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Chromalloy is a global engineering & solutions company. We are a leadings provider of aftermarket parts, repairs, and solutions that safely & reliably extend the life of aircraft engines and gas turbines. We develop, manufacture and repair critical turbine components for a range of engine platforms. Our solutions support the engines running the aerospace, energy and defense industries around the world. Video: What We Do Why work at Chromalloy? Chromalloy employees are proud, passionate problem-solvers who strive to live our values every day. A career with Chromalloy is an opportunity to learn from top industry experts, work with important technologies, and unlock a passion for innovation. Join our team of experts, innovators and problem-solvers delivering world-class solutions for our customers. As a global company, we are committed to creating an inclusive environment where all employees feel represented, heard, and able to bring their best selves to work every day. Be part of something bigger with Chromalloy! Our Total Rewards Program is designed to support you today and in the future. • Comprehensive and flexible benefit options starting on day one, including medical, dental, vision, EAP, wellness incentives, and 401(k) with employer matching. • Development & progression opportunities for every employee – regular performance conversations, training and development curriculum, and engineering fellowship programs. • Paid time off, including vacation, sick time, paid holidays, floating holidays, and parental leave—all eligible on your first day of employment! • Competitive pay, including eligibility for quarterly and annual bonuses, depending on role and site. Eligibility for individual benefit plans may vary based on employment status. A Production Operator I assembles, fabricates and repairs FAA components by utilizing various hand tools and equipment and are responsible for overall work assignments under the supervision of the Cell Supervisor/Work Lead. Hand tools subject to use but are not limited to: Sandblasters, masking, use of hand-held motors, belt and wire wheel sanders. Core Duties and Responsibilities • Work safely following all health, safety, and environmental rules and policies. • Demonstrate high ethical standards and integrity as set forth in our Code and Conduct • Demonstrate the ability to effectively participate in a team environment that promotes the company's goals and objectives. • Ability to understand instructions delivered via oral, written, or diagram form. • Ability to read, write, speak, and effectively communicate in English. Essential Duties and Responsibilities • Can repair parts using sandblasters, masking, use of hand-held motors, belt and wire wheel sanders. • Calculate dimensions and tolerances using knowledge of mathematics. • Must be able to work independently, but also demonstrate an ability to work productively within the department team. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Any additional requirements are representative of the knowledge, skills, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience • High school diploma (or equivalent work experience) • 1 year in a production role preferred Physical Demands 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. Occasionally: Sit, lift, and/or move up to 30 pounds. Regularly: Lift and/or move up to 50 pounds. Push or pull using material handling equipment up to 500 pounds. Frequently: Stand, walk, stoop, kneel, crouch, talk, hear, and reach with hands and arms. Use hands to type, handle, or feel. Close vision, distance vision, color vision, and focus adjustment. Initial and annual hearing and vision exams must be successfully passed. If this position requires access to export-controlled technology and technical data, as defined in the Export Administration Regulations and or the International Traffic in Arms Regulations, any offer of employment is contingent upon Chromalloy’s determination, in its sole discretion, if any additional authorization for the employee to access such technology is required and obtainable in a manner that meets its immediate business needs prior to beginning work. Chromalloy participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Any offer of employment will also be conditioned upon the successful completion of a background investigation and drug screen in accordance with company policy and applicable federal and state regulations. Chromalloy is an equal opportunity employer - vets/disabled. In the United States, if you need a reasonable accommodation for the online application process due to a disability, please contact: https://www.chromalloy.com/contact-us/
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. Machine Operators • Technicians • Packaging • Inspection • Janitorial CAPTEK® is ACCEPTING APPLICATIONS for Production and Manufacturing positions. Responsibilities Include: • Operating equipment to defined standards and product requirement goals • Supporting a safe working environment by adhering to all plant safety, policies and procedures, including wearing appropriate Preventative Protective Equipment (PPE) • Conducting required quality checks on products to ensure customer satisfaction • Extensive amounts of reading, writing, and documenting • Working up to 8 hours per day in a loud/noisy, powdery, sometimes smelly environment • Must be able to perform tasks such as lifting, walking, climbing, stooping, standing, pushing and/or pulling We will hire and train candidates who are self-motivated. We promote from within and offer excellent growth opportunities for anyone looking for a career not just a job. Benefits Include: • Medical Insurance • Dental Insurance • Vision Insurance • Life Insurance • Long Term Disability • $500 Referral Bonus Program • 401k • 401k Matching • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Tuition Reimbursement We comply with E-Verify, Background Checks and Drug Screens. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. We are actively hiring for 2nd Shift (2:00 PM - 10:15 PM)! Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. Machine Operators • Technicians • Packaging • Inspection • Janitorial CAPTEK® is ACCEPTING APPLICATIONS for Production and Manufacturing positions. Responsibilities Include: • Operating equipment to defined standards and product requirement goals • Supporting a safe working environment by adhering to all plant safety, policies and procedures, including wearing appropriate Preventative Protective Equipment (PPE) • Conducting required quality checks on products to ensure customer satisfaction • Extensive amounts of reading, writing, and documenting • Working up to 8 hours per day in a loud/noisy, powdery, sometimes smelly environment • Must be able to perform tasks such as lifting, walking, climbing, stooping, standing, pushing and/or pulling We will hire and train candidates who are self-motivated. We promote from within and offer excellent growth opportunities for anyone looking for a career not just a job. Benefits Include: • Medical Insurance • Dental Insurance • Vision Insurance • Life Insurance • Long Term Disability • $500 Referral Bonus Program • 401k • 401k Matching • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Tuition Reimbursement We comply with E-Verify, Background Checks and Drug Screens. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Summary: To monitor and care for the finished gelatin product. Ensure that all tracking log are maintained and executed for all gelatin receivers Essential Duties and Responsibilities: • Follows company policies, SOPs, cGMPs and GDP • Maintains a safe and clean work environment in the gelatin staging area • Must maintain all gelatin tracking logs throughout the shift • Assists the softgel encapsulation operators in finding and moving receivers to the correct location • Assists and check the softgel encapsulation operators connect the correct gelatin • With the assistant of a lead, check and record the viscosity when necessary. • Ensures that oldest lot numbers/ materials/gelatin batches are used first (FIFO) • Consistently monitors gelatin temperature throughout the shift • Make sure all gelatins left-over is accounted it for and documented on batch record. • Ensures that temperature probes are maintained, washed and ready to use for the following shift • Reports any damaged or broken tools, receivers and equipment to the manager • The ability to communicate and interact with other departments (nutrient, encapsulation, maintenance quality assurance etc.) • Executes proper shift change and communicates all information pertaining to the operator's area of responsibility • Anticipates and minimizes down time to ensure completion of order in a timely manner • Assists with janitorial duties as needed • Ensures work area is clean and organized at all times and mop at least once a day • Remove trash at the end of each shift • Communicates solutions and ideas on how to improve department to the department manager • Complies with company policies and procedures and maintains regular work attendance • Performs other duties as assigned Educational Qualification: • Some High school credit and any work experiences Required Skills / Experience: • Able to read and write • Able to lift up to 25 kg Work Environment: • The work environment characteristics described here are representative of those an employee encounters while performing 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 occasionally exposed to work near moving mechanical parts; fumes or airborne particles and risk of electrical shock. • The noise level in the work environment is usually moderate Physical Demands: • 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 • The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision and Ability to adjust focus. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands and fingers to handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. 3rd Shift: 10:00 PM - 6:30 AM Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. Machine Operators • Technicians • Packaging • Inspection • Janitorial CAPTEK® is ACCEPTING APPLICATIONS for Production and Manufacturing positions. Responsibilities Include: • Operating equipment to defined standards and product requirement goals • Supporting a safe working environment by adhering to all plant safety, policies and procedures, including wearing appropriate Preventative Protective Equipment (PPE) • Conducting required quality checks on products to ensure customer satisfaction • Extensive amounts of reading, writing, and documenting • Working up to 8 hours per day in a loud/noisy, powdery, sometimes smelly environment • Must be able to perform tasks such as lifting, walking, climbing, stooping, standing, pushing and/or pulling We will hire and train candidates who are self-motivated. We promote from within and offer excellent growth opportunities for anyone looking for a career not just a job. Benefits Include: • Medical Insurance • Dental Insurance • Vision Insurance • Life Insurance • Long Term Disability • $500 Referral Bonus Program • 401k • 401k Matching • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Tuition Reimbursement We comply with E-Verify, Background Checks and Drug Screens. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
