Cleaning Validation Specialist
About this role:
We are seeking a skilled Cleaning Validation Specialist to support our multi-product drug substance manufacturing facility. The successful candidate will play a key role in maintaining and updating the Cleaning/Validation Master Plan, developing and implementing cleaning strategies for fixed and mobile parts, and generating and executing cleaning validation protocols as required.
Key responsibilities include:
* Maintain and update the Cleaning/Validation Master Plan.
* Develop and implement cleaning strategies for fixed and mobile parts.
* Generate and execute cleaning validation protocols.
About you:
To be successful in this role, you will need to have a strong understanding of cleaning validation/verification, quality systems, and regulatory requirements across multiple health authorities. You should also have experience in Technical Services / Manufacturing / Technical Development/Quality Support in a biological bulk drug substance manufacturing organisation, with at least 2+ years' experience.
This is an excellent opportunity to work with a leading biopharmaceutical organisation that paves the way with state-of-the-art technology on their one-of-a-kind manufacturing facility. You will have the opportunity to work on a variety of projects, develop your skills and knowledge, and contribute to the success of our team.