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Entry Level Production Technician - (Night-Shift) Compensation: $20.00 per hour Employment type: Full-time Job title: Production Technician l Toray is a Worldwide manufacturer of high-quality water treatment products in Poway, who is seeking a motivated production assembler! This position is direct-hire, temporary, employment. We are seeking workers who can work the following shift (shift openings are based on business need/availability): Schedule: 11-hour Shift (6 pm - 6 am, with two (2) 30-minute unpaid meal breaks): Rotating Shift Schedule (Week 1 you work: Mon, Tues, Fri, Sat; Week 2 you work Sun, Wed, Thur) Requirements: An ability to read, understand, and communicate (both oral and written) in English. Basic math skills. An ability to safely use measuring and cutting tools. Good manual dexterity. Physical ability to lift, push, or pull up to 50 lbs. Awareness of the importance of attendance and good attendance records. Experience in a manufacturing environment is a plus but not required. Benefits: 100% Employer paid health care 401k with match 11 paid holidays a year PTO (Paid Time Off) and Sick time Yearly performance reviews EAP (Employee assistance programs) All candidates considered for hire must successfully complete a background check and employment health screening and must be able to maintain regular, reliable attendance in compliance with company policy. About Toray Membrane USA, Inc. Toray Membrane USA, Inc. is a worldwide manufacturer of high-quality water treatment products in north San Diego, CA. We strive to build long-lasting relationships with our employees, customers, business partners, and stakeholders. Since our establishment in 2007 in Poway, CA, as a subsidiary of Toray Industries, Inc. (founded in 1926 and headquartered in Tokyo, Japan), Toray Membrane USA, Inc. has experienced steady growth. With products backed by years of R&D and experience, such as reverse osmosis (RO), nanofiltration (NF), ultrafiltration (UF), microfiltration (MF), and membrane bioreactor (MBR) membranes manufactured in the United States, we have evolved into a critical player in Toray's water treatment business in North America, providing a solid foundation for our stakeholders' confidence in our partnership. Why work for us? At Toray Membrane, in addition to competitive salaries and outstanding employee benefits, we believe that the company's success can only be achieved with each employee's success. Supporting our employees' professional development and success is one of our high-priority missions. Employees are allowed to develop and achieve a variety of long-term career plans in a collaborative, cooperative team setting. Who are we looking for? Toray Membrane USA, Inc. seeks hardworking, accountable team players who are passionate about their work. We highly value the initiative to achieve goals proactively, the ability to collaborate with team members, and the desire to grow in your work, which could lead to a rewarding career.
Summary: The QA Technician executes quality assurance activities to ensure dietary supplements, topical products, and cosmetics are manufactured, packaged, labeled, tested, and stored in compliance with applicable cGMP, cosmetic GMP, OSHA safety requirements, and internal procedures. Essential Duties and Responsibilities * Perform in‑process inspections, line clearance, and verification of manufacturing, compounding, filling, and packaging operations for dietary supplements, topicals, and cosmetics against approved MMRs/BPRs, formulas, and SOPs. * Review batch production records and associated documentation for all product types (oral, topical, cosmetic) for accuracy, completeness, and compliance prior to QA release. * Conduct routine environmental, sanitation, and equipment cleanliness checks in manufacturing, compounding, and filling areas; document results per procedural requirements. * Perform receiving inspection and sampling of raw materials, cosmetic ingredients, excipients, packaging components, labels, and finished goods; verify documentation such as CoAs, specifications, safety data, and label proofs. * Execute sampling of raw materials, in‑process blends, bulk topicals, and finished supplement and cosmetic products in accordance with SOPs and sampling plans. * Support QA disposition of materials and products (approve/reject, quarantine, and release) based on specifications, test results, safety assessments where applicable, and documentation review. * Initiate and document deviations, non‑conformances, and quality events; support investigations, root‑cause analysis, and implementation of CAPA. * Maintain QA logs, forms, and electronic records (including material review, batch release, deviation/CAPA, and complaint records) to meet data integrity and recordkeeping expectations. * Perform QA line clearance, label verification, and reconciliation for supplement and cosmetic packaging lines to prevent label or artwork mix‑ups and misbranding. * Follow OSHA and company safety policies at all times, including proper use of PPE, safe handling of chemicals, and adherence to hazard communication, lockout/tagout, and machine‑guarding