R&R Industries is looking to hire _*full-time Production Workers ASAP*_ in our Silk Screen Decorating Department. This position is hiring ASAP! _*¡Hablamos Español!*_ *Starting at $19 per hour* *Work shift is 6am - 2:30pm, Monday through Friday. *_*Overtime available during peak seasons.*_ *Key Responsibilities include:* * Support receiving garments from the production dryer belt * Conduct quality inspection of the quantity and quality of printed goods * Responsible for handling and repetitively counting hundreds of items daily * Ensure each order is physically accurate and matches our ERP System, meeting and/or exceeding customer satisfaction * Package and label orders in a timely manner * Ability to multi-task while paying attention to quality of printed products * Ability to meet daily orders and print targets * Work alongside a garment dryer where the surrounding temperature is warm * Keep the general maintenance of work area clean and organized * Perform other responsibilities as needed *Requirements: * * Must be able to regularly lift up to 40lbs. * Must be able to stand for extended periods of time * Frequent repetitive hand motion * Must be able to keep up in fast paced production environment & consistent workflow *Thank you for your interest in R&R Industries!* *About Us - *R&R Industries, Inc. is an apparel manufacturer specializing in high-visibility clothing. We decorate our customer's logos on-site that include but are not limited to construction, airlines, and landscaping industries, etc. We literally see the fruit of our labor most everywhere we go! If this sounds like a fit, what are you waiting for? *Apply now!!!* *Note:* No agencies. All candidates/resumes submitted by an agency or 3rd party will be considered a referral. We are an E-Verify Employer. We are an equal opportunity employer and value diversity at R & R Industries, Inc. We do not discriminate on the basis of race, religion, color, national origin, gender or gender identity, sexual orientation, age, marital status, veteran or disability status, or any other characteristic protected by law. Job Type: Full-time Pay: From $19.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Referral program * Vision insurance Ability to Commute: * San Clemente, CA 92672 (Required) Ability to Relocate: * San Clemente, CA 92672: Relocate before starting work (Required) Work Location: In person
RASIRC is seeking a passionate and dynamic Senior Quality Engineer to join our team. If you're someone who thrives in a fast-paced environment, enjoys collaborating with diverse teams, and is committed to making a meaningful impact, we want to hear from you! U.S. Citizenship: Please note that RASIRC does not assume the responsibility to sponsor employees, US citizenship or Permanent Resident Certificate (Green Card) is required for this job. Company Culture: We value versatility where team members wear multiple hats and contribute across various functions. Our values are at the forefront of our tasks and interactions every day both with coworkers as well as customers. These values include: Customer Focused Innovation Integrity Teamwork Open Communication Efficiency Learning Position Overview: We are seeking a highly skilled and detail-oriented Senior Quality Engineer to join our team. This role will facilitate and oversee quality aspects of product development, design and process changes, and root cause analysis of field failures. In this role you will guide engineering teams on development of product requirements, risk analysis, Design History File (DHF) completeness, drive failure analysis and root cause investigations, and serve as a customer-facing partner for field issue resolution. The position also supports product and materials compliance activities for global markets. You will collaborate closely with Product Development, Manufacturing Engineering, and other teams to deliver robust, compliant, and reliable solutions. Key Responsibilities: Design Quality & Risk Management Facilitate and support creation of design requirement based on market requirements Lead dFMEA and pFMEA development and maintenance. Ensure DHF completeness. Failure Analysis & Corrective Actions Oversee structured failure analysis on returned units and its documentation. Ensure structured root cause analysis and implementation of effective corrective and preventive actions. Customer-Facing Quality Act as the quality contact for customers on field failures and corrective actions. Communicate investigation results and improvement plans clearly and professionally. Compliance & Certification Support activities for product, electrical and materials compliance to meet target market requirements. Quality Systems & Audits Contribute to ISO 9001 quality system maintenance and participate in internal and external audits. Supplier evaluation and improvement Evaluate new suppliers to ensure compliance with quality standards and assess long-term viability. Track and report supplier performance metrics; drive improvement plans where needed. Data-Driven Quality Utilize statistical tools (SPC, DOE, MSA) to monitor and improve product and process performance. Coaching & Leadership Mentor engineers on quality tools, risk analysis, design controls, and problem-solving methodologies. Documentation and Reporting: Maintain accurate and up-to-date records Prepare and present quality reports to management and other stakeholders. Qualifications: Required Bachelor's degree or higher in Chemical Engineering, Mechanical