Oct 12, 2017
Responsible for the implementation of aseptic processing of Pharmaceutical components and products in a cGMP manufacturing environment.
Participate in the design of facilities for aseptic processing and filling of pharmaceutical products.
Perform technology transfer of developed processes and procedures to scale up activities;
Engage team members to drive to true root cause of errors and seek ways to improve and optimize the process to eliminate mistakes;
Provide guidance on key decisions with front line leaders and junior to mid-level employees.
Understand controlled environment and aseptic processing principles.
Understand manufacturing safety regulations and comply with current Good Manufacturing Practices.
Experience in implementing and maintaining clean room aseptic processing qualification.
Experience in performing environment monitoring.
Must have experience managing and developing high functioning teams
Must be a “go-getter” who can drive change, drive improvements, and deliver results
The successful candidate will hold a degree in Pharmaceutical Sciences, Chemical Engineering or equivalent education.
Min 2 years related pharmaceutical industry experience in sterile manufacturing.