General SummaryThe Sterile Processing Quality Assurance Specialist (QA) is responsible for ensuring the accuracy and proper assembly of instrument trays according to pick sheets. This role includes verifying instrument placement, checking for good working order, and preparing trays for processing. The QA specialist provides immediate feedback and coaching, documents data in provided software, and identifies discrepancies/errors in count sheets.Additionally, the QA specialist may assist in developing, recommending, and implementing educational needs, internal standards, policies, and procedures to improve the quality and effectiveness of patient care and sterile processing. Participation in hospital, departmental, and multidisciplinary programs, committees, and special projects may also be required.Values StatementThe Sterile Processing Quality Assurance Specialist embodies the hospital’s core values in all interactions with patients, families, and colleagues.Duties NoticeThe following statements describe the essential duties of the person assigned to this job. They are not intended as an exhaustive list of all job duties and responsibilities. In the event of a public health emergency, you may be asked to assume additional duties in other areas of the organization if needed.Principal Duties and ResponsibilitiesKit Review and Accuracy: Maintains review kits for accuracy and instrument functionality. Ensures every kit is audited and entered into the database.Error Trend Identification: Identifies trends in kit errors and reports findings from SPM collation to monthly staff meetings.Immediate Feedback and Coaching: Provides immediate feedback to assemblers, offers coaching to staff when gaps arise, and recognizes staff that are unreceptive to coaching. Recommends focused needs to educators and specialty training.Staff Evaluation: Recognizes staff that are unreceptive to feedback and reports findings and trends.Case Cart Review: Reviews and inspects case carts for accuracy and completeness. Helps create a missing/priority list to complete case carts.Discrepancy Reporting: Accurately reports all discrepancies.Quality Assurance Support: Supports enterprise programs for quality assurance needs.Other Duties: Performs other duties as assigned.Certification/RegistrationCertification/Registration Required: SPD Certification, Level II TechCertification/Registration Preferred: CISEducationRequired Education: High School Diploma or Surgical TechnologistPreferred Education: Bachelor’s DegreeWork ExperienceRequired Work Experience: Certification in SPD, 5+ years of experiencePreferred Work Experience: None specifiedKnowledge, Skills, and AbilitiesAnalytical Skills: Ability to resolve complex problems requiring the application of clinical, scientific, or technical principles, theories, and concepts and in-depth, cross-functional, experienced-based knowledge.Communication Skills: Effectively deal with conflicting views or issues, mediate fair solutions, and possess well-developed writing skills.Interpersonal Skills: Ability to communicate effectively with supervisors, coworkers, and all levels of hospital staff, including the Operating Room and physicians.Multi-tasking: Capable of planning, organizing, and multi-tasking projects. Flexible and self-motivated.Technical Reading: Ability to read and understand applicable IFU and SPM count sheets.Customer Centric Behavior: Demonstrated customer-centric behavior.OR Workflow Knowledge: Familiarity with OR workflow, procedures, medical terminology, and instrumentation.Infection Control: Knowledge of infection control and health & safety policies and procedures.Cultural Sensitivity: Sensitivity to recognize, appreciate, and incorporate differences, diversity, and preferences into the provision of care.Software Proficiency: Thorough working knowledge of Microsoft Office applications and the capability to learn software programs.

Are you a CNC Machinist looking to take your career to the next level KARL STORZ is seeking aSenior CNC Machinist/Programmerto join our dynamic team, specializing in the precision manufacturing of medical device components. In this role, you’ll leverage your programming and machining skills to produce high-quality parts that make a difference.Shift hours:3:30 p.m. - 12:00 a.m., Monday through FridayWhat you'll be doing:Set up and operate CNC lathes, mills, and Swiss-style machines to deliver flawless results.Create, edit, and optimize CNC programs under engineering direction.Troubleshoot machining challenges and ensure parts meet tight tolerances.Lead projects to improve processes through Lean manufacturing initiatives.Train and mentor junior machinists, sharing your expertise and driving team success.What you will need to be considered:5–10+ years of CNC programming and machining experience, including exotic metals like nitinol and stainless steel.Proven ability to read blueprints, inspect parts, and maintain GMP compliance.Advanced problem-solving skills for tooling, setup, and machine alignment.Experience with FDA QSR, ISO 13485, and ISO 9001 standards.A passion for precision, innovation, and collaboration.Why Join Us Be part of a cutting-edge team revolutionizing medical device manufacturing.Competitive compensation and benefits package.Opportunities for leadership, growth, and professional development.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.Make an impact where precision meets purpose. APPLY NOW TO JOIN OUR TEAM!#LI-BL1

