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Veridiam is a strategic manufacturing partner with over 60 years of experience serving the aerospace, industrial, medical, and nuclear markets. Our roots were formed in the exacting nuclear and aerospace industries, expanded into Medical where we have supplied critical components to a global customer base. We currently provide elegant solutions across a broad range of customers and diverse markets. At Veridiam we recognize that talent is at the forefront of our organization and define who we are in today's industry. POSITION SUMMARY Develop, implement and optimize manufacturing and production processes. Establish processes to improve efficiency, ensure product quality and drive continuous improvement initiatives while maintain compliance with safety and regulatory standards. ESSENTIAL DUTIES AND RESPONSIBILITIES Analyze production data to identify areas for efficiency, cost savings and quality improvements. Design and implement manufacturing processes, workflows and equipment layouts. Prepare process documentation including but not limited to Standard Operating Procedures (SOPs), work instructions, job aids and specifications. Optimize equipment utilization and reduce downtime. Ensure processes comply with industry standards including but not limited to ISO, FDA, OSHA. Implement Lean Manufacturing, Six Sigma or other continuous improvement methodologies. Collaborate with Quality Assurance teams to resolve product quality issues. Partner with cross-functional teams to resolve issues and report on improvements. Identify bottlenecks, failures or inefficiencies and troubleshoot process issues and recommend corrective actions. Support new product introduction and scale up activities. Provide or recommend training and guidance to production staff on process requirements. May participate in cross functional meetings to communicate applicable changes or challenges. Collaborate with supply chain and production teams to ensure data integrity. Demonstrates ability to appear for work on time, follow directions from a supervisor, interact well with co-workers, understand and follow work rules and procedures, comply with company policies and procedures, goals and objectives, and accepts constructive feedback. Other duties as assigned, requested or needed. POSITION REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. Education and Experience: Bachelor’s degree in industrial or manufacturing/mechanical engineering. Minimum five (5) years’ experience in manufacturing or process engineering roles or equivalent of education and experience. Prior experience in highly regulated industries (i.e. aerospace, medical devices). Knowledge, Skills and Abilities: High level knowledge of manufacturing process design, equipment and/or industrial systems. Strong analytical, time management, problem solving, technical knowledge and communication skills. Familiarity with Lean, Six Sigma, Kaizen or other continuous improvement tools. Ability to prioritize and handle high level of workflow. Read and comprehend verbal and written instructions. Ability to multi-task and maintain organization. The above statements are intended to describe, in broad terms, the general functions and responsibility levels assigned to this classification. Management has the right to change duties at any time to meet business needs. Pay Rate: The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience with the industry, education, geographic location, etc. Veridiam is an Equal Employment Opportunity/Affirmative Action Employer. Veridiam will recruit, hire, train and promote persons into all jobs without regard to age, race, color, religion, ancestry, medical condition, sex, sexual orientation, gender identity, national origin, status as a veteran or status as an individual with a disability or any other characteristic or classification protected by law. Access to our facility (and, therefore, employment) is restricted under the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR) to U.S. Citizens, lawful permanent residents of the United States and properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes.
Introduction to the Job Are you ready to help shape the future of technology? At ASML, we are committed to innovation and excellence. As a Manufacturing Technician, you will play a key role in delivering advanced semiconductor equipment to customers around the world. Your work will directly contribute to our mission: enabling groundbreaking technology that changes lives. Role and Responsibilities As a Manufacturing Technician, you will help assemble, test, and troubleshoot high-tech systems in a dynamic, team-oriented environment. Your attention to detail and commitment to quality will help us deliver solutions that meet the highest industry standards. Assemble, test, and calibrate manufacturing equipment according to documented procedures Inspect components and systems for quality and accuracy Troubleshoot and resolve technical issues using established guidelines Document work performed and communicate findings to team members Follow all safety protocols and maintain a clean work area Collaborate with engineers and other technicians to improve processes Support continuous improvement initiatives within the department Education and Experience High school diploma or GED required; associate degree or technical certification preferred Experience working in a manufacturing or production environment (Minimum 2+ years preferred). Basic understanding of mechanical and electrical systems Familiarity with hand tools, power tools, and measurement equipment Skills We welcome candidates who are committed to learning and teamwork. The ideal Manufacturing Technician is detail-oriented, adaptable, and values clear communication. These skills are essential for success in our fast-paced environment. Strong problem-solving skills Ability to follow detailed instructions Effective verbal and written communication Teamwork and collaboration Time management and organization