The CQV develops documentation of the commissioning, qualification and validation for RGD’s clients for their equipment and processes to qualification and production.
Write protocol, execution, field verification and summary reports
Investigate and resolve discrepancies in protocol
Develop tech reports and summary reports
Read and verify facility and equipment drawings
Develop Standard Operating Procedures, Validation Plans, Turnover Packages and other documentation
Conduct validation testing for equipment to meet qualifications for production
Facilitate turnover of equipment to be qualified and put into production
Also seeking candidates for Project Managers, Construction Managers, Project Engineers, and Project Controls Engineers (schedule & cost).
At least 5 years proven experience in the planning, engineering, construction, commissioning, or validation of pharmaceutical facilities and operations.
Understanding of standard operating procedures and documentation in the pharmaceutical industry.
Bachelor’s and/or Master’s degree preferred or equivalent experience in engineering or construction roles.
Direct experience with regulated environments (i.e. cGMP, OSHA, EPA) required.
Internal Number: CQV1
About RGD Project Management
RGD Project Management, Inc. is a growing company based in Cary, North Carolina. Our employees specialize in providing Project Management, Construction Management and Technical Support Services to Pharmaceutical, Bio-Tech, High Tech and Industrial Companies. For over 20 years, we have set our standards high to ensure that our team is one of the best in the industry. Safety, efficiency, quality, cost and schedule are our foundation.