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

• Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
• Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects.
• Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.

Qualifications

• Ability to interpret and apply GLPs and GMPs
• Data integrity experience (ALCOA, ALCOA+, etc.)
• Familiarity with documentation in a highly regulated environment
• Ability to operate specialized laboratory equipment and computers as appropriate
• Familiarity with validation processes
• Good Documentation Practices
• English Proficient
• Change control experience
• Technical Writing (Validation Documentation)

Education

• Doctorate degree or Master’s degree and 3 years of Engineering experience or 
• Bachelor’s degree in Engineering and 5 years of Engineering experience.

• Willing to work as Independent Contractor

• Candidates should send resume in Word or PDF format.