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Ascential Medical and Life Sciences is a leader in delivering precision engineering and automation solutions for medical devices, diagnostics, and life sciences. We are looking for a Sr Manufacturing Engineer to join our multidisciplinary team, contributing to cutting-edge projects that drive innovation in healthcare and diagnostics. POSITION SUMMARY: The Senior Manufacturing Engineer is a hands-on technical leader responsible for developing, improving, and sustaining manufacturing processes for regulated instruments and devices, including FDA Class II products. This role plays a critical part in driving operational excellence through built-in quality, lean manufacturing, structured new product introduction (NPI), and alignment with plant-level SQDC goals (Safety, Quality, Delivery, Cost). The ideal candidate thrives in a low- to mid-volume, high-mix environment and excels at cross-functional collaboration, process rigor, and systems thinking. ESSENTIAL FUNCTIONS: Process Development & Built-In Quality: Lead the design, development, validation, and implementation of robust assembly and test processes, including IQ/OQ/PQ and equipment qualification. Apply Built-in Quality principles to manufacturing line design, including: Single-piece flow where applicable Right-sized and ergonomically optimized workstations Task segmentation to reduce complexity and rework 5S workplace organization and visual controls Integration of poka-yoke (error-proofing) mechanisms Design and release work instructions, process documentation, and in-process controls to ensure repeatable and scalable manufacturing. Continuous Improvement & Lean Manufacturing: Drive continuous improvement initiatives using Lean tools (e.g., value stream mapping, standard work, visual management). Conduct time and motion studies, line balancing, and workstation optimization to improve efficiency and reduce waste. Support tier-based escalation and visual factory systems to monitor and resolve Safety, Quality, Delivery, and Cost (SQDC) issues on the floor. Implement data-driven process controls to reduce variability and increase yield. Lead root cause investigations and corrective actions (CAPA) to address systemic production issues. New Product Introduction (NPI) & Client Integration: Act as the manufacturing lead for NPI, owning process development and validation deliverables throughout the product lifecycle. Collaborate with R&D, client engineering, and internal stakeholders to ensure design-for-manufacturability (DFM), smooth design transfer, and process readiness. Define and execute NPI activities such as PFMEA, pilot build support, validation plans, and readiness reviews. Serve as the technical point of contact for client engagements, audits, and feedback loops related to manufacturability and scalability. Documentation, Change Control & Compliance: Maintain controlled documentation including work instructions, BOMs, test protocols, and validation records in accordance with ISO 13485 and FDA 21 CFR 820. Initiate and process Engineering Change Orders (ECOs) and Document Change Orders (DCOs) to ensure technical documentation is up to date and reflects approved changes. Ensure robust configuration control across drawings, specifications, and revision history. Own or support Nonconformance Reports (NCRs) by conducting root cause analysis, implementing containment and corrective actions, and collaborating with Quality and Production. Participate in or lead Material Review Boards (MRBs) to disposition nonconforming material and drive resolution. Cross-Functional Collaboration: Work closely with Quality, Supply Chain, Planning, and Production teams to resolve issues, implement improvements, and meet customer and regulatory requirements. Translate client product requirements into manufacturable solutions and operational procedures. Represent manufacturing in client meetings, audits, and design reviews. Leadership & Mentorship: Provide technical mentorship to junior engineers and manufacturing support staff. Lead Kaizen events, RCCA investigations, and continuous improvement initiatives across departments. Contribute to the development and tracking of engineering and production metrics in alignment with SQDC performance indicators. Support tier-based daily management systems to ensure timely escalation, resolution, and communication of key operational issues. EDUCATION, EXPERIENCE, SKILLS AND ABILITIES REQUIRED: Education & Experience: Typically requires 5+ years of experience, and a mechanical, electrical or industrial engineering Bachelor’s degree from four-year College or university, or the equivalent combination of education, experience and training that provides the required knowledge, skills and abilities. Job Complexity: Works on problems of diverse scope and high complexity, often with incomplete or ambiguous information. Requires in-depth analysis and a strong understanding of manufacturing systems, regulatory constraints, and client expectations. Exercises sound judgment in selecting methods, techniques, and evaluation criteria to develop scalable and compliant solutions. Independently drives initiatives while building strong internal and external relationships across engineering, quality, production, and client teams. Knowledge, Skills & Abilities: Strong knowledge of manufacturing principles including Lean, Built-in Quality, 5S, single-piece flow, poka-yoke, throughput, utilization, and process capability. Skilled in PFMEA, control plans, process validation (IQ/OQ/PQ), and test method development. Experienced with root cause analysis (8D, 5 Whys, fishbone), CAPA, SPC, Gage R&R, and risk-based quality tools. Proficient in interpreting mechanical drawings, GD&T, electrical schematics, and BOMs. Familiar with mechanical and electromechanical components (motors, gears, sensors, adhesives, fasteners, fluidic systems, optics systems, and PCBAs). Understanding of fabrication and assembly methods including machining, molding, welding, and surface treatments. Knowledge of FDA 21 CFR 820, ISO 13485, and regulatory compliance practices (CE, UL). Experience with ECOs, DCOs, NCRs, MRB, and configuration control processes. Ability to support NPI from prototype through production and engage directly with clients on design transfer and manufacturability. Effective in cross-functional collaboration and tiered issue escalation aligned with SQDC (Safety, Quality, Delivery, Cost) performance metrics. Proficient in CAD (SolidWorks preferred), ERP/document control systems, and MS Office; experience with test automation or simulation tools is a plus. Strong communication, problem-solving, presentation, and mentorship skills. EFFORT REQUIRED: Physical Activities: This position primarily requires the ability to sit at a desk and work on a computer for extended periods of time, including frequent use of a keyboard and other standard office equipment for written and electronic communication. The role occasionally involves walking through production areas, standing during inspections or meetings, and lifting objects up to 25 pounds. Telephone communication may also be required intermittently. The work environment includes both office and manufacturing floor settings, with a typical noise level that is moderate. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. TRAVEL: This position may require some travel for up to 10% of the time. This is an on-site position in San Diego with an annual salary range of $100,000 - $137, 000, based on experience and qualifications Compensation is based on several factors including experience, skills, education, and job-related knowledge. In addition to base salary, Ascential offers a comprehensive benefits package.
Company Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $18.00 - $21.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Quality Inspector you will: The Quality Inspector is responsible for upholding current safety policies and oversees the product development process to ensure that all products meet quality standards. The Quality Inspector is also responsible for performing tests on products at various stages of production to ensure that customer specifications, blueprint, and Purchase Order requirements are being met and company quality standards are followed. What will my responsibilities include? Final inspection of product to ensure compliance to customer technical specifications, blueprint and Purchase Order requirements. Inspect, test and/or measure materials or products being produced. Document FAI measurement results and complete AS9102 First Article Inspection Reports. Act as liaison with other departments and organizations. Provide leadership, technical advice and council to team members. Investigate, recommend, and implement process improvements that effect quality, cost and speed. Reports quality problems or finds to QA Manager and follows up to ensure corrective action takes place. Maintains record of inspections and prepares lists of defects, interacts with other departments to ensure compliance with specifications and to facilitate the acceptance of parts. Ensure that all quality check procedures put in place by the company are followed during every production phase. Must take full responsibility for product that is shipped to Customers Other reasonable duties as business and operational needs dictate Qualifications What key skills and experience do I need? Minimum 1 year of experience related to QA engineering in a manufacturing environment Ability to read and interpret blueprint drawings Knowledge of measuring gauges, calipers, and instruments Must be able communicate and interact effectively with employees at all levels of the organization, both verbally and written Education and Experience: High School Diploma or equivalent Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor
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