Engineering, or related field. Minimum 4 years in quality engineering. Expertise in Risk Management, dFMEA/pFMEA, DHF, and design control processes. Proven experience in failure analysis, root cause investigation, and CAPA execution preferably utilizing 8D methodology. Strong writing and communication skills with experience interfacing directly with customers and suppliers. Proficiency in statistical analysis preferably utilizing JMP. Experience with ISO 9001 or other standards such as ISO 13485, ISO 14971, etc. Familiarity with electronic QMS platforms (especially QT9) and stage-gate development processes. Ability to work in a fast-paced, dynamic environment and manage multiple priorities. Ability to work independently and as part of a team. Preferred ASQ CQE, Six Sigma, or other quality certifications Experience with semiconductor capital equipment, vacuum, or hazardous gas systems. Knowledge of global compliance requirements (CE, RoHS/REACH, etc.). Other Requirements: Ability to stand for extended periods and perform repetitive tasks. Ability to lift and move up to 35 pounds. Must be willing and able to work in environments that require frequent bending, reaching, and lifting. Use of personal protective equipment (PPE) as required. Ability to work in an ISO Class 6 cleanroom with required cleanroom garb. This role requires working with dangerous and toxic liquids and gaseous chemicals and strictly following all safety protocols. What We Offer: The salary range for this position is $95,000 - $125,000/year depending on experience and qualifications. RASIRC values employee growth and development and with that has a comprehensive training program to ensure that you reach the goals of your position, as well as provide the resources needed for your future career goals. Health and Wellness Benefits: RASIRC pays 77% of a designated base plan with a multiple plan private exchange for employee health insurance for employees. Paid Time Off 401k with company match Equal Opportunity Employer: RASIRC is an equal opportunity employer and values diversity in the workplace. We encourage candidates of all backgrounds to apply. Join us in shaping the future of Semiconductors and making a difference in the world!
Description Looking for an opportunity to make an impact? At Leidos, We are seeking a highly skilled Lead Quality Engineer (QE) to oversee Quality Engineering efforts on a key AS9100 program. This role will be responsible for managing a team of QEs, driving quality assurance activities, ensuring compliance with AS9100 and customer requirements, and leading continuous improvement initiatives. The Lead QE will work cross-functionally with Engineering, Manufacturing, Supply Chain, and Program Management to ensure product integrity and compliance throughout the lifecycle. . Your greatest work is ahead! Leidos’ Defense Systems Aerospace sector is seeking a Program Quality Lead Engineer to join our team This position will require the candidate direct all quality aspects of a new program. The candidate should have knowledge of manufacturing practices. These activities will include but no limited to: Assembly operations / controls, testing, Non-conformances, root cause investigation, internal and 3rd party audits. This position will manage the non-conformances, managing the Quality flow downs to suppliers, Inspection instructions. This position will follow up on all internal audit findings to drive the closure of the open issues. This job will audit and ensure all operation steps are being followed per the instructions. The candidate should have a knowledge of Space programs and how they operate. This job will have occasional travel to other sites and will be required to submit Weekly, monthly and Quarterly Quality reports If this sounds like the kind of environment where you can thrive, keep reading! Leidos Defense Systems Sector provides a diverse portfolio of systems, solutions, and services covering land, sea, air, space, and cyberspace for customers worldwide. Solutions for Defense include enterprise and mission IT, large-scale intelligence systems, command and control, geospatial and data analytics, cybersecurity, logistics, training, and intelligence analysis and operations support. Our team is solving the world’s toughest security challenges for customers with “can’t fail” missions. To explore and learn more, click here! Are you ready to make an impact? Share your resume with us today! Primary Responsibilities • Leadership & Team Management • Lead and mentor a team of Quality Engineers supporting the AS9100 program. • Assign responsibilities, set priorities, and provide guidance on quality-related tasks. • Develop and support training programs to enhance team capabilities. • Quality Engineering & Compliance • Ensure adherence to AS9100, customer, and regulatory requirements across the program. • Lead risk management, root cause analysis, and corrective/preventive action (RCCA/CAPA) initiatives. • Drive First Article Inspections (FAIs), PPAP, and process validations per industry standards. • Support Design Reviews, Manufacturing Readiness Reviews (MRRs), and Configuration Control Boards (CCBs). • Program Support & Customer Interface • Act as the primary quality representative for the program, ensuring alignment with customer expectations. • Lead customer audits, source inspections, and quality reviews. • Collaborate with Program Management and Engineering to resolve quality-related challenges. • Continuous Improvement & Data-Driven Decision Making • Utilize metrics and data analysis to identify trends, drive improvements, and reduce defects. • Lead