CIP - CQV Engineer

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.

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