Asssociate Director, Clinical Supply Operations,Logistics

Job Responsibilities:

The candidate will lead the Materials Management team in New Brunswick under
Clinical Supply Operations Logistics department. The area of responsibility
includes the following operations: •Materials management supporting the
pilot facilities to manufacturing API and intermediates •Materials
management supporting the pilot facilities to manufacturing solid and sterile
clinical formulated drug product •Materials management supporting clinical
packaging The candidate working across CSO sites, will develop, implement and
manage processes and procedures related to clinical supplies materials
management activities for New Brunswick. He/she is expected to understand and
ensure materials management compliance with all GMP requirements (e.g., CFR21,
ICH Guidelines). The candidate is expected to develop and maintain effective
interfaces with key customers (external and internal) and will be viewed by
peers as a leader with a high level of respectability and knowledge of the
clinical supplies and supply chain process and strategies. In addition, the
candidate will manage all facilities related projects within the scope of New
Brunswick distribution and materials management operations. The candidate is
also expected to identify and facilitate business process improvements
initiatives within CSO Logistics and broader CSO leading to a more effective
supply chain and organization.

Job Requirements/Education:

A B.S./B.A., preferably MS/MBA in pharmacy, engineering, business, or life
sciences with 7-10 years experience in Biotech/pharmaceutical/medical device
industry. Expertise in supply chain, materials management, purchasing, and/or
logistics operations and concepts with the working knowledge of MRP systems,
preferably with SAP. Thorough understanding of GMP requirements as applied to
materials management, warehousing, and distribution including cold chain
management. Prior supervisory experience with demonstrated ability to work with
and manage people/teams in a culturally diverse, complex, changing environment.

Salary will be commensurate with experience.
Bristol-Myers Squibb is an equal opportunity employer. M/F/V/D