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Manufacturing Associate l Monday – Friday 5:00am to 1:30pm About Us At Argen, we’re in the business of creating healthy, confident smiles one case at a time. Argen is a global leader in dental manufacturing with headquarters in San Diego, CA, subsidiaries in Canada, Germany, UK, and China, and sales in 105 countries worldwide. We are 500 team members strong. Founded more than 50 years ago as a precious metals company in South Africa, Argen has grown to become the largest dental zirconia manufacturer in North America, largest dental alloy provider worldwide, and leader in digital dentistry solutions with a product offering that spans fixed, removable, ortho, implants, and equipment. Our 140,000 square foot manufacturing center houses more than 150 3D printing and milling machines and operates six days a week. Argen’s products are held to the highest standards of quality, and are FDA 510(k) cleared, ISO 13485 certified, and MDSAP compliant. Argen embodies a culture of innovation, continuous improvement, and LEAN practices in support of our mission to help our dental laboratory customers succeed. About the Opportunity The Manufacturing Associate l is responsible for producing standard and/or custom medical devices to meet customer and Quality requirements by following standard work instructions and company policies while manufacturing Argen products in a team environment. In this role, the successful candidate will: Follows department SOPs and work instructions and adheres to customer and Argen standards for manufacturing products. Adheres to work instructions to properly operate and maintain equipment as needed. Visually inspects product quality & escalates issues. Identifies and recommends disposition of defective items for rework or scrap. Understands the product manufacturing process from initial steps through final inspection. Completes all documentation and training as required. Maintains a safe and clean work area, wears appropriate PPE, and adheres to safety standards. Cross trains in one or more areas of manufacturing. Other duties as assigned. What does it take to be successful? High school diploma or equivalent required. One plus years of experience working in a manufacturing environment preferred. 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 production goals. Ability to learn technical concepts by reading work instructions and standard operating procedures, and completing on-the-job training. 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 Plans Dental Plans Vision Plan 401k with Employer Match Paid Time Off and Paid Holidays 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
*Production Operator – Water Plant* Innovive, LLC, a high-growth manufacturing company serving the Biomedical Research community, is seeking a production operator to join our team. This person will work with the production teams of our bottle filling/water purification. This position requires a great team spirit and a generally positive attitude while donning proper PPE in a cleanroom environment. Must be able to evolve with a high level of thoroughness throughout the day. *Job Duties:* · Setup the production equipment and supplies before executing the job orders · Operate equipment safely and effectively for production processing · Ensure that equipment is maintained in good and safe working condition · Inspect equipment to identify any replacements, malfunctions, and repairs · Perform regular equipment check/maintenance to ensure production capacity and quality · Work under the guidance of the Lead/Supervisor to perform and complete the assigned duties in a timely manner · Evaluate equipment performance and recommend improvements · Follow safety procedures and company policies for equipment operation · Recommend process improvements to enhance operational efficiency and safety · Identify and report unsafe operations to Supervisor immediately · Maintain a clean, safe, and organized work area · Position requires heavy lifting. Must be able to lift 50lbs. · Pack boxes and palletize product *Knowledge, Skills, and Abilities:* · Previous experience with cleanroom or laboratory environments is a plus · Ability to do repetitive tasks; detail-oriented; understanding of industry and safety standards · Thrives to work in a faced-paced working environment · Ability to lift 50lbs above the head · Familiarity with water treatment operations and methods preferred · Working knowledge of automated operations, ideally with experience in filling and/or packaging · 2+ years of manufacturing experience preferred · Bi-lingual in Spanish and English preferred *About Innovive LLC* Innovive, LLC serve the global laboratory research market with products and services that allow animal research facilities to dedicate more of their efforts towards scientific discovery than was previously possible. Our patented Disposable IVC Rodent Caging System empowers the husbandry industry with the option of eliminating traditional cage wash operations, freeing up capital funding, space, time, labor, utilities, and other valuable resources. At Innovive we are committed to providing the highest *quality products and services* to our customers, backed by an unparalleled level of *customer service* while integrating *sustainable practices* into everything we do. *Employment Type: *Full-Time, Hourly *First Shift: *Mon-Thurs, 3:30am - 2:00pm Job Type: Full-time Pay: From $21.50 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Retirement plan * Vision insurance Experience: * Production Operator: 1 year (Required) Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
