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

Pay: $80000 per year - $80000 per yearAt Great Wolf, theAssistant Director of Engineeringsupervises maintenance operations and physical condition of the facility to ensure the highest quality standards of guest satisfaction within the allotted budget.Essential Duties & ResponsibilitiesMeets maintenance operational standards by contributing maintenance information to strategic plans and review; implementing production, productivity, quality, and customer-service standards; resolving problemsEvaluates functionality and reliability of facility systems and associated equipment by conferring with operating departments; identifying problems and requirementsMaintains function and reliability of facility systems and associated equipment by implementing a preventive maintenance program; operating and testing systems and equipment; restoring, repairing, rebuilding, or replacing faulty or inoperative components and partsImproves function and reliability of facility systems and associated equipment by studying performance results; identifying, recommending, and implementing changes, expansions, and additionsPerform supervisory responsibilities by selecting, training, scheduling, coaching and counseling with disciplinary measures, as necessaryEvaluate performance of the team and recommending compensation actionsMaintains safe and healthy work environment by following standards and procedures; complying with legal codes and regulationsUpdates job knowledge by participating in educational opportunities, staying up to date with the industryAccomplishes maintenance and organization mission by completing related results as neededBasic Qualifications & SkillsAssociate's degree or equivalent experience5+ years experience with hands-on equipment maintenance; must include experience with solving electronics failures, using such tools as test clips for device packages along with grabbers, SMD tweezers, probes, and insertion/extraction tools3+ years experience with supervising work for a team of technically skilled individualsDesired Qualifications & TraitsPlumbing License, Certified Pool & Spa (CPO) License, Aquatic Facility Operator (AFO) CertifiedPrevious experience in leadership role in resort/waterpark settingAble to develop, implement, and monitor programs that adhere to all appropriate regulations, including: Ergonomics, Emergency Response, Injury and Illness Prevention, and Hazard CommunicationsExcellent people management skills including resolving conflict, coaching and developing others, promoting teamwork, and performance managementPhysical RequirementsAble to lift up to 15 lbsAble to bend, stretch, and twistAble to sit or stand for long periods of timeAble to climb multiple flights of stairs on daily basis and walk frequentlyThis contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, national origin, and for inquiring about, discussing or disclosing compensation. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

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 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:Provides engineering leadership to the assigned areas of the Stafford Springs manufacturing plant – establishes a network of resources and contacts to meet business goals and customer needs.Implement safety, productivity, and yield improvements, through project leadership or Kaizen events, with ownership for key manufacturing processes and products.Leads local implementation of Management of Change projects in support of global safety, product quality, and service goals.Engagement and involvement in daily operations, supports/participates in Lean Management system, and provides direction/support of maintenance and capital improvement projects.Monitors ongoing productivity of assigned areas and initiates continuous improvement projects as well as supports site resources with technical knowledge and problem-solving skillset.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 (completed and verified prior to start) from an accredited institution in Engineering.ORHigh School Diploma/GED (completed and verified prior to start) AND 4 years experience working within a manufacturing and/or process engineering environment.Additional qualifications that could help you succeed even further in this role include:Bachelor’s degree or higher in Chemical or Mechanical Engineering from an accredited universityThree (3) years working within a manufacturing and/or process engineering environment.One (1) year of experience with Continuous Improvement and Business ExcellenceThree (3) years working with cross-functional teamsSelf-starter/self-directed that leads with high energy and passionEffective facilitation, communication, and teaching skillsAbility to multi-task and handle large workloads under time constraintsWork location:Onsite [(Stafford Springs, CTTravel: May include up to 10% domestic/internationalRelocation 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.

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

Join our team of more than 34,000 team members, supporting our members and communities in our Club Support Center, 235+ clubs and eight distribution centers. BJ’s Wholesale Club offers a collaborative and inclusive environment where all team members can learn, grow and be their authentic selves. Together, we’re committed to providing outstanding service and convenience to our members, helping them save on the products and services they need for their families and homes. The Benefits of working at BJ’s• BJ’s pays weekly•Eligible for free BJ's Inner Circle and Supplemental membership(s)*• Generous time off programs to support busy lifestyles* o Vacation, Personal, Holiday, Sick, Bereavement Leave, Jury Duty• Benefit plans for your changing needs* o Three medical plans**, Health Savings Account (HSA), two dental plans, vision plan,flexible spending • 401(k) plan with company match (must be at least 18 years old)*eligibility requirements vary by position**medical plans vary by locationJob Summary:Responsible for partnering with BJ’s suppliers to develop packaging solutions for our Own Brand products. Works closely with a cross functional Own Brand team (comprised of Own Brand Management, Sourcing, Product Development and Quality) to execute a roadmap of projects that deliver top and bottom-line Own Brand growth. Accountable for delivering primary and secondary (transit) packaging solutions that protect the quality of the product, minimize waste and optimize product cost. Responsibilities and Key Accountabilities:Partners with the Own Brand Manager to understand the strategic initiatives of the business and implement packaging solutions in partnership with BJ’s suppliersPerforms technical and competitive benchmarking to define critical vs optional primary and secondary packaging attributes to engineer the right quality at the best costDefines a roadmap of opportunities for quality engineering to deliver value to our members and profitability for BJs. Responsible for identification and validation of package materials and suppliers through the development process and provides feedback to BJ’s suppliers. Partners with BJ’s suppliers to document the packaging specification for each product in BJ’s portfolioEnhances and validates package components and packaging processes to ensure packaging can maintain integrity throughout the Supply ChainEvaluate, recommend, develop and implement packaging materials/systems based on multiple factors and influenceDefines sustainability standards for packaging that support waste and cost reductionInfluences the Own Brand cross functional team with a strong understanding of the interactions among product, processes and packaging to deliver consistent and strong product quality Validates the packaging quality achieves the specification through the commercialization phase of product development in partnership with BJ’s suppliers to deliver a high-quality product for our membersPartner with external suppliers and internal cross-functional teams to identify, develop, trial and commercialize new packaging formats for current and innovative Own Brand products. Monitors and manages on-going packaging quality to ensure products remain competitive and initiates continuous improvement projects when opportunities ariseQualifications:Bachelor’s Degree- preferred in Packaging Engineering5-15 years' experience in a retail owned brand or consumer packaged goods R&D / packaging teamFood, personal care and/or household packaging development experience – including understanding of cost drivers, quality management and technical feasibilityTrack record of driving exceptional results in a cross functional environmentWorking knowledge of product manufacturing (CPG experience desired)Strong curiosity, problem solving and strategic thinking skillsOutstanding communication and collaboration skills – thrives in a team environmentProject management skillsExceptional prioritization ability focused on delivering against most important outcomesKnowledgeable about packaging design for logistics/warehousing optimizationIn-depth knowledge of packaging, material compatibility and technologies related to development, testing and implementation of new product packaging and delivery systemIn accordance with the Pay Transparency requirements, the following represents a good faith estimate of the compensation range for this position. At BJ’s Wholesale Club, we carefully consider a wide range of non-discriminatory factors when determining salary. Actual salaries will vary depending on factors including but not limited to location, education, experience, and qualifications. The pay range for this position is starting from $98,500.00.

