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How will you make an impact? The Supervisor Quality Assurance (QA) will provide engineering support and conduct activities to approve incoming inspection and manufacturing of Class III medical devices. This individual will work with cross functional departments to resolve product quality (mainly incoming inspection) issues. The QA Supervisor will ensure all procedures and records meet regulatory and Glaukos requirements. What will you do? Receiving Inspection: · Manage the daily activities of the department personnel by setting priorities, coordinating activities to meet project deadlines, and troubleshooting technical difficulties. · Monitor inspection activities to ensure compliance to internal procedures. · Compile data and provides reports to monitor health of the RI function. · Investigate and disposition nonconforming components identified during receiving inspection. · Initiate and investigate NCR and CAPA as appropriate. · Assist engineering in choosing proper metrology equipment such as Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. · Provide feedback to suppliers through the SCAR process. · Monitor inspection results and ensure tightening or reducing AQLs are performed according to procedure. · Assist, mentor, and guide inspectors as needed to achieve program goals. Quality System Maintenance: · Review supporting documentation for component and process changes at suppliers and component drawings and specification at Glaukos. · Monitor and ensure procedures for receiving inspection are being adhered to and in compliance with regulations. · Support the Quality System, including the CAPA process, collaborating with owners to ensure effective root cause analysis and the development of innovative, long-term solutions. · Lead process improvements in the area of receiving inspection including corrective and preventive actions and responding to audit findings. This position will also perform other duties as assigned. How will you get here? Experience · Bachelor’s Degree · 2-5+ years of relevant work experience · Knowledge of medical device manufacturing preferred · Working understanding of GDP, GMP and ISO 13485 requirements · Experience in GD&T. Able to program CMM and Smartscope is preferred. · Working knowledge of statistics as it applies to verification/ validation testing and process control, and previous use of statistical analysis software, such as Minitab · A work style of hands-on involvement with all phases of projects · Excellent documentation skills, attention to detail and accuracy · Team player, flexible multitask, good written/oral communicator · Must be organized and able to coordinate activities with internal departments and outside vendors · Experience in supplier audit and ASQ certification is a plus
Kingspan Light + Air is an award-winning innovator of high-performance daylighting and ventilation solutions for building envelopes. Our translucent walls, skylights, canopies, and smoke vents are engineered to optimize the role that natural light and air play in the design of buildings and the health and well-being of its occupants. We are currently seeking an Manufacturing Engineer who will provide engineering and technical support to ensure manufacturing goals are met. The Manufacturing Engineer will assist in reviewing existing design and developing new design of manufacturing equipment and processes. Daily tasks may include suggesting and/or implementing equipment purchases, modifications or calibration changes that result in improved productivity or reduced costs related to production. The right candidate will be familiar with standard concepts, practices, and procedures within manufacturing and will rely on experience and judgment to plan and accomplish goals. Key Responsibilities: Assist with prototyping of new designs and provide feedback to engineers regarding product design improvements. Assist in the design, fabrication, automation, and/or assembly of product and related manufacturing fixtures and tools to improve manufacturing process. Work with Engineering department to develop/implement new methods and procedures that improve flow, reduce cost, and/or improve quality, maximizing efficiency using Lean methods and tools. Performs office and computer-aided studies and prepares periodic and special reports based on findings from research, studies, and surveys; and makes recommendations on findings. Works with Engineering department to generate and implement continuous improvement ideas. Drives product/process improvement activities and provides technical leadership where appropriate. Develops, evaluates and assists in the direction of improving processes for all production activities. Establishes operating metrics which measure departmental performance on a regular basis and communicate this information to management and employees. Ensures coordination among appropriate departments in order to meet lead times and deadlines. Responsible for maintaining an environment where employees take individual responsibility for sustainable safety and quality in all aspects of their job. Ensures damage prevention of equipment through good manufacturing practices. Ensures that production labor is monitored to produce high quality standards. Qualifications: Bachelor’s degree (from ABET-accredited institution preferred) in a related engineering discipline (Mechanical, Manufacturing, Design, etc.) or equivalent experience. 5-7 years of experience in manufacturing, development and documentation (prototyping to production) required. Computer competency in word processing, spreadsheet, database, and SolidWorks software. Ability to analyze, prioritize, and multitask. Strong communication, organization and team leadership skills. Excellent mechanical and technical aptitude. G Familiar with test and measurement equipment. Ability to travel between Vista and Santa Ana facilities. At Kingspan, we believe our employees are our greatest resource. Therefore, we offer a competitive salary, benefits, and vacation package for all full-time permanent positions. Kingspan is proud to be an equal opportunity employer. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
