Senior Specialist Compliance Process Excellence, Commercial Operations

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. Ensures GMP compliance within Manufacturing by owning documentation, quality events, risk assessments, and inspection readiness activities. The role supports deviation management, change control and audit responses while contributing to defect library training and Communities of Practice. Through hands‑on execution and collaboration, the position supports continuous improvement and sustained regulatory compliance. Duties/Responsibilities GMP Manufacturing Documentation & Training * Author and maintain manufacturing GMP documentation, including SOPs, forms, and logbooks * Act as document owner, ensuring lifecycle management and compliance Manufacturing Quality Events & Compliance Processes * Initiate and own activities from initiation to closure for: * Actions coming form the QMS (e.g. CAPA, Proactive initiatives, standalone actions, Supplemental Actions, Change Action...) * Change Controls * Findings arising from self-inspections * Quality event without root cause analysis * Initiate and own deviations from creation through deviation assessment * Participate to deviation investigation when needed * Initiate Supplier Corrective Action Requests (SCARs) * Participate to Communities of Practice (CoPs) Risk Management * Own, perform, and maintain risk assessments, including: * Manufacturing Risk Assessments * Data Integrity Risk Assessments (DIRA) and associated summary reports Defect library * Participate to staff training to the defect library Audit & Inspection Readiness * Act as Manufacturing SPoC for inspection readiness, * Actively contribute to manufacturing inspection-readiness * Continue to responses coming from audit observations and inspection findings Continuous Improvement * Support local continuous improvement initiatives related to compliance, process effectiveness, and inspection readiness * This job description is not intended to be exhaustive; additional duties and responsibilities may be assigned as needed to meet business requirement. Qualifications * Bachelor’s degree in Life Sciences or related field * 3-5 years in GMP compliance * Good collaboration and communication skills * 3-5 years of experience in pharmaceutical environement * Business Level in French and English * Experience in GMP inspections and audits If 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 Careers With 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 a supportive culture, promoting global participation 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. On-site...