Qureos Mentor

Eli Lilly

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
Lilly&rsquo;s Purpose
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 35,000 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&rsquo;re looking for people who are determined to make life better for people around the world.
The Enterprise Data Platforms Organization enables the business functions with an integrated and intuitive Enterprise platform services in the field of Databases, Integration and Analytical Platform services.
Roles &amp; Responsibilities: SaS Platform Grid/Viya Administrator: (3-10 Years of Experience)
SAS Platform Administration<ul><li>
Install, configure, and maintain SAS 9.4 Grid / Viya in Linux environments.</li><li>
Deploy and manage SAS Grid on AWS EC2&rsquo;s with EFS as shared file storage.</li><li>
Configure SAS Metadata Server, Compute nodes and Mid-Tier.</li><li>
Apply SAS hotfixes, perform password rotations and manage version upgrades(Life Cycle Management).</li><li>
Configure and maintain SAS libraries, authentication, and metadata security.</li><li>
Troubleshoot any issues and get Root Cause Analysis(RCA). If needed collaborate with SAS vendor.</li><li>
Maintain 100% availability of the SAS Grid platforms.</li></ul>
Linux &amp; AWS Infrastructure Management:<ul><li>
Administer Linux servers used for SAS Grid (Red Hat / Amazon Linux).</li><li>
Manage AWS resources for SAS deployment &ndash; EC2, EFS, Security Groups, IAM roles.</li><li>
Aware and used different filesystems(both Windows and Linux based protocols).</li><li>
Implement high availability and disaster recovery strategies in AWS.</li><li>
Collaborate with multiple platform teams(Linux/Windows/Storage/Network/VM)</li></ul>
Automation &amp; Monitoring:<ul><li>
Develop custom monitoring scripts (Bash, Python, Perl) for Grid job performance, disk usage, metadata health, and system availability.</li><li>
Automate access provisioning and de-provisioning processes via scripts and metadata APIs.</li><li>
Integrate SAS monitoring with enterprise tools (Splunk, Grafana, CloudWatch, etc.).</li><li>
User Support &amp; Governance - Provide technical support for SAS developers, analysts, and business users in case of any Grid related issues</li><li>
Manage metadata security, roles, and permissions.</li><li>
Document SOPs for SAS platform maintenance and deployment.</li><li>
On-call support for any P1/P2 Incidents.</li><li>
Weekend on-call support and available for any maintenance activities.</li></ul>
Required Skills &amp; Experience:<ul><li>
Graduation with 3-10 years of working experience on SAS Grid Platform.</li><li>
SAS Grid Platform Administration &ndash; SAS 9.4 Grid on Linux and Viya 4.0 on AWS EKS</li><li>
SAS Desktop tools(SAS EG, PC SAS) installation and maintenance.</li><li>
Knowledge of SAS Viya cloud deployments and administration.</li><li>
Knowledge of JMP tool, R administration</li><li>
Basics of Clinical trial process and steps.</li><li>
Exposure to tools like Python and R.</li><li>
Hands on fundamental experience with Base SAS and basic SAS Macros.</li><li>
Experience with LSF/GSUB for job scheduling and workload balancing</li><li>
Strong understanding of SAS Metadata security and authentication</li><li>
Configure SAS Environment Manager and expertise</li><li>
AWS &ndash; EC2 provisioning, EFS configuration, networking, security</li><li>
Linux Administration &ndash; Server setup &amp; monitoring, performance tuning, troubleshooting</li><li>
Knowledge in VMs concept and usage.</li><li>
Understanding on Citrix setup and its usage</li><li>
Monitoring &amp; Automation &ndash; Bash/Python scripts, SAS logs monitoring, SAS environments monitoring, automated provisioning</li><li>
Familiarity with backup and Disaster Recovery processes in AWS and On-prem.</li><li>
Integration with LDAP/AD for user authentication</li><li>
Filesystem with Windows, Linux and multi-protocol based solution.</li><li>
Familiarity with CloudFormation / Terraform for infrastructure automation</li><li>
Experience with monitoring tools like CloudWatch, Splunk</li><li>
Tickets handling with Service Now or any other ticketing tools.</li><li>
Expertise in Documentations for maintaining Security/CSQA standards.</li><li>
Must have excellent communication and interpersonal skills.</li><li>
Handle business requirements and queries.</li></ul> 
Additional Details:<ul><li>
Availability to work flexible work hours is/may be required. This team will support continuous operations across two shifts and therefore, this role will require non-standard work hours, and some work on weekends and holidays. Appropriate adjustments in benefits will be provided for employees working non-standard hours where applicable.</li><li>
This role is open across experience levels, and the final designation will be determined based on the interview and assessment outcomes.</li></ul>
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</div>

