Exceptional Quality Assurance Specialist sought for a challenging role in the biopharmaceutical industry. The ideal candidate will possess strong expertise in managing quality records, identifying and resolving deviations, and driving process improvements.
About the Role
We are seeking a skilled Quality Assurance Specialist to join our team in South Dublin. As a key member of our operations team, you will be responsible for ensuring the highest standards of quality in our manufacturing processes.
Key Responsibilities:
* Act as disposition manager, ensuring that batch disposition activities are managed efficiently.
* Manage and drive Quality records to closure, including deviation records and investigation reports.
* Initiate Quality records for supplier-related changes.
* Collaborate with Complaints team to request assessments, review complaint reports, and address comments.
* Provide data to support Quality Management Processes.
* Participate in operational and quality improvement initiatives, programs, and projects.
Requirements
To be successful in this role, you will need:
* A university degree in an engineering or science related discipline.
* Minimum 4 years' experience in a cGMP manufacturing environment, with a strong understanding of regulatory requirements and expectations.
* Ability to positively impact others, affect behaviors, and connect with colleagues.
* Previous experience in batch release activities.
* Good working knowledge of SAP.
Benefits
This is a fantastic opportunity for a motivated individual to take their career to the next level. We offer a dynamic work environment, competitive salary, and opportunities for professional growth and development.
Contact Information
Applicants must have a Stamp 1G or a Stamp 4 visa. Please note that we cannot provide visa sponsorship.