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

Join our team of more than 34,000 team members, supporting our members and communities in our Club Support Center, 235+ clubs and eight distribution centers. BJ’s Wholesale Club offers a collaborative and inclusive environment where all team members can learn, grow and be their authentic selves. Together, we’re committed to providing outstanding service and convenience to our members, helping them save on the products and services they need for their families and homes. The Benefits of working at BJ’s• BJ’s pays weekly•Eligible for free BJ's Inner Circle and Supplemental membership(s)*• Generous time off programs to support busy lifestyles* o Vacation, Personal, Holiday, Sick, Bereavement Leave, Jury Duty• Benefit plans for your changing needs* o Three medical plans**, Health Savings Account (HSA), two dental plans, vision plan,flexible spending • 401(k) plan with company match (must be at least 18 years old)*eligibility requirements vary by position**medical plans vary by locationAs a Lead Site Reliability Engineer, you will be responsible for designing, building, monitoring, and continuously improving our ecommerce platform's infrastructure and processes. Leveraging your expertise in observability tools such as New Relic, Scalyr/Splunk, bash scripts, and Python scripts, you will play a pivotal role in ensuring the reliability and performance of our Java microservices-based architecture. Key Responsibilities:Design and manage Java based microservices, bash scripts, Redis, High-Availability design, while strictly adhering to Site Reliability Engineering (SRE) principles. Thrive in high-pressure environments, working swiftly and reliably to maintain system integrity and meet service level objectives (SLOs) and service level indicators (SLIs). Proactively identify and address potential issues before they impact operations, utilizing observability tools like New Relic, Scalyr/Splunk, bash scripts, and Python scripts. Lead initiatives to enhance current systems and implement innovative solutions in collaboration with a fast-paced, mission-driven team, focusing on the implementation of SRE best practices. Conduct thorough root-cause analyses for production incidents and generate high-quality RCA reports, leveraging SRE methodologies to prevent recurrence. Apply software engineering principles to rectify operational challenges and optimize system performance, with a specific focus on implementing SRE-driven solutions. Ensure the availability, latency, performance, efficiency, and security of our infrastructure, adhering rigorously to SRE principles and best practices. Design and maintain robust production monitoring systems to ensure timely detection and resolution of issues, following SRE guidelines for effective monitoring and alerting. Utilize a diverse array of tools to troubleshoot performance and stability issues effectively, employing SRE methodologies to identify and mitigate bottlenecks. Evaluate and enhance application and environment security measures, integrating SRE-driven security practices into the development and deployment pipelines. Provide support for globally distributed, multi-cloud (public and/or private) environments, implementing SRE strategies for resilience and fault tolerance. Automate repetitive tasks at scale to streamline operational workflows and enhance efficiency, focusing on the implementation of SRE-driven automation solutions. Adhere to change management processes during implementations and utilize version control for application infrastructure, following SRE principles for reliable and auditable change management. Foster a SRE mindset throughout the organization, promoting collaboration and shared responsibility for reliability and performanceQualifications:Bachelor's Degree in Computer Science or related field, or foreign equivalent. Demonstrated curiosity and self-drive to tackle complex challenges and drive change in a diverse organizational landscape. Excellent written and verbal communication skills, with the ability to effectively communicate with engineering management, developers, and leadership. Proven ability to adapt to new technologies and learn quickly. Minimum of 5 years of experience in Site Reliability Engineering (SRE) or related roles. Job Conditions:Collaborate within a diverse and global team environment. Participate in cross-training with other team members across different regions. Rotate in an on-call schedule as required to ensure 24/7 availability and support for critical systems. In accordance with the Pay Transparency requirements, the following represents a good faith estimate of the compensation range for this position. At BJ’s Wholesale Club, we carefully consider a wide range of non-discriminatory factors when determining salary. Actual salaries will vary depending on factors including but not limited to location, education, experience, and qualifications. The pay range for this position is starting from $109,000.00.

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