Senior Manager, MSAT Cell Therapy Engineering Support, Process Data Steward

Company: Disability Solutions
Location: Bothell
Posted on: May 3, 2024

Job Description:

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 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 Summary: The Sr. Manager is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply at the Bristol Myers Squibb Cell Therapy Manufacturing Plant in Bothell, WA. This role is an individual contributor, owning and advancing the Process Monitoring/Statistical Process Control program at the Bothell site, interfacing with global data stewards to drive network-wide alignment, and driving data organization/acquisition from manufacturing control systems for current and new products. Work will involve data analysis using best fit tools to determine statistical relevance and practical significance of trends.The Sr. Manager sits on the Cell Therapy Engineering Support (CTES) leadership team driving strategic alignment with business and quality deliverables that require process data backed decisions. They will support other members of CTES and MSAT when process data and/or analysis is required. Work will heavily involve management of stakeholder relationships with Quality Assurance, global MSAT (Technical Operations), Manufacturing, Information Technology, and Automation.This role is site based at the Bothell, WA BMS manufacturing facility. 50% on-site presence is required. May require entry to the controlled classified manufacturing space on occasion to support process improvements and other projects. Roles and Responsibilities:

• Own and execute the BMS Bothell Process Monitoring (ProMo) program.
• Implement Statistical Process Control (SPC) into the ProMo program.
• Analyze and manipulate process data to elucidate potential patterns and trends.
• Enable identification of process improvement from identification of patterns and trends in process data.
• Support global improvement of SPC and alignment of ProMo programs across sites.
• Facilitate routine engagement with the ProMo program for local and global stakeholders.
• Facilitate access to additional sources of manufacturing process data. Systems include but are not limited to MES, DeltaV, LIMS, etc.
• Lead cross-functional teams at and above site to enable effective collaboration.
• Support the identification of implements effective Key Performance Indicators (KPIs) to drive engagement and performance.
• Work with team members to identify barriers to execution, identify solutions, and execute or escalate for resolution/recommendation.
• With minimal supervision, lead multiple projects and contribute to more complex projects and initiatives for the broader site. Lead complex technical project teams and cross-functional teams.
• Enforce and master team processes, supporting the understanding of benefits and tradeoffs of decisions. Frequently challenges the team processes, looking for ways to improve them.
• Measurable tactical achievements and 360 feedback highly indicative of confidence in ability to lead initiatives of limited scope. Some measurable strategic achievements and 360 feedback indicative of confidence in ability to lead a mid-high level initiatives and teams.
• Strong ability to lead and influence others. Mentor others to accelerate their career-growth and encourage them to participate. Proactively support other team members within area capability and help them to be successful.
• Demonstrate multiple BMS values (Integrity, Innovation, Passion, Urgency, Inclusion, Accountability) and work to address perceived deficiencies. Begin to demonstrate all BMS values at higher levels with tangible examples of each category.Education/Experience:
  • Bachelor's Degree in life sciences/engineering/STEM or equivalent; Master's Degree preferred
  • 8+ years of manufacturing or analytical experience, preferably within biopharma, cell therapy, GMP, FDA regulated, or other regulated environments; or equivalent combination of education and experience
  • Experience analyzing complex data sets to identify relevant trends and patterns (utilizing a variety of statistical techniques such as univariate control charts and multi-variate analysis/PCA/PLS)
  • Experience with Process Monitoring of a manufacturing process utilizing statistical process control applications (ex, SAS/JMP, Statistica, etc.)
  • Experience creating and owning a program/process and driving continuous improvement over time
  • Experience utilizing key performance indicators to drive process improvement
  • Possess the professionalism and technical competency required to represent the department before our customers, regulatory agencies, and management.
  • Strong knowledge of GMP compliance, regulations and manufacturing operations
  • Experience driving projects and actions in a cross functional environment with timely and effective communications and a sense of urgency to achieve immediate and future goals
  • Ability to work in a fast-paced environment and manage multiple projects and objectives in parallel.
  • Must be able to identify risks in a timely manner to keep deliverables on track.
  • Proven logic and decision-making abilities, critical thinking skills.
  • Lean / Six Sigma Experience is desired The starting compensation for this job is a range from $114,000 - $144,000, plus incentive cash and stock opportunities (based on eligibility). The starting pay takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation is decid ed based on demonstrated experience. For more on benefits, please visit our BMS Careers si te. Eligibility for specific benefits listed in our careers site may vary based on the job and location. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. TRAVEL REQUIREMENTS:--- Not Applicable-NAInfrequent visits to other BMS Cell Therapy sites and the Seattle, WA facility may be required.WORKING CONDITIONS (US Only):This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management within reason.BMSCART VETERAN 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 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 Protocol BMS has a diverse 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 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.

Keywords: Disability Solutions, Federal Way , Senior Manager, MSAT Cell Therapy Engineering Support, Process Data Steward, Executive , Bothell, Washington