- Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations
- Perform data analysis and final result reporting to support product lot release with adherence to turnaround times.
- Perform all activities with respect to GMP/GDP compliance
- Support thorough GMP investigations for out of specification test results and other quality events
- Support technical problem solving for issues pertaining to GMP Quality Control
- Support product stability programs including execution of stability testing, stability data analysis and trending, and final reporting of stability data
- Assist in the generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs and change controls
- Perform peer review of laboratory data and logbooks
- Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
- Support Health Authority inspections
- Provide input to functional laboratory team meetings
Job Type: Contract
Salary: From $42.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
- Night shift
- Weekends as needed
Work setting:
- In-person
Education:
- Bachelor's (Preferred)
Experience:
- Pharmaceutical: 3 years (Preferred)
- Quality control: 3 years (Preferred)
- Flow cytometry: 1 year (Preferred)
- ELISA: 1 year (Preferred)
- NC200: 1 year (Preferred)
- GMP: 1 year (Preferred)
Work Location: In person