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HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. At HME you will have the opportunity to learn and grow while developing our future products. Come join our team! We are currently recruiting for a Factory Service Operations Supervisor. What you will do in the position: Supervision, Coordination, and Training of Staff Monitors inventory levels and customer demand and manages work assignments as needed to meet requirements Hires and trains staff Conducts performance appraisals and makes salary recommendations Monitors day-to-day performance and provides feedback to employees and management Follows HME employee policies and ensures department personnel follow them as well Resolves employee complaints or work performance issues on a timely basis Owns training program for supervised personnel, ensuring work instructions are maintained and followed to maximize productivity and quality Ensures personnel are cross-trained on different tasks to drive ergonomic work diversity and maintain department agility and flexibility Engages and challenges personnel to leverage their talents and interests to achieve world-class performance Develops and spotlights personnel with potential leadership capability and interest to create a bench of future HME leaders Advises Factory Service Manager of anticipated manpower and expense requirements to support the budgeting process Process Ownership Works with other departments as appropriate to assure efficient and accurate execution of assigned responsibilities Implements plans and changes to maximize assigned functional quality Ensures work area is clean and organized, providing an environment conducive to a world-class operation Owns internal processes for operational tasks, maximizing productivity and quality Works with IT department to enhance and improve company ERP systems Responsible for Factory Repair unit and material inventory accuracy and availability Works with Factory Service Manager to plan for material obsolescence Responsible for Factory Service label system Performs all other job responsibilities as assigned. What you will need to succeed: Strong supervisory and customer service skills. Excellent verbal and written communication skills. Experience delivering presentations to senior management desired Working knowledge of PC operations and programs including Outlook and Teams Strong data analysis skills. Experience with Microsoft Office Suite including Word, Excel & PowerPoint. Experience with LEAN manufacturing principles Experience with ERP systems required, Microsoft AX preferred. Experience with inventory control systems and processes 6+ years related experience Associates Degree - strongly preferred Travel: 0% The posted pay range, $72,500 - $86,000, is what we reasonably expect to pay for the role. This may vary depending on experience and other factors. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment 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. The employee will occasionally lift and move up to 50 pounds with assistance. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities 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 (https://www.eeoc.gov/poster) notice from the Department of Labor.
*Join Foster Display Group – Leaders in Experiential Design and Fabrication* Foster Display Group is one of the *fastest-growing experiential agencies in the country*, recognized twice on the *Inc. 5000 Fastest-Growing Companies in America* list and celebrated as one of the *Top 50 Fabrication Companies in North America* by Event Marketer Magazine. Our mission? To create unforgettable brand experiences that captivate audiences and leave lasting impressions. From *movie premieres in New York City* to *pop-up shops in Las Vegas*, *music festivals in Southern California*, and the *world’s largest comic conventions in San Diego*, our work spans the spectrum of innovation. Partnering with industry leaders like *Universal Pictures, eBay, DreamWorks, and Citizen Watches*, we stay at the forefront of cutting-edge design and execution. We are currently seeking a *Warehouse Coordinator – Trade Show Production* to join our dynamic team at our *state-of-the-art fabrication shop in Oceanside, CA*. This is the beating heart of our business, where creativity meets craftsmanship to bring our clients’ visions to life. If you thrive in a fast-paced, hands-on environment and are ready to be part of something extraordinary, we want to hear from you. *About the Role* As a *Warehouse Coordinator*, you will play a pivotal role in ensuring our projects are executed seamlessly from conception to installation. Working closely with our operations and fabrication teams, you’ll manage everything from organizing materials to assisting with fabrication and traveling to some of the nation’s most iconic venues for onsite builds. This position offers a *unique blend of creativity, logistics, and craftsmanship*, with opportunities for career growth, national travel, and hands-on experience at premier events. *What You’ll Do* * *Fabricate and Prepare Exhibits:* Assist in the creation of custom displays and booth elements that dazzle clients and attendees alike. * *Coordinate Warehouse Operations:* Manage materials, organize inventory, and ensure tools, furniture, and electronics are event-ready. * *Shipping & Logistics:* Pack and unpack crates, load trucks, and coordinate shipping and receiving schedules. * *Maintain Organization:* Keep the warehouse running smoothly with an eye for detail and a commitment to safety standards. *What We’re Looking For* We’re seeking a *high-energy team player* with a passion for creative problem-solving and a drive to deliver excellence. While experience is a bonus, the *right attitude, willingness to learn, and teamwork mindset* are paramount. *Basic Requirements:* * Ability to lift 50 lbs and work with ladders. * Strong organizational and verbal communication skills. * High school diploma or GED. * Driver’s license and reliable transportation. *Preferred Skills:* * Forklift certification. * Knowledge of lighting, electrical, and exhibit assembly techniques. * Leadership experience and a willingness to take charge when needed. *Work Style:* * Thrive in a *fast-paced, deadline-driven environment*. * Flexible to work long hours and weekends during event builds. * A natural *self-starter* who enjoys both teamwork and independent challenges. *Why Join Foster Display Group?* At Foster Display Group, we foster a culture of *innovation, collaboration, and growth*. We value our team and are committed to creating an environment where *hard work is recognized, and talent thrives*. Here’s what you can expect: * *Opportunities for Career Advancement* in a rapidly growing industry. * A *Fun, Fast-Paced Environment* where no two days are the same. * The chance to work on projects with *global brands* and make a tangible impact. *Ready to Elevate Your Career?* Join a company where your skills and creativity will shine. Apply today and become part of a team that’s transforming the exhibit industry, one extraordinary experience at a time. Job Type: Full-time Pay: $18.00 - $25.00 per hour Benefits: * 401(k) * 401(k) matching * Paid time off Ability to Commute: * Oceanside, CA 92056 (Required) Ability to Relocate: * Oceanside, CA 92056: Relocate before starting work (Required) Work Location: In person
We understand that the world we want tomorrow starts with how we do business today, and that’s why we’re inspired to make A Better World for Pets. Antech is comprised of a diverse team of individuals who are committed to each other’s growth and development. Our culture is centered on our guiding philosophy, The Five Principles: Quality, Responsibility, Mutuality, Efficiency and Freedom. Today Antech is driving the future of pet health as part of Mars Science & Diagnostics , a family-owned company focused on veterinary care. Current Associates will need to apply through the internal career site. Please log into Workday and click on Menu or View All Apps, select the Jobs Hub app, then click the magnifying glass to Browse Jobs. The Target Pay Range for this position is $23- $26 hourly. At Antech, pay decisions are determined using factors such as relevant job-related skills, experience, education, training and budget. Job Purpose/Overview The Production Technician will be working in the Production operations area, in a team environment, with other technicians and intra-department personnel to configure, test, manufacture, repair and continuously improve the products that we sell and support. Essential Duties and Responsibilities Assemble, test, and troubleshoot computers and Digital Radiography, Laser, X-Ray, Ultrasound and Network related products. Interpret and apply information from technical manuals; communicate on technical issues with individuals with varying degrees of product familiarity. Troubleshoot hardware and software problems on RMAs and identify, research and resolve technical problems Offer solutions and advice on field problems for customer service staff and peers. Assist, troubleshoot and repair sales department and tradeshow equipment. Develop and follow all administrative procedures as required for manufacturing and repair processes. Process RTV requests for equipment returning to vendor for repair or further evaluation and communicate with vendors on a technical level. Knowledge in system configuration for network communication. Prepare and maintain accurate records of manufactured product (e.g. Production logs, End of Line Certificates). Education and Experience High school diploma required. AA/AS in electronics or 2-5 years experience in manufacturing environment. Minimum 2 years of equivalent experience. Strong teamwork capabilities including the ability to effectively work with leadership, peers and other internal and external individuals through projects, making sure project deadlines are met and projects enhance the goals and strategic direction of the company. Ability to effectively work with executive leaders, team leads, and peers through projects, making sure project deadlines are met. Strong written and oral communication skills. Must work well independently and work in a matrix based organization with minimal direction. Must be able to handle multiple projects and be able to adapt to changes in priority. Technical Experience Experience with installing, maintaining, and repairing hardware and software for business computers and related equipment. Must be familiar with manufacturing pressures and work environments and must be able to communicate effectively, work cross-functionally and assist others as required. Have experience with inputting, accessing, analyzing and integrating data using a computer. Physical requirements Must be able to bend, stoop and lift up to 50lbs. About Antech Antech is a leader in veterinary diagnostics, driven by our passion for innovation that delivers better animal health outcomes. Our products and services span 90+ reference laboratories around the globe; in-house diagnostic laboratory instruments and consumables, including rapid assay diagnostic products and digital cytology services; local and cloud-based data services; practice information management software and related software and support; veterinary imaging and technology; veterinary professional education and training; and board-certified specialist support services. Benefits Antech offers an industry competitive benefits package and continues to invest in and evolve benefits programs that meet the health, wellness and financial needs of our associates. Benefits eligiblity is based on employment status. Paid Time Off & Holidays Medical, Dental, Vision (Multiple Plans Available) Basic Life (Company Paid) & Supplemental Life Short and Long Term Disability (Company Paid) Flexible Spending Accounts/Health Savings Accounts Paid Parental Leave 401(k) with company match Tuition/Continuing Education Reimbursement Life Assistance Program Pet Care Discounts Commitment to Equal Employer Opportunities We are proud to be an Equal Opportunity Employer - Veterans / Disabled. For a complete EEO statement, please see our Career page at Antech Careers . Note to Search Firms/Agencies Antech Diagnostics, Inc. and its subsidiaries and affiliates (Antech) do not compensate search firms for unsolicited assistance unless they have a written search agreement with Antech and the requisition is position-specific. Any resumes, curriculum vitae, and other unsolicited assistance from search firms that do not have a written search agreement or position-specific requisition submitted to any Associate of Antech will be deemed the sole property of Antech and no fee will be paid in the event the candidate is hired by Antech.
The Sr. Quality Assurance Specialist fulfills a critical role in Quality Assurance. This individual will contribute an advanced level of understanding of GMP system improvements, technical documents, and review of GMP documentation and reports. This individual must also provide GMP and related guidance, data analysis, and technical review of QC data. in some instances, this role may act as the deputy for the Manager, Quality Assurance. What you will do Perform all duties pertaining to a QA specialist I, II, III, in addition to those listed below. Support real time batch record review in a timely manner and with high accuracy, performing usage decisions in electronic batch release systems. Suggest and implement improvements in quality systems and SOPs taking into account LEAN GMP approaches. Reviewing and approval of all GMP documentation, which includes BPRs, validation protocols, data, reports, etc. Reviewing, analyzing, and trending data to extract relevant information. Work closely with other functions and sites to close out quality records, investigations e.g., OOS, and approval of documents and changes e.g., MBPRs, analytical procedures, protocols, reports, and specifications/global specifications. Suggests/recommends and implements new policies and procedures to improve existing processes and products. Problem resolutions with GMP systems as well as guiding on GMP topics. Be an active part in increasing the quality culture in the organization e.g., by guidance and training of other departments and sites. Perform GMP audits for internal operations, GMP compliance improvements and provide GMP compliance guidance to other departments and BAM Sites as needed. Support actively and able to take the lead in customer/authority audits. Writing new and revising current standard operating procedures (SOPs), specifications, etc. In addition, provide technical assistance on production and quality systems documents. Qualifications Bachelor's Degree in organic chemistry or related field required or Master's Degree in organic chemistry or related field preferred Bachelor's Degree in a science related field and a minimum of 5 years' experience in a GMP manufacturing setting required or Associate's Degree in a science related field and a minimum of 7 years' experience in a GMP manufacturing setting required 4-6 years experience in Quality Assurance required 4-6 years experience with GMP document control, validation, qualification and calibration preferred 4-6 years Ability to work in ISO7 and ISO8 control environment and support real time batch record review required 4-6 years experience in internal auditing as well as working with regulatory agencies preferred Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint Ability to effectively organize, multitask and work in fast-paced, deadline driven work environment. Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Detail oriented with the ability to troubleshoot and resolve problems. Ability to work independently and manage one's time. Communicate effectively and ability to function well in a team environment. Certified Quality Process Analyst - ASQ preferred or CQA preferred or CQE certification desired preferred Annual Salary Range: $97,174.20 - $133,614.80 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. At Bachem, you’ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation—regardless of age, gender, background, religion, or sexual orientation. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
To ensure Bachem can meet the demands of its evolving business and diverse customer base, the Senior Director, Technical Operations leads the local Technical Operations organization and ensures that site manufacturing technology, technical capabilities, and operational readiness are aligned with site strategy, customer needs, global standards, and regulatory expectations. The role provides senior leadership for technical operations across manufacturing science, technology transfers, product stewardship, process optimization, validation support, automation and digitalization initiatives, technical documentation, and lifecycle management. The Senior Director, Technical Operations leads scientists, chemists, engineers, technical writers, process specialists, and other technical experts supporting clinical and commercial manufacturing, major capital investments, new product introductions, and transfers within the Bachem network or from client sites to BAM. The role partners closely with Manufacturing, Quality, Engineering, Supply Chain, R&D, Project Management, and global TechOps to strengthen process robustness, inspection readiness, operational excellence, and future site capabilities. This position reports to the Vice President of Global Technical Operations. What you will do Ensure adequate technical support for clinical and commercial products through Process Performance Qualification (PPQ), technology transfer, process monitoring, troubleshooting, product stewardship, validation support, manufacturing readiness, lifecycle management, complex troubleshooting, and process optimization activities requiring expertise beyond the capabilities of the Commercial Manufacturing Team (CMT), ensuring robust, compliant, and reliable manufacturing operations. Lead technology transfer activities including internal site transfers and transfers from client sites to BAM, ensuring robust transfer governance, technical risk assessment, process understanding, validation readiness, clear documentation of transfer requirements and lessons learned. Establish and maintain structured checklists, standards, governance processes, and sustainable knowledge-transfer practices for intra-site and inter-site technology transfers. Lead and implement efforts to improve manufacturing efficiency, process robustness, and operational excellence for clinical and commercial products, including troubleshooting manufacturing deviations, root cause investigations, process change controls, implementation and effectiveness reviews of CAPAs, data analytics, data mining, trending, process simulations, and digital process-intelligence approaches that strengthen process understanding and monitor commercial process health. Lead technical support for manufacturing activities, special events, site ramp-up activities, and new product introductions, ensuring effective coordination with Manufacturing, Quality, Engineering, Supply Chain, R&D, and Project Management to support successful execution and operational readiness. Establish and ensure alignment of technology requirements, technical capabilities, automation and digitalization priorities, and platform technologies with site strategy, future product needs, global standards, and long-term operational excellence objectives while identifying opportunities to leverage emerging technologies and industry best practices. Serve as a member of the site leadership team and the extended science and technology network, representing Technical Operations in site strategy, global TechOPS alignment, operational readiness, cross-site harmonization of technical standards, risk-management practices, and long-term technical strategy development across the network. Coach, develop, and retain internal technical talent by building future-ready capabilities, conducting after-action reviews, strengthening knowledge management, establishing best-practice guidelines, fostering accountability, innovation, and continuous improvement, and building a high-performing Technical Operations organization. Partner with cross-functional and global stakeholders across Supply Chain, Quality Control, Quality Assurance, Procurement, Production, Facilities, Engineering, Project Management, R&D, and Global TechOPS to drive COGS improvement, strengthen risk portfolio management, support regulatory inspections and inspection readiness, participate in GEMBA walks, oversee process-validation and PPQ activities, support pre-approval inspection preparation, and ensure appropriate technical documentation and CMC-related technical content. Promote process safety, equipment stewardship, and a state-of-the-art technical work environment. Qualifications Master's Degree in chemical, biochemical engineering, pharmaceuticals sciences or any other chemistry or engineering related fields or PhD in chemical, biochemical engineering, pharmaceuticals sciences or any other chemistry or engineering related fields 10+ years of GMP experience in pharmaceutical, biotech, CDMO, process development, manufacturing science, technical operations, or manufacturing operations, with strong exposure to clinical and commercial manufacturing environments. 5+ years of senior leadership experience in Technical Operations, manufacturing science, process development, or related technical functions, including leadership of cross-functional or matrix teams, technology transfers, process optimization, validation support, technical documentation, lifecycle management, and digital or data-driven improvement initiatives. Strong knowledge of GMP, quality systems, regulatory frameworks, validation expectations, process safety principles, and inspection-readiness requirements for pharmaceutical manufacturing. Demonstrated decision-making, analytical, troubleshooting, and problem-solving skills; familiar with Lean Six Sigma, operational excellence, data analytics, trending, and proactive process-monitoring approaches in manufacturing environments. Proven ability to lead and develop managers, technical experts, and cross-functional teams with diverse scientific, engineering, manufacturing, quality, and documentation backgrounds. Strong project and stakeholder management skills with the ability to communicate effectively with site leadership, global functions, customers, regulatory interfaces, and external stakeholders. Good understanding of business financial management, budget planning, CAPEX support, COGS improvement opportunities, and business-case development for technical operations and manufacturing technology investments. Proven ability to collaborate across multiple sites and functions, influence without direct authority, align stakeholders through matrix leadership, and implement global technical standards in local operations. Proven ability to build a high-performing Technical Operations organization, develop future-ready talent, drive change, and integrate new technologies, automation, digital tools, and innovation for operational excellence. Strong technical understanding of manufacturing processes, equipment, technology transfer, product stewardship, lifecycle management, CMC-related technical documentation, FMEA, SOPs, qualification protocols, ERP/MES systems, and process-intelligence tools. Annual Salary Range: $141,566.40 - $194,653.80 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. At Bachem, you’ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation—regardless of age, gender, background, religion, or sexual orientation. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
Job Purpose: Our Testing Lab Technician will perform a variety of laboratory procedures of technical nature ensuring compliance with company, customer, industry and regulatory requirements. This position supports the business and our customers by performing standardized tests, producing and documenting reliable results, preparing technical reports and maintaining safe laboratory environment. Job Responsibilities: Conduct testing such as ISTA distribution and cold chain tests. Document test data and test reports using Good Documentation Practices. Interpret and execute industry test standards from organizations such as ISTA, ASTM, and customer protocols. Safely operate test lab equipment. Work on multiple projects simultaneously. Maintain responsive communication with sales reps and customers regarding test status, updates, and results. Work collaboratively with internal departments. Perform other duties as assigned. Additional Responsibilities & Qualifications: Minimum 1 year industry or testing lab experience or packaging related degree. Have a basic understanding of packaging principles and types of corrugated boxes. ISTA Packaging Dynamics Professional certification preferred. Ability to work independently, successfully manage accounts, work under pressure, and adapt to changes in the work environment is essential. CAD software experience (ArtiosCAD, Solidworks) preferred. Work Experience: 1-3 years of related job experience. Ability to work in a team environment. Ability to work quickly and efficiently. Excellent verbal, written, people, and diplomacy skills are required. Must be highly motivated, flexible and deadline driven. Proficient with Microsoft Office Suite. Strong customer service skills (friendly, courteous and helpful). Strong planning and organization skills are required. Strong problem-solving and attention to detail skills are required. Education: Bachelor's Degree Preferred Working Conditions and Physical Requirements: Ability to lift and move up to 50 pounds. Frequent standing, walking, bending, and reaching. Ability to handle packaging samples and testing equipment safely. Ability to work in both laboratory and warehouse environments. What We Offer Engaging and inclusive culture with employee-led Employee Resource Groups, Veritiv Cultural Alliance, recognition platform, etc. Extensive training opportunities, professional development programs, career pathing, and mentorship opportunities. Collaborative atmosphere with our customers and suppliers to create healthier, safer and more sustainable communities through our responsible operations and innovative solutions. Healthcare benefits (including medical, dental, vision, and health savings account), life, AD&D, and disability insurance, 401k, paid time off, tuition reimbursement, employee assistance program, and other fringe benefits. About Veritiv Together with its subsidiaries, Veritiv is the leading full-service provider of packaging solutions. Veritiv also provides JanSan, hygiene, print and publishing products and services. Veritiv serves customers in a wide range of industries, through team members around the world helping shape the success of its customers. For more information, visit www.veritiv.com and connect with the Company on LinkedIn. Veritiv is an Equal Opportunity/Affirmative Action employer. EEO Policy US | EEO Policy Mexico This description does not attempt to define the job's essential functions as defined by applicable disabilities law.
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under supervision, the Composite Technician Assembler is responsible for fabricating, assembling, and repairing advanced composite structures using materials such as carbon fiber, Kevlar, and fiberglass. This role involves reading and interpreting blueprints, preparing molds, and performing material lay-up, curing, and finishing processes. The technician assembles components by trimming, drilling, bonding, and fastening parts to meet precise engineering specifications. They ensure quality through detailed inspections and collaborate with other teams to resolve assembly challenges. Maintaining a safe and organized work environment is essential, as is adherence to safety procedures and documentation requirements. This position requires strong attention to detail, manual dexterity, and experience with composite materials or aerospace components. DUTIES & RESPONSIBILITIES: Part Alignment & Fit-Up: Precisely align and fit composite parts and subassemblies according to engineering drawings and specifications, ensuring proper orientation and fit between components. Bonding & Joining: Apply structural adhesives, sealants, and bonding agents to join composite components. Use proper techniques to ensure strong, durable bonds and prevent contamination. Mechanical Fastening: Install fasteners such as rivets, bolts, and screws using hand and power tools. Verify torque values and fastener placement according to specifications. Component Integration: Assemble complex structures by integrating hardware (inserts, bushings, brackets) and mating composite parts with metallic or non-metallic elements. Surface Preparation: Prepare bonding surfaces by sanding, cleaning, and treating as required to ensure optimal adhesion and structural integrity. Tooling & Fixtures: Set up and use assembly jigs, fixtures, and templates to maintain dimensional accuracy and repeatability during assembly processes. Functional Testing: Perform basic functional checks (fit, movement, alignment) and preliminary inspections to verify assembly quality before final inspection. Documentation: Record assembly steps, process parameters, and any deviations from standard procedures. Communicate findings and issues to supervisors or engineering teams. Collaboration: Work closely with engineering, quality, and fabrication teams to resolve assembly challenges and improve processes. Assist in the preparation of molds and forms. Mark and cut tape, woven material, honeycomb, adhesive and similar materials following templates, guides or specific dimensions and sequences following specific instruction. Route, drill, trim and sand to blueprint dimensions and tolerances. Maintain records as required. Support quality process by maintaining work area in an orderly condition by returning tools, equipment and material to storage areas. 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. Additional Functions: 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 High School diploma or equivalent. Must be customer focused and desirable knowledge of safety practices, OSHA, tool, equipment and materials used in the field. Knowledge of surface preparation, material and techniques for surface finishing. Must possess ability to read and interpret drawings to understand customer requirements. Physical ability to lift to 50 lbs. and ability to work from ladders. Interpersonal skills and written communication skills to work as a team. Be able to interface with employees and upper management from other departments and effectively communicate status of job and estimated completion dates. Ability to obtain and maintain a DoD secret clearance is required. Job Category Manufacturing 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? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Chemist will be a part of the Small Volume Manufacturing team in Carlsbad supporting the small-scale manufacturing process and the experimental products M4Ward™program. The Small Volume team works closely with the R&D, Marketing, Quality Control and Engineering teams. The Small Volume team works to scale up and optimize production of new chemicals transferred from R&D and assist in transitioning production to high volume scale up as needed. Chemical SDS review to conduct and participate in safety reviews Supporting chemical purification by running purification systems and providing technical input on small scale chemical purifications. Perform chemical sampling and packaging and providing technical input on complex container fills and chemical handling Vessel cleaning and break down Maintaining a current chemical inventory Performing equipment setup, maintenance, and troubleshooting Maintaining a clean and efficient lab environment Physical Attributes: Wearing full face air-purifying respirator and other PPE Lifting to 50 pounds Standing, sitting, or walking for up to 8 hours Raising arms up to and possibly above 90-degree angle This is a Day-Shift position: Sunday – Thursday Hours operations 5am-1:30pm Who You Are Minimum Qualifications: Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science discipline. Preferred Qualifications: Knowledge of P&ID’s and basic engineering principles Experience working in gloveboxes Chemical distillation and sublimation knowledge Prior chemistry lab experience handling highly toxic chemicals, acids and bases Strong troubleshooting, documentation, and communication skills A strong focus on quality and safety Experience using Microsoft suite including (Word, Excel, Access, SharePoint) Experience using SAP, Intelex MOC, and LIMS systems Strong data analysis, attention-to-detail and organizational skills Pay Range for this position: $32.00-$50.00 per hour. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are looking for a Production Equipment Maintenance Technician onsite at our San Diego location. The Production Equipment Maintenance Technician is responsible for the maintenance of production equipment and equipment verification in an ISO 13485 compliant manufacturing facility. Assigned tasks will be conducted in both routine and non-routine conditions. *Some Essential Duties and Responsibilities:* · Perform routine preventive maintenance and repairs on automated pneumatic and electromechanical medical device manufacturing equipment. · Troubleshoot equipment issues and implement solutions to minimize downtime. · Ensure the acceptance, daily maintenance, and timely repair of production equipment. · Collaborate with other departments to identify and implement process improvements. · Maintain equipment accounts, maintenance records, and malfunction maintenance records of production equipment. · Perform validation of equipment in production and other departments as needed. · Assist in training operators on standard equipment operation, adjusting and optimizing equipment operation procedures. · Adhere to all safety protocols and guidelines. *Education and /or Experience:* * High school diploma or equivalent required; technical certification or degree preferred, or an equivalency using a combination of education and experience. * Minimum of 3 years' experience in automated equipment maintenance in an FDA-regulated manufacturing environment. *Required Knowledge, Skills and Abilities:* * Experience with operating manual and semi-automated manufacturing equipment using gross and particularly fine motor skills are required. * Expected to display Good Manufacturing Practice (GMP) documentation habits and workmanship in a manufacturing environment according to SOPs or directed work instructions. * Must be able to communicate effectively across multiple audiences in a professional demeanor. * Ability to adapt and handle multiple and simultaneous assigned tasks. * Knowledge of quality systems for medical devices (ISO 13485 and FDA QSR) is preferred. * English fluency required. Bilingual in English/Spanish a plus. 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 ACON 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 $30.00 -$40.00 per hour. ACON offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and ACON may amend, terminate, or enhance the benefits provided, as it deems appropriate. Job Type: Full-time Pay: $30.00 - $40.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Life insurance * Vision insurance Application Question(s): * How many years of experience do you have in automated equipment maintenance in an FDA regulated manufacturing environment? * How much experience do you have troubleshooting PLC or HMI systems? Experience: * Electrical troubleshooting: 3 years (Preferred) Work Location: In person
Position Summary Utility workers are responsible for the essential job functions related to keeping their specific department running. Utility workers will be responsible for general duties involving physically handling products, materials, supplies and inspecting products to ensure high quality. Schedule 5:00 AM - 1:30 PM Wednesday-Sunday (1), or Thursday-Monday (1), Sunday-Thursday (1), with flexibility for overtime. Please note that schedules are limited and are not guaranteed to be available. Available schedules will be offered to candidates based on business needs and staffing availability. Essential Duties and Responsibilities Manual labor including but not limited to: Loading HPP torpedoes. Unloading HPP torpedoes. Standing bottles up at HPP discharge. Running the HPP dumper. Making/pre-building boxes. Bringing in fiber/packaging materials for the lines. Loading caps into cap hoppers. General labor related to the bottling process. General labor related to shipping/pack-out/receiving/inventory, etc. Building pallets, lifting, moving/stacking cases up to 50 lbs. Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Regular and reliable attendance. Non-Essential Job Duties May perform similar and incidental duties as required. Experience Manufacturing experience is a plus but not required. Abilities Ability to work well under time constraints and prioritize work to meet commitments/deadlines. Ability to work cross-functional with other departments. Attention to detail and a commitment to maintaining high product quality. Flexibility to work in a fast-paced and dynamic production environment. Language Skills Ability to communicate, read, listen, and understand English. Bilingual is a plus. Working Environment Regular exposure to wet, cold manufacturing environments (temperatures as low as 35°F) Occasional exposure to dry warehouse spaces or freezer conditions (down to -10°F) Frequent exposure to high noise levels (above 85 dBA) Requires use of PPE including safety glasses, ear protection, gloves, and steel-toed footwear Physical Requirements Ability to stand and walk for the full duration of the shift Must be able to frequently lift/move hoses, equipment, and chemical containers weighing up to 50 lbs. Ability to push/pull up to 100 lbs. with continuous motion Must be able to bend, kneel, squat, climb stairs/ladders, and reach overhead regularly Must have sufficient hand strength and manual dexterity to operate sanitation tools and machinery Must be able to pass a pre-employment physical Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Pay rate: $18.00 an hour Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #INDHP Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay Education Preferred High School or better Licenses & Certifications Preferred Drivers License 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 (https://www.eeoc.gov/poster) notice from the Department of Labor.
Quality Engineer Department: Quality Reports To: Quality Manager Salary Range: $80-$95,000 depending on experience This role is onsite in Escondido, CA. Why Join Us? Gain exposure to new technologies, automated inspection systems, and cross-functional leadership opportunities Competitive pay, PTO, and benefits Strong team culture focused on quality and improvement About Us ARCH Global Precision manufactures high-precision components and engineered solutions for customers in demanding industries. Through advanced manufacturing capabilities, technical expertise, and a strong commitment to quality, we help our customers bring innovative products to market with confidence. About the Role We are seeking an experienced Quality Engineer to join our Quality team. This position plays a critical role in ensuring customer satisfaction, reducing internal scrap, driving continuous improvement initiatives, and supporting product and process validations. The ideal candidate is detail-oriented, analytical, and thrives in a fast-paced manufacturing environment while collaborating effectively with cross-functional teams. Key Responsibilities As a Quality Engineer, you will: Develop and maintain quality plans, inspection plans, control plans, work instructions, and PFMEAs. Support new product introductions, product revisions, and process development activities. Participate in product qualifications, validations, and change control processes. Collaborate with Engineering to review drawings and ensure customer requirements are clearly defined and understood. Conduct measurement system analyses including GR&R studies and establish effective inspection methods. Lead or support Material Review Board (MRB) activities and nonconformance investigations. Manage customer complaints, CAPAs, NCMRs, and corrective action activities. Utilize quality tools such as Root Cause Analysis, FMEA, Risk Analysis, SPC, and 8D problem-solving methodologies. Perform internal audits and support external audits as required. Analyze process data and conduct process capability studies to drive continuous improvement. Train employees on quality requirements, inspection methods, and metrology practices. Support equipment validations and qualification activities in partnership with Maintenance, IT, and Operations teams. Drive initiatives to improve manufacturing quality, efficiency, and customer satisfaction. Required Qualifications Bachelor's degree in Manufacturing Engineering, Quality Engineering, or a related technical discipline, or an equivalent combination of education and experience. Minimum of 3 years of quality engineering experience in a manufacturing environment. Strong knowledge of quality systems, methodologies, and problem-solving tools. Experience with CAPA programs, process capability studies, GR&R, PFMEA, and SPC. Knowledge of ISO standards, preferably ISO 13485, and FDA regulations including 21 CFR Part 820. Strong written and verbal communication skills. Proficiency in Microsoft Office applications including Word, Excel, Outlook, and PowerPoint. Ability to work effectively in a cross-functional team environment. Preferred Qualifications ASQ Certification (CQE, CSQE, Six Sigma Black Belt, Lean, or equivalent). Strong GD&T knowledge and experience. Experience with Minitab. Experience using automated inspection equipment such as CMMs, Keyence, Vertex, or similar systems. Experience developing manufacturing quality plans and driving process optimization projects. What We're Looking For High energy and self-motivation. Strong attention to detail and accountability. Excellent analytical and problem-solving abilities. Effective interpersonal and communication skills. Ability to manage multiple priorities in a fast-paced environment. Commitment to continuous improvement and operational excellence. Physical Requirements Ability to sit, stand, walk, talk, and hear frequently throughout the workday. Regular computer use. Ability to lift up to 20 pounds occasionally. Equal Opportunity Employer Additional Notes ARCH Global Precision is an Equal Opportunity Employee and wholeheartedly supports diversity in the workplace as a basic premise for business success. All employees of ARCH Global Precision are employed on an at-will basis. This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employee(s) will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. A review of this position has excluded the marginal functions of the position that are incidental to the performance of fundamental job duties. All duties and responsibilities are essential job functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbent(s) will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. 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 (https://www.eeoc.gov/poster) notice from the Department of Labor.
*About Us* At L.F. Industries, we’ve built over 40 years of expertise in precision machining for the aerospace, defense, commercial, and semiconductor industries. We specialize in low-volume, high-mix work where every day brings new challenges. We are seeking a highly skilled CNC Programmer to join our precision manufacturing team. In this role, you will be responsible for creating, optimizing, and maintaining multi-axis machining programs using GibbsCAM. You will support floor operations by developing efficient toolpaths for a diverse lineup of 3, 4, and 5-axis mills and horizontal machining centers to produce parts for aerospace, defense, commercial, and semiconductor industries. *What You’ll Do* * Generate and optimize CNC programs for 3,4 and 5 axis mills using GibbsCAM software. * Develop comprehensive setup sheets, tooling lists, and work instructions to ensure smooth handoffs to setup machinists and operators. * Assist with initial first-article prove-outs, working closely with shop personnel to adjust feeds, speeds, and toolpaths for maximum efficiency. * Set-up machines as required to prove out new or existing part programs. *What We’re Looking For* * 3+ years of dedicated CNC programming experience in a precision job shop environment. * Demonstrated proficiency using GibbsCAM software or similar CADCAM software. * Strong understanding of machining dynamics, custom workholding strategies, and modern cutting tool technologies. * Strong ability to read and interpret detailed blueprints, engineering models, and complex GD&T specifications. * Excellent problem-solving ability and sharp attention to detail. *Preferred Skills* * Experience setting up 3, 4, and/or 5 axis mills with Fanuc controls. * Background in low-volume, high-mix job shop environments. * CAD/CAM programming experience *Why Join Us?* * Competitive pay based on your experience and capability. * Work in a clean, well-equipped, and collaborative shop environment. * Be part of a company where your skill and independence are valued. * Opportunities to grow alongside a stable and respected precision machining company. * Excellent benefits - we pay 90% of your medical insurance, 100% dental and vision coverage. 401K +Match, Profit Sharing, PTO, Paid Holidays If you’re a hands-on problem solver who thrives programming machined parts and takes pride in precision, we’d love to hear from you. Apply today and bring your expertise to L.F. Industries! Pay: $40.00 - $60.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Profit sharing * Vision insurance People with a criminal record are encouraged to apply Work Location: In person