Process Engineer - CIP Cycle Development Subject Matter Expert (SME)

Company Name:
Hyde Engineering + Consulting
Since 1993, Hyde has been a worldwide leader and global service provider to pharmaceutical and biopharmaceutical industries. Our projects result in the successful design, construction, commissioning, and validation of manufacturing facilities and equipment.
As a member of the Hyde team, you'll be part of providing state-of-the-art solutions for some of the industry leaders. As we continue to grow our operations around the world, we need the best talent--men and women dedicated to quality and innovation. We offer a collaborative culture, challenging projects, and excellent compensation and benefits. You will find these values reflected in our company:
Family Happiness
Integrity
Friendship
Wisdom
Adventure
Position: Process Engineer, Subject Matter Expert in CIP Cycle Development
The process engineer is responsible for cleaning cycle development for downstream equipment in the biotech and pharmaceutical industries.
Responsibilities
Act as process engineering lead for developing cleaning development strategy.
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 risk assessment and gap analysis for site cleaning programs.
Perform batch record review, including verifying calibration and in-process data.
Perform spray coverage testing, cleaning verification/validation swabbing, and risk sampling.
Perform 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
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.
Proven experience with: CIP cycle development, 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.

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