Address
Form of workJob Description
QC Analyst
Onsite in Sellersville
Pharma domain
No visa restrictions
Length of contract assignment:
Describe the project and why the client is doing it?
This position is responsible for running all QC chemistry analytical testing of pharmaceutical raw material and finished product.
Onsite in Sellersville
Pharma domain
No visa restrictions
Length of contract assignment:
- 6 months. Possibility to extend.
- 40 hours, onsite fulltime
- No remote or hybrid option
- 8am to 5pm
- CDMO providing a complete end to end solution for the development and manufacture of oral dosage and topical pharmaceuticals.
Describe the project and why the client is doing it?
This position is responsible for running all QC chemistry analytical testing of pharmaceutical raw material and finished product.
- Test instrumentation and methods include HPLC, GC, Dissolutions, Particle Size Analyzer, FTIR (Fourier Transform Infrared) Spectroscopy, pH, Dissolution Testing, Viscosity and TOC (Total Organic Carbon) Testing.
- Interpretation and Presentation of analytical testing data to QC Data Review and Manufacturing stakeholders prior to product release.
- This role will be responsible for the bench testing and wet chemistry activities of all raw materials and finished products.
- This role will also be responsible for all HPLC and GC activity and generating chromatograms and troubleshooting the processes when issues are identified with the results.
- Waters Empower, HPLC
- Malvern, Particle Size Analyzer
- Karl Fischer Method
- LabVantage LIMS
- Bench testing of raw materials and finished products using Empower HPLC, Malvern Particle Size Analyzer and Waters Gas Chromatograph.
- Performing wet chemistry testing including viscosity, pH and dissolution.
- Documentation of results into LabVantage LIMS.
- Developing trend reports to share with QC Data Review team
- Review of chromatograms for data accuracy
