The CIP Engineer / Consultant is responsible for CIP cycle development on a variety of equipment including process vessels and lines, chromatography skid/column, UF/DF skid, centrifuge, glass/parts washers, and portable processing equipment, and subsequent commissioning, qualification and validation. Must have CIP System/Circuit experience. SHIFT WORK

Responsibilities
• Perform commissioning and provide automation support for CIP systems, including PLC and SCADA/Delta V systems.
• Responsible for GDP documentation.
• Consult with clients/vendors as a department representative regarding major problems or developments.
• Reviews engineering specifications for compliance with ordinances and engineering requirements.
• Perform batch record review, including verifying calibration and in-process data.
• Review piping design and flow calculations for CIP systems.

Required Qualifications
• A minimum of six (6) years of pharmaceutical manufacturing experience or in a GMP Environment and a BS in chemical engineering or related field.
• Experience with CIP systems and circuits, cleaning validation, protocol development, execution, and summary reports.
• Experience with CIP troubleshooting, preferred
• Familiarity with cleaning of process equipment, including CIP cycle development and optimization, piping design, and fluid dynamics.
• A minimum of five (5) years Commissioning, Qualification, and Validation of pharmaceutical manufacturing equipment.
• Reviews engineering specifications for compliance with ordinances and engineering requirements.
• Familiarity with plant control software, including PLC and SCADA/Delta V systems.
• Strong verbal and written communication skills.
• Strong computer knowledge including Microsoft Office products
• Willingness to travel as needed