SIP CIP Validation Engineer
Katalyst HealthCares & Life Sciences
- Lincoln, NE
- Permanent
- Full-time
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.