Company description: WuXi Biologics is a world-class biologics services provider (from discovery, through to commercialisation) with global clients in the biopharmaceutical and healthcare industries. Our mission is to accelerate and transform discovery, development and manufacturing in the fast growing field of biologics to benefit patients worldwide. The company has sites/offices in China, US, EU and Asia. The company currently employs over 5,000 employees worldwide, and are providing services to over 200+ clients globally, including 13 of the top 20 biopharmaceutical companies. Job description: QA Compliance Specialist As QA Compliance Specialist you will be responsible for supporting the QA GMP supplier and service provider management processes, regulatory surveillance, the internal audit program, inspection readiness, Client audits and Health Authority inspections, support the provision of the GDP orientation, GMP orientation and GMP refresher training programs, generation of PQRs, approval of risk assessments, change controls & deviations on behalf of the quality department Organization Description As QA Compliance Specialist, youll be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives. In this role you will report into the QA Senior Manager. Essential Duties and Responsibilities: Support the qualification of new material suppliers and GMP service providers and support the maintenance of the Approved Supplier and Service Provider Lists Participate in auditing of GMP suppliers and GMP service providers from time to time. Act as SAP Key User for material supplier data. Support the review and approval of GMP supplier and service provider changes, including coordinating change control activities with internal and external cross functional teams. Support the resolution of quality deviations and closure of CAPAs. Support the internal audit program, including managing the schedule, conducting the internal audit and maintenance and reporting of metrics relating to internal audits. Participate and follow-up on audits and/or inspections carried out at the site by Regulatory Authorities or Clients. Participate in initiatives and action plans for the development of QA and improvement of GMP compliance. Manage and provide support for the site electronic quality management system (EQMS). Provide site metrics and KPIs as required for the Quality Management System (QMS). Provide support for the Quality Management Review (QMR) as applicable. Review and Approve Risk Assessments, change controls, deviations and complaint investigations and collate PQRs. Support the site regulatory surveillance. Management of product & material complaints. Execute Mock recall. Assist in preparation and presentation of GMP orientation and refresher training programmes. Perform all duties in accordance with GMP requirements, SOPs and controlled documents. Will be flexible to take on additional tasks and responsibilities at the discretion of the QA Senior Specialist/QA Senior Manager/ QMS Lead. Will act as a role model for the Quality Assurance function and the wider organisation in adherence to the WuXi corporate core values and PROUD culture Your Profile The ideal candidate for this position will have the following: Education: A Bachelors degree in a technical discipline (e.g. biochemistry, chemistry, engineering) would be an advantage. Knowledge/Experience: Demonstrated knowledge of Quality Management System and continuous/process improvement tools. Experience in the biotechnology and/or pharmaceutical industry within a Quality role. Candidates from Manufacturing Operations, Validation, Engineering, and other technical disciplines within the biotechnology and/or pharmaceutical industry will be considered but knowledge of Quality Management System, pharmaceutical regulations and continuous/process improvement tools will be required to be demonstrated. Experience in performing internal audits and risk assessments would be an advantage. Technical Competencies: Required: Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures). Strong knowledge of cGxP requirements and regulations Knowledge of trouble shooting and problem-solving skills, e.g. formal root cause analysis such as Ishikawa diagrams, FMEA etc. An Auditor qualification would be an advantage Demonstrated knowledge of Quality Management System and continuous/process improvement tools. Behavioural Competencies Adaptable, able to multi-task and handle tasks with competing priorities effectively to deliver site priorities. Demonstrated organisation and collaboration skills with a teamwork mindset. Excellent communication skills (written and oral). Analytical with demonstrated problem solving & root-cause analysis skills Proactive attitude with good attention to detail Other Requirements There may be a requirement for occasional travel to locations within Ireland and overseas to support business needs. Must be willing to travel when required. As we extend our global reach, we need colleagues interested in change, in challenge, and in building a new future together. Reach beyond yourself and discover your true potential If you can thrive in a dynamic and fast-paced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our mission - Any drug can be made, and any disease can be treated - dont miss out on this opportunity to join us and reach beyond yourself and discover your true potential. Apply now Would you like to know more before you apply? Please visit us at or contact us via WuXi Biologics is an equal opportunities employer. Skills: Attention to Detail Quality Oversight QMS Stakeholder Management Benefits: Bonus Parking Pension VHI