ASSOC. DIR., GMP COMPLIANCE

Job Responsibilities: This position will report to the Devens, Massachusetts site. Manages overall
regulatory and cGMP compliance as it relates to the Devens Biotechnology
Operations and Critical Systems including change control, documentation, GMP
and supplier auditing, regulatory inspection management, and GMP training.
Designs and develops a successful strategy for QA oversight within Operations
and Facilities. This position requires an extensive amount of independent
decision making and decisions made in conjunction with Operations and key QC QA
personnel within the site and other BMS facilities. Significantly contributes
to the creation of a team based, collaborative environment, promoting candor
and receptivity, clarity of purpose and goals, and high commitment to achieve
business goals. Demonstrates appropriate examples for compliance behaviors and
attitudes, thereby shaping the culture. Will meet and exceed all safety
expectations and adhere to all BMS Core Behaviors.

Job Requirements/Education:

This position requires at a minimum a M.S. degree in a Scientific and or
Managerial Discipline, as well as 5 years experience in cGMP or Regulatory
management. Some experience with GMP training applications is preferred. Must
have proven ability to work and motivate a diverse groups of people, have
excellent organizational skills and excellent oral and written communication
skills. Must also have proven ability to establish, develop and communicate a
compelling vision of the Quality Assurance Unit and have proven experience in
leading cross functional and cross departmental Teams.

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