Sr. Associate - Medicines Quality Organisation

<p>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.</p><p></p><p></p><p>Associate / Senior (Sr) Associate / Principal Associate</p><p>Medicines Quality Organisation (MQO) <b>(R1-R3) / R4</b></p><p><b><span>Job Description:</span></b></p><p>The purpose of the Associate / Sr Associate / Principal Associate – MQO International role is to support the development and implementation of quality systems strategy and activities to support International Business Unit (IBU) goals and objectives for assigned countries or regions.</p><p>In support of this mission, the purpose of this role within an Affiliate/Region is to act as a quality consultant and leader in integrating the quality requirements into the business processes.  The role will implement the quality plan and ensure consistency between the global requirements and local requirements.  This includes the implementation of Safety and Efficacy quality system/procedures and assuring that this system/procedures is aligned with appropriate quality and regulatory requirements. Provide updates on internal/external GxP trends and changes through the country/regional affiliate leadership team(s). Acting as a contact person regarding quality and business process compliance concerns between affiliates and global.</p><p>Primary Responsibilities: This job description is intended to provide a general overview of the job requirements.</p><p></p><p><b>Implement and Manage Quality Systems</b></p><ul><li>Contribute to the development and review of country/region specific quality system documents to ensure requirements and accountabilities are represented.</li><li>Approve regional and/or local required tools, resources, forms, templates.</li><li>Assist in interpreting relevant regulations and guidelines and act as a contact person for global and affiliates.</li><li>Recommend new procedures or changes to existing procedures where applicable.</li><li>Responsible for deviations, change controls, Notification to Management (NTM), ensuring events are appropriately documented, escalated, and completed.</li><li>Conduct root cause analysis and implement Corrective Action and Preventative Action (CAPA) process.</li><li>Support the business on the application and facilitation of quality systems (deviations, notification to management, change control).</li><li>Support activities and processes related to external party management (such as, third-party organizations, business alliance partners) as assigned.</li><li>Perform quality self-assessments, as needed.</li></ul><p></p><p><b>Provide Quality Oversight for business area(s)</b></p><ul><li>Monitors and provide quality oversight for compliance to Safety &amp; Efficacy Quality System (SEQS) in at least one of the following business areas, Clinical operations, Regulatory or Drug Safety.</li><li>Communicates and escalates compliance issues to management locally and globally, as appropriate.</li><li>Provide consultation on the interpretation and practical application of external requirements, standards, and procedures.</li><li>Ensure implementation of regional and/or affiliate Quality Plan(s) as necessary. Monitor progress of actions and provide updates to business and quality leadership.</li><li>Analyze trends, identify areas of weaknesses/gaps and recommend corrective actions.</li><li>Monitor completion of quality related required actions such as: CAPA associated with deviations, change controls, audit or inspection commitments.</li><li>Provides input into risk assessments, audit planning and/or quality plans based on identified signal/risks/gaps.</li><li>Share key learning to drive simplification and replicate best practices in the region and globally.</li><li>Coordinate quality improvement initiatives.</li><li>Seek and implement simplification and process improvement.</li></ul><p></p><p><b>Audits and Inspections</b></p><ul><li>Facilitate audits/inspections (for example,  <span>preparation/readiness,</span> coordination, back room, front room, responses).</li><li>Manage audit and/or inspection responses</li><li>Communicate and ensure inspection readiness requirements are in place, being organisation and availability of documents such as training records, job description, backroom and/or front room organization.</li><li>Ensure completion of audit or inspection CAPA plans and timely resolution.</li></ul><p></p><p><b>Partnership with other area(s) </b></p><ul><li>Functions as the initial point of consultation for business areas on quality related questi