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AEM website: https://aem.com.sg/ Check us out on Linked In: https://www.linkedin.com/company/aem-holdings/ *ABOUT AEM:* AEM is a global leader in test innovation. We provide the most comprehensive semiconductor and electronics test solutions based on the best-in-class technologies, processes, and customer support. We deliver customized, application-specific solutions to meet our customers’ application needs. With full-stack test capabilities for advanced engineering to high-volume manufacturing, we provide innovative test solutions to drive successful customer outcomes in innovation. AEM has a global presence across Asia, Europe, and the United States. At AEM, we are curious, creative, and collaborative, embracing agility in the way we work and think. We approach challenges from all perspectives to fuel innovation. We have a purpose: A Zero Failure World! We are a diverse team of proactive and creative problem solvers with a shared purpose. We have a culture of strengthening confidence, where ownership is encouraged, learning is supported, and ideas are empowered. You will be a valuable contributor for a unified organization, an industry leader with an innovation focus, and where being customer-centric means first investing in our people and culture. If you’re ready to Test Innovation and join the AEM family, apply today! *Position Summary* We are seeking a highly skilled *Mechanical Engineer with strong expertise in process flow development and tooling design for LTCC, HTCC, MLCC, PCBs*, and similar components. This role will support early-stage process development and lead the design, improvement, and maintenance of mechanical tooling, fixtures, and production equipment used in the manufacturing, assembly, and testing of various custom products. The ideal candidate brings hands-on experience in developing custom tooling solutions that improve throughput, accuracy, and overall manufacturability within automated production environments. This role requires a strong combination of technical expertise and process engineering capabilities. *Key Responsibilities* * Develop manufacturing process flows, progressing from high-level concepts to detailed work routings and comprehensive work instructions. * Generate documentation for production operations including manufacturing and equipment instructions, validation protocols, design control, and control plans. * Design and develop *tooling, jigs, fixtures, and assembly aids* for *LTCC, HTCC, MLCC and similar components* used in fabrication, assembly, and testing. * Create detailed *CAD models, drawings, and specifications* using mainly SolidWorks. * Support *New Product Introduction (NPI)* with custom fixtures and tooling by designing and implementing custom fixtures and tooling for both prototype and production builds. Collaborate closely with R&D to develop and refine new manufacturing techniques for various proof-of-concept initiatives. * Perform *Design for Manufacturability (DFM)* evaluations to optimize equipment performance, capacity improvements and usability. * Troubleshoot tooling and fixture-related issues and implement corrective actions. * Maintain documentation, BOMs, and engineering revisions within PDM systems. *Required Qualifications* * Bachelor’s degree in *Mechanical Engineering* or related field. * *10+ years* of experience in mechanical design, manufacturing engineering, or related areas. * Demonstrated experience designing *fixtures and tooling for LTCC, HTCC, MLCC, or PCB manufacturing.* * Proficiency in Solidworks 2023 or higher. * Strong understanding of mechanical tolerances, GD&T, and engineering standards. * Experience with machining, sheet metal, 3D printing, and rapid prototyping. * Strong analytical and troubleshooting skills. * Hands-on prototyping skills. *Preferred Qualifications* * Experience in microelectronic development and manufacturing industries. * Experience with *automation tooling* or semi-automated assembly systems. * Familiarity with thin-film and/or thick-film manufacturing environments. * Lean Manufacturing or Six Sigma exposure. *Soft Skills* * Excellent communication and teamwork abilities. * Ability to work independently and manage multiple concurrent projects. * Strong attention to detail and commitment to continuous improvement. *Company Benefits in the U.S.:* * Health insurance * Dental insurance * Vision insurance * Company Paid Life insurance * Paid time off * Sick time * EAP * 401(k) * 401(k) matching * An awesome work environment for a company who cares for their employees! *EEO Statement: * AEM is an Equal Opportunity Employer encouraging diversity in the workplace. We celebrate diversity and are committed to creating an inclusive environment for all employees. *Classification: Exempt (Salaried)* *Reports to: Engineering/Manufacturing Manager* *Job Type: Full-time. Onsite.* Job Type: Full-time Pay: $110,000.00 - $160,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Vision insurance Work Location: In person
Lead Quality Assurance Inspector Monday – Friday 8 am-4:30 pm About the Opportunity Coordinates the Quality Assurance Inspectors to inspect incoming materials, work in-process and finished goods in the production/assembly of dental parts/assemblies/finished goods to ensure conformance as defined by ISO 13485:2016, FDA regulated standards, customer specifications, and Argen requirements. In this role, the successful candidate will: Ensures Quality Inspection area is running efficiently. Makes on-the-spot personnel adjustments to keep processes on times, and communicates all adjustments to the Supervisor. Communicates clear instructions to team members. Ensures safety guidelines are followed. Facilitates team participation. Acts as a liaison between inspectors and the Supervisor. Assists the Supervisor to conduct and document training. Ensures compliance to all applicable regulations to FDA, ISO, MDSAP, OSHA, etc. Ensures completeness and accuracy of quality inspection documentation. Assists inspectors by answering questions and demonstrating inspection processes. Confirms all Quality Inspectors are up to date on their training requirements in