General/Dexa/Fluoro Technologist

General/Dexa/Fluoro Technologist Overview We are seeking a skilled and dedicated General Technologist to join our healthcare team. Iowa Radiology is a patient-centered practice that promotes a more compassionate approach to medicine. We provide our employees the ability to bring their authentic selves to work every day, providing compassionate care for our patients in a collaborative, supportive work environment. Location: Des Moines Metro Schedule: Monday - Friday, 8:00 AM - 5:00 PM Flexible full-time schedule of 32 or 40 hours per week We want YOU to join the Iowa Rad family! We truly care about our employees, their health and well-being, and their career goals and aspirations. The ideal candidate will play a crucial role in helping us continue to be the premier provider of radiologic services in Iowa by providing high-quality imaging services, ensuring patient safety, and delivering accurate diagnostic information. Mammography training is available for anyone interested! Responsibilities: Producing diagnostic exams following established protocols and guidelines. Utilizing general x-ray, bone densitometry and fluoroscopy to assist in the diagnosis and treatment of patients. Demonstrate proficiency in medical terminology and anatomy knowledge to accurately communicate imaging findings. Collaborate with radiologists, physicians, and other healthcare professionals to ensure high-quality patient care. Stay updated on the latest advancements in technology and techniques to provide optimal services to patients. Following established protocols for infection control and patient safety during all procedures. Qualifications: ARRT certification and a current Iowa permit to practice in general radiography is required. Excellent patient care and communication skills are essential Some lifting is involved with this position. Competitive Benefits Package including but not limited to: Health, Dental, and Vision Insurance Life Insurance Short-term and Long-term Disability Insurance Paid Time Off and Paid Holidays 401k Retirement Plan Referral Program Iowa Radiology, Professional Medical Management (PMM), and Iowa Diagnostic Imaging and Procedure Center (IDIPC), are equal opportunity employers. We are committed to fostering a diverse, inclusive, and respectful workplace. All qualified candidates are given equal employment opportunity without regard to race, color, national origin, sex, gender identify, sexual orientation, age, disability, religion, or any other characteristic protected by federal, state, or local law. We celebrate diversity and are committed to creating an inclusive environment for all employees. Reasonable accommodations are available to individuals with disabilities from the application process and throughout employment with any of our companies. Work Location: Multiple locations PI26fa221357bb-5727

RN - Registered Nurse - Cardiology - Multiple Shifts

Position Overview Department: 7 North Cardiology Schedule: Shifts Available: Work Location: UAB St. Vincent's East Benefits for eligible positions only include: Generous Paid Time Off, Paid Parental Leave, Associate Assistance Program, Tuition Reimbursement Program, and More 15 Telemetry beds and 8 IMC beds What You Will Do Provide direct nursing care in accordance with established policies, procedures and protocols ofthe healthcare organization. Implement and monitor patient care plans. Monitor, record and communicate patient condition as appropriate. Serve as a primary coordinator of all disciplines for well-coordinated patient care. Note and carry out physician and nursing orders. Assess and coordinate patient's discharge planning needs with members of the healthcare team. What You Will Need Licensure / Certification / Registration: BLS Provider obtained within 1 Month (30 days) of hire date or job transfer date required. American Heart Association or American Red Cross accepted. Licensed Associate Professional Registered Nurse credentialed from the Alabama Board of Nursing obtained prior to hire date or job transfer date required. Education: Diploma from an accredited school/college of nursing AND Required professional licensure at time of hire. Additional Preferences No additional preferences. About UAB St. Vincent's UAB St. Vincent's, a proud part of UAB Medicine, is a trusted provider of health care, serving Alabama for more than 125 years. With five hospitals and numerous clinics, we're a health care community deeply rooted in compassion, service, and respect for all, guided by the rich legacy of the St. Vincent's name. We're committed to extending kindness and personalized care to patients, their families, and each other. We address the physical, psychological, social, and spiritual needs of our patients. We believe in the power of teamwork and unity, and foster a collaborative spirit among our more than 4,800 employees. As one of Alabama's best hospitals as recognized by U.S. News & World Report, improving the health and lives of those we serve is at the heart of our mission. Join us in continuing our legacy of service and healing in central Alabama, where we can make a lasting impact together.

