CIP - CQV Engineer

International Association of Plumbing and Mechanical Officials (IAPMO); Raleigh, Northern (NC, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Hyde Engineering + Consulting is seeking an Associate CIPConsultant to support upstream and downstream processes and manufacturing support equipment in a GMP environment. The role requires CIP system experience and involves commissioning, validation, and collaboration with clients and vendors from Raleigh, NC.

Responsibilities include reviewing specifications, developing CIP cycles, and ensuring data accuracy across batch records and process equipment.

Qualifications

• Strong verbal and written communication skills.
• Experience with CIP systems and CIP troubleshooting preferred.
• BS degree or higher in chemical engineering or a related engineering discipline.

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 CIP systems and 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/DeltaV systems.

Skills

Strong communication skills

Education

BS in Chemical Engineering or related field

Tools

SCADA/DeltaV

PLC

Microsoft Office

Job description

The Commissioning & Qualification CIPConsultant is responsible for providing support to various upstream, and downstream processes and/ormanufacturing 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

Hyde Engineering + Consulting is an equal opportunity, affirmative action employer.

Associate