Manufacturing technician jobs in National City, CA - 225 jobs

About the Opportunity Argen Corporation currently has an exciting opportunity for a Manufacturing Associate I to join a growing, technology-focused and service-oriented team. If you thrive in a fast- paced and dynamic environment, and want to be a part of an organization with an unwavering commitment to quality dental solutions, then explore our career opportunities and get to know Argen. Schedule: Monday - Friday, 7:00am - 3:30pm In this role, the successful candidate: Follow department work instructions and adhere to customer and industry standards for dental products. Adhere to work instructions to properly operate mechanical equipment as needed. Visually check medical devices and perform operations according to work instructions. Identify and recommend disposition of defective items for rework or scrap. Understand the product manufacturing process from initial steps through final inspection. Complete all documentation as required. Maintain a safe and clean work area. Cross training in one or more areas of manufacturing. What does it take to be successful? High school diploma or equivalent required. One plus years of experience working in a Manufacturing environment with minimal supervision preferred. Proficiency in one or more areas of Argen manufacturing. Ability to work in a team environment. Ability to follow instructions and readily accept additional responsibilities. Attention to detail and quality focused. Passionate about industry and desire to contribute where needed. Schedule adherence and dependability. Ability to meet tight deadlines and meet production goals. Ability to follow detailed directions in a manufacturing Good Manufacturing Practices (GMP) environment is required. Ability to learn technical concepts by reading work instructions and standard operating procedures, and completing on-the-job training. Knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD) R Sch3 preferred. Our Awesome Benefits! Medical, Dental and Vision Plans 401k with Employer Match Paid Time Off and Holidays Employee Events Wellness Programs Discounts for home, travel, entertainment and so much more! About Us Argen is a family-owned and privately held company based in San Diego, CA with a state-of-the-art manufacturing center that provides high quality dental solutions to dental labs of all sizes. Founded as a precious metals company in South Africa, Argen has evolved into a dynamic, technology-based manufacturing organization focused on three key business segments, including dental alloys, zirconia, and digital dentistry solutions. Argen continues to invest in innovative research and development, continually improving on our current products and developing new solutions for the dental industry. Argen provides our global customers with affordable, high-performance products and industry-leading customer service. Argen's products are FDA regulated and ISO certified.

About Artiva: Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artiva's lead program, AlloNK, is an allogeneic, off-the-shelf, non-genetically modified NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK is delivered in the outpatient setting with no required hospitalization. AlloNK is currently being evaluated in three ongoing clinical trials for the treatment of B-cell driven autoimmune diseases. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjögren's Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases. Artiva's pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cell's NK cell manufacturing technology and programs. Artiva is headquartered in San Diego, California. For more information, visit ****************** Job Summary The Manufacturing Associate will support manufacturing of Artiva's off-the-shelf cell therapy platforms in our new, state of the art, cGMP facility. The successful candidate will develop and adhere to written procedures (SOPs) related to GMP facility operations, monitoring of equipment and facilities, and manufacturing of cell therapies internally at Artiva. The ideal candidate will demonstrate in-depth knowledge of cGMP compliance and will support manufacturing activities across multiple programs. Duties/Responsibilities Assist in setting up cGMP manufacturing suites and equipment/fixtures as needed. Perform facility and equipment monitoring activities. Assist in authoring manufacturing standard operating procedures and batch production records that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Perform cGMP manufacturing and support operations described in standard operating procedures and batch records across multiple programs. Complete documentation required by process tech-transfer protocols, validation protocols, standard operating procedures, and batch records following cGDP standards. Perform tasks in a manner consistent with Artiva's safety policies, quality systems, and GMP requirements. Complete training assignments and qualifications to ensure the necessary GMP manufacturing, and process related technical skills and knowledge. Required Skills & Experience Bachelor's degree in relevant science or engineering discipline, or equivalent work experience. Minimum 2 years of experience in cGMP biologics or cell culture manufacturing, experience in biotech or cell therapy manufacturing preferred. Experience in the following preferred: Aseptic gowning and manufacturing in an ISO 7 clean room environment. Cell counting on various platforms Cell culture and expansion using bag systems, single use large scale bioreactors, and others where applicable. Sartorius systems experience a plus. Experience with transduction using Lentiviral vectors Cell harvesting and washing processes both automated and manual. Experience with kSep a plus. Cell selection and depletion techniques using Miltenyi CliniMACS Prodigy. Fill finish and Cryopreservation processes and equipment in both bags and vials. AT-vialing a plus Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. Working Conditions and Physical Requirements Will require working with cells and cell lines of human origin as well as viral vectors Position may require occasional weekend or evening work at Artiva. Why you should apply: We have a fantastic team and philosophy! We are passionate - we deeply care about our team, our science, and improving the lives of patients. We are tenacious - laser-focused on our mission and undeterred in our commitment to deliver life-saving medicines for cancer patients. We are innovative - pushing into new frontiers for patient benefit. We are transparent - believers in flat, accessible, and open communication paths. We are inclusive - committed to the diversity of our team and ensuring that all voices are heard. In addition to a great culture, we offer: • An entrepreneurial, highly collaborative, and innovative environment • Comprehensive benefits, including: Medical, Dental, and Vision Group Life Insurance Long Term Disability (LTD) 401(k) Retirement Plan Employee Assistance Program (EAP) Flexible Spending Account (FSA) Paid Time Off (PTO) Company paid holidays, including the year-end holiday week Our recognition program, Bonus.ly, is where you can trade in points earned for things you want. If all this speaks to you, come join us on our journey! Base Salary: $75,000 - $100,000. Exact compensation may vary based on level, skills and experience.

