Job Description
A Cleaning Validation Engineer is needed for a 12-month contract with a global Pharmaceutical company.
Main Responsibilities:
* Taking Cleaning Validation samples alongside Upstream/Downstream processing and collaborating with manufacturing to ensure CIP/SIP and dirty holds are completed correctly.
* Developing, executing, and reviewing validation protocols.
* Generating, reviewing, and approving protocols.
* Reporting writing duties.
* Maintaining and updating the Cleaning Validation Plan.
Qualifications & Preferential Experience:
* Degree in Engineering or Science discipline.
* At least 3 years of relevant experience.
* Aseptic technique expertise.
* Experience with Gowning for ISO7/ISO8 environments.
* Technical writing skills.
* Deviation/Change control writing experience.
* Understanding of baseline studies for new equipment.