SAS Platform Grid/Viya Administrator

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
JOB SUMMARY 
Medical Science Liaisons (MSL) are field based medical professionals with deep content knowledge about specific disease states, Lilly and competitor compounds along with having knowledge on current issues in the therapeutic areas they represent. MSLs recognize and communicate feedback and insights of strategic importance from their interactions with Scientific Experts, to better inform Lilly&rsquo;s strategic direction for research and commercialization. By facilitating scientific exchange between industry and the scientific community, MSLs have the opportunity to shape the future of healthcare by providing needed information that addresses important clinical and scientific questions.<div> 
JOB RESPONSIBILITIES 
Maintain and effectively communicate deep scientific knowledge: 
<ul><li>Engage and ensure continuous learning to maintain the highest level of technical expertise within their respective therapeutic area. This will enable the MSL.</li><li>Be equipped to answer deep scientific questions and be sought after by their customers based on peer-credible knowledge and expertise.</li><li>To establish oneself as a reliable, trusted, resource of unbiased, accurate, up-to-date, medical and scientific knowledge requested and desired by customers.</li></ul>
Excellence at customer engagement and support medical/scientific information needs of scientific experts:</div><ul><li>Ensure customer facing engagement through mutually beneficial 2-way dialogues with scientific experts.</li><li>Act as the primary interface between Lilly medical and scientific experts to deliver the best-in-class customer experience through application of effective emotional intelligence and deep understanding of customer needs.</li><li>Connect scientific experts with Lilly resources or internal business partners as appropriate and identify possible collaborative research or external collaborations.</li></ul><div>
Strategic vision and leadership: 
<ul><li>Synthesize complex data and effectively communicate meaningful clinical insights and unanswered customer questions received from Scientific Experts to Lilly medical and cross -functional teams (CFT).</li><li>Use reactive problem-solving skills and utilize internal resources effectively to execute upon solutions.</li><li>Use a principle-based decision-making approach to make decisions independently or escalate them appropriately.</li><li>Cultivate internal networks and collaborate effectively across functions with an active contribution to medical planning and strategy in the affiliate.</li></ul></div><div>
Territory ownership: 
<ul><li>Demonstrate strategic analysis, planning, and prioritization to maximize efficiency.</li><li>Implement and evaluate a strategic territory plan prioritizing core activity and take personal accountability for results.</li><li>Execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws, demonstrating good judgement at all times.</li></ul></div><div>
Professional Development: 
<ul><li>Keep up to date on trainings for professional development.</li><li>Ensure Performance Management objectives are completed in line with company process.</li><li>Understanding of all company policies and procedures.</li></ul></div><div> 
JOB QUALIFICATIONS 
EDUCATION 
<ul><li>Medical Doctor</li></ul>
EXPERIENCE 
<ul><li>Proven experience to work as an individual and team contributor.</li><li>Proven experience to engage medical professionals.</li></ul></div><div>
Desirable 
<ul><li>Minimum of 1 years&rsquo; MSL experience within a multinational company.</li><li>Experience in Oncology &amp; Hematology therapeutic areas preferred.</li><li>Experience with academic communities, medical research, and medical education process.</li></ul>
SOFT SKILLS 
<ul><li>High learning agility to comprehend and effectively communicate large amounts of complex scientific content in a clear and concise fashion.</li><li>Independent contributor to be able to work alone in the field effectively managing multiple priorities and projects.</li><li>Strategic and critical thinking to analyze, assess and evaluate information and interpret impact or relevance to future states.</li><li>Strong verbal and written communication skills.</li><li>Resiliency in managing complex challenges.</li><li>Strong teamwork and interpersonal skills.</li><li>High emotional intelligence.</li><li>Strong relationship building and networking.</li><li>Strong planning and organization.</li></ul>
TECHNICAL SKILLS</div><ul><li>Advanced presentation and computer skills with expertise in literature identification.</li><li>Ability to use field-based electronic or other communication tools needed for role.</li></ul>
OTHER QUALIFICATIONS 
<ul><li>Ability to travel 80% of the time (role is pre-dominantly field based)</li><li>Will require domestic travelling and may require international travel.</li><li>May require evening/weekend work.</li></ul>
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</div>