*Overview* We are seeking a talented and motivated Manufacturing Engineer to join our dynamic team in a fast-paced manufacturing facility. The ideal candidate will be responsible for designing, implementing, and optimizing manufacturing processes to enhance productivity and efficiency. This role requires a strong background in mechanical and industrial engineering, along with proficiency in CAD software and an understanding of robotic programming. *Responsibilities* * Develop and improve manufacturing processes to enhance efficiency and reduce waste. * Utilize CAD software, such as SolidWorks, to create detailed designs and specifications for new equipment or modifications. * Program and integrate robots into the manufacturing process to automate tasks and improve production rates. * Collaborate with cross-functional teams to troubleshoot production issues and implement effective solutions. * Conduct feasibility studies for new projects, including cost analysis and resource allocation. * Implement vision inspection systems to ensure product quality and compliance with specifications. * Oversee the fabrication of components and assemblies within the manufacturing facility. * Maintain documentation related to engineering changes, process flows, and production metrics. *Qualifications* * Bachelor’s degree in Mechanical Engineering, Industrial Engineering, or a related field. * Proficiency in CAD software (SolidWorks preferred) for design purposes. * Experience with CNC machinery and programming is highly desirable. * Knowledge of robot programming techniques and applications within a manufacturing context. * Familiarity with vision inspection systems used in quality control processes. * Strong analytical skills with the ability to solve complex engineering problems effectively. * Excellent communication skills to collaborate with team members across various departments. * A proactive approach to continuous improvement initiatives within the manufacturing environment. Join us in driving innovation within our manufacturing processes while ensuring high-quality standards are met. We look forward to welcoming a dedicated Manufacturing Engineer who is eager to contribute their expertise to our team. Job Type: Contract Pay: $39.01 per hour Work Location: In person
_*Position Summary*_ Sol-ti is in search of an individual who will add value to our growing company with focused high energy and a positive attitude. The Quality Assurance Technician will monitor quality assurance activities from the receipt of raw materials to processing into the finished products and ensuring the product is within guidelines and QC specifications. A Quality Assurance Technician will convey strong leadership, ambition, and the desire to join a positive, winning team. Our ideal candidate is a resourceful, responsible, self-driven individual who would like to improve their abilities in while growing with Sol-ti. _*Career Responsibilities*_ * Inspects quality of incoming fruit loads and test samples. * Obtain and taste juice samples and juice blends and test using laboratory equipment and instruments according to lab procedures. Verifies that results conform to QC specs. * Ensures that test data is recorded on an established spreadsheet and bulk manifest daily. * Use, maintain and calibrate various laboratory equipment and instruments. * Load, unload, dispatch and receive tankers and/or other bulk juice containers. Responsible for completing related paperwork. * Completes paperwork for HACCP, juice blends, batch codes & water. Includes a visual check for water safety and chemical storage daily. * Tracks and verifies where juice is stored and ensures that data is recorded on bulk manifest on an ongoing basis daily. * Checks and verifies stock of supplies like hairnets and facemasks for QC and Production. * Updates bottling board daily and as needed throughout the shift. * Produces retain and micro samples from bottled and tanker samples. * Responsible for inspecting and maintaining chlorine titration on fruit conveyor. Also responsible for filling hand dips and footbaths as needed throughout the shift. * Verify and record temps for coolers, freezers and juice tanks and fill out QC Lab reports daily. Prep and distribute a blank grade out report to the production area _*Career Requirements/What we ask of you:*_ · Comply with all Plant, State, and Federal OSHA, EPA, FDA, HACCP, and SQF regulations. · Conduct all verification activities to assure finished products comply with food safety and quality specifications. · Responsible for No GE SGS Supply Chain Standards. · Responsible for assuring Organic Certificates of Analysis are on file. · Proficiency in Microsoft Office _*Schedule*_ Weekends as needed Monday - Friday 8pm-4:30am Job Type: Full-time Pay: $25.00 - $30.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Schedule: * 8 hour shift * Night shift * Weekends as needed Work Location: In person
