QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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• Work on the Process Monitoring (Continue process verification) for Parenteral and Solid products.
• Provide support to investigations by participating in the root cause analysis.
• Own/lead investigations and corrective action implementations.
• Knowledge on parenteral and solid processes (Formulation, Granulation, Filling, Compression, Coating, etc.).
• Statistical knowledge and proficient in the use of Minitab and JMP, R-coding recommended.
• Knowledge in data retrieval/data analysis/presentation tools (OsiSoft PI, Spotfire, Smartsheet, Tableau etc), as well as MS Office (including Excel, Word and PowerPoint).

• Master’s degree and 3 years of directly related experience or
• Bachelor’s degree and 5 years of directly related experience, Science degree (Statistics, Biology, Biochemistry, Math or Chemistry Preferred) or Engineering (Industrial Engineering Preferred).
• Excellent technical writing skills
• Fully bilingual (Spanish/English)

• It is a Non-Standard shift.