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*Job Type:* Full-Time, Monday – Friday *Pay Range:* $22.00 – $28.00 per hour (DOE) About the Role: Axycut Precision Machining is seeking an experienced CNC Machinist / Precision Operator to run CNC Lathes (DMG Mori / Fanuc-style controls) and/or CNC Mills (Haas / Fanuc-style controls) producing tight-tolerance components for aerospace and commercial precision applications. This is *not an entry-level trainee role*. Candidates must be capable of independent part inspection, tool wear offset adjustments, and interpreting engineering blueprints to maintain tolerances down to +/- .0005" Key Responsibilities: * Set up, operate, and tend CNC turning centers and vertical milling machines. * Load raw materials (aluminum, stainless steels, alloy steels) and cycle parts to production standards. * Monitor tool wear, adjust geometry and wear offsets, and perform routine insert and tool changes. * Conduct first-article and in-process inspections using micrometers (OD/ID, blade, depth), dial bore gages, calipers, and height gages. * Accurately interpret blueprints, including geometric dimensioning and tolerancing (GD&T) callouts. * Maintain complete and accurate traveler documentation and quality inspection logs. * Deburr parts and maintain clean, organized workstations and fluid levels per shop standards. Minimum Requirements * *Minimum 2 years of hands-on CNC machining experience* in a precision metal job shop or production manufacturing environment (aerospace or defense background preferred). * Demonstrated experience operating CNC turning centers (DMG Mori, Fanuc-based) and/or Haas vertical machining centers. * Proven proficiency reading technical drawings and applying standard GD&T symbols. * Demonstrated competency with precision hand measurement tools (0.0001'' reading micrometers, bore gages, calipers). * Practical understanding of tool wear, cutting parameters, and basic G-code navigation. * Reliable, punctual, and able to stand for extended periods in an active machine shop environment. Preferred Qualifications * Proven ability to perform complete independent machine setups (setting work coordinate systems, tool touch-offs, and verifying first-article parts). * Experience machining tough alloys (300/400-series stainless, nickel alloys, Hastelloy, hardened steels). * Experience with shop travelers/ floor tracking. Pay: $22.00 - $28.00 per hour Expected hours: 40.0 per week Application Question(s): * Which CNC controls have you directly operated or set up? * When a bore is running 0.0008'' undersized on a lathe or mill, explain briefly how you identify and adjust the offset to bring it into nominal tolerance. Experience: * paid shop-floor CNC machining: 2 years (Required) Work Location: In person
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: An experienced team member in a manufacturing environment providing quality guidance and support for product launches, sustaining engineering, and quality system activities to assure conformance to established specifications and risk reduction. Works independently to optimize and continuously improve internal operations to meet department, business unit and company objectives. Also provides expertise and guidance to ensure quality systems are in place across the hardware development organization that improves quality of our devices as well as our business operations. The Senior Quality Engineers at Tandem are also responsible for: Serves as a Quality lead on sustaining engineering, production, and quality system activities. Reviews and approves product and process changes/new designs to ensure they are developed, verified, validated and documented in accordance with regulatory requirements. Assures all actions required to optimize the quality, manage the risk, and maintain the compliance of all products, planned and completed, and that the results drive quality and quality system actions. Analyzes and solves quality related problems with products and processes. Provides input to IQ/OQ/PQ development for processes and equipment. Supports the non-conforming material report (NCR) process and lead monitoring and tracking for open NCRs and ensure timely closures. Reviews and approves CO’s as well as provides quality input. Provides quality input to Complaint, First Article, CAPA investigations. Independently completes activities in Risk Analysis, Process Capability Analysis (Cpk),, Design Reviews, Gage R&R, DOEs, V&V Testing, and reliability testing activities. Facilitates or participates in cross-functional or cross-divisional process improvement teams to drive product development quality excellence and cost savings initiatives. Reviews and analyzes project and customer requirements, and assists project teams in tailoring and using company procedures, methods, templates and tools. Collects process metrics and lessons learned, reviews and evaluates processes and work products and recommends improvements as appropriate. Supports and leads, internal and external audits as scheduled to build the quality system and reduce risk. Confirms completion of required training plan before assuming job responsibilities. Ensures work is performed in compliance with company policies including Privacy/HIPAA and other regulatory, legal, and safety requirements. Other responsibilities as assigned. WHEN & WHERE YOU’LL WORK: This role is on-site five days a week at our Barnes Canyon office due to the nature of the work involved. WHAT YOU’LL NEED: Bachelor’s degree in a technical field, preferably Mechanical Engineering or the equivalent education and applicable work experience. 