- As a Micro QC Scientist, you will perform chemical, in-vitro, or in-vivo biological assays of clinical and/or commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process & cleaning validation samples, package samples and components as well as some specialized techniques
- You will identify basic technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems and participate in the investigation to resolve and correct
- Assays are qualitative, quantitative and investigational in nature and are performed in compliance with USP, FDA and other regulatory body requirements, Pfizer standard operating procedures, and approved license requirements
- Results are compared with specifications and documented
- You will have mastered most or all of fundamental technical and quality concepts
- Water Sampling/Testing in a Laboratory Setting Required 1-3 years of experience
- Applicants MUST have knowledge of Microbial Water Testing, Bioburden
- Knowledge of Endotoxin and Microbial Limits is a HUGE plus
- Applicants MUST have 3 -4 years SOLID Pharma experience (not school work or internships)
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