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Full Time
3/25/2025
Boston, MA 02298
(9.1 miles)
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.
Full Time
4/1/2025
Bellingham, MA 02019
(40.3 miles)
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
Full Time
4/1/2025
Nashua, NH 03064
(35.4 miles)
Our Production Team is Kind of a Big Deal! UniFirst is seeking a reliable and hardworking Production Team Partner to join our UniFirst Family. As a Team Partner in the Pre-Tunnel Inspection Department, you will be working on a team to help ensure quality assurance for our customers by inspecting garments as you process them through our steam tunnel. At UniFirst we have a 5-day work week, enjoy Saturday and Sunday off!! We have an immediate opening and provide on the job training. Pay & Benefits: On the job training & great hourly pay + 401K with Company Match, Profit Sharing, Health Insurance, Employee Assistance Program, Life Insurance, Paid Time Off, Direct Payroll Deposit, Tuition Reimbursement, 30% Employee Discount, Employee Referral Bonuses. What’s in it for you Training: Our Team Partners receive ongoing cross-training, exposing them to different areas of production. Cross training enhances their performance and assists them with their career potential and advancement. Work Life Balance: We offer a 40-hour work week. Enjoy weekends off! Career Growth: Some companies like to promote from within, we love to! Many of our managers started at UniFirst working on the production floor! Culture: Our family culture is what makes UniFirst an organization that stands out from the rest. Diversity: At UniFirst, you'll find an environment packed with different cultures, personalities, and backgrounds. We believe our diversity makes us who we are, and we strive every day to build a culture where everyone feels welcome. What you’ll be doing: Count garmentsHang garments to be processed through the steam tunnelVisually inspect all garments for tears, holes, stains, and damageEnsure all garments pass the UniFirst 20-point uniform inspection processFollow all safety policies, HACCP and medical guidelines. *Perform other duties as described by area supervisor or management QualificationsWhat we’re looking for: High school education and/or GED equivalent preferredMust be at least 18 years of age or older.Ability to stand for 8-hour shiftAbility to read, write, and communicate clearly with managementAbility to perform basic mathematical functions using American standard units in weight, measurement, volume, and distanceAbility to lift up to 10 lbs. and push up to 25 lbs. About UniFirst The fabric of UniFirst is woven from its very unique family culture where our Team Partners enjoy a small company feel while taking advantage of the resources and stability that come with being a 2-billion-dollar organization. UniFirst is an international leader in the $18 billion-dollar garment services industry. We currently employ over 14,000 team partners who serve 300,000 business customer locations throughout the U.S., Canada, and Europe. We were included in the top 10 of Selling Power magazine’s “Best Companies to Sell For” list and recognized on Forbes magazine’s “Platinum 400 – Best Big Companies” list. As an 80-year old company focused on annual growth, there’s never been a better time to join our team. UniFirst is an equal opportunity employer. We do not discriminate in hiring or employment against any individual on the basis of race, color, gender, national origin, ancestry, religion, physical or mental disability, age, veteran status, sexual orientation, gender identity or expression, marital status, pregnancy, citizenship, or any other factor protected by anti-discrimination laws.
Full Time
4/1/2025
Medway, MA 02053
(34.6 miles)
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.
Full Time
4/1/2025
Boston, MA 02298
(9.1 miles)
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
Full Time
4/1/2025
Boston, MA 02298
(9.1 miles)
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.
Full Time
3/25/2025
Burlington, MA 01805
(28.2 miles)
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
Full Time
3/25/2025
Waltham, MA 02254
(28.2 miles)
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.
Full Time
4/1/2025
Bellingham, MA 02019
(40.3 miles)
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
Full Time
4/1/2025
Bellingham, MA 02019
(40.3 miles)
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
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