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. **Educational Requirements:** Bachelor's degree in Chemical Sciences. **Language Requirements:** Fluent spoken and written English (C1 level). **Experience Requirements:** Prior experience not required. **Additional Information:** Availability to work afternoon shifts from Monday to Friday. **Personal Skills:** * Interpersonal skills: Teamwork, customer orientation (internal/external), initiative and decision-making, strong oral and written communication, active listening, problem-solving ability. * Organizational skills: Ability to organize workspace and daily activities to ensure maximum quality. Ensure a safe environment to prevent incidents and/or accidents. Attention to detail. Ability to handle multiple tasks simultaneously and prioritize objectives... * Technical skills: Knowledge of Good Manufacturing Practices regulations, GMP policies and procedures. Ability to work in a highly regulated environment. * Computer skills: Proficiency in office software at user level, as well as knowledge of computer systems controlling daily operational activities. **Key Responsibilities:** * Ensure training completion for all assigned tasks. Recognize deviations and initiate, participate in, and/or conduct root cause investigations. * Conduct and/or approve analytical investigations and deviations. * Develop and/or review Quality Control technical documentation required for the role based on learning and experience, ensuring compliance with applicable quality standards. * Develop and/or review laboratory change controls related to the position (e.g., analytical documentation, equipment). * Manage internal Quality Control documents (e.g., laboratory notebooks, analytical methods). * Collaborate in the review of analytical data for release of finished product batches, raw materials, stability studies, and Quality Control service samples. * Promptly and properly report any incidents arising in the area’s activities to the group supervisor. * Participate in audits and self-inspections. * Identify job-related improvements and support implementation efforts. * Contribute to quality system improvements through creation and review of documentation. * Participate in and propose Continuous Improvement initiatives within the team. * Ensure compliance with safety regulations and wear appropriate work attire and necessary personal protective equipment for each task. * Perform job-related tasks safely, complying with all safety and hygiene requirements. * Identify and report any situation that could pose a risk to personnel. * Participate in behavior observations and company initiatives aimed at identifying potential risks. Lilly is dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities when applying 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