This job board retrieves part of its jobs from: Toronto Jobs | Emplois Montréal | IT Jobs Canada

Check out new job offers everyday

To post a job, login or create an account |  Post a Job

Bristol Myers Squibb: Manager, Msat Process And Product Support

Bristol Myers Squibb

This is a Full-time position in Bothell, WA posted December 27, 2020.

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.

PURPOSE AND SCOPE OF POSITION: The Manufacturing Science and Technology (MSAT) Process and Product Support Team at our manufacturing plant in Bothell, WA is responsible for maintaining the site’s Right to Operate and enables excellence in manufacturing by providing technical support to the production and quality organizations while driving continuous production improvements.

The MSAT Process and Product Support Manager manages a team of process engineers responsible for monitoring, troubleshooting, and improving cell therapy unit operations, provides strategic and technical leadership both within and outside of the site, establishes site-specific support practices, and assures on-time completion of his/her team’s deliverables.

DUTIES AND RESPONSIBILITIES: Lead team of process engineers with varying levels of experience from entry level to senior/principal engineer Effectively manage MSAT Process and Product Support Team in the following areas: Immediate response and resolution of emergent production issues including troubleshooting on a 24/7 basis Support deviations and investigations using systematic based approaches to identify root cause Identification and implementation of immediate corrective or preventative actions to ensure continued compliant operation Lead and/or support identification and implementation of near and long-term changes including root cause analysis and ownership/sponsorship of CAPAs Lead and/or support process FMEAs to understand process and product risks May support and/or lead a change controls related to product/process improvements and product lifecycle Collaborate with: Manufacturing Operations and Operational Excellence to identify, prioritize and drive continuous improvements and other readiness operational maintenance activities to reduce safety risks, operational costs, lead times, and scrap/discrepancy rates across all aspects of production Quality Assurance in maintaining high compliance standards Global MSAT and other site-MSAT functions to design reliable and robust processes Establish process and product support best practices, strategies, and maintenance/management of these processes, share best practices across the cell therapy network Provide input to revised and new site-specific as well as global policies and procedures Maintain the team’s constant state of inspection readiness Function as a primary contact for internal and Health Authority audits and driving audit observation corrective actions to closure Serve as MSAT representative on cross-functional and multi-site teams Build and maintain effective collaborative relationships across the site and network Establish, monitor, and drive to completion MSAT Process and Product Support team’s annual goals Mentor and develop direct reports by providing an environment that encourages professional development and ensuring they have the appropriate knowledge, skills, and growth opportunities Establish and track team’s performance metrics, provide progress reports to stakeholders REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Education: BS/BA in life sciences, physical sciences, engineering or an equivalent combination of education and work experience Experience Basic Qualifications: 5 years relevant experience in cGMP environment for Biologics/CMC/Vaccines 2 years managing direct reports with varying levels of experience Strong knowledge of GMP compliance, regulations and manufacturing operations Experience leading a high performing team driving an environment of collaboration, timely and effective communications, a sense of urgency to achieve immediate and future goals Experience representing technical operations during internal as well as US and international-specific health authority audits, particularly pre-licensure inspections (PLIs) Excellent organizational skills and the ability to make sound decisions when allocating resources and managing team’s priorities Ability to communicate clearly and professionally both in writing and verbally Preferred Qualifications: Experience with cell therapies highly desired Knowledge of Six Sigma a plus WORKING CONDITIONS (US Only): Employee will work in typical office conditions (sit/stand desk, lighting, temperature, noise-level, office equipment and air quality) with occasional work in the manufacturing cleanroom for specific tasks.

Ability to lift a desired weight is not needed 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.

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.