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General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. Under general supervision, this position supports the manufacturing production process with focus on the design, development, and implementation of new or revised production processes for the efficient and economical fabrication of parts, components, sub-assemblies, and final assemblies. DUTIES AND RESPONSIBLITIES: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub- assemblies, and final assemblies. Applies technical knowledge to analyze, investigate and resolve manufacturing and engineering related problems. Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery. Collaborates with product design engineering on technical specifications that will best utilize equipment and manufacturing techniques. Investigates, dispositions and justifies product, drawing, and specification non conformances. Estimates manufacturing costs and determines time standards. Ensures that production processes and procedures are in compliance with regulations. Maintains records and reporting systems for coordination of manufacturing operations. Performs supplier audit and oversight as necessary to ensure conforming product being delivered. Communicates technical responses to supply base questions during proposal efforts, manufacturing efforts and post manufacturing efforts. Supports on-site supplier kick off meetings to discuss manufacturing plan, schedule and supplier deliverables. Assist with development, status and needs of the project plan to the Control Account Manager. Maintains the strict confidentiality of sensitive information. Performs other duties as assigned. 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. 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 bachelors in engineering or a related technical field as well as two or more years of manufacturing engineering experience. May substitute equivalent experience in lieu of education. Experience participating teams as a key contributor to up-scale production lines across the entire manufacturing process using lean principles (Define Value, Value Stream Mapping, Creating Flow, Establish Pull, ect). Knowledge in both Operations and Manufacturing Engineering disciplines related to complex welded and machined parts preferred Bachelors in engineering or a related technical field as well as Manufacturing Engineering and/or Operations experience is desired. Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables. Good communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team. Ability to obtain and maintain DoD Secret Clearance Job Category Engineering Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 68,770 Pay Range High 116,193 Travel Percentage Required 25% - 50% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. Under general direction this position is responsible for inspecting cables, parts, assemblies, tooling fixtures and material to ensure compliance with customer requirements, company specifications, and quality requirements. Sets up, operates, inspects, tests, and adjusts new and reworked tools, dies, gauges, jigs and fixtures for conformance to engineering drawings and specifications. Maintains, processes, and updates confidential and sensitive electronic and hard copy reports, records and statistics. DUTIES AND RESPONSIBILITIES: Inspects cables, machined parts, components, assemblies and materials to ensure compliance with appropriate regulatory guidelines (Military Standards, ASTM and ANSI, and ASME Code). Provides various electronic and hard copy reports of inspections and notifies appropriate parties including project engineers. Sets up and calibrates measuring and test equipment and schedules service and repair of equipment. May maintain calibration computer databases. May observe testing and provide oversight, as necessary, to verify compliance with requirements. May perform nondestructive examinations on various metallic and nonmetallic materials, parts, and assemblies using methods such as penetrant, hi-pot and hardness testing. May interact with regulatory agencies and customers during audits and review of company inspection and calibration activities. May monitor and verify quality in accordance with statistical process or other control procedures. 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 Duties 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, trade school certificate, military training or equivalent in quality inspections or certification by a professional group such as ASQ or AWS, and one or more years of progressive experience in electrical, mechanical, electromechanical or metrology inspection and calibration. May substitute additional experience in lieu of formal education and training. Must possess: Ability to read and understand engineering drawings and specifications, and perform mathematical computations; Good communication skills to effectively interface with all levels of employees including management; Ability to interpret non-routine information and respond to non-routine issues; Ability to maintain the confidentiality of sensitive information.; and Good computer skills. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Experience with IPC-A-610, IPC-D-620, JSTD-001, AS9100 are desirable. Job Category Quality Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 52,020 Pay Range High 77,325 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
Job Information Number ICIMS-2026-10349 Job function Other Job type Full-time Location Werfen - San Diego - WBH - 6260 Sequence Drive San Diego, California 92121 United States Country United States Shift 1st About the Position Introduction Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Job Summary The Staff Manufacturing Engineer applies advanced technical insight, hands-on experience, and deep knowledge of electrical systems to support complex Manufacturing Engineering activities focused on instrument electronics and printed circuit board assemblies (PCBAs) in the instrument area. This role is responsible for solving multifaceted issues in new product design transfer, manufacturing process development and optimization for medical diagnostic instruments, electrical integration, sustaining engineering, and daily production operations. The Staff Manufacturing Engineer will lead cross-functional teams on continuous improvement projects, develop and execute validation protocols and final reports, and drive manufacturing activities to ensure high-yield, reliable production of complex electromechanical instruments. The annual base salary range for this role is currently $145,000 to $175,000. This is a bonus-eligible position. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs. Responsibilities Key Accountabilities Function as a lead team member for design control project teams; ensure design requirements are met and comply with applicable standards. Work as a lead project team member to complete all activities needed to conclude projects per plans. Develop and implement process controls for new products and for transfer to manufacturing. Develop statistically based sampling plans for design verification, design and process validation activities, new/existing product test methods, and incoming inspection to ensure they meet their predetermined requirements. Oversee validation project teams; prepare agendas, issue meeting minutes, and participate in development of quality plans. Write, review, and approve validations (installation qualification IQ/operational qualification OQ/performance qualification PQ protocols, Standard Operating Procedures (SOP), technical reports and final reports) for new products, processes, and equipment; ensure systems, utilities, and processes comply with the Food and Drug Administration (FDA) and industry standards. Function as an advanced support resource; lead training initiatives of department staff as directed. Provide statistical analysis of process and test data to support validation reports and continuous improvement. Ensure all projects/processes are following FDA, Good Manufacturing Practices (GMP), Quality System Requirement (QSR), ISO-13485:2003 and other applicable requirements. Actively participate in FDA inspections, ISO audits, and internal/customer audits as a subject matter expert on instrument electronics. Provide cross-functional support by delivering required technical documentation and data to meet compliance needs. Identify and implement opportunities for continuous improvement in Instrument yield, cycle time, and first-pass quality. Coordinate activities with cross-functional departments, external CMs/vendors, and customers. Maintain fiscal responsibility and budget compliance. Ensure and maintain compliance with the company’s quality system requirements through training and adherence to policies, procedures, and processes. Other duties as assigned. Networking/Key relationships To be determined based on business needs. Qualifications Minimum Knowledge & Experience for the position: Bachelor’s degree (Mechanical or Electrical Engineering) or equivalent years of experience; advanced degree a plus. Eight (10) to ten (15) years previous manufacturing engineering experience preferred; previous experience within a regulated medical device or pharmaceutical environment strongly preferred. Skills & Capabilities: Six Sigma Green Belt or Black Belt methodology a plus. Strong Electrical Engineering background with deep proficiency in electrical schematics, BOM management, and electromechanical instrument integration. In-depth knowledge of instrument electronics and PCBA technologies, including sustaining support, integration, and technical oversight of contract manufacturers. Excellent troubleshooting and root-cause analysis skills for electrical and instrument-level failures in a production/CM environment. Expertise in writing and performing validations in a GMP and ISO9001 regulated environment. This also includes URS/FAT for new equipment acquisition. Strong working knowledge of statistical tools including Design of Experiments (DOE), Statistical Process Control (SPC), process capability analysis (Cp/Cpk), and sampling plans to support validation and quality control. Thorough understanding of FDA 21 CFR Part 820, GMP, ISO 13485, and OSHA regulations, with demonstrated experience supporting regulatory audits. Excellent communication, organizational, and time management skills; ability to pay close attention to detail. Excellent technical writing, verbal communication, and cross-functional leadership skills with the ability to clearly convey complex electrical and manufacturing concepts. Good leadership ability with experience coordinating and providing technical guidance to external CMs/vendors. Travel requirements: Able to travel to visit vendors processes. If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact [email protected] for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. www.werfen.com
Description: Production Scheduler II will be responsible for maintaining a high level of OTS, customer satisfaction and clear concise communication between Operations, outsourced supplies and Commercial. This role will be integral in monitoring our incoming workflow and giving realistic, aggressive timelines. Requirements: ESSENTIAL JOB FUNCTIONS: Serve as the primary on-site point of contact during night shift for production and equipment-related issues Monitor all orders over 5k and ensure we will be able to ship out on time. This means getting ahead of surprises like rebuilds & failed builds. Work closely with project technicians to ensure that they are building parts on time and scheduling builds with enough time to recover. Work with commercial team to ensure smooth production on time production of order Collaborate with external suppliers to align delivery timing and quality standards, minimizing production disruptions. Drive cross-functional and external workflows to align resources and processes in support of on-time delivery objectives. Collaborate cross-functionally with the Purchasing Coordinator to coordinate internal and external workflows that support production execution. Make independent scheduling and prioritization decisions to balance capacity, material availability, and delivery commitments. Exercise discretion in adjusting production plans in response to supply chain disruptions or changing business needs. Be able to quickly respond to issues such as downed equipment, material shortage. Working with manufacturing leads to help identify opportunities for improvement such as efficiency, 5S, and lean manufacturing. Work closely with Manufacturing Engineering to resolve any issues impacting OTS. Providing detailed reasons to commercial on why schedules weren’t kept. Responsible for managing the Production daily ship list and updating the Forecast PM Team with questionable geometry, issues, concerns and schedules that can’t be met. Own production scheduling outcomes, including on-time delivery performance and production flow efficiency. Accountable for identifying and resolving schedule conflicts that impact production or customer commitments. Proactively identify scheduling risks and develop mitigation plans to prevent production delays. Analyze constraints and recommend corrective actions to leadership when delivery targets are at risk. Maintain an OTD of 95% or better in accordance with MJF metrics Enter to the QA database Work closely with the MJF Supervisors, Engineering, Project Technicians and the Shipping Department Perform work instructions as detailed on the Job Sheet Visually inspect parts for defects Reject any parts that cannot meet the customer’s needs and create an appendix Ensure that all jobs make it to the QC and shipping department on time Maintain a safe work environment Promote a positive work environment Miscellaneous duties as assigned SKILL REQUIREMENTS/QUALIFICATIONS: High School Diploma or equivalent required. Previous experience or interest in 3D Printing/Additive Manufacturing/Manufacturing or tech, and willingness to learn more is preferable Bachelor's degree in Engineering, Business, Supply Chain Management, Operations Management, or related field; OR 3-5 years of equivalent experience in a technical manufacturing environment Project management experience in a manufacturing setting, preferably in additive manufacturing, machining, or contract manufacturing Experience with contract review, negotiation, and management (customer and/or supplier contracts) Experience with technical customer service and consultative sales approaches Ability to read, understand, and execute work with detailed job instructions. Excellent hand skills and coordination. Keen attention to detail. Strong analytical and problem-solving skills. Solid organizational skills. Excellent verbal and written communication skills. Ability to work within a team as well as individually. Ability to multitask when needed. Ability to accomplish tasks without constant supervision. WORK ENVIRONMENT: The performance of this position will require exposure to the manufacturing areas where all areas require the use of personal protective equipment such as safety glasses, hearing protection, steel toe shoes, and other mandatory safety equipment. For the most part, ambient temperatures are climate controlled due to production requirements PHYSICAL DEMANDS: Ability to stand and walk for extended periods (up to 8–10 hours per shift) on a manufacturing floor Frequent use of hands for handling, sanding, polishing, grinding, and finishing parts Ability to lift, carry, push, and/or pull materials weighing up to 25–50 pounds, with or without assistance Frequent reaching, bending, stooping, kneeling, and crouching Manual dexterity and hand-eye coordination required to operate finishing tools and equipment Ability to wear required personal protective equipment (PPE), including respirators, gloves, safety glasses, and protective clothing Ability to work in a manufacturing environment that may include exposure to dust, fumes, noise, chemicals, and varying temperatures Ability to distinguish colors, finishes, and surface defects as needed for quality inspection Sufficient vision (with or without correction) to inspect detailed parts and surfaces Ability to safely operate finishing equipment such as grinders, sanders, bead blasters, or similar tools SAFETY AND POLICY PRACTICES: Each employee must be knowledgeable of standard safety policies and procedures and adhere to the same while supporting the goals and objectives of the organization and recognizing the Company’s need to achieve its business objectives. Each employee is responsible for complying with company hazardous waste disposal procedures. AFFIRMATIVE ACTION: ADDMAN Engineering is proud to be an Equal Opportunity Employer of Minorities, Women, Protected Veterans, and Individuals with Disabilities. All terms and conditions of employment will be administered without regard to an individual’s sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected veteran status, or any other characteristic protected by applicable law. NOTE: This job description is intended to describe the general level of work being performed. This job description is not intended to be all-inclusive. The duties of this position may change from time to time, and the employee may perform other related duties to meet the ongoing needs of the organization. ADDMAN Engineering reserves the right to add, delete or modify these duties and responsibilities at its discretion. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Employment is at-will, and nothing in this job description is intended to create or imply a contractual relationship or alter the at-will status of the employee.
*Overview* *Job Overview:* We are seeking a detail-oriented and technically proficient *Technical Designer* to manage all production files for printing and CNC machines. This role requires close collaboration with our manufacturing team and designers to refine production details, optimize fabrication methods, and ensure production packages accurately reflect fabrication processes. The *Technical Designer* will also be responsible for generating *Bills of Materials (BOMs)* and providing project and production managers with a detailed list of all required hardware and materials for signage production. *Key Responsibilities:* * Prepare and refine production-ready files for *printing and CNC machining*, ensuring accuracy and manufacturability. * Collaborate with *designers and manufacturing teams* to clarify production details and optimize fabrication processes. * Create and maintain *Bills of Materials (BOMs)* for projects, specifying all materials and hardware required. * Work closely with *project managers and production managers* to provide comprehensive lists of materials, ensuring efficient procurement and production workflows. * Troubleshoot and resolve any technical issues related to production files, ensuring seamless execution during fabrication. * Ensure adherence to *industry standards* and best practices for file preparation and manufacturing techniques. * Maintain a well-organized digital library of production files, templates, and project documentation. *Qualifications & Skills:* * *Experience in technical design*, production file preparation, or a related field, preferably within the signage, printing, or manufacturing industry. * *Proficiency in design and CAD software*, such as Adobe Illustrator, Rhino, and CNC Software. * Strong understanding of *printing and CNC machining processes*, including file formatting, cutting paths, material specifications, and production constraints. * Excellent attention to detail and problem-solving skills to ensure accuracy in production files and material specifications. * Ability to effectively communicate with *designers, fabricators, and project managers* to align production details with manufacturing capabilities. * Knowledge of *signage materials and hardware* is highly preferred. * Strong organizational skills and ability to manage multiple projects simultaneously. Job Type: Full-time Benefits: * Health insurance * Paid time off Ability to Commute: * San Diego, CA 92121 (Required) Ability to Relocate: * San Diego, CA 92121: Relocate before starting work (Required) Work Location: In person
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 general supervision with detailed instruction for new work or a special assignment, this position is responsible for performing a wide variety of repetitive or standard electronic and /or mechanical assemblies and subassemblies. Determines and/or follows methods and sequence of operations in performing assembly tasks such as wiring, component installation, hand soldering and cable harnessing on assembly units. May monitor and verify quality in accordance with control procedures. DUTIES & RESPONSIBILITIES: Assembles components, assemblies or sub-assemblies. Makes setups and adjustments holding tolerances to specifications. May perform duties as required in assembly of electronic equipment such as cables, harnesses, chassis, and printed circuit boards, or may perform mechanical assembly of panels, LRU's, batteries, and servo motors. May disassemble, modify, rework, and reassemble assemblies or subassemblies. 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 May assist in training lower level assemblers. Performs housekeeping and cleanup duties upon completion of assigned tasks. 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 Typical requires a high school diploma or equivalent and three or more years experience. Proficient in the use of hand tools and torque wrenches; must have a solid understanding of prevailing torque and its proper application. Must be customer focused and possess: The ability to read and interpret engineering drawing and wire lists. Good understanding of the general aspects of the job with limited technical comprehension. Knowledge of computer operations and applications pertinent to the position. Familiarity with use of soldering and compression connection tools. 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 Manufacturing Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 44,590 Pay Range High 66,295 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
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. This position is responsible for performing complex functions related to machine tools. Plans, lays out work, sets up and operates all types of lathes, mills or grinders to machine or grind developmental, production or maintenance parts to exacting tolerances and dimensions. DUTIES AND RESPONSIBILITIES: Plans sequence of machine operation as required using drawings, sketches or other written or verbal instructions. Ideal candidate to have knowledge in CAM system programming IE. Mastercam, Hypermill etc. along with knowledge in CNC setup on mill or lathe operations. Reviews engineering drawings, sketches, graphic illustrations or verbal/written correspondence to compute angular and linear dimensions. Determines cutting tools to be used, method of holding, and machine speeds and feeds. May monitor and verify quality of work performed by equal or lower level personnel, such as first part inspection. Sets up tooling and production stock to be machined using a wide variety of both conventional and CNC machining equipment to perform machining of complex parts by drilling, reaming, boring, tapping, slotting, and dovetailing on ferrous and non-ferrous metals and their alloys. Designs, fabricates, and/or improvises tooling, and tooling aids to assist in machine setups utilizing various shop equipment. Performs preventive maintenance and makes machine adjustments as required using hand tools and precision measuring instruments. May provide guidance or training to equal or lower level machinist. 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 a high school diploma, technical/trade school training or equivalent and two or more years related experience. Must be customer focused and possess the ability to perform semi-routine set-up and fabrication of machined parts. Good knowledge of machining equipment including ability to use judgment and safe practices. Ability to read and understand engineering blue prints and diagrams. Skills to maintain the flow of work within the unit. Good interpersonal skills and written communication skills to interface with employees and supervisor. Basic computer skills. Must be able to work both independently and in a team environment. Flexibility to work extended hours as required. Job Category Engineering Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 44,590 Pay Range High 66,295 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
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. This is a second shift position that is responsible for performing complex functions related to machine tools. Plans, lays out work, sets up and operates all types of lathes, mills or grinders to machine or grind developmental, production or maintenance parts to exacting tolerances and dimensions. DUTIES AND RESPONSIBILITIES: Second Shift Plans sequence of machine operation as required using drawings, sketches or other written or verbal instructions. Ideal candidate to have knowledge in CAM system programming IE. Mastercam, Hypermill etc. along with knowledge in CNC setup on mill or lathe operations. Reviews engineering drawings, sketches, graphic illustrations or verbal/written correspondence to compute angular and linear dimensions. Determines cutting tools to be used, method of holding, and machine speeds and feeds. May monitor and verify quality of work performed by equal or lower level personnel, such as first part inspection. Sets up tooling and production stock to be machined using a wide variety of both conventional and CNC machining equipment to perform machining of complex parts by drilling, reaming, boring, tapping, slotting, and dovetailing on ferrous and non-ferrous metals and their alloys. Designs, fabricates, and/or improvises tooling, and tooling aids to assist in machine setups utilizing various shop equipment. Performs preventive maintenance and makes machine adjustments as required using hand tools and precision measuring instruments. May provide guidance or training to equal or lower level machinist. 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 a high school diploma, technical/trade school training or equivalent and two or more years related experience. Must be customer focused and possess the ability to perform semi-routine set-up and fabrication of machined parts. Good knowledge of machining equipment including ability to use judgment and safe practices. Ability to read and understand engineering blue prints and diagrams. Skills to maintain the flow of work within the unit. Good interpersonal skills and written communication skills to interface with employees and supervisor. Basic computer skills. Must be able to work both independently and in a team environment. Flexibility to work extended hours as required. Job Category Engineering Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 44,590 Pay Range High 66,295 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
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. This role combines business process analysis, technical writing, and project coordination to support engineering execution within a Quality Management System (QMS). The position focuses on process mapping for Engineering Design Procedures, collaborator process assessments, and Design Assurance support to ensure audit-ready documentation, clear process definition, and effective milestone planning across the full engineering design lifecycle. DUTIES AND RESPONSIBILITIES: Develop, document, and maintain engineering procedures, Design Assurance processes, checklists, templates, and training materials in alignment with QMS and contractual requirements. Perform process mapping and continuous improvement activities to standardize Engineering Design Procedures and enhance process clarity and efficiency. Gather, analyze, and synthesize technical data from engineering artifacts (e.g., drawings, specifications, test procedures) and subject matter experts to produce clear, accurate, and user-focused documentation. Ensure audit-ready documentation, including traceability, configuration control, and alignment with design reviews, verification activities, and milestone planning. Coordinate and support technical and process reviews, ensuring proper stakeholder engagement, documentation tracking, and record retention. Conduct collaborator process assessments and support alignment with internal processes and external requirements. Identify process gaps, risks, and inefficiencies; support resolution and continuous improvement efforts with engineering and program teams. Ensure compliance with company policies, regulatory requirements, and safety practices. 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 Bachelors degree in a related field and six or more years experience as a business process analyst working with computerized management systems to include, but not limited to, product life cycle systems. May substitute equivalent experience in lieu of education. Experience developing and maintaining controlled technical documentation, procedures, and process artifacts. Working knowledge of QMS and Design Assurance principles, including document control, traceability, configuration management, and design review processes. Familiarity with regulated environments (e.g., AS9100, CMMI) preferred. Proficiency with document management and collaboration tools (e.g., SharePoint or similar systems). Strong analytical, organizational, and communication skills, with the ability to translate complex technical concepts into clear documentation. Ability to work independently and collaboratively in a team environment while maintaining confidentiality. Ability to obtain and maintain DOD security clearance is required. Job Category Engineering Experience Level Mid-Level (3-7 years) Workstyle Hybrid Full-Time/Part-Time Full-Time Salary Pay Range Low 73,700 Pay Range High 128,780 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
Introduction: Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview: Job Summary The Staff Manufacturing Engineer applies advanced technical insight, hands-on experience, and deep knowledge of electrical systems to support complex Manufacturing Engineering activities focused on instrument electronics and printed circuit board assemblies (PCBAs) in the instrument area. This role is responsible for solving multifaceted issues in new product design transfer, manufacturing process development and optimization for medical diagnostic instruments, electrical integration, sustaining engineering, and daily production operations. The Staff Manufacturing Engineer will lead cross-functional teams on continuous improvement projects, develop and execute validation protocols and final reports, and drive manufacturing activities to ensure high-yield, reliable production of complex electromechanical instruments. The annual base salary range for this role is currently $150,000 to $175,000. This is a bonus-eligible position. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs. Responsibilities: Key Accountabilities Function as a lead team member for design control project teams; ensure design requirements are met and comply with applicable standards. Work as a lead project team member to complete all activities needed to conclude projects per plans. Develop and implement process controls for new products and for transfer to manufacturing. Develop statistically based sampling plans for design verification, design and process validation activities, new/existing product test methods, and incoming inspection to ensure they meet their predetermined requirements. Oversee validation project teams; prepare agendas, issue meeting minutes, and participate in development of quality plans. Write, review, and approve validations (installation qualification IQ/operational qualification OQ/performance qualification PQ protocols, Standard Operating Procedures (SOP), technical reports and final reports) for new products, processes, and equipment; ensure systems, utilities, and processes comply with the Food and Drug Administration (FDA) and industry standards. Function as an advanced support resource; lead training initiatives of department staff as directed. Provide statistical analysis of process and test data to support validation reports and continuous improvement. Ensure all projects/processes are following FDA, Good Manufacturing Practices (GMP), Quality System Requirement (QSR), ISO-13485:2003 and other applicable requirements. Actively participate in FDA inspections, ISO audits, and internal/customer audits as a subject matter expert on instrument electronics. Provide cross-functional support by delivering required technical documentation and data to meet compliance needs. Identify and implement opportunities for continuous improvement in Instrument yield, cycle time, and first-pass quality. Coordinate activities with cross-functional departments, external CMs/vendors, and customers. Maintain fiscal responsibility and budget compliance. Ensure and maintain compliance with the company’s quality system requirements through training and adherence to policies, procedures, and processes. Other duties as assigned. Networking/Key relationships To be determined based on business needs. Qualifications: Minimum Knowledge & Experience for the position: Bachelor’s degree (Mechanical or Electrical Engineering) or equivalent years of experience; advanced degree a plus. Eight (10) to ten (15) years previous manufacturing engineering experience preferred; previous experience within a regulated medical device or pharmaceutical environment strongly preferred. Skills & Capabilities: Six Sigma Green Belt or Black Belt methodology a plus. Strong Electrical Engineering background with deep proficiency in electrical schematics, BOM management, and electromechanical instrument integration. In-depth knowledge of instrument electronics and PCBA technologies, including sustaining support, integration, and technical oversight of contract manufacturers. Excellent troubleshooting and root-cause analysis skills for electrical and instrument-level failures in a production/CM environment. Expertise in writing and performing validations in a GMP and ISO9001 regulated environment. This also includes URS/FAT for new equipment acquisition. Strong working knowledge of statistical tools including Design of Experiments (DOE), Statistical Process Control (SPC), process capability analysis (Cp/Cpk), and sampling plans to support validation and quality control. Thorough understanding of FDA 21 CFR Part 820, GMP, ISO 13485, and OSHA regulations, with demonstrated experience supporting regulatory audits. Excellent communication, organizational, and time management skills; ability to pay close attention to detail. Excellent technical writing, verbal communication, and cross-functional leadership skills with the ability to clearly convey complex electrical and manufacturing concepts. Good leadership ability with experience coordinating and providing technical guidance to external CMs/vendors. Travel requirements: Able to travel to visit vendors processes. Closing: If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact [email protected] for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. www.werfen.com
How You’ll Make an Impact: The Quality Control Manager in San Clemente, CA oversees all QC laboratory operations and testing activities. This role supervises QC staff, ensures compliant and efficient lab execution, maintains cGMP compliance and data integrity, and provides technical leadership while keeping the laboratory inspection-ready and supporting project teams as needed. What You’ll Do: General laboratory Management Oversees and assigns raw material, in-process, finished product, and stability testing across multiple pharmaceutical products to ensure timely batch release and stability commitments Manages cGMP stability programs for clinical and commercial products and performs trend analysis to identify risks or emerging issues Oversees the internal reference standard qualification, lifecycle management, and documentation program Oversees method validations, verifications, transfers, and feasibility studies to support product development and commercialization Oversees audit trail review process and 21 CFR Part 11 compliance Evaluates internal versus external testing strategies and recommends improvements to optimize efficiency, cost, and compliance Recommends laboratory equipment, instrumentation upgrades, and new technologies to support future QC capability needs Oversees qualification and calibration of analytical equipment and approves vendor qualification documentation, may include URS development, IQ/OQ/PQ approval authority, equipment lifecycle planning, obsolescence strategy Monitors contract testing laboratories, reviews external analytical data, and ensures CRO/CMO compliance with quality standards Identifies and resolves technical challenges impacting method transfer, assay implementation, and laboratory operations Responsbile for laboratory budget management such as headcount forecasting, consumables planning, and alignment on capital expenditure planning Documentation & Compliance Reviews and approves analytical data, laboratory documentation, and Certificates of Analysis to ensure accuracy, completeness, and data integrity Oversight of audit trail review process Authors and/or reviews laboratory investigations (OOS, OOT, deviations) and ensures appropriate root cause analysis, impact assessment, and corrective actions Authors, reviews, and approves analytical methods, validation protocols, qualification reports, and stability reports to ensure regulatory compliance Provides annual product quality review analytical input Ensures QC documentation, laboratory systems, and practices comply with ICH, USP, Pharm. Eur., JP, and applicable global regulatory guidelines Supports regulatory submissions by preparing or reviewing technical summaries Contributes to SOP development, process improvements, and continuous improvement initiatives within the laboratory Inspection Readiness & Regulatory Activities Ensures QC maintains inspection readiness, compliance, and a culture of data integrity Serves as the primary technical lead for QC investigations and escalates significant quality risks appropriately Analyzes and interprets complex analytical data and provides scientifically sound conclusions to support quality and regulatory decisions Participates in regulatory inspections and supports responses to regulatory agencies as required Owns QC laboratory performance metrics and drives continuous improvement initiatives to improve efficiency and compliance Team Leadership & Cross-Functional Support Supervises QC chemists, sets priorities, and ensures compliant execution of laboratory activities in accordance with cGMP requirements Responsible for QC chemist training matrix updates in coordination with training team Provides technical leadership, mentorship, development, and performance management for QC chemists Participates in cross-functional development and manufacturing meetings as QC representative Communicates QC priorities, timelines, and risks to stakeholders and leadership Collaborates with R&D to assess and implement specialized analytical approaches, when applicable Ownership of QC lab related change control or technical impact assessments and CAPA approval authority Employing technical knowledge to assist with Quality risk management (FMEA) and risk management during Quality investigations Digital and Automation Strategy Oversee implementation of LIMS / electronic notebooks Improve digital data analytics How You’ll GetThere: 8+ years of experience in analytical chemistry within Pharmaceutical QC environment. Minimum of 1 year of previous management experience in Pharmaceutical QC laboratory, including supervision of QC chemists. Demonstrated leadership skills with the ability to prioritize workload, mentor staff, and ensure inspection readiness and cGMP compliance. Experience managing and overseeing external contract testing laboratories (CROs/CMOs) is preferred. Understanding of analytical platforms including HPLC, FTIR, UV/Vis, and Drug Release. Experience overseeing analytical method validation, verification, method transfer activities, and management of cGMP stability programs. Working knowledge of ICH guidelines, major pharmacopoeias (USP, Ph. Eur., JP), CTD structure, and global regulatory expectations. Strong analytical skills (interpret data, summarize data, present data). Strong written and verbal communication skills. · Motivated and able to work independently, as well as within a team. Exhibits personal integrity, credibility, and responsibility. · Excellent organizational skills and ability to work on multiple projects/tasks. · Meets milestones and schedules. Bachelor’s degree in a scientific discipline is required
Job Summary The RAW Machine Operator is responsible for operating, monitoring, and adjusting production equipment used in our salami manufacturing plant. This role ensures machines run safely, efficiently, and according to quality and food safety standards, supporting consistent production of finished products. Essential Functions and Responsibilities (not restrictive) Operate and monitor food processing equipment including Poly-clip, Stuffers, Grinder, Mixer Line, and other equipment. Set up machines at the start of shift, perform machine adjustments to maintain proper speeds, weights, cuts, and product specifications. Support changeovers, cleaning, and equipment teardown/assembly. Verify process parameters and document results according to HACCP, GMP, and USDA/FSIS requirements; perform routine operational checks to ensure product quality, weight accuracy, and product integrity. Document production data accurately and completely. Identify and troubleshoot minor mechanical issues; escalate problems to Lead, Maintenance or Supervisor when needed. Maintain clean and sanitized work areas and equipment following sanitation and food safety practices. Follow all safety procedures, including lockout/tagout, PPE use, equipment guarding, and safe material handling. Communicate production issues, downtime, supply needs, or quality concerns promptly to leadership. Education, Training: High school diploma or equivalent; formalized training in Machine Operation or mechanics helpful Experience Required: Minimum of 2 years’ experience in food manufacturing or similar environment, including experience operating machinery. Experience in a USDA-regulated environment preferred. Pay Range : $21/hr Starting rate of pay may vary based on factors including, but not limited to, position offered, location, education, training, and/or experience. #Ollicareers