Job ID NumberR5060Employment TypeFull timeWorksite FlexibilityOnsiteJob SummaryAs Quality Control Specialist, you will conduct inspections and testing on a variety of parts and products to ensure compliance with customer specifications and quality standards.Job DescriptionWe are looking for a Quality Control Specialist. This position will be a full-timeand onsite contract opportunity in Medway, MA. What You’ll DoTo conduct first piece and in-process inspection, final inspection and testing on a variety of parts and products in a manner which will consistently ensure compliance with pre-established customer specifications and quality standardsConducts assigned inspection and testing activities consistent with Quality policies, procedures, and standardsPerforms standard surface plate and coordinate measuring machine inspectionCreate and maintain inspection plansUses precision measuring instruments and makes, or assists in making, precision inspection set-upsConducts, or assists in conducting, random audits during operations to ensure that machined parts comply with process and final drawing specificationsTrains new employees in the use of equipment and on inspection proceduresPerforms receiving inspection and testing of vendor parts, services, and materials were requiredAssists in reviewing the calibration status of inspection equipment, ISO Standards, and reports problems as appropriateReviews inspection equipment and methods utilized by manufacturing personnel and offers assistance/recommendations as neededUpdates and maintains daily inspection logs in a timely and accurate mannerMaintains work area in a neat and orderly conditionWorks safely, and complies with all established safety rules and work practicesComplies with Company, Department, and quality policies and procedures as applicableKeeps the Quality Supervisor informed of job related problems and other information related to work activityMaintains a positive work attitude and promotes a “team’ approach throughout the DepartmentPerforms related work as apparent or assignedWhat You'll NeedRequired:High school education or equivalent, plus at least 1 year of appropriate technical training including geometric dimensioning and tolerancingNeed experience with hand tools such as calipers, micrometer, pin gauges etc.Knowledge of and experience with surface plate inspection, small tool mechanical measurements, and coordinate measuring machinesWorking knowledge of ISOAbility to work from blueprints, inspection specifications, and/or written or verbal instructionsPreferredAbility to utilize manufacturing software systemsAt least 2 years of first piece and in-process mechanical inspection experience in a close tolerance machining job shop environment is preferredPhysical DemandsAbility to safely and successfully perform the essential job functions consistent with the ADA and other federal, state, and local standardsWhile performing the duties of this job, the employee is occasionally required to walk; sit; use hands to finger, handle, or feel objects, tools or controls; reach with hands and arm; balance; stoop; talk or hearThe employee must occasionally lift and/or move up to 40 poundsSpecific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focusWork environment: General office and machine shop environment#LI-AL1Reasonable Accommodation StatementIf you require a reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employment selection process, please direct your inquiries to or (888) 824 – 8111.Equal Employment Opportunity Policy StatementIt is the policy of CAI not to discriminate against any employee or applicant due to race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or being a protected veteran. It is also the policy of CAI to take affirmative action to employ and to advance in employment, all persons regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or being a protected veteran, and to base all employment decisions only on valid job requirements. This policy shall apply to all employment actions, including but not limited to recruitment, hiring, upgrading, promotion, transfer, demotion, layoff, recall, termination, rates of pay or other forms of compensation and selection for training, including apprenticeship, at all levels of employment. Employees and applicants of CAI will not be subject to harassment due to race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or being a protected veteran. Additionally, retaliation, including intimidation, threats, or coercion, because an employee or applicant has objected to discrimination, engaged or may engage in filing a complaint, assisted in a review, investigation, or hearing or have otherwise sought to obtain their legal rights under any Federal, State, or local EEO law is prohibited.