We’re seeking experienced Cable Assemblers to join a high-performing team working on precision electronic and mechanical assemblies. This role involves tasks such as wiring, soldering, cable harnessing, and interpreting schematics and blueprints. *Responsibilities:* * Assemble cables, harnesses, and subassemblies using hand tools and schematics * Perform soldering and compression connections * Inspect and verify quality in accordance with control procedures * Disassemble, modify, and reassemble components as needed * Maintain a clean and safe work environment * Participate in training and continuous improvement activities *Qualifications:* * High school diploma or equivalent * Minimum 3+ years of experience in cable or electronic assembly * Ability to read schematics, blueprints, and wire lists * Familiarity with tools such as soldering irons, calipers, and tape measures * Ability to obtain a DOD security clearance * IPC620 certification and soldering certification preferred * Willingness to work overtime and flexible shifts * No C2C, C2H or similar candidates will be considered. *Apply Today!* If you’re detail-oriented, quality-driven, and ready to take on a hands-on role in a dynamic environment, we’d love to hear from you. Apply now! Job Types: Temp-to-hire, Contract Pay: $24.00 - $29.00 per hour Expected hours: No less than 40 per week Benefits: * 401(k) * Dental insurance * Health insurance * Vision insurance Application Question(s): * To be eligible for a DOD security clearance, candidates must pass a drug test and background check and be a U.S. citizen. Can you confirm that you meet these requirements? * Currently, no Corp to Corp, C2H, or similar candidates will be considered. Would that be a problem for you? Experience: * Long Haul Cable Assembly: 3 years (Preferred) License/Certification: * IPC-610 Certification (Preferred) Location: * Poway, CA 92064 (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Work Location: In person
*Job Title: Manufacturing Engineer* *Job Details:* * Manage and support capital projects (emergent and major) at the plant * Oversee up to 20 small projects simultaneously * Collaborate with operations and reliability engineering * Develop scopes, technical specs, and manage project paperwork * Coordinate contractors, equipment quotes, bidding, material delivery, and installation * Use ProjectWise for drawings and documentation * Frequent use of Excel and Microsoft Office tools (Outlook, Teams, SharePoint) * Primarily internal collaboration, with some external vendor and consulting engineer interaction *Qualifications:* * Bachelor’s degree in Engineering (Mechanical, Electrical, Civil, or related) * 2+ years engineering experience, preferably in plant/manufacturing or power plant environment * Experience with project management, budget oversight, and contractor management * Strong teamwork, communication, multitasking, and initiative skills * Familiarity or interest in Fundamentals of Engineering (FE) exam preferred, but not required Job Type: Contract Pay: $42.00 per hour Benefits: * Health insurance Work Location: In person
Assembly Technician (1st Shift) 10949 Technology Pl STE A. San Diego, California 92127 Full-Time Who We Are: PSYONIC is redefining what it means to be human through advances in bio-integrated technologies. We achieve this not only by making scientific breakthroughs in bionic prosthetic devices, but by also making them accessible to more people than ever before. In the next ten years, we expect our devices to seamlessly integrate with the human neuromuscular system. Join our bionic revolution. Responsibilities: Follow and adhere to Standard Operating Procedures, Work Instructions, assembly methods, product handling methods, current Good Manufacturing Practices, and Safety Requirements. Successfully complete training on production tasks for multiple sub-assemblies and operations. Understand the Ability Hand subassemblies, and be able to name and identify all materials and subassemblies. Understand how to use custom testing equipment needed for product builds. Perform equipment set-up, operation, and in-process inspection in order to accomplish assigned task(s). Achieve quotas set weekly and communicate progress when necessary. Perform assembly operations in other departments as required. Perform Inventory Counts. Labeling and Packaging of Medical Products. Understand and perform in-process inspection to assure workmanship and quality. Ability to train and communicate effectively with other Technicians. Skills and Abilities: Have good organization skills, personal skills, and a strong work ethic. Be able to work independently and take initiative on completing tasks. Have good communication skills. Follow instructions, respond to management direction. Understand 6S Methodology or willingness to learn. Ability to physically handle small, delicate parts. Ability to read and understand work instructions, process guidelines, and visual workmanship standards. Ability to perform delicate and repetitive tasks. Be able to use a torque screwdriver, drill, and clamps. Be able to solder. Job Type: Full-time Pay: $20.00 - $22.00 per hour Benefits: Dental insurance. Health insurance. Paid time off. Vision insurance. Schedule: 1st Shift: Monday to Friday 7am to 4pm (Flexible) 3rd Shift: Monday to Friday 1am to 9am Experience: Assembly: 2 years (Recommended) Expectations: Be able to handle repetitive tasks and keep on schedule for tasks. Assemble from motor up to drivetrain sub-assembly and memorize all components and steps. Ability to keep inventory from tasks finished and report to manager when tasks are completed. Be able to learn new skills necessary to create new components. About Psyonic: PSYONIC is redefining what it means to be human through advances in biointegrated technologies. We achieve this not only by making scientific breakthroughs in bionic prosthetic devices, but by also making them accessible to more people than ever before. In the next ten years, we expect our devices to seamlessly integrate with the human neuromuscular system. Join our bionic revolution.
Assembly Technician (3rd Shift) 10949 Technology Pl STE A. San Diego, California 92127 Full-Time Who We Are: PSYONIC is redefining what it means to be human through advances in bio-integrated technologies. We achieve this not only by making scientific breakthroughs in bionic prosthetic devices, but by also making them accessible to more people than ever before. In the next ten years, we expect our devices to seamlessly integrate with the human neuromuscular system. Join our bionic revolution. Responsibilities: Follow and adhere to Standard Operating Procedures, Work Instructions, assembly methods, product handling methods, current Good Manufacturing Practices, and Safety Requirements. Successfully complete training on production tasks for multiple sub-assemblies and operations. Understand the Ability Hand subassemblies, and be able to name and identify all materials and subassemblies. Understand how to use custom testing equipment needed for product builds. Perform equipment set-up, operation, and in-process inspection in order to accomplish assigned task(s). Achieve quotas set weekly and communicate progress when necessary. Perform assembly operations in other departments as required. Perform Inventory Counts. Labeling and Packaging of Medical Products. Understand and perform in-process inspection to assure workmanship and quality. Ability to train and communicate effectively with other Technicians. Skills and Abilities: Have good organizational skills, personal skills, and a strong work ethic. Be able to work independently and take initiative on completing tasks. Have good communication skills. Follow instructions, respond to management direction. Understand 6S Methodology or willingness to learn. Ability to physically handle small, delicate parts. Ability to read and understand work instructions, process guidelines, and visual workmanship standards. Ability to perform delicate and repetitive tasks. Be able to use a torque screwdriver, drill, and clamps. Be able to solder. Job Type: Full-time Pay: $20.00 - $22.00 per hour Benefits: Dental insurance. Health insurance. Paid time off. Vision insurance. Schedule: 1st Shift: Monday to Friday 7am to 4pm (Flexible). 3rd Shift: Monday to Friday 1am to 9am. Experience: Assembly: 2 years (Recommended) Expectations: Be able to handle repetitive tasks and keep on schedule for tasks. Assemble from motor up to the drivetrain sub-assembly and memorize all components and steps. Ability to keep inventory from tasks finished and report to manager when tasks are completed. Be able to learn new skills necessary to create new components. About Psyonic: PSYONIC is redefining what it means to be human through advances in biointegrated technologies. We achieve this not only by making scientific breakthroughs in bionic prosthetic devices, but by also making them accessible to more people than ever before. In the next ten years, we expect our devices to seamlessly integrate with the human neuromuscular system. Join our bionic revolution.
Manufacturing Operator Job Description Revised July 2020 Supervisor’s Title: Manufacturing Supervisor Department: Manufacturing Location: Carlsbad, CA Exempt Status: Non-Exempt Position Backed Up By: Manufacturing Supervisor 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 X2 Label bags 410 60 125, Zip tie liners, Tape filled boxes, Palletize boxes Hand clean separators, air flows, heat sealers, conveyors, scales, metal detectors 460 95 005, 460 95 023460 95 024, 460 95 004 and 510 95 000 Prepare cell for wash - cover electronics, remove scan gun, apply appropriate LOTO Able to identify status of equipment and cell 410 80 030 Operate hand jack Inspection of raw material and /or fill IBC (no set up) 350 60 060 Gather tools and supplies from tool room for blends or wash 410 60 004 Operate conveyor metal detector, includes HACCP metal checks 510 00 020 510 00 010 Scale Check 900 05 019 Scan in blends to NOAX Manufacturing and Inspection Cell Release 460 60 005 Seal foil and plastic liners Able to assist the operator with all blending, milling, packing tasks Identify ingredient name, lot number and item number Read and understand sequence of steps on BPR 410 80 037Screen, 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. 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 (Safe Quality Foods, Food and Drug Admin, and State Ordinance) Additional Functions Perform other duties as assigned Qualifications High School Diploma or GED preferred. Completion of all training and development requirements of a Manufacturing Operator II 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.
Who are we: Magnaflow is a leading manufacturer and supplier based in Oceanside, CA of premium products to the automotive aftermarket industry such as catalytic converters, performance exhaust and replacement exhaust. Through the Camburg division in Huntington Beach, CA. Magnaflow also supplies race-inspired performance suspension products and vehicle uplifting services, Magnaflow is focused on future growth through both new business development and new product introduction. our websites are www.magnaflow.com and www.camburg.com. Salary Range: $21.50 to $31.00 USD *Final agreed upon compensation will be based on a variety of factors including but not limited to an individual’s related experience, education, certifications, skills, and work location. A Manufacturing Machine Operator is responsible for setting up, operating, and maintaining machines used in the production process. They ensure that machinery runs smoothly, produces quality products, and operates efficiently while adhering to safety and quality standards. Responsibilities: Set up and calibrate machines and equipment for production runs based on job specifications and production schedules. Operate various machines, such as CNC machines, injection molding machines, lathes, or presses, to manufacture products according to the design and quality standards. Monitor and inspect machine outputs to ensure products meet required specifications and quality standards. Perform quality checks and adjust machines as needed. Identify and resolve issues related to machinery, product defects, or production delays. Perform basic maintenance or repairs on machines as needed. Conduct routine maintenance and cleaning of machines to ensure optimal performance and prevent breakdowns. Track production progress and adjust processes to meet deadlines. Report any irregularities or issues to supervisors. Maintain production logs, including machine settings, quantities produced, and any issues encountered during the production process. Follow all safety protocols and use personal protective equipment (PPE). Report any safety hazards or unsafe practices immediately. Work with other team members, such as maintenance technicians, quality inspectors, and supervisors, to ensure smooth production flow and resolve any operational issues. What’s in it for you? Competitive Salary PTO, Sick Pay, Birthday Holiday, Paid Holidays Medical, Dental, Vision 401k Matching (Up to 5%) Education assistance Company sponsored events Growing department and team Skills & Qualifications: Experience in operating manufacturing machinery (CNC, injection molding, presses, lathes, etc.). Basic knowledge of machine functions, troubleshooting, and maintenance procedures. Ability to monitor machine performance and ensure products meet required quality standards. Strong troubleshooting skills to quickly address machine malfunctions or production issues. Ability to stand, lift, and perform manual tasks in a manufacturing environment. Knowledge of safety procedures related to machine operation and manufacturing processes. Ability to meet production targets while maintaining quality standards. Strong collaboration and communication skills to work with other operators and team members. Education & Experience: High school diploma or equivalent (some positions may require vocational training or technical certifications in machine operation). Previous experience as a machine operator or in a manufacturing environment is typically preferred but may not be required. On-the-job training may be provided.
Quality Control Manager- Camp Pendleton Competitive Salary and EMPLOYER PAID INSURANCE! EMI Services is hiring a Quality Control Manager (QCM) to work directly with the project manager, the operations manager, the safety supervisor, as well as the United States Government. This position assures quality services to customers: reports performance levels and degrees of compliance with an established QC program. The QCM is required to test and inspect services and work performed for compliance with contract requirements and performance standards. Evaluate data and write reports to validate or indicate deviations. Recommend modifications or necessary actions to achieve optimum quality. Monitor building conditions for possible QC issues or violations, in conjunction with the Safety Supervisor. Also, monitor work assignments and projects for safety or health issues. In addition, the QCM produces and analyzes reports and makes recommendations for quality improvements, as well as, investigates complaints and report’s findings to the project manager. The ideal EMI Quality Control Manager promotes quality and customer services excellence. Salary Starting at $100,000 (DOE) plus employer paid insurance! Key Responsibilities Work closely with Project Manager, FSM, SSHO, subcontractors and QCI Staff ALL aspects Quality Control Inspection and documentation of Service and Maintenance work Develop and maintain quality surveillance and tracking system for maintenance shops and subcontractors Develop and implement QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting Advise the Project Manager on quality control and environmental program status, strategies, issues and potential problem areas Monitor and track specialized qualifications or credentials such as licenses, certificates, degrees or training needed by personnel Enforce all regulatory, base and company specific safety rules Manage Quality Control Inspectors Lead monthly QCM with Government Execute additional duties and responsibilities as assigned and/or required to complete the project Essential Skills Effective oral and written communication skills Strong organizational, interpersonal skills Type; operate a personal