Medical Science Liaison, Oncology, Türkiye

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
Organization Overview:
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&rsquo;re looking for people who are determined to make life better for people around the world.
Lilly is currently constructing a cutting edge facility for the manufacture of new modalities including Gene Therapy in Lebanon, Indiana. This facility will be Lilly&rsquo;s most technically advanced manufacturing site focused on the delivery of the next wave of innovative products at Lilly. It will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety, quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to start up the facility for both clinical and commercial supply.
This is an exciting opportunity to help start up a state-of-the-art facility and build a manufacturing supply chain from ground-up. The Supply Chain organization has responsibility for scheduling the manufacturing processes for Lebanon Advanced Therapies site and supporting manufacturing with all inbound and outbound material flows.
The Master Data Analysts play a critical role within the Supply Chain organization by maintaining the fundamental master data set residing in SAP. The initial phase of the project will require extensive cross-functional work with procurement, quality, and warehouse operations to deliver an operational SAP system. As the site transitions to the production phase, the team will also be involved in tracking supply chain metrics and driving continuous improvement. They will work closely with multiple teams across the site to manage data change requests, solve technical issues, and contribute to continuous improvement activities around Master Data.
Responsibilities:<ul><li>
Develop and maintain key data and data design in SAP (Material Master, Bill of Materials, Recipes, Resource, Purchasing-Info Records and Warehousing) and associated systems</li><li>
Create and maintain Standard Operating Procedures (SOPs) and training materials</li><li>
Ensure global data consistence and conformance to SOPs while managing master data updates due to process or system changes.</li><li>
Serve as a key member of the SAP Implementation Project Team during the greenfield site construction/startup phase.</li><li>
Contribute to global initiatives for Master Data Management, as required, and attend select Power User forums to share best practices with peers</li><li>
Generate OSSCE (Operational Standards for Supply Chain Excellence) metrics and Pareto analyses</li><li>
Drive process improvement initiatives which could include developing process flows for setup of new materials and leveraging appropriate tools/reports to track maintenance efforts, data accuracy, and data completeness</li><li>
Participate in annual standard costing assessment in readiness for Business Planning and drive the annual review of planning data</li><li>
Troubleshoot SAP or MES execution problems, identify root causes, and implement solutions</li><li>
Investigate deviations and provide impact assessments for change management</li><li>
Maintain a safe workplace through proper ergonomic practices</li><li>
Maintain a state of compliance (learning plan, SOP adherence, etc.)</li></ul>
Basic Requirements:<ul><li>
Bachelor&rsquo;s degree</li></ul>
or<ul><li>
high-school diploma with 5+ years relevant SAP work experience</li></ul>
Additional Preferences:<ul><li>
SAP / Master Data experience in Material Master creation and maintenance</li><li>
Knowledge / Experience in Manufacturing, Packaging, and/or Customer Service</li><li>
Strong organizational and Project Management skills</li><li>
Strong interpersonal skills</li><li>
Customer-oriented</li><li>
Excellent Computer skills (e.g., MRP, SAP, Excel)</li></ul>
Other Information:
<ul><li>8 hour work days &ndash; Monday through Friday</li><li>
May need to be available off shift and respond to operational issues as-needed</li><li>
Minimal travel required (&lt;5%)</li></ul>
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$58,500 - $137,500
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Master Data Analyst - Advanced Therapies

