Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. 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 Benefits for this position, subject to applicable eligibility requirements. Medical Insurance Dental Insurance Vision Insurance Company Paid Life Insurance 1X annual Salary Voluntary Life Insurance Long-Term Disability Insurance and Short-Term Disability Insurance Flexible Spending Account and Health Saving Account 401(K) Retirement Plan 10 Days of Paid Time Off 10 Paid Holidays Annually The pay range for this position is between $27.00 - $32.00 per hour. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. Position and Scope The purpose of this position is to assist in establishing and managing a microbiology program that oversees aseptic fill/finish activities, environmental monitoring, gowning qualification, and the establishment of compendial microbiology assays that include endotoxin, bioburden, and sterility. The position is responsible for ensuring all activities are performed within an appropriate level of cGMP compliance. Previous experience with aseptic filling operations and controls and drug product process validation is highly desired. This role is 100% On-Site, Monday – Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00am and 9:00am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Serve as a subject matter expert (SME) for Microbiological assays and methods during internal/external audits, risk assessments, investigations, and client visits Supports assay transfer, qualification, and validation activities for microbial based assays or clients' specific methods Author, revise, and review Quality Control (QC) standard operating procedures (SOPs) and assay qualification protocols and reports Perform analysis on in-process samples, APIs, raw materials, and stability samples using existing methods Perform routine and non-routine environmental monitoring (EM) of GMP and GLP manufacturing facilities for total particulates, air viables, and surface viables. Initiate and participate in the investigation of environmental monitoring excursions and assesses potential impact on product quality Support a Gowning Qualification Program for all manufacturing and QC personnel Perform routine monitoring of pharmaceutical water and gas systems Perform Bioburden, Growth Promotion, Endotoxin, Gram Stain, Microscopy, TOC, Conductivity, and Nitrates testing Maintain QC lab equipment and provide assistance, as needed, during equipment and facility qualification activities Assist in trending EM data and generate quarterly and yearly reports Participate in inspection readiness activities Interact closely with other departments to ensure efficient, compliant, and timely execution of project activities Provide assistance as needed to maintain a functioning QC Laboratory, including material ordering, inventory control, general housekeeping, and other duties Assist in investigation and review of GMP quality events, including but not limited to deviations, non-conformances, and audit findings Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results with a client driven focus Safely operate laboratory equipment in accordance to established practices and SOPs Assist in training of additional team members Under minimum supervision, support special projects as needed Operates to the highest ethical and moral standards. Adheres to quality standards set by regulations and Argonaut Manufacturing Services policies and procedures Communicates effectively with supervisors, staff, and clients Participate in projects within a team and as an individual Support continuous improvement projects related to QC Multi-task, prioritize workload, document properly and interpret data accurately Follow laboratory safety requirements to promote a safety-first culture Requirements and Qualifications Combination of Undergraduate courses and on-the-job experience in Microbiology or a related discipline (e.g., biology, chemistry, or biological sciences) Minimum three (3) years' experience in Quality Control and environmental monitoring of GMP facilities High intelligence and problem-solving skills Excellent oral and written communication and listening skills High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business is preferred General knowledge of one or more of compendial methods such as: Bioburden, Endotoxin, Growth Promotion, Sterility, and other microbiological methods Knowledge in environmental excursion investigations, root cause analysis, out of specifications, and knowledge of cleanroom practices is preferred Direct experience with endotoxin, bioburden, and growth promotion methodologies. Experience in sterility testing is highly desired. Experience with transfers and qualification/validations of large molecule focused analytical methods Must have experience with Microsoft Office applications Experience with quality software and 21 CFR 11 applications preferred 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 with all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