Vivaldi. Reinforces proper adherence to required Personal Protective Equipment (PPE) for the area. Utilizes microscope, digital calipers, micrometer, optical comparator, vision measurement system, and other related equipment with optimal accuracy. Provides in-process/final inspection and testing as required. Provides inspection of outside processing (receiving inspection). Maintains proper inspection and test records. Assures that non-conforming material has been properly identified. Advises the responsible production personnel of the acceptability of products or materials based on results of testing and/or inspection. Provides solutions to technical problems and assists on special projects. Maintains lot traceability, log sheets, and good housekeeping practices at all times. Maintains a working knowledge of safety policies and regulations to ensure duties of self and others are performed in a safe manner. What does it take to be successful? High school diploma required. Previous experience working in a GMP facility a plus. 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. Knowledge of scientific products and services. Conform to all customer requirements for background checks, health and safety issues, security clearance. Exhibits leadership skills and accountability. Fast learner with high attention to detail. Strong communication skills. Excellent Customer Service Skills; display a professional can-do attitude. Perform duties with the highest regard for safety and quality. Ability to understand and follow site protocols, policies and procedures Must be flexible, forward- thinking, motivated, and have the ability to act independently. Basic computer skills including Microsoft Office with proficiency in Word and Excel. Ability to prioritize tasks and meet deadlines. Problem-solving skills. 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 and entertainment. 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. Monday – Friday 8 am-4:30 pm
Nordson Electronics Solutions, a global leader in assembly and advanced packaging stage solutions, is seeking an experienced and highly motivated individual to join our team. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment. Summary of the role As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected. Not applicable - temp to hire Interested? If you are interested in being a part of a team and creating an inclusive and diverse workplace, please apply online with your CV. About Nordson Electronics Solutions Nordson Electronics Solutions is a trusted surface treatment and precision fluid dispensing equipment supplier within the global electronics manufacturing industry, working closely with semiconductor, printed circuit board, and precision assembly manufacturers. By joining our team today, you will help us bring innovative ideas to life. Nordson Electronics Solutions is a global team that works to create machines and systems that improve the electronics and semiconductor manufacturing process. We offer a supportive culture in a growing and dynamic work environment. Whether you're just beginning your career or you're a seasoned professional, there's a place for you to belong at Nordson Electronics Solutions. We offer hourly and salary positions in production, maintenance, customer service, quality, engineering, and more. We actively invest in our teams to help you build your skillsets and advance your career.
Role: Delivery & Production Finishing Specialist at AlphaGraphics - 1205 Linda Vista Dr. Suite A, San Marcos, CA 92078 The Production Finishing Specialist is responsible for the finishing and completion of projects in the center. This Production Finishing Specialist also sometimes includes the staging/preparation of completed jobs to be delivered or shipped to our client’s final destination. BENEFITS/PERKS: Competitive Compensation Flexible Scheduling Hard work, collaboration, humanity, fun, and laughter Career path development COMPANY OVERVIEW: As an established leader in the Printing, Marketing, and Design industry, our mission is to partner with customers from local small businesses to Fortune 500 organizations and provide them with the tools and expertise needed to grow their businesses. Our tight-knit team, AlphaGraphics - US554 is actively seeking a Bindery Specialist to join us full-time. Our Production Finishing Specialist is primarily responsible for operating various machines and equipment to finish products that have been printed so they can be delivered. More than anything, we’re looking for highly-collaborative and dependable teammates who are driven by the opportunity to contribute to the success of a local business. We are a small, passionate, and fast-paced team that is fully invested in the success of our company, and we value contributions from each team member. WHAT WE EXPECT OF YOU: Read work orders to determine instructions and specifications for finishing of projects. The ability to work under pressure and manage multiple projects while meeting deadlines Operate finishing machine devices, such as cutters, folders, collators/stitchers, and other production finishing machines as available in the center to facilitate the final assembly of finished products. Maintain records, such as daily production records, using specified forms. Follow all quality control procedures as instructed by the owner or manager of the center. Any other essential functions/duties that are needed to provide the highest quality customer service and product output. WHAT YOU BRING TO THE TABLE: 2+ years of experience in operating finishing equipment associated with the print, signage or associated industries Positive, Professional Attitude Strong Work Ethic Problem Solving Skills Cooperative interpersonal skills Demonstrated ability to work quickly and neatly while multi-tasking Basic math skills and ability to use a computer Ability to lift 50 lbs safely and work over a waist-high table Strong Multi-Tasking Ability Effective Communication Skills (oral and written) Ability to follow instructions and prioritize workload Apply now if you want to become a Production Finishing Specialist with AlphaGraphics! *AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.
