Source description
About the role
Job Title: Cleaning Validation Engineer Location: Lincoln Park, NJ Experience: 5+ years
Job Summary: We are seeking an experienced Cleaning Validation Engineer to manage and coordinate engineering activities related to Cleaning in Place (CIP) and Sterilization in Place (SIP) processes. The role involves working closely with internal teams and external partners to ensure effective design, validation, and implementation of CIP/SIP systems.
Key Responsibilities:
Review and assess CIP/SIP system designs.
Develop and implement CIP/SIP validation strategies.
Review and validate user requirements for CIP/SIP systems.
Coordinate with internal stakeholders and external partners to ensure alignment and proper execution of CIP/SIP processes.
Requirements
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Minimum 5 years of experience in cleaning and sterilization, with a focus on validation or engineering in the pharmaceutical industry.
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Hands-on experience with autoclaves.
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Strong knowledge and experience in CIP and SIP system design and validation within the pharma sector.
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Bachelor’s degree in Mechanical or Chemical Engineering, or equivalent technical training and experience.
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