*Job Summary* We are seeking a motivated and detail-oriented Composite Lay-up Technician to join our dynamic manufacturing team. In this role, you will be responsible for assembling composite materials using precise lay-up techniques to create high-quality parts and components. Your expertise will contribute to the production of durable, lightweight, and innovative composite structures. This position offers an exciting opportunity to work with advanced materials and fabrication processes in a fast-paced, team-driven environment. The ideal candidate is energetic, eager to learn, and possesses a strong mechanical aptitude. *Duties* * Prepare composite lay-up molds and work surfaces, ensuring cleanliness and proper setup for each project * Cut, trim, and handle composite materials using hand tools, power tools, and fabrication equipment with precision * Follow detailed work instructions and technical drawings to accurately assemble layers of fiberglass, carbon fiber, or other composite fabrics * Use forklift and materials handling equipment to move raw materials and finished parts safely within the workspace * Operate machinery such as machining tools or carpentry equipment to support fabrication and assembly tasks * Inspect finished components for quality standards, ensuring proper layering, curing, and surface finish * Maintain a clean and organized work area, adhering to safety protocols at all times *Experience* * Prior experience in manufacturing, fabrication, or assembly environments is preferred but not required; training will be provided for the right candidate * Familiarity with hand tools, power tools, and basic carpentry or machining techniques is highly desirable * Warehouse experience involving materials handling or forklift operation is a plus * Knowledge of composite materials, millwork, or construction processes will be advantageous * Strong mechanical knowledge with an ability to interpret technical drawings and specifications * Experience working with manufacturing or fabrication equipment such as CNC machines or similar machinery is beneficial Join us in creating innovative composite solutions! We value energetic individuals who thrive in collaborative settings and are committed to producing top-quality products through precision craftsmanship. This role provides a hands-on opportunity to develop skills in advanced manufacturing while contributing to exciting projects across various industries. Job Type: Full-time Pay: $25.00 - $30.00 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Flexible schedule * Flexible spending account * Health insurance * Life insurance * On-the-job training * Paid time off * Safety equipment provided * Vision insurance Work Location: In person
Cabinet Assembly Technician Job Summary The Cabinet Assembly Technician is responsible for the disassembly and reassembly of approximately 120 MS cabinets, including the installation of new hardware components. This temporary position requires attention to detail, the ability to follow structured instructions, and careful handling of freshly painted materials to prevent damage. This role is project-based and expected to last approximately 1–2 months, depending on workflow, material returns, and potential additional units. Key Responsibilities Disassemble MS cabinets in accordance with provided guidelines Reassemble cabinets with newly installed hardware components Follow detailed instructions for proper hardware installation Handle freshly painted cabinet components carefully to prevent scratching, denting, or breakage Use small hand tools efficiently and safely Perform repetitive assembly tasks with consistency and attention to detail Move and position cabinets within the workspace as needed Maintain a clean and organized work area Qualifications & Requirements Familiarity and comfort using small hand tools Ability to follow written and verbal instructions Strong attention to detail Ability to perform repetitive tasks for extended periods Physical ability to lift, move, and maneuver cabinets (strength and coordination required) Ability to work in a warehouse and/or climate-controlled environment Work Environment Variable warehouse and climate-controlled workspace Project-based role lasting approximately 1–2 months Timeline may extend depending on paint/hardware returns and additional unit volume Work Authorization Must have the legal right to work in the United States without sponsorship Position Type/Expected Hours of Work Hours of work are Monday through Friday, 7:00 a.m. to 3:30 p.m., 40 hours per week. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Salary: $17.75
Position Description Carlsmed is seeking an experienced Senior Quality Engineer to support New Product Introduction (NPI), design transfer, product sustaining, and supplier quality activities for spine implants and instrumentation. This senior individual contributor role owns quality deliverables for design transfer and leads supplier selection, qualification, auditing, performance monitoring, and change management activities within an ISO 13485 and MDSAP certified Quality Management System. Responsibilities Own quality engineering activities for NPI and design transfer, including planning, execution, and approval of quality deliverables. Serve as Quality core team member for product development programs supporting implants, instruments, and additive manufacturing. Ensure effective translation of design and risk outputs into manufacturing