SIP CIP Validation Engineer
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.
- 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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