5 plus years experience working as a Quality Engineer in an FDA-regulated hardware development environment, medical device development, or an FDA-regulated industry. Demonstrates proficient knowledge of Quality Engineering policies, principles and best practices. Proficient knowledge of quality standards (ISO 13485, FDA QMSR, ISO 14971). Proficiency with querying, navigating, and analyzing datasets Understands the use of all test and quality measurement equipment. Strong proficiency of statistical techniques including sampling theory, probability, capability analysis, and SPC. Previous experience generating and analyzing quality metrics. Demonstrated experience using problem solving methodologies: why-why analysis, fault tree analysis, cause and effect diagram etc. Ability to work independently to identify potential quality issues and propose solutions. Basic understanding of mechanical drawings & specifications including geometric dimensioning and tolerances (GD&T). Able to recognize non-conformances from accepted and documented practices. Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information. Skilled at promoting team cooperation and a commitment to team success. Adept at seeing change as an opportunity to improve business performance and campaigning for it when necessary. Ability to effectively use MS Office suite (Word, Excel, Outlook) and MiniTab and other applicable software packages. EXTRA AWESOME: Experience in a ISO environment preferred. COMPENSATION & BENEFITS: The starting base pay range for this position is $110K - $121K annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package. YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.
_Filger Manufacturing has been a leader in producing Aerospace, Medical and Space components for over 70 years. We are looking to hire an experienced CNC Machinist to set-up (using Fanuc controls) and produce critical/tight tolerance parts on either our CNC Kia lathe turning center or Hardinge lathe turning centers. Candidate needs to have experience setting up and running single operation lathes. Must be efficient and autonomous at set ups and operation of close tolerance +/- .0002 aerospace parts. Parts will be run complete from first article to end of production run. Job start time is 6:00am and workday is 8+ hours per day with proper meal and rest periods. Opportunity for overtime depending on workload. Our current workload is stacked._ _Responsibilities/daily tasks_ _Duties Include:_ * _Daily production of metal machined components_ * _Select tools and materials for the job_ * _Operate CNC Lathes (Kia and Hardinge)_ * _Verifying 1st Article piece with Foreman_ * _Set up CNC Lathes (Kia and Hardinge) using Fanuc controls_ * _Troubleshoot machinery_ * _Making program changes as needed_ * _Review blueprints for specifications of job_ * _Measure parts using micrometers, calipers, CMM and other measuring equipment_ * _Perform offsets_ * _Inspect parts for accuracy_ * _Meet production goals_ * _Maintain machines and overall shop cleanliness_ * _Completing any other duties assigned by Management_ _Applicant must complete and pass a basic background check prior to employment. Employer will also request references to call and confirm prior employment job title, duties, and length of employment. Applicant must possess the ability to lift 50+lbs. and have the ability to stand at a machine for 10+ hours per day. Applicant must be able to work in a noisy environment. Must be have 5+ years experience setting up and running CNC. Must be efficient and autonomous at set ups and operation of close tolerance +/- .0002 aerospace parts. Must be able to set up a machine quickly and accurately and identify changes that need to be made. Must be able to measure using micrometers , calipers and inspect using an eye loupe. Ability to stay focused and produce high-tolerance, demanding machined components with little to no errors. Must be able to follow work instructions and feel comfortable ask questions if something is unclear. Must be able to work well with others and independently. This is a 40+ hour per week position. Position pays hourly and hourly rate depends on experience. Company offers 401k, profit sharing, and end of the year bonus. Medical and Dental benefits after 60 days. Life Insurance offered after 60 days. We are an equal opportunity employer._ _*We are looking forward to hearing from you and finding another member of our tenured, growing, and skilled team!*_ Job Type: Full-time Pay: $25.00 - $40.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off Experience: * cnc lathe machinist: 3 years (Required) Ability to Commute: * San Clemente, CA 92672 (Required) Work Location: In person
*Job Summary* DeepWater Exploration develops advance vision products for mapping and sensing the seafloor. We are a young team that is quickly growing and to meet production demands, we are seeking a skilled Assembly Technician to join our team. As an Assembly Technician, you’ll build and inspect components and products using technical drawings, production documents, and established work instructions. You will work at our lab in San Diego, collaborating with our engineering team to assemble high-quality vision solutions for customers. *Responsibilities* * Perform mechanical assembly using hand tools, power tools, pneumatic tools, and specialized industrial tools. * Read schematics and instructions; interpret mechanical blueprints, technical drawings, and production documents to guide each task. * Measure and verify parts with calipers, micrometers, and other measuring instruments. * Complete assigned manufacturing tasks, including soldering and machining, as required by the work. * Follow safe work practices, including proper manual handling and personal protective equipment (PPE) use; report quality or safety concerns. *Qualifications* * Demonstrated mechanical knowledge and ability to perform assembly work with