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:Solventum is seeking Production Operator candidates to join our team in Stafford Springs CT!Starting Pay: $21.06/hour + Shift PremiumsOther production positions within the site have increased pay opportunities dependent on experience.Solventum Purification & Filtration businessWe are pleased to announce that Solventum has entered into a definitive agreement to sell our Purification & Filtration business to Thermo Fisher Scientific. This transaction is anticipated to be completed by the end of 2025, subject to the satisfaction of customary closing conditions, receipt of regulatory approvals, and country specific information and consultation needs where required. This is a significant milestone for the P&F business and will allow for the strategic investment and resources needed for sustaining growth and delivering customer solutions. By joining us during this transitional period, you will be able to work alongside an energized and mission-driven team who is experiencing this transition along with you. Until then, Solventum will continue to operate as a unified entity, and employment is subject to all applicable terms and conditions as set forth in our employment agreement and company policies.The Impact You’ll Make in this RoleAs a Production Operator, 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:Operating production lines in accordance with written work instructions and process parameters and making necessary adjustments within qualified ranges to ensure equipment is running properly.Performing routine area and equipment cleaning, preventative maintenance, and reporting any malfunctions/problems to supervision.Completing tests to ensure proper quality standards are achieved and entering test/run data into the quality data base.Following all site and department safety rules and reporting all safety hazards to supervision.Processing, inspecting and packing material as it comes off the line.Performing changeovers from one product line to another.Ensuring accuracy while preparing and inspecting paperwork, labels, and batch numbers for material to be run.May require handling hazardous waste and other miscellaneous duties (including training) assigned by department supervision/leadership.Possessing the ability to clearly speak, understand, and write in English to communicate effectively in both verbal and written contexts.Your Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:High School Diploma/GED or higher (completed prior to start)Additional qualifications that could help you succeed even further in this role include:One (1) year of manufacturing experience.Ability to successfully follow instructions.Possess good communication skills.Work location: Onsite – 32 River Rd, Stafford Springs, CT 06076Travel: No TravelRelocation Assistance: Not 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.The starting rate of pay for this position is $21.06/hour, with the potential to reach $22.10/hour. 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.

WHO WE ARE LOOKING FORAs our Footwear Production Artist II, you will combine your experience, problem solving abilities, and creativity to bring to life the seasonal creative narratives through graphic design that is trend relevant to the consumer across performance and lifestyle footwear. You will assist in creating original graphic and/or textile designs that appropriately reflect Nike's design ethos. This position amplifies footwear design by ensuring flawless execution of production-ready files and serves as a trusted resource in footwear construction and graphic execution within product triads. Candidates should possess a creative mindset and the ability to manage multiple projects in a fast-paced environment, maintaining forward-thinking design principles.WHAT YOU WILL WORK ONYou will proactively create and finalize the execution of all footwear product details, including providing the appropriate materials to designers, developers, account managers to ensure manufacturability. For textiles, you will produce textile repeats for production purposes.You will do this by leveraging 2D and 3D tools to communicate design intent. A typical day could include cross-functional meetings and discussions, high-volume technical sketch creation to Nike authoring standards, presenting to development, attending prototype reviews, maintain updates on all appropriate files until final approval. This could include schematic building for embroidery, trim, and various printing processes. You will also maintain and document process that bring product to life. You will get to learn new tools and advocate for efficiencies in the product creation life cycle.WHO YOU WILL WORK WITHYou will report directly to the Footwear Production Art Senior Manager, while working in collaboration with fellow Footwear Graphic Production Artists and Footwear Graphic Designers. Outside of the Studio, your primary partners will be Footwear Development, Color Design, Material Design and Product Design.WHAT YOU BRINGBachelor’s degree in graphic design or related field or equivalent combination of education and experience.2+ years experience in progressively technically sophisticated graphic design experienceProven ability to apply and perform graphic design skills, including drawing/sketching, typography, ideation, color theory, use of texture, spacing, and scale, visual presentation development and layout that is supported by a portfolio of non-computer-based creative art and graphic design.Product creation experience is a plusPassion for sport, culture and/or the Nike brandExperience working in complex, matrixed environment is a plusExpert in Adobe Creative SuiteColor separation experience is a plusExcellent attention to detail in a high-volume production environmentAbility to work independently as well as collaboratively in a team environment.Strong organizational skillsDeep curiosity for learningStrong ability to multitask amidst competing prioritiesStrong communication and prioritization skillsStrong listening skillsAbility to find efficiencies in workflowAbility to take on projects benefitting Studio collectiveTO BE CONSIDERED, YOU MUST INCLUDE A PORTFOLIO OR WORK SAMPLES WITH YOUR APPLICATION