and supplier controls. Support sustaining quality activities including MRB, NCR, and SCAR investigations. Lead supplier selection, evaluation, qualification, and approval activities. Plan and execute supplier audits; document findings and ensure timely closure of nonconformances. Develop, implement, and maintain supplier scorecards and performance metrics. Coordinate and approve supplier process, material, and site changes. Support internal and external audits including ISO 13485 and MDSAP. Act as a senior technical mentor within the Quality organization. Process and equipment validation (IQ/OQ, PQ). Analyze quality data and supplier performance metrics to drive continuous improvement and support data-driven supplier decisions. Lead and review risk management activities, risk controls, and verification of risk mitigation effectiveness. Qualifications Bachelor’s degree in Engineering or related technical discipline. 7+ years of progressive medical device quality engineering experience. Experience owning design transfer activities. Strong knowledge of ISO 13485 and MDSAP requirements. Experience with supplier auditing and supplier quality management. Experience supporting machined instruments, additive manufacturing, sterilization, and packaging suppliers. Ability to travel up to 10%. Equal Opportunity Employer Carlsmed is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Carlsmed is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know. Compensation We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families. including paying 100% of monthly healthcare, dental & vision insurance premiums, a 401(k) plan with employer matching and unlimited PTO. The expected pay range is: $130,000 to $145,000 annually. Compensation may vary based on related skills, experience, and relevant key attributes.
Machinist Maintenance Location: Camp Pendleton, CA 92057 Job Summary We are seeking a skilled Machinist Maintenance professional to join our team at Camp Pendleton, CA. The ideal candidate will be responsible for maintaining, repairing, and fabricating precision parts and equipment to ensure optimal operation of machinery and systems. This role requires strong technical skills, attention to detail, and the ability to work independently or as part of a maintenance team. Key Responsibilities HVAC & Refrigeration, Chiller & Cooling Tower Maintenance is performed in accordance with Contractor's PM program and work schedule. HVAC and refrigeration systems are maintained at the required temperature. HVAC and refrigeration systems are in compliance with environmental regulations. Seasonal start-up and shutdown work shall be completed in compliance with the Contractor’s approved recurring service program schedule. Sampling and testing are accomplished in accordance with the Contractor's program and schedule. Radiant Heater, Boiler systems, Testing, inspection, and certification of boilers performed and completed in accordance with the Inspection, Testing, and Certification Program and Schedule. Boilers are promptly returned to service upon issuance of certification. Boilers are prepared for inspection and certification. Sampling and testing are accomplished in accordance with the Contractor's program and schedule. Seasonal start-up and shutdown work is completed in accordance with the Contractor’s approved Recurring Service Program schedule. Compressed Air Systems Maintenance is performed in accordance with Contractor's PM program and work schedule. Compressed Air Systems are fully functional per OEM standards. Perform routine and preventive maintenance on various types of machinery and equipment. Operate machine tools such as lathes, milling machines, grinders, and drill presses to fabricate or repair parts. Read and interpret blueprints, technical drawings, and schematics to determine machining requirements. Diagnose mechanical issues and perform necessary repairs or adjustments. Maintain accurate records of maintenance activities, repairs, and parts inventory. Ensure compliance with safety standards and company policies during all maintenance operations. Collaborate with engineering and maintenance teams to improve equipment reliability and performance. Use precision measuring instruments to verify dimensions and tolerances of machined parts. Qualifications High school diploma or equivalent; technical or vocational training in machining or maintenance preferred. Proven experience as a machinist or maintenance machinist in an industrial or manufacturing environment. Proficiency in operating machine tools and using precision measuring instruments. Ability to read and interpret blueprints, technical drawings, and manuals. Strong mechanical aptitude and problem-solving skills. Familiarity with safety regulations and best practices in a maintenance setting. Good communication skills and ability to work effectively in a team environment. Willingness to work flexible hours or overtime as needed. Work Environment This position is based at Camp Pendleton, CA, and involves working in an industrial or manufacturing environment. The role may require standing for extended periods, lifting heavy objects, and working with machinery and tools. Adherence to safety protocols is essential. How to Apply Interested candidates are encouraged to submit their resume and cover letter detailing their qualifications and experience relevant to the Machinist Maintenance position. ```
