We are seeking a highly experienced Quality Assurance Specialist to lead our validation efforts in a leading Biopharmaceutical Facility in Ireland.
About the Role
The successful candidate will be responsible for ensuring quality oversight of qualification/validation activities across facilities, utilities, and equipment. This includes reviewing validation documentation, plans, and reports for conformance to SOPs and cGMP requirements.
Additionally, the QA Specialist will provide support during regulatory inspections and client audits, and maintain the validation status of the facility through expert QA validations.
About You
* Bachelor's degree in a scientific or engineering discipline (e.g., biochemistry, chemistry, engineering).
* 5+ years of experience in quality engineering, quality assurance, or quality validations for biologics or pharmaceutical/medical device manufacturing in a regulated environment.
* Stamp 1G or Stamp 4 visa required for contracting positions in Ireland's pharmaceutical industry.
What We Offer
This is an excellent opportunity to join a dynamic team and take your career to the next level. With our strong commitment to quality and customer satisfaction, you will have the chance to make a real impact and grow with us.