SIP CIP Validation Engineer

Overview

On Site
Full Time

Skills

Management
Collaboration
Pharmaceutical Industry
SIP
Pharmaceutics
Mechanical Engineering
Technical Training

Job Details

Job Description:
Responsible for the management and coordination of engineering activities related to CIP (Cleaning in Place) and SIP (Sterilization in Place) with external partners and internal stakeholders.
Responsibilities:
  • Review CIP/SIP design.
  • Develop and implement CIP/SIP strategy.
  • Review user requirements for CIP/SIP.
  • Coordinate with external parties and internal stakeholders to ensure overall alignment and coordination of CIP/SIP design.
Requirements:
  • Minimum 5 years of experience in cleaning and sterilization, specifically in validation or engineering within the pharmaceutical industry.
  • Autoclave experience.
  • Extensive knowledge and experience with CIP & SIP validation and design in the pharma sector.
  • Engineering Degree (Mechanical or Chemical) or equivalent technical training and experience.
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