process improvement initiatives (e.g., Lean, Six Sigma, Zero Defect initiatives). • Champion a culture of quality and accountability within the organization. Basic Qualifications. • Bachelor’s degree with 8-12 years of prior relevant work experience or Masters degree with 6-10 of prior relevant work experience in a AS9100 regulated aerospace/defense environment. • 3+ years of experience leading or managing Quality Engineers. • Strong knowledge of AS9100, NADCAP, and aerospace industry standards. • Hands-on experience with FAI (AS9102), PPAP, RCCA (8D, 5-Why), and quality tools. • Proficiency in GD&T, statistical analysis, and risk management tools (FMEA, PFMEA, DFMEA). • Experience working with customer quality representatives, suppliers, and regulatory bodies. • Candidate must have a BS degree and 8 years of relevant experience. In lieu of a degree, a High School diploma/GED or equivalent education with 10 years of relevant experience will be considered. • Candidate must have experience working with non-conforming material, performing failure analysis, identifying root cause and implementing corrective action. • Candidate must be a US Citizen and possess ( as well as maintain) a Final Secret Clearance Preferred Qualifications. • Optics Background is preferred but not required • Certified Quality Engineer (CQE), Six Sigma Green/Black Belt, or AS9100 Lead Auditor certification. • Experience with DoD, NASA, or hypersonic programs. • Familiarity with APQP, MSA, and digital transformation initiatives in quality. • Candidate should have at least 3 years of quality experience in an ISO9001/AS9100 system or equivalent experience in DOD, Aerospace, or Automotive manufacturing quality control. At Leidos, we don’t want someone who "fits the mold"—we want someone who melts it down and builds something better. This is a role for the restless, the over-caffeinated, the ones who ask, “what’s next?” before the dust settles on “what’s now.” If you’re already scheming step 20 while everyone else is still debating step 2… good. You’ll fit right in. Original Posting: September 3, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range: Pay Range $89,700.00 - $162,150.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
GLAUKOS #DareToDomore Manufacturing Technician II – San Clemente, CA Founded in 1998, Glaukos is a publicly traded ophthalmic medical technology and pharmaceutical company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases. Our global headquarters is in Aliso Viejo, California, and we have additional locations in the United States, Canada, United Kingdom, Germany, Japan, Australia and Brazil. How will you make an impact? The Manufacturing Technician II, based in San Clemente, CA, will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements. What will you do? The Manufacturing Technician II , based in San Clemente, CA will be responsible for the following: Prepare components and build assemblies Ability to perform activities under a microscope Prepare bulk drug formulations Perform the following: Filing, capping, and crimping operations Packaging and labeling operations Sampling Visual inspections Documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Additional responsibilities will include: Maintain proper cleanroom environment, including gowning, room cleaning, and supplies Follow, execute and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches Perform basic calculation and data entry Assemble, disassemble, and clean process equipment Clean, etch, passivate, assemble, and inspect components Process and assemble components in accordance with documented specifications and procedures Perform in-process inspection of assemblies and finished products in accordance with specification criteria Ability to perform validation and qualification activities (IQ/OQ/PQ/TMV/PV) Organize and clean the work areas Perform additional duties and projects as required How will you get here? To be successful in this role, you will need to have the following industry (medical device, pharmaceutical, and/or biotechnology) and educational experience. It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards. Level - II 2 – 4 years experience with high school diploma. Less than 1 year experience with an Associate’s degree in science or engineering Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family. Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we’re a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others. We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Check out our profile on The Muse to get an inside look at our company culture. Glaukos Corporation has been Certified as a Great Place to Work the last three years! Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
*Overview* We are seeking a skilled Manual Machinist to join our team. The ideal candidate will possess a strong mechanical knowledge and experience in various machining processes. This role requires proficiency in operating manual machines, interpreting blueprints, and utilizing precision measuring instruments to produce high-quality components. The Manual Machinist will play a crucial role in ensuring that our products meet stringent specifications and quality standards. *Responsibilities* * Operate manual lathes, milling machines, and other machining equipment to fabricate parts according to specifications. * Interpret and analyze blueprints, technical drawings to determine machining processes. * Utilize precision measuring instruments such as calipers, micrometers, bore gauges, and coordinate measuring machines to ensure accuracy. * Conduct routine maintenance