Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
WHO ARE WE Sonaca North America is driven by a passion for innovation and a commitment to excellence. As a leading provider of aerospace and defense solutions, we are dedicated to making air and space travel safe and sustainable. We have 13 locations across North America and our engineering expertise and operational excellence set us apart from the competition. Since the beginning in 1948, we have a proven track record of delivering high-quality products and services that are reliable, safe, and efficient. Our team of experts is dedicated to staying ahead of the curve in the aerospace and defense industry, utilizing the latest technologies and processes to ensure that we deliver the best possible solutions to our customers. POSITION SUMMARY We are currently seeking a Quality Engineer (QE). The QE responsible for interpreting Customer contract requirements, engineering drawings & data sets, specifications, and other technical information to ensure compliance and proper implementation in the Quality Management System (QMS). The role of the QE spans the entire scope of the QMS, from contact/proposal review through final delivery and documentation of quality acceptance. In all actions, the QE will support Strategy, Quality Policy, and Values by supporting our commitment to total customer satisfaction, quality products and services, and employee development. ESSENTIAL JOB RESPONSIBILITIES The essential duties and responsibilities of the QE will vary depending upon the assignment within a particular operation and manufacturing location at Sonaca North America. The following list represents the key activities typical of this role: Identify and communicate Customer contractual requirements Provide interface to the Customer for quality related activities Host and provide support for customer or industry quality audit or certification activities Create Quality Assurance Program Plans, as applicable Update and maintain procedures and work instructions to ensure compliance with Customer requirements Conduct process and product audits in support of quality compliance Participate in design review, design verification, and Integrated Product Team (IPT) support, as required Create inspection plans, and methods for the manufacturing operations, including inspection equipment and tools necessary to provide efficient inspection processes. This would include the creation of First Article Inspection (FAI) plans, as required. Assist and train personnel in procedures and processes establishing and documenting inspection criteria and process improvements including process auditing Participate in and lead team based corrective action and continuous improvement efforts related to continuous quality improvement Utilize qualitative and statistical methods and tools to collect, summarize, analyze, interpret and communicate process capability and performance. This would include the use of key statistical process control (SPC) tools. EDUCATION AND EXPERIENCES Bachelor's degree from four-year College or University with major course work in engineering, quality, or science preferred along with 3-5 years Quality Engineering experience in the aerospace industry. Equivalent combination of education and experience will be accepted. Knowledge of the Aerospace industry is preferred. Inspection of detail parts, tooling and assemblies required. Aerospace inspection experience and knowledge of computer aided design systems and digital product definition o5r model based definition objects is preferred. Auditing experience required, preferably to AS9000/AS9100. Lead Auditor certification for AS9000/AS9100 preferred. Experience in performing root cause analysis and corrective action development. Excellent computer skills in Microsoft Office Suite and the ability to use enterprise applications (e.g., material resource planning, product lifecycle management) and a variety of special software applications on a daily basis. Certification to the Body of Knowledge for ASQ Quality Engineering preferred. US Citizenship. WHY CHOOSE SONACA NORTH AMERICA? We take care of our people. 401(k) retirement savings plan with a percentage company-match contribution Competitive wages Paid holidays Paid time off Medical, dental, vision, life, and accidental insurance Short-term disability Long-term disability Employee assistance plan — for access to counseling, consulting and other community resources Wellness program Tuition assistance Subject to eligibility, terms, and conditions Pay Range - $85,000-$95,000 annually This job description is only a summary of the typical functions of the job, not an exhaustive or comprehensive list of all possible job responsibilities, tasks, and duties. The responsibilities, tasks, and duties may differ from those outlined in the job description and other duties, as assigned, may be required. This document does not create an employment contract. Employees of the Company are employed on an “at will” basis and may be terminated at any time. Sonaca North America is an equal employment opportunity employer. Consistent with applicable law, Sonaca North America provides access and opportunities to those with disabilities. This includes providing reasonable accommodation to individuals with disabilities and disabled veterans who seek to access the company’s online application system. If an applicant is unable to fully access the online application system, Sonaca North America will provide a reasonable accommodation. Applicants with disabilities may contact us at 636-916-2400 for assistance accessing the on-line application system. Callers should have a detailed description of the requested accommodation, their name and preferred method of contact ready for Sonaca North America‘s Human Resources Department. Sonaca North America will make every effort to respond within two (2) business days. This phone number is not for the general submission of application materials. Sonaca North America is an E-Verify Employer. Sonaca North America is an Equal Employment Opportunity /Disability/Veterans Employer NOTICE ON FRAUDULENT JOB OFFERS It has been brought to our attention that there have been instances of fraudulent job offers, purporting to be from Sonaca North America and/or its affiliates (“LMI Aerospace”). This type of fraud is normally carried out through online services such as false websites, or through fake e-mails or call from people claiming to be from the company. These persons offer fraudulent employment opportunities to applicants and often ask for sensitive personal and financial information. The fraudsters may also request recipients to provide personal information and/or to make payments as part of their fake recruiting process. Sonaca North America d oes not ask for any financial commitments from candidates as a pre-employment requirement and will always require candidates to formally apply for positions via the Careers Page or job postings. Sonaca North America has no responsibility for fraudulent offers and if you believe you have been a victim of a fraudulent job offer concerning Sonaca North America, please email [email protected] .
