EDUCATION

• Bachelor’s degree in scientific or engineering subject area required.
• Master’s degree in a scientific, engineering, or business subject area preferred.

EXPERIENCE

• 6-8 years of validated experience in either cell therapy operations, commercial drug substance manufacturing, or commercial drug product manufacturing in an FDA regulated environment is required.
• 5 years consistent track record of leading teams.
• Experience with engaging externally facing customers within a contract development and manufacturing organization (CDMO) highly preferred.
• Commercial biologics manufacturing experience is required.

KNOWLEDGE, SKILLS, ABILITIES

• Ability to work within a matrixed cross-functional team structure.
• Ability to balance multiple projects and results simultaneously.
• Capable of leading people in multi-disciplinary technical and scientific teams.

PHYSICAL REQUIREMENTS / WORK ENVIRONMENT

• Exposure to life sciences Biosafety level 2 R&D laboratory, manufacturing space and office environment.
• Flexibility to work after hours depending on business needs.
• Up to 10% travel may be required.

Please refer the Job description for details