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Pharmaceutical Engineer - CIP experience required

  • Pharmaceutical Engineer - CIP experience required job type Posted on: Oct 27, 2026
  • Pharmaceutical Engineer - CIP experience required experience level Hyde Engineering + Consulting
  • Pharmaceutical Engineer - CIP experience required employment type Boulder, Colorado
  • Pharmaceutical Engineer - CIP experience required salary Salary: $75 per hour
  • Pharmaceutical Engineer - CIP experience required employment type Onsite
  • Pharmaceutical Engineer - CIP experience required salary Full-time

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Job Title :

Pharmaceutical Engineer - CIP experience required

Job Type :

Full-Time

Job Location :

Boulder Colorado United States

Remote :

No

Jobcon Logo Job Description :

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 Salary range, DOE: $75 - $110K annually 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. Associate  

Jobcon Logo Position Details

Posted:

Oct 27, 2026

Reference Number:

10440_4403660733

Employment:

Full-time

Salary:

$75 per hour

City:

Boulder

Job Origin:

APPCAST_CPC

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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 Salary range, DOE: $75 - $110K annually 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. Associate  

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