DPI Direct, Inc. is a rapidly growing, dynamic one-source printing, digital label, packaging and marketing company located in Poway, CA. The right candidate will be offered competitive pay with a competitive benefits package. We have an immediate full time opening in our Digital Division for an experienced *2nd Shift Press Operator I (HP Indigo 100k series) * **Minimum one-year hands-on experience on Indigo 100k or 120k or newer machine series is required.* *Monday through Friday: 2:00PM to 10:30PM with opportunities for overtime. *Job description Includes but is not limited to:* * Set up, operate, and adjust the equipment, and in addition, diagnose, solve, and correct operating problems affecting the quality and timeliness of the service or product or function. * Follow schedule to determine next job ticket from online job schedule. * Track all work activity in job data collection tablet. * Obtain tools and materials needed for the job ticket. * Ensure proper operation and maintenance of equipment and work area. * Consistently follow safety protocol and guidelines in performing assigned tasks. * Perform all other duties as assigned by management. *Skill and Experience:* To be successful in this role, candidate must have the following: * Good math skills, time management, strong work ethic. * High School Diploma or G.E.D. (General Educational Development) * *Minimum 2-years current hands-on experience on HP Indigo 7k and 100k or newer machine series is required.* * *Must be HP Certified for 7k and 100k.* * Experience with other Digital Printing/Press equipment operation (Mechanically inclined) is highly preferred. * Willingness to learn, grow, and adapt to new machines and unique tasks. * Must have computer skills and ability to perform mathematical calculations correctly. * Must have excellent time management, able to organize/prioritize tasks and problem solve to deliver expected results timely. * Ability to understand and follow both written and verbal instructions/specifications. Bilingual is fine. * Must communicate effectively and work well with diverse management and other team members. * Ability to commit and work full-time hours from Monday to Friday with occasional overtime (early morning, evenings & or weekends) to complete jobs is required. * Regularly lift up to 15 lbs. and periodically be able to lift up to 50 lbs. * Ability to bend, squat, walk, and stand for long periods of time. Job Type: Full-time Pay: $23.00 - $25.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Experience: * Press Machine: 1 year (Required) * press printing: 1 year (Required) * digital or labels printing: 1 year (Preferred) Work Location: In person
What you'll bring to the team Do you have a passion for the environment and sustainability? Join the team helping LEGOLAND California Resort become Zero Waste by 2030. As a Waste Management Technician, you'll play a vital role in maximizing landfill diversion. You'll be responsible for the daily collection, transportation, and processing of all organic, inorganic, and hazardous waste generated on site. Each day, you will work with five to six other technicians to collect resort waste and dispose of it in an efficient and environmentally friendly manner. Generally, you will work behind the scenes using hand tools, powered equipment and company vehicles, such as light duty trucks, to complete your tasks. For more information about the day-to-day responsibilities of a Waste Management Technician, refer to the Scope and Responsibilities section below Merlin - It's where we play Merlin Entertainments Merlin Entertainments 2.24K subscribers Watch on Scope and Essential Job Functions: Perform daily rounds of collection, segregation, and disposal of solid waste and recyclable material. Operate heavy equipment, such as light duty trucks, trailers, compactors, balers, forklifts, etc. Dismantle unwanted equipment and assist in the recovery of recyclable materials using a variety of tools. Perform daily inspections to ensure department equipment and vehicles are in good working order. Maintain a clean and safe working environment by sweeping, cleaning equipment, reporting hazards, etc. Notifies Assistant Manager of service interruptions, including blocked containers, closed pathways, equipment failure or potential safety hazards. Works closely with Assistant Manager to improve route efficiencies and identify best practices. Notifies Assistant Manager of any incidents, accidents, injures, or property damage. Performs all duties as scheduled by the Assistant Manager and assists other technicians as directed to meet resort needs. Builds cooperative rapport with all departments and serves as an ambassador for resort sustainability and landfill diversion. This role is seasonal, and will sunset on Monday, February 24th, 2026. Qualifications & Experience Qualifications: Successfully complete and pass pre-employment drug screen and background check. Legally eligible to work in the United States. Hold a current class C driver’s license, clean driving record, and meet California minimum liability car insurance requirements. Must be 18 years of age. Must be willing to work flexible hours, including evenings, weekends and Holidays to support park operations. Requires excellent verbal English skills. Background and Experience: Experience within the waste management industry, operating heavy equipment such as trucks, single axle trailers, front-end loaders or compactors, forklifts is desired but not required. Education: High school diploma or general education degree (or equivalent education and experience) is required. Safety: While performing duties, the individual is regularly required to stand and walk for prolonged periods of time. Use of hands and fingers are used to handle and/or grip objects, tools, and controls. Pushing, lifting, and pulling objects will be performed during time of duties. Individual is occasionally exposed to chemicals, hazardous chemicals, fluorescent lamps or batteries, hazardous waste; will be exposed to loud work environment. All candidates offered a position must complete safety induction training, which includes but is not limited to the following topics: Emergency Action Plan for Waste Management Services HazCom Training Chemical Release Response and Hazardous Waste Management Autism Awareness Human Trafficking Awareness Sexual Harassment Prevention Training Physical Demands G Roles Standing: Constant 100% Walking: Constant 100% Sitting: None 0% (e.g., except during breaks) Lifting/Carrying: 0–10 lbs: Constant 80% 10–25 lbs: Constant 80% 25–50 lbs: Constant 80% 50+ lbs: Constant team lift: 80% of the time Pushing/Pulling: Frequent 80% (equipment used: [e.g., carts, product pallet jacks, machinery]) Reaching: Below waist: Frequently 90% Waist to shoulder: Frequently 90% Overhead: Occasionally 10% Bending/Stooping: Frequently 100% Twisting: Frequently 100% Kneeling/Crouching: Frequently 100% Climbing (stairs/ladders): Occasionally 50% Manual Dexterity (hands/fingers): Typing, handling small objects, tools, handling cardboard-Frequently 100% Vision Requirements: close vision, distance, color vision, depth perception-Frequently 100% Noise Exposure: Moderate-Frequently, Loud-Frequently 100% Temperature Exposure: Indoor / Outdoor / Seasonal variations / Extreme conditions, anywhere from 25 degrees to 101 degrees. Frequently 100% Work Environment: wet surfaces, heights, confined spaces, chemicals, working both indoors and outdoors Frequently 100% Additional Requirements: N/A Accommodation Statement: Reasonable accommodations will be made in accordance with applicable California law. Benefits Benefits of Merlin Entertainments · Excellent health care options (medical, dental, and vision that encourage preventative care). · Outstanding Paid Time Off (PTO) that allows for adventure, rest, relaxation, or recuperation. · Merlin Magic Pass for friends and family to enjoy the parks & attractions · Recognition Programs and Rewards · 401(k) program with company match · Tuition reimbursement programs · Numerous learning and advancement opportunities Pay Range Compensation between USD $19.50/Hr.-USD $19.50/Hr. At Merlin we welcome the world to our magical attractions and resorts every day and we want to reflect that same multicultural mix inside our business too. We strive to create an inclusive and diverse workplace where people can be themselves, have the same opportunities and thrive together. Because at Merlin, everyone matters! Together, we work to create a workplace where everyone feels valued, no matter their age, race, gender, disability or sexual orientation. Although we understand that we'll always be learning and growing, we aim to be the most inclusive and flexible employer in our industry.
The Position This role is a vital part of our Manufacturing team at Genentech Oceanside, which is dedicated to delivering high-quality biopharmaceuticals safely and reliably to patients worldwide. As a key technical and compliance leader within this department, you will collaborate closely with cross-functional partners across MSAT, Quality Assurance, Facilities & Engineering, and Compliance. In this collaborative environment, you will drive operational excellence, lead root-cause investigations, and ensure continuous adherence to cGMP standards across our biomanufacturing operations. The Opportunity As a Principal Manufacturing Compliance Engineer, you will serve as a primary technical subject matter expert to manage and resolve complex technical, regulatory, and compliance issues across biomanufacturing operations. You will lead cross-functional problem-solving initiatives, ensure full cGMP compliance, and safeguard production integrity through robust quality systems, investigations, and continuous improvement efforts. Manage and resolve complex technical, quality, and compliance issues in biomanufacturing in close partnership with Quality, MSAT, and Facilities & Engineering. Act as a Discrepancy Owner Lead, leading Root Cause Analysis (RCA) sessions and coordinating corrective and preventative action (CAPA) implementations within required timelines. Perform critical technical and operational reviews and approvals for process validation protocols, engineering changes, planned/unplanned variance reports, and controlled documentation. Serve as a Manufacturing Subject Matter Expert (SME) to regulatory agencies and contribute strategically during site inspections. Identify and mitigate technical, procedural, or equipment risks—including microbial contamination risks in cleanroom environments—that could impact production or compliance. Drive operational excellence initiatives and mentor manufacturing personnel to foster a strong compliance mindset and operational ownership across the site. Track, analyze, and present departmental performance metrics and environmental monitoring data to promptly address adverse trends. Who You Are Education & Experience: Bachelor’s degree (BS/BA) in Life Sciences, Engineering, or a related field with at