The Test Technician Engineer plays a critical role in supporting manufacturing by executing, designing, and sustaining test procedures that validate products against design standards and quality requirements. This position encompasses configuring and conducting electrical, mechanical, and software testing, diagnosing issues, evaluating test results, and contributing to the enhancement of production testing systems. Core Responsibilities: Configure, run, and service production testing equipment and fixtures to confirm product functionality and performance standards Conduct root cause investigations of test anomalies and recommend solutions for identified issues Partner with engineering teams across design, process, and quality disciplines to deploy new testing methodologies or refine current protocols Perform calibration and upkeep of test instruments to maintain measurement accuracy and consistency Maintain and revise testing documentation, including procedures, test reports, and operational instructions Support validation activities for newly developed products and manufacturing processes Verify that all testing activities adhere to internal quality standards, client specifications, and applicable regulations Provide real-time technical support to production personnel by resolving test-related challenges Engage in continuous improvement and lean manufacturing programs to enhance testing efficiency and output quality Provide training to operators and production staff on correct testing procedures and equipment operation Document findings and compile comprehensive reports on collected testing data Execute product evaluations for safety, capacity, regulatory compliance, and performance metrics Utilize precision measurement tools and instruments Compare test outcomes against established specifications Propose enhancements to manufacturing and testing processes Oversee equipment maintenance and recordkeeping Verify adherence to regulatory requirements Execute modifications to testing protocols as necessary Communicate concerns and findings through proper organizational channels Work Setting: This position operates within a production facility featuring appropriate lighting, climate control, and moderate ambient noise levels. The standard schedule is 40 hours across five days per week, with flexibility for additional hours based on operational requirements. Required Qualifications: Education Associate's or Bachelor's degree in Electrical Engineering, Mechatronics, or a comparable technical discipline Professional Background 2-5 years of manufacturing test experience Demonstrated competency with automated testing equipment, data collection systems, and measurement instruments (such as oscilloscopes, multimeters, and power supplies) Working knowledge of root cause methodologies and failure analysis techniques Technical Competencies Advanced analytical and problem-solving capabilities Ability to interpret engineering blueprints, circuit diagrams, and testing specifications Programming or scripting experience (LabVIEW, Python, C#, etc.) preferred Superior documentation and interpersonal communication abilities Knowledge of workplace safety protocols and electrostatic discharge (ESD) prevention Physical Requirements and Working Conditions Capability to maintain standing or seated positions for prolonged durations while operating testing equipment Physical capacity to lift objects weighing 25-40 pounds

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. **Monday - Friday** **6:30AM - 3:00PM** The **Manufacturing Technician 1** performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. **PRIMARY RESPONSIBILITIES:** + Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals + Detailed cleaning of equipment/facilities to MSP/cGMP standards. + Complete technical training profile as required. + Strict adherence to Dept. Safety Rules + Bulk processing and filtration involving monitoring processing parameters (i.e. pH, weights, separation, assay results..) + Perform real-time documentation during the production run. **ADDITIONAL RESPONSIBILITIES** English fluency both verbal and written. Basic math skills with proficiency in metric system. Accurate documentation skills are a must. Basic computer skills. Mechanical aptitude. Must be available to work any shift, including weekends. Ability to work well with others in a team environment is essential. Self-starter with the ability to work independently and use good judgment. Must be able to handle multiple priorities. Must be proactive, results oriented, and have strong attention to detail **EDUCATION** High school diploma or GED required. Associates Degree or Bachelor's degree preferred. Manufacturing, or experience in pharmaceuticals/biologics processing in a GMP environment is preferred. **EXPERIENCE** 1-2 years' experience in a manufacturing environment preferred. **SKILLS & ABILITIES** Accurate documentation and attention to detail oriented. Usage of a 10-key calculator. **OCCUPATIONAL DEMANDS** Ability to lift/push 50 lbs. All work is performed in a clean room (sanitized) manufacturing environment and must gown up. Must be able to work in a cold environment, job requires bending or standing for prolonged periods. This is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned. _EEO Minorities/Females/Disability/Veterans_ **BENEFITS** + The estimated pay scale for the Manufacturing Technician I role based in Vista, CA is $21.51 - $32.26/hour depending on experience + Additionally, the position is eligible to participate in up to 5% of the company bonus pool + We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement + Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data \#biomatusa Learn more about Grifols (************************************************* **Req ID:** 538071 **Type:** Regular Full-Time **Job Category:** MANUFACTURING

