Pharmaceutical Validation Professional
4 days ago
About the Role
This Pharmaceutical Validation Professional position offers an excellent opportunity to work with an award-winning organization based in Dublin.
The successful candidate will provide technical expertise in validation activities, ensuring compliance with regulatory requirements.
Key Responsibilities
The role involves validation oversight of External Manufacturing sites, including process, cleaning, filter, and sterilization/sanitization validation activities.
The candidate will also be responsible for validation document author/approver, ensuring validated parameters are correctly incorporated in Master Batch Records.
Regulatory aspects, such as Aseptic processing system oversight, will also be part of the role.
Other key responsibilities include validation change control assessment, performing Person in Plant activities, and authoring applicable MA filing sections.
The ideal candidate will have a strong background in validation and regulatory aspects, with at least 5 years (ideally 8 years +) of biotech or pharmaceutical industry experience.
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