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Associate Director, RR COE Technical Lead Client: Bristol Myers Squibb
Location: Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 85f024a1fb6e
Job Views: 109
Posted: 03.03.2025
Expiry Date: 17.04.2025
Job Description: Working with Us
Challenging.
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 Ireland Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, haematology, immunology, cardiovascular and neuroscience.
Our employees work every day to transform patients' lives through science.
Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units.
The Role The Global SC Planning Excellence organisation is seeking to recruit an Associate Director, RR COE Technical Lead for its operation based in Dublin.
The person will be accountable for the successful deployment, business adoption and continuous improvement of planning capabilities in Rapid Response.
This includes:
Business Technical Lead with in-depth knowledge of system design Business Technical Lead 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 Technical Lead for all Company project/workstreams impacting Rapid Response, providing technical guidance, support, or acting as the RR CoE lead when required.
Key Duties and Responsibilities: As the Business Technical Lead, 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.
Represents the RR CoE as the business technical lead on company projects/workstreams.
Forges a seamless relationship with planning SME's, ensuring planning needs are fully understood and planning capabilities are fully supported.
Forges a seamless relationship with IT, ensuring business needs are being represented and communicated accurately at all times.
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.
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.
Owns the annual update on all technical training documents including offline Single Point Lessons, in-system task flows, workbook help, worksheet help.
Owns the annual update on all business relevant system generating alerts.
Represents the Rapid Response Center of Excellence in multiple meetings / workstreams.
Qualifications, Knowledge and Skills Required: Undergraduate degree in supply chain, life science, business administration and/or engineering or equivalent required Minimum 10+ years managing supply planning operations for a reputed global BioPharma or Consumer Product company Experience in implementing world class, global supply chain planning processes and tools management Experience in working in a fast paced, reputed, global pharmaceutical/Biotechnology or Consumer company organized in a matrix structure Strong Project Management capability skills Demonstrated 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 requirements Thorough understanding of and experience with some aspect of technical operations.
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 solutions Excellent verbal, written and interpersonal communication skills at all levels of the organization.
Additional professional and personal requirements include: Executing for Results: Maintains high standards of performance for himself/herself and follows through on commitments.
Leading / Supporting Cross Functional Teams: Ability to lead strong, diverse teams of people.
Building Relationships: Establishes credibility and earns respect with a diverse set of cross functional stakeholders.
Why you should apply You 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.
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