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
Location: Dubai, UAE 
Department: Digital Marketing / Commercial Operations 
Reports to: Associate Director, Consumer Engagement &amp; Innovation - META
Job Summary:
We are looking for a consumer-first strategist to join our Consumer Experience &amp; Innovation Team. The role will focus on developing Lilly&rsquo;s digital business model through advancing e-commerce and digital partnership strategies that expand access to Disease State Education (DSE) and enhance the consumer journey. You will play a critical role in shaping the future of how we engage externally with patients and consumers, as well as educating and upskilling the internal organization on this novel capability.
Key Responsibilities:<ul><li>
Design and implement consumer-centric DSE experiences that support patient, consumer, and caregiver needs.</li><li>
Identify and evaluate emerging and established platforms, such as digital health platforms, e-pharmacies, telehealth services, e-commerce channels, and other relevant marketplaces, to integrate DSE solutions.</li><li>
Build and manage strategic partnerships to expand the reach of DSE content and drive personalized consumer journeys.</li><li>
Lead the development of a scalable digital business model and Insite program optimization across owned (e.g., Lilly Direct) and third-party channels, ensuring a seamless experience from awareness to diagnosis, prescription, and fulfillment.</li><li>
Analyze performance metrics to optimize digital initiatives, drive ROI, and inform future strategy.</li><li>
Stay ahead of e-commerce and digital health trends by identifying new growth opportunities and technologies to expand the digital ecosystem.</li><li>
Ensure all digital content and tactics are compliant with industry regulations and undergo proper Medical, Legal, and Regulatory (MLR) review.</li><li>
Collaborate with cross-functional teams (e.g., brand, B2B, Medical, Legal, IT, BI&amp;A, OCE) to align on strategy, execution, and measurement.</li><li>
Manage and optimize MarTech platforms (such as Adobe Experience Cloud, Salesforce Marketing Cloud, Veeva CRM, Google Analytics, and Customer Data Platforms) for targeting, automation, and insights.</li><li>
Champion innovation by piloting and scaling digital initiatives that improve patient and consumer outcomes.</li></ul>
Required experience and skills:<ul><li>
Proven track record in managing and optimizing digital campaigns through KPIs such as ROAS, CAC, LTV, and conversion rates.</li><li>
Strong understanding of the digital health ecosystem, including digital business models, consumer journeys, and direct-to-consumer solutions.</li><li>
Experience in designing consumer- and patient-centric journeys that drive measurable outcomes.</li><li>
Excellent communication and presentation skills, with the ability to influence and educate internal stakeholders.</li><li>
Start-up mentality with an entrepreneurial mindset, driving novel concepts from ideation to implementation.</li></ul> 
Qualifications:<ul><li>
Bachelor&rsquo;s degree in marketing, business, digital media, or a related field (MBA is a plus).</li><li>
5+ years of experience in digital marketing, e-commerce, preferably within FMCG, OTC, and health tech.</li></ul>
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</div>