on machinery and tools to ensure optimal performance. * Collaborate with engineering teams on tooling design and process improvements. * Apply GD&T principles to ensure proper tolerances are maintained throughout the manufacturing process. * Implement lean manufacturing principles to enhance efficiency and reduce waste. * Assist in assembly processes as required, including the use of hand tools and power tools. *Qualifications* * Proven experience as a Manual Machinist with a solid understanding of machining processes. * Strong mechanical knowledge with the ability to troubleshoot equipment issues effectively. * Basic math skills for accurate measurements and calculations. * Experience with tooling setup, adjustment, and maintenance. * Strong attention to detail with a commitment to producing high-quality work. Job Type: Part-time Pay: From $17.50 per hour Expected hours: No less than 15 per week Work Location: In person
HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. At HME you will have the opportunity to learn and grow while developing our future products. Come join our team! We are currently recruiting for a Quality Assurance Coordinator. What you will do in this position: Determines initial routing and/or disposition of Return For Credit (RFC) material [i.e., Defective on Arrival (DOA), Trade-In, and Demo equipment] to Quality Engineering or the Material Review Board (MRB) as prescribed by the governing Standard Operating Procedures (SOP). Enters all applicable data and disposition comments into the Returned Material Tracking (RMT) of the MRP system and completes any hardcopy documents (e.g. NCR's) as required. Process and accurately record data relevant to QA-evaluated DOA material in Enterprise Resource Planning system. What you will need to succeed: Qualifications Working knowledge of basic statistical quality control, data collection methods, and inspection methods and terms. Ability to create and use control charts. Computer literacy in Windows environment. Software proficiency: Microsoft Word, Excel, and Access. Working knowledge of ERP system and Report Wizard or ODBC preferred. Experience 4+ years Education High School Diploma - Required Travel: 0% The posted pay range, $23.80 to $31.74, is what we reasonably expect to pay for the role. This may vary depending on experience and other factors. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment 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. The employee will occasionally lift and move up to 25 pounds. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
HIRING AT: Urban Stone is a fabrication and installation stone company located in Fallbrook, CA. Hiring a full time self-motivated and organized individual, for Polisher. *Position Summary * As a Polisher, you will ensure that the various materials, such as quartz, marble, granite, are smooth and shiny when completed. You will use a variety of tools and techniques to remove imperfections, scratches, or rough spots from surfaces, enhancing their appearance and quality. *Essential Duties and Responsibilities* The essential functions include, but are not limited to the following: * Inspect materials for imperfections, scratches, or blemishes that need to be corrected. * Clean surfaces to remove dirt, dust, grease, or other contaminants before polishing. * Select appropriate polishing tools and abrasives based on the material type, finish requirements, and surface condition. * Use hand-held or powered polishing equipment, such as rotary buffers, sanders, or grinding machines, to polish surfaces. * Apply polishing compounds, pastes, or solutions to surfaces to facilitate the polishing process and achieve desired results. * Perform polishing operations with precision and attention to detail, ensuring consistent quality and uniformity across surfaces. * Remove scratches, burrs, or defects from surfaces by gradually refining the finish through successive polishing steps. * Inspect polished surfaces for uniformity, smoothness, and overall appearance, making adjustments as needed to achieve desired results. * Verify compliance with quality standards and specifications for finish, gloss, and surface texture. * Operate polishing equipment and tools safely, following proper procedures and using appropriate personal protective equipment (PPE). * Maintain polishing equipment and tools in good working condition, performing routine maintenance and cleaning as necessary. * Report any equipment malfunctions, safety hazards, or maintenance issues to Shop Foreman. *Qualifications (Knowledge, Skills, and Abilities)* 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, skill and/or ability required. * Excellent communication and interpersonal skills. * Knowledge of polishing techniques, materials, and equipment. * Familiarity with different types of surfaces and their polishing requirements. * Ability to prioritize tasks and work independently. * Ability to problem-solve and troubleshoot polishing issues. * High school diploma, or related field experience preferred *Physical Demands * The physical demands include, but are not limited to the following: · Constant standing · Occasional sitting · Constant use of hands · Constant walking · Repetitive tasks to operate polishing equipment. · Loud environment · Carrying, lifting, pushing, and pulling items up to 75 lbs. · Constant grasping and pinching with hands. HOURS- 6:30-5:00pm Monday-Thursday. (4/10 Shift) Job Type: Full-time Pay: $18.00 - $25.00 per hour Benefits: * Dental insurance * Employee discount * Health insurance * Life insurance * Vision insurance Work Location: In person