At Glanbia Nutritionals Inc., our portfolio centers on dairy and non-dairy nutritional ingredients. We co-innovate and deliver ingredient solutions and precision premixes for use in the mainstream food and beverage, infant and clinical, and functional nutrition markets. We are the number one provider of whey-based nutritional ingredients globally and the number one producer of American-style cheddar cheese. Our protein systems have transformed the bar and beverage categories — bringing increased levels of protein, cleaner labels and greater product functionality to market. We have a direct presence in 21 countries, with manufacturing facilities in the US, Germany and China, and international sales and technical offices around the world. Job Summary Responsible for the preparation, production and packaging of blend material. Provides assistance to the operator and fills in for basic operator duties as assigned. Maintain blend equipment and production area cleanliness. Must complete all applicable SOP and QA trainings. Essential Functions Box Room duties - tape boxes, insert foil/plastic liners, apply labels to boxes Label bags, Zip tie liners, Tape filled boxes, Palletize boxes Hand clean separators, air flows, heat sealers, conveyors, scales, metal detectors Clean drains Prepare cell for wash - cover electronics, remove scan gun, apply appropriate LOTO Able to identify status of equipment and cell Operate hand jack and power jack (certified) Inspection of raw material and /or fill IBC Gather tools and supplies from tool room for blends or wash Operate conveyor metal detector, includes HACCP metal checks Basic Sampling / Aseptic Sampling Scale Check Scan in blends to NOAX Manufacturing and Inspection Cell Release Discharge blenders out of separator (not at line speed) Seal foil and plastic liners Able to assist the operator with all blending, milling, packing tasks Identify ingredient name, lot number and item number Operate High Pressure washer and Foamer Read and understand sequence of steps on BPR Screen, blend and package a variety of amino acids, vitamins and minerals, including those which are allergenic. Responsible for following the procedures for the preparation of blends and final blend product. Proper cleaning, blending, packaging and material inspection per Standard Operating Procedures. Proper cleaning of manufacturing equipment and production floor. Assist with routine maintenance on manufacturing equipment as requested by the Operator. Regular attendance is an essential function of this position. Following and living Glanbia values: Showing Respect, Winning Together, Finding a Better Way, Performance Matters, and Customers Champion. Each employee shall comply with occupational safety and health standards and all rules, regulations, and orders issued pursuant to the Occupational Safety and Health Act which are applicable to his/her own actions and conduct. Complies with all applicable food safety regulations and mandates Additional Functions Perform other duties as assigned Qualifications High School Diploma or GED preferred. Ability to work with amino acids, vitamins and fine chemicals in powder and liquid form as well as allergen products. Ability to follow direction and work with Standard Operating Procedures. Must be able to work flexible hours to include overtime and weekends on short notice Clear command of the English language both verbal and in writing. Basic computer knowledge. Typical Physical Activity Physical Demands The physical demands described represent those that must be met by an employee and the work environment characteristics are those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Regularly involves talking or listening, sitting, and the use of hands and fingers. · Regularly involves going up and down stairs. · Frequently involves reaching with hands and arms, standing and walking. · Occasionally involves crouching, stooping, kneeling and/or climbing or balancing. Physical Requirements Must be able to lift and carry items weighing up to 55 pounds. Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. Involves moderate physical activity performing non-strenuous daily activities of a primarily administrative nature. Should be able to identify and distinguish colors, see clearly at 20 inches or closer and 20 feet or more, observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point, judge distances and spatial relationships, and adjust the eye to bring an object into sharp focus. Typical Environmental Conditions May be exposed to moderate noise levels (i.e. office equipment, light traffic). May be exposed to moderate to high noise levels (i.e. production equipment, forklifts, heavy traffic). May be exposed to humidity, intense heat and cold, outdoor weather conditions, and fumes and toxic chemicals. May work in areas with mechanical moving parts, above ground with risk of fall, or areas with risk of electrical shock. Travel Requirements N/A Disclaimer Must perform the essential duties and responsibilities with or without reasonable accommodation efficiently and accurately without causing significant safety threat to self or others. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia our culture will celebrate individuality, knowing that together we are more.
