




Job Summary: We are seeking a Quality Engineer to monitor GMP services, participate in qualifications, and ensure compliance with standards in the pharmaceutical industry. Key Responsibilities: 1. Monitor GMP services and participate in qualification/validation projects. 2. Ensure quality system management according to established standards. 3. Provide technical and quality advice for continuous improvement. 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. **JOB DESCRIPTION** · Monitor GMP services at the facility. · Actively participate in qualification/validation projects for GMP equipment and systems, providing the Quality Assurance perspective. · Ensure that quality systems directly related to facilities, utilities, equipment, automated equipment, and ISA 95 Level 1 distributed control systems are managed in accordance with established quality standards. · Provide technical and quality advice to Maintenance and Engineering departments to achieve continuous improvement and ensure functional excellence. · Ensure that facilities, utilities, equipment (both factory and Quality Control Laboratory equipment), automated and non-automated, and ISA 95 Level 1 distributed control systems remain validated throughout their entire lifecycle by participating in periodic review and change control processes. **EDUCATION REQUIREMENTS** Engineering degree, preferably Chemical or Industrial. **EXPERIENCE REQUIREMENTS** Not required. Internship experience in the pharmaceutical sector is considered a plus. **LANGUAGE REQUIREMENTS** Fluent English \- spoken and written (C1\). **PERSONAL SKILLS** · Interpersonal skills: teamwork, customer orientation (internal/external), decision-making, strong oral and written communication. · Organizational skills: ability to prioritize objectives; highly organized and detail-oriented individuals. · Technical skills: knowledge of Good Manufacturing Practices (GMP), quality concepts, and their application in the pharmaceutical industry; staying informed about new trends in facilities and utilities and their application in the pharmaceutical industry. · Computer proficiency: familiarity with commonly used office software at the user level, as well as knowledge of information systems controlling business processes. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace\-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. \#WeAreLilly


