Associate Director, Supply Planning, Business Technical Lead > Boudry > Joboolo CH :
Company : Bristol Myers Squibb Location : Boudry Neuchâtel From : Neuvoo CH
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The Rapid Response Center of Excellence BusinessTechnicalLead is accountable for the successful deployment, business adoption and continuous improvement of planning capabilities in Rapid Response.
This includes:
BusinessTechnicalLead with in-depth knowledge of system design BusinessTechnicalLead with in-depth knowledge of all planning capabilities deployed, including use cases and best practices Forges a seamless relationship with IT and planning teams to drive best in class planning capabilities Owns the RR CoE Issue/Remediation process with a focus on providing best-in-class service to our customers Responsible for overseeing and approving all configuration changes and cutover activities going into production environment Owns the design and successful implementation of RR CoE initiated regression testing and planner completed user acceptance testing (UAT) with a focus on accuracy/efficiency Acts as the TechnicalLead for all Company project/workstreams impacting Rapid Response, providing technical guidance, support, or acting as the RR CoE lead when requiredKey ResponsibilitiesAs the BusinessTechnicalLead, he/she is accountable to have an in depth understanding of the system landscape including all inbound/outbound interfaces, data transformation and planning activities/capabilities.
Knowledge needed to lead a world class system issue/remediation workstream and implement change effectively, with best-in-class accuracy/efficiency.Represents the RR CoE as the businesstechnicallead on company projects/workstreams.
Owns or has direct oversight on all technicalbusiness requirements handed off to IT for configuration changes initiated by the RR CoE or extended stakeholder projects.Forges a seamless relationship with planning SME’s, ensuring planning needs are fully understood and planning capabilities are fully supported.
Aligns on all proof-of-concept testing, UAT testing, push to prod activities, project cutover activities and training, ensuring no lost time in production environment.
Forges a seamless relationship with IT, ensuring business needs are being represented and communicated accurately at all times.
Leads or has direct business oversight over system improvements workstreams.
This includes the overall workplan including design discussions/tradeoffs, proof of concept testing, sprint testing, regression testing, UAT, training, cutover and hyper care, as needed.Responsible for partnering with IT and Planning SME’s to design a world class SIT/UAT process focused on improving efficiency/accuracy on all changes to the planning system, including incorporating the roll out of new out-of-box capabilities with minimal effort.Partners with IT and Kinaxis CoE to resolve high priority planning needs with out-of-box solutions.Owns the Advanced Planning Toolbox, a formal document highlighting all advanced planning capabilities currently deployed, including control mechanisms, behaviors and demonstrated use case examples to be highlighted during planner community of practice presentations.Owns the annual update on all technical training documents including offline Single Point Lessons, in-system task flows, workbook help, worksheet helpOwns the annual update on all business relevant system generating alerts.Represents the Rapid Response Center of Excellence in multiple meetings / workstreamsQualifications & Experience Undergraduate degree in supply chain, life science, business administration and/or engineering or equivalent requiredMinimum 10+ years managing supply planning operations for a reputed global BioPharma or Consumer Product company utilizing world class planning and execution processes and supported by ERP and Advanced Planning Systems (experience with SAP suites and Kinaxis Rapid Response software)Experience in implementing world class, global supply chain planning processes and tools management through deployment of global advanced planning and scheduling systems as well as performance managementExperience in working in a fast paced, reputed, global pharmaceutical/Biotechnology or Consumer company organized in a matrix structureStrong Project Management capability skillsDemonstrated Operational Excellence and Continuous Improvement skill set and delivery.
Preferred:
Good understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirementsThorough understanding of and experience with some aspect of technical operations; interest and demonstrated ability to learn across several disciplines (manufacturing, quality, supply chain, technical development, regulatory, patient experience, finance, operations, etc.) Personal Competencies Desired/Required:
Demonstrated experience in developing, aligning, socializing, monitoring, adapting, and delivering on complex deliverables in dynamic, rapidly changing environments.Interprets business challenges and recommends best practices-based solutionsExcellent verbal, written and interpersonal communication skills at all levels of the organization; excellent presentation skills, both material creation and delivery Additional professional and personal requirements include:
Executing for Results:
Maintains high standards of performance for himself/herself and follows through on commitments.
Demonstrates integrity, conveys a sense of urgency and drives issues to closure.
Leading / Supporting Cross Functional Teams:
Ability to lead strong, diverse teams of people with multiple perspectives and talents.Building Relationships:
Establishes credibility and earns respect with a diverse set of cross functional stakeholders.
Is highly articulate and makes arguments in a clear and compelling manner.
Can achieve win-win outcomes in difficult situations.
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 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.
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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.
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