Production Artist 2 –Sport Apparel Digital Design, Global Jordan.The Jordan Design team is inspired by the Greatest of All Time, and is focused on continuing to deliver product that is made and engineered to the exact specification of championship athletes. On and off the court, we want our consumers and athletes to feel confident in the way they look and feel, the same way the greatest player who ever played the game felt every time he laced up his J’s. Jordan Design is a high performance team that works together, pushes the boundaries, and always stays focused on delivering the best product for the consumer.WHO WE ARE LOOKING FORWe are looking for an exceptional Product Artist 2 to combine their experience, problem solving abilities, communication skills and creativity to help create the future of Jordan Sport.The ideal candidate is a highly creative problem solver, who doesn’t settle for anything less than the best Design solutions to meet the needs of our consumer and athletes. This person will be focused on elevating the consumer experience by focusing on both the art and science of Graphic and Print design, and driving Graphic excellence through the connection of trend, design, development, and manufacturing of Apparel and some Footwear graphics.WHAT YOU WILL WORK ONIf this is you, you’ll be partnering with the Jordan Sport Team - Apparel Designers, Product Line Managers, Product Development Teams - to bring to life seasonal stories on performance apparel (and some footwear) products for various sports and athletes.From creating seasonal collections, presenting and collaborating with different internal and external functions and working with manufacturing partners, the daily responsibilities of this role are wide ranging, challenging, and rewarding.WHO YOU WILL WORK WITHThis role does not have direct reports, and reports directly to the Jordan Product Graphics – Senior Manager, while regularly partnering with other Apparel Cut & Sew Designers, Color Designers, Product Line Managers and outside partners.WHAT YOU BRINGQUALIFICATIONS:• Bachelor's degree or combination of relevant education, experience, and training• Minimum 2-3 years of graphic design experience• Demonstrated passion and understanding of trend and visual culture• Elevated skills in type, illustration and image creation• Understanding of apparel product creation• Understanding ofproduct development process – creating mechanicals, schematics and tech packs• Good communication and presentation skills using a variety of formats – Keynote, Miro, Adobe Acrobat• Ability to seek out opportunities to elevate product graphics though craft and construction• Proficient in Adobe CC and comfortable working within new digital spaces•Ability to work cooperatively and share ideas•Ability to manage multiple and competing work priorities, demands, and changes.• Passion for discoveryRESPONSIBILITIES:• This teammate embodies communication skills with the ability to translate complex ideas into focused, consumer-right design narratives• Design support and collaboration for high level designers• This role requires passion and creativity, with focus to see designs through the product creation process• A typical day could include everything from creating visual centers and building design presentations, to attending fit sessions and reviewing prototypes with our development partners• You will be guiding the creative through the design season while working with a team of designers, developers, product managers, and merchants to deliver creative in line with the Jordan Design EthosWe offer a number of accommodations to complete our interview process including screen readers, sign language interpreters, accessible and single location for in-person interviews, closed captioning, and other reasonable modifications as needed. If you discover, as you navigate our application process, that you need assistance or an accommodation due to a disability, please complete the Candidate Accommodation Request Form.