AXILLON AEROSPACE specializes in the use of fiber-reinforced polymer composites, specialty polymers, and ceramics across the low- and high-temperature thermoset and thermoplastic spectrum. Learn more at axillonaerospace.com JOB SUMMARY: The successful Manufacturing Technician performs a variety of manufacturing processes such as pre-stacking, kitting, presses, molding, layup, noodles and deflashing associated with the fabrication of aerospace composite materials in connection with production contracts. Operations vary in complexity and difficulty requiring differential compensation based on experience and mastery of techniques and processes. Mastery of progressive skills typically involves cross-training and certification/sign-off from a qualified trainer. ESSENTIAL DUTIES AND RESPONSIBILITIES: Layup and cure composite parts using prepreg fabric, uni-tape, SMC, BMC and dry materials. Assemble, demold, and bond components and parts. Prepare parts and perform bonding and finishing by filling, sanding, grinding, and cleaning. Fit components by cutting, deburring, trimming and hand working materials. Use hand and power tools, measurement devices and equipment to perform production operations. Follows written instructions, work instructions, travelers and procedures when producing hardware. Fills out production records, travelers and logs as work is completed. Logs and records material traceability information on travelers. Stamps and dates operations complete on travelers when they are complete and the work performed satisfies all documented quality requirements. Ensures that all material used in deliverable products is within its shelf-life and allowable out-time. Identifies expired material and completes applicable non-conformance reports. Works with the team Lead, Value Stream Manager, and/or project Engineer to identify root causes and corrective actions required to fix and prevent discrepancies. Maintains and cares for tools, molds, machines and equipment. Maintains the order and cleanliness of production work areas, ensuring that all tools, materials and supplies are returned to their designated locations at the end of each shift. Facilitates the flow of production parts to and from other manufacturing operations and locations. Delivers parts and materials to the next operation. Participates in and contributes to process improvement, lean manufacturing and other initiatives. Recommends process improvements to the Lead, Value Stream Manager, Manufacturing Operations Manager or Manager of Continuous Improvement. Performs all other duties and responsibilities as assigned. QUALIFICATIONS: Education: Required High School diploma or equivalent Experience: Must have 3-5 years of experience working in manufacturing, assembly, layup or composite fabrication. Aerospace experience preferred. Skills: Must be able to lift, hold and carry up to 40 pounds unaided and be able to perform the necessary physical requirements of the job. Must be able to use various production hand tools. Must be willing to work overtime when required. PC Proficiency in Microsoft Word and Excel preferred PC Proficiency in sending and writing emails using Outlook or equivalent preferred Excellent verbal and written communication skills required. Organized and self-motivated. Strong attention to detail and high level of accuracy. Ability to manage multiple duties, set priorities and follow tasks through completion. Capable of working in an environment in which demands and priorities change. Schedule: Monday-Friday, 5:00am-2:30pm (9/80 workweek) 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: $23.00/hour - $28.00/hour. Trade Compliance restrictions require all candidates to be US Persons. See below for more information. Axillon is an Equal Opportunity and Affirmative Action 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.

Zenith Talent specializes in staffing professional positions in Information Technology, Engineering, Marketing, Sales, Finance, HR and Operations. We have the knowledge and skills to supply candidates that fit perfectly in your organization. As a minority owned company, we understand the benefits of a diverse workforce, which is why we have built strong alliances with many diverse organizations, directly linking their members to opportunities within your organization. Job Description Minimum qualifications Skills: • Excellent familiarity with standard laboratory practices. • High level of familiarity with lasers, laser-optics, electro-optics, electronics or related technical field required. • Communicate well with supervisor and other employees. • Experience with SOPs, travelers, ECOs, and GMP is a plus. Education: • High school diploma or equivalent required. • Some college level science courses or training are a plus. Additional Information If our requirement matches your resume, then please do reply on my email id "***********************************" or call me on ************

