Job Title: Senior Quality Assurance Systems Specialist
Job Description:
We are seeking a highly skilled and experienced Senior Quality Assurance Systems Specialist to join our team in Dublin. As a key member of our quality assurance department, you will play a vital role in ensuring the highest standards of quality in our pharmaceutical organization.
This is an excellent opportunity for anyone looking to work in a leading multinational company that is renowned for its commitment to excellence. You will be responsible for developing and maintaining site quality systems, quality compliance and related procedures and processes.
* Responsibility and oversight for the development and maintenance of site quality systems, quality compliance and related procedures and processes, including but not limited to, Documentation Management, Change Control, Deviation/CAPA processes, oversight of applicable QMS systems supporting and the overall Quality Management Review process.
* Provide Quality direction and input at Change Control and Deviation Review Boards and assume oversight of change control and Deviation/CAPA records; ensuring scope of record is clear and implementation activities are robust and timely.
* Oversee and implement Quality Agreements relating to area of responsibility.
* Keep abreast of regulatory initiatives and new guidance/requirements and for the communication of revised guidelines associated to Quality Systems.
* Responsible for sustained compliance initiatives, including execution of gap assessments in support of revised operating Standards and/or Corporate policies & procedures.
* Oversight and management of Quality Risk Management (QRM) Processes and for the embedding of QRM principles within the quality framework.
* Ownership, accountability and provision of Subject Matter Expertise for key quality Systems, including Change Control, Deviation/CAPA processes and Documentation Management.
* Responsible for trending programs associated with Deviation/CAPA, Change Control, Complaints, Periodic Reviews, QRM, ensuring that trend programs and outputs are providing key indicators as to program efficacy.
* Responsible for challenging current procedures and practices, interpretation of trend data and for making any necessary revisions to quality programs to afford optimisation and further development of existing quality standards and overall compliance.
* In line with business requirements, these responsibilities may expand or otherwise include additional areas of responsibility which are not described in this specification but are associated with the role. The knowledge and skills necessary to perform the duties of the QA Specialist are typically acquired through the following combination of education, experience and knowledge.
* Ensuring that the self-inspection, audit and key compliance systems are effectively implemented, revised and optimised to ensure a continuous drive to improve product and process quality at site.
Required Skills and Qualifications:
* University degree. Engineering or Science related discipline preferred.
* Relevant experience (8yrs +) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role.
* Experience working in aseptic operations, protein formulation, vial and syringe filling.
Benefits:
As a Senior Quality Assurance Systems Specialist, you will have the opportunity to work in a dynamic and fast-paced environment where you can make a real difference in ensuring the highest standards of quality in our organization.
Others:
If you are interested in this position, please feel free to contact us for further information.