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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.Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Industries
Biotechnology Research and Civil Engineering
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