least 5 years of experience in the pharmaceutical or biopharmaceutical industry (or an equivalent combination of education and experience). Technical Expertise: Direct, hands-on experience with mammalian cell culture and/or purification of biopharmaceutical products, alongside thorough working knowledge of cGMPs, FDA, ICH, and European regulatory guidelines. Quality Systems Mastery: Proven expertise in Deviation Management Systems (DMS) as a Discrepancy Owner, including proficiency with CAPA execution and Change Control processes. Problem Solving & Technical Writing: Demonstrated ability to lead complex Root Cause Analysis (RCA) investigations and write or revise high-quality technical documents, including Standard Operating Procedures (SOPs) and process validation reports. Leadership & Communication: Strong written and oral communication skills, with a track record of driving cross-functional alignment, prioritizing assignments independently, and mentoring teams under minimal supervision. This is an on-site position. Relocation benefits are approved for this posting. The expected salary range for this position based on the primary location of California is $95,200 - $176,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this link. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
The Position Join our Oceanside team and take on a meaningful role at the heart of biochemical manufacturing. You’ll collaborate across teams to resolve challenges, maintain quality system records, and ensure compliance with regulatory standards using cGMP and SOPs. Your responsibilities will include owning and investigating deviations, supporting tech transfer and commercial manufacturing, reviewing and approving technical documentation, supporting continuous improvements, and partnering with MSAT, Site Operations, and Quality Assurance to tackle quality issues and improve our compliance standing and understanding. In addition, you’ll lead operational excellence initiatives to improve processes, solve complex problems, and uphold high standards for safety, quality, and compliance. Your contributions will help ensure our products consistently meet customer and regulatory expectations. This role centers on broader compliance knowledge, with expertise in inspection strategies, risk assessment, and various compliance programs, such as environmental monitoring, personnel flow, and gowning procedures. The Opportunity Manage and resolve technical and compliance issues with Quality, Technology, Maintenance, Facilities, Calibration & EH&S. Solve a wide range of difficult issues that impact multiple functions following cGMP regulations and Genentech standards by applying advanced theory, technical principals and expert judgment. Troubleshoot and direct the resolution of Quality issues by fostering effective interdepartmental and cross-functional partnership. Lead and and/or facilitate Root Cause Analysis sessions for more complex issues and serve as a coach and process owner for DMS Event Observer/DO Community within their function on best practices Be able to act as SME to regulatory agencies Implement and follow through on corrective and preventative actions (CAPA) in accordance with timelines. Who you are Engineer: BS/BA in Life Sciences/Engineering preferred, and 0-2 years of experience in the pharmaceutical, biopharmaceutical industry or a combination of education and experience. Senior Engineer: BS/BA in Life Sciences/Engineering preferred, and 3-7 years of experience in the pharmaceutical, biopharmaceutical industry or a combination of education and experience. Ability to make sound decisions about scheduling, allocation of resources and managing of priorities. Preferred Strong oral and written communication skills. Ability to make sound decisions with minimal supervision. Possess thorough knowledge and understanding of cGMPs and familiarity with FDA, ICH and European guidelines. Manage assignments that are complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations. Experience in technical writing, such as, creation and revision of Standard Operating Procedures or other technical reports/evaluations is desirable Work Environment/Physical Demands/Safety Considerations Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Work in clean room environment with large mechanical equipment, piping, and pumps connecting to tanks serviced by high-pressure steam, water and air together this creates a load environment. May work with hazardous materials. Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of Oceanside, CA is $80,500 - $149,500 annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
Job Description Goodtron Electronics LLC is looking for a reliable *Part-Time Production Assistant* to support our electronics manufacturing and assembly operations. This is an entry-level position. *Some previous production, manufacturing, assembly, or warehouse experience is preferred, but extensive experience is not required.* We are willing to train the right candidate. Responsibilities * Assist with daily production and assembly tasks * Support PCB/PCBA and electronics assembly operations * Prepare materials and components for production * Perform basic visual inspection and quality checks * Assist with packaging, labeling, and organizing finished products * Maintain a clean and organized production area * Follow production instructions and safety procedures * Assist the production team with other tasks as needed Qualifications * Some production, manufacturing, assembly, or similar hands-on experience preferred * No extensive electronics experience required * Detail-oriented and able to follow instructions * Reliable and punctual * Comfortable performing hands-on production work * Willing to learn * *Chinese or Japanese language ability is preferred.* Schedule * Part-time * Schedule can be discussed based on production needs and availability Work Location Vista, California On-site About Goodtron Electronics LLC Goodtron Electronics LLC is an electronics manufacturing company specializing in PCB assembly (PCBA), SMT assembly, prototyping, and low-volume production. We are a small and growing team looking for dependable people who are interested in learning and growing with the company. Pay: $18.00 - $20.00 per hour Work Location: In person
Looking to be part of a team where craftsmanship, teamwork, and innovation come together? Welcome to Caseman GPC—where we don’t just build cases, we build solutions that work in the real world. Our production team plays a critical role in bringing custom-designed cases and packaging solutions to life, here in Poway, California. Our mission is simple but powerful: To deliver packaging solutions that go beyond storage, providing the perfect balance of presentation value, protection, and usability. Every case we create helps our customers protect what matters, and you will play a key role in making that happen. At our core, we believe in: Integrity, Quality, and Customer Focus! The vibe? Warm, welcoming, and full of possibility. People stick around not just for the work, but for the team. If you're looking for a place where you can grow your skills and genuinely make a difference, you’ll feel right at home here. How You Will Make an Impact: Assemble and finish custom cases, packaging solutions, and foam inserts according to specifications and quality standards. Operate production machinery, power tools, and equipment safely and efficiently to support daily manufacturing goals. Coordinate the movement of materials between receiving, warehouse, and production areas to maintain an efficient workflow. Leverage company technology, systems, and tools to drive productivity, ensure data accuracy, and support continuous improvement. Review production instructions, inspect finished products, and maintain high standards of quality and consistency. Collaborate with team members to meet production targets while maintaining a clean, organized, and safe work environment. To Be Successful in This Role, You Must: Work with attention to detail to ensure every product meets Caseman GPC’s standards. Communicate effectively with team members to support a smooth production flow. Adapt quickly to a changing work environment and manage competing demands. Be reliable, proactive, and committed to working safely. Be willing to learn and grow with new tools, processes, or responsibilities. Ensure deadlines are met without compromising quality. To Qualify for This Role, You Must Have: Ability to work in a fast-paced, team-oriented environment. Strong work ethic and reliability. Attention to detail to ensure product meets quality standards. Physical ability to lift, move, and handle materials as needed. Experience using a computer, Windows, Office, and ClickUp, or other relatable software and programs. Preferred: Experience using a bandsaw. Prior experience in production, assembly, or manufacturing. Familiar with case assembly. Pay, Perks & Benefits: Medical, dental, and vision insurance Paid vacation, holidays, and sick time 401(k) with 4% match Growth opportunities in a creative, forward-thinking environment Ready to Apply? If you're ready to take your skills to the next level in a company where thoughtful design and meaningful work come together, we’d love to meet you.
Thick Film Printer Technician – Level 1 Full Time + Benefits (Medical, Dental, Vision, 401k with Company Match, PTO) Job Type: Onsite Hourly Range: $20.00 - $25.00, DOE Shift: 1st Location: Poway, CA Fralock is an engineered solutions provider of specialty components and subassemblies using advanced materials for high reliability, severe environment, and technically challenging applications. We develop and manufacture custom integrated solutions. Established in 1967, we are a critical solutions provider to Fortune 500 corporations, government, and targeted OEMs in a variety of industries including Semiconductor Equipment Manufacturing, Medical and Life Science, Aerospace and Defense , Industrial, Electronics, and Energy. Fralock is headquartered in Valencia, CA with manufacturing locations located throughout Northern and Southern California. VISION To be recognized by our customers as a leading solutions provider of proprietary engineered advanced materials for high reliability, severe environment, and technically challenging applications. MISSION To create value, profitably grow, and share our success with all stakeholders. CULTURE Respect – We treat others the way they want to be treated. Integrity – We practice a high standard of ethics in our business dealings with customers,suppliersand employees. Responsiveness – We have a sense of urgency in responding to internal and external requests and work proactively to solve problems. Excellence/Competence – We empower our people to continuously improve and execute high quality work. Teamwork – We work together to achieve Fralock businessobjectivesby communicating ata high level, by listening and having clarity in our expectations of one another. Individual Accountability