At Glanbia Nutritionals Inc., our portfolio centers on dairy and non-dairy nutritional ingredients. We co-innovate and deliver ingredient solutions and precision premixes for use in the mainstream food and beverage, infant and clinical, and functional nutrition markets. We are the number one provider of whey-based nutritional ingredients globally and the number one producer of American-style cheddar cheese. Our protein systems have transformed the bar and beverage categories — bringing increased levels of protein, cleaner labels and greater product functionality to market. We have a direct presence in 21 countries, with manufacturing facilities in the US, Germany and China, and international sales and technical offices around the world. Job Summary Responsible for the preparation, production and packaging of blend material. Provides assistance to the operator and fills in for basic operator duties as assigned. Maintain blend equipment and production area cleanliness. Must complete all applicable SOP and QA trainings. Hourly Pay: $21.12 Essential Functions Box Room duties - tape boxes, insert foil/plastic liners, apply labels to boxes Label bags, Zip tie liners, Tape filled boxes, Palletize boxes Hand clean separators, air flows, heat sealers, conveyors, scales, metal detectors Clean drains Prepare cell for wash - cover electronics, remove scan gun, apply appropriate LOTO Able to identify status of equipment and cell Operate hand jack and power jack (certified) Inspection of raw material and /or fill IBC Gather tools and supplies from tool room for blends or wash Operate conveyor metal detector, includes HACCP metal checks Basic Sampling / Aseptic Sampling Scale Check Scan in blends to NOAX Manufacturing and Inspection Cell Release Discharge blenders out of separator (not at line speed) Seal foil and plastic liners Able to assist the operator with all blending, milling, packing tasks Identify ingredient name, lot number and item number Operate High Pressure washer and Foamer Read and understand sequence of steps on BPR Screen, blend and package a variety of amino acids, vitamins and minerals, including those which are allergenic. Responsible for following the procedures for the preparation of blends and final blend product. Proper cleaning, blending, packaging and material inspection per Standard Operating Procedures. Proper cleaning of manufacturing equipment and production floor. Assist with routine maintenance on manufacturing equipment as requested by the Operator. Regular attendance is an essential function of this position. Following and living Glanbia values: Showing Respect, Winning Together, Finding a Better Way, Performance Matters, and Customers Champion. Each employee shall comply with occupational safety and health standards and all rules, regulations, and orders issued pursuant to the Occupational Safety and Health Act which are applicable to his/her own actions and conduct. Complies with all applicable food safety regulations and mandates Additional Functions Perform other duties as assigned Qualifications High School Diploma or GED preferred. Ability to work with amino acids, vitamins and fine chemicals in powder and liquid form as well as allergen products. Ability to follow direction and work with Standard Operating Procedures. Must be able to work flexible hours to include overtime and weekends on short notice Clear command of the English language both verbal and in writing. Basic computer knowledge. Typical Physical Activity Physical Demands The physical demands described represent those that must be met by an employee and the work environment characteristics are those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Regularly involves talking or listening, sitting, and the use of hands and fingers. · Regularly involves going up and down stairs. · Frequently involves reaching with hands and arms, standing and walking. · Occasionally involves crouching, stooping, kneeling and/or climbing or balancing. Physical Requirements Must be able to lift and carry items weighing up to 55 pounds. Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. Involves moderate physical activity performing non-strenuous daily activities of a primarily administrative nature. Should be able to identify and distinguish colors, see clearly at 20 inches or closer and 20 feet or more, observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point, judge distances and spatial relationships, and adjust the eye to bring an object into sharp focus. Typical Environmental Conditions May be exposed to moderate noise levels (i.e. office equipment, light traffic). May be exposed to moderate to high noise levels (i.e. production equipment, forklifts, heavy traffic). May be exposed to humidity, intense heat and cold, outdoor weather conditions, and fumes and toxic chemicals. May work in areas with mechanical moving parts, above ground with risk of fall, or areas with risk of electrical shock. Travel Requirements N/A Disclaimer Must perform the essential duties and responsibilities with or without reasonable accommodation efficiently and accurately without causing significant safety threat to self or others. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia our culture will celebrate individuality, knowing that together we are more.
POSITION SUMMARY: Manages the Manufacturing Engineering department, responsible for developing, improving, and sustaining manufacturing processes to support both daily production and new product introduction (NPI). This role oversees the design and deployment of production methods, tooling, fixtures, and test strategies to ensure efficient, compliant, and scalable operations. The manager ensures that manufacturing engineering practices align with Safety, Quality, Delivery, and Cost (SQDC) objectives and support consistent execution of the Ascential Production System. This includes driving operational readiness, supporting production issue resolution, and enabling effective design transfer through close collaboration with cross-functional partners in Engineering, Quality, Supply Chain, and Production. This role emphasizes continuous improvement, operational excellence, and the successful integration of new technologies and corporate initiatives. The manager is also responsible for resource planning, technical mentorship, performance development, and fostering a culture of accountability and problem-solving across the department. ESSENTIAL FUNCTIONS: These may include, but are not limited to: Directly manage and develop manufacturing engineering staff, including goal setting, performance reviews, and individual development plans. Lead the evaluation and