Intern

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 Learns and performs well-defined procedures. Attain a basic understanding of cGMP’s and compliance in a GMP manufacturing setting performing both supervised and unsupervised tasks. Perform basic laboratory tasks (pH and conductivity measurement, water sampling, etc). Perform routine sanitation tasks to maintain facility standards. Ensuring manufacturing supplies and batch records are readily available for next 24 hours production activities. Apply and upkeep 6S concept and housekeeping in MFG suites. 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, knows 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). #J-18808-Ljbffr