Job Title:
We are seeking an experienced professional to join our team at a Pharmaceutical organization based in Cork.
This is an excellent opportunity for anyone looking to work with a leading multinational company that excels in its field.
Duties:
* Compile relevant documentation from contractors, suppliers, and other departments for inclusion in reports.
* Prepare reports for executed protocols for review and approval.
* Initiate and implement change control activities in accordance with site procedures.
* Track and resolve exceptions/events/deviations.
* Prioritize MSAT activities in line with the project schedule.
* Coordinate document review and approval.
* Collate and organize files for turnover to QADC.
* Assist in the development of training material.
* Participate in cross-functional teams as required.
* Deputise for the Manager or other team member where required.
* Domestic and international travel may be required.
Education & Experience:
* Bachelor's Degree in a scientific/technical discipline is required.
* Experience in Cleaning Validation is essential.
* Experience in other Validation areas such as Process Validation Support (e.g. Mixing Studies, Media Challenge), Thermal Validation, and Process Validation is desirable.