Specialist I, Manufacturing Compliance & Support

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. Background The Specialist, Manufacturing Compliance & Support contributes in a team that directly support Manufacturing floor operations. The Manufacturing Compliance team is a part of the overall manufacturing team and is organized around floor-enabling deliverables through compliance programs, quality systems, training, finite scheduling and equipment lifecycle support. We are looking for multiple specialist positions at different levels within this team. Responsibilities · Provide front line support for manufacturing operations · Investigates and coordinate the resolution of deviations through use of Root Cause Analysis tools and product impact assessments. · Support manufacturing continuous improvement projects · Collaborating with appropriate stakeholders to write and/or revise applicable SOPs, batch records, and other operational related documents · Conducts technical training for manufacturing operations · Other tasks and duties as assigned by Management Experience & Qualifications The ideal candidate for this position of Manufacturing Compliance and Support Specialist is highly skilled flexible worker with strong people skills and an extensive background in cGMP manufacturing. · Bachelor’s or Master's degree in sciences (for instance: Biochemistry, Life Science & Technology, Biology). · A minimum of 3 years of cGMP production experience · Sound knowledge and understanding of process, documentation requirements, systems and equipment to troubleshoot problems and provide solutions to management · Knowledgeable of Current Good Manufacturing Practices (cGMPs) · Expert knowledge of electronic quality systems. · Knowledge of equipment and systems related to manufacturing operations (i.e., MES, eBR, Sepax, CliniMACs, LOVO, etc.) · Experienced in providing and assessing performance related to manufacturing operation technical training Skills · Excellent verbal, technical writing and interpersonal skills · Excellent communication skills in English, both written and spoken · Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities · Ability to work efficiently and accurately on multiple projects simultaneously to meet set goals and timelines. Around 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.