Sr. Process Engineer

Job Responsibilities:

As a member of the Core Team, the Sr. Process Engineer will be knowledgeable in
both Upstream and Downstream, with Downstream expertise. The Sr. Process
Engineer will be directly responsible for process fit, technical transfer and
validation of cell culture purification processes to third party manufacturing
and other internal manufacturing facilities. The Sr. Process Engineer will also
responsible for the critical interfaces with Development, Analytical
Biochemistry, QA QC,Global Engineering and Manufacturing Operations, including
direction and training of others, where applicable. Position will also be
required to prepare, produce and or review critical regulatory documents and
other technical reports.

Job Requirements/Education:

The successful candidate will have PhD in Biochemical Engineering or related
discipline and 3 to 5 years of relevant industrial experience. Direct
experience with development and validation of protein therapeutic processes and
cGMP manufacturing experience are essential. Experience in all aspects of
technical transfer of processes between facilities is required. Significant
travel required, up to 50 percent, both domestic and international. Strong
experience and ability in Technical report writing and review essential, as is
critical reading of reports and other regulatory documents. Strong business
acumen, proven organizational, multi tasking, time management and writing and
communication skills required. Proven ability to balance business requirements
and technical work scope. Ability to work effectively as a member of larger
cross functional teams.

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