Territory Sales and Service Representative

Want to build a brighter, bolder future and cultivate your career? Join Ecolab’s team and help create a world in which we all thrive. Our Institutional team enhances customer success in sectors like hospitality, foodservice, long-term care, commercial, education, and government by focusing on satisfied guests, protected reputations, and efficient operations. Committed to building lasting relationships, we leverage our industry expertise and science-based guidance in cleanliness, food safety, and public health. Through our collaborative partnerships, we empower customers to elevate their service and ensure the highest safety standards. Ecolab is seeking a Territory Sales and Service Representative to join our team in the Gainesville, GA market. As an industry leader, we're growing and need talented people like you to help us continue to protect the world's most vital resources. You will serve as the face of Ecolab, managing your territory, servicing laundry and dish machines, dispensing equipment and systems, and selling new solutions for our customers to help achieve our mutual goal of a cleaner, safer & healthier environment for all. How You’ll Make an Impact: Leverage tools and technology (including tablet and mobile phone apps) to conduct customer visits and recommend unique programs and solutions to customers Communicate our total value to the customer to meet their needs and grow sales within existing customer accounts Use your problem-solving skills to conduct preventative and corrective maintenance on laundry and dish machines, dispensing equipment, and systems Provide emergency service to existing customers via phone or in person, as needed Assist in the installation of equipment and solutions Demonstrate safe equipment use, ensuring your customers' operations are fully functional Manage equipment, parts, and inventory to control costs Position Details: This is a field-based position and may require travel to the following locations and surrounding areas: Gainesville, GA ; Toccoa, GA; Cornelia, GA During your training program, you will be required to travel to Ecolab Corporate Headquarters in Eagan, Minnesota for 2 of the 12 weeks. The remaining weeks will be in-field training. Ecolab will arrange and pay for your travel and certain travel-related expenses. You are responsible for having the proper documentation to fly such as a Real ID or other acceptable form of identification. After completing an initial training program, you will be managing, servicing, and selling to established customers including restaurants, hotels, schools, long-term care facilities, and more within an assigned territory. In some cases, where a territory is not immediately available, associates will be assigned a supporting role until a territory assignment becomes available. Weekend Rotation: Generally, 1 in 4 weekends are required (based on business demand) What’s Unique About This Role: Access to best-in-class resources, tools, and technology Independent work environment where you will manage your monthly schedule Thrive in a company that values a culture of safety to include top-notch safety training and personal protection equipment An award-winning paid training program (including paid travel time) at a state-of-the-art training facility in Eagan, MN. This program utilizes a blended approach incorporating digital learning, classroom training, live demonstrations, and on-the-job training with field professionals to ensure associates are safe, confident, and proficient in their roles. Receive a company service vehicle and cell phone for business use. We pay for fuel, drive time to customer sites, and time for service maintenance on your vehicle Grow your income as you drive growth Opportunities for growth and development: carve out a long-term, advanced career path towards service, sales, or management with an opportunity for tuition reimbursement ​ Minimum Qualifications: High School Diploma or equivalent 2 years of sales, mechanical service, customer service, food service or hospitality industry-related experience Availability to work overnight shifts and provide emergency assistance which may occur at night, on weekends and over holidays Position requires a current and valid Driver’s License with no restrictions No Immigration Sponsorship available for this position Physical Requirements of Position : Lifting 50 lbs Pushing/pulling Standing/bending/stooping Working in confined spaces Distinguishing color (tools may be accommodated) Availability to work overtime Driving a company vehicle as required to perform job duties (pre-employment and ongoing motor vehicle record checks will be performed to determine eligibility to drive a company vehicle) Ecolab is committed to providing reasonable accommodation to qualified individuals with a disability. Preferred Qualifications: Associate’s degree or other advanced training or certifications Previous mechanical problem-solving experience (e.g. plumbing, electrical, HVAC and/or mechanical experience) in industries related to food service, laundry, housekeeping, hospitality and/or pool and spa What’s in it For You: Starting on Day 1 : Access to our comprehensive benefits package including medical, dental, vision, matching 401K, company-paid pension, stock purchase plan, paid parental leave, select discounted childcare resources, and more! The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, and healthy environments. The ability to make an impact and shape your career with a company that is passionate about growth. The support of an organization that believes it is vital to include and engage diverse people, perspectives, and ideas to achieve our best. About Ecolab: At Ecolab, we prioritize our talent-first philosophy by creating the most capable and diverse team to excel at our nearly three million customer sites. Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based solutions, data-driven insights and world-class service to advance food safety, maintain clean and safe environments, and optimize water and energy use, and improve operational efficiencies and sustainability for customers in the food, healthcare, life sciences, hospitality and industrial markets in more than 170 countries around the world. Our solutions not only enhance operational efficiency but also contribute to sustainability and public health, making a positive impact on the world. We are committed to eliminating unnecessary complexities and embracing a beginner's mindset, continuously seeking new perspectives and innovative solutions to stay ahead in a rapidly changing world. Annual or Hourly Compensation Range The total Compensation range for this position is $58,700-$88,100 which includes base pay and target incentive based on performance, per plan terms. Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws. Benefits Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click here to see our benefits. If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here. Potential Customer Requirements Notice To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to: - Undergo additional background screens and/or drug/alcohol testing for customer credentialing. Americans with Disabilities Act (ADA) Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website. Our Commitment to a Culture of Inclusion & Belonging At Ecolab, we believe the best teams are inclusive. We are on a journey to create a workplace where every associate can grow and achieve their best. We are committed to fair and equal treatment of associates and applicants and recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance. In all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement, we will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, disability, or status as a covered veteran. In addition, we are committed to furthering the principles of Equal Employment Opportunity (EEO) through Affirmative Action (AA). We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York City Fair Chance Act.

