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!

Sr Engineer with knowledge and experience with:

• cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment.
• Change control, non-conformace, corrective and preventive actions, and validation practices.   
• Maximo.
• Working and/or submitting Purchase Orders (PO).
• Working and escorting vendors. 

• Doctorate or Master's  Degree +2 years of engineering experience or
  Bachelor in Engineering +4 years of engineering experience (Mehcanic, Electrical or Chemical)
• Technical Writing 
• Bilingual (Spanish/English)(Write/Speak)
• Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.

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