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.Eli Lilly Italia is seeking a QC Laboratory Support Associate to lead cross-functional projects in the Tech Agenda, focusing on laboratory instrumentation and systems.As the Laboratory Secondary Loop Coordinator, you'll be the go-to expert for all things related to lab instrumentation and systems.
You'll ensure that the introduction, qualification, and updates of lab equipment and systems comply with company procedures, pharmacopeias, GMP standards, and applicable GQS/LQS.
Your role is crucial in maintaining GMP and corporate standards within your assigned area.Key Responsibilities:Lead and coordinate lab instrumentation and systems projects, ensuring timely implementation.Assist laboratory Process Teams with the introduction of new lab instruments and system upgrades.Ensure GMP, GQS/CQP, and pharmacopeia standards are applied within your area of expertise.Maintain an appropriate escalation process.Handle investigations related to deviations in your area.Approve procedures within your scope.Approve qualification and requalification documentation for lab instruments (IOQ, PQ, QP, etc.
).Independently manage complex instrumentation/equipment projects.Propose and oversee changes in your sector.Potentially act as System Owner for computerized systems.Assist in managing budget expenses and capital expenditures.Ensure continuous improvement in your area of expertise.Requirements:Master's degree in Engineering or Technical/Scientific disciplines (e.G., Chemistry and Pharmaceutical Technologies)Understanding of manufacturing processes, GMP regulations, and international pharmaceutical standards.Strong analytical skills for data/results analysisFluent in EnglishProblem-solving and decision-making skillsProactivity and autonomyPlanning, prioritization, and unexpected event management skillsContinuous Improvement mindsetWhat we offer:Step into a role where your expertise is recognized, appreciated, and rewarded.
As a member of our team, you can expect:Competitive Salary : We offer a competitive base salary supplemented by an annual variable component based on achieving objectives.Relocation Package: You will be eligible for a relocation package based on your location.Comprehensive Benefits : Enjoy a well-rounded welfare package, including an extensive insurance plan.Annual Salary Review : We recognize and reward your continued effort with an annual salary review, providing opportunities for advancement based on your performance.
As part of our commitment to your future, you may also be eligible to receive a stock option package, aligning your success with the company's growth.#J-18808-Ljbffr
