Bristol Myers Squibb: Quality Control Associate Iii, Cell Therapy

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.Position Overview:The primary focus of the Quality Control Associate III is to provide support for sample management and routine laboratory operations. This role is responsible for performing and coordinating sample accessioning, testing, shipping, and data handling. Primary ResponsibilitiesCoordinate the logistics of sample receipt, internal testing and external testing.Ensure delivery of samples to internal testing labs prioritized by required turnaround times.Coordinate and ship samples to external test labs and prepare associated paperwork.Ensure QC test data packets are assembled on time for lot release.Perform inventory maintenance.Maintain QC data files and perform data archival as required.Maintain instrumentation and supporting documentation in a GMP compliant manner.Respond to equipment alarms.Perform equipment maintenance tasks.Conduct regular meetings with external testing laboratories.Assist the implementation of new products and functionality in LIMS.Provide site specific LIMS application support, problem reporting and resolution SME for Sample Management supporting quality events.Train new staff in Sample Management. Supporting user acceptance testing in support of validation activities. Required QualificationsAbility to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects.Sample Management Experience Required.Experience as a LIMS Business Analyst preferred.Strong analytical and communication skills.Strong Decision-Making AbilityThe ability to work effectively with others.Computer proficiency as well as the ability to master new software programs.Experience working in a regulated (GxP) environment. Education RequirementsBS Degree in a scientific discipline with 5+ years of relevant analytical testing or QC experience in a GMP-related industry required, or equivalent combination of education and experience. BMSCART 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. 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 …@bms.com. Visit careers.Bms.Com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Associated topics: ascp, blood collection, laboratory, medical lab science, medical laboratory science, medical technologist, microbiology, pathology, technologist, toxicology