and Personal Responsibility – We do what we have committed to do when we committed to doing it. Continuous Improvement across all segments of the company This position requires access to information controlled under the International Traffic in Arms Regulations (ITAR) or the Export Administration Regulations (EAR), the successful candidate must be a "U.S. person" as defined in the ITAR and EAR (which generally means ( i ) be a citizen or national of the United States; or (ii) be a lawful permanent resident of the United States; or (iii) have been admitted to the United States as a refugee, or have been granted asylum, as specified under applicable law. Main Functions We are seeking an energetic and detail-oriented Thick Film Printer Technician - Level 1 to join our growing technical manufacturing team. In this entry-level role, you will work closely with senior technicians and production staff to perform routine printer operations, material staging, and basic preventative maintenance tasks. This is a hands-on opportunity to build your technical skills in precision screen printing, support daily manufacturing output, and contribute to a clean, safe, and efficient production environment. Key Responsibilities Routine Operation & Staging: Assist with basic machine loading, substrate staging, andoperatingsemi-automated thick film screen printers under direct supervision. Material Preparation & Handling: Prepare, mix, and stage conductive/resistive Inks following strict recipes;assistwith screen cleaning, reclamation, and proper storage. Basic Inspection & Quality Support: Perform visual inspections of printed substrates under magnification to check for obvious flaws, smearing, or misalignments, reporting defectsimmediatelyto senior staff. Preventative Maintenance & Support: Perform scheduled basic housekeeping and routine preventative maintenance tasks on printing platforms and cleanroom equipment. Documentation & Yield Tracking: Accurately log production counts, lot numbers, traveler sign-offs , and scrap data into the manufacturing execution system (MES) or ERP platform. Continuous Improvement & 5S: Participatein plant 5S, cleanroom housekeeping, and Lean manufacturing initiatives to keep the print area organized, safe, and contamination-free. Safety & Compliance: Strictly complywith all safety rules, chemical handling guidelines, ESD (electrostatic discharge) protocols, cleanroom regulations, and proper Personal Protective Equipment (PPE) usage. Required Skills Technical Expertise: Foundational mechanical aptitude and familiarity with precision hand tools and inspection instruments. Willingness and capability to learn how to read process travelers, engineering blueprints, and equipment operating manuals. Basic understanding of cleanroom protocols, contamination control, and handling delicate microelectronic substrates. Eagerness to develop foundational knowledge of paste rheology, screen mechanics, and printing parameters. Core Competencies: High levelof enthusiasm, eagerness to learn, and strong willingness to receive constructive feedback and mentorship. Good interpersonal and communication skills for interacting effectively with peers and production operators. Strict dedication to workplace safety rules, chemical handling standards, andmaintaininga clean, orderly work environment. Education Requirements High School Diploma or GEDrequired. Coursework or vocational training in electronics, manufacturing technology, or a related field is a strong plus. Experience Requirements 0 to 2 years of hands-on experience in a manufacturing, cleanroom, or precision assembly environment, or an equivalent combination of technical education and aptitude. Basic mechanical aptitude and comfort working with delicate parts and precision machinery. Willingness to learn optical microscope inspection techniques and measurement tools. Eagerness to develop operational competence on thick film screen printing systems. Basic comfort using computers, touchscreens, and manufacturing software to log data and check production schedules. Physical Requirements Ability to stand forlong periods, perform repetitive fine-motor tasks, use precision microscopes, and lift up to 30 lbs. regularly. Flexibility to work assigned shifts and occasional overtime as required . Required to wear mandatory Personal Protective Equipment (PPE) and cleanroom garments at all times (smocks, hairnets, gloves, safety glasses, and steel-toe footwear where designated). Strict adherence to chemical safety, ESD protocols, and SOPs is required. Work is performed in a cleanroom and manufacturing floor environment, which includes adherence to strict contamination controls, handling chemical pastes, and exposure to varying temperature conditions near thermal equipment. May require working specific assigned shifts (day, swing, or graveyard), occasional weekend support, and overtime to accommodate production demands and scheduled maintenance windows. All offers of employment at Fralock are contingent upon clear results of a background check. Background checks may include some or all the following depending on job title and responsibilities: Social Security Verification Prior Employment Verification Criminal History Personal and Professional References Motor Vehicle Records (only if applicable for the position) Credit History (only if applicable for the position) Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of a position. Fralock 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.
Manufacturing Lead - Zirconia Mfg. 2nd Shift (1:30 pm to 10 pm) Argen Corporation currently has an exciting opportunity for a Manufacturing Lead to join a growing, technology-focused and service-oriented team. Do you thrive in a fast- paced and dynamic environment? If you would like to be a part of an organization with an unwavering commitment to quality dental solutions, then explore our career opportunities and get to know Argen. About Us Argen is a family-owned and privately held company based in San Diego, CA with a state-of-the-art manufacturing center that provides high quality dental solutions to dental labs of all sizes. Founded as a precious metals company in South Africa, Argen has evolved into a dynamic, technology-based manufacturing organization focused on three key business segments, including dental alloys, zirconia, and digital dentistry solutions. Argen continues to invest in innovative product improvement initiatives through its Quality Management System to provide our global customers with affordable, high-performance products and industry-leading excellent service. Argen’s products are FDA regulated and ISO certified. About the Opportunity A Manufacturing Lead produces standard and/or custom medical devices to meet customer requirements by following standard work instructions and company policies while manufacturing Argen products in a team environment. In this role, the successful candidate: Follow department SOPs and work instructions and adhere to customer and Argen standards for manufacturing products. Adhere to work instructions to properly operate and maintain equipment as needed. Visually inspect product quality, troubleshoot and escalate issues when necessary. Report & escalate equipment per work instructions. Ensure team meets daily Service Level Agreement (SLA) expectations. Identify and recommend disposition of defective items for rework or scrap. Understand the product manufacturing process from initial steps through final inspection. Make line balancing personnel adjustments as required to maintain production flow and communicate all adjustments to the Supervisor. Clearly communicate instructions and operational expectations to team members. Periodically inspect product to ensure quality levels are maintained. Complete all documentation and training as required. Assist in authoring and/or revising SOPs and work instructions as needed. Support R&D Engineering products as requested by supervisor. Maintain a safe and clean work area, wear appropriate PPE, and adhere to safety standards. Ensure safety guidelines are followed by all team members. Train all manufacturing associates on all SOPs and work instructions in area. Serve as a subject matter expert in area. Other duties as assigned. What does it take to be successful? High school diploma or equivalent required. Five plus years of experience working in a manufacturing environment preferred. Strong knowledge of all manufacturing procedures with the ability to train others. Possesses leadership qualities and leads a manufacturing team in achieving results in a high-volume manufacturing environment. Possesses leadership qualities such as self-awareness, team focus, ability to translate learning into action, and train others to do so, as well as drive success. Ability to work in a team environment. Ability to follow instructions and readily accept additional responsibilities. Attention to detail and quality focused. Passionate about industry and desire to contribute where needed. Schedule adherence and dependability. Ability to meet tight deadlines and meet production goals. Ability to learn technical concepts by reading work instructions and standard operating procedures, and completing on-the-job training. Ability to effectively communicate in both written and verbal form. Ability to follow detailed directions in a Good Manufacturing Practices (GMP) environment required. Knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3 preferred. Our Awesome Benefits! Working for a growing innovative company like Argen means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, Argen is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes: Health/Dental/Vision Plans 401k with Employer Match Paid Vacation, Holiday and Sick Time Employee Events Wellness Programs Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more! EOE/M/F/Vet/Disabled VEVRAA Federal Contractor
Overview Join our dynamic team as a Packaging Associate in Carlsbad, CA, 92010! We are looking for motivated individuals who are passionate about quality and efficiency in packaging. In this role, you will play a crucial part in ensuring our products are packaged safely and effectively, ready to reach our customers with the highest standards. If you thrive in a fast-paced environment and enjoy hands-on work, we want to hear from you! Responsibilities Prepare and package products according to specifications and quality standards. Operate packaging machinery and equipment safely and efficiently. Inspect finished products for quality assurance and report any defects. Maintain a clean and organized work area, adhering to safety protocols. Collaborate with team members to meet production goals and deadlines. Assist in inventory management and restocking supplies as needed. Participate in training sessions to improve skills and knowledge of packaging processes. Qualifications High school diploma or equivalent preferred. Previous experience in packaging or manufacturing is a plus. Strong attention to detail and ability to follow instructions accurately. Ability to work in a fast-paced environment and meet production targets. Good communication skills and ability to work well in a team. Willingness to learn and adapt to new processes and technologies. Physical ability to lift and move packages as required.
PrideStaff is seeking a CNC Set Up/Machine Operator. Interested in this position? Give us a call at (760) 438-0161. Position: CNC Set Up Operator/ Machine Operator Pay Rate: $22 - $25/hr DOE Hours: 7am to 3:30pm Monday through Friday Location: Escondido, CA Job Duties and Responsibilities: Setting up and operating machinery Running lathes and vertical machines Must know how to read blueprints Must be able to know how to use basic hand tools Knowledge of measuring instruments miscellaneous job functions throughout the shop REQUIREMENTS: 1+ years’ experience operating conventional latheand verticalmachines Team player Responsible and dependable
*Position Summary* Steel Traditions is seeking a skilled and detail-oriented *Machinist / Material Preparation & Fabrication Technician* to support the production of custom steel doors and windows. The ideal candidate will have experience in machining, metal fabrication, architectural metal, door and window manufacturing, or a comparable precision manufacturing environment. This position is responsible for accurately cutting, machining, deburring, and preparing steel components for fabrication. The successful candidate must be mechanically inclined, comfortable working with production equipment and precision measuring tools, and capable of reading and interpreting fabrication drawings and cut lists. *1. MATERIAL CUTTING & PRODUCTION PREPARATION* *Responsibilities* * Review approved cut lists, shop drawings, and production documentation before processing material. * Verify material type, profile, wall thickness, and dimensions. * Accurately measure and cut steel tube, bar stock, plate, flat bar, angle, channel, and other materials. * Operate cold saws, band saws, and other approved cutting equipment. * Produce accurate straight cuts, miter cuts, and specialty cuts as required. * Deburr cut material and remove sharp edges and excessive burrs. * Ensure material is properly prepared and safe for handling before moving into fabrication. * Verify first-piece accuracy and perform routine dimensional checks. * Organize, identify, and stage completed material for fabrication. * Identify discrepancies or potential issues before material is processed. * Minimize material waste through accurate measuring and efficient cutting practices. *2. MACHINING & COMPONENT PREPARATION* *Responsibilities* * Perform drilling, tapping, countersinking, counterboring, and other basic machining operations. * Machine components for hinges, locks, handles, closers, pivots, guides, and other hardware. * Accurately locate and machine holes based on approved drawings and dimensions. * Operate drill presses, milling machines, and other applicable machining equipment. * Select and maintain appropriate tooling for each operation. * Perform threading and tapping operations. * Machine or modify brackets, mounting plates, stops, guides, spacers, and specialty components as required. * Verify completed components using appropriate measuring tools. *Measurement Skills* The candidate should be comfortable using: * Tape measures and steel rules * Combination squares * Digital calipers * Micrometers and depth gauges, when required * Angle and layout tools * Thread gauges and templates *3. DRAWING & DOCUMENT INTERPRETATION* *Responsibilities* * Read and interpret fabrication drawings, cut lists, and production documentation. * Accurately understand fractional and decimal dimensions. * Verify dimensions and material requirements before cutting or machining. * Identify missing, conflicting, or questionable information. * Follow current revision-controlled drawings and production documents. * Communicate documentation or dimensional issues before material is processed. *4. QUALITY RESPONSIBILITIES* This position is responsible for ensuring work is accurate before it moves into the next stage of production. *Responsibilities* * Inspect cut and machined components for accuracy. * Verify critical dimensions, angles, hole locations, and hardware preparation. * Check for burrs, damaged material, excessive saw marks, or machining defects. * Confirm proper thread quality and hardware fitment when applicable. * Identify and report nonconforming material or production issues. * Help prevent avoidable errors, rework, and material waste. *Quality Standard:* Do not pass a known error to the next stage of production. *5. MACHINE & WORK AREA RESPONSIBILITIES* *Responsibilities* * Perform basic daily inspections of assigned equipment. * Maintain cutting and machining equipment in a clean and safe condition. * Monitor saw blades, drill bits, taps, end mills, and other tooling. * Replace worn tooling or report equipment issues. * Keep the cutting and machining areas clean and organized. * Maintain proper organization of tools, fixtures, and measuring equipment. *6. CONTINUOUS IMPROVEMENT* *Responsibilities* * Identify opportunities to improve cutting and machining processes. * Recommend or assist with the development of jigs, fixtures, and repeatable production methods. * Help reduce material waste and improve production efficiency. * Assist with improving organization and workflow within the cutting and machining areas. * Participate in the development and improvement of standard operating procedures. *7. SAFETY RESPONSIBILITIES* *Responsibilities* * Follow all company safety procedures and equipment requirements. * Wear required personal protective equipment. * Never bypass machine guards or safety devices. * Secure material properly before cutting or machining. * Maintain awareness of sharp edges, rotating equipment, and other workplace hazards. * Keep work areas clean and free from unnecessary hazards. * Report unsafe conditions or damaged equipment immediately. *REQUIRED QUALIFICATIONS* *Minimum Qualifications* * Experience operating metal cutting equipment. * Basic machining experience, including drilling and tapping. * Experience with precision measurement and layout. * Basic knowledge of metal fabrication and manufacturing processes. * Ability to accurately read a tape measure and work with fractional and decimal dimensions. * Ability to read and interpret fabrication drawings, cut lists, or technical documents. * Strong mechanical aptitude and attention to detail. * Ability to work independently and manage production priorities. * Ability to safely operate production and machining equipment. *Preferred Qualifications* * Experience in door and window manufacturing. * Experience in architectural steel or architectural metal fabrication. * Experience with manual milling machines or similar machining equipment. * Experience creating or using jigs and fixtures. * Experience with custom fabrication or precision manufacturing. * Familiarity with CAD-generated cut lists or production drawings. * Forklift experience or willingness to become certified. *IDEAL CANDIDATE* The ideal candidate is a hands-on, mechanically skilled problem solver who takes pride in producing accurate, high-quality work. Experience in *doors and windows, architectural metal, precision machining, custom fabrication, or a similar manufacturing environment* is highly desirable. This is a hands-on production position requiring a combination of *machining skills, precision measurement, material cutting experience, mechanical aptitude, attention to detail, and the ability to work effectively in a fast-paced custom manufacturing environment*. Pay: $26.00 - $29.00 per hour Benefits: * 401(k) * Paid time off Work Location: In person