Sr. Specialist, CTO Site Supply Chain Compliance

4 weeks ago

Summit, United States Bristol-Myers Squibb Full time

Working with UsChallenging. Meaningful. Life-changing. Those arent 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. Youll 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. Read more: careers.bms.com/working-with-us.Position SummaryThe Sr. Specialist, Site Supply Chain Compliance is responsible for the coordination, communication, management and support of various projects and information within the Site Supply Chain Compliance Team. The position has analytical and documentation responsibilities across CTO SMW Site Supply Chain to maintain a compliant, effective, and efficient operation that meets business needs. The Sr. Specialist will manage and coordinate Global & Change Controls, Deviations & CAPAs across the site.Key ResponsibilitiesWork within a team of approximately 3-4 people, that encompasses subject matter experts in various supply chain compliance activities (i.e., Audit Action Items, Deviation / CAPA management, Documentation ownership & required updates, etc.)Collects, analyzes, and reports key information impacting the department.Lead cross-functionally to support the training requirements associated with deviations, change controls, and CAPAs using a process-based approach.Assist in the implementation of departmental business processes for the regular oversight of quality records including KPIs, investigations, and cross-functional forums to drive end-to-end solutions.Lead a team responsible for the oversight and management of the quality documentation processes including but not limited to supply chain change controls, CAPAs and deviations.Manage projects and compliance initiatives which directly support network and GxP initiatives, to effectivity implement strategic business objectives in driving quality, compliance, and safetyEnsures that CAPAs are issued, investigated, root cause is determined/documented and that they are closed on time with appropriate and effective corrective action/resolutionsSupport the creation of storyboards for key supply chain events for use in GMP audit and inspectionsDevelop, and author GMP SOPs, work instructions and training guides for supply chain processesKey contributor for project related Change Control Review Board (CCRB) impacting site operationsSupports investigations and CAPA requests associated with warehouse process and ensure that the training remains in alignment Promote a mindset of continuous improvement, problem-solving and preventionBuild and maintain positive relationships with all functions at the S12 site, as well as with external customers and stakeholders.Performs other tasks as assigned.Qualifications & ExperienceBachelors degree in supply chain, engineering, life sciences, business management or related fields; advanced degree preferred.10+ years relevant work experience within a regulated pharmaceutical manufacturing environment7+ years direct experience in business system implementation including project planning, change control and user acceptance testing (UAT)Independent decision-making capability and ability to think conceptually and understand impact of decisionsCapable of balancing multiple projects and prioritize deadlines within the teamDemonstrated high level of verbal and written communication skillsAn equivalent combination of education, experience and training may substitute.BMSCARTVETERAN#LI-HybridIf you come across a role that intrigues you but doesnt 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.On-site ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in 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.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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