At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.SUMMARYTo assist the Quality Assurance function as technical support in issues affecting manufacturing. To support and drive corrective action efforts.ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.· Ensure capability studies are performed on critical processes.· Perform first article inspection and review visual aids.· Perform defect analysis reporting.· Perform MRB on sustained products.· Participate in CAC meetings – support continuous improvement.· Perform line and product audits.· Assist Quality Engineering in APQP.· Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.· Comply and follow all procedures within the company security policy.MINIMUM REQUIREMENTSBachelor's degree preferred; or equivalent combination of education and experience.BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact the Federal Bureau of Investigations internet crime hotline (www.ic3.gov), the Federal Trade Commission identity theft hotline (www.identitytheft.gov) and/or your local police department. Any scam job listings should be reported to whatever website it was posted in.Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.Accessibility AccommodationIf you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to or calling with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong#AWorldofPossibilities#EarlyCareer

Are you a detail-oriented engineer passionate about compliance and technology Join KARL STORZ as a R&D Quality Engineer IVand play a crucial role in shaping the future of medical technology! What you'll be doing:You will oversee global component planning, establish standards, and solve complex vendor-related issues while ensuring compliance with regulatory requirements.Collaborate with other Engineering teamsto analyze components, reduce costs, and set specifications.Manage compliance with regulations like China RoHS and REACH, working closely with QA teams.Facilitate end-of-life (EOL) projections and manage component replacements.Maintain the global parts library and provide training on compliance standards.Participate in product development teams to manage Design History Files and ensure adherence to FDA/QSR and ISO regulations.Conduct internal audits and respond to corrective actions promptly.What you'll need to be considered:Bachelor’s degree in Mechanical, Electrical, or Software Engineering preferred.Minimum of 10 years in component engineering, with 8+ years in a medical device environment.Experience with reusable medical devices and familiarity with FDA Quality System Regulation (21 CFR Part 820) and ISO standards (13485, 9001).Ability to evaluate electronic component data sheets in circuit designs is a plus.Who we are:KARL STORZ is an independent, family-owned supplier of advanced medical technology. For 80 years, we’ve pioneered the most groundbreaking innovations in endoscopy, surgical imaging, and OR integration to benefit patients and healthcare providers alike.Every day, we apply cutting-edge technology, precision engineering, and award-winning customer support to help healthcare facilities manage costs, streamline operations, and deliver exceptional patient outcomes. With facilities across the country and countless opportunities in the field, we attract a diverse and talented staff, motivated by the chance to make a lasting positive impact. At KARL STORZ, it’s not just about the tools we create it’s about the lives we change, together.Apply Today to make an impact in the medical device industry!#LI-BL1

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.Job Description:Manufacturing Engineer (Solventum)3M Health Care is now SolventumAt Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.The Impact You’ll Make in this RoleAs a(n) Manufacturing Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:Leads and implements improvements related to safety, quality, customer service, and cost (productivity).Drives cost and productivity through Lean Six Sigma projects utilizing a technical approach, standard work, and kaizen events.Develops and implements cross-functional projects, plans, programs in support of the business strategic plans, new process start-ups, new technology integration, aggressive cost reduction and supply chain improvement using Lean Six Sigma tools.Proactively communicates project direction and status to appropriate personnel.Engagement and involvement in daily operations, supports/participates in Lean Management system, and provides direction/support of maintenance and capital improvement projects.Drives understanding of key customer needs and monitors process capabilities.Responsive to a manufacturing environment that operates 24 hours a dayYour Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:Bachelor’s degree or higher from an accredited university in mechanical, Industrial, or Chemical EngineeringPreferred Qualifications:Three (3) years working within a manufacturing and/or process engineering environment.One (1) year of experience with DMAIC and Business ExcellenceThree (3) years working with cross-functional teamsDemonstrated strength in engineering/technical skillsSelf-starter/self-directed that leads with high energy and passionProven track record of continuous process improvementEffective facilitation, communication, and teaching skillsAbility to engage and influence the organizationAbility to multi-task and handle large workloads under time constraintsWork location: Onsite [Meriden]Travel: May include up to [10% ][domestic/international]Relocation Assistance: May be authorizedMust be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).Supporting Your Well-beingSolventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.Applicable to US Applicants Only:The expected compensation range for this position is $95,825 - $117,120, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-RewardsResponsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of @solventum.com. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.Solventum Global Terms of Use and Privacy StatementCarefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with theterms.

