Responsible Scientist – Quality Control Microbiology Lab (m/w/d)

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.  At Lilly in Germany, we are currently planning and building a high-tech production facility in Alzey (Rhineland-Palatinate), which will expand our production of injectable drugs from 2027 and employ up to 1,000 specialists. To make the most of our innovative production site, we are looking for motivated reinforcements who, together with us, will ensure the supply of Lilly medicines in Germany, Europe, and worldwide, in line with the three Lilly values of "Excellence," "Integrity," and "Respect for People." Join our Lilly team in Alzey and start as soon as possible as: Responsible Scientist – Quality Control Microbiology Lab (m/w/d) What tasks await you? The Responsible Scientist utilizes their technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and completes thorough investigations of aberrant data and results. Outcomes of these activities including results, conclusions, and action plans are thoroughly and accurately documented by the Responsible Scientist and may be published in regulatory and/or technical documents. The position is responsible for technical mentoring of lab staff, sharing technical information and best practice within the work group and across plant sites. Responsibilities / Deliverables: Technical review, interpretation, and release of raw material, in-process, and finished product data. Contributes to annual product reviews and process validations as required. Perform technical training and mentor analysts through formal process/program. Initiate, author, and review change controls and deviations. Utilizes technical skills to lead or perform in-depth investigations into out of spec results and aberrant data. Draws conclusions and performs root cause analysis investigations and recommends solutions to prevent reoccurrence. Develop investigational testing protocols and perform testing as required. Author and assist in execution of method verifications, transfers, and validations. Monitor method and process performance. Improve lab quality systems; develop content, review, and approve SOPs and training as necessary. Contribute to development and implementation of Global Lab Quality Standards. Comply with and implement safety standards. Provide technical oversight for Periodic Management Reviews. Interacts effectively with business partners to communicate and resolve issues and gain a clear and accurate understanding of each other's requirements. Types of communication include: Notification to management of quality issues. Interaction with other functions and auditors. Participation in internal/external audits. How do you convince us? Master's or bachelor's degree with extensive relevant work experience in a science field related to microbiology. 5-10 years of demonstrated relevant experience in a GMP, Microbiology Laboratory, preferably associated with GMP manufacturing. Demonstrated proficiency in laboratory analysis including, but not limited to endotoxin, bioburden, sterility, bioassay, particulate matter, and organism identification. Strong oral and written communication skills and demonstrated through documentation and presentation skills Fluent in English & German Additional Information: Primary location is Alzey, Germany Ability to travel (approximately 10-20 %) On-site