- Prepare equipment and materials for GMP clinical production and operate equipment such as AKTA chromatography skids, pumps, pH meters, and filtration units.
- Work as part of a team in close collaboration with R&D Quality to perform various routine manufacturing tasks under cGMP guidelines and established procedures.
- Accurately document data and complete batch records.
- Research and develop new medicines for unmet medical needs.
- Assess, monitor, and ensure products meet clinical safety standards.
- Conduct sophisticated analysis.
- Manage research information systems and technical documentation.
- Establish relationship with regulatory authorities to establish and maintain registration licenses to sell products globally.
- Associate or Bachelor's degree in Science or Engineering required.
- Relevant experience in manufacturing, equipment operation, and good documentation is required.
- Ability to follow instructions and direct supervision.
- Driven and detail oriented with demonstrated ability to follow detailed directions in a GMP manufacturing environment.
*This position is 100% on-site work*
Schedule: Monday-Friday, 8am-4:30pm