Manager - E-Commerce & Digital Partnerships, META

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.<div>
JOB RESPONSIBILITIES</div><div></div><div><div><div><div><div><div><div><div><div>
Brand Team Support<ul><li>
Serve as a key medical point of contact for the brand team.</li><li>
Contribute clinical, scientific, and strategic input to support the cross functional team.</li><li>
Medical launch support</li><li>
By offering scientific and creative input, contribute to the development (local materials) and/or review (global/regional materials) of promotional materials for the brand teams.</li><li>
Effectively communicate and transfer knowledge of the therapeutic available solutions environment, the clinical landscape and relevant medical and scientific information</li><li>
Support the medical training needs of internal business partners such as sales and marketing.</li><li>
Support the planning &amp; implementation of symposia, advisory boards, scientific exchange, and educational meetings/events with HCP&rsquo;s.</li></ul>
Customer Support &amp; Experience<ul><li>
Respond to external customer questions and needs, including escalations by Med Info &amp; sales in accordance with company-wide requirements for responding to unsolicited requests for information.</li><li>
The local coordination of activities and engagement of Thought Leaders</li><li>
Speaker training</li><li>
Develop and maintain collaborations and relationships with relevant professional societies.</li><li>
Deliver scientific, educational, and promotional presentations internally and to customers.</li><li>
Collaborate cross-functionally to drive improvement in customer engagement through Digital innovation.</li><li>
Oversee the collation and analysis of customer information to drive understanding and insights.</li></ul>
Scientific Expertise and Medical Affairs Delivery<ul><li>
Develop and/or contribute to the affiliate / therapeutic area medical plan and strategies.</li><li>
Support data analysis and the development of slide sets and publications (abstracts, posters, manuscripts)</li><li>
Keep up to date with medical and other scientific developments relevant to the product or portfolio.</li><li>
Be aware of current trends, issues and projections for clinical practice and access.</li><li>
Partner with other existing medical affairs roles to achieve a seamless medical team aimed at delivering exceptional customer experiences.</li><li>
May serve as the affiliate medical/scientific leader including research and regulatory deliverables.</li></ul>
QUALIFICATIONS<ul><li>
Advanced degree (MD) in health sciences min. 3 years of relevant clinical, therapeutic experience or relevant scientific industry experience</li><li>
Cardiometabolic Health experience preferred</li><li>
Good planning and organization skills</li><li>
Strong communication skills</li><li>
Ability to effectively partner across multiple functions.</li><li>
Advanced interpersonal, project management and presentation skills</li><li>
Fluent in English (both verbal and written)</li><li>
Ability to &lsquo;translate&rsquo; scientific data into meaningful, clear, and compliant content for customer communications and engagement.</li><li>
Commercial/business acumen</li><li>
Location: Based in Istanbul</li></ul></div></div></div></div></div></div></div></div></div>
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</div>

Director - Medical, CMH, Türkiye

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
Organization and Function Overview
Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a pioneering center that integrates advanced manufacturing and drug development. As the first facility of its kind, the Foundry is designed to accelerate innovation in manufacturing processes, expand capacity for clinical trial medicines, and speed Lilly innovative medicine to Clinics, and reduce both costs and environmental impact.
The Process Translation and Execution (PTE) team translates API/DS process knowledge into clinical supply readiness, oversees technology transfer, implements phase-appropriate control strategies, and ensures right-first-time clinical manufacturing for a variety of modalities, including synthetic molecules, biologics, peptides, oligonucleotide, and bioconjugates (ADC,ARC etc.)
Through cross-functional collaboration, PTE influences process design, revolutionizes clinical manufacturing, builds capabilities in emerging technologies and aligns with corporate and LRL goals, drives scientific excellence and innovation to accelerate manufacturing advancements and propels the site toward long-term business success.
In the Foundry Construction and Project Delivery/Startup Phase (2025 To 2028), roles will be &#64258;uid and dynamic as we build a new organization, design and implement the necessary systems and business processes required to enable operational readiness, support the project delivery, and build the site culture. Success will require significant collaboration, creativity, and resilience as the Lilly Medicine Foundry transitions from design to startup and ultimately to steady-state operations and continuous improvement. This period presents a unique opportunity for learning, growth, and making a lasting impact.
We are seeking enthusiastic scientists and engineers to join the PTE team and help bring the Lilly Medicine Foundry&rsquo;s vision to life.
Key Responsibilities:<ul><li>
Tech transfers: Lead or support the transfer of API/DS processes from Process Development (PD) into the cGMP facility. Translate process knowledge and control strategies into manufacturing documentation/procedures; author and review essential tech transfer documentation; conduct facility fit assessments and establish lab models; design and execute needed lab studies to ensure a successful process transfer into GMP production.</li><li>
Manufacturing campaign support: Provide on-the-floor support for critical operations, real-time technical expertise during clinical manufacturing campaigns. Daily attendance at process team meeting ideally physically in the control room.</li><li>
Process troubleshooting and investigations: Serve as the technical lead for process deviations, quality events, and non-conformances. Perform root cause analysis and develop effective corrective and preventive actions (CAPAs).</li><li>
Data Analysis&amp; Process Monitoring: Analyze manufacturing data to monitor process performance, identify trends, and ensure the process remains in a state of control.</li><li>
Documentation: Author, review technical documents, including tech transfer plan, standard operating procedures (SOPs), batch records, campaign summary reports, and deviation reports.</li><li>
Cross Functional Collaboration: Work with development, manufacturing operations, quality assurance, and regulatory affairs to achieve project and manufacturing goals.</li><li>
Process improvement: Apply scientific knowledge to identify areas for improvement and implement new technologies or procedures.</li><li>
Training/mentoring: Provide training/mentoring to junior scientists, technicians/operators, or in laboratory procedures, data analysis and all PTE activities.</li></ul>
Basic Requirements<ul><li>
BS or MS in Chemistry, Biology, Biochemistry, Chemical/Biological Engineering, or related disciplines</li><li>
Experience: BS with 10+ years, or MS with 7+ years in Pharmaceutical Manufacturing Science and Technology (MSAT), Technical Service Manufacturing Science (TSMS), or Process Development; experience in manufacturing environments for synthetic molecule API, biologics DS is preferred.</li></ul>
Additional Skills and Preferences<ul><li>
Problem-solving skills: Proven ability to analyze data, perform root cause analysis, and resolve complex technical challenges.</li><li>
Communication skills: Excellent written and verbal communication skills for technical report writing, presentations, and effective collaboration across teams.</li><li>
Collaboration: Demonstrated success in cross-functional, dynamic, and matrixed environments.</li><li>
Regulatory knowledge: Solid understanding of biopharmaceutical manufacturing principles and cGMP requirements.</li><li>
Project management: Experience leading small projects, coordinating activities, and managing timelines to meet project goals.</li></ul>
Other Information:<ul><li>
Initial location at Lilly Technology Center, Indianapolis.</li><li>
Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.</li><li>
Limited domestic and international travel (&lt; 5%) may be required for this role</li><li>
Role requires ability to work in manufacturing and laboratory environments.</li></ul>
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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$79,500 - $171,600
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Senior Principal Scientist Process Translation and Execution Lilly Medicine Foundry