Adaptability to changing priorities Commitment to safety and quality Basic computer literacy Respect for diverse perspectives Continuous improvement mindset Other Information Location: San Diego, CA Anticipated work hours: 6:30pm - 7:00am, Sunday-Tuesday, and every other Wednesday. Department: Manufacturing/Production Seniority Level: Entry to mid-level Work Environment: Primarily on-site, in a cleanroom or production area Physical Requirements: Standing, walking, and lifting up to 30 lbs may be required The current base annual hourly range for this role is currently: $22.54-37.56 Pay scales are determined by role, level, location and alignment with market data. Individual pay is determined through interviews and an assessment of several factors that that are unique to each candidate, including but not limited to job-related skills, relevant education and experience, certifications, abilities of the candidate and pay relative to other team members. The Company offers employees and their families, medical, dental, vision, and basic life insurance. Employees are able to participate in the Company’s 401k plan. Employees will also receive eight (8) hours of vacation leave every month and (13) paid holidays throughout the calendar year. For more information, please contact the Recruiter or click on this link Compensation & Benefits in the US. All new ASML jobs have a minimum application deadline of 10 days. This position requires access to controlled technology, as defined in the United States Export Administration Regulations (15 C.F.R. § 730, et seq.). Qualified candidates must be legally authorized to access such controlled technology prior to beginning work. Business demands may require ASML to proceed with candidates who are immediately eligible to access controlled technology. Inclusion and diversity ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that inclusion and diversity is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions. Request an Accommodation ASML provides reasonable accommodations to applicants for ASML employment and ASML employees with disabilities. An accommodation is a change in work rules, facilities, or conditions which enable an individual with a disability to apply for a job, perform the essential functions of a job, and/or enjoy equal access to the benefits and privileges of employment. If you are in need of an accommodation to complete an application, participate in an interview, or otherwise participate in the employee pre-selection process, please send an email to [email protected] to initiate the company’s reasonable accommodation process. Please note: This email address is solely intended to provide a method for applicants to initiate ASML’s process to request accommodation(s). Any recruitment questions should be directed to the designated Talent Acquisition member for the position.
Position available for an energetic EXPERIENCED SHEET METAL INSTALLER. Experience required in residential and commercial architectural sheet metal. Well-established (we rarely advertise a position) small custom shop emphasizes high-quality workmanship and superior customer service - attention to detail, excellent communication skills and the ability to follow directions are essential. This is a great opportunity in a congenial environment for a motivated team member -- we value someone of strong character who is confident in their skills, mature, trustworthy and reliable. We offer highly subsidized medical/dental, paid holidays and vacation and 401k matching after vesting. You must have a clean driving record (this means a VALID CALIFORNIA DL!!) and clean background check, which includes a pre-employment physical. We want a SOLID candidate and we provide a SOLID position! Job Type: Full-time Pay: $25.00 - $33.00 per hour Benefits: * 401(k) matching * Company truck * Dental insurance * Health insurance * Paid time off Work Location: In person
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 14 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $195,000 - $205,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The Director of Quality Control is responsible for leading and managing all aspects of laboratory operations within QC Chemistry and Microbiology programs. This role ensures compliance with Good Manufacturing Practices (GMP) and other regulatory requirements while supporting organizational growth initiatives. The Director will oversee daily operations, including scheduling, staffing, training, troubleshooting, and continuous improvement efforts. Additionally, this position plays a critical role in managing analytical method transfers, instrument qualification, deviation investigations, and CAPA implementation. The Director will collaborate closely with cross-functional teams, providing strategic leadership in quality control while maintaining high standards of compliance, efficiency, and data integrity. The ideal candidate will have extensive experience in regulatory compliance (ISO-13485, ISO 14971, GMP/GLP, QSR, ICH guidelines), audit management, and client communications. This individual will bring a hands-on leadership approach, fostering a culture of excellence, accountability, and continuous improvement within the Quality Control team. This role is 100% on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Lead and manage daily laboratory operations for QC Chemistry and Microbiology programs, ensuring compliance with SOPs, GMP, and safety regulations. Oversee scheduling, staffing, training, and troubleshooting to maintain efficient workflows and high-quality standards. Write and review protocols, reports, and investigation documentation, including deviations, OOS, CAPAs, and change controls. Manage analytical method transfers, including phase-appropriate qualification and validation of test methods. Direct instrument qualification (IOQ) and ensure proper placement and maintenance of analytical equipment. Develop and implement process improvements to enhance efficiency, compliance, and data integrity. Support strategic planning, team development, and professional growth initiatives. Ensure objective product quality assessments through accurate and timely data generation. Lead audits, client interactions, and regulatory inspections, providing technical expertise and compliance assurance. Recruit, mentor, and develop a high-performing quality control team, fostering a culture of accountability and excellence. Requirements and Qualifications Bachelor's, Master's, or Ph.D. in a Life Science discipline (e.g., Chemistry, Microbiology, Molecular Biology, or Biochemistry). 10+ years of progressively increasing leadership experience in the medical device or pharmaceutical industry. Proven track record in FDA-regulated environments, including direct involvement with audits from the FDA, regulatory agencies, and clients. Experience managing 3rd-party contract laboratories. Strong analytical background in Chemistry and Microbiology, with the ability to execute objective and thorough OOS (Out of Specification) and failure investigations. Experience in a growth-oriented, contract manufacturing organization with a focus on compliance. Demonstrated success in strategic planning, process improvements, and professional development initiatives. In-depth knowledge of ISO-13485, ISO 14971, GMP/GLP, QSR, ICH Q1A/Q2, and 21 CFR 820.30. Strong understanding of analytical method validation, stability programs, and CAPA implementation. Ability to manage IOQ activities related to analytical instrumentation placement and validation. Proven credibility as a leader with a "hands-on" management style. Strong negotiation skills to maximize value in client and regulatory discussions. Excellent oral and written communication skills, including experience engaging with clients during audits, tours, and meetings. Ability to recruit, mentor, and develop high-performing teams within budget constraints. High level of personal and professional integrity with the ability to work independently and collaboratively. Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
*The Position:* The *Quality Administrator *is tasked with assisting in quality, inventory, and customer service administrative functions while supporting daily lab operations, case management, and training initiatives. *The Company:* Advanced Test Equipment Corporation is a leading provider of test and measurement equipment based in San Diego and is known for the great care we take with clients and employees alike. *Benefits*: ATEC provides a generous and competitive benefits package to meet you and your family’s needs. It includes medical, dental, vision, life, disability, FSA, 401k with match, sick time, and PTO. *Requirements:* * Minimum of 2 year quality and customer service experience preferred * ISO 9001 or ISO 17025 background. * Strong attention to detail, communication, and data entry skills * Strong ability to multitask *Responsibilities:* * Maintains and organizes quality documentation, including standard operating procedures (SOPs), quality manuals, policies, and compliance records, ensuring accuracy and accessibility. * Performs case management activities, including closing cases, updating notes, ensuring accuracy in spreadsheets/CRM, and maintaining handling time metrics. * Supports inventory processes (restock, cycle count, scrap, accessory kit verification), ensuring compliance with WKIs and SOPs. * Assists in inventory audits, address discrepancies, and maintain accurate inventory records. Track stock levels to ensure inventory availability. * Compiles and analyze survey feedback (e.g., SurveyMonkey) to generate actionable insights for improving processes and customer satisfaction. * Organizes and maintains the parts room, ensuring bins are completed, items are labeled correctly, and records are updated in GP/CRM. * Documents and escalates technical or case-related issues to relevant teams as needed. * Assists with incoming calls by responding to customer inquiries and concerns in a timely and professional manner. Collaborate with internal teams to address issues and enhance customer experience. * Performs CRM data updates related to customers to ensure accurate and up-to-date information. * Assist with first-level technical support for product or service-related issues, ensuring continuous follow-up until case closure with customer satisfaction, and overseeing the completion of billing tickets, RMAs, and other necessary tasks. * Coordinates and participates in internal and external quality audits, ensuring compliance with quality standards. Track audit findings and assist in implementing corrective actions. * Maintains accurate and organized records to support the QMS, including order process dashboards, in-service lists, and work order verifications. * Facilitates the change control process by tracking change requests and ensuring proper approvals are obtained before implementation by tracking CRs, updating WKIs, and ensuring proper approvals are obtained before release. * Identifies and implements process improvements to enhance operational efficiency, ensuring continuous quality improvement. * Maintains key quality metrics and provide regular reports on quality performance. *Our Work Environment:* * Fast paced and dynamic environment with a focus on achieving results. * Collaborative team setting with a strong emphasis on innovation and continuous improvement. * Resources for personal and professional development. * Work/life balance. * Comfortable and accessible. Job Type: Full-time Pay: $25.00 - $30.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Tuition reimbursement * Vision insurance Education: * Bachelor's (Preferred) Experience: * Quality audits: 2 years (Preferred) * Quality systems: 2 years (Preferred) * Internal audits: 2 years (Preferred) Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
We are looking for FULL TIME Production Associate / Machine Operator to set up, maintain and operate multiple machines at one time to produce products for medical devices.. Being a team player is necessary since all tasks will require collaboration with co-workers. A great team member is reliable and able to work with attention to detail and safety standards. You will receive on-the-job training. EXCELLENT EYESIGHT AND MANUAL DEXTERITY ARE ESSENTIAL. *Responsibilities* * Set up machines (cleaning etc.) to start a production cycle * Feed raw material or parts to machines. Check output to spot any mistakes or flaws * Monitor processes, materials and surroundings. * Fix issues that might occur due to machine-related mistakes or flaws * Keep records of manufacturing activities and acceptable/defect units products * Build products according to written work instructions and verbal training. * Follow Good Manufacturing Practices (GMP) guidelines and comply with quality and safety requirements. * Read and comprehend assembly and work instructions. * Work with miniature components that may require visual magnification/microscopes. * Excellent eyesight is absolutely required to properly perform job. * Comply with all in-house training and procedures. * Performs all other duties, as assigned. * Must possess good verbal and written communication skills.. * Mechanical aptitude/dexterity and the ability to lift up to 20 lbs. General physical duties - must be able to stand for long periods of time. * Must be capable of using basic hand tools to operate production equipment. * Basic knowledge of relevant techniques, approaches, guidelines, policies and procedures in the job area. * Familiarity with medical device manufacturing is helpful., but not required. * Excellent eyesight, manual dexterity, and the ability to stand for long periods is required to effectively perform the job functions. Job Type: Full-time Pay: $20.00 per hour Work Location: In person
*Responsibilities* * Operate Flexo press/ Digital Hybrid to produce jobs according to specifications. * Prepare the press for printing and die-cutting. * Load substrate, install tooling, mount plates, set print impression, and adjust the press. * Ensure that substrate, ink, and tooling meet required specifications. * Adjust ink distribution, speed, and temperature in the drying chamber. * Troubleshoot and correct print issues quickly to minimize downtime and material waste. * Perform routine maintenance, including oiling, cleaning, and minor repairs. *Requirements* * Must have proven experience operating a Mark Andy, Nilpeter, MPS, Omet, or other servo-driven narrow web press. * Team-oriented with excellent communication skills. Job Type: Full-time Pay: $25.00 - $38.00 per hour Application Question(s): * Can you operate Mark Andy, Nilpeter, MPS, Omet press ? * This job is for Second Shift 4pm-2:30 AM- Mon-Thursday. Are you Ok with this shift ? Work Location: In person
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. With limited direction, 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 & Responsibilities: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub- assemblies, and final assemblies. Conducts tests throughout all stages of production to determine control over applicable variables and troubleshooting and resolving manufacturing problems that are extremely complex and require the regular use of ingenuity and creativity. Designs the arrangement of manufacturing equipment to ensure most efficient and productive layout. Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery. Interfaces and collaborates with design engineering in coordinating the release of new products. Provides guidance to product design engineering on technical specifications that will best utilize equipment and manufacturing techniques. Estimates manufacturing cost, determines time standards, and makes recommendations for tooling and process requirements of new or existing product lines. Ensures that production processes and procedures are in compliance with regulations. Maintains records and reporting systems for coordination of manufacturing operations. Develops appropriate documentation of findings and implemented solutions and communicates results to staff. May be required to make technical presentations to staff. May provide direction to less experienced professionals, design staff or technicians. 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.51660 Job Qualifications: Typically requires a bachelors in engineering or a related technical field as well as nine or more years of manufacturing engineering experience. May substitute equivalent experience in lieu of education. Demonstrates an extensive technical expertise and application of manufacturing engineering principles, concepts, theory, and practice with the ability to organize, plan, schedule, conduct, and coordinate workloads to meet established deadlines or milestones with some experience in project leadership. Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment. Customer focused, formulates plans based on the development of innovative new designs in resolving extremely complex manufacturing engineering problems. Strong communication, presentation, and interpersonal skills are required enabling an effective interface with other departments and/or professionals, and capable of representing the organization as a prime technical contact, as well as providing leadership and guidance to less experienced professionals. Must be able to work both independently and in a team environment. Able to work extended hours as required. Travel is required and operations are on a 9X80 schedule with every other Friday off. Salary:$98,100 - $171,398Travel Percentage Required 0 - 25Relocation Assistance Provided Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. Under general direction, this position is responsible for support for a major project through the planning, preparing, issuing and controlling of production schedules and coordinates with material requirements to ensure a controlled flow of approved materials timed to meet production requirements. Oversees budget, performance monitoring, analysis reports and may provide directions to support staff. Advises management of the status of work in progress, material availability, and potential production problems to ensure that personnel, equipment, materials and services are provided as needed. Duties & Responsibilities: Advises management of the status of work in progress, material availability, and potential production problems to ensure that personnel equipment, materials, and services are provided as needed. Keeps management appraised of potential schedule or fiscal problems by tracking, reviewing and evaluating plans, schedules and/or budgets for inaccuracies, inconsistencies or interface/support problems. Analyzes task/project cost and/or schedule variances and informs management. Provides manpower resource planning and allocation. Generates manufacturing work orders using Material Requirement Planning (MRP) planned order requirements as well as generating purchase requisitions for outside process and outside manufacturing services. Processes work orders and material transactions for non-conformance material dispositions. Interprets engineering change orders (ECO), implements dispositions affecting stock, work in progress, and NEXT assembly. Schedules equipment and personnel, confirms material supply and demands, prepares purchase orders. Provides budgeting input and program funding tracking and pursuit. Alerts and/or recommends solutions to operating or project management to deviation from established norms. Prepares milestone coordination and reports. Develops and monitors overhead, capital, research and development, marketing and other budgets. Interfaces with operating and support groups (Purchasing, Finance, QA) to collect data for preparation of schedules and reports as well as providing status reports to internal and external contacts. Works in close coordination with outside fabricators and processors. May provide work direction to professional and/or support personnel. 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 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.51657 Job Qualifications: Typically requires a Bachelors degree in Business Administration with an emphasis in Planning, Engineering, Production Control or a related discipline and six or more years progressive experience in planning, scheduling, budgeting and performance measurement. May substitute equivalent experience in lieu of education. Must have a complete understanding of manufacturing planning principles, theories and concepts as well as ability to understand accounting and manufacturing systems in a research or production environment and to apply advanced planning tools and techniques; and ability to read, interpret and explain engineering drawings. Must be customer focused and possess: The ability to develop and communicate new concepts and apply them accurately throughout an evolving environment. Ability to organize, schedule and coordinate work phases. Ability to determine the appropriate approach at the project level and provide innovative solutions to a range of moderately complex technical problems. Organization skills to maintain flow of work within the unit. Strong interpersonal, verbal and written communication skills to interface with internal employees and external representatives and to accurately document, report and present. Ability to maintain the strict confidentiality of sensitive information. Knowledge of computer operations and applications and word processing and spreadsheets. Ability to work both independently and in a team, environment is essential as is the ability to work extended hours as required. Travel is required and operations are on a 9x80 schedule with every other Friday off. Salary:$68,770 - $116,193Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? No Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. With limited direction, 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 & Responsibilities: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub- assemblies, and final assemblies. Conducts tests throughout all stages of production to determine control over applicable variables and troubleshooting and resolving manufacturing problems that are extremely complex and require the regular use of ingenuity and creativity. Designs the arrangement of manufacturing equipment to ensure most efficient and productive layout. Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery. Interfaces and collaborates with design engineering in coordinating the release of new products. Provides guidance to product design engineering on technical specifications that will best utilize equipment and manufacturing techniques. Estimates manufacturing cost, determines time standards, and makes recommendations for tooling and process requirements of new or existing product lines. Ensures that production processes and procedures are in compliance with regulations. Maintains records and reporting systems for coordination of manufacturing operations. Develops appropriate documentation of findings and implemented solutions and communicates results to staff. May be required to make technical presentations to staff. May provide direction to less experienced professionals, design staff or technicians. 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.51659 Job Qualifications: Typically requires a bachelors in engineering or a related technical field as well as nine or more years of manufacturing engineering experience. May substitute equivalent experience in lieu of education. Demonstrates an extensive technical expertise and application of manufacturing engineering principles, concepts, theory, and practice with the ability to organize, plan, schedule, conduct, and coordinate workloads to meet established deadlines or milestones with some experience in project leadership. Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment. Customer focused, formulates plans based on the development of innovative new designs in resolving extremely complex manufacturing engineering problems. Strong communication, presentation, and interpersonal skills are required enabling an effective interface with other departments and/or professionals, and capable of representing the organization as a prime technical contact, as well as providing leadership and guidance to less experienced professionals. Must be able to work both independently and in a team environment. Able to work extended hours as required. Travel is required and operations are on a 9X80 schedule with every other Friday off. Salary:$98,100 - $171,398Travel Percentage Required 0 - 25Relocation Assistance Provided Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
Job Information Number ICIMS-2025-9513 Job function QA&RA Job type Temporary Location San Diego - WBH - 6260 Sequence Drive San Diego, California 92121 United States Country United States Shift 2nd About the Position Introduction Werfen 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 Position Summary: The QC Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Technologist III supports investigations and assists in trending and statistically analyzing finish product testing data. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $29-$34/hr, depending on experience. Responsibilities Key Accountabilities Essential Functions: Perform and organize testing of biological raw materials and finished goods per relevant SOP with minimal supervision; subject matter expertise in at least one product line. Assist with planning of method, product and process validations on existing products; perform and organize testing as needed. Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required. Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team. Responsible for tracking relevant trends. Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments. Document all test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. As required, coordinate and assist with investigation and resolution of complaints, non-conforming material and product performance issues. Submit complex change orders to update procedures as required. As required, work cross-functionally to investigate and resolve issues deriving from finish product testing. Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor’s degree in Science or equivalent experience preferred. A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required; previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred. Thorough understanding of Good Laboratory Practices (GLP) required. Practical experience with laboratory controls, internal audits, and lab training/maintenance. Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Proficiency with common laboratory techniques, such as pipetting and use of balances. Proficiency with Microsoft Office suite. Proficiency with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems preferred. 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
AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. JOB SUMMARY The Quality Supervisor manages and maintains a set of multiple Coordinate Measurement Machine (10+ CMMs) manned by a team of Quality Inspection (QI). Supervises the team and ensures that products meet the quality standards of materials and workmanship as set forth by quality assurance, or engineering function. Ensure compliance to Axillon Aerospace Standard Procedures and Work Instructions. ESSENTIAL DUTIES AND RESPONSIBILITIES The primary duties of this job require the smooth operation of CMM equipment and management of a team of full-time inspectors. Responsibilities include: Maintaining product flow through CMM inspection to serve the program demand. Debugging and resolving software / program related issues to meet expectations on daily number of inspections. Interviewing, selecting, hiring and training inspectors; setting and adjusting rates of pay and work hours. Conducting regular performance appraisal to ensure team competencies and capabilities to reach business goals and recommend promotions or changes in status. Handling employee complaints and grievances; disciplining employees. Providing for the safety and security of the employees. Supervises the QI team on the inspection of raw materials, parts, assemblies, finished parts and machined parts to assure quality products. Provides CMM expertise and training for operation and first level maintenance to maintain a smooth flow of operations. Promotes working relationships between inspection personnel and other departments. Maintains and tracks quality KPI for the purposes of analysis, control, and management reports. Conducts other responsibilities as assigned. Consistent exercise of independent judgment and discretion in matters of significance is required. JOB SPECIFICATIONS Education: Post-Secondary degree in engineering / physics (metrology) or equivalent of relevant education and work experience that will allow successful performance of job expectations. Certifications: CMM Operator Certification and GD&T certified; ASQ Certified Inspector is a plus. Years Experience: 5 - 7 years or more of relevant experience including supervisory responsibilities. Skills: Proven ability to plan and direct technical efforts to meet quality targets. Ability to operate and read CMM program (CAMIO and or PCDMIS language is plus). Skilled at performing examinations and quality control inspections on products, materials, components and parts on all types of standard and special products. Experienced in analyzing and determining quality methods and procedures. Demonstrated judgment to identify and resolve day-to-day technical and operational problems. Effective interpersonal skills to influence and lead a team. Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $100K-$120K. Axillon is an Equal Opportunity Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position is subject to meeting export compliance eligibility requirements. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. (“Minority / Female / Disability / Veteran / VEVRAA Federal Contractor”) If you would like more information about Equal Employment Opportunity as an applicant under the law, please go to Know Your Rights: Workplace Discrimination is Illegal (eeoc.gov) and Genetic Information Discrimination.