common hand and power tools. * Ability to read blueprints, interpret technical drawings and production documents, and apply basic shop math. * Familiarity with calipers, micrometers, and other precision measuring instruments. * Experience with manufacturing, mechanical assembly, soldering, or machining is helpful; requirements may vary by assignment. * Ability to use pneumatic and specialized industrial tools and follow PPE and manual-handling procedures. *Along with your salary, you'll receive perks including:* * Competitive insurance (including a Silver/Gold HMO plan or other options) * 401k matching up to 4% of salary * A pet-friendly office * PTO Please note that we are currently unable to sponsor employment visas, so candidates must be independently authorized to work in the United States. We appreciate diverse perspectives and life experiences, and we're committed to building a team that reflects a wide range of backgrounds. We look forward to reviewing your application! Pay: $24.00 - $30.00 per hour Expected hours: 40.0 per week Benefits: * Health insurance * Paid time off Work Location: In person
SPEED & SPIRIT is what we look for in our candidates, defined by some simple values that inspire us to BE DRIVEN in our performance, BE VIBRANT in our sporting legacy, BE TOGETHER in our team spirit, and BE YOU to let our individual talent and experience shine. Applying for a job at PUMA is easy. Simply click APPLY ONLINE and follow the steps to upload your application. Your mission Club Assembly Provide strategic operational leadership and direction for Manufacturing facilities in North America Responsible for all aspects of Club Assembly operation, including Stock and Custom. Set, track and monitor Club Assembly operation budget. Work closely with Finance to ensure that the monthly budgets are met. Work closely with Sourcing, Program Management and Product Development teams to ensure all assembly process can meet output and quality requirements for the business. Establishes, implements, and reports on metrics for measuring operational performance. Production Planning Manage production planners to ensure Club assembly operations are building appropriate clubs to meet sales needs. Work closely with Warehouse team to ensure proper components are staged for club assembly in a timely manner. Manage Custom Assembly plant to meet KPI to meet “Customer Happy” core value. Custom Club Planning Manages custom orderbook through Custom Club Team to optimize the flow of orders from order intake to assembly Creates, establishes, and maintains business processes for managing the custom business from order taking to product shipment Oversees team who are the liaison between Customer Service, Sales Support Representatives, and the field on Custom Club business Leadership & Team Management This role will focus on the Cobra Golf operation, including Club Assembly, Global Quality and production planning for golf club categories. Implement a culture of “Continuous Improvements”, striving to get better each day. Find process improvement opportunities to drive efficiencies. Leads the Operations team in executing best practices and measuring performance through agreed upon Key Performance Indicators (KPIs). Proactively develop others within the Cobra operation organization through sharing of best demonstrated processes and knowledge transference. Your talent 10+ years materials management/procurement experience with at least 7 years management experience Bachelor’s degree in Supply Chain or an equivalent combination of education and experience Experience and a solid understanding of ERP systems in a manufacturing and distribution environment; advanced capability in balancing procurement, inventory management, and customer satisfaction within the ERP system settings Relationship quality: communication, listening, diplomacy Superior analytical skills with demonstrated expertise in MS Excel Must have excellent problem-solving skills Must be able to work in a fast-paced complex manufacturing environment. Exceptional technical aptitude: ability to quickly learn new systems Strong relationship-building skills Ability to prioritize departmental activities and set effective (SMART) goals and objectives for buyer planners. Golf Industry experiences a strong plus. The hiring range base pay for this position is $135,600 - $187,795 + Bonus + Benefits (Benefit Summary Corporate) Pay may vary depending on job-related knowledge, skills, and experience. Our principles PUMA provides equal opportunities for all job applicants, regardless of race, color, religion, national origin, sex, gender identity or expression, sexual orientation, age, or disability. Equality for all is one of the core principles at PUMA and we do not tolerate any form of harassment or discrimination. At PUMA, every application is reviewed by real people who are committed to fairness, transparency, and equal opportunity - no matter your background, identity, or experience. To ensure our process stays true to these values, no automated systems or AI tools are used to make hiring decisions. Every decision is made by real people -with real judgment and accountability. We may use functions supported by Artificial Intelligence (AI) to carry out isolated organizational steps, such as scheduling interviews. These functions have no influence on decisions in the application process. We believe in creating spaces where everyone is welcome, celebrated, and empowered to contribute authentically. Because at PUMA, whoever wants to play, can play. PUMA is a global sports brand creating footwear, apparel, and accessories that inspire athletes and everyday movers. The PUMA Group owns PUMA, Cobra Golf, and stichd, operates in 120+ countries, and has around 22,000 employees worldwide.
