Associate Director, Life Cycle Mgmt Job in New York (NY), Operations Career, Full Time Jobs in Novartis Pharmaceuticals
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Associate Director, Life Cycle Mgmt job in Melville

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Novartis Pharmaceuticals jobs
New York (NY), Melville
Job Code:  245849BR
Employer:  Novartis Pharmaceuticals
Category:  Operations
Job Type:  Full Time

Location
Country:  United States
State:  New York (NY)
City:  Melville
Map: 
09/05/2018

Description
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage.

The Associate Director Life Cycle Management acts as a project lead at Site for TechOps technical/manufacturing/engineering projects during the life-cycle of a given product, e. g. product launches, changes, transfers, new business/volume opportunities, pruning, divestment and other special Tech-Ops projects (acts as site SPOC ensuring coordination and alignment across global and local functions).

Setup and lead local cross-functional teams, to ensure optimal realization of Site strategies (considering LEAN methodology, pipeline re-design, sourcing strategies, assortment optimization/complexity management) and ensure Site objectives can be reached during ongoing life-cycle activities regarding: Customer service level, COGS, Inventory and Compliance.

Skilled in project management, presentation skills, and business case development,

Must be able to manage multiple priorities and customers simultaneously; influencing without authority

Able to adapt quickly and easily to change

Travel less than 10% of the timeBS degree required

MBA or Masters degree a plus English

10+ years of experience in MS&T, Commercial Operations, supply chain, engineering

Continuous improvement or project management certification a plus

Experience with manufacturing, technical transfers, validation and demonstrated success in the above areas

Thorough knowledge of GMP, pharmaceutical regulatory requirements and other relevant regulations

Adept at using SAP MS Project, MS Excel, PowerPoint, Documentum, databases
ref: (245849BR)
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