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!

Specialist Quality Control with experience in:

• Scientific Data Analysis
• Strong Technical Writing (English and Spanish) mainly focuses
• Strong knowledge of Microsoft Excel as a Tool for Data Analysis
• Project Management
• Sample Management
• Ability to develop inspection or qualification protocols in a short timeframe period.
• Strong negotiation skills

Knowledge in:

• Computer System and Method Validation (Experience preferable)
• Strong knowledge and experience with quality process management
• Basic Knowledge on equipment preventive maintenance and troubleshooting
• Agile on prioritization of critical tasks

• Doctorate or Masters + 2 years of directly related experience or
  Bachelors + 4 years of directly related experience or
  Associates + 8 years of directly related experience (Engineering (Chemical, Environmental, Mechanical, Electrical), or Chemist/Biology (with experience in Equipment Validation)
• Bilingual (Spanish/English)(Speak/Write)
• Computer Literacy 

• Doctorate or Master +2 years of directly related experience or
  Bachelors +4 years of directly related experience or
  Associates + 8 years of directly related experience
• Preferable Scientific Background (Science or Engineering) with experience in the Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management Method Validation, Method Transfer and Quality processes. Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering.
• Bilingual (Spanish/English)(Write/Speak)
• ​Good Communication skills