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 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $130,000 - $140,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product and stability test samples. Further support services includes processing and testing of environmental monitoring and raw material samples. QC personnel are responsible for compliance to QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. This role is an 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. Responsibilities and Duties Management of incoming samples utilizing a laboratory information system (LIMS) or other means. Perform detailed chemical analysis of samples from production, routine monitoring, stability and validation or qualification studies using compendial and non-compendial methods Utilize advanced instruments such as HPLC/UHPLC, SoloVPE, Maurice (cIEF and SDS Page), FTIR and UV/Vis Spectrophotometers Author protocols and reports including but not limited to, method qualification, method verification, method validation and method suitability. Apply and adhere to data integrity principals to sample handling and analysis Manage deviation/OOS investigations and implement CAPAs and change controls per GMP requirements Author and revise QC related SOPs as required Interface with product Sponsors on QC related inquiries. Participate in the review and approval of Manufacturing Batch Records for QC related activities Execute analytical method transfer activities, including product-specific test methods Train junior personnel in appropriate laboratory and safety procedures Execute Installation and Operational Qualification of analytical instrumentation where applicable Directly contributes to daily laboratory operations for QC Chemistry in full compliance with applicable SOPs and safety guidelines Requirements and Qualifications Undergraduate degree (B.A. or B.S.) in a Life Science discipline A minimum of 7 years' experience in a GMP-compliant Quality Control function within the medical device and/or biopharmaceutical fields A high level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction Analytical experience in the following methodologies: Buffer Characterization (pH, conductivity, osmolality), Concentration (UV/Vis and/or Fluorescence), Chromatography (HPLC, Electrophoresis) The ability to work effectively within cross functional teams comprised of Manufacturing, Tech Transfer, Quality Assurance, and Senior Management An affinity for precise and detailed documentation skills. The ability to effectively influence and contribute to a dynamic and fast-paced work environment A strong work ethic and a high level of accountability Strong oral and written communication and listening skills Excellent Problem-solving skills 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.
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 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $71K - $80K annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The Quality Systems Specialist will identify, document, and resolve quality issues, deviations, and non-conformances related to sterile drug product manufacturing operations. They will perform root cause analysis, assess risks, and determine Corrective and Preventive Actions (CAPA) to ensure strict compliance with FDA and cGMP standards. The Quality System Specialist will also participate in internal and external audits (client and supplier) and facilitate any corrective actions identified. The role is a key Quality contact at Argonaut and requires the ability to independently manage timelines and effectively communicate with team members, cross-functional stakeholders, and clients while helping to maintain site Quality Systems in a state of inspection readiness. This role is an 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 investigations into batch deviations, out-of-specification results, and product failures by independently evaluating evidence, determining root causes, assessing product impact, and recommending appropriate corrective and preventive actions (CAPAs). Direct and conduct investigations of customer complaints by reviewing manufacturing records, interviewing personnel, evaluating potential product impact, and determining appropriate investigative strategies and follow-up actions. Interpret and apply FDA, cGMP, ISO, and other regulatory requirements to ensure investigation outcomes, documentation, and quality system activities remain compliant and inspection ready. Analyze quality system trends and performance metrics, evaluate operational risks, and provide recommendations to management regarding quality improvements and regulatory compliance. Serve as the Quality lead by providing technical guidance to cross-functional teams during investigations and ensuring investigations meet regulatory and quality system requirements. Lead quality training sessions as needed Evaluate investigation processes and recommend and implement improvements that enhance regulatory compliance, operational efficiency, and overall quality system effectiveness Lead internal audit program; assist in hosting and responding to client and regulatory audits Other duties may be assigned Requirements and Qualifications Bachelor's degree in Life Sciences (Biology, Chemistry), Engineering, or a closely related field is strongly preferred Level II Associate: 2 - 4 years of experience in pharmaceutical or biotech manufacturing, heavily focused on GMP (Good Manufacturing Practices) and performing investigations. Analytical mindset, root-cause analysis skills, exceptional technical writing, and a solid working knowledge of FDA guidelines and ICH requirements. Must have a high attention to detail, and excellent communication skills Must be able to effectively communicate within the department and cross-functionally with other divisions Experience with MasterControl and NetSuite a plus Superior attention to detail, organizational skills, and the ability to multi-task in a time-line driven environment Ability to make decisions regarding quality of product and material Strong initiative and willingness to take ownership and drive projects to completion 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.
*Job Summary* We are seeking a highly motivated and detail-oriented Technician specializing in Thermal Imaging Sensors and Camera Manufacturing. In this role, you will be integral to the assembly, testing, and troubleshooting of advanced thermal imaging components and systems. Your expertise will ensure the production of high-quality sensors and cameras used in a variety of innovative applications. This position offers an exciting opportunity to work with cutting-edge electro-mechanical components, develop your technical skills, and contribute to the advancement of thermal imaging technology. *Responsibilities* * Assemble Thermal Camera Assemblies, SOP's and other engineering documents. * Read and interpret electrical schematics, blueprints, and technical drawings to guide assembly processes accurately. * Use hand tools, power tools, soldering irons, and electro-mechanical assembly equipment to build electrical panels, wiring harnesses, and mechanical assemblies. * Perform machining or mechanical assembly tasks as needed for sensor housing or camera enclosures. * Assist in the calibration, testing, and validation of thermal imaging sensors to meet performance specifications. * Maintain detailed documentation of assembly steps, test results, and troubleshooting procedures to support manufacturing quality assurance. *Experience* * Knowledge of programmable logic controllers (PLCs), electrical panel building, and troubleshooting automation equipment is preferred. * Experience working with mechanical assembly processes including machining or component fitting is advantageous. * Ability to use hand tools, power tools, ohmmeters, and other diagnostic equipment confidently during manufacturing processes. * Understanding of electro-mechanical components used in thermal imaging sensors or cameras will be beneficial. Join us to be part of a dynamic team dedicated to pushing the boundaries of thermal imaging technology! We value innovation, precision craftsmanship, and continuous learning—offering a rewarding environment where your skills make a real impact in cutting-edge manufacturing processes. Pay: $23.00 - $32.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Health savings account * Life insurance * On-the-job training * Paid sick time * Paid time off * Vision insurance Work Location: In person
Position Summary To safely and effectively run equipment related to HPP/Bottling/Packaging and Pack Out. Operator 2 will demonstrate the ability to run all machines within one department e.g. All machines associated with the Bottling department. Schedule 1:00 PM - 9:30 PM Wednesday-Sunday (1) or Tuesday–Saturday (1), with flexibility for mandatory overtime. Please note that schedules are limited and are not guaranteed to be available. Available schedules will be offered to candidates based on business needs and staffing availability. 2-Week Training Schedule: Sunday–Thursday, employees will start with this schedule and then transition to their regular assigned schedule. Essential Duties and Responsibilities Including but not limited to: To run all machines safely and effectively within your department including but not limited to: Fillers, HPP’s, Labelers, Case Packers, Bundlers, Sleevers, Palletizers, etc. Plan to ensure you have the correct materials, equipment, and ingredients for each day. Communicate with your Shift Lead/Supervisor/Manager to advise of any issues/concerns. Communicate well with other employees. Follow all OSHA rules regarding safe machine operation. Keep your work area clean, organized, and safe always. Keep your work area clean, organized, and safe always Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Ability to understand and follow verbal and written instructions related to safety, equipment operation, and daily work assignments. Regular and reliable attendance. Department Machine Bottling Depal GRX Unscrambler F4 F5 Shot Filler Carbonated Filler HPP HPP 1 - 2 HPP 3 - 4 Trines Sleever Packaging/Pack Out Bundlers (Dimac, KHS, SMI) Drop Packer Unscrambler Non-Essential Job Duties May perform similar and incidental duties as required. Job Qualifications Experience: 2+ years’ experience working in a manufacturing/warehouse environment Skills & Abilities Must have strong leadership skills. Problem solver skills Be able to work independently with moderate supervision Ability to think ahead. Responsibilities may require an adjusted work schedule, overtime, evening/weekend hours in order to meet deadlines. Ability to work cross-functional with other departments. Attention to detail and a commitment to maintaining high product quality. Flexibility to work in a fast-paced and dynamic production environment. Language Skills Ability to communicate, read, listen, and understand English. Bilingual is a plus. Working Environment Regular exposure to wet, cold manufacturing environments (temperatures as low as 35°F) Occasional exposure to dry warehouse spaces or freezer conditions (down to -10°F) Frequent exposure to high noise levels (above 85 dBA) Requires use of PPE including safety glasses, ear protection, gloves, and steel-toed footwear Physical Requirements Ability to stand and walk for the full duration of the shift Must be able to frequently lift/move hoses, equipment, and chemical containers weighing up to 50 lbs. Ability to push/pull up to 100 lbs. with continuous motion Must be able to bend, kneel, squat, climb stairs/ladders, and reach overhead regularly Must have sufficient hand strength and manual dexterity to operate sanitation tools and machinery Must be able to pass a pre-employment physical Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Pay rates starting at $18.00-$19.00 an hour Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #ZR #INDHP Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
Position Summary Utility workers are responsible for the essential job functions related to keeping their specific department running. Utility workers will be responsible for general duties involving physically handling products, materials, supplies and inspecting products to ensure high quality. Schedule 1:00 PM - 9:30 PM Monday-Friday (1), Sunday-Thursday (1), or Tuesday–Saturday (1), with flexibility for mandatory overtime. Please note that schedules are limited and are not guaranteed to be available. Available schedules will be offered to candidates based on business needs and staffing availability. 2-Week Training Schedule: Sunday–Thursday, employees will start with this schedule and then transition to their regular assigned schedule. Essential Duties and Responsibilities Manual labor including but not limited to: Loading HPP torpedoes. Unloading HPP torpedoes. Standing bottles up at HPP discharge. Running the HPP dumper. Making/pre-building boxes. Bringing in fiber/packaging materials for the lines. Loading caps into cap hoppers. General labor related to the bottling process. General labor related to shipping/pack-out/receiving/inventory, etc. Building pallets, lifting, moving/stacking cases up to 50 lbs. Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Regular and reliable attendance. Non-Essential Job Duties May perform similar and incidental duties as required. Experience Manufacturing experience is a plus but not required. Abilities Ability to work well under time constraints and prioritize work to meet commitments/deadlines. Ability to work cross-functional with other departments. Attention to detail and a commitment to maintaining high product quality. Flexibility to work in a fast-paced and dynamic production environment. Language Skills Ability to communicate, read, listen, and understand English. Bilingual is a plus. Working Environment Regular exposure to wet, cold manufacturing environments (temperatures as low as 35°F) Occasional exposure to dry warehouse spaces or freezer conditions (down to -10°F) Frequent exposure to high noise levels (above 85 dBA) Requires use of PPE including safety glasses, ear protection, gloves, and steel-toed footwear Physical Requirements Ability to stand and walk for the full duration of the shift Must be able to frequently lift/move hoses, equipment, and chemical containers weighing up to 50 lbs. Ability to push/pull up to 100 lbs. with continuous motion Must be able to bend, kneel, squat, climb stairs/ladders, and reach overhead regularly Must have sufficient hand strength and manual dexterity to operate sanitation tools and machinery Must be able to pass a pre-employment physical Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Pay rate starts at $18.00 an hour Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #INDHP Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay Experience Preferred 1 year(s): CPG experience a plus Education Preferred High School or better Licenses & Certifications Preferred Drivers License Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
*Position Summary:* QP Technologies (formerly Quik-Pak) is a leading provider of microelectronic packaging and assembly, wafer preparation, and substrate design and development services and our service offerings enable our customers to target a range of end markets, including commercial, RF, power, industrial, automotive, medical and mil-aero. The Quality Assurance Inspector will support the Quality Assurance function. Inspect incoming, in-process parts and final assemblies to conform to requirements and task instructions. May use precision measuring instruments to inspect, test or measure materials to determine specifications. May perform data collection and analysis and produce relevant Quality Management System (QMS) metrics and reports. *Essential Duties:* · Perform incoming, in-process, and final inspection of mechanical components, subassemblies and final assemblies using visual inspection protocol · Generate Certificates of Compliance · Follow QA task instructions and the QMS · Evaluate quality of materials or product · Maintain all necessary paperwork and quality records · Meets schedule, quality, and quantity requirements in an organized manner *Other Duties & Responsibilities (Optional)* · Assist production personnel in complying with all relevant aspects of the Quality Management System (QMS) *Minimum Qualifications:* · Practical working knowledge of Microsoft Office Suite, Outlook email · Must be able to read/write in English · Must have basic math skills · Experience using digital multimeters, calipers, micrometers, and microscope · Good manual hand dexterity · Must be a US Person *Key Competencies:* · Ability to exercise discretion · Must be able to effectively communicate *Preferred Skills:* · Prior experience in a contract manufacturing environment · Experienced in working with ISO 9001 and ITAR environments · Experience with MIL-STD-883 requirements · IPC-610 Certified *Work Environment:* While performing the duties of the job, the employee is regularly required to sit, stand and/or walk for extended periods of time; use hands and fingers; reach with hands and arms; and talk and hear. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Will wear common ESD and protective equipment as necessary. This position is in an indoor, environmentally controlled cleanroom. Job Type: Full-time Pay: $21.00 - $24.00 per hour Benefits: * 401(k) * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Referral program * Tuition reimbursement * Vision insurance Work Location: In person
*Experienced Production Seamstress | Industrial Sewing Experience Required* *Versión en español abajo. We are hiring a full-time experienced seamstress for our San Marcos, CA workshop. Sewing experience is required, this is not an entry-level position. We are looking for someone who already knows how to sew well on industrial machines and can work quickly, accurately, and with excellent attention to detail. *Requirements* * Experience using industrial sewing machines: Walking Foot, Single Needle, and Overlock/Serger * Experience sewing a variety of fabrics * Excellent attention to detail * Able to sew quickly while maintaining consistent quality * Able to follow patterns, measurements, and sewing instructions * Reliable and able to work independently *A sewing test is required as part of the interview process.* *Pay:* $21-$25 per hour, depending on experience and skill *Schedule:* Monday–Friday, 6:30 AM–3:00 PM (occasional overtime available) *Location:* San Marcos, CA *Schedule and interview, please text:* Eric: 413-222-2857 — English Ahide: 760-805-3480 — Hablamos Español — *Costurera de Producción con Experiencia | Se Requiere Experiencia en Costura Industrial* Estamos contratando una costurera con experiencia para trabajar tiempo completo en nuestro taller en San Marcos, CA. Se requiere experiencia en costura. Este no es un puesto de nivel inicial. Buscamos a alguien que ya sepa coser bien con máquinas industriales y que pueda trabajar rápido, con precisión y con excelente atención a los detalles. *Requisitos:* * Experiencia usando máquinas de coser industriales: Walking Foot, Single Needle y Overlock/Serger * Experiencia cosiendo diferentes tipos de telas * Excelente atención a los detalles * Capacidad para coser rápidamente manteniendo una calidad constante * Capacidad para seguir patrones, medidas e instrucciones de costura * Responsable y capaz de trabajar de manera independiente *Se requiere una prueba de costura como parte del proceso de entrevista.* *Pago:* $21-$25 por hora, dependiendo de la experiencia y habilidad *Horario:* Lunes a viernes, 6:30 AM–3:00 PM (ocasionalmente hay horas extras disponibles) *Ubicación:* San Marcos, CA *Para programar una entrevista, envíe un mensaje de texto a:* Ahide: 760-805-3480 — Hablamos Español Eric: 413-222-2857 — Inglés Job Type: Full-time Pay: $21.00 - $25.00 per hour Expected hours: 40.0 per week Benefits: * Paid time off Experience: * Industrial Seamstress: 2 years (Required) Shift availability: * Day Shift (Required) Work Location: In person
Production Painter – Put Your Craftsmanship on the Cutting Edge of Aerospace Innovation Bring Precision, Pride, and Performance to Every Coat You Apply PDS Tech Commercial is seeking a skilled Production Painter to join our team in San Diego, CA, supporting a leading innovator in the aerospace industry. If you take pride in producing high-quality finishes, enjoy hands-on work, and want to contribute to the creation of advanced aerospace structures, this is your opportunity to make a lasting impact. As a Production Painter, you'll play a critical role in protecting and enhancing aerospace components that help power some of the industry's most sophisticated technologies. Your expertise will directly contribute to product quality, performance, and mission success. Position Details Job Title: Production Painter Job Type: Full-Time Consultant (12-Month Assignment) Location: San Diego, CA 92121 Schedule: Monday–Friday | 9/80 Work Schedule Pay Rate: $31.84 per hour Make an Impact Join the Paint/Wet Chemistry Department and become part of a team responsible for preparing, priming, and painting aerospace structures that demand exceptional quality and precision. Every surface you coat helps protect critical components while ensuring they meet stringent aerospace standards. This role offers the opportunity to apply your craftsmanship in a high-tech environment where attention to detail and quality workmanship truly matter. What You'll Do Apply protective and decorative coatings to aerospace parts, assemblies, and finished products. Prepare surfaces for painting and finishing operations. Select, mix, and prepare paints, primers, enamels, lacquers, varnishes, and other coating materials. Utilize spray guns to apply coatings according to specifications and quality requirements. Apply coatings with brushes and rollers in areas inaccessible to spray equipment. Prime and paint a variety of aerospace structures and components. Inspect finished surfaces to ensure quality, consistency, and compliance with standards. Support quality verification activities and statistical process control initiatives when required. Follow established safety procedures and maintain a clean, organized work area. Collaborate with production and quality teams to meet schedule and performance goals. Required Qualifications Experience applying paint, primer, coatings, or finishes in a manufacturing, production, automotive, marine, aerospace, or industrial environment. Ability to safely operate painting equipment, including spray guns and related tools. Strong attention to detail and commitment to quality workmanship. Ability to follow detailed instructions, specifications, and safety procedures. Ability to work effectively in a team-oriented production environment. Strong reliability, work ethic, and commitment to meeting production schedules. Preferred Qualifications Previous aerospace painting or coating experience. Experience working within a paint, wet chemistry, or manufacturing production environment. Familiarity with quality inspection standards and process controls. Knowledge of aerospace coatings, primers, and finishing techniques. Experience working in highly regulated industries where precision and quality are critical. Why Join PDS Tech Commercial? At PDS Tech Commercial, we're dedicated to connecting talented professionals with opportunities that make a difference. When you join our team, you'll gain: The chance to work alongside a respected leader in the aerospace industry. Hands-on experience supporting advanced aerospace programs and technologies. A collaborative culture built on safety, innovation, quality, and teamwork. Competitive pay and valuable industry experience. Opportunities to grow your skills and expand your professional network. Potential contract-to-hire opportunity aligned with a full-time Production Painter role.* *While conversion to direct employment is intended, it is not guaranteed. Ready to Paint Your Future in Aerospace? If you're passionate about quality craftsmanship, precision finishing, and contributing to industry-leading aerospace programs, we want to hear from you. Apply today and take your painting career to new heights with PDS Tech Commercial and a premier aerospace industry partner.* **This position requires use of information or access to facilities subject to the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR). These regulations may limit access of controlled technologies: 1) to U.S. Persons, including U.S. Citizens, lawful permanent residents, and other narrow categories including refugees and asylees, or 2) to certain foreign nationals that have received an export license. ** Pay Details: $31.84 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.pdstech.com/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. You should be proficient in: Blueprint Reading
Are you looking for an opportunity to make a difference? At Mesa Labs we’re passionate about protecting the vulnerable by enabling scientific breakthroughs, ensuring product integrity, increasing patient and worker safety, and improving quality of life around the world. At Mesa Labs we offer competitive wages, including bonus opportunity, and a comprehensive benefits package. Base Compensation Range: $24.1587 to $30.1683 USD This position is eligible for an annual 10% bonus opportunity in addition to the base salary Outstanding Benefits and Perks: We are proud to offer a variety of benefits that meet the diverse needs of our employees: Eligible for benefits the first day of the month after you start Tiered Medical, Dental and Vision Insurance options Health savings (HSA), healthcare & dependent care flexible spending (FSA) accounts Company paid short term and long-term disability (unless covered by a state disability plan) Company paid life insurance and AD&D 3 weeks of accrued vacation time; accruals begin on Day 1 Paid sick leave of 48 hours per calendar year Eligible employees may receive four (4) weeks paid Care Giver leave after 1 year of service or in accordance with state leave laws 401(k) plan that provides a 4% Safe Harbor company match on a 4% employee contribution that begins on Day 1 Employee Wellness and Financial Assistance Resources through Cigna and NY Life Nine (9) paid company holidays per year Overtime opportunities Agena: Agena Bioscience® empowers research laboratories worldwide to deliver scalable targeted genomic data. Our open, advanced platform, the Mass ARRAY® System, provides researchers with insights through a highly multiplexed solution in the areas of mutation profiling, liquid biopsy, pharmacogenetics, and more. Job Summary: The Production Process Operator IV is responsible for operating and monitoring complex production processes, ensuring efficient and safe manufacturing operations. This position requires an experienced operator who has advanced technical knowledge, leadership capabilities, and expertise in optimizing production processes, troubleshooting issues, and maintaining high product quality standards. Duties/Responsibilities: Process Operation & Monitoring: Operate and monitor sophisticated production equipment and machinery to ensure safe and efficient production. Set up, calibrate, and adjust machines as necessary, following standard operating procedures (SOPs) and work instructions. Monitor critical process parameters such as temperature, pressure, flow rates, and material levels, adjusting settings as needed to maintain product quality. Ensure all production processes are running within specified limits to meet production targets. Troubleshooting & Problem Solving: Identify process abnormalities or equipment malfunctions and troubleshoot to resolve issues quickly, minimizing downtime. Work with maintenance personnel and other technical staff to perform root cause analysis and implement corrective actions to improve process reliability. Continuously improve equipment and process performance to maximize efficiency. Quality Assurance & Compliance: Ensure product quality standards are met by conducting routine inspections and quality checks during production. Document results of quality tests, including any deviations, and take corrective actions when necessary. Ensure compliance with all regulatory requirements, safety standards, and quality assurance protocols (e.g., FDA, GMP, ISO). Maintain accurate records of production activities, including batch records, logs, and other documentation. Safety & Environmental Compliance: Maintain a safe work environment by adhering to all safety protocols and actively promoting safety awareness among team members. Follow proper handling, storage, and disposal procedures for hazardous materials and waste, adhering to environmental regulations. Participate in safety training, hazard assessments, and emergency drills as needed. Process Optimization & Continuous Improvement: Participate in continuous improvement projects to increase production efficiency, reduce waste, and lower costs. Utilize Lean Manufacturing, Six Sigma, or other process improvement methodologies to identify areas for process optimization. Propose and implement changes to improve production throughput and reduce variability. Team Collaboration & Training: Serve as a mentor and leader to junior operators, providing guidance and training on process operations, troubleshooting techniques, and safety procedures. Collaborate with production teams, quality control, maintenance, and engineering to ensure smooth production flow. Assist in the development and training of new SOPs, work instructions, and best practices for operational excellence. Data Entry & Reporting: Accurately record production data, machine settings, maintenance activities, and quality checks. Generate and submit reports related to production performance, downtime, material usage, and any process-related incidents. Equipment Maintenance: Perform basic maintenance tasks on equipment and machinery, such as cleaning, lubrication, and minor adjustments. Notify maintenance personnel of any equipment malfunctions or maintenance needs that require professional attention. Experience/Education: High school diploma or equivalent required. Minimum of 4 - 6 years of experience in a manufacturing or production environment. Knowledge & Skillsets Required: Strong understanding of manufacturing processes, equipment, and production methods. Proficient in reading and interpreting technical documentation such as blueprints, schematics, and process diagrams. Ability to troubleshoot mechanical, electrical, and process issues effectively. Strong attention to detail and ability to work with precision. Excellent communication skills, both written and verbal, to coordinate with other team members, supervisors, and departments. Ability to work under pressure and manage multiple tasks to meet production deadlines. Strong commitment to safety, quality, and regulatory compliance. Physical Demands (US Only): Standing or walking: Frequently during production processes and equipment operation. Lifting: Handling and moving materials or products, sometimes heavy. Manual dexterity: Using tools and operating machinery with precision. Bending and crouching: Accessing machinery or performing tasks in confined spaces. Repetitive motions: Repeatedly performing assembly or production tasks. Environmental Conditions (US Only): Workspace: Climate control (air conditioning or heating) to ensure comfort. Lighting: Artificial lighting Noise Levels: Light to moderate Ergonomics: Ventilation: Good ventilation to ensure a comfortable working environment, though this can vary depending on the building. Mesa Labs is an Equal Employment Opportunity Employer. Mesa Labs prohibits unlawful discrimination and harassment against applicants or employees based on age, race, sex, color, religion, creed, national origin or ancestry, disability, military status, sexual orientation, or any other status protected by applicable state or local law. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of five, 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: Under limited supervision, the CNC Production Machine Operator performs standardized CNC machining operations and provides technical assistance to production associates and operations leadership as needed. POSITION TYPE AND SCHEDULE: This position is a temporary role and is expected to last 4-6 months. Schedule is either Tues-Sat or Sun-Thurs, 3rd shift (7:30pm-5:00am) on a 9/80 workweek. ESSENTIAL DUTIES AND RESPONSIBILITIES: Assists in setting up complex production equipment and conducts tests, analyses and calibrates assemblies in accordance with company policy and safety procedures. Installs, maintains, repairs, rebuilds and operates a variety of machining tools including lathes, milling machines, drill presses, etc. Diagnoses problems, disassembles, determines extent of repair necessary or feasible, repairs, refits or replaces worn or defective parts and reassembles. Makes ordinary replacements of new parts and/or complete new assemblies and selects materials, plans and performs machining operations on new or replacement parts. Works to specifications, from both oral and written instructions, sketches, blueprints, engineering drawings and manuals with little supervision. Other responsibilities as assigned. Regular, consistent and punctual attendance is required. May need to work additional hours as necessary. JOB SPECIFICATIONS: Education: High School Diploma or equivalent. Certifications: Vocational training, apprenticeships or the equivalent experience in related field. Years Experience: 2-5 years or more of relevant experience. Skills: Experience in semi-repetitive specialized machine operations. Strong experience in machining tools Ability to use hand tools and machinery. Able to follow instructions, sketches, blueprints, engineering drawings and manuals. Capable of problem-solving: Exercises judgment, based on previous experience, practices and precedents, to identify and solve problems that arise with little or no precedent. Effective oral and written communication. Please note that the salary range information is only applicable for California. Compensation is based on variety of factors, candidate experience, qualifications, and location as well as market and business considerations. Pay Range: $28.00/hour - $32.00/hour (Plus $3.50/hour 3rd shift differential) depending on experience. 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.
AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of five, 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 Mechanical Quality Inspector inspects a range of components, parts and/or products for the area assigned as prescribed by all applicable specifications and quality assurance Instructions. Identifies moderately difficult quality issues in design, process or other inefficiencies to meet quality requirements. POSITION TYPE AND SCHEDULE: This position is a temporary role and is expected to last 4-6 months. Schedule is Monday-Friday, 2nd shift (2:30pm-12:00am) on a 9/80 workweek. ESSENTIAL DUTIES AND RESPONSIBILITIES: Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards. Participates in analysis statistical data from processes to either confirm compliance with established standards or identify deviations from standards. Performs visual inspections of soldered connections, mechanical inspections of assemblies and subassemblies. Prepares and completes all necessary documentation for reporting. Acceptance/rejection of inspected and/or tested items. Identifies design, process or other inefficiencies and reports quality concerns and issues. Performs routine quality inspections on engineering designs, assemblies, piece parts, final assemblies and tooling. Conducts Internal audits and corrective action follow ups. Other responsibilities as assigned. Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary. JOB SPECIFICATIONS: Education: High School Diploma or equivalent. Experience: 2-5 years relevant experience, or vocational training and/or relevant apprenticeships Skills: Ability to follow established job instructions and procedures with minimal supervision. Able to apply a systematic QA approach while using existing procedures to solve a range of technical issues. Skilled at measuring and using test equipment as prescribed by job assignment. Capable of following instructions and applying processes and procedures to standard routine tasks Must be able to interpret and follow written and verbal instructions, including engineering drawings, charts, diagrams, and sketches. Proficient computer skills. 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: $25.00/hour- $30.00/hour (Plus $2.00/hour 2nd shift differential). 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.