JOB DESCRIPTION: MANAGER, MANUFACTURING ENGINEERING Burlington, MA, USA Poly6 is enabling production of complex turbine engine designs by combining additive manufacturing with advanced materials. Our technology is uniquely suited to both increase the efficiency of complex manufacturing processes and advance engineering design capabilities, while achieving the long-term benefit of reducing greenhouse gas emissions. You will have the opportunity to work alongside a highly talented team to solve problems in one of the world's most complex engineering industries: aviation. JOB SUMMARY The Manufacturing Engineering Manager, reporting directly to the Plant Manager, is a dynamic technical leader responsible for overseeing a team of engineers. This role is accountable for driving continuous improvement in process capability, operational efficiency, and cost productivity within manufacturing operations, while ensuring that safety is integral to the DNA of the engineering team. The manager ensures the development and maintenance of reliable, predictable production processes that align with the company's ambitious growth strategy, including multi-site expansion and achieving a 20X increase in production volume over the next five years. RESPONSIBILITIES • Lead and develop the engineering team, providing leadership, mentorship, and development opportunities to ensure a high-performing and engaged workforce. • Oversee all production processes, including the creation, maintenance, and improvement of process documentation, ensuring adherence to quality and regulatory standards. • Implement and maintain best practices to enhance workplace safety across all manufacturing operations. • Improve yield, process capability, efficiency, capacity, and cost-effectiveness to meet production and business goals. • Develop, procure, install, validate, and support new manufacturing equipment and processes to support production demands and innovation. • Collaborate with cross-functional teams to scale new processes from prototype to full production. • Serve as the technical lead for knowledge transfer and standardization in support of a multi-site expansion project. • Develop and execute a vision for multi-site team expansion and ongoing execution. • Partner with facilities and maintenance teams to ensure seamless integration of manufacturing equipment and processes. • Define, measure & control KPVs, correlating to, and measuring against, product requirements. • Track business key performance indicators (KPIs) related to safety, quality, delivery, productivity, and cost, providing regular updates to leadership. • Champion Lean, Six Sigma, and other continuous improvement methodologies to enhance production processes and overall operational efficiency. • Work closely with R&D, quality, supply chain, and operations teams to align engineering initiatives with business objectives. QUALIFICATIONS • B.S. with 7-10 years' experience, or 12+ years' experience in a related field including chemical processing, injection molding, 3D printing, or ceramics manufacturing. • Minimum of 5 years' experience in an ISO 9001 or similar production manufacturing environment. • Minimum of 3 years' experience in a Fixed Process environment, preferably aerospace. • 5+ years' experience in engineering people management. • Proficiency in management of operational and quality metrics like OEE, yield, process capability. • Proficiency in Minitab, JMP or SAS engineering analysis tools. • Six Sigma Green Belt and 3+ years' applied Six Sigma engineering experience or 5+ years' applied Six Sigma engineering experience. • Experience managing across various TRL and MRL levels, with demonstrated capability for multi-site technology transfer. PREFERRED EXPERIENCE • Advanced proficiency in Minitab, JMP, or SAS engineering analysis tools. • 5+ years' experience in ceramic core for aerospace casting. • Six Sigma Black Belt. This position requires access to information protected under U.S. export control laws, including the International Traffic in Arms Regulations and/or the Export Administration Regulations. Please note that any offer for employment may be conditioned on authorization to receive software or technology controlled under these US export laws without sponsorship for an export license. Poly6 is an equal opportunity employer. We do nThis is a management positionThis is a full time position