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. We are seeking a Manufacturing Technician at nVent Sydney facility. The candidate will play a pivotal role in nVent manufacturing process in-house and field service and support duties as required, ensure smooth execution of production orders, meet business contractual commitments, satisfy stakeholders and drive continuous improvement while adhering to nVent health, safety and environmental standards. Key role responsibilities * Assist with nVent Electrical & Fastening production work on site and in the field * Ensure the production workflow comply to nVent EH&S guidelines. * Oversee production assets to ensure equipment are serviced at recommended intervals * Responsible for the accuracy and timely completion of work orders with optimal use of resources * Responsible for coordinating production schedules on a daily and weekly basis to meet customer work order requirements. * To maintain a clean and safe work environment on site * Manage business in accordance with quality standards * Serve as a point of escalation for problems/issues to ensure a prompt resolution * Establish and maintain co-operative business relationships with internal and external stakeholders * Manage and monitor expenses and assets to meet assigned goals * Maintain systematic audit trails to keep accurate inventory in the production cell * Generate manufacturing related metrics as requested by management * Strive to improve efficiency and quality of the operation through processes and procedures in order to meet ongoing and future demand * Maintain and implement any ISO related Quality requirements on site qualifications and experience * Associate Diploma in Production / Engineering or relevant experience in a manufacturing environment * Understanding of production methodology and equipment maintenance * Restricted Electrical license preferred * Good Computer Literacy, ERP exposure a plus * Good communication skills Special REQUIREMENTS * NSW Drivers License * Forklift License WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Job Description MAST Technologies seeking a Manufacturing Technician 1 who tends to production machines such as spray booth, clicker press, dip machine, presses, rubber mills, sander, laminator and includes various touch labor activities. About MAST: MAST Technologies is an industry leader in advanced RF and EMI absorbing materials. We create engineered solutions that support mission-critical defense and aerospace applications worldwide. Our employees contribute directly to cutting-edge innovation and enjoy a collaborative environment focused on quality, technical excellence, and continuous improvement. Job Accountabilities: Rubber processing area operates rubber mills and hydraulic presses. Foam processing area operates spray booth and dip tank. Material processing area operates laminator, clicker press to die cut material and touch labor to clean and process material. Sanding area operates sander and with critical measurement of material thickness. Technicians for all areas must be able to read job specifications and procedures to determine any machine adjustments and the material requirements, in addition the operator must maintain accurate process logs of all activities Must be familiar with basic machine functions in order to perform the tasks stated above. Must be able to accurately work with scales. Must have ability to safely work with cutting knifes and steel rule dies. Pushes button or depresses pedal to activate machine. Observes machine operation to detect workpiece defects or machine malfunction. Measures workpiece dimensions to determine accuracy of machine operation. Performs minor machine maintenance such as oiling machines, dies, or workpieces. Sets up and breakdown of processes on equipment. Operates any equipment needed to perform job. Detects and reports defective material or questionable conditions to the department supervisor. Maintain the work area in a clean and orderly condition. Follows all safety guidelines and rules. Performs other work-related duties as assigned. Must be able to work overtime to meet production schedule. Job Specifications: Education: High School diploma or general education degree (GED) or equivalent combination of education and experience Years' Experience: Three to six months' related experience and/or training Skills: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to read and interpret metal rules. Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations. Able to communicate well with supervisor and follow work instructions. Benefits: At MAST Technologies, we recognize how important your career and benefits are to you and your family. We offer a full suite of benefits, including medical, dental, vision, short and long-term disability coverage, accident insurance, critical illness insurance, basic and supplemental life insurance, employee assistance plan, retirement savings and matching, and other developmental opportunities. We are committed to supporting the way you live and work. MAST is an Equal Opportunity Employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status. Applicants requiring reasonable accommodation to complete the application process may contact Human Resources. This position requires access to information subject to the International Traffic in Arms Regulations (ITAR). Employment is contingent upon the applicant being a “U.S. person” as defined by ITAR (22 CFR §120.15), which includes U.S. citizens, lawful permanent residents, refugees, or asylees, as required by U.S. export control laws. (Actual placement within the salary range is dependent on multiple factors, including but not limited to skills, education, experience and location)

