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 Quality Engineer Specialist to provide senior- level and documentation support for facilities, assets, utilities and maintenance processes. 

Functions:

• Create, review or approve documentation
• Author and progress investigations, conducting root cause analysis
• Draft, route and support implementation of change control
• Review and approve qualification and commissioning documentation
• Facilitate risk assessments (review & approve)
• Maintenance documentation/Work orders
• Monitor and trend qualified-utilities performance against internal specifications and applicable regulations, escalating excursions and drafting related assessments for QA Engineer review.

• Bachelor in Chemical, Biotechnology, Biomedical or Mechanical Engineering with 5 years of experience,
• Technical Writing
• Bilingual (Spanish/English)
• Computer Literacy 

Benefits

What We Offer

• Opportunities for learning, development, and professional growth.
• A collaborative and supportive work environment.
• The opportunity to work with industry-leading clients on impactful projects.

Your information will be kept confidential according to EEO guidelines.