Associate Director, Bioprocess Development

Job Responsibilities:

The Associate Director of Bioprocess Development will have overall
responsibility for the department and its staff of approximately 20 to 25
scientific and engineering professionals. Responsibilities include oversight of
technical groupsresponsible for the development of biologics manufacturing
processes. The Associate Director, Bioprocess Development will report to the
Director of Biotechnology Development. He or she should have solid demonstrated
leadership qualities and be results oriented. He or she will be an innovative,
visionary and strategic individual with a drive for continuous improvement.
Additional attributes desired include superior intelligence, sound judgment,
high energy, a strong work ethic, flexibility, motivational and empowerment
skills and dedication. Specific responsibilities will include providing
tactical and strategic oversight to the Bioprocess Development group and
leadership in the linkages with Quality Operations, Bioprocess Engineering,
Development Support, and Biotechnology Operations. The Associate Director will
also be responsible for the recruiting, retention and development of talent in
the Bioprocess Development organization the development and alignment of
objectives with partner organizations and maintaining relationships with
internal and external partners involved in Bioprocess Development projects.

Job Requirements/Education:

The ideal candidate will have a Ph.D. in biochemical engineering or a relevant
biological science, strong academic credentials, a solid history of technical
accomplishments with at least 5 years of industrial experience in biotechnology
and successful, demonstrated supervisory experience. Specific qualifications
desired include a demonstrated knowledge of biologic manufacturing processes
and process science, and demonstrated skills in budget management.

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