Hotel Manager

Job description The Hotel Manager is responsible for overseeing the daily operations of the front desk, maintenance and housekeeping department ensuring the highest level of guest satisfaction. This role involves managing front desk staff, handling guest inquiries and complaints, ensuring smooth check-in and check-out processes, and maintaining a welcoming environment for all guests. It will also include managing housekeeping staff, maintenance, budgeting, inventory control, and maintaining a safe and hygienic environment throughout the hotel. ESSENTIAL DUTIES AND RESPONSIBILITIES Staff Management Recruit, train, and supervise front desk staff and housekeeping staff. Follow up and assign tasks to maintenance department including work orders and PMs. Schedule staff shifts and ensure adequate coverage. Conduct performance evaluations and provide feedback. Foster a positive work environment and encourage teamwork. Guest Services Ensure a high standard of customer service is maintained. Handle guest inquiries, requests, and complaints in a timely and professional manner. Monitor guest feedback and implement improvements as needed. Ensure VIP guests and special requests are attended to. Operations Management Oversee the check-in and check-out procedures. Ensure all front desk operations comply with hotel policies and procedures. Maintain accurate records of bookings, payments, and guest information. Manage room inventory and coordinate with housekeeping to ensure room availability. Perform weekly room inspections and daily property walks. Conduct daily stand-up meetings. Inventory and Supplies Management Monitor and manage inventory levels of cleaning supplies, linens, and guest amenities. Order and replenish supplies as needed, ensuring cost-effective purchasing practices. Maintain accurate records of inventory usage and expenses. Financial Responsibilities Handle all billing and reconciliation of hotel accounts. Prepare and manage the front desk, housekeeping & maintenance budgets and inventory. Monitor and report hotel expenses. Administrative Duties Prepare reports on hotel activities and performance. Ensure compliance with health and safety regulations. Maintain an organized and tidy front desk and public areas. Implement and oversee front desk training programs. Communication Efficiently communicate with other departments daily to ensure smooth operations. Communicate effectively with guests, staff, and management. Address and resolve any inter-departmental issues. Maintain a neat and efficient office environment. Other duties as assigned by direct supervisor. Requirements Good communication skills, both verbal and written. Strong team leadership in most tasks performed in a team environment. Must possess computer skills. Must have open and flexible schedule and ability to work evenings, holidays and weekends. Extensive knowledge of the hotel, its services and facilities. Ability to input and access information in the property management system. Minimum Qualifications Two to four years' experience in hotel front office/housekeeping/guest services role, with at least two years in a supervisory role is required. Physical Requirements Ability to lift, push, pull, and carry items up to 50 pounds. Ability to stand, walk, bend, and reach for extended periods. Capability to operate housekeeping tools and equipment safely. Job Type: Full-time Location: Round Rock, TX (Relocate before starting work) Work Location: In person Pay: $50,000.00 - $55,000.00 per year Benefits 401(k) Dental insurance Employee discount Health insurance Paid time off Vision insurance J-18808-Ljbffr