Location: San Diego, CA, US, 92121 Business Unit: Energy Conversion Solutions Posting Date: Feb 12, 2026 Job Description: About Us: Join AMETEK Programmable Power, a leader in cutting-edge programmable power solutions and systems. We specialize in designing and delivering precision AC and DC programmable power supplies, electronic loads, power subsystems, and compliance test solutions. If you're ready to work at the forefront of differentiated power technologies, this is your opportunity to make an impact in a fast-paced, high-tech environment! Job Summary: Lead a team of Assemblers to perform assembly and sub-assemblies build according to production plan. This position will perform electrical and mechanical assembly operations of complex assemblies and sub-assemblies and be responsible for training and directing daily functions of the assembly group and will support daily production schedules and maintain standard Quality workmanship in the area. In addition, this position will interface with engineering, management and production personnel as needed and will perform electrical and mechanical assembly operations of complex assemblies and sub-assemblies. 1st Shift: Monday through Friday, 5:30 AM to 2:00 PM Overtime: Ability to work overtime Monday through Friday and on weekends as needed/occasionally. Key Responsibilities: Lead team and distributes work daily throughout the shift to meet production schedule. Audits the Quality for compliance to ISO 9001:2015 and AMETEK Workmanship Standards. Coordinate/provide cross training to reduce bottleneck and eliminate Single-Point-Of-Failure. Monitor efficiency to set working standards to achieve daily productivity. Help resolve/escalate issues impacting production. Observes/help enforce all AMETEK Policies/Processes/Procedures and Safety rules/policies. Leads 6S activities (Safety, Sort, Set in Order, Shine, Standardize, Sustain) and Conducts monthly Gemba walks. Hold individuals accountable for tools and equipment preventive maintenance and record keeping. Provide input to annual Performance Appraisal in his/her group. Working lead role/responsibilities - Split 30% leading and 70% working Hold team accountable to perform daily housekeeping at the end of the shift. Run daily Tier 1 meeting with team. Facilitate SQDIP (Tier 2) meeting in the absence of a Supervisor/Manager. Must be available to work a flexible schedule including overtime and weekends. Performs related duties as assigned. Minimum Qualifications: Must require a minimum of 3 - 5 years of related experience. Assembler levels 3 - 5 will vary based on years of experience and scope of responsibility High school diploma or equivalent Must possess good to excellent assembly blueprint reading experience/skills Must be able to use hand tools (i.e. torque wrench, drills and inspection tools) Ability to properly read a variety of measuring devices including rulers, tape measures, and scales Must be able to communicate effectively with others Performs other duties as assigned Due to the nature of Programmable Power programs and products, applicants must have the legal right to work in the U.S. and additionally must be legally authorized to access export-controlled information and source code Desired Qualifications: Intermediate computer skills IPC-610 and J-STD 001 certification Efficient MS Word and Excel user What’s in It for You: Competitive compensation, holiday pay, and paid time off Great benefits package that includes health, vision, and dental insurance 401(k), plus matching Flexible spending accounts (FSAs), health savings account (HSA) with AMETEK contribution, life insurance, disability insurance, and family medical leave Employee referral program Tuition reimbursement program Employee assistance program Exciting, fast-paced environment where you could make a true impact Opportunities for career advancement within our business unit and across all other AMETEK business entities Additional Details: Location: This role is based in San Diego, California, a city renowned for its idyllic blend of sun, sea, and vibrant culture. With a coastal climate and over 70 miles of stunning coastline, it's a haven for beach lovers and outdoor enthusiasts year-round. Explore diverse museums, the historic Gaslamp Quarter, and Balboa Park's gardens and world-famous zoo. Enjoy an active lifestyle with parks, trails, and water sports. Relish international cuisine and experience unique neighborhoods like lively North Park and coastal La Jolla. San Diego offers an irresistible mix of relaxation and adventure. Salary Range: The annual pay range for this position generally ranges between $20.00 - $25.00. Actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition, AMETEK provides a variety of benefits to employees, including health insurance coverage, an employee assistance program, life and disability insurance, a retirement savings plan, paid holidays and paid time off. To learn more about our company and our job opportunities, visit us at: https://www.ametek.com/careers To learn more about the business unit you’ll be joining, visit us at: Programmable Power: https://www.programmablepower.com/ VTI Instruments: https://www.vtiinstruments.com/ Compensation Employee Type: Hourly Salary Minimum: $40,000 Salary Maximum: $55,000 Incentive: No Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location. For more information on AMETEK's competitive benefits, please click here. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 22,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK is a component of the S&P 500. Visit https://www.ametek.com/careers for more information. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call 1 (866) 263-8359.
