| QC Data Reviewer for Sellersville, PA at Sellersville, Pennsylvania, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=663533&uid= Job Description Job Title: QC Data Reviewer Visa: No H1B & CPT Location: Sellersville, PA (Onsite) Rate: $50/Hr C2C(MAX) Duration : 6 months + extensions Job Description: Please note: This is not a QC Analyst position; this is a Data Reviewer position. We are looking for someone senior enough who has the analyst experience but has taken the next step in their career and has experience reviewing the data that the analysts provide. 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 supporting the QC department with review of analytical data obtained from analytical testing of pharmaceutical 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. Review, Interpretation and Presentation of analytical testing data to QC and Manufacturing stakeholders prior to release This role will be responsible for the review of documentation, SOPs and reports related to the QC analysis of each pharmaceutical product. This role will also be responsible for all deviation investigations including event summary and process/equipment overview. Technology environment the consultant will be working in: Waters Empower, HPLC Malvern, Particle Size Analyzer Karl Fischer Method LabVantage LIMS Consultants day to day responsibilities: Bench testing of pharma products using Empower HPLC and Malvern Particle Size Analyzer Performing wet chemistry testing including viscosity, pH, and dissolution. Documentation of results into LabVantage LIMS. Developing trend reports, presenting to QC, and Manufacturing stakeholders Writing and reviewing analytical testing SOPs for individual products Writing deviation investigations/reports in partnership with QC leadership Work schedule/typical work week/daily start and end time: Expected hours, can you work off site/remote Is there flexibility 40 hours, onsite fulltime No remote or hybrid option 8am to 5pm Avinsh Nagar| Senior Technical Recruiter Disclaimer: This is not meant to be an unsolicited email, so if you dont want to receive any emails from me and QSP Infotech, you can click on -> . Do not hesitate to contact me back for any questions . -- Keywords: information technology green card Pennsylvania http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=663533&uid= |
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| 12:57 AM 21-Sep-23 |