hiring of new employees that meet the required technical qualifications and interpersonal skills. Collaborate with leadership team to prioritize team workload across multiple programs, balancing sustaining support, CI initiatives, and NPI deliverables. Implement and manage resource planning and project management tools. Actively manages the SIOP process as related to manufacturing engineering resources. Monitor progress toward key project milestones, ensuring engineering deliverables meet deadlines, quality standards, and cost targets. Serve as a key liaison between Engineering, Production, Quality, Supply Chain, and Client teams. Support business development by contributing to proposals, estimating manufacturing engineering scope, and allocating preliminary resources during quoting or early engagement phases. Provide technical direction on meeting regulatory and quality system requirements, including FDA 21 CFR 820, ISO 13485, and client-specific standards. Guide risk management activities such as PFMEAs, control strategies, and mitigation planning throughout the product lifecycle. Ensure engineering practices support design transfer, traceability, and compliance with documentation, testing, and production readiness standards. Provide oversight and resource alignment for New Product Introduction (NPI), including process development, design transfer, manufacturability, and production readiness. Support corporate initiatives by preparing NPI programs for transition to lower-cost sustaining sites once production is stabilized. Actively engages in manufacturing engineering activities across multiple projects, demonstrating leadership by example. Monitor and evaluate project and department progress and results. Execute the Ascential Production System by owning and maintaining the Manufacturing Engineering Tier board. Monitor key KPIs and lead the department’s alignment with SQDC metrics. Utilize the PDCA process to identify, prioritize, and resolve production issues, and ensure engagement of the manufacturing engineering team across all projects. Drive the application of Lean and Built-in Quality principles, including right-sized workstations, single-piece flow, poka-yoke, and 5S implementation. Lead cross-functional process improvement events—including 3P, Kaizen, and value stream mapping (VSM)—by assessing operational needs, planning and facilitating workshops, and delivering executive-level report-outs on outcomes and recommendations. Coach and mentor team members through standard work, Gemba practices, structured problem-solving, and root cause analysis Track departmental budgets and support cost control initiatives tied to SQDC goals. Ensure all manufacturing engineering projects, initiatives, and processes are in conformance with organization’s established policies and objectives Prepare and deliver internal reports and client-facing updates as needed. Perform administrative functions such as approving expenditures, approving timecards, enforcing rules, and making decisions about the purchase of materials or services. Assess and manage capital expenditure needs for equipment, tooling, and test systems; lead justification, approval, and implementation processes. Serve as a key contributor to site-level execution of corporate strategic initiatives, including MES deployments, QMS enhancements, and the integration of emerging technologies such as AI and advanced analytics. Contribute to process governance and continuous improvement at both the site and enterprise level, ensuring better alignment in tools, processes, and KPIs across sister facilities. EDUCATION, EXPERIENCE, SKILLS AND ABILITIES REQUIRED: Education: Bachelor’s degree from accredited four-year college or university (preferably in engineering), or a combination of education, certification and experience which fulfill the essential knowledge, skills and experience required for this position. Experience: 8+ years of manufacturing/process development experience, with technical staff management experience. Prior experience in medical device manufacturing preferred. Essential Knowledge, Skills & Abilities: Solid technical foundation in one of the engineering disciplines. Experience with statistical techniques (e.g., DOE, SPC). Experience with Lean manufacturing techniques, value stream mapping, and continuous improvement methodologies. Solid people management and communication skills. Solid knowledge of GMP, ISO regulations. Prior experience leading Lean and 6 Sigma initiatives Demonstrated leadership skills. Ability to “get things done” in a growing organization – willingness to fill gaps and wear multiple hats. Knowledge of key manufacturing processes and methodologies. Knowledge and understanding of effective manufacturing principles (line layout, throughput, utilization, cycle time, process capability, process control, ECO process). Excellent communication and presentation skills (written and oral). Ability to predict key risk areas and determine mitigation steps. Ability to assess complex situations, review possible alternatives, and determine the best path forward (often with incomplete data). Ability and willingness to have challenging program conversations with clients and/or employees when required (in a timely and professional manner). Knowledge of Design Transfer processes, complexities, and best practices. Knowledge and understanding of root-cause analyses and problem solving tools (8D, FMEA, fishbone diagrams, and other decision making tools, etc.) Knowledge of regulatory processes and requirements (CE, UL, FDA, etc.) Job Complexity: Works on issues where analysis of situations or data requires an in-depth knowledge of organizational objectives. Implements strategic policies when selecting methods, techniques, and evaluation criteria for obtaining results. Establishes and assures adherence to budgets, schedules, work plans, and performance requirements. Supervision: Monitors work operations of exempt and/or non-exempt employees on a daily basis and actively assists or provides direction to staff as required. Responsible for department results, including costs, methods and staffing. Basic Office Skills: Equipment: PC, scanners, voice mail and e-mail systems, and common office machines or ability to be trained. Software Knowledge: Windows, MS Office (Word, Excel, Access, PowerPoint) Effort Required: Physical Activities: On a continuous basis, sit at desk for a long period of time; write or use a keyboard to communicate through written and oral means. Intermittently answer telephone. Some walking and lifting up to 20 lbs. may be required. The noise level in the work environment is usually moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Travel: This position may require some travel (domestic and international). This is a regular fulltime on-site position in San Diego. Starting salary range based on experience and business need: $147,000-$165,000