<div>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&rsquo;re looking for people who are determined to make life better for people around the world.
Responsibilities:
The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site&rsquo;s sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy.
Key Objectives/Deliverables:<ul><li>
Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level.</li><li>
Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to; Airflow Pattern Testing, Environmental Monitoring Performance Qualifications, Aseptic Process Simulations, Cleaning, Sanitization, and Disinfection, Gowning within GMP Classified Areas, Aseptic Processing Techniques, Contamination Control</li><li>
Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established.</li><li>
Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established.</li><li>
Lead/assist with support and/or provide technical expertise for developing the site&rsquo;s contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies.</li><li>
Lead/assist with support and/or provide technical expertise for the facility&rsquo;s cleanroom gowning and aseptic technique strategy/program.</li><li>
Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination.</li><li>
Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.</li><li>
Lead or provide technical support for root cause investigations associated with sterility assurance programs.</li><li>
Participate and/or provide technical sterility assurance support during internal and external audits.</li><li>
Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs.</li><li>
Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives.</li></ul>
Basic Qualifications:<ul><li>
Bachelor&rsquo;s or Master&rsquo;s Degree in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline.</li><li>
Demonstrated understanding and relevant experience of scientific principles required for manufacturing of parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing.</li></ul>
Additional Skills/Preferences:<ul><li>
Possess strong interpersonal skills to work cross-functionally within a team.</li><li>
Possess strong self-management and organizational skills.</li><li>
Possess strong oral and written communication skills for communicating to colleagues, management, and other departments.</li><li>
Experience with data analysis and trending.</li><li>
Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing, warehouse, or laboratory areas.</li><li>
Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities.</li></ul>
Additional Information:<ul><li>
Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and / or off-hour work may be required.</li><li>
Tasks may require repetitive motion and standing or walking for long periods of time.</li><li>
Travel may be required during the project phase for training and implementation of sterility assurance programs</li></ul>
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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$66,000 - $171,600
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Scientist / Senior Scientist - TSMS Sterility Assurance

Join Eli Lilly and explore 15   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.