Contract-to-Hire | $20-$26/hr DOE The Manufacturing Technician II/III supports production operations within an ISO 13485 and cGMP-regulated environment. This role is responsible for executing manufacturing activities, maintaining accurate documentation, operating production equipment, and ensuring compliance with quality and safety standards. Key Responsibilities Work within an ISO 13485 and cGMP production environment and ensure compliance with all quality system requirements Execute and review documentation in accordance with cGMP and GDP procedures Perform daily documentation review and support post-manufacturing documentation completion Conduct visual inspection of lyophilized products and packaging heat seals Operate and monitor large automated and semi-automated manufacturing equipment Report equipment alarms or issues to Lead Technician or Supervisor Clean and sanitize manufacturing and support areas Perform daily arithmetic calculations related to volumes, concentrations, and unit conversions (gravimetric and volumetric) Operate production equipment including pipettes, balances, pH meters, and heat sealers Ensure equipment is operating properly and within calibration Participate in Quality Working Teams and Continuous Improvement initiatives Assist in training and mentoring new team members Assist with creation, updates, and revisions of Standard Operating Procedures (SOPs) Author Manufacturing Non-Conformance Reports (NCRs) and risk analysis memos as needed Receive and distribute materials to production areas Perform NetSuite transactions including material issuance, work order completion, and closing Assist with review of Quality Assurance logbooks Manage hazardous waste in compliance with company procedures and all applicable regulations Perform safety and cGMP inspections or observations Perform additional duties as assigned Education & Experience Requirements Manufacturing Technician II Bachelor's degree in Biotechnology, Molecular Biology, Biochemistry, or related field with 1+ year of cGMP manufacturing experience OR Associate's degree in a related field OR High school diploma/equivalent with 3+ years of cGMP manufacturing experience Manufacturing Technician III Bachelor's degree in a related field with 2+ years of cGMP manufacturing experience OR Associate's degree in a related field with 3+ years of experience OR High school diploma/equivalent with 5+ years of cGMP manufacturing experience Required Skills & Knowledge Reliable attendance and punctuality Ability to read, understand, and follow detailed written instructions Strong verbal and written communication skills Proficiency in English (reading, writing, and speaking) Knowledge of cGMP manufacturing processes and SOP compliance Experience with visual inspection of components and finished goods Understanding of basic chemical and biological safety procedures Familiarity with formulation, filling, kitting, labeling, and packaging operations #MS-CBMFG

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 Pay range for this position is $20.00 - $26.00 per hour, depending on experience. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. This is a temp to hire position. Position Overview The Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Start time for this position is 6:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Ability to work within an ISO 13485 and cGMP production environment and ensure compliance with our quality system. Execute documentation based on cGMP and GDP procedures, as well as perform documentation review post manufacturing execution. Participate in Quality Working Teams and Continuous Improvement Teams. Visual inspection of lyophilized product and heat seals of packaging. Clean and sanitize manufacturing and associated support areas. Responsible for monitoring machinery and reporting alarms to lead technician or Supervisor. Conduct daily documentation review. Participate in Quality Working Teams and Continuous Improvement Teams. Operate large machinery and monitor automated. Employee may be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. Perform daily arithmetic calculations as it pertains to total volume and liquid concentrations. Perform daily unit conversions as it pertains to gravimetric and volumetric measurements. Operate production equipment such as pipettes, balances, pH meter and heat sealers. Monitor department equipment for proper operation that is within calibration. May perform safety and cGMP inspections or observations. Ensure compliance with SOP/cGMP and cGDP requirements. Assist in training/ leading of new team members in production activities. Assist in updating and new revision of standard operating procedures (SOP). May need to be an author for any MFG Non-Conformance Reports (NCR) and risk analysis memos. Receive and distribute supplies into the production area as necessary. Perform NetSuite transaction, issue material, completion and closing of work orders. May assist with review of quality assurance logbooks. May perform other duties as assigned. Education Requirements Level II Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment. Level III Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment. Required Skills and Knowledge Punctuality and reliable attendance required. Ability to read and follow detailed written instructions; strong verbal and written communication skills. Proficient in reading, writing, and conversing in English to understand cGMP manufacturing processes and SOPs. Knowledge of manufacturing production processes related to product integrity, including visual inspection of components and finished goods, manual and semi-automated packaging, and product labeling. Understanding of basic chemical and biological safety procedures. Basic knowledge of formulation, filling, and kitting operations and capabilities. 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.

DEPARTMENT: Manufacturing - Sensors REPORTS TO: Manufacturing Manager STATUS: Non-Exempt JOB SUMMARY: The Production Technician's responsibilities include assembling, testing, calibrating, inspecting, and packaging temperature sensors. Operating various machinery and equipment, interpreting work orders, and ensuring product quality are essential aspects of this role. This position contributes to the delivery of high-quality products to both internal and external stakeholders. RESPONSIBILITIES: Operating Machinery/Equipment: Operate various machinery and equipment, including a cutoff saw, sanding belts, buffing wheels, crimping machine, wire strippers, sand blaster, soldering iron, TIG welder, and measurement equipment (e.g., ruler, calipers, multimeter). Manual Fabrication & Assembly: Fabricate and assemble parts in accordance with Procedures and Work Instructions. Parts Management: Identify and pull parts as required. Interpret complex work orders to determine assembly requirements. Quality Control & Documentation: Conduct quality assessments with minimal training, ensuring product acceptability through process inspection sheets and workstation measuring and test equipment. Recognize and document quality issues and defects. Effectively communicate issues to co-workers and supervisors for potential process improvement. Accurately indicate acceptable products on work orders as per established procedures. Read and understand blueprints. Specific duties will vary on a daily basis. Qualifications MINIMUM QUALIFICATIONS: Proficiency in the English language (speaking, writing, and reading). Computer literacy (e.g., MS Word, Excel, internet) with a willingness to learn new programs. Reliable transportation to and from work (40-hour work week). Ability to stand for up to 8 hours. Strong manual dexterity and good eyesight (for reading blueprints). Ability to follow written instructions. Willingness to learn new skills. Strong work ethic, emphasizing efficiency on repetitive tasks and tackling technical problems. TIG welding skills and experience. PREFERRED SKILLS: Mechanical inclination, such as working on cars, building models, or having experience in final assembly. Soldering skills. Experience with calipers and multimeters. Ability to thrive in an environment with shifting priorities and prioritize work without direct supervision. Previous experience in a factory/production environment. Problem-solving abilities.

Job DescriptionDescription: Launch your career by helping build and test systems that power critical operations. Radeus Labs designs and manufactures advanced computing and communications systems for aerospace, defense, and commercial markets. As a Production Tech 1, you will support the assembly and basic testing of electronic and mechanical components. This is an entry-level position ideal for someone detail-oriented, eager to learn, and ready to grow in a hands-on technical environment. What Success Looks Like: You follow detailed instructions, complete work accurately, and maintain a clean and organized work area. You ask questions when needed, show up on time, and take pride in the quality of your work. You grow in skill and confidence as you learn new tasks and processes. Mindset: Learning-focused, dependable Soft Skills: Follow instructions carefully Ask clarifying questions Demonstrates reliability (attendance, punctuality) Leadership Expectation: None yet - focus on becoming a solid team member Responsibilities: Assemble basic electronic and mechanical components using hand tools and work instructions Perform visual inspections to check for defects or missing parts Assist with basic testing under supervision Maintain cleanliness and organization in your work area Follow safety procedures and quality standards Communicate effectively with team leads and trainers Accurately document work performed on travelers or checklists Requirements: High school diploma or equivalent Strong attention to detail and manual dexterity Willingness to learn and follow instructions Dependable, punctual, and safety-conscious Basic computer and documentation skills No prior experience required - training provided

SOMACIS, Inc. - Global Printed Circuit Board Manufacturer for 50+ Years Company Overview: SOMACIS, Inc. is a leading manufacturer of Printed Circuit Boards (PCBs), serving a diverse range of industries, including Aerospace, Avionics, Military, Commercial, and Medical Applications. Our commitment to quality and innovation has earned us a reputation as a trusted partner and supplier of high-performance PCBs. Position Description: SOMACIS, Inc. is a well-established, advanced technology, high-reliability printed circuit board manufacturer located in Poway, California. We are looking for motivated, team-oriented individuals (both entry-level and experienced) for multiple areas within the production department. Key Responsibilities: Motivated individuals with a "Go-Getter" attitude Be punctual to work and ensure equipment start-up and material gathering for job duties Take responsibility and hold yourself accountable for the quality of the work produced Willingness to learn and cross-train on other pieces of equipment and/or departments Seek critical feedback and adjust based on the information shared Fully embody the Somacis Quality Policy in all activities Exhibit a team-player mentality and help out when needed Thrive in a fast-paced environment Required Knowledge, Skills, and Abilities: Motivated, adaptable, innovative, and responsible individuals who produce quality results Ability to set up, operate, and maintain manufacturing equipment CNC, Lathe, and Drill machine experience is a plus Ability to read and understand customer specifications, prints, and related documents Basic visual inspection skills Strong communication skills, both oral and written Ability to perform basic mathematical calculations High school graduate or equivalent Physical Requirements: Regularly required to use hands for handling objects, tools, or controls and talk or hear Occasionally required to stand, walk, and reach with hands and arms Ability to move around the facility and production floor Physical endurance to lift and/or move up to 30 pounds Specific vision abilities required include close vision, distance vision, depth perception, and the ability to adjust focus Strong listening skills to gather and process requests and respond accordingly Benefits: Medical, Dental, and Vision Insurance 401(k) Program Company-Sponsored Life & Long-Term Disability Insurance Voluntary Insurance Options: Life, Long-Term Disability, Short-Term Disability, AD&D, Accident, Hospital Indemnity, Critical Illness, and Legal Insurance Health Savings Account (HSA) and Flexible Spending Account (FSA) Options Paid Time Off (PTO) Program Employee Referral Program Education Reimbursement Program 14 Company Holidays Shift Differential Eligibility: Qualified applicants must hold U.S. Citizenship, Permanent Residency, Asylee, or Refugee Status. Note: Job descriptions provide accurate overviews of roles but are not exhaustive. They serve as reference points for fair pay considerations. SOMACIS is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. Standard First Shift: 6:00 am - 2:30 pm Standard Second Shift: 2:00 pm - 10:30 pm

