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Validation Engineer
2 months ago
Job Summary:
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
- 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