3497 Program Management Intern jobs in Princeton,NJ

Bachelor's degree in Science, Engineering or related field or equivalent experience required
A minimum of two (2) to four (4) years of operations experience within a cGMP environment in the biotech/biopharma industry is preferred
Prior experience in an aseptic manufacturing environment and leadership positions
Prior experience in manufacturing, quality, or engineering is required
Experience with Operational Excellence and/or Lean Manufacturing is an asset
Excellent communication and organizational behaviors skills are required
Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook) is required
Ability to accommodate changes in the schedule including working in other shifts as per operational needs is required
Experience working in cGMP systems including MES lite, eLIMs, Siemens, and SAP is preferred
Ability to lift a minimum of 25 lbs. and to stand for a long period of time are required
This position may require up to 10% of domestic travel
Knowledge of cGMP regulations and FDA guidance related to manufacturing of drug substance products, and cleanroom behaviors
Must exhibit strong Leadership skills and ability to effectively communicate and influence Operations associate and convey information to Management
Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively
Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members
Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability
An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment
Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures
Ability to accommodate shift work including evenings and weekends as required by the process
Sufficient vision and hearing capability to work in job environment with physical dexterity sufficient to use computers and document production records
A working leader who can participate in production runs in critical situations when needed
This position is based in Raritan New Jersey