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. This position within the Airframe Project Engineering Team supports MQ-1C Gray Eagle and Mojave STOL production and integration activities. The role will focus on resolving manufacturing and aircraft-integration engineering issues, supporting production operations, and coordinating implementation of engineering changes. This is a multi-faceted position requiring collaboration with a broad range of technical disciplines and stakeholders throughout the project life cycle. The position will interface with multiple engineering disciplines, Manufacturing, Quality, Supply Chain, suppliers, and field service organizations to resolve complex technical issues, improve processes, support aircraft builds, and develop corrective actions. Under general supervision with limited review, this position is responsible for determining and developing effective approaches for resolving a wide range of challenging engineering problems. Assignments are normally outlined in terms of overall objectives and anticipated results. Work is reviewed at milestones or at completion for adequacy in meeting objectives. Documents findings, communicates results to engineering staff, and makes technical presentations as required. May coordinate segments of a specific project and may have frequent inter-organization, supplier, and customer contact on difficult technical issues. Provides direction to design or technical staff and may provide direction to less experienced professional staff. DUTIES AND RESPONSIBILITIES Supports operation of engineering systems by evaluating and interpreting manufacturing, integration, and production needs and problems and develops effective approaches to resolving those issues. Troubleshoots, analyzes, and resolves airframe, aerostructure, mechanical-system, installation, and integration issues in assigned areas by utilizing standard engineering and scientific principles. Works with Manufacturing and Integration to resolve engineering issues and support aircraft builds for MQ-1C Gray Eagle and Mojave STOL platforms. Leads cross-functional issue-resolution efforts with Manufacturing, Quality, Supply Chain, suppliers, and functional engineering groups to resolve complex production and integration issues. Performs and coordinates root-cause analyses and corrective actions to address production and integration issues, improve processes, and prevent recurrence. Coordinates and monitors engineering issue resolution and design-development activities through regular presence in manufacturing shops, aircraft-integration areas, Quality Assurance, Manufacturing Engineering, and functional engineering groups. Supports the planning and coordination of engineering changes, including configuration impacts, cut-in plans, production incorporation, and fielding activities. Coordinates with suppliers, as required, to resolve technical issues affecting airframe components, assemblies, installations, production schedules, or quality. Plans and coordinates the maintenance of engineering solutions, including documentation, issue tracking, reporting, and technical presentations, in accordance with established processes. Delivers technical presentations to assess and communicate the viability of proposed solutions in an evolving environment. Supports engineering estimates and proposals in response to customer and program management direction. Directs the activities of designers, technicians and may direct the activities of less experienced professional staff. May represent the organization in providing solutions to technical issues associated with specific projects. Maintains strict confidentiality of sensitive information. Performs other duties as assigned. Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from an accredited institution and progressive engineering experience as follows; four or more years of experience with a bachelors degree or two or more years of experience with a masters degree. May substitute equivalent engineering experience in lieu of education. Must have a complete understanding of engineering concepts, principles, codes, and theory; experience demonstrating a broad application of those concepts; and expanding knowledge of principles, concepts, theory, and practices in related technical specialties. Must possess the ability to understand new concepts quickly; apply them accurately throughout an evolving environment; organize, schedule, and coordinate work phases; and determine the appropriate approach at the task level or, with assistance, at the project level to provide solutions to a range of complex problems. Must have excellent communication, computer, documentation, presentation, and interpersonal skills, ability to work independently and as part of a team; able to perform complex tasks in one engineering area; and lead a team of less experienced professional employees on semi-routine tasks. Must possess the ability to understand new concepts quickly; apply them accurately throughout an evolving environment; organize, schedule, and coordinate work phases; and determine the appropriate approach at the task level or, with assistance, at the project level to provide solutions to a range of complex problems. Able to work extended hours as required. A Professional Engineering License is desirable. Able to obtain a DoD secret security clearance in required. Job