TECHNICAL INVESTIGATOR

Job Responsibilities:

Overall responsibility for completion of projects on preestablished agreed
timelines for technical transfer of product to Third Party Manufacturing.
Assure compilation, distribution, and data accumulation related to projects at
various stages. Involvement in investigation and trouble shooting issues
supporting Third Party Manufacturing. Coaching mentoring and developing people.
Project transfer, training, and maintenance responsibility in the processes
involved. Individual contributor initially with potential for growth in the
organization. Represent Manufacturing Technology and work closely with the
respective functional manager and project team members in all areas of the
company. Informs management about the critical issues related to product
manufacturing and validation process and packaging. Direct all activities of
planning, organizing and implementing the research and development activities
of a Manufacturing Technology group focusing on formulation process
optimization. Supports and ensures leadership of the Manufacturing Technology
Department to effectively support product transfers. Implement transition of
transferred and or revised formulation into production in cooperation with
outside departments. Plan, conduct, and evaluate scientific investigation in
the respective field of manufacturing processes. Transfer all product and
process technology to the designated manufacturing site. Monitor and evaluate
joint venture development programs through personal contact with scientists,
engineers, by literature search and by market trend to develop innovative
technologies. Evaluate recommend and substantiate the need for new equipment
and instruments. Train and motivate the staff in the group, evaluate the
individual performance on a regular basis focusing on leadership and project
management.

Job Requirements/Education:

Chemical Engineer or Pharmacist with minimum 3 years of experience in
manufacturing of sterile biological drug product and fundamental knowledge of
aseptic operation. Knowledge of SOPs, cGMP s and GLP s and the know how to work
and manage within a regulatory environment. Knowledge of BMS product portfolio
and manufacturing processes preferred. Fundamental knowledge of pharmaceutical
manufacturing and packaging processes and Environmental, Health and Safety
issues. Working knowledge of computer software. Requires up to 40 travel.

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