Company Description
QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!
Job Description
Specialist QA is responsible for leading quality assurance activities across manufacturing operations, including the review and approval of validation protocols, risk assessments, CAPAs, and change controls. Quality Professional with Validations and Commissioning & Qualifications of manufacturing equipment and laboratory bench equipment experience (IOQ, PQ, Functional Test). In addition to Technical Writing, Quality Systems (Deviations, Change Control) and Maintenance (PM, Work Orders, Job Plans review and approval) knowledge. Technical Documents review (Validation Reports, Procedures, Forms).

Qualifications

• Doctorate Degree OR
• Masters Degree + 2 years of directly related experience OR
• Bachelors Degree + 4 years of directly related experience OR
• Associates Degree + 8 years of directly related experience OR

Sciences or Engineering background
Additional Information
All your information will be kept confidential according to EEO guidelines

Please refer the Job description for details