The Commissioning & Qualification CIP Consultant is responsible for providing support to various upstream, and downstream processes and/or manufacturing support equipment. Must have CIP System/Circuit experience.

SHIFT WORK

Responsibilities Reviews engineering specifications for compliance with ordinances and engineering requirements. Consult with clients/vendors as a department representative regarding major problems or developments. Prepares special periodic reports and records. Perform cleaning cycle development for a variety of equipment including process vessels and lines, chromatography skid/column, UF/DF skid, centrifuge, glass/parts washers, and portable processing equipment. Perform batch record review, including verifying calibration and in-process data. Review piping design and flow calculations for CIP systems. Perform commissioning and provide automation support for CIP systems, including PLC and SCADA/Delta V systems. Required Qualifications A minimum of three (3) years of pharmaceutical manufacturing experience or in a GMP Environment Experience with CIP systems

• Experience with CIP troubleshooting, preferred

• A minimum of three (3) Commissioning, Qualification, and Validation of pharmaceutical manufacturing equipment. Reviews engineering specifications for compliance with ordinances and engineering requirements.. Consult with clients/vendors as a department representative regarding major problems or development. Prepares special periodic reports and records. BS degree or higher in chemical engineering or a related engineering or scientific discipline. Familiarity with cleaning of process equipment, including CIP cycle development and optimization, piping design, and fluid dynamics. Familiarity with plant control software, including PLC and SCADA/Delta V systems. Familiarity with engineering project management.

Experience with:

CIP systems and circuits, cleaning validation, protocol development, execution, troubleshooting, and summary reports. Strong verbal and written communication skills. Industry experience related to cGMP drug manufacturing, validation, programming, or chemical process design. Strong computer knowledge including Microsoft Office products Willingness to travel as needed Are you looking for a meaningful career that makes a difference in the world? Consider joining the Hyde Engineering

+ Consulting team where you will do just that. Hyde E+C contributes to helping people live longer, healthier lives by ensuring pharmaceutical and biopharmaceutical manufacturers can effectively and safely produce their life-enhancing and often life-saving medicines. To read more about Hyde's culture and benefits, visit our website: www.hyde-ec.com Hyde Engineering

+ Consulting is an equal opportunity, affirmative action employer. #LI-JS1 #LI-Hybrid Associate