Compensation Type: Yearly Highgate Hotels: Highgate is a premier real estate investment and hospitality management company widely recognized as an innovator in the industry. Highgate is the dominant player in U.S. gateway markets including New York, Boston, Miami, San Francisco and Honolulu, with a rapidly expanding presence in Europe, Latin America, and the Caribbean. Highgate’s portfolio of global properties represents an aggregate asset value exceeding $20B and generates over $5B in cumulative revenues. The company provides expert guidance through all stages of the hospitality property cycle, from planning and development through recapitalization or disposition. Highgate also has the creativity and bandwidth to develop bespoke hotel brands and utilizes industry-leading proprietary revenue management tools that identify and predict evolving market dynamics to drive out performance and maximize asset value. With an executive team consisting of some of the industry’s most experienced hotel management leaders, the company is a trusted partner for top ownership groups and major hotel brands. Highgate maintains corporate offices in London, New York, Dallas, and Seattle. Location: Overview: The Chief Engineer is responsible for the day-to-day operations of the engineering division. Responsibilities: Developing and implementing plans to maintain property, equipment, grounds and other assets in a safe and acceptable state of repair.Ensure the hotel is in compliance with all local, state and federal laws.Supervise and train all Engineering staff in Customer Service, Empowerment, Standard Operating Procedures and Loss Prevention.Create and implement preventative maintenance program for all hotel equipment.Ensure all emergency and life safety equipment and systems are inspected, tested and certified per Highgate Hotel standards.Actively participate in energy conservation programs.Review all guest and meeting planner comment cards to ensure problems are identified and corrected in a timely manner.Ensure compliancewith the Americans with Disabilities Act (ADA).Assist with the administration of all vendor contracts controlled by the engineering department.Ensure that room maintenance requests are handled in a prompt and courteous manner.Follow up on all alarms immediately to determine the exact location and cause.Determine emergency status and report findings to Front Desk.Take immediate action as necessary.Assist as necessary with special projects and renovations.Support and participate in all Highgate Hotel programs.Participate in Highgate Hotel Safety Committee. Qualifications: At least 3 years of progressive facilities management experience in a hotel or a related field; or a 2-year college degree and 1 year of related management experience.High school diploma or equivalent required.Stationary Engineer’s license if required by local code.HVAC, electrical, plumbing, boiler operations and general maintenance skills required.Long hours sometimes required.Heavy work – Exerting up to 100 pounds of force occasionally, and /or 50 pounds of force frequently and/or up to 20 pounds of force constantly to lift, carry, push, pull or otherwise move objects.Maintain a warm and friendly demeanor at all times.Must be able to effectively communicate both verbally and written, with all level of employees and guests in an attentive, friendly, courteous and service oriented manner.Must be effective at listening to, understanding, and clarifying concerns raised by employees and guests.Must be able to multitask and prioritize departmental functions to meet deadlines.Approach all encounters with guests and employees in an attentive, friendly, courteous and service-oriented manner.Attend all hotel required meetings and trainings.Participate in M.O.D. coverage as required.Maintain regular attendance in compliance with Highgate Hotel Standards, as required by scheduling, which will vary according to the needs of the hotel.Maintain high standards of personal appearance and grooming, which include wearing nametags.Comply with Highgate Hotel Standards and regulations to encourage safe and efficient hotel operations.Maximize efforts towards productivity, identify problem areas and assist in implementing solutions.Must be effective in handling problems, including anticipating, preventing, identifying and solving problems as necessary.Must be able to understand and evaluate complex information, data, etc. from various sources to meet appropriate objectives.Must be able to maintain confidentiality of information.Perform other duties as requested by management.

ADVANCING OUR OPERATIONSIn order for us to complete our missions, our technology simply cannot fail. Covering a wide range of specialties ranging from aeronautical and computer systems to flight test and mechanical, Developmental Engineers provide advanced skill and knowledge of their particular specialties. Responsible for everything from the planning to implementation of their projects, these experts are essential to the success of operations all over the world.REQUIREMENTSYou must meet several requirements before joining the Air Force. These concern your background, overall health and other standards set by the Air Force, Department of Defense and federal law.Minimum EducationBachelor’s degree in engineering related to one of the following specialties: aerospace, aeronautical, astronautical, computer, electrical, electronics, communication or mechanicalQualificationsCompletion of the Defence Acquisition UniversityFundamentals of SystemsAcquisition Management course or Acquisition Fundamentals courseCompletion of the Air Force Flight Test Engineer course or comparableMinimum of 24 months of experience in qualified position or a master’s degree in a specified discipline and 12 months’ experience or a Doctor of Philosophy degree in a specified disciplineCompletionof Officer Training School (OTS), AirForce Academy (AFA) or AirForce Reserve Officer Training Corps (AFROTC)Must be between the ages of 18 and have not reached your 42ndbirthday

Shape the Future of Medical Technology with KARL STORZ!Are you an experienced engineer passionate about designing life-changing medical devices KARL STORZ is seeking a Senior Mechanical Engineer – Product Enhancement & Development to lead the development of cutting-edge flexible endoscopes and associated technologies. This is your opportunity to work on impactful projects that enhance patient care worldwide.What you’ll be doing:Lead the design, prototyping, testing, and production of new medical devices, focusing on flexible endoscopes and accessories.Drive product development from concept to production, ensuring on-time delivery with global cross-functional teams.Identify opportunities for product improvements, cost reduction, and production yield enhancements.Develop and refine test protocols, conduct data analysis, and lead root cause investigations.Collaborate with international engineering teams to implement design changes and maintain compliance with global medical device standards (FDA, ISO 13485, ISO 9001).What’s in it for me Innovative Environment: Work on groundbreaking products that improve patient outcomes.Global Impact: Collaborate with a diverse, international team to bring medical technologies to market.Career Growth: Advance your career with a company that values professional development and technical leadership.Global Experience: Opportunities for up to 20% travel (domestic and international) allow you to gain valuable global perspectives and work with diverse teams.Contribution to Health: Play a key role in developing life-saving medical devices, making your work impactful and rewarding.What you will need to be considered:B.S degree in Mechanical Engineering (or equivalent mechanical design-based degree). 9+ years of experience in design/project engineering.5+ years of experience in a medical device development.Strong expertise in SolidWorks, statistical analysis, and MS Project/Server.Proven track record in leading teams and delivering innovative product solutions.Experience in manufacturing transitions, process development, and prototype fabrication.Who we are:KARL STORZ is an independent, family-owned company headquartered in Germany’s renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and OR integration to benefit patients and healthcare providers alike.With a 9000+ employees worldwide, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support. In doing so, we help healthcare facilities manage costs, streamline operations, and deliver positive patient outcomes.It's not just about the tools we createit’s about the lives we change, together.Ready to make a difference Apply now and be part of a dynamic team at the forefront of medical innovation.#LI-BL1

Ready to make a difference We're looking for a Design Verification/Test Engineer who is passionate about quality and innovation to help us deliver life-changing medical devices that meet the highest standards of excellence.What you’ll be doing:Develop & Execute: Create and carry out design verification test plans and procedures.Analyze & Report: Collect data, troubleshoot, and report test outcomes to drive improvements.Collaborate & Innovate: Work closely with engineering teams to design custom test fixtures for electrical, optical, and mechanical systems.Ensure Compliance: Uphold FDA, ISO 13485, and ISO 9001 quality standards.What you’ll need to be considered:Educational Background: B.S. in Electronics Technology/Engineering with 3-5 years of experience, or MS with 0-3 years.Technical Expertise: Proficient in C#, Matlab, LabView, or similar tools. Experience with automated testing is a plus.Problem-Solving Mindset: Strong analytical skills with attention to detail.Team Spirit: Excellent communication skills and ability to work collaboratively across departments.Why Join Us Impactful Work: Contribute to products that change lives.Growth Opportunities: Be part of an innovative environment that supports your career development.Inclusive Culture: Join a team that values diversity, creativity, and collaboration.Who we are:KARL STORZ is an independent, family-owned company headquartered in Germany’s renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and OR integration to benefit patients and healthcare providers alike.With a 9000+ employees worldwide, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support. In doing so, we help healthcare facilities manage costs, streamline operations, and deliver positive patient outcomes. It's not just about the tools we createit’s about the lives we change, together.#LI-BL1