*Position Summary* The Quality Assurance (QA) Specialist is responsible for supporting and maintaining compliance with Good Laboratory Practice (GLP) regulations, internal SOPs, and applicable regulatory requirements within a preclinical contract research laboratory. This role performs study-based and process-based audits, manages document control and archiving activities, supports sample accountability oversight, assists with equipment validation activities, and contributes to successful client and regulatory inspections. The QA Specialist works cross-functionally with scientific, operations, and management teams to promote data integrity, quality systems effectiveness, and continuous improvement. *Key Responsibilities* *GLP Study Auditing & Quality Oversight* · Conduct GLP compliance audits including protocols, amendments, raw data, reports, and in-process inspections. · Perform facility, process, and systems audits to verify adherence to SOPs and regulatory requirements (FDA GLP 21 CFR Part 58, OECD GLP). · Document audit findings clearly and objectively; track responses and corrective/preventive actions (CAPAs). · Verify protocol compliance and data integrity (ALCOA+ principles). · Verify proper use of validated systems · Contribute to QA statements and study inspection reports. *Document Control & Archiving* · Maintain controlled documents including SOPs, forms, templates, and policies. · Manage document lifecycle processes (creation, review, approval, revision, distribution, archival). · Ensure proper indexing, retrieval, and retention of study records and raw data. · Oversee secure and compliant GLP archive operations and record transfers. · Conduct periodic archive audits and inventory checks. *Sample Management & Control Oversight* · Audit sample receipt, labeling, storage, tracking, and disposition processes. · Verify chain-of-custody documentation and sample accountability. · Ensure storage conditions and environmental monitoring meet protocol and GLP requirements. · Participate in sample reconciliation and inventory reviews. *Equipment Validation & Quality Systems Support* · Support validation lifecycle activities (IQ/OQ/PQ), equipment qualification, and computerized system validation (CSV). · Review validation protocols, reports, and change control documentation. · Verify calibration and maintenance compliance during audits. · Assist with deviation, CAPA, and change control processes. *Inspection & Client Audit Support* · Assist with preparation and hosting of regulatory inspections and client audits. · Compile documentation packages and support inspection readiness activities. · Participate in mock inspections and internal gap assessments. · Track commitments and responses following inspections. *Quality Systems & Continuous Improvement* · Support training compliance tracking and QA metrics. · Assist in SOP development and quality system improvements. · Participate in risk assessments and process improvement initiatives. *Qualifications* *Education & Experience* Bachelor’s degree in life sciences, quality assurance, or related scientific field required. 2–5 years of QA or laboratory experience in a GLP-regulated environment preferred. Experience in preclinical CRO, pharmaceutical, biotechnology, or regulated research setting highly desirable. *Knowledge & Skills* · Working knowledge of FDA GLP regulations (21 CFR Part 58), OECD GLP, and data integrity principles (ALCOA+). · Familiarity with auditing techniques and quality management systems. · Understanding of document control, archival processes, and equipment validation. · Strong written communication and technical documentation skills. · Ability to interact professionally with clients and regulatory inspectors. · Strong attention to detail and organizational skills. · Quick turn-around on requests, with accuracy and thoroughness being critical. · Ability to handle multiple tasks, respond quickly and efficiently, and keep situations under control in a fast-paced, dynamic work environment · Ability to adapt to changing procedures, policies, and work environments. · Ability to compose clear, concise, and professional written communication. · Ability to meet deadlines and work under pressure. · Flexibility and adaptability with workload, shifting priorities as needed. · Perform tasks for experiments following step-by-step protocols. · Ability to work