_Quality Assurance Associate_ *Qualifications:* * Bachelor’s degree, biology or related field preferred but not required * Familiarity with cGMP, ISO 13485 requirements, FDA, and international quality * Computer skills *Duties and Responsibilities* * Stay current with all regulatory procedures and documentation in order to maintain compliance with GMP, QSRs, FDA, ISO, CE and customer requirements. * Develop procedures and practices to optimize product quality, safety, and reliability. * Work with Production and R&D to review and optimize or develop validation protocols. * Ensure compliance of product labeling and advertising. * Examine product release lot packets and review/verify product quality for product releasing. * Document and maintain accurate records of quality assurance activities, including but not limited to lot packets, SOPs, water quality records, temperature records and other investigations. * Develop or edit QSR SOPs; Production SOPs; product design history files, Instruction for Use, etc. * Make sure all documents complying with ISO13485:2016, US FDA and MDSAP standards, and fit Epitope’s operational procedures. * Prepare quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. * Participate in internal audits and assessments to identify non-compliances and areas for improvement. * Participate in the validation of equipment, procedures, and systems to ensure compliance with quality standards. * Take on growing responsibilities for FDA audit, ISO surveillance audits and customer audits. * Assist in EU IVDR, FDA 510(k) and other countries product registrations. * Play a key role in daily department operation to achieve delivering quality products to customers and reach customer satisfaction. It is the policy of Epitope Diagnostics to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Epitope Diagnostics will provide reasonable accommodations for qualified individuals with disabilities. Job Type: Full-time Pay: $52,000.00 - $72,000.00 per year Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off Work Location: In person
About Our Company MDI Advanced Systems USA Inc. was established in February 2024 as the U.S. branch of MDI (Mitsuboshi Diamond Industrial Co., Ltd., Osaka, Japan). MDI is a leading equipment manufacturer specializing in precision processing technologies, including scribing, breaking, drilling, and patterning. We provide proprietary cutting tools, laser systems, and automated equipment designed to achieve high productivity. Since 1935, we have applied patented cutting technologies to glass and other hard and brittle materials. Our equipment and tools also support multi-layered structures, including metal and organic materials. Position Overview * Job Title: Process Engineer * Job Type: Full-time * Classification: Exempt (Managerial / Professional) * Visa Sponsorship: Not available * Location: San Diego, CA 92121 – Onsite * Work Schedule: Monday–Friday (Saturday, Sunday, and holidays off) * Relocation: Candidates must be willing to relocate prior to start date * Travel: Domestic and international travel required (including Japan); travel allowance provided Job Description As a Process Engineer, you will: * Test and evaluate customer samples using our singulation (cutting/dividing) equipment * Interact closely with customers and collaborate with headquarters in Japan * Prepare detailed technical reports * Analyze and interpret test results * Travel as needed for business purposes Minimum Qualifications * Bachelor’s degree in Engineering or a related field * Entry-level candidates encouraged to apply * Ability to work onsite and travel internationally * References required after interview _Note: Relocation assistance is not provided._ Compensation * Salary: $66,560 – $85,000 per year Benefits * 401(k) Plan with Matching * Health, Dental, and Vision Insurance * Paid Time Off (PTO) and Sick Leave * Travel allowance for business trips We provide a competitive compensation and benefits package along with a flexible work schedule that supports work-life balance. Equal Employment Opportunity & Background Check MDI Advanced Systems USA Inc. is an Equal Opportunity Employer. Employment is contingent upon successful completion of a background check in accordance with applicable law. At-Will Employment Employment with MDI Advanced Systems USA Inc. is on an at-will basis. This means that either the employee or the company may terminate employment at any time, with or without cause or notice, in accordance with applicable law. Job Type: Full-time Pay: $66,560.00 - $80,000.00 per year Benefits: * 401(k) matching * Dental insurance * Health insurance * Vision insurance Ability to Relocate: * San Diego, CA 92121: Relocate before starting work (Required) Work Location: In person
Malin Space Science Systems (MSSS) is a private technology company that designs, develops and operates space camera systems for government and commercial aerospace customers and provides services in spacecraft instrument operations and space science research. As a member of our multidisciplinary space imaging systems design team, the Flight Assembly Technician is responsible for high-level assembly of prototype and spaceflight electronics under the direction of the Production Manager, utilizing applicable preferred certifications and technical expertise to run production equipment. *Essential Functions* * Assembles electronic, mechanical, optical, and cable harness assemblies by following detailed work instructions and applicable NASA and IPC workmanship standards. * Responsible for operating Surface-Mount Technology (SMT) reflow machine. * Processes and operates X-Ray machine per project guidelines. * Operates Automated Optical Inspection (AOI) machine. * Prepares and operates Parylene conformal coating machine. * Maintains detailed assembly records according to company and industry standards. * Assists hardware engineering in assembly of prototype electronics and cable harnesses, testing, troubleshooting, and mechanical integration. * Maintains all required NASA and IPC trainings and recertifications. * Performs ESD check-in on a daily basis. * Cross-trains in assembly disciplines to support all aspects of work completion. * Participates in team meetings and provides updates on work status. * Maintains work area, tools and equipment. Performs required maintenance as needed. * Prior to entering assembly, test, storage or development