Job DescriptionSaronic Technologies is a leader in revolutionizing autonomy at sea, dedicated to developing state-of-the-art solutions that enhance maritime operations through autonomous and intelligent platforms. Job OverviewWe're seeking an Electromechanical Technician to ensure the operational readiness and reliability of our autonomous surface vessels for the DoD. You will be responsible for diagnosing, repairing, and maintaining ASVs and remain instrumental in sustaining mission-critical assets and ongoing operations.Responsibilities Conduct comprehensive diagnostic assessments of ASVs and their components to identify issues and malfunctions Perform timely and efficient repairs, replacements, and adjustments to restore ASVs to optimal functionality Collaborate closely with engineering and technical teams to troubleshoot complex problems and implement effective solutions Conduct thorough testing and quality assurance procedures to validate repairs and ensure compliance with performance standards Document all repair activities, including findings, procedures, and outcomes, adhering to company protocols and industry regulations Maintain an organized inventory of spare parts, tools, and equipment necessary for depot repair operations Assist in the development and optimization of repair procedures and protocols to enhance efficiency and effectiveness Provide technical support and training to field technicians and end-users as needed Qualifications Associate degree or technical certification in electronics, mechanical engineering, or a related field. Bachelor's degree preferred Experience in depot-level repair and maintenance of complex electronic and mechanical systems, preferably in the maritime or defense industry Proficiency in troubleshooting, diagnosing, and repairing electrical, electronic, and mechanical components and systems Familiarity with autonomous systems, marine navigation, and control systems is preferred Strong analytical and problem-solving skills with attention to detail Experience working with the DoD or government contracts is a plus Benefits Medical Insurance: Comprehensive health insurance plans covering a range of services Saronic pays 100% of the premium for employees and 80% for dependents Dental and Vision Insurance: Coverage for routine dental check-ups, orthodontics, and vision care Saronic pays 99% of the premium for employees and 80% for dependents Time Off: Generous PTO and Holidays Parental Leave: Paid maternity and paternity leave to support new parents Competitive Salary: Industry-standard salaries with opportunities for performance-based bonuses Retirement Plan: 401(k) plan Stock Options: Equity options to give employees a stake in the company's success Life and Disability Insurance: Basic life insurance and short- and long-term disability coverage Additional Perks: Free lunch benefit and unlimited free drinks and snacks in the office Physical Demands Ability to perform physically demanding work for extended periods of time, up to 12 hours/day Frequently and repetitively, lift, push and carry up to 20 lbs. The ability to carry 20 lbs. up and down stairs Ability to work outside for an extended period of time Frequently and repetitively, bend, lift and reach to install vehicle parts of varying size and weight overhead, accurately and in allotted timeframes Ability to stand and walk for up to 12 hours/day, including over varied and uneven terrain Stoop, lay, bend, reach, squat, kneel, crouch, twist and crawl for extended periods of time, including up to 12 hours/day Climb and maintain balance on ladders, platforms, or other high structures Ability to find issues in a work process and be alert to safety signals using sight, touch, and hearing Demonstrated ability to handle and manipulate tooling and mechanically fasten bolts within required cycle time Exposures to hazardous materials and ability to follow waste handling/disposal procedures Wearing Personal Protective Equipment, including but not limited to safety glasses, safety shoes, hearing protection, gloves and adhering to prescribed safety rules and guidelines This role requires access to export-controlled information or items that require “U.S. Person” status. As defined by U.S. law, individuals who are any one of the following are considered to be a “U.S. Person”: (1) U.S. citizens, (2) legal permanent residents (a.k.a. green card holders), and (3) certain protected classes of asylees and refugees, as defined in 8 U.S.C. 1324b(a)(3). Saronic does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits.