occasional weekend, early morning, or late-night shifts as required. *Preferred Qualifications* · QA auditing certification or formal GLP training. · Experience with LIMS, electronic data capture systems and Quality Management Systems (e.g., Provantis, Pristima, Xybion). · Experience hosting or supporting FDA, USDA, AAALAC or client inspections. · Experience in FDA (GLP), USDA, AAALAC, OLAW, DEA. · Knowledge of computerized system validation and data integrity assessments. *Work Environment* · Office and laboratory environment within a GLP preclinical research facility. · May involve review of laboratory procedures and study activities in animal research settings. · Occasional extended hours during inspections or audit periods. *Key Competencies* Regulatory compliance focus Critical thinking and risk assessment Professional communication Confidentiality and integrity Collaboration and teamwork Pay: $90,000.00 - $100,000.00 per year Benefits: * 401(k) * Dental insurance * Flexible schedule * Health insurance * Paid time off * Tuition reimbursement * Vision insurance Work Location: In person
Join Reva Medical LLC as a Full-Time Extrusion/Assembly Technician and become part of a pioneering team dedicated to revolutionizing medical devices. This onsite role offers a thrilling opportunity to work hands-on with cutting-edge technology, contributing to life-changing innovations in the healthcare industry. You'll play a vital role in the assembly process, collaborating with passionate experts who value problem-solving and integrity. At Reva Medical, our culture fosters high performance and forward-thinking, allowing you to grow professionally while making a tangible impact on patients' lives. Your contributions will directly affect product quality and operational efficiency, enhancing the future of medical care. You will receive great benefits such as Medical, Dental, Vision, 401(k), and Life Insurance. If you are eager to embrace challenges in a traditional yet dynamic environment, this position is your perfect fit! Apply now and help shape the future of medical technology. WHAT IT'S LIKE TO BE A EXTRUSION/ASSEMBLY TECHNICIAN AT EXTRUSION/ASSEMBLY TECHNICIAN As a new Extrusion/Assembly Technician at Reva Medical LLC, you will be responsible for operating extrusion machinery, ensuring precise setup and calibration for optimal performance. Your day-to-day tasks will include inspecting materials and components for quality, following strict assembly protocols, and adhering to established safety standards. You will collaborate closely with team members to troubleshoot any issues that arise during the extrusion and assembly processes. Additionally, you will document production data and maintain accurate records to support continuous improvement efforts. Engaging in routine maintenance and cleaning of equipment will also be essential to ensure operational efficiency. You'll participate in team meetings to share insights and contribute ideas for innovation, helping to foster a culture of high performance. Overall, your role will be pivotal in driving quality and consistency in our medical device manufacturing processes. REQUIREMENTS FOR THIS EXTRUSION/ASSEMBLY TECHNICIAN JOB To be successful as an Extrusion/Assembly Technician at Reva Medical LLC, strong attention to detail is paramount, as you'll be working with intricate components that require precision and accuracy. Excellent problem-solving skills will be essential for identifying and addressing issues during the manufacturing process. A hands-on approach and mechanical aptitude will help you navigate equipment effectively and perform troubleshooting as needed. Additionally, strong communication skills are crucial for collaborating with team members and sharing insights that promote innovation. Time management abilities will enable you to prioritize tasks effectively and meet production deadlines without compromising quality. Adaptability is also key, as you'll be working in a dynamic environment that values forward thinking and continuous improvement. Finally, a commitment to maintaining high standards of integrity and professionalism will ensure you thrive in our high-performance culture, contributing meaningfully to our mission in the medical device industry. MAKE YOUR MOVE Applying for this position is a walk in the park if you feel it's a good fit for you. Best of luck!
Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Operations Technician 1 – Night Shift will be part of the Chemical Manufacturing team in Carlsbad, CA. The team of Operations Technicians are responsible for filling and completing orders for customers. Hours : Tuesday – Saturday 9:00pm-5:30am, including a 15% shift differential Position will start out on the day shift for 1-3 months and will move to a night shift once fully trained Pull needed vessel(s) for assigned orders Chemical Packaging (Filling with chemical) Conduct safe work practices Ensure quality standards are met Maintain a clean and organized manufacturing environment Comprehend written and verbal instructions Complete assigned day to day tasks other than filling orders Perform data entry Physical Attributes: Use of a full-face air-purifying respirator and other PPE Lift up to 50 pounds Who You Are Minimum Qualifications: High school diploma or GED 6+ months in a role requiring quality and safety 6+ months experience using Microsoft suite including (Word, Excel, Access, SharePoint) Preferred Qualifications: Previous experience handling chemicals Experience with Six Sigma methodologies Previous experience in a fast-paced manufacturing environment Strong troubleshooting, documentation, and communication skills Ability to read and understand Safety Data Sheets and written work instructions Strong focus on quality and safety Experience using SAP and LIMS systems Ability to use hand tools Pay Range for this position - $25/hr - $40/hr The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
*CNC Mill Set Up Machinist Needed (POWAY)* Employment type: *full-time* Job title: *CNC Mill Setup Machinist* Premier CNC machine shop in San Diego County. We are looking for 1st shift CNC Mill setup machinists with a minimum of 5 years of experience. Shift is 7AM-3:30PM M-F Job requirements: * Experience setting up CNC mills (either 3, 4, or 5 axis are acceptable) * Ability to check your own work with various types of basic inspection equipment * Able to read blueprints and have an understanding of dimensioning and tolerancing * Ability to follow instructions and provide consistent quality * Must work well with others in a team environment What this position offers: * Steady paycheck as we have long-term customers and a stable workload * 401K/profit sharing * Health/Dental insurance * We pay top dollar for the right candidate Recruiters please do not reply CNC, Setup, Set-up, S/U, mill, haas, fanuc, mori, matsuura, doosan Job Type: Full-time Pay: $26.00 - $35.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Parental leave * Retirement plan * Vision insurance Education: * High school or equivalent (Required) Experience: * CNC machining: 2 years (Required) Shift availability: * Day Shift (Preferred) Work Location: In person
*Job Summary* The Production Planner will be responsible for planning and coordinating production activities to ensure timely delivery of products. This role involves scheduling, material sourcing, and close collaboration with engineering, procurement, and production teams. This position works under the guidance of Project Managers and the Director of Engineering and Operations to align planning activities with overall project and organizational goals. This role requires an understanding of manufacturing processes, ERP systems, and continuous improvement methodologies to enhance overall production efficiency and product quality. *Work Environment:* This role operates in both an office setting and a production warehouse. The Production Planner is expected to communicate with production personnel and front office staff to ensure successful completion of work. A typical day may include, but is not limited to: working with Epicor to plan jobs, updating or editing router (job traveler) documents, walking the shop floor to check job status, verifying material or part availability, checking condition of parts to determine usability or need for rework, and communicating with procurement, engineering, sales, and production departments to stay updated on current status. *Key Responsibilities:* * Create and update Methods of Manufacturing in Epicor ERP * Print and distribute travelers (routers) for production jobs * Communicate with sales, engineering, and production teams regarding job priorities and details * Develop and maintain production schedules to meet customer demand * Source and identify materials required for production * Coordinate with procurement and production to ensure material availability and workflow efficiency * Monitor job progress and adjust schedules as needed to meet deadlines * Qualifications: * Education: High School Diploma required; some college preferred * Experience: 1–3 years in production planning or related field * Technical Skills: Experience using an ERP system (Epicor experience preferred), Microsoft Office Suite (Excel, Word, Outlook), Project management tools or Task management tools. * Warehouse awareness and safety * Understanding of engineering drawings. *Preferred Skills:* * Exposure to Lean Manufacturing Principals * Comfort identifying different types of material types and their various alloy types. * Open to learning and continuous improvement * Sense of urgency and ability to handle multiple projects at same while maintaining high quality work. *Company Culture:* We foster an environment of accountability, high-quality work, ownership, empowerment, and collaboration. Team members are encouraged to take initiative and contribute to process improvements. *Performance Metrics:* * Schedule Adherence: % of jobs completed on time * Accuracy of Travelers/Routers: Error rate in documentation * Material Availability: % of jobs started without material delays * Communication Effectiveness: Timeliness and clarity of updates to engineering and production * ERP Data Accuracy: Completeness and correctness of manufacturing methods and job details * Continuous Improvement Contributions: Number of process improvement suggestions implemented *Benefits: Full Time* * Competitive pay * 401K with match * Medical, Dental & Vision Insurance benefits * Overtime opportunities * Collaborative work environment * Growth and learning opportunities *Equal Employment Opportunity Statement:* Flotron Inc. is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Job Type: Full-time Pay: $30.00 - $37.00 per hour Expected hours: No less than 40 per week Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Health savings account * Paid time off * Vision insurance Work Location: In person