Category
Regulatory, Quality and Clinical
Description
Tasks For The Function
- Adheres to the established manufacturing schedule for all assigned batches from start to completion.
- Assists in the manufacture of pharmaceutical oral dosage products for use in clinical studies.
- Follows all written procedures, SOPs, cGMP regulations and safety requirements during manufacturing.
- Carries out operations with strict adherence to cGMP and OSHA requirements.
- Participates in all manufacturing activities of assigned batches and completes all required documentation.
- Performs equipment setup, batch execution including completion of associated batch documentation and equipment logs and equipment cleaning.
- Enters data into computer terminals when required.
Education Requirements
- Two-year Associate Degree in Science related to pharmaceutical development or equivalent.
- Proficiency in use of computer programs/systems is essential.
- Technicians must maintain their skills and knowledge current with advances in the field of pharmaceutical development.
- Incumbents may attend internal or external training courses as approved by management.