Category Engineering Experience Level Mid-Level (3-7 years) Workstyle Hybrid Full-Time/Part-Time Full-Time Salary Pay Range Low 84,000 Pay Range High 140,625 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About this role: The Quality technician will review device history records and approve final release documentation. This role will also complete appropriate quality records within company GMP (Good Manufacturing Process) and GDP (Good Documentation Practice) guidelines, policies and procedures. The Quality Technician performs inspection, in-process inspections, and final inspections, review of device history records of manufacturing/batch records per control/quality plans The Quality Technician will keep track of Non-Conformance material and documentation, place or remove required label of the product/materials involved in the non-conformance. Open Shifts 1st Shift - 6:00am-2:30pm 2nd Shift - 2:30pm-11:00pm Work Mode At Boston Scientific, we value collaboration and synergy. This role follows a onsite work model, requiring employees to be in our local office five days per week. Relocation Relocation assistance is not available for this position at this time. VISA Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time. Your responsibilities will include: Knowledge handling and reviewing device history records is a key responsibility in this position. Review incoming or production documentation for conformance that may include engineering drawings, schematics, and specifications; process standards and specifications; and production or process plans (IPC-A-610 certification is recommended). Knowledge handling Non-conformance documentation for manufacturing batch records and identifying GDP (Good Documentation Procedures) errors. Accept or reject device history records or first article inspection; identify and document non-conformance and notify appropriate personnel of potential rejection/correction of items. Refer/document unusual inspection problems to supervision, lead or Project Quality Engineer. Knowledge using a variety of measuring tools including electrical test sets, multimeter, fixed, limit, plug-gages, steel rules, scales, micrometers, calipers, and surface plate. Assist in the writing and updating of inspection procedures, protocol, and checklists. Transferring, releasing or quarantining material physically according to inspection status Documenting and maintaining inspection and test records Understand the importance of product conformity. Understand lot numbers and traceability. Understand ISO 13485 quality assurance standards and the related documentation in support of. Maintains safe and clean work environment by keeping shelves, workstations, etc. neat and complying with procedures, rules and regulations. Complete respective paperwork/documentation. Required Qualifications: Education: Minimum of High School Diploma or AA degree in a scientific discipline and two years or more working experience in a relevant, cGMP/FDA regulated industry. Require Experience: Be able to identify GDP errors Be able to apply and remove material labels. Be able to read and understand mechanical drawings and dimensions Be able to read and interpret drawing notes and able to understand configuration management (revision control) Be able to use basic measuring tools such as calipers, go-no/go gauges, torque wrenches, and others as necessary Experience with electrical test sets, multimeter, vision measuring system is a plus Experience working with an ERP system and data entry Experience with Outlook and MS Office. Good communication and organizational skills. Must possess good math fundamentals, comprehend written work instructions, and communicate well. Knowledge, Skills, and Abilities: Knowledge of medical device records use within manufacturing Working understanding of GDP and GMP Excellent documentation skills, attention to detail and accuracy Team player, flexible multitask, good written/oral communicator Must be organized and able to coordinate activities with internal departments and outside vendors Experience assisting regulatory inspections and/or audit Other Duties/Standards: The above descriptions are intended to describe the general nature and level of work being performed. This job description is not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. Boston Scientific utilizes the multi-skill concept and expects the employee to perform other job disciplines. Boston Scientific retains the discretion to add or change the functions and duties of the position at any time. Requisition ID: 636866 Minimum Salary: $ 39416 Maximum Salary: $ 66976 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Manufacturing Technician II – Monday – Friday, 1st Shift Where you come in: Perform product builds, equipment setups, changeovers, and shutdowns Execute defined manufacturing processes and approved equipment operations Support build readiness reviews to ensure materials, tooling, equipment, and documentation are in place Participate in pilot manufacturing builds, including development and refinement of new processes Set up, operate, and maintain manufacturing equipment Troubleshoot equipment and process issues to determine root cause and corrective actions Execute approved equipment or tooling changes and communicate updates across the team Analyze process and production data and monitor live performance indicators (KPIs) Support continuous improvement initiatives and evolving processes Read and interpret LHRs, MPIs, and engineering study instructions Document troubleshooting actions, observations, and build issues Collaborate cross-functionally with Engineering, Quality, and Equipment teams Assist with equipment qualifications (IQs, OQs, PQs) Perform other duties as assigned What makes you successful: Ability to interpret engineering study protocols Advanced manufacturing or pilot build experience Strong problem-solving and root cause analysis skills Ability to work independently in a production environment Effective cross-functional collaboration skills What you’ll get: A front row seat to life-changing CGM technology Comprehensive benefits program Global growth and career development opportunities Innovative, industry-leading work environment Typically 4+ years of related manufacturing experience · Pilot or R&D manufacturing experience preferred Travel Required: 0% Experience and Education Requirements: • Typically requires a minimum of 2-4 years of related experience and a High School diploma/certificate or equivalent. Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at [email protected]. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at [email protected]. Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications. AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people. Salary: $23.70 - $35.52 #DexcomUS
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. We have an exciting opportunity for a CNC Machinist to join our Inertial Fusion Technology (IFT) division within the Energy group. This position is located in San Diego (Torrey Pines), CA. The components to be machined are normally high-precision, small quantities, and typically millimeter in scale with micro-size features and tolerances. Production schedules are reasonable but due dates are often inflexible. Salary potential commensurate with willingness/ability to grow professionally. DUTIES AND RESPONSIBILITIES: Set-up and operate micro CNC shop equipment such as lathes, mills, and saws. Being able to follow all safety procedures in working and machining in a laboratory that works with beryllium components. NC programming in both manual (i.e., plain G-code and parametric G-code) and CAD/CAM (Creo). Inspect parts using mics, calipers, digital height gages, measuring microscope, indicators, gage blocks, surface plates, etc. as required. Inspect parts using high level inspection tools such as CT and white light optical profilers. Record and document machining data, including both in‑process and final inspection results, in the database or designated Excel templates, and archive them on the server. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Performs other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires high school diploma or equivalent. Must possess: Proficiency with common manual shop equipment such as lathes, mills, and saws. Some experience setting-up and operating NC mills and lathes. Some experience with NC programming (both G-code and CAD/CAM). Proficiency with common manual inspection tools such as micrometers, calipers, digital height gages, indicators, gage blocks, surface plates. Knowledge of computer operations and applications pertinent to the field required. Customer focus. Ability to use good judgment and safe practices in a shop environment. Time management skills to maintain the flow of work within the unit. Good interpersonal skills and written communication skills to interface with employees and supervisor; and basic computer skills. Ability to work in a large lab research environment requiring long periods of standing, walking, bending and lifting up to 50 lbs. Ability to work both independently and in a team environment. Ability to handle parts under 10 mm in size Flexibility to work extended hours as required. Must be willing to work with hazardous and radioactive materials Must have the ability to obtain and maintain a DoE Q Level Security clearance. Job Category Manufacturing Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 39,000 Pay Range High 58,125 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level DOE - Q Search Jobs at | General Atomics and Affiliated Companies
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: An experienced senior team member in a sustaining, manufacturing environment with ample knowledge and experience in sterilization, bacterial endotoxin testing, and cleanroom activities providing quality guidance and support for product launch, sustaining engineering, and quality system activities to ensure conformance to established specifications and risk reduction. Works independently to optimize and continuously improve internal operations to meet department, business unit and company objectives. Also provides expertise and guidance to ensure quality systems are in place across the hardware development organization that improves patient safety, product quality and business operations. The Senior Quality Engineers at Tandem are also responsible for: · Serves as a Quality lead on sustaining engineering, production, and quality system activities. · Reviews and approves product and process changes/new designs to ensure they are developed, verified, validated and documented in accordance with regulatory requirements. · Assures all actions required to optimize the quality, manage the risk, and