computer, with emphasis on accuracy, mental alertness, and neatness Demonstrated ability to work accurately, follow procedures and schedules, and prioritize multiple tasks Ability to read and understand blueprints, specifications, and contract requirements Proficiency with all MS Office products (Word, Excel, Access, PowerPoint) Ability to work successfully in a team environment, aligning with company culture and processes Must possess a strong work ethic and values that are above-reproach Understand and adhere to policies and procedures as set by EMI Services Promote and maintain a positive image of EMI Services Maintain confidentiality of information related to EMI Services, our customers, vendors and employees Be adaptable and flexible in work situations. Establish priorities to ensure completion of tasks in a timely manner Inform the Project Manager of all pertinent problems, irregularities, and other important information within area of responsibility Adhere to safety policies and procedures to include proper use of personal protective equipment Requirements High School Diploma or equivalent 5 + years of experience as a Quality Control Manager working federal projects Experience with Government Contracts and Personnel ASQ CMQ/OE Certification Safety Certification OSHA 30 hour Construction Quality Management course within 5 years Valid driver’s license compliant with REAL ID Act or are you willing and able to obtain one Pass a pre-employment drug screening and background check Regular, dependable attendance required U.S. citizenship to obtain and maintain access to military installations *This individual is subject to Government approval Preferred Qualifications Bachelor’s degree or equivalent experience (1:2 ratio) with maintenance and repair facilities Physical Requirements Carrying objects/boxes/print-outs short distances Extensive work with a personal computer Lifting and moving as much as 50 pounds with assistance Use of hands, reaching with hands and arms, talking, and walking Prolonged periods of sitting, bending, squatting, standing, twisting, or stooping Climbing ladders and entering confined spaces Work both indoors and outdoors in various temperatures (some extreme) and weather conditions *Physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Click here to follow EMI Services on Facebook Benefits Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) Employee Stock Ownership Plan (ESOP) Short Term and Long Term Disability Term Life Insurance What We Do EMI is an industry-leading provider of DoD base operation support services, facilities maintenance, and logistics. Our goal is to contribute to the repair and maintenance of buildings and equipment. EMI consistently delivers cost-saving through best-value innovations and quality service that exceeds our clients’ expectations. What Sets Us Apart The Right Partner: EMI has grown by gaining our customers’ trust and our employees’ loyalty. We’ve successfully performed over 60 service contracts and we understand the unique challenges facing today’s military. We offer exceptional responsiveness and a strong commitment to customer satisfaction. We demonstrate this commitment by consistently earning some of the highest customer satisfaction ratings in the industry. The Right Team: The EMI team includes over 250 high-achieving professionals, administrative and trades personnel deployed in various locations throughout the United States. At times, we augment our in-house capabilities with proven and capable business partners. The Right Approach: EMI brings vast expertise and proven solutions to augment our clients’ operations. We provide a platform that delivers seamless mission support and exceptional customer service in a very cost-effective and repeatable solution. #emiservices
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role We are seeking an Associate Operator role. Under close supervision, this position is responsible for a variety of assembly and non-assembly functions in support of manufacturing goals. This position will be located onsite in Carlsbad, CA. The Responsibilities Operates equipment used to manufacture products Checks and inspects products against departmental procedures Responsible for recognizing product or equipment problems that arise during the manufacturing process Maybe required to assist with the set-up and clean-up of manufacturing equipment Responsible for Lean Initiatives Carries out duties in compliance with established business policies Performs other duties & projects as assigned The Individual Required: 0 - 2 years of related experience Basic knowledge of regulations (FDA, ISO, OSHA, etc.) Demonstrates commitment to the development, implementation and effectiveness of Quidel Quality Management System per ISO, FDA and other regulatory agencies Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities Preferred High school diploma or equivalent Experience in medical device manufacturing MS Office and manufacturing systems The Key Working Relationships Internal Partners: Operators, mechanics, engineers and management The Work Environment The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Works on assignments that are routine in nature. The Physical Demands Position requires ability to lift up to 50 lbs. on a regular basis. May be required to perform repetitive manufacturing processes (e.g., manual lamination, manual cassette assembly, pouch inspection, etc.) up to 90% of workday. Walking, standing, and/or sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted. Salary Transparency The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $36,000.00 - $45,000.00 annually. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at [email protected] . #LI-HF1