procedures. * Promptly identify and report unsafe conditions, near misses, and incidents; participate in safety inspections, safety training, and implementation of corrective actions to support a strong safety culture. * Assist with internal audits and inspection readiness activities for regulatory and third‑party audits, including document retrieval and implementation of audit‑related actions. * Collaborate with Production, Compounding, QC, R&D, Warehouse, and EHS/Safety personnel to resolve quality and safety issues and support continuous improvement across all processes. * Perform other duties assigned, including support for material receipt, status labeling, inventory quality status updates, complaint intake/documentation, and product release activities across all product categories. Qualifications * Associate or Bachelor’s degree in a scientific or related field preferred. * 1–3 years of QA/QC or inspection experience in dietary supplements, cosmetics, pharmaceuticals, or related regulated manufacturing environments. * Working knowledge of cGMP for dietary supplements and familiarity with cosmetic GMP and basic OSHA workplace safety principles, or willingness to learn quickly. * Strong attention to detail, documentation accuracy, and adherence to SOPs, quality standards, and safety rules. * Proficiency with basic computer applications and quality/ERP or QMS systems. Work Conditions * Manufacturing environment with exposure to powders, liquids, semi‑solids, fragrances, cleaning agents, and moving equipment; use of PPE and adherence to safety procedures required. Benefits * Health Insurance and Dental * 401K after 3 months Pay: $24.00 - $30.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance Work Location: In person
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 At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Associate Operator. 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 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 and projects assigned The Individual Required: 0 - 2 years of related experience required 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. This position is not currently eligible for visa sponsorship. Preferred: High school diploma or equivalent Experience in medical device manufacturing MS Office and manufacturing systems The Key Working Relationships Internal Partners: Mechanics, Engineers and Management External Partners: Vendors and Contractors 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 $41,365.59 - $52,741.13 and is bonus eligible. 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 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 the 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
Founded in 1954, Vibrant Ingredients is a leading provider of natural, clean label ingredients and systems that power extraordinary food and beverage experiences. The company’s broad portfolio — including natural flavors, botanical extracts, functional nutrition, cold brew coffee, tea essences, and food protection solutions — enhances taste, texture, color, shelf life, and performance across a wide range of applications. Vibrant operates four state-of-the-art facilities across the United States and works with leading brands, manufacturers, and foodservice operators. With vertically integrated capabilities and a proven track record of innovation and execution, Vibrant helps customers accelerate to market without compromise. About the Role: We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, we are a true partner. We collaborate with our customers in ways that respect people and the environment. A commitment to Purely Better™ drives our innovation team to discover new, on trend solutions. As a Roasting & Grinding Operator you play a crucial role in the manufacturing process by ensuring that raw materials are transformed into high-quality products. This position involves operating and maintaining roasting and grinding equipment to achieve optimal flavor profiles and consistency. The operator will monitor the roasting process, adjusting parameters as necessary to meet production standards and specifications. Additionally, they will be responsible for conducting quality checks and maintaining cleanliness and safety standards in the work area. Ultimately, the success of this role directly impacts product quality and customer satisfaction. How will you contribute: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions. Essential job functions and duties include, but are not limited to: Operate and monitor roasting and grinding machinery to ensure efficient production. Adjust equipment settings based on product specifications and quality standards. Conduct regular quality control checks on roasted and ground products. Maintain a clean and organized work environment, adhering to safety protocols. Collaborate with team members to optimize production processes and resolve any issues. The required skills for this role include mechanical aptitude and attention to detail, which are essential for operating and troubleshooting machinery effectively. Strong observational skills are necessary for conducting quality checks and ensuring that products meet established standards. Preferred skills such as knowledge of food safety regulations will enhance the operator's ability to maintain compliance and uphold product quality. Effective communication skills are important for collaborating with team members and reporting any issues that arise during production. Overall, a combination of technical and interpersonal skills will contribute to a successful and efficient manufacturing process. Minimum Requirements/Qualifications: High school diploma or equivalent. Previous experience in a manufacturing or food processing environment. Basic understanding of machinery operation and maintenance. Preferred Qualifications: Experience with roasting and grinding equipment. Knowledge of food safety regulations and quality control processes. Certification in food handling or safety. Work Environment: May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame. What Vibrant Ingredients can offer you: Generous time off for vacations Paid Holidays 401(k) with company match Tuition reimbursement Medical/Dental/Vision Health & Wellness programs More about us: Vibrant Ingredients, headquartered in Lake Mary, FL, is one of the world's leading independent providers of natural ingredients. With a legacy spanning over 70 years, we deliver a diverse portfolio of clean label ingredients and innovative system solutions to the food and beverage industry. Our commitment to quality and performance is reflected in our American-made products, which enhance both taste and functionality. Backed by advanced manufacturing capabilities, we specialize in fermentation, patented cold brew extraction, custom flavor development, and a range of drying and blending technologies. Operating from four state-of-the-art facilities strategically located across the U.S., we ensure the accessibility of real, high-quality ingredients—helping our customers create better-for-you food and beverage for consumers. "Improving the food and beverages consumed by providing real ingredients from nature that work." This position is currently classified as on-site. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Holidays, Vacation, Tuition Reimbursement Program. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. The Company reserves the right to modify, update, change and/or make corrections to this job description, at the sole discretion of senior management, at any time during the employee’s employment term, at the sole discretion of management. EEO Statement Vibrant Ingredients is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Vibrant Ingredients will work with applicants to meet accommodation needs that are made known to Vibrant Ingredients in advance. **Please no external recruiters** Mon - Fri (8:00pm - 4:30am; Overtime and occasional weekend work)
Founded in 1954, Vibrant Ingredients is a leading provider of natural, clean label ingredients and systems that power extraordinary food and beverage experiences. The company’s broad portfolio — including natural flavors, botanical extracts, functional nutrition, cold brew coffee, tea essences, and food protection solutions — enhances taste, texture, color, shelf life, and performance across a wide range of applications. Vibrant operates four state-of-the-art facilities across the United States and works with leading brands, manufacturers, and foodservice operators. With vertically integrated capabilities and a proven track record of innovation and execution, Vibrant helps customers accelerate to market without compromise. About the role: We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, we are a true partner. We collaborate with our customers in ways that respect people and the environment. A commitment to Purely Better™ drives our innovation team to discover new, on trend solutions. As a Packaging Operator, you will be responsible for operating and monitoring packaging equipment to ensure the safe and efficient packaging of products. This position plays a critical role in ensuring that our products are properly packaged and meet the quality standards set by the company. How will you contribute: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions. Essential job functions and duties include, but are not limited to: Operate and monitor packaging equipment including filling machines, labeling machines, and sealing machines Perform quality checks on packaged products to ensure they meet the company's standards Take corrective actions if any issues or deviations are identified during the packaging process Collaborate with the production team to ensure a smooth and efficient packaging process Maintain a clean and organized work area, adhering to all safety and hygiene regulations Complete production and packaging logs accurately and in a timely manner Assist with equipment setup, changeovers, and troubleshooting as needed Communicate effectively with team members and supervisors Minimum Requirements/Qualifications: High school diploma or equivalent Prior experience as a Packaging Operator or in a similar role is preferred Strong attention to detail and commitment to producing high-quality products Ability to follow instructions and work safely and efficiently Basic computer skills for data entry and equipment operation Good communication and team collaboration skills Ability to work the assigned shift schedule, including overtime hours and weekends as needed Work Environment: May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame. What Vibrant Ingredients can offer you: Generous time off for vacations Paid Holidays 401(k) with company match Tuition reimbursement Medical/Dental/Vision Health & Wellness programs More about us: Vibrant Ingredients, headquartered in Lake Mary, FL, is one of the world's leading independent providers of natural ingredients. With a legacy spanning over 70 years, we deliver a diverse portfolio of clean label ingredients and innovative system solutions to the food and beverage industry. Our commitment to quality and performance is reflected in our American-made products, which enhance both taste and functionality. Backed by advanced manufacturing capabilities, we specialize in fermentation, patented cold brew extraction, custom flavor development, and a range of drying and blending technologies. Operating from four state-of-the-art facilities strategically located across the U.S., we ensure the accessibility of real, high-quality ingredients—helping our customers create better-for-you food and beverage for consumers. "Improving the food and beverages consumed by providing real ingredients from nature that work." This position is currently classified as on-site. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Holidays, Vacation, Tuition Reimbursement Program. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. The Company reserves the right to modify, update, change and/or make corrections to this job description, at the sole discretion of senior management, at any time during the employee’s employment term, at the sole discretion of management. EEO Statement Vibrant Ingredients is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Vibrant Ingredients will work with applicants to meet accommodation needs that are made known to Vibrant Ingredients in advance. **Please no external recruiters**
Diazyme, an affiliate of General Atomics, is a cGMP and ISO 13485 certified medical device manufacturer. Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Their products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes. Under close supervision with detailed instruction and intermittent review, this position is responsible for performing repetitive assembly line filling, packaging and labeling for the production of test kits and bulk reagents in clinical diagnostic products. DUTIES & RESPONSIBILITIES: Performs repetitive tasks for assembly line filling, packaging labeling operations of diagnostic test products. Makes setups and adjustments holding tolerances to specifications. May assemble, disassemble, and assist in repair of routine instruments according to specifications. Monitors quality in accordance with quality specifications. Performs tests and verify quality of products in accordance with control procedures. Performs housekeeping, lab ware cleaning and other cleanup duties. Performs other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a high school diploma or equivalent and two or more years experience. Must be customer focused and possess: The ability to communicate and understand written and verbal communication. The ability to read assembly documentation such as diagrams, drawings, specifications, work instructions and wire lists. Familiarity with use of soldering and compression connection tools. Knowledge of computer operations and applications pertinent to the position. Good visual perception and ability to distinguish between colors. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Job Category BioTech Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 38,230 Pay Range High 56,838 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? No Clearance Required? No
Diazyme, an affiliate of General Atomics, is a cGMP and ISO 13485 certified medical device manufacturer. Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Their products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes. Under close supervision with detailed instruction and intermittent review, this position is responsible for performing repetitive assembly line filling, packaging and labeling for the production of test kits and bulk reagents in clinical diagnostic products. DUTIES & RESPONSIBILITIES: Performs repetitive tasks for assembly line filling, packaging labeling operations of diagnostic test products. Makes setups and adjustments holding tolerances to specifications. May assemble, disassemble, and assist in repair of routine instruments according to specifications. Monitors quality in accordance with quality specifications. Performs tests and verify quality of products in accordance with control procedures. Performs housekeeping, lab ware cleaning and other cleanup duties. Performs other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a high school diploma or equivalent and two or more years experience. Must be customer focused and possess: The ability to communicate and understand written and verbal communication. The ability to read assembly documentation such as diagrams, drawings, specifications, work instructions and wire lists. Familiarity with use of soldering and compression connection tools. Knowledge of computer operations and applications pertinent to the position. Good visual perception and ability to distinguish between colors. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Job Category BioTech Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 38,230 Pay Range High 56,838 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? No Clearance Required? No
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. We have an exciting opportunity for a Sr CNC Machinist to join our Inertial Fusion Technology (IFT) division within the Energy group. This position is located in San Diego (Torrey Pines), CA. The components to be machined are normally high-precision, small quantities, and typically millimeter in scale with micro-size features and tolerances. Production schedules are reasonable but due dates are often inflexible. Salary potential commensurate with willingness/ability to grow professionally. DUTIES AND RESPONSIBILITIES: Set-up and operate micro CNC shop equipment such as lathes, mills, and saws. Being able to follow all safety procedures in working and machining in a laboratory that works with beryllium components. NC programming in both manual (i.e., plain G-code and parametric G-code) and CAD/CAM (Creo). Inspect parts using mics, calipers, digital height gages, measuring microscope, indicators, gage blocks, surface plates, etc. as required. Inspect parts using high level inspection tools such as CT and white light optical profilers. Record and document machining data, including both in‑process and final inspection results, in the database or designated Excel templates, and archive them on the server. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Performs other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires an associate's degree, technical/trade school training or equivalent and seven or more years related experience. Additional experience may be substituted for formal education. Must possess: Proficiency with common manual shop equipment such as lathes, mills, and saws. Some experience setting-up and operating NC mills and lathes. Some experience with NC programming (both G-code and CAD/CAM). Proficiency with common manual inspection tools such as micrometers, calipers, digital height gages, indicators, gage blocks, surface plates. Knowledge of computer operations and applications pertinent to the field required. Customer focus. Ability to use good judgment and safe practices in a shop environment. Time management skills to maintain the flow of work within the unit. Good interpersonal skills and written communication skills to interface with employees and supervisor; and basic computer skills. Ability to work in a large lab research environment requiring long periods of standing, walking, bending and lifting up to 50 lbs. Ability to work both independently and in a team environment. Ability to handle parts under 10 mm in size Flexibility to work extended hours as required. Must be willing to work with hazardous and radioactive materials Must have the ability to obtain and maintain a DoE Q Level Security clearance. Job Category Technicians Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 65,410 Pay Range High 99,888 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level DOE - Q
There’s a Place for You at OneSource Distributors A career at OneSource is more than a job. You’re investing in a brighter, more sustainable future together and joining a team that makes a real difference for our customers. OneSource offers electrical products and services to contractors. If it helps bring electricity to an office, home, factory or other building – you can find it here. We operate throughout Arizona, Hawaii, and all of California. We are part of the Sonepar group, the world’s #1 electrical distributor with over 45,000 associates around the globe. Being “Powered by Difference” means we respect and value diverse perspectives. At OneSource, we offer a supportive culture and great benefits, and as part of the larger Sonepar group, we can provide exciting opportunities to grow your career. What you will do: · Perform all the duties and responsibilities of an Assembler II proficiently. · Reads and deciphers schematics, blueprints, and assembly instructions. · Cut, strip and crimp cables per schematics requirements. · Populate panels boards with material / components per schematic layout. · Wire panel boards per Wiring diagram. · Operate, print, and attach labels to project per Labeling diagram. · Analyze and troubleshoot problems with builds. · Ground bar testing to ensure there are no shortages. · Maintains a safe and clean working environment by complying with procedures, rules, and regulations. · Documents actions by completing production and quality forms. What you will bring: · Electrical, Industrial and/or distribution experience preferred but not required · High School diploma or G.E.D.; or · 6 months of related experience and/or training; or · Equivalent combination of education and experience. · Forklift certified- internal. Physical Requirements and Work Environment: · Long and varied hours required occasionally · Ability to work mandatory physical inventory · Ability to work in extreme hot or cold environment · Ability to work in dusty conditions · Ability to use power tools, including drills, impact drivers, etc Location: This role is based in Miramar, CA. Work hours: 5:00am – 1:30pm Salary Range: · This is a non-exempt position and pays between $19.33 – $22.55 per hour. This salary range reflects figures based on the primary location, within California. What We Offer You As a full-time associate, you are eligible to participate in the following benefits: Healthcare plans Dental & vision Paid time off Paid parental leave 401(k) retirement savings with company match Professional and personal development programs Opportunity to become a shareholder Employer-paid short and long-term disability Employer-paid life insurance for spouse and dependents Robust wellness program Gym reimbursement Employee Referral Program Employee Assistance Program (EAP) We’re proud to be a military-friendly company, and our many employee resource groups (ERGs) help you make connections and feel supported. Learn More About Us Get to know us on YouTube, LinkedIn, Facebook, and Instagram to learn how we’re “Powering Progress for Future Generations.” YouTube: https://www.youtube.com/c/OneSourceDistributors LinkedIn: https://www.linkedin.com/company/309791/ Facebook: https://www.facebook.com/onesourcedist/ Instagram: https://www.instagram.com/onesourcedist/ Learn more about OneSource at https://www.1sourcedist.com/about OneSource Distributors is part of the Sonepar family of brands: https://www.soneparusa.com/us-en/about-us OneSource Distributors is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, or any other categories protected by federal, state or local law. OneSource is committed to the full inclusion of all qualified individuals. In keeping with our commitment, we will take the steps to assure that people with disabilities are provided reasonable accommodations. Accordingly, if a reasonable accommodation is required to fully participate in the job application or interview process, to perform the essential functions of the position, and/or to receive all other benefits and privileges of employment, please call 760-966-4500 or email [email protected] OneSource Distributors is a M/F/Disabled and Vet EEO/AA employer
The application window is expected to close on: 05/03/2026Job posting may be removed earlier if the position is filled or if a sufficient number of applications are received. Meet the team: You will be a key collaborator within the CBM organization, working extensively with internal Cisco teams including Sales Operations, Demand Planning, Shipping& Receiving, and Accounting& Finance. You will also engage externally with contract manufacturers both domestically and overseas. We are looking for an inquisitive, collaborative, and proactive professional who thrives in a dynamic, ERP-centric environment and enjoys working multi-functionally to orchestrate solutions for our diverse product portfolio. Your Impact: You are accountable for the systematic flow of materials through our ERP systems, ensuring all data remains synchronized and accurate. You will champion progressive supply planning policies, processes, and metrics designed to support CBM’s technologically advanced portfolio of semiconductor and optics products. Your core responsibilities include: • Managing and owning the tactical execution of solutions to align systems. • Driving critical initiatives across the supply chain using best-in-class problem-solving techniques and methodologies. • Collaborating with business and data teams to understand and support strategic supply chain objectives. • Ensuring all tasks are performed with an uncompromising dedication to accuracy and quality. Minimum Qualifications: • BA/BS Degree with equivalent work experience. • Minimum 6 years of experience in supply chain operations. • Minimum 4 years of experience in semiconductor or electronics manufacturing. • Minimum 4 years of experience with Oracle or similar cloud-based ERP systems that utilize a planning engine to track supply requirements. • Proven program management expertise and a track record of driving efforts with large, cross-functional teams. Preferred Qualifications: • Experience leading system design, integration, and deployment in a complex, integrated environment. • Hands-on supply chain expertise spanning operations and contract manufacturing. • Results-oriented, ambitious, and flexible mindset. • Ability to adapt quickly in a fast-paced, changing environment. • Strong analytical skills with the ability to translate strategic objectives into tactical system solutions. Why Cisco? At Cisco, we’re revolutionizing how data and infrastructure connect and protect organizations in the AI era – and beyond. We’ve been innovating fearlessly for 40 years to create solutions that power how humans and technology work together across the physical and digital worlds. These solutions provide customers with unparalleled security, visibility, and insights across the entire digital footprint. Fueled by the depth and breadth of our technology, we experiment and create meaningful solutions. Add to that our worldwide network of doers and experts, and you’ll see that the opportunities to grow and build are limitless. We work as a team, collaborating with empathy to make really big things happen on a global scale. Because our solutions are everywhere, our impact is everywhere. We are Cisco, and our power starts with you. Message to applicants applying to work in the U.S. and/or Canada: The starting salary range posted for this position is $88,900.00 to $112,900.00 and reflects the projected salary range for new hires in this position in U.S. and/or Canada locations, not including incentive compensation*, equity, or benefits. Individual pay is determined by the candidate's hiring location, market conditions, job-related skillset, experience, qualifications, education, certifications, and/or training. The full salary range for certain locations is listed below. For locations not listed below, the recruiter can share more details about compensation for the role in your location during the hiring process. U.S. employees are offered benefits, subject to Cisco’s plan eligibility rules, which include medical, dental and vision insurance, a 401(k) plan with a Cisco matching contribution, paid parental leave, short and long-term disability coverage, and basic life insurance. Please see the Cisco careers site to discover more benefits and perks. Employees may be eligible to receive grants of Cisco restricted stock units, which vest following continued employment with Cisco for defined periods of time. U.S. employees are eligible for paid time away as described below, subject to Cisco’s policies: • 10 paid holidays per full calendar year, plus 1 floating holiday for non-exempt employees • 1 paid day off for employee’s birthday, paid year-end holiday shutdown, and 4 paid days off for personal wellness determined by Cisco • Non-exempt employees** receive 16 days of paid vacation time per full calendar year, accrued at rate of 4.92 hours per pay period for full-time employees • Exempt employees participate in Cisco’s flexible vacation time off program, which has no defined limit on how much vacation time eligible employees may use (subject to availability and some business limitations) • 80 hours of sick time off provided on hire date and each January 1st thereafter, and up to 80 hours of unused sick time carried forward from one calendar year to the next • Additional paid time away may be requested to deal with critical or emergency issues for family members • Optional 10 paid days per full calendar year to volunteer For non-sales roles, employees are also eligible to earn annual bonuses subject to Cisco’s policies. Employees on sales plans earn performance-based incentive pay on top of their base salary, which is split between quota and non-quota components, subject to the applicable Cisco plan. For quota-based incentive pay, Cisco typically pays as follows: • .75% of incentive target for each 1% of revenue attainment up to 50% of quota; • 1.5% of incentive target for each 1% of attainment between 50% and 75%; • 1% of incentive target for each 1% of attainment between 75% and 100%; and • Once performance exceeds 100% attainment, incentive rates are at or above 1% for each 1% of attainment with no cap on incentive compensation. For non-quota-based sales performance elements such as strategic sales objectives, Cisco may pay 0% up to 125% of target. Cisco sales plans do not have a minimum threshold of performance for sales incentive compensation to be paid. The applicable full salary ranges for this position, by specific state, are listed below: New York City Metro Area: $100,300.00 - $146,300.00 Non-Metro New York state& Washington state: $88,900.00 - $129,800.00 * For quota-based sales roles on Cisco’s sales plan, the ranges provided in this posting include base pay and sales target incentive compensation combined. ** Employees in Illinois, whether exempt or non-exempt, will participate in a unique time off program to meet local requirements.
Air Supply Tools seeks a full time Waterjet and Laser Operator with experience setting up and operating Flow waterjet machines but we are willing to train someone with machining experience. Must be able to setup and run multiple machines. Capable of checking setups and part dimensions and quality using various inspection tools e.g. calipers, micrometers, and pin gages. Experience operating a forklift is preferred. Experience working with AutoCad preferred. Creating of DXF files. Your benefits will include: -Competitive pay. -Paid vacation and sick pay. -Opportunity to earn overtime. -Clean & safe work environment with friendly staff. -Growth & expansion potential within the company. Job Type: Full-time Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off * Vision insurance Pay: $25.00 - $27.00 per hour Work Location: In person
*COMPANY OVERVIEW* Envases Group is a global leader in packaging solutions, offering a diverse range of aluminum, tin, rigid plastic, and pharmaceutical containers. With a strong commitment to innovation and sustainability, the company serves industries including food, personal care, home care, and pharmaceuticals. Founded in 1995, Envases Group operates globally, focusing on minimizing environmental impact while providing high-quality and functional packaging designs. The organization is dedicated to ethical business practices and creating sustainable solutions that meet the needs of its customers and communities worldwide. *POSITION SUMMARY / OBJECTIVE * The Production Supervisor is responsible for overseeing the daily operations of both the Injection Molding and Blow Molding production areas in our SQF-certified facility. This role ensures compliance with food safety and quality standards, supervises Packers,operators and technicians, optimizes production processes, and leads continuous improvement initiatives. The ideal candidate will have experience in both blow and injection molding operations within a regulated manufacturing environment and a strong understanding of SQF (Safe Quality Food) principles. *ESSENTIAL FUNCTIONS* * Supervise daily production operations across both the Injection and Blow Molding departments, ensuring compliance with SQF certification standards, food safety, hygiene, and quality requirements. * Arrive 15 minutes prior to start of shift * Lead, coach, and develop a team of machine operators and technicians, fostering a culture of accountability, teamwork, and safety. * Maintain production schedules, ensuring efficiency, minimal downtime, and adherence to operational targets. * Monitor, adjust, and optimize machine settings to maximize efficiency, product quality, and yield, reducing scrap and defects. * Troubleshoot and resolve operational issues, including equipment malfunctions, material handling problems, and production delays. * Collaborate with maintenance and quality control teams to ensure equipment reliability and consistent product quality. * Implement continuous improvement processes to drive production efficiency, cost reduction, and quality enhancement. * Conduct and document quality control checks and inspections to meet customer specifications and regulatory standards as needed * Maintain accurate production records, including log sheets, process parameters, and quality reports. * Assist with internal and external audits related to SQF certification, and support corrective action plans as necessary. * Collaborate with planning and inventory control teams to manage inventory levels of raw materials and production supplies, while ensuring timely restocking to prevent downtime. * Assist with month end paperwork verification * Approve and coordinate employee scheduling, time-off requests, and shift assignments. * Document and promptly report all safety hazards, incidents, or concerns to the appropriate supervisor or department to ensure compliance with company policies and regulatory standards. Including confidentiality. * Follow all safety procedures and policies, maintaining a safe and clean work environment at all times. * Other duties as assigned. *PREFERRED EDUCATION & EXPERIENCE* * *High school diploma or equivalent* (Associate’s or Bachelor’s degree in a related field is a plus). * *Minimum of 2 years of experience in injection and/or blow molding production*, with at least *3-5 years in a supervisory role*. * *Knowledge of SQF standards, GMPs, and food safety regulations*. * Strong expertise in *injection molding and blow molding processes, machinery, and troubleshooting techniques*. * Intermediate to Advanced experience with *process optimization, equipment maintenance, and quality control procedures*. * *Ability to read and interpret* technical documents, blueprints, and machine operation manuals. * *Basic computer skills*, including proficiency in production management software, ERP systems, and Google Suite (Docs, Sheets, Drive). * Strong *leadership, problem-solving, and organizational skills* with the ability to handle multiple tasks and meet deadlines. * Knowledge of *Lean Manufacturing, SixSigma, 5s, Continuous Improvement, and Statistical Process Control (SPC) methodologies* is a plus. *PHYSICAL REQUIREMENTS* * Ability to stand, walk, and move continuously for up to 8+ hours. * Must be able to lift and carry or otherwise move 25 pounds regularly/occasionally and up to 50 pounds with assistance. * Ability to bend, stoop, crouch, or reach overhead as needed. * Must be able to ascend and descend ladders, stairs and work in confined spaces and in proximity to loud equipment. * Fine motor skills and hand-eye coordination to operate tools, equipment, or machinery. * Visual acuity to read, operate equipment, or monitor surroundings. * Hearing ability to understand instructions and respond to safety signals in a noisy environment. * Ability to tolerate exposure to varying temperatures, humidity, and outdoor/indoor environments. * Must be able to respond quickly to sounds. * Must be able to move safely over uneven terrain * Ability to wear required personal protective equipment (PPE) for extended periods, including masks, gloves, or safety glasses. * Ability to perform repetitive motions, including [e.g., typing, or operating tools]. 2nd Shift Hours: 2:00 pm to 10:30 pm Job Type: Full-time Pay: $25.00 - $30.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person