and escalate as appropriate.Support and carry-out process-related investigations and assist in QA audit activities.Lead cross-functional teams and operational meetings.Act as Incident Controller for the site during adverse or emergency events.Drive Right-First-Time execution on shift & front-line support/resolution of manufacturing issues.Role model and support a culture of continuous improvement and operational excellence.Ownership and promotion of improvement projects for manufacturing work practices and a safe working environment by application of sound scientific, engineering and lean principles.Role model of the BMS behaviors and Safety culture.Qualifications & Experience The successful candidate must possess a Bachelor/Masters in Engineering, or Science related subject.A minimum of 5 years' management experience in process operations together with previous supervisory experience in an automated bio pharmaceutical manufacturing facility.Project management, technical transfer and validation experience are desirable.Ability to adapt to a changing environment and handle multiple priorities.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
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