Biopharmaceutical Quality Oversight Specialist Opportunity
About the Role
We are seeking a highly skilled Biopharmaceutical Quality Oversight Specialist to join our team in Louth. As a key member of our facility, you will be responsible for ensuring the quality oversight of qualification/validation activities.
* Review validation documentation and associated data for conformance to Standard Operating Procedures (SOPs) and specifications.
* Provide Quality Assurance oversight for events/deviations, investigations, and change evaluations during qualification/validation activities.
Key Responsibilities:
* Ensure all validation documentation is reviewed and approved by Quality Assurance.
* Support Regulatory inspections and Client audits.
* Contribute QA Validations expertise to maintain validation status of the facility.
About You
To be successful in this role, you will require a Bachelor's degree in a scientific or engineering-related discipline and experience in Quality Engineering/Quality Assurance/Quality Validations roles for Biologics or related pharmaceutical/medical device manufacturing in a FDA/EU regulated environment.
You must possess a Stamp 1 G or a Stamp 4 visa for contracting positions in Ireland's pharmaceutical industry.
Candidates should have strong analytical skills and excellent communication skills.
This opportunity offers a chance to work with a leading biopharmaceutical facility, contributing to the development of high-quality products that improve patient outcomes.