KARL STORZ is seeking a passionate and innovative Mechanical Engineer – Product Enhancement & Development to join our dynamic team. In this role, you will drive the design and development of advanced medical devices, collaborating with cross-functional international teams to ensure our products meet the highest standards of quality and efficacy.As a Development Engineer III, here's what's in it for you:Innovative Projects: Work on cutting-edge medical device technologies, particularly in the design and development of flexible endoscopes and their components. You'll lead projects from concept to market, which provides a strong sense of ownership and accomplishment.Leadership and Collaboration: Lead international teams of engineers and technicians, enhancing your leadership, project management, and collaboration skills across global teams.Professional Growth: Engage in cross-functional work with R&D, production, and quality teams, expanding your technical knowledge and experience with medical device standards and manufacturing processes.Problem Solving: Tackle complex engineering challenges, from product failures to process improvements, strengthening your analytical and problem-solving skills.Career Advancement: Gain exposure to project management and new product development in a high-impact industry, positioning yourself for future roles in leadership or technical expertise.Global Experience: Opportunities for up to 15% travel (domestic and international) allow you to gain valuable global perspectives and work with diverse teams.What you’ll be doing:Lead new product development, upgrades, and improvements for flexible endoscopes.Design, test, and develop prototypes, including manufacturing transition.Develop and refine test protocols and process documentation.Investigate product failures and recommend corrective actions.Support manufacturability of designs, ensuring product performance meets specifications.What you’ll need to be considered:BS in Mechanical Engineering or related field with a focus on mechanical design.6+ years of experience in design or project engineering.3+ years in medical product development.Proficiency in SolidWorks and Microsoft Office (Word, Excel, MS Project).Experience leading project teams or supervising technical staff.Tool shop experience and strong knowledge of standard engineering practices.Additional experience that will make you stand out:International communication and collaboration skills.Proven project management experience.Strong problem-solving abilities, attention to detail, and multitasking in a fast-paced environment.Tool/machine shop experience.Who we are:KARL STORZ is an independent, family-owned company headquartered in Germany’s renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and OR integration to benefit patients and healthcare providers alike.With a 9000+ employees worldwide, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support. In doing so, we help healthcare facilities manage costs, streamline operations, and deliver positive patient outcomes.It's not just about the tools we createit’s about the lives we change, together.#LI-BL1

