Working with UsChallenging. 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: Position SummaryCruiserath Biologics is seeking a Senior Manager of Quality Control to Project Manage the Quality Control start-up activities in support of the transition of storage and testing of Drug Product Stability from the BMS Devens facility to Cruiserath. This position will provide Strategic Guidance & Oversight, technical and compliance support as a QC Leader to support QC Operations at BMS Cruiserath.Reporting to the Quality Control Director, this position has responsibility for developing the Project Strategy, Defining the Project Schedule, managing Schedule adherence, QC Hiring strategy, QC Laboratory Facility / operational Design, QC Stability Governance across Technical Transfer, Operational Readiness and Capital Expense. This position is responsible for the overall QC readiness for the new Drug Product Stability Storage and Testing. This is a 12 month fixed term contract.Key ResponsibilitiesOverall accountability for timely delivery of the QC operational readiness requirements for testing switch-on in 2026Overall accountability for timely delivery of the QC requirements for on-site storage readiness in 2027Responsible for the Drug Product Stability Storage facility design and GMP certificationOverall responsibility for identifying, defining, scheduling, coordinating and driving to completion all Quality Control activities within the remit of the Drug Product Stability readiness operations.Work with the Site Projects team to ensure the delivery of Storage for Long term, Stressed and Accelerated StabilityWork with the QC Projects team & the Global Stability Team to ensure the delivery of Method Transfer activities under the remit of Drug Product Stability.Principal Quality Control Liaison with each of the main Stability workstreams (Technical Transfer, Operational Readiness and Capital Expense)Responsible for the development of the QC Stability Hiring Plan with accountability to adhere to the phased hiring scheduleCompliance with all BMS Policies, Standard Operating Procedures and Registered Specifications.Ensure the QC Organisation is set up to meet the needs of the new Drug Product Stability Program at CruiserathEnsure the new Stability Storage Facility is set up in a safe manner with safety as a primary concern in its design.Work closely with each of the QC teams to ensure they are informed of critical milestones, progress and support requirements.Provide an effective and efficient QC Service to the Global Stability and Site Project teams through strong communication and focus on key priority milestonesKeeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and Stability TestingReview and Approval of project strategy reports, protocols and associated Project documentation.Participate in regulatory agency inspections as required.Strategically plan and implement procedures and systems to maximise operating efficiency through the use of Operational Excellence tools.Manage and contribute to the achievements of department productivity and quality goals.QC Point of contact at all Drug Product Stability meetings, liaison with network SMEs such as Method Lifecycle Microbiology Centre of Excellence, Analytical Science Organisation and Manufacturing Science & TechnologyResponsible for building the QC detailed schedules and ensure delivery timelines are metManage headcount and hiring schedule in line with agreed timeframe. Ensure new hires ready to support key activities and meet site timelines.Support any Equipment Qualification timelines requiredEnsure all equipment, lab design, methods are accounted for and can be introduced successfully into the current LOC LaboratoriesTroubleshooting issues and resolving problems in a timely mannerInspires transformative thinking and motivates employees to deliver benchmark performance.Leads and fosters an environment of continuous improvement.Qualifications & ExperienceThe successful candidate must possess a Bachelor/Masters in Science or Science related discipline. A minimum of 10 years' experience in the Pharmaceutical Industry.Deep and demonstrated understanding and experience of the principles of GMP / GDPAn accomplished team leader of project teams with the ability to motivate and develop QC teams through effective feedback and coachingThe candidate will have proven success working well in a team environment, as well as proven leadership skills to manage a project in a dynamic environment.Demonstrated ability to influence work cross functionally in a matrix environment during startup and into commercial manufactureExperience with technical transfer of new products is essential, as well as experience interacting with regulatory agencies.Experience with a stability testing program is desirableMust be experienced in managing large complex projects. Experience in building and designing laboratories is desiredExtensive knowledge of US and EMA GMP regulations and guidance.Demonstrated leadership, interpersonal, communication, and motivation skills.Demonstrated understanding of test methods and instrumentation associated with the testing of biopharmaceutical processes including microbiological, chemical & functional testingPlanning and organizing skills are required to plan, execute and manage resources against timelines and project commitments; must be able to adjust to changing priorities and a dynamic work environment.The candidate will have demonstrated strong leadership and people / project management abilities, proven decision making ability and the ability to work well with and influence all levels of management and staff. Additionally, the successful candidate must be able to interact with a broad range of disciplines and exert positive influence within internal matrix teams across a variety of functions.This is a EG-120 position.Why you should applyYou 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, 27 days of annual leave, life assurance and on-site gym 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 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 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 ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.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 Visit 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.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.