ShiftCode Analytics
(2) QC Analysts
ShiftCode Analytics, United, Pennsylvania, us, 15689
Title: (2) QC AnalystsVisa: Any visa except H1B, OPT, CPTLocation: On-site Sellersville, PADuration: 6 MonthsMode Of Interview: Video Call
Must have LinkedIn I'd
Length of contract assignment:
6 months. Possibility to extend.Work schedule/typical work week/daily start and end time:
Expected hours, can you work off site/remote? Is there flexibility?
40 hours, onsite fulltimeNo remote or hybrid option8am to 5pmClient description:
CDMO providing a complete end to end solution for the development and manufacture of oral dosage and topical pharmaceuticals.Project description: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.Technology environment the consultant will be working in:
Waters Empower, HPLCMalvern, Particle Size AnalyzerKarl Fischer MethodLabVantage LIMSConsultant's day to day responsibilities:
Bench testing of raw materials and finished products using Empower HPLC, Malvern Particle Size Analyzer and Waters Gas Chromatograph.Supporting technical services director with tech transfer activities.Performing wet chemistry testing including viscosity, pH and dissolution.Documentation of results into LabVantage LIMS.Developing trend reports to share with QC Data Review teamReview of chromatograms for data accuracy
Must have LinkedIn I'd
Length of contract assignment:
6 months. Possibility to extend.Work schedule/typical work week/daily start and end time:
Expected hours, can you work off site/remote? Is there flexibility?
40 hours, onsite fulltimeNo remote or hybrid option8am to 5pmClient description:
CDMO providing a complete end to end solution for the development and manufacture of oral dosage and topical pharmaceuticals.Project description: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.Technology environment the consultant will be working in:
Waters Empower, HPLCMalvern, Particle Size AnalyzerKarl Fischer MethodLabVantage LIMSConsultant's day to day responsibilities:
Bench testing of raw materials and finished products using Empower HPLC, Malvern Particle Size Analyzer and Waters Gas Chromatograph.Supporting technical services director with tech transfer activities.Performing wet chemistry testing including viscosity, pH and dissolution.Documentation of results into LabVantage LIMS.Developing trend reports to share with QC Data Review teamReview of chromatograms for data accuracy