areas within the Camera Systems Group unescorted, receive initial and ongoing annual training in the fundamentals of Electrostatic Discharge (ESD). *Non-Essential Functions* * Travels to customers and/or vendors as required. * Performs other duties as required or requested which may become essential to this position. *Minimum Qualifications* * High-School Graduate / GED required. Some college or Trade School / ROP certification desired. * Minimum of 3 years of solder assembly experience. * Minimum of 5 years of operating experience with either SMT, AOI, Parylene or X-Ray machines. * Excellent hand soldering, cable harness assembly, mechanical assembly, documentation, organization, and communication skills. * Excellent attention to detail and ability to work closely with each member of a production team. * Must be able to read schematics and mechanical drawings and precisely follow detailed written instructions. * J-STD-001 certification is required. Space Addendum certification is preferred and is a requirement to perform the position. * Polymerics mix and application experienced preferred; will be required to obtain NASA-STD 8739.1 certification. * Must be computer literate with knowledge of MS Excel and Word. * Results-oriented, self-motivated and dependable. * Hands-on machinist experience for manufacturing test fixtures is preferred. * Ability to work outside of regular business hours. * Occasional travel to customers and/or vendors may be required. *Physical Requirements* Must be able to remain in a stationary position operating lab equipment for periods of time. Must be able to perform repetitive soldering tasks under a microscope to properly position hardware. Ability to inspect parts and assemblies under a microscope to determine product placement. Ability to work and move around in a cleanroom environment, wearing required outer garments including smock/coveralls, shoe covers, mask, goggles, hood, gloves and ESD wrist strap. Must be able to communicate clearly with a variety of people on a daily basis. Must be able to traverse spaces in and around the office, labs, and machine shop as applicable. Ability to lift and carry up to 10 lbs. as needed. Possess mental acuity at a level which will facilitate execution of complex technical instructions. Ability to practice safe driving habits while following all state safety regulations and standards.Ability to handle high stress levels in connection with multiple conflicting priorities and deadlines. High tolerance for ambiguity and shifting expectations. Ability to travel to customers and/or vendors locations. *Disclaimer* The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. The Employer retains the right to change or assign other duties to this position. _MSSS is committed to providing equal employment opportunities to all individuals, regardless of any protected status, including veterans and individuals with disabilities._ Job Type: Full-time Pay: $32.00 - $34.00 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Life insurance * On-the-job training * Paid sick time * Paid time off * Parental leave * Vision insurance Work Location: In person
*Engineering Manager, Product Development* Location: Carlsbad, California Schedule: Full Time, Day Shift, On-Site *Position Summary* Lumos Diagnostics is seeking an Engineering Manager, Product Development to lead engineering execution supporting the FebriDx platform and future product initiatives. This is a hands-on leadership role responsible for delivering technically sound, manufacturable, and compliant engineering solutions across the product lifecycle. The Engineering Manager leads a small team of engineers while actively contributing to product and process development, ensuring alignment with business priorities, project timelines, and quality standards. This role partners closely with Product, R&D, Quality, Manufacturing, and Operations to advance product improvements, support manufacturing readiness, and strengthen engineering processes as the organization continues to scale. *Essential Duties and Responsibilities* · Lead engineering execution in support of new product development and enhancements to existing product lines · Provide technical direction to engineers to ensure solutions are feasible, manufacturable, and aligned with performance and quality requirements · Support projects from development through commercialization while maintaining accountability for engineering deliverables and timelines · Identify technical risks early and collaborate with cross-functional partners to develop mitigation plans · Participate in design reviews and support verification, validation, and documentation activities within regulated quality systems · Directly manage engineers by providing coaching, feedback, and performance management · Prioritize workload, set expectations, and ensure team members are positioned for success · Foster a collaborative and accountable team culture · Partner cross-functionally with Product, R&D, Quality, Manufacturing, and Operations to support technical execution · Support transfer to manufacturing activities including process development, yield improvement, validation, and production support · Communicate progress, risks, and recommendations clearly to stakeholders and leadership · Contribute to development and refinement of engineering best practices and processes · Support root cause analysis and corrective actions related to product or manufacturing issues · Perform other duties as assigned *Minimum Qualifications* · Bachelor’s degree in Engineering or related technical discipline such as Mechanical, Manufacturing, or similar · Five or more years of progressive engineering experience in product development or regulated environments · Prior experience leading or supervising engineers · Experience supporting cross-functional product development initiatives · Experience with design for manufacturability and process development · Experience supporting product transfer to manufacturing and production scale · Experience working within FDA or ISO 13485 regulated environments · Strong technical problem solving and execution skills · Demonstrated ability to manage competing priorities and deliver projects against timelines · Strong interpersonal skills with the ability to collaborate effectively across cross-functional teams *Compensation* Annual salary range: $140,000 to $170,000 depending on internal equity, experience, and qualifications This position is eligible for a discretionary annual performance bonus based on individual and company performance *Benefits* Comprehensive benefits package including medical, dental, vision, life