General Summary *Evening Shift* *Overnight Shift also available*The Sterile Processing Quality Assurance Specialist (QA) is responsible for ensuring the accuracy and proper assembly of instrument trays according to pick sheets. This role includes verifying instrument placement, checking for good working order, and preparing trays for processing. The QA specialist provides immediate feedback and coaching, documents data in provided software, and identifies discrepancies/errors in count sheets.Additionally, the QA specialist may assist in developing, recommending, and implementing educational needs, internal standards, policies, and procedures to improve the quality and effectiveness of patient care and sterile processing.Values StatementThe Sterile Processing Quality Assurance Specialist embodies the hospital’s core values in all interactions with patients, families, and colleagues.Duties NoticeThe following statements describe the essential duties of the person assigned to this job. They are not intended as an exhaustive list of all job duties and responsibilities. In the event of a public health emergency, you may be asked to assume additional duties in other areas of the organization if needed.Principal Duties and ResponsibilitiesKit Review and Accuracy: Maintains review kits for accuracy and instrument functionality. Ensures every kit is audited and entered into the database.Error Trend Identification: Identifies trends in kit errors and reports findings from SPM collation to monthly staff meetings.Immediate Feedback and Coaching: Provides immediate feedback to assemblers, offers coaching to staff when gaps arise, and recognizes staff that are unreceptive to coaching. Recommends focused needs to educators and specialty training.Staff Evaluation: Recognizes staff that are unreceptive to feedback and reports findings and trends.Case Cart Review: Reviews and inspects case carts for accuracy and completeness. Helps create a missing/priority list to complete case carts.Discrepancy Reporting: Accurately reports all discrepancies.Quality Assurance Support: Supports enterprise programs for quality assurance needs.Other Duties: Performs other duties as assigned.Certification/RegistrationCertification/Registration Required: SPD Certification, Level II TechCertification/Registration Preferred: CISEducationRequired Education: High School Diploma or Surgical TechnologistPreferred Education: Bachelor’s DegreeWork ExperienceRequired Work Experience: Certification in SPD, 5+ years of experiencePreferred Work Experience: None specifiedKnowledge, Skills, and AbilitiesAnalytical Skills: Ability to resolve complex problems requiring the application of clinical, scientific, or technical principles, theories, and concepts and in-depth, cross-functional, experienced-based knowledge.Communication Skills: Effectively deal with conflicting views or issues, mediate fair solutions, and possess well-developed writing skills.Interpersonal Skills: Ability to communicate effectively with supervisors, coworkers, and all levels of hospital staff, including the Operating Room and physicians.Multi-tasking: Capable of planning, organizing, and multi-tasking projects. Flexible and self-motivated.Technical Reading: Ability to read and understand applicable IFU and SPM count sheets.Customer Centric Behavior: Demonstrated customer-centric behavior.OR Workflow Knowledge: Familiarity with OR workflow, procedures, medical terminology, and instrumentation.Infection Control: Knowledge of infection control and health & safety policies and procedures.Cultural Sensitivity: Sensitivity to recognize, appreciate, and incorporate differences, diversity, and preferences into the provision of care.Software Proficiency: Thorough working knowledge of Microsoft Office applications and the capability to learn software programs.

If you are a skilled CNC Machinist with a passion for precision and continuous improvement, we encourage you to apply and join the innovative team at KARL STORZ U.S.!Shift Hours:6:00 a.m. - 2:30 p.m., Monday through FridayWhat you'll be doing:Set up and operate CNC machines (lathe, mill, Swiss-style) and ensure accuracy to blueprint specifications.Edit CNC programs and troubleshoot any issues during setup or operation.Inspect and measure parts to ensure conformance to print and record relevant data.Perform basic Total Productive Maintenance (TPM) to keep machines in good working order.Work with exotic metals such as nitinol, stainless steel, and nickel alloys, ensuring high-quality production.Participate in Lean manufacturing and process improvement activities.Collaborate with engineers, quality teams, and management to meet production schedules and quality standards.What you'll need to be considered:High school diploma or general equivalency (GED)3-5+ years of CNC machining experience.Proven ability to read blueprints and inspect parts according to specified tolerances.Experience with exotic metals and machining medical device components is preferred.Ability to edit CNC programs and troubleshoot machine issues.Basic to intermediate computer skills for program edits and record-keeping.Strong attention to detail and commitment to maintaining quality and safety standards..Must be able to lift up to 50 lbs and stand for extended periods.Must adhere to FDA Quality System Regulations (QSR), ISO 13485, and ISO 9001 standards.Willingness to learn and grow in a dynamic manufacturing environmentAbility to work effectively with engineers, management, and coworkers.Strong problem-solving skills and the ability to make decisions regarding machining processes.Excellent interpersonal communication skills and the ability to maintain organized records.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.Ready to make an impact Apply today and help us shape the future of medical technology atKARL STORZ.#LI-BL1

