Job Description
Duties and Responsibilities:
- Perform operations necessary for quality testing and plays a role in implementing new technology within quality control.
- At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.
- Complete routine inspection (i.e. visual and dimension inspection/testing) and sampling of raw materials, in accordance with SOPs for material release and validation.
- Aid in the development of test methods.
- Conduct data review and preliminary evaluation of results.
- Solve problems using limited predetermined options such as repeating the inspections when parameters are not met to determine the cause, etc.
- Provide input to the technical composition of operating documentation.
- Work is closely supervised.
- Follows standard practices to obtain solutions.
- Contribute to the completion of routine technical tasks.
- Failure to achieve results can normally be overcome without serious effect on schedules and programs.
- Contacts are primarily with immediate supervisor and other personnel in the section or group.
Requirements:
- 1-3 years of experience in related role.
- GMP related a plus, or pharm related —MS Office, Word, Excel, Power Point.
- Exposure to chemicals: Isopropyl Alcohol, bleach, disinfectant.
- GMP experience, CAPA, deviations seen as a plus –Pharma/ biotech experience –SAP.