**Cleaning Validation Specialist**
We are seeking a highly skilled and experienced Cleaning Validation Specialist to join our team on a 12-month contract based in Dublin.
About the Role:
* The successful candidate will be responsible for maintaining and updating the Cleaning/Validation Master Plan to support multi-product drug substance manufacturing facilities.
* They will develop and implement cleaning strategies for fixed and mobile parts, as well as optimize cleaning cycles/methods/recipes for buffer and media preparation systems, bioreactors, equipment trains, parts washers, and supporting process equipment.
* Additionally, the individual will generate and execute cleaning validation protocols as required, and author and review process transfer/cleaning documentation, risk assessments, technical protocols and reports, verification/validation documents, and supporting documentation.
Required Skills and Qualifications:
* At least 2 years' experience in Technical Services, Manufacturing, or Quality Support in a biological bulk drug substance manufacturing organization is essential.
* The ideal candidate will have technical and operational knowledge of cleaning validation/verification, quality systems, and regulatory requirements across multiple health authorities.
* Experience in cleaning validation and verification of downstream processing equipment is also desirable.
Benefits:
This role offers an exciting opportunity to work with a leading pharmaceutical organization and contribute to the development of innovative cleaning validation strategies.
Others:
The successful candidate will have the opportunity to work in a collaborative environment and contribute to the growth and success of the organization.