Pharmaceutical Engineer - CIP experience required

Hyde Engineering + Consulting

Mumbai

On-site

INR 800,000 - 1,200,000

Full time

14 days+

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Job summary

Hyde Engineering + Consulting in Mumbai is seeking a CIP Engineer / Consultant responsible for cleaning cycle development across a variety of equipment. The candidate will perform commissioning, provide automation support for CIP systems, and consult with clients regarding issues. Candidates should have a BS in chemical engineering or related field, a minimum of three years in pharmaceutical manufacturing, and experience with CIP systems. This position requires strong communication skills and a willingness to travel as needed.

Qualifications

  • Minimum of three years of experience in pharmaceutical manufacturing or GMP environment.
  • Experience with CIP systems and circuits, cleaning validation, protocol development.
  • Familiarity with cleaning of process equipment, CIP cycle development and optimization.

Responsibilities

  • Perform commissioning and provide automation support for CIP systems.
  • Responsible for GDP documentation.
  • Consult with clients/vendors regarding major issues.

Skills

CIP System experience
Pharmaceutical manufacturing experience
PLC and SCADA/Delta V systems
Cleaning validation
Strong communication skills
Microsoft Office Knowledge

Education

BS in chemical engineering or related field

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.

Hyde Engineering + Consulting is an equal opportunity, affirmative action employer.

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