maintain the compliance of all products, planned and completed, and that the results drive quality and quality system actions. · Analyzes and solves quality related problems with products and processes. May · Provides input to IQ/OQ/PQ development for processes and equipment. · Manufacturing and/or test fixture qualification (requirements, protocols, execution, test report) · Support the non-conforming material report (NCR) process and lead monitoring and tracking for open NCRs and ensure timely closures. · Lead and support sterilization validation activities, including dose establishment, dose audits, requalification, and routine monitoring in compliance with ISO 11137, ISO 13485, FDA QMSR, and applicable regulatory requirements. · Evaluate bioburden and sterility assurance data, investigate sterilization-related nonconformances, assess the impact of manufacturing or design changes on validated sterilization processes, and ensure continued state of control through data trending, risk assessment, and supplier oversight. · Review and approves COs as well as provides quality input. · Lead and support cleanroom environmental control programs to ensure compliance with ISO 14644, applicable regulatory requirements, and internal quality standards. · Monitor and trend environmental monitoring data, including viable and non-viable particulate results, investigate excursions and out-of-specification conditions, assess the impact of manufacturing changes on cleanroom performance, and drive corrective and preventive actions to maintain a validated state of control. · Review and approve environmental monitoring protocols, reports, and cleanroom qualification documentation. · Support cleanroom design, validation, requalification, and contamination control strategy activities. · Conduct investigations and root cause analyses for environmental monitoring excursions, contamination events, and adverse trends. · Collaborate with Manufacturing, Facilities, Microbiology, Validation, and Regulatory Affairs to ensure ongoing cleanroom effectiveness. · Evaluate gowning, cleaning, disinfection, and personnel monitoring programs for compliance and effectiveness. · Support risk assessments and change control activities affecting controlled manufacturing environments. · Provides quality input to Complaint, FA, CAPA investigations Independently completes such activities in Risk Analysis, Process Capability Analysis (Cpk), DFM, Design Reviews, Gage R&R, DOEs, V&V Testing, and reliability testing activities. · Facilitates or participates in cross-functional or cross-divisional process improvement teams to drive product development quality excellence and cost savings initiatives. · Reviews and analyzes project and customer requirements and assists project teams in tailoring and using company procedures, methods, templates and tools. · Collects process metrics and lessons learned, reviews and evaluates processes and work products and recommends improvements as appropriate. · Supports and leads, internal and external audits as scheduled to build the quality system and reduce risk. · Confirms completion of required training plan before assuming job responsibilities. · Ensures work is performed in compliance with company policies including Privacy/HIPAA and other regulatory, legal, and safety requirements. · Other responsibilities as assigned. WHEN & WHERE YOU’LL WORK: This role is on-site five days a week at our Barnes Canyon office due to the nature of the work involved. WHAT YOU’LL NEED: · Bachelor’s degree in a technical field, preferably Mechanical Engineering or the equivalent education and applicable work experience. · 5 plus years’ experience working as a Quality Engineer in an FDA-regulated hardware development environment, medical device development, or an FDA-regulated industry. · Demonstrates proficient knowledge of Quality Engineering policies, principles and best practices. · Proficient knowledge of quality standards (ISO 13485, FDA QMSR, ISO 14971). · Proficient knowledge and experience with sterilization, bacterial endotoxin testing, and cleanroom standards (ISO 11137-1, ISO 11137-2, ISO 11737-1, ISO 11737-2, ISO 11737-3, AAMI ST72, ISO 14644-1) · Understands the use of all test and quality measurement equipment. · Strong proficiency of statistical techniques including sampling theory, probability, capability analysis, and SPC. · Previous experience generating and analyzing quality metrics. · Demonstrated experience using problem solving methodologies: why-why analysis, fault tree analysis, cause and effect diagram etc. · Ability to work independently to identify potential quality issues and propose solutions. · Basic understanding of mechanical drawings & specifications including geometric dimensioning and tolerances (GD&T). · Able to recognize non-conformances from accepted and documented practices. · Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information. · Skilled at promoting team cooperation and a commitment to team success. · Adept at seeing change as an opportunity to improve business performance and campaigning for it when necessary. · Ability to effectively use MS Office suite (Word, Excel, Outlook) and MiniTab and other applicable software packages. EXTRA AWESOME: · Experience in a ISO environment preferred. COMPENSATION & BENEFITS: The starting base pay range for this position is $110K - $121K annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package. YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow. #LI-Remote #LI-KL1
*Job Summary:* We are seeking a skilled and dedicated *Fire Sprinkler Technician* to join our team. This is a *Permanent position*, offering opportunities for *on-the-job training, education, and long-term career growth* in the fire protection industry. The ideal candidate will assist with the *installation, maintenance, and repair* of fire sprinkler systems in both commercial and residential settings. This role requires strong mechanical aptitude, attention to detail, and the ability to work safely on active construction sites. *Responsibilities:* * Assemble and install fire sprinkler systems in accordance with specifications, building codes, and safety regulations * Perform pipe threading, tube bending, and layout of fire protection piping * Operate power tools and equipment safely and efficiently * Conduct inspections and perform maintenance on fire sprinkler systems * Troubleshoot and repair system issues as needed * Coordinate with other construction team members to ensure timely project completion * Maintain accurate documentation of work performed *Qualifications:* * Mechanical knowledge with experience in plumbing, pipefitting, or fire protection systems preferred * Familiarity with pipeline construction techniques; welding experience is a plus * Ability to read and interpret blueprints and technical drawings * Strong problem-solving skills and attention to detail * Comfortable working in various environments, including active construction sites * Effective communication and teamwork skills * *Must have reliable transportation* * *Must be willing to learn, grow, and develop within the company* * *Must be willing to work overtime when needed, especially during busy periods* * Certification in fire protection systems is a plus but not required *Why Join Us?* * Hands-on *training and educational support* * Be part of a growing team contributing to life-saving fire protection work * Competitive pay and potential for increased hours during peak workloads Pay: $18.00 - $23.00 per hour Expected hours: 40.0 per week Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Education: * High school or equivalent (Required) Experience: * Pipefitter: 1 year (Required) Language: * English (Required) * Spanish (Preferred) License/Certification: * Cal-Fire Fitter Card (Preferred) Security clearance: * Confidential (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Ability to Commute: * Temecula, CA 92590 (Preferred) Willingness to travel: * 100% (Required) Work Location: In person
*Job Summary:* We are seeking a skilled and dedicated *Fire Sprinkler Fitter (Journeyman Level)* to join our growing team. This is a *permanent position* offering hands-on training, continued education, and long-term career growth within the fire protection industry. The ideal candidate will assist in the *installation, maintenance, and repair* of fire sprinkler systems in *commercial and residential* environments. This position requires mechanical aptitude, a strong work ethic, attention to detail, and a commitment to working safely on active job sites. *Responsibilities:* * Assemble and install fire sprinkler systems in compliance with specifications, NFPA codes, and local building regulations * Perform pipe threading, tube bending, and layout of fire protection piping systems * Safely operate power tools and construction equipment * Conduct routine inspections and preventive maintenance on fire sprinkler systems * Diagnose and repair issues within existing fire protection systems * Work closely with general contractors, supervisors, and other trades on-site * Maintain accurate jobsite documentation and material tracking * Adhere to safety protocols and company standards at all times *Qualifications:* * Journeyman-level experience in fire sprinkler fitting or similar trade (plumbing, pipefitting, etc.) * *Valid CAL FIRE Fitter Certification (Required)* * Experience with pipeline construction methods * Ability to read and interpret blueprints, technical drawings, and schematics * Strong mechanical and troubleshooting skills * Reliable transportation to job sites * Willingness to work overtime as required, particularly during peak project periods * Must be adaptable to varying work conditions, including indoor and outdoor environments * Strong communication skills and ability to work as part of a team * Commitment to learning, development, and contributing to a safety-first culture *Why Join Us?* * Permanent full-time position with advancement opportunities * Industry-specific training and continuing education support * Not your average fire sprinkler company. * Be part of a mission-driven team that plays a crucial role in life safety and code compliance *To Apply:* Please submit your resume to [email protected] Pay: $27.00 - $32.00 per hour Expected hours: 40.0 per week Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Education: * High school or equivalent (Required) Experience: * Pipefitter: 3 years (Required) Language: * English (Preferred) * Spanish (Preferred) License/Certification: * Cal-Fire Fitter Card (Required) Security clearance: * Confidential (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Ability to Commute: * Temecula, CA 92590 (Preferred) Willingness to travel: * 100% (Preferred) Work Location: In person