The Manufacturing Intern role is responsible for the support of therapeutic protein manufacturing under cGMP conditions. This individual works within the clean room environment in a team led by a Section Lead. The Intern will be assigned to a specific operational area (Small Scale, Large Scale, Centralized Operations), with a focus in either Upstream, Downstream, Solution Preparation or Production Support function.
Primary Responsibilities
Other Departmental Duties
Instruction may be provided by co-workers, supervisors, or cross-departmental representatives to facilitate continued production within GMP, with the consent of the immediate Supervisor.
Supervision Received
Daily supervision on routine work and detailed instructions on new assignments, including organizing and planning of tasks to ensure timely completion. Documentation of tasks performed when required. Basic decision making, knowing when to seek help and who to contact. Coaching on manufacturing process flow.
Requirement:
ITE/Diploma/Degree in relevant science discipline (Biotechnology, Pharmaceutical Science, Chemical Engineering, Chemistry, Biochemistry or Biology).