The Quality Engineer IV is a senior-level professional responsible for supporting the quality assurance of both sterile and non-sterile products, focusing on KARL STORZ’s Advanced Machining Center (AMC) and Single Sterile Use (SSU) production. The role ensures compliance with quality and sterilization standards, focusing on patient safety and regulatory requirements.What's in it for me Leadership Opportunities: You’ll take a lead role in quality initiatives, process improvements, and compliance, with the chance to mentor and supervise technicians.Professional Growth: You’ll work with advanced technologies like sterilization processes and cleanroom environments, gaining specialized expertise in medical device manufacturing and regulatory standards (FDA, ISO, MDR).Cross-functional Collaboration: You’ll engage with various teams (engineering, production, regulatory) to drive high-impact projects and continuous improvement.Job Security and Impact: You’ll play a crucial role in ensuring patient safety and product quality, contributing directly to healthcare innovation.Advanced Tools and Systems: Access to cutting-edge tools, quality systems, and software (SAP, Six Sigma, SPC) enhances your technical skill set.Challenging and Diverse Work: Exposure to a variety of processes, including process validation, defect analysis, audits, and environmental monitoring, ensures dynamic day-to-day responsibilities.What you’ll be doing:Provide sterilization expertise and oversee sterilization release processes.Support continuous improvement in product and process quality, including validation, defect analysis, CAPA, and internal audits.Ensure compliance with FDA, ISO, and MDR regulations, supporting both internal and external audits.Lead initiatives to improve quality systems, lean manufacturing, and Six Sigma activities.Analyze quality data, prepare inspection procedures, and review engineering changes.Supervise and mentor technicians and provide training to QA and manufacturing teams.Ensure environmental monitoring and product sterility requirements are met.What you need to be considered:Bachelor’s degree in engineering and 5+ years of experience in medical device manufacturing and quality assurance.Knowledge of sterilization, clean rooms, machining, and injection molding.Proficiency in statistics, SPC, and quality engineering tools.Strong communication, problem-solving, and organizational skills.Experience with MS Office, SAP, and quality tools like Six Sigma and Minitab preferred.Who we are:KARL STORZ is an independent, family-owned company headquartered in Germany’s renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and OR integration to benefit patients and healthcare providers alike.With a 9000+ employees worldwide, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support. In doing so, we help healthcare facilities manage costs, streamline operations, and deliver positive patient outcomes.It's not just about the tools we createit’s about the lives we change, together.#LI-BL1

The CNC Machining/Manufacturing Engineer at KARL STORZ provides hands-on engineering support to the Advanced Machining Center in Franklin, MA, producing high-quality components for medical devices. The role focuses on continuous improvement, process implementation, and solving machining problems. It also supports the introduction of new products, processes, and equipment.What's in it for me :Technical Mastery: Enhance your expertise in CNC programming, automation, and machining technologies while working with advanced equipment and processes.Innovation and Problem-Solving: Lead continuous improvement initiatives, develop solutions for machining challenges, and play a key role in the introduction of new products, equipment, and processes.Cross-functional Collaboration: Work closely with R&D, Project Engineering, Quality, and Operations teams, giving you exposure to various disciplines and broadening your skill set.Leadership Opportunities: Take ownership of projects like equipment qualification, process optimization, and cost-reduction strategies, driving significant impact in the manufacturing process.Career Growth: Gain valuable experience in cutting-edge areas like cobot integration, machine learning, and automation, positioning yourself for future leadership roles in manufacturing engineering.What you'll be doing:Collaborate with R&D, Operations, and Quality teams to launch and support manufacturing processes.Design and qualify tooling and fixtures for machining.Troubleshoot and validate existing processes and equipment.Insourcing of new parts and selecting/qualifying equipment (IQ/OQ/PQ).Optimize product line layout and implement flow and quality improvements.Lead cost reduction initiatives and author Engineering Change Orders (ECOs).What you need to be considered for this role:BS in a Technical/Engineering discipline.Extensive experience in CNC machining process development, automation, and programming.Proficient in problem-solving methods like Six Sigma, Kaizen, and DMAIC.Ability to design and qualify tooling, fixtures, and equipment.Proficiency in Solidworks, SPC, GD&T, and process yield improvement analytics.Additional experience that would make you stand out:Experience working with international teams and willingness to travel.Knowledge of cobot integration, machine monitoring, and learning systems.PLC programming, troubleshooting, and HMI/SCADA experience.Background in Quality Control and inspection processes.Who we are:KARL STORZ is an independent, family-owned company headquartered in Germany’s renowned MedTech manufacturing region. For 80 years, we've pioneered the most groundbreaking innovations in endoscopic surgery, video imaging, and OR integration to benefit patients and healthcare providers alike.With a 9000+ employees worldwide, we pride ourselves on harnessing cutting-edge technology, precise workmanship, and unrivaled customer support. In doing so, we help healthcare facilities manage costs, streamline operations, and deliver positive patient outcomes.It's not just about the tools we createit’s about the lives we change, together.#LI-BL1