Pharmaceutical Engineer - CIP experience required

Description

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

Requirements

• Familiarity with plant control software, including PLC and SCADA/Delta V systems.
• A minimum of three (3) years of pharmaceutical manufacturing experience or in a GMP Environment and a BS in chemical engineering or related field.
• A minimum of three (3) Commissioning, Qualification, and Validation of pharmaceutical manufacturing equipment.
• Familiarity with cleaning of process equipment, including CIP cycle development and optimization, piping design, and fluid dynamics.
• Experience with CIP troubleshooting, preferred
• Strong computer knowledge including Microsoft Office products
• Experience with CIP systems and circuits, cleaning validation, protocol development, execution, and summary reports.
• Strong verbal and written communication skills.
• Willingness to travel as needed

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance