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Summary of Essential Duties and Responsibilities Provides technical engineering support to new and existing product development and sustaining engineering teams. Applies knowledge of manufacturing principles and quality engineering techniques to development efforts as a member of one or more cross-functional development team(s). Develops and implements procedures and processes to ensure products are developed and tested in accordance with applicable industry standards, regulatory requirements, and customer requirements. Provides quality engineering support for regulatory submissions. Duties / Responsibilities Follows the procedures and instructions in the REVA Medical Quality System in the execution of all relevant tasks and responsibilities. Develop and implement quality test procedures, including the design of tests, testing mechanisms and test equipment. Develop and execute test equipment IQ/OQ/PQ protocols and reports. Conduct test method qualifications and validations. Develop gauge reliability and repeatability studies for test and production-related equipment. Develop equipment calibration procedures. Develop sampling plans for incoming materials and in-process and finished product testing based on appropriate statistical methods. Responsible for product-related investigations and corrective actions. Maintain a working relationship with suppliers to ensure resolution of supplier-critical issues and investigations. This may include supplier visits to technically assist in the resolution of issues and investigations. Ensure that all corrective/preventive measures meet acceptable reliability standards, and that documentation is compliant with requirements. Participate in customer product complaint analyses, evaluation and investigation. Perform investigational activities including evaluation of returned products and complaint trending analysis. In conjunction with product development, participates in the updating, maintaining, and approving of risk analysis/risk management documentation in accordance with ISO14971 Reviews production data and performs statistical analysis to track metrics and to analyze trends. As part of the quality organization, reviews and approves assigned controlled documents (e.g. work instructions, quality specifications, engineering specifications, procedures and validations protocols/reports). Assist in "troubleshooting" problems related to the manufacture, test, validation and documentation. Also represents quality assurance function in project team meetings. Participates in internal/supplier audits and interacts with external regulatory inspectors as subject matter expert. Provides quality engineering support to support regulatory submissions and requests from external regulatory bodies Participates in and manages special projects and other duties as assigned. Education and/or Experience At minimum, bachelor's degree in technical discipline, preferably engineering or science. MS or advanced degree desirable. A minimum of 4 plus years' experience in Medical Device or Pharmaceutical Quality Engineering, a master's degree in a scientific discipline with at least 2 years' experience in Medical Device or Pharmaceutical Quality Assurance/Engineering or a Doctorate in a scientific discipline directly relevant to Quality Assurance or Quality Engineering. Demonstrated ability to work independently and produce professional work products. Strong written and verbal communication skills Experience participating on project teams. Experience in related areas, including R&D or manufacturing, may also be applicable if experience includes work responsibilities listed above. Strong work ethic and demonstrated ability to deliver assignments on time. Experience implementing an eQMS is highly desired. Experience working with Drug/Device Combination devices is highly desired. Experience working with and/or validating analytical equipment for polymer manufacturing, such as HPLC, GPC, and GCMS is highly desired. Required Knowledge/Skills Knowledge of global combination drug/device product regulations including The Food Drug and Cosmetic Act (FD&C), Good Manufacturing Practices (GMP's), EUMDR, and ISO13485. Quality system regulations, Device classification, medical device submission and registration requirements, labeling and advertising requirements and restrictions, MDR reporting, recall procedures, and FDA and International regulations related to assigned duties. Thorough familiarity and ability to work with office automation programs and corporate database tools. Communicates effectively, both orally and in writing. Demonstrates excellent interpersonal skills with personnel at all levels and exhibits a high degree of initiative and motivation. Physical Demands/Working Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to sit or stand for prolonged periods of time, frequently in front of a computer. Must be able to travel occasionally.
*Position: Package Assembler* *Location:- San Diego, CA (Onsite Role)* *Contract Position* Assists with the packaging operations. Runs the packaging machines, loads items into containers. May weigh and label containers. May perform quality checks for defective items. Keeps records of materials and shipments. Shift - 12:00 pm - 8:30 PM PST Pay: $18.00 - $20.00 per hour Work Location: In person
Production Brewer, San Diego Job Description Production Brewer Last Updated: 05/21/2026 Notice to California Residents: Please review the California Employee and Applicant Privacy Policy prior to submitting your application At Athletic Brewing, we are on a mission to revolutionize the beer industry and we are doing it with a team of doers. We move quickly, we hold a high bar, and we reward performance. We are a company of hard workers and dedicated professionals who take ownership, drive results, and want their impact to be visible. We believe in merit, accountability, and earning opportunities through contribution. High performers grow here. If you are motivated by building, improving, and winning as a team, you will thrive at Athletic. Through our products and our people, we believe we can positively impact health, activity, and opportunity in our communities. We actively seek representation from diverse backgrounds and experiences and are committed to building a team that reflects the communities we serve. About the Role The Brewing team reflects Athletic Brewing’s commitment to quality through meticulous brewing processes, strict sanitation standards, and continuous product verification to ensure every beer meets the highest standards. The position also allows for significant innovation, as team members contribute to a pioneering and rapidly growing segment of the craft beverage industry focused on award-winning non-alcoholic beer. To be a member of this team is to be collaborative, creative, self motivated and have a high attention to detail to ensure our beer is best - always. The Brewing team is at the heart of Athletic Brewing's commitment to quality. This is a hands-on, process-driven role where you will execute world class brewing procedures, uphold the highest sanitation standards, and perform continuous product verification to ensure every beer we produce meets the highest bar — always. Brewing team members are major contributors to an innovative and rapidly growing segment of the craft beverage industry focused on award-winning non-alcoholic beer. This role is deeply connected to the broader Athletic community — from the teammates you collaborate with on the floor to the fans who trust what's in every can. Job Responsibilities: Reports to the Brewing Supervisor. Participate in basic brewing operations including receiving/ storing/ handling raw materials including but not limited to hops, grain, adjuncts, and processing aids. Participate in all aspects of wort production including but not limited to: Preparing ingredients, milling, weighing, mashing, boiling, transfer, aeration, monitoring and recording in written and digital format. Participate with all cellar activity including but not limited to: Monitoring and recording, filtration media changes, filtration using a centrifuge, transfers, tank additions, cleaning and sanitation. Participate in quality assurance by doing carbon dioxide and oxygen measurements, CIP verification, pH and gravity readings as well as in-process and finished-product sensory verification Professional and meticulous use of all chemicals in the brewery. Participate in yeast sample collection, harvest and pitching. Participate in flash pasteurization. Responsible for product blending. Maintain a clean and safe working environment and work with supporting departments to address deficiencies. Abide by all safety and good manufacturing practices to maintain a sanitary, food safe and audit-ready environment included but not limited to: Meticulous record keeping, cleaning and sanitation, participation in cross-departmental floor walks, as well as any additional duties as mandated by production and quality May assume Assistant Brewer responsibilities when needed. Maintain confidentiality of Athletic brewing process. Process is not to be discussed or repeated unless on a need to know basis. Other duties, responsibilities, and activities may change or be assigned at any time with or without notice. Desired Experience/ Traits Who You Are: Personal curiosity in learning and developing new skills. Strong time management skills with a proven ability to meet deadlines. Strong organizational skills, attention to detail, listening, critical thinking, verbal and written communication skills. Honest, dependable, high integrity, team player, and passionate. Skills and Experience: High School Diploma or GED required. Experience in cellaring and brewing production. Strong technical understanding of the brewing process and sanitation. Experience with brewery maintenance and upkeep. Experience with troubleshooting and root cause analysis. Experience operating both manual and automated brewing equipment. Experience with operating a centrifuge filtration system. Experience with sanitation and cleaning systems. Experience with documentation, manual and electronic. Strong communication skills to work interdepartmentally. Job Details: Location: San Diego, CA Salary: Commensurate with experience - Starting rate: $27.50 Benefits: Company Paid health, vision, dental, life, 401k with 5% company match, and Paid Parental Leave Community Program: In addition to Paid Time Off, all team members receive one paid day per month to dedicate to volunteering activities. We value internal mobility and team equity. We are an equal opportunity employer – we thrive when we champion diversity and inclusion. We are welcoming, respectful, and supportive at work and in our community. We encourage and welcome members of traditionally underrepresented communities to apply. Physical Demands The physical demands described here represent those that must be met by an employee to successfully perform the essential functions of this job. Regularly required to stand, walk, climb, balance, stoop, kneel, crouch, and crawl. Frequent use of hands to handle, feel, and operate equipment and tools. Regularly lift, move, and/or carry up to 50 pounds without assistance; occasional lifts up to 85 pounds may be required. Ability to work on feet for extended periods, often for the duration of a shift. Work in a production environment with varying temperatures, noise levels, and exposure to wet or slippery surfaces. May be required to climb ladders, work at heights, and navigate tight or confined spaces. Specific vision abilities include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus. Ability to wear and use required personal protective equipment (PPE) as determined by the hazard assessment, including eye and face protection, protective footwear, hearing protection, and hand protection, for the duration of the shift, as applicable. Ability to recognize and respond to instructions and alert signals in the work environment.
***CANDIDATES MUST APPLY AT WWW.LWWD.ORG/EMPLOYMENT-APPLICATION*** *SALARY:* $34.48 - $43.10 hourly *JOB TYPE:* Full Time Position *LOCATION:* 1960 La Costa Avenue, Carlsbad, California *OPENING DATE: *July 13, 2026 *CLOSING DATE:* *August 14, 2026 by 4:30 p.m.* *APPLICATION DEADLINE: *Any applications received after August 14, 2026 will only be considered if the position is not filled. *THE ORGANIZATION:* Leucadia Wastewater District is an independent special district, located in Carlsbad, California that provides wastewater collection services to the Leucadia and Village Park areas of Encinitas and the La Costa area of Carlsbad. Our mission is to serve the public by collecting, transporting, recycling and treating wastewater in a safe, reliable, efficient, cost effective and environmentally responsible manner, while providing excellent service to our customers. The District offers an excellent benefit package and employees work a 9/80 work schedule. *BRIEF JOB DESCRIPTION:* Under close supervision, the Field Services Technician-in-training performs a wide variety of manual labor tasks associated with the maintenance and repair of wastewater collection and treatment facilities, including pumping stations, sewer lines, other sanitary sewer collection system structures and water reclamation plant facilities. Candidates must be willing and able to work any shift; work holidays, weekends and emergency overtime as needed. _Essential duties and responsibilities include, but are not limited to:_ * Assists in the maintenance, repair and cleaning of sewer lines utilizing power operated equipment. * Cleans precipitates such as grit, sludge, grease, and other debris from pump station wet wells, manholes and other sanitary sewer collection system structures. * Lubricates equipment such as pumps, motors and valves. Assists with pump and motor overhauls. * Properly and safely operates light-weight equipment and light-to medium-weight vehicles. Uses hand and power tools and equipment to perform maintenance and repair tasks. * Performs building and grounds maintenance at District facilities. _Required Certificates and Licenses_ * Must possess a valid California Class 'C' driver’s license and be able to obtain a valid California Class ‘B’ driver’s license (with tanker and air brake endorsements) within one (1) year of hire. * Must be able to obtain a California Water Environment Association collection system operator certification within six (6) months of hire and water treatment operator (T1) certification within one (1) year of hire. _*For the full job description, please visit our website’s job descriptions page: https://www.lwwd.org/departments/human-resources/job-descriptions*_ *APPLICATION PROCEDURE:* To be considered, please complete LWD’s application, and provide a current resume. Applications may also be picked up at 1960 La Costa Avenue, Carlsbad, CA 92009, Monday through Friday between 8:00 a.m. and 4:30 p.m. Please submit the application and resume online, or via email to [email protected], or at our office by *August 14, 2026 by 4:30 p.m.* *DISTRICT OFFICE LOCATION:* 1960 La Costa Avenue Carlsbad, CA 92009 760-753-0155 Attention: Trisha Hill, Administrative Services Supervisor Job Type: Full-time Pay: $34.48 - $43.10 per hour Benefits: * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid time off * Retirement plan * Tuition reimbursement * Vision insurance Work Location: In person
*This position is very dynamic. If you aren't completely sure you are qualified, but are still interested, I encourage you to still apply*. *Those with CNC/Machining/Manufacturing experience is a huge plus.* This position is somewhat unique. I don't generally run a 9-5; I'm a growing small business looking to hire someone detail-oriented and comfortable taking on different responsibilities as production needs change. I'm willing to work with full time, part time, or custom schedules as I'm pretty flexible. Mechanical inclination strongly preferred, but not required. *I value people who enjoy creating and working on their own projects. When applying and if you're comfortable, please tell me about any personal projects, hobbies, or hands-on interests you pursue outside of work. Domain or genre doesn't matter, creativity and industriousness is something I value!* *Job Title:* Production, Logistics, and Operations Associate *Job Summary:* I am seeking a versatile, hands-on Production & Operations team member to support the daily activities of a growing small manufacturing company. This is a multi-role position involving product manufacturing, 3D printing, assembly, finishing, inventory management, order fulfillment, equipment maintenance, and general business operations. The ideal candidate is dependable, detail-oriented, mechanically inclined, and comfortable taking on different responsibilities as production needs change. This role is well suited for someone who enjoys making physical products, solving practical problems, and helping improve the systems behind a growing manufacturing operation. *Responsibilities:* * Operate and monitor 3D printers and other small-scale manufacturing equipment. * Prepare machines, materials, and digital files for production. * Remove, clean, inspect, and post-process manufactured parts. * Perform product assembly, sanding, fitting, painting, finishing, and packaging as needed. * Inspect finished products for dimensional accuracy, appearance, function, and overall quality. * Identify production defects and assist with troubleshooting equipment, materials, or manufacturing processes. * Maintain organized production, inventory, storage, and work areas. * Track raw materials, components, work-in-progress, and finished inventory. * Package and prepare customer orders for shipment. * Assist with shipping, receiving, purchasing, and supplier coordination. * Document production procedures and help develop repeatable manufacturing processes. * Support prototype development, product testing, and design improvements. * Perform basic equipment maintenance and keep machinery clean and operational. * Help manage production schedules and prioritize orders based on deadlines. * Assist with product listings, customer inquiries, and other administrative tasks when needed. * Take on additional responsibilities as the company grows and new products or equipment are introduced. *Qualifications:* * Bachelor's degree in Business, Engineering or related field/something similar (Preferred, but **not required**). * Experience with 3D printing, manufacturing, fabrication, automotive parts, model making, or a related hands-on field. (Strongly Preferred) * Familiarity with basic hand tools, power tools, measuring tools, and shop equipment. (Preferred) * Strong attention to detail and commitment to producing high-quality work. * Ability to troubleshoot problems and work independently. * Comfortable learning new machines, software, materials, and production techniques. * Good organizational and time-management skills. * Basic computer skills and familiarity with digital files and order-management systems. * CAD, painting, finishing, electronics, mechanical, or equipment-maintenance experience. (Preferred) * CNC/Machining experience ( Preferred) * Ability to be creative (Strongly Preferred) * Manufacturing experience/interest (Strongly Preferred) * Excellent communication, critical thinking, and interpersonal skills. * Comfort in a varied work environment. *Benefits:* * Extremely flexible schedule. * Business development bonuses. * Professional development and training opportunities. * Extremely laid-back, flexible, and supportive work environment. * Strong Employee retention incentives. *What We Value* * Craftsmanship and attention to detail * Willingness to learn * Practical problem-solving * Organization and efficiency * Flexibility in a multi-role environment * Genuine interest in manufacturing and product development * Integrity and communication Job Types: Full-time, Part-time Pay: $25.00 - $30.00 per hour Work Location: In person
Position Summary The Quality Systems Engineer is the primary owner and administrator of the XLR8 EMS Quality Management System (QMS). This role is responsible for maintaining, monitoring, and continuously improving the company's quality system to ensure compliance with ISO 13485, AS9100, ISO 9001, ITAR, customer requirements, and applicable regulatory standards. The position is focused exclusively on quality system management, compliance, audits, document control, CAPA administration, training compliance, and certification maintenance, and does not have responsibility for manufacturing process quality, supplier quality, inspection activities, or product quality engineering. Key Responsibilities Maintain compliance with ISO 13485, AS9100, ISO 9001, ITAR, and customer-specific requirements. Develop, revise, review, and control quality system procedures, policies, forms, and records. Manage document control processes, revision control, approvals, distribution, and record retention. Develop and execute the internal audit program and conduct system and compliance audits. Coordinate registrar, customer, and regulatory audits and ensure audit readiness. Administer the Corrective and Preventive Action (CAPA) system, including tracking, closure, and effectiveness verification. Support Management Review activities and prepare quality system performance metrics and reports. Maintain employee training matrices, competency records, and quality system training compliance. Monitor and implement changes related to quality standards, regulatory requirements, and customer requirements. Administer and maintain electronic quality management systems (eQMS) and related quality databases. Drive continual improvement of quality system processes and overall compliance effectiveness. Required Qualifications Bachelor's degree in Engineering, Quality, Regulatory Affairs, Industrial Technology, or related field. 3–7 years of experience in Quality Systems, Quality Assurance, or Compliance within a regulated manufacturing environment. Working knowledge of ISO 13485, AS9100, ISO 9001, and ITAR requirements. Experience planning, conducting, and managing internal and external audits. Strong understanding of document control, CAPA systems, training management, and quality records management. Excellent organizational, communication, and project management skills. Preferred Qualifications ASQ Certified Quality Auditor (CQA) or similar certification. AS9100 and/or ISO 13485 Lead Auditor certification. Experience in Electronics Manufacturing Services (EMS). Experience supporting Medical Device, Aerospace, and Defense industries. Experience with eQMS platforms and compliance management systems. Benefits 401(k) 401 (k) matching Dental insurance Health insurance Vision insurance Paid time off
Company Overview Solecta is an exciting early-stage, high-tech company focused on solving real customer issues and commercializing polymeric industrial filtration products. Solecta has manufacturing facilities in Oceanside, CA. The company is backed by True North Venture Partners, an investing firm that specializes in commercializing and scaling disruptive innovations. Position Summary To support the manufacturing of company products by completing production processes with direction and supervision. To support a highly empowered, world-class team to deliver excellent safety, quality, delivery and efficiency results. To assist in the continuous improvement of production processes. Essential Duties and Responsibilities To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or ability required. Other duties as assigned. Duties: Prepare, blend and compound membrane materials (e.g. polymers, coatings, additives) to meet specifications. Weigh or measure materials, ingredients, or products to ensure conformance to requirements. Perform inline testing, maintain cleanliness/sanitation, and ensure compliance with quality and GMP standards. Operates blending, coating, or compounding equipment, troubleshooting and maintaining machinery. Complete and maintain SOPs, work instructions and production records. Meets safety, quality, productivity, and efficiency standards. Follows documented standard work instructions and procedures. Runs and sets up processes and equipment. Performs product inspection. Competent in multiple workstations. Subject matter expert who can perform process audits in multiple workstations. Ability to cross train multiple workstations. Demonstrated performance across all product types and families. Collects data from process and completes paperwork with production information. Uses computer to collect required production data. Leads 5S in assigned production area. Reads and understands information and ideas presented in English. Assists production continuous improvement efforts. Performs work as assigned by supervisor/lead. Performs simple equipment maintenance. Maintains work area and equipment in a clean and orderly condition. Identifies and assists with troubleshooting, and in resolving machine issues. Skills Proficiency in ready and interpreting GMP documentation Strong attention to detail and safety. Basic knowledge of compounding equipment and processes Mathematical Skills (add, subtract, multiply, & divide quickly and correctly). Basic computer skills (Microsoft Excel, Word & Email). Organizational skills and attention to detail. Time management skills with a proven ability to meet production demands. Abilities Ability to read work orders or other instructions to determine product specifications or material requirements. Ability to follow compounding and mixing standards Ability to safely handle manufacturing chemicals and raw materials in accordance with Safety Data Sheets (SDS). Ability to function well in a high-paced and at times stressful environment. Ability to Communicate information and ideas clearly. This includes the ability to speak, read and write clearly and accurately in English. Ability to follow written and verbal instructions in English Ability to work in a team environment. Ability to multi-task. Ability to wear protective equipment such as safety glasses, hair net, and hearing protection Ability to work extended hours as needed. Minimum Qualifications High School Diploma or G.E.D. Prior experience in manufacturing, food/pharmaceutical compounding, or membrane/water treatment manufacturing is preferred Good verbal and written communication skills in English. Highly Dependable with ability to report on-time to start of company working shifts. Manufacturing experience. Experience with assembly/equipment/automated manufacturing. Experience in Membrane Filtration industry. Lean Manufacturing knowledge preferred. Continuous Improvement mindset. Forklift certification preferred. Netsuite experience preferred. Physical Requirements Must be able to operate mixing machinery. Must be able handle ingredients or substances to be used in production processes. Wear protective safety equipment such as safety shoes, gloves, glasses, coats, etc. Prolonged periods of standing and walking through the factory. Must be able to lift 50 pounds at times. Visual acuity to inspect products and machinery. Hearing and speaking to exchange information Dexterity of hands and fingers to demonstrate activities Operate a computer and other office productivity machinery Bending at the waist, kneeling or crouching Work Environment The work environment described here is representative of those an employee encounters while performing the essential functions of this job. Fast-paced manufacturing environment. This role routinely involves standard office equipment such as computers, photocopiers, filing cabinets, etc. The role is exposed to a variety of conditions that may be found while walking the production floor. No travel will be required for this position. 100% of the time spent on the production floor. Work extended hours as needed. Solecta, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Monday - Friday, 5:00 am - 1:30 pm
Description: We are seeking a Test Technician to join our team. In this role, you will be responsible for performing cabinet functional testing, troubleshooting, debugging, and modifying cabinet per instructions and specifications in a timely manner. Duties and Responsibilities Perform cabinet functional test. Perform assembly functional test. Troubleshoot and debug if necessary. Furnish and certify test results. Perform process quality checks on sub-assemblies and finished product. Utilize small hand tools, calibrated instruments, measurement equipment, and test fixtures. Work with engineers, QA, and technicians to resolve line issues and suggest improvements. Maintain accurate records/documentation related to quality, work in process, test results, labor (timecards) and special projects. Perform other job-related duties as assigned. Requirements: Must be able to read electrical wiring and schematics. Must be able to use DVM, scope, and other electronic test equipment. Must have computer skills, i.e.: able to use Great Plains, etc. Must be creative and able to work as a member of the cabinet test team. Must keep the area neat, organized and safe. Must maintain the highest level of professionalism under pressure. Ability to work in a high-paced environment. Ability to be flexible. Ability to handle multiple tasks. Ability to work independently with minimal supervision. Ability to interact with customers and all levels of personnel in a professional manner. Ability to manage several projects at the same time and meet deadlines. Must have working experience in a manufacturing/production environment. An electronics background is strongly desired. Familiarity with document control is helpful. Physical Conditions / Requirements No unusual physical requirements. It requires no heavy lifting, and nearly all work is done in a comfortable indoor facility. Occasional – Routine deadlines; usually sufficient lead time; variance in work volume seasonal and predictable; priorities can be anticipated; some interruptions are present; involves occasional exposure to demands and pressures from persons other than immediate supervisor. Job frequently requires sitting and handling objects with hands. Job occasionally requires standing, walking, bending, reaching, talking, hearing, and lifting up to 10 pounds. Hearing requirements: Ability to hear people over the telephone and in person; hear noises in surrounding areas, i.e., forklifts in the warehouse for safety purposes. Vision requirements: Ability to see information in print and/or electronically. As a member of our team, you will enjoy A GREAT work environment with fun, friendly, knowledgeable and helpful team members. Benefits package to support you and your family’s health. From medical, dental, and vision, to flexible spending accounts for both health and dependent care. Educational reimbursement to help keep your career undated. Save money on tickets to the San Diego Zoo, other amusement parks, movies, indoor skydiving and so much more with our employee discount program. Paid time off, holidays, company-matched 401(k) plan and more! Join SWARCO McCain. We look forward to receiving your resume.SWARCO McCain is an equal opportunity employer and participates in E-Verify.
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. Meet the team: Welcome to our dynamic team, where we pioneer the development of processes and equipment for all iterations of Dexcom wearables and applicators. From cutting-edge research concepts to the efficient production machinery responsible for crafting millions of sensors annually, our team plays a pivotal role in shaping the future of Dexcom technology. Join us in this exceptional and thrilling work environment within a stellar company, where your technical prowess and creative contributions directly influence the lives of our customers daily, both now and in the days to come. Where you come in: You will design and integrate equipment and processes to manufacture R&D scale builds that will eventually scale into commercial processes You will develop processes and evaluation systems to support DOEs for R&D Projects. You will develop and maintain project timelines and provide updates and feedback to project leadership. You lead material characterization, dispensing, and cure-related projects, including root-cause analysis, material qualification, and second sourcing. You design and develop fixtures and equipment components required to meet process goals from concept to implementation. You will design, document, and optimize new manufacturing processes, assembly steps, and operating procedures for new stations, equipment, and processes within a regulated quality system. You demonstrate hands-on process understanding and provide guidance and training to pilot plant operators on engineering-level builds. You create and release equipment specifications and drawings, establish calibration, and preventative maintenance requirements. You will set up infrastructure for data to be acquired in you measurement and fabrication processes and you will process large data sets to draw conclusions. You provide technical oversight and coordinate Research and Development builds within a pilot production facility for multiple projects and project teams. You implement, characterize, and optimize processes, mechanical tests, and fixtures/jigs for assembly, inspection, and test through the implementation of measurement systems, part inspections, MSA, and capability analysis. You identify process risks and track mitigations through standard methods. You assist in scaling up equipment and processes from prototype to pilot to full-scale manufacturing, providing design and assembly requirements within the scope determined by business and schedule needs. You exercise judgment within defined procedures and policies to determine appropriate action. What makes you successful: You have the ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D environment. You can deal with ambiguity and uncertainty, and you are willing to try new and challenging things. You have experience with operating and programming signal processing equipment &/or automated liquid handling robotics platforms and complex laboratory systems. You have proven ability to work hands-on in a fast-paced environment. You have previous direct involvement in the medical device industry. You are proficient in the use of SolidWorks or equivalent CAD software. You are familiar with data analysis methods and analysis software, with experience in JMP preferred. You are detail-oriented with strong time management skills. You have excellent communication (written and verbal) and personal interaction skills. You have knowledge of high reliability, high volume manufacturing processes and designs. What you’ll get: A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community . A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in-house learning programs and/or qualified tuition reimbursement. An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve. Travel Required: 0-5% Experience and Education Requirements: Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 5-8 years related experience or Master’s degree and 2-5 years equivalent industry experience or a PhD and 0-2 years experience. 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. Salary: $105,800.00 - $176,300.00
Job Overview: The Quality Assurance Manager will be directly responsible for ensuring that products meet certain thresholds of acceptability. Will plan, direct or coordinate quality assurance programs and formulates quality control policies. Responsible for maintaining a Quality Management System in compliance with AS9100 Aerospace Standard requirements. Duties & Responsibilities: Develops quality assurance plans by conducting hazard analyses, identifying critical control points and preventive measures, establishing critical limits, monitoring procedures, corrective actions, and verification procedures and inventories. Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits. Ensures that products adhere to quality standards. Reviews statistical data from the production lines. Investigate and respond to customer complaints. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Schedules Quality Control Inspectors to run daily quality inspection for daily production requirements. Manages product quality throughout the manufacturing areas. Creates a teamwork environment by coaching and promoting a teamwork attitude throughout the quality control area and constantly seeking improvement to the quality assurance processes, inspection methods, inspection tooling, and equipment. Writes, trains and controls quality assurance procedures. Ensures quality process documentation is current, controlled and accurate. Monitors daily inspections discrepancy report. Maintains compliance to AS9100 standard, QMS System. Provides training to new hires and implements quality assurance procedures and policies. Documents and implements preventative maintenance procedures. Resolve conflicts among personnel. Conduct performance reviews for direct reports. Maintains positive working relationships with Knowles customers and Knowles product representatives. Support accurate and timely maintenance of all approved electronic and manual record keeping systems. Periodically reviews department work instructions to ensure correct processes are being followed. Maintains a continuous effort to learn all aspects of the department including administrative processes, philosophy, acceptable and preferred internal and external communications methods, language and techniques. Strives to learn how to effectively do the job of others to prepare for personal advancement or effectively fill in when vacancies occur. Maintains a high level of cooperation within and between departments. Follow and support all safety practices by wearing proper personal protective equipment (PPE), following all Standard Operating Procedures (SOP) and complying with safety signs and placards, maintaining good housekeeping, communicating unsafe practices and conditions to your local or PD EHS teams, and reporting all safety incidents (including near misses) as they occur. Performs other duties as assigned. Qualifications & Skills: This position requires U.S. citizenship due to the nature of the work performed and access to classified information. Candidates must be able to obtain and maintain security clearance. Bachelor's Degree in a technical field required Excellent communication skills. Planning and project management skills. Leadership and management skills. Familiar with quality standards and processes. Attention to detail and Ability to Multitask Computer operating experience using Microsoft products. Accurate typing skills. Experience conducting customer contract reviewing and evaluating quality clauses within customer purchase orders. Ability to produce written inspection reports for nonconforming material discrepancies. Ability to produce First Article Inspection Reports. Able to manage and lead a team. In-depth knowledge and experience with AS9100 Quality Management Systems. Demonstrated experience utilizing A3 problem solving tools Experience monitoring and tracking customer Non-Recurring Engineering (NRE) Supervisory Responsibilities: Directly supervises the QA employees Work/Physical Requirements: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Occasional stooping, bending and reaching may be necessary. Individual must be comfortable sitting for long periods of time. Prolonged periods standing and walking throughout the facility. Repetitive motion (mousing and keyboarding). Must be able to lift up to 25 pounds at occasionally. Usually work indoors. Often exposed to loud sounds and distracting noise levels. Exposed to hazardous equipment. Exposed to contaminants. May share work space with others. Shift: First Shift Compensation: $90,000 - $110,000 annually Additional Details : Knowles is a leading manufacturer of specialty electronic components. We design parts that perform unique, critical functions for innovative technologies. Through extreme reliability, custom engineering, and scalable manufacturing, we enable businesses to succeed in the most demanding applications across medtech, defense, and industrial markets. Our high-performance capacitors, RF and microwave filters, advanced medtech microphones, balanced armature speakers, and miniaturization products enable and enhance the performance of technologies with the power to change, improve, and save lives. Founded in 1946 and headquartered in Itasca, Illinois, Knowles has grown into a global organization with employees spanning 11 countries. "What's in it for you on Day 1: * Medical, dental and vision insurance plans * Prescription Drug Plans * Basic Life Insurance * 401k plan with company match * Tuition Reimbursement Program * Employee Referral Program * Hourly Overtime opportunities * Paid Time Off * Paid Holidays Exciting Onsite Perks: * Free coffee available at our cafeteria * Employee Appreciation Events Knowles is committed to providing a competitive and fair total compensation package for all employees. Individual compensation decisions are based on a number of factors, including but not limited to previous experience and skills acquired prior to joining Knowles, cost of living in the assigned work location, assigned schedule, and salaries of similarly situated peers at the company. It is to be expected that candidates will come to us with different sets of skills and experiences and therefore will be paid at different points in the stated range. We recognize that the person(s) we select for hire may be less experienced or more experienced than the role as posted; if this is the case, any updates to available salary ranges will be communicated with candidates during the recruitment process. Equal Opportunity Statement: Knowles Precision Devices prohibits pay discrimination and discrimination of any kind based on race, color, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation, or other legally protected status. ITAR Statement: Please note that this position may require access to technical data controlled under the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants must be U.S. persons (citizens, lawful permanent residents, or individuals granted refugee or asylee status) or have the necessary authorization to access controlled technical data. Compliance with ITAR and EAR regulations is a condition of employment. Notice to Staffing Agencies, Search Firms and Recruitment Agencies: The recruitment process at Knowles is managed through the Human Resources department. Knowles does not accept resumes submitted from 3rd party agencies outside of our system. To submit resumes, 3rd party agencies will need to be a pre-approved vendor with a valid contract in place, be actively engaged by Knowles to recruit for a specific position and have agency log in credentials to submit candidates to our careers portal. Please do not submit resumes via e-mail, through our external website or directly to our employees. Any resumes submitted in this way become the property of Knowles and will not be eligible for any placement fee."
Description: Department: Industrial Machining Reports to: Production Supervisor Position Type: Hourly, RFT About the Company: DwyerOmega is a globally trusted leader in manufacturing innovative instrumentation solutions for the Process Measurement, Automation, Control and HVAC markets. With very strong brand recognition and high levels of customer loyalty, DwyerOmega has an unmatched reputation for providing customized solutions that meet and exceed customer needs. Our team of engineering experts help our customers select technical, and often configured, product solutions for their unique applications. The company offers over 300,000 state-of-the-art products for process measurement and control of temperature, humidity, pressure, strain, force, flow, level, pH, conductivity, and indoor air quality, and is a recognized global leader in the digital marketing of technical products. The products that we manufacture are used to control and drive process efficiency, creating safe and sustainable environments. At DwyerOmega, we enable our customers to improve the world – one measurement at a time. We achieve this through our unwavering commitment to technology, customer service, and overall continuous improvement. Every day, we strive to cultivate a culture of ingenuity, empowerment, accountability, adaptability, and speed. The company’s corporate headquarters are based in Michigan City, Indiana, and Norwalk, CT with manufacturing locations and sales offices located throughout the world. Position Summary: The Assembler is responsible for performing electro-mechanical assembly operations of light to moderate complexity in support of production goals. This role requires attention to detail, manual dexterity, and adherence to safety and quality standards to ensure products meet design and performance requirements. Essential Job Functions: Prepare, clean, and organize parts and components prior to assembly. Perform electro-mechanical assembly work of light to moderate complexity, requiring fitting, alignment, and adjustment of components, using job orders, drawings, and other documentation. Conduct basic functional testing of completed assemblies, including dielectric and insulation resistance testing. Rework and repair non-conforming production assemblies in accordance with established procedures. Follow all safe work practices and company safety policies. Participate in required safety training programs. Promptly report unsafe conditions, near misses, or accidents to supervision. Safety Responsibilities: Understand and support the company’s quality policy and applicable elements of the quality management system. Take responsibility for reducing, eliminating, and preventing quality deficiencies, including product escapes. Initiate action to prevent nonconformities related to products, process, or quality systems. Identify quality issues and elevate concerns through appropriate channels for corrective action. Exercise authority and responsibility to uphold quality standards in daily work. Quality Responsibilities: Understand and support the Quality Policy and applicable elements of the Quality Management System relevant to assigned work areas. Take proactive action to reduce, eliminate, and prevent quality deficiencies, including product or process escapes. Initiate actions to prevent nonconformities related to products, processes, and quality systems. Exercise responsibility and authority to identify quality concerns and elevate issues for timely resolution within the quality system. Communication: Communicate effectively in English, both verbally and in writing. Maintain professional, constructive, and collaborative working relationships with internal teams and external stakeholders. Essential/Preferred Skills: 0–2 years of experience in electro-mechanical assembly or repair of electro-mechanical devices, instruments, or units preferred. High School diploma or GED preferred. Demonstrated manual dexterity and mechanical aptitude, including proficient use of hand tools. Ability to perform repetitive assembly, testing, and potting operations with consistency and accuracy. Ability to read and follow general procedures, assembly drawings, and wiring diagrams. Ability to follow detailed instructions and established procedures with minimal supervision. Ability to perform repetitive tasks in a production or manufacturing environment while maintaining quality and efficiency. Requirements: Work Conditions and Physical Requirements: Work is performed in a manufacturing and production environment with regular exposure to moving mechanical parts, hand tools, and test equipment. May involve exposure to electrical components, adhesives, solvents, and potting materials, with appropriate safety controls and required use of personal protective equipment (PPE). Noise levels are generally moderate and may vary based on production activity. Work may be performed while standing or sitting at an assembly workstation for extended periods. Requires repetitive use of hands and wrists for assembly, testing, inspection, and material handling tasks. Requires fine motor skills, manual dexterity, and the ability to use hand tools and test instruments with precision. Requires the ability to bend, reach, walk, and move within the work area as needed throughout the shift. Must be able to lift, carry, push, and pull materials weighing up to 25 pounds, with or without reasonable accommodation. Requires the ability to visually inspect small components, read drawings, labels, and computer screens, with or without corrective lenses. At DwyerOmega, we’re committed to fair, transparent compensation. All U.S. job postings include a good-faith salary range that reflects the role, location, experience, and internal equity. We encourage open conversations about pay and are happy to discuss compensation at any stage of the hiring process.
Overview: Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger. The Quality Engineer provides customer and factory facing quality support. The position includes managing the interface between Resonetics, its customers and suppliers quality organization, assisting with transition and sustaining of laser manufacturing processes, and support for our quality management system. The Quality Engineer position uses Quality Engineering techniques including: Problem solving using Lean Six Sigma methodology, Process Validations and Verifications, Process Development and optimization, Gage R&R, and reducing dependence on inspection along with ISO 13485 and/or 21CFR820 compliance. Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you. Responsibilities: Monitoring and disseminating customer quality alerts and process deviations as required. Generating process deviations, Customer Change Notices, validation protocols & reports. Lead troubleshooting Quality opportunities during product launches and assisting with the Product Development Process. Leading development of metrology equipment Developing and maintaining quality/control plans and PFMEA. Ensuring Quality Management Systems procedures and appropriate regulations and industry standards are being utilized throughout the product development and process development processes. Developing Risk documentation in compliance with the QMS and regulatory standards, such as PFMECAs. Conducting Gage R&R studies and Design of Experiments Developing Quality Procedures and conducting training to all personnel as appropriate Approving Nonconformance disposition Analyzing production and validation data with advance statistic such as Anova & Regresion CPK, PPK & CP Control Charts SPC Gage R&R Design of Experiments Working on continual improvement and process assessment projects as assigned Author protocols or provides support in performing qualification validation protocols in support of design control deliverables. As a lead Quality Engineer on development projects, directly contribute and/or provide guidance to others to establish appropriate Design History File / Device Master Record documentation and provide detailed planning for product builds. Support Equipment Calibration and Maintenance per the applicable procedures. Required Qualifications: Minimum 5 years’ experience in a Quality Engineering role for a medical device manufacturer and/or start-up company, or equivalent engineering experience Demonstrated technical writing and communication skills. Working knowledge of Statistical software and/or Minitab Bachelor’s degree or equivalent experience Interact with customer and supplier companies in a professional manner; proactively communicates with them to ensure an ongoing two-way exchange of information. Auditing and qualification of new suppliers may be required. Experience with databases and Business Intelligence (PowerBi, Tableau, etc) Preferred Qualifications: CQE and/or Six Sigma Green or Black belt BS degree; Physics, Optics, Mechanical, Chemical, Plastics, Engineering preferred. Strong attention to detail and satisfactory organizational skills. Able to self-manage project task Physical Demands: Light office work only; position may include up to 10% domestic and international travel Compensation: The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $70,304 - $102,000. For temp, temp-to-hire, and regular full-time positions, our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.