Join Our Team at KARL STORZ U.S. – Elevate Quality and Drive Continuous ImprovementAre you passionate about quality and regulatory compliance in the medical device industry Do you thrive in a leadership role, guiding teams to achieve excellence If so, we want you to join our team as a Quality Assurance Manager at KARL STORZ, a global leader in endoscopy, medical device technology, and healthcare solutions.Why KARL STORZ Be Part of Innovation: Drive continuous improvement and contribute to products that impact healthcare worldwide.Leadership Impact: Lead and develop a talented team, influencing quality initiatives and shaping the future of medical technology.Career Growth: With our commitment to ongoing learning, you’ll have ample opportunities to advance and expand your skill set in a dynamic environment.What you will be doing:Quality System Oversight: Ensure compliance with FDA, ISO, EN, and MDR standards, leading audits, CAPA processes, and driving quality improvement initiatives.Data Analytics: Analyze field failure data to identify trends, make recommendations for design or process improvements, and reduce costs and service impact.Audits & Compliance: Host and manage internal and external audits, ensuring quality system adherence across global operations.Leadership & Mentoring: Lead a team, provide training, and foster a collaborative, high-performance culture. Drive continuous improvement across the quality system.Cross-Functional Collaboration: Work closely with departments like engineering, production, and customer service to resolve issues and improve quality and compliance.What you will need to be considered:Experience: 7+ years in quality management roles within the medical device industry; 3-5 years in quality auditing.Education: Bachelor’s degree in a relevant field.Certifications: Lead Auditor training for ISO 9001/ISO 13485, CQE or CQM certifications preferred.Skills: Strong knowledge of FDA regulations, ISO standards (13485, 14971), and experience with ERP systems like SAP. Proficiency in Microsoft Office tools.Leadership: Proven ability to lead and mentor teams, delivering high-quality results and driving cross-functional collaboration.What’s in it for you Competitive Compensation: Attractive salary and benefits, including healthcare, retirement plan, and more.Career Advancement: Access to ongoing training, leadership development, and internal growth opportunities.Work-Life Balance: Flexible work environment with minimal travel required (up to 20%).Impactful Role: Make a tangible difference in the quality of healthcare products, ensuring they meet the highest standards.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.Ready to make an impact Apply today and help us shape the future of medical technology at KARL STORZ.#LI-BL1

Are you looking for work that is fulfilling Have you considered working with a company that is making a difference in people's lives every day At KARL STORZ U.S., we are recruiting for a 2nd shift Assembler III in Charlton, MA, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours:3:30 p.m. - 12:00 midnight, Monday through FridayWhat you'll be doing:Assemble/disassembleand inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 2-4years ofmanualassembly experience, medical products a plus.Basic computer skills using Microsoft Office programs.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to operate moderately complicated machinery.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Things that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Prior fiber optic assembly experience preferred, but not required.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.What’s In It For You Competitive Compensation:Enjoy a strong salary and benefits package that rewards your hard work and experience.Career Advancement:Take advantage of opportunities for training and development, with potential for growth within the company.Dynamic Work Environment:Thrive in a fast-paced, collaborative atmosphere where your contributions directly affect production outcomes.Job Stability:Join a well-established company with a commitment to continuous improvement, providing you with long-term career stability.Work-Life Balance:Enjoy overtime options when necessary, while maintaining regular hours and a structured work environment.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.If you're looking for a hands-on, fast-paced role where precision and quality matter, we encourage you to apply today!It's not just about the tools we createit’s about the lives we change, together.

Are you ready to work in a great environment on 1st shift on products that change peoples lives Join our team atKARL STORZ U.S.as an Assembler III on 1st shift, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours:5:00 a.m. - 3:30 p.m., Monday through ThursdayWhat you'll be doing:Assemble and inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Complete sub-assembly soldering and basic laser welding.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 2-4year experience assembling medical products preferred.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Things that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.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.If you're looking for a hands-on, detail-oriented role where you can grow in the medical device industry, we encourage you toAPPLY TODAY!#LI-BL1