insurance, and disability coverage 401(k) with employer match Three weeks of vacation accrued annually Sick time, paid holidays, and a floating holiday *About Lumos Diagnostics* Lumos Diagnostics develops, manufactures, and commercializes innovative diagnostic solutions that deliver reliable results at the point of care. Our culture is guided by our core values Take Ownership Engage Openly Act with Integrity Move Together *Work Environment* This role is primarily performed on-site in an office, laboratory, and manufacturing environment working standard day shift hours *Why Join Lumos* You will have the opportunity to lead impactful engineering initiatives, work cross-functionally, and contribute to innovative product development in a collaborative environment *Screening Question Instruction Note* All screening questions must be answered in full for consideration for this role. Incomplete applications may not be reviewed. Pay: $140,000.00 - $170,000.00 per year Benefits: * 401(k) * 401(k) 4% Match * 401(k) matching * AD&D insurance * Dental insurance * Disability insurance * Employee assistance program * Employee discount * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid jury duty * Paid time off * Parental leave * Professional development assistance * Tuition reimbursement * Vision insurance Application Question(s): * How many years of progressive engineering experience do you have in product development or regulated environments? * Do you have experience working in a regulated environment such as FDA, ISO 13485, or similar quality systems? * Do you have prior experience leading, supervising, or managing engineers or technical teams? * How many years of people leadership experience do you have? * Do you have experience supporting product development from concept through commercialization? * Do you have experience with design for manufacturability and supporting transfer to manufacturing? * 9. Which of the following areas do you have hands-on experience with? • Product development engineering • Process development • Manufacturing support • Validation activities • Root cause analysis and CAPA • Automation or equipment development • None of the above * This role is a full-time, on-site position in Carlsbad, California working a day shift schedule. Are you able to meet these requirements? * 13. This role has an annual salary range of $140,000 to $170,000 depending on experience and internal equity. Are you comfortable with the offered range? Education: * Bachelor's (Required) Shift availability: * Day Shift (Required) Ability to Commute: * Carlsbad, CA 92010 (Required) Work Location: In person
Position Summary The Quality Assurance Technician ensures food safety, quality, and compliance across all production activities. This role is critical in supporting manufacturing by identifying risks, conducting inspections, and verifying that all regulatory and Suja standards are met. This is an on-site position within a production environment and reports to the QA Supervisor. Schedule 1:00 PM - 9:30 PM Sunday-Thursday, with flexibility for OT on Friday's Essential Duties and Responsibilities Monitor production conditions, specifications, process controls and tracking controls Monitor wash line concentrations and test ppm concentrations for sanitation bucket and floor solutions Monitor a system that will verify checks on existing production control forms and be audited on the same forms that meet all program requirements. Collect Lab retain samples Verify all CCPs on-line and take corrective actions whenever necessary to assist in determining the root cause and development of a preventative action plan Responsible for checking the pH levels, temperature and brix of each batch of juice produced and is with in product specifications Verify and document Facility Operation Inspections & Good Manufacturing Practices Enforce Good Manufacturing Practices (GMPs) throughout the manufacturing areas Perform Standard Sanitation Operational Procedures (SSOPs) verification and ATP swabs Tracks non-conforming product (Holds) Perform pre-operational inspection procedures of all production/bottling equipment and facility Verify equipment calibrations. Verify volumes, lot codes, torques & bottle weights are within product specification. Complete and enter into database all pallet tags and CCP forms for production and bottling. Record cycles and verify that all HPP settings and information is correct Perform metal mesh, magnet and sock mesh inspections Verify production lot codes, labels, mold number and packaging are within product specification Shipping and receiving verifications. Verification of all raw materials being delivered and labelled with accurate information at Receipt (product name, lots, expirations, quantity received) COA Reviewing, comparing to the specification, approving and filing the COA. Escalating or placing on hold any items that are out of compliance. Review and Verify receiving documents and logs. Monitors production conditions, specifications, process controls and tracking controls as they specifically relate to raw materials used in production. Document and maintain records for all raw materials used in the production process including disposals, usage, and pre-batching of ingredients. Materials will be logged on the appropriate batch ticket for raw material commodity of interest. Commodities include raw produce, frozen juice, frozen puree, dry ingredients and aseptic products. Inspect raw materials for deficiencies relating to appearance, texture, and/or odor before production use. Inspect incoming trailers to ensure compliance with receiving standards. Report any food safety problems to the SQF Practitioner or Department Supervisor in a timely manner so that corrective actions may be performed. Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Regular and reliable attendance. Job Qualifications 1–2 years of experience in Quality Control and/or the food industry preferred Familiarity with food safety regulations is a plus Other Skills & Abilities Excellent communication skills Strong computer proficiency Sharp critical thinking and problem-solving abilities Flexible and able to adapt to change Capable of working independently with moderate supervision Comfortable in a fast-paced production setting Working Conditions This role operates in a food manufacturing environment. Frequent standing, walking, and exposure to cold or wet areas are expected. Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Hourly Pay: $20.00 Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #ZR #INDHP Suja Life is proud to be an equal-opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay.