QC Analyst at Sellersville, Pennsylvania, USA |
Email: [email protected] |
http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=640976&uid= From: Manpreet, Intime Infotech [email protected] Reply to: [email protected] Hi, I am hiring a consultant for one of my client's requirement. Job Description for the same is written below. If you find yourself comfortable with the requirement please reply back with your updated resume. I would really appreciate if you can give me a call back at my contact # 302-401-6677 Ext- 533. Job Title QC Analyst Location Sellersville PA Duration 6 months /Contract JOB DESCRIPTION Interview Mode: Video Visa: USC GC GC-EAD 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 and presenting to QC and Manufacturing stakeholders Writing and reviewing analytical testing SOPs for individual products Writing deviation investigations/reports in partnership with QC leadership Keywords: access management information technology green card Pennsylvania http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=640976&uid= |
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10:53 PM 14-Sep-23 |