Are you ready to work in a great environment on products that change peoples lives Join our team atKARL STORZ U.S.as an Assembler II on 1st shift, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours: 5:00 a.m. - 3:30 p.m., Monday through ThursdayWhat you'll be doing:Assemble and inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Complete sub-assembly soldering and basic laser welding.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 0-1 year experience assembling medical products preferred.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Things that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.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.If you're looking for a hands-on, detail-oriented role where you can grow in the medical device industry, we encourage you toAPPLY TODAY!#LI-BL1

Are you looking for an opportunity to work with a company that is making a difference in people's lives We are recruiting for a 2nd shift Assembler I atKARL STORZ U.S.in Charlton, MA, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours:3:30 p.m. - 12:00 midnight, Monday through FridayWhat you'll be doing:Assemble/disassembleand inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 1-2years ofmanualassembly experience, medical products a plus.Basic computer skills using Microsoft Office programs.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Things that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Prior fiber optic assembly experience preferred, but not required.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.What’s In It For You Competitive Compensation:Enjoy a strong salary and benefits package that rewards your hard work and experience.Career Advancement:Take advantage of opportunities for training and development, with potential for growth within the company.Dynamic Work Environment:Thrive in a fast-paced, collaborative atmosphere where your contributions directly affect production outcomes.Job Stability:Join a well-established company with a commitment to continuous improvement, providing you with long-term career stability.Work-Life Balance:Enjoy overtime options when necessary, while maintaining regular hours and a structured work environment.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.If you're looking for a hands-on, fast-paced role where precision and quality matter, we encourage you to apply today!It's not just about the tools we createit’s about the lives we change, together.

Are you a detail oriented person looking to work with a company that makes a difference in people's lives every day We are recruiting for a 2nd shift Assembler II atKARL STORZ U.S.in Charlton, MA, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours:3:30 p.m. - 2:00 a.m., Monday through ThursdayWhat you'll be doing:Assemble/disassembleand inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 1-2years ofmanualassembly experience, medical products a plus.Basic computer skills using Microsoft Office programs.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Things that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Prior fiber optic assembly experience preferred, but not required.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.What’s In It For You Competitive Compensation:Enjoy a strong salary and benefits package that rewards your hard work and experience.Career Advancement:Take advantage of opportunities for training and development, with potential for growth within the company.Dynamic Work Environment:Thrive in a fast-paced, collaborative atmosphere where your contributions directly affect production outcomes.Job Stability:Join a well-established company with a commitment to continuous improvement, providing you with long-term career stability.Work-Life Balance:Enjoy overtime options when necessary, while maintaining regular hours and a structured work environment.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.If you're looking for a hands-on, fast-paced role where precision and quality matter, we encourage you to apply today!It's not just about the tools we createit’s about the lives we change, together.#LI-BL1

Are you looking for an opportunity on 1st shift to work in a great environment on products that change peoples lives Join our team at KARL STORZ U.S. as an Assembler I, where you’ll be responsible for assembling high-quality endoscope subassemblies.Hours: 6:00 a.m. - 2:30 p.m., Monday through FridayWhat you'll be doing:Assemble and inspect miniature precision medical products following detailed assembly procedures.Use tools such as microscopes, small hand and power tools, adhesives, and solvents to perform tasks.Complete sub-assembly soldering and basic laser welding.Maintain detailed records, data entry, and material movement transactions.Work collaboratively with coworkers to resolve issues and meet production goals.Follow safety guidelines and comply with environmental and safety policies.What you'll need to be considered:High school diploma or equivalent; 0-1 year experience assembling medical products preferred.Ability to read and follow assembly drawings and written instructions.Strong manual dexterity, attention to detail, and keen vision.Ability to perform detailed work under a microscope for extended periods.Ability to work overtime and adhere to attendance guidelines.Ability to handle chemicals and adhesives safely.Thing that would make you stand out:Strong team player with the ability to communicate effectively with coworkers.Willingness to learn and adapt quickly to new processes.Basic knowledge of FDA regulations, ISO 13485, and ISO 9001 (a plus).Commitment to safety and quality standards.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.If you're looking for a hands-on, detail-oriented role where you can grow in the medical device industry, we encourage you to APPLY TODAY!#LI-BL1