Responsibilities
- Provide subject matter expertise to key engineering projects to startup and cycle development projects.
- Directs other employees in the execution of a variety of projects.
- Reviews engineering specifications for compliance with ordinances and engineering requirements.
- Consult with clients/vendors as a department representative regarding major problems or developments.
- Prepares periodic reports and records.
- Advises and answers a variety of technical questions.
- Create cleaning cycle development strategies 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.
- Perform piping design and flow calculations for CIP systems.
- Hydraulic Calculations: Flow Rate, Reynolds Number, Pump Sizing, etc.
- Consult with clients/vendors as a department representative regarding major problems or development.
- Perform commissioning and provide automation support for CIP systems, including PLC and SCADA/Delta V systems.
- A minimum of ten (10) years of pharmaceutical manufacturing experience or in a GMP Environment and BS in chemical engineering or related field.
- Experience with: CIP cycle development, cleaning validation, protocol development, execution, troubleshooting, and summary reports.
- Experience with CIP shakedowns and troubleshooting
- Experience with CIP change parameters and parameter adjustment
- Experience with CIP cycle runs
- Hydraulic Calculations: Flow Rate, Reynolds Number, Pump Sizing, etc.
- Familiarity with plant control software, including PLC and SCADA/Delta V systems.
- Familiarity with engineering project management.
- Strong verbal and written communication skills.
- Strong computer knowledge including Microsoft Office products.
Hyde Engineering + Consulting is an equal opportunity, affirmative action employer.
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