Automation, Biotech and Pharmaceutical, CIP (Clean-in-Place), Calibration, Centrifuge, Chemical Engineering, Cleaning Equipment, Column Chromatography, Commissioning, Communication Skills, Consulting, Data Processing, Documentation, Drug Manufacturing, Fluid Mechanics and Dynamics, GMP (Good Manufacturing Practices), Identify Issues, Manufacturing Equipment, Medical Products, Microsoft Office, Microsoft Product Family, Piping, Presentation/Verbal Skills, Programmable Logic Controller (PLC), Supervisory Control and Data Acquisition (SCADA), Validation Plan, Willing to Travel, Writing Skills
The CIP Engineer / Consultant is responsible for cleaning 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.
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 three (3) 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 three (3) 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
Are you looking for a meaningful career that makes a difference in the world? Consider joining the Hyde Engineering + Consulting team where you will do just that. Hyde E+C contributes to helping people live longer, healthier lives by ensuring pharmaceutical and biopharmaceutical manufacturers can effectively and safely produce their life-enhancing and often life-saving medicines. To read more about Hyde's culture and benefits, visit our website: www.hyde-ec.com
Hyde Engineering + Consulting is an equal opportunity, affirmative action employer.
#LI-KH1
Associate
H
Hyde Engineering + Consulting Inc
Hyde Engineering + Consulting is a global design and consulting organization providing process system design, commissioning and validation, FDA compliance, and state-of-the-art cleaning technologies to pharmaceutical, bioprocess and other regulated process industries.
Global capabilities and offices throughout the United States, Europe and Asia gives Hyde clients the convenience of a single worldwide partner. Our staff of over 200 professionals are dedicated to understanding client needs and exceeding their expectations.
Regardless of the size of the facility or complexity of the project, Hyde provides peace of mind through global expertise.
100 to 499 employees
Biotechnology/Pharmaceuticals