Country Medical Director, Germany

Country Medical Director, GermanyApplylocations: Germany Remotetime type: Full timeposted on: Posted Todayjob requisition id: R35379BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General Description:The Country Medical Director (CMD) is accountable for medical affairs leadership, oversight, and governance for Germany and plays a key role in the design, implementation, and governance of the Medical Affairs strategy to support marketed products and products in development.The role primarily serves to provide and enable executive scientific direction, ensuring medical excellence, and aligning Germany medical strategies with European and Global Medical Affairs priorities.The role reports to the Vice President of Medical Affairs in Europe.Essential Functions of the Job:Responsibilities include, but are not necessarily limited to, the following:* Lead the Medical Affairs organization for Germany, with accountability for the development, prioritization, and governance of the local medical strategy, including evidence-generation plans, appropriate to Germany context.* Serve as the senior scientific leader within the German leadership team, providing expert guidance, strategic challenges, and decision-making support at key milestones.* Ensure compliance with German, regional, and corporate directives, including those governing promotional material, medical training materials, and medical information, acting as the senior accountable medical authority within Germany.* Be accountable for fostering effective cross-functional collaboration at Country level, ensuring Medical Affairs acts as a strategic partner to Commercial, Market Access, Regulatory, Clinical Development, and Corporate Affairs. This includes aligning priorities, facilitating constructive dialogue across functions, and enabling timely, integrated decision-making in the best interest of patients and the overall business.* Act as a regional medical leader, contributing as an active participant in European Medical Affairs leadership forums, with the objective of supporting the overall success and cohesion of the European Medical Affairs organization. This includes shaping aligned regional strategy, governance, and priorities across clinical development, safety oversight, investigator-initiated research, and payer-relevant evidence generation.* Oversee the alignment of medical strategy, communication plans, resources, and budget to ensure Medical Affairs activities effectively deliver Medical Plans and support Country business needs while preserving scientific independence.* Provide strategic oversight, critical evaluation, and endorsement of local evidence generation activities, including IITs and HEOR, required to support reimbursement and access discussions at Country level, ensuring these activities are conducted at the highest standards of scientific integrity, compliance, and governance.* Be accountable for medical input into R&D and lifecycle management activities, ensuring Country teams are empowered to provide timely perspectives that are appropriately represented in regional and global plans.* Provide strategic direction and oversight to Country Medical TA Leads and Field Medical Teams, enabling high-quality scientific exchange and consistent, compliant medical communication.* Provide senior scientific leadership and matrix influence across relevant functions (e.g., safety, regulatory, local clinical development), ensuring alignment with Country needs while coordinating with European and Global line management as appropriate.* Establish and maintain strategic relationships with key opinion leaders and external stakeholders, positioning the CMD as a catalyst for scientific exchange, partnership, and reputation-building, while enabling appropriate delegation to Medical Affairs team members.* Provide leadership for Country-level medical and scientific forums (e.g., advisory boards, educational meetings), ensuring strategic focus, scientific rigor, and alignment with patient and business priorities.* Provide executive medical oversight and challenge for promotional and non-promotional materials and learning content, with involvement focused on strategic review and risk mitigation.* Act as a senior medical spokesperson for BeOne products and significant medical topics within Germany, in coordination with Corporate Communications and General Management, focusing on high-impact, strategically relevant, and scientific engagements.* Recommend, prioritize, and govern Country-level medical activities, initiatives, and investments, in alignment with European and Global Medical Affairs strategy and evolving Country needs.Qualifications:* M.D. Physician / Scientist with significant experience in all aspects of clinical trials and professional knowledge and skills working with hematology and oncology therapeutics in solid tumor and hematologic indications.* Relevant pharmaceutical or related industry experience (7 years) in oncology with proven track record as country medical director with contribution to commercial, medical and/or clinical development strategies (in country).* Solid peer relationships with and exposure to external scientific and clinical experts and Key Opinion Leaders; demonstrated ability to proactively engage internal and external leaders and serve as a medical expert for the oncology disease area.* Understanding of commercial and scientific needs on a local and global basis.* Intimately familiar with applicable rules and regulations and actions of EU regulatory bodies within the assigned Region.* Recognized expertise in clinical and/or research experience (including publications) in therapy area is desired; specialty training and/or clinical experience in oncology is highly preferred.* Proven ability to translate and appropriately align commercial and scientific goals and objectives and to interact productively with both commercial and scientific colleagues.* Highest ethical standards in corporate medical governance.* Experience delivering effective and persuasive communications on complex and controversial topics to both corporate management and scientific audiences.* Successful track record of initiating and leading cross-business/cross-functional planning, collaborating and solution building.* Strong interpersonal skills to allow for successful interaction with peers across the organization to achieve corporate goals.* Excellent written and oral communication skills.Supervisory Responsibilities: The incumbent will build, lead, and develop the Country Medical Affairs organization, with direct line management responsibility for Medical Affairs staff within Germany.Computer Skills:Proficient with Microsoft Office Suite, experienced with electronic CRM systems.Other Qualifications:Fluency in both verbal and written English and German necessary; any other major European language is of advantage.Travel:Ability to travel.Salary Range MD: 192,000.00 EUR - 240,000.00 EUR J-18808-Ljbffr

Director, Drug Product - SMDD

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. 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 are looking for people who are determined to make life better! 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 35,000 employees 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 are looking for people who are determined to make life better! Position Brand Description The Synthetic Molecule Design and Development (SMDD) department within Lilly Research Labs is involved in key activities for the advancement of small molecules, peptides, and oligonucleotides from early discovery phases to commercialization. Our scientists and engineers develop innovative technical and business solutions across a portfolio of projects using their deep technical expertise to accelerate testing of the clinical hypothesis and overall drug development. Through recognizing the value of a hardworking, diverse, and inclusive workforce, SMDD delivers on these responsibilities and helps bring the next generation of life changing medicines to patients. Our team is looking for highly motivated and creative candidates who will work on the integration of early drug discovery, preclinical, and clinical activities with a focus on drug product design and development. Responsibilities Our team is looking for candidates interested in further advancing formulation, manufacturing platform technologies and commercialization of solid drug products. The candidate will collaborate with other development scientists/engineers and manufacturing groups to provide technical leadership in the design and implementation of formulation and manufacturing technology platforms, with special focus on continuous manufacturing. The position presents possibilities to work across multiple subject areas, sites, and networks! Top candidates for this position will be encouraged to: Apply experience in both batch and continuous solid drug product manufacturing unit operations to accelerate product development. Understand the interaction between raw material properties and processability as well as how unit operations can be used to improve manufacturability. Build comprehensive material and manufacturing process risk assessments that will guide formulation selection, development, and experimental work-plans. Improve product design through definition of drug product critical quality attributes (CQAs). Drive the implementation of new platforms such as continuous manufacturing, process analytical technologies (PAT), and modeling and simulation tools. Design robust and globally acceptable manufacturing process control strategies as well as partner with manufacturing teams to transfer those control strategies. Lead short and long-term development activities including prioritization of technical agendas and timelines. Partner with multi-functional teams such as Product Delivery, Project Management, Quality, Manufacturing, and Regulatory to execute and deliver material and information for clinical trials and regulatory submissions. Engage and influence the external environment as well as demonstrate the ability to recognize and adopt external innovation across Lilly’s drug product portfolio. Embrace learning agility to apply fundamental knowledge/experience to novel problem statements in order to accelerate drug product development. Lead the development of regulatory strategies including authorship of INDs, NDAs, and response to regulatory inquiries. Embrace diverse thought, background, and experience to deliver creative solutions that address unmet technical needs. Basic Requirements Ph.D. in chemical engineering or pharmaceutical sciences with 5 years of experience . or M.S. with 15 years or B.S. with 20 years of demonstrated equivalent experience in a related field of expertise Experience with developing solid drug product formulations, manufacturing processes and technical transfer of processes into manufacturing Demonstrated leadership capabilities in a team environment Additional Skills/Preferences Sound fundamentals and understanding of biopharmaceutics Awareness of non-standard (e.g. modified release, peptide) oral drug delivery landscape Experience in continuous manufacturing Experience in developing pharmaceutical dosage forms as a formulation scientist or process engineer Knowledge and experience with management of a technical project Experience supervising or guiding the work of others Strong communication and a sustained tendency for collaboration Good verbal and written communication skills Ability to prioritize multiple activities and handle ambiguity Demonstrated initiative, risk-taking, and ability to drive and accept change Engagement and awareness of the external scientific and regulatory landscape Additional Information Potential exposure to chemicals, allergens, and loud noises. Travel: 0 to 10% Position Local: Onsite Monday through Friday, Indianapolis, IN, LTC-N Lilly is an EEO/Affirmative Action Employer, and does not discriminate on the basis of race, gender, protected veteran status, disability or any other legally protected status. 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’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’s education, experience, skills, and geographic location. The anticipated wage for this position is $148,500 - $217,800 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’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. 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