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!

Process Development Specialist with experience in regulated industry.

• Proficient creating and executing validation and qualification documentation.
• Provide support to vision inspection qualification and characterizations.
• Knowledge in automated vision inspection systems. (A plus)
• Knowledge in CSV Support CQV documentation and execution. (A plus)

Willing to work during regular business hours, night shift, and/or weekends, as needed to meet the projects’ schedule.​

• Doctorate degree in Sciences or Master’s degree in sciences and 2 years of directly related experience
  Bachelor’s degree and 4 years of directly related experience
• Excellent communication skills with suppliers and other sites
• Bilingual (Spanish/English)
• Willing to work during regular business hours, night shift, and/or weekends, as needed to meet the projects’ schedule.

All your information will be kept confidential according to EEO guidelines.