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 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.