We are seeking a Manufacturing Technician to join our reagent formulation team. The ideal candidate will perform assigned manufacturing tasks for reagents and buffers, troubleshoot formulations, filling processes, and conduct Quality Control procedures for consumables. This role involves working collaboratively in a fast-paced environment with a multi-disciplinary team to support R&D and process improvement activities. Responsibilities + Perform assigned manufacturing tasks for reagents and buffers. + Troubleshoot formulations, filling processes, and packaging. + Conduct Quality Control procedures for consumables. + Perform data collection and analysis. + Process work orders to complete products for inventory. + Execute and improve batch records and standard operating procedures (SOPs). + Identify gaps and weaknesses in SOPs and formulations. + Maintain accurate inventory of materials through cycle counts, ordering, and receipt of materials. + Operate effectively in a fast-paced environment with rapidly shifting priorities. + Collaborate with scientists, engineers, and manufacturing personnel to support R&D and process improvement activities. + Lead kit and fill support lines. + Formulate simple buffers under 50L. + Perform additional duties as assigned. Essential Skills + Experience with formulations, reagents, and Quality Control. + Proficiency with general laboratory skills and equipment such as UV-VIS, pH meters, and conductivity meters. + Hands-on experience with SOPs, batch records, and work instructions. + Strong analytical, verbal, and written communication skills. + Ability to work independently and as part of a team. + Detail-oriented and highly organized. + Experience with developing and updating Bill of Materials (BOMs). Additional Skills & Qualifications + Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or related life science discipline preferred. + 0-2 years of relevant experience in consumable manufacturing or equivalent combination of education and experience. + Preferred experience in formulation, filling, packaging, and chromatography in a laboratory setting. Job Type & Location This is a Contract to Hire position based out of San Diego, CA. Pay and Benefits The pay range for this position is $25.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Jan 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. The Manufacturing Technician II position will be responsible for leading CNC programming improvements, conducting advanced tooling trials, and provide troubleshooting support on all equipment as assigned utilizing internal and external resources. This position will be a direct support function to operations that will serve as the front line of defense against machine and process issues. This will help insure exceptional customer delivery and quality control. This position will also support Engineering, Maintenance, and on-site Lean groups. WHAT YOU WILL EXPERIENCE IN THIS POSITION: * Generate solutions for machining quality issues reported by machine operators. * Recommend improvements for tool life and cycle times in existing CNC programs. * Troubleshoot mechanical, electrical, hydraulic, and pneumatic issues with maintenance personnel to ensure customer delivery. * Perform mechanical re-alignments of CNC equipment and work holding independently. * Assist in creating manufacturing documentation and work instructions for new and existing CNC equipment. * Support Manufacturing Engineering with process, equipment, and tooling improvements. * Communicate effectively with Maintenance, Engineering, Supervisors, and outside vendors regarding projects and equipment repair problems. * Help relocate and install large machinery. * Understand engineering drawings, schematics, maintenance work orders, or manufacturers' manuals. * Handle various assignments and changing priorities. * Perform basic preventative maintenance on industrial machinery. * Use basic hand and power tools, machine tools, and precision measuring equipment. YOU HAVE * High school diploma or equivalent. Technical or trade school preferred. * 3-5 years of direct CNC machining setup experience. * Good organizational skills with strong attention to detail. * Excellent print reading skills: GD&T, 3D modeling, and CAD proficiency is a plus * Computer skills with ability to use Microsoft Excel, Word, and Outlook. WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

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 Pay range for this position is $20.00 - $26.00 per hour, depending on experience. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. This is a temp to hire position. Position Overview The Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Start time for this position is 6:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Ability to work within an ISO 13485 and cGMP production environment and ensure compliance with our quality system. Execute documentation based on cGMP and GDP procedures, as well as perform documentation review post manufacturing execution. Participate in Quality Working Teams and Continuous Improvement Teams. Visual inspection of lyophilized product and heat seals of packaging. Clean and sanitize manufacturing and associated support areas. Responsible for monitoring machinery and reporting alarms to lead technician or Supervisor. Conduct daily documentation review. Participate in Quality Working Teams and Continuous Improvement Teams. Operate large machinery and monitor automated. Employee may be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. Perform daily arithmetic calculations as it pertains to total volume and liquid concentrations. Perform daily unit conversions as it pertains to gravimetric and volumetric measurements. Operate production equipment such as pipettes, balances, pH meter and heat sealers. Monitor department equipment for proper operation that is within calibration. May perform safety and cGMP inspections or observations. Ensure compliance with SOP/cGMP and cGDP requirements. Assist in training/ leading of new team members in production activities. Assist in updating and new revision of standard operating procedures (SOP). May need to be an author for any MFG Non-Conformance Reports (NCR) and risk analysis memos. Receive and distribute supplies into the production area as necessary. Perform NetSuite transaction, issue material, completion and closing of work orders. May assist with review of quality assurance logbooks. May perform other duties as assigned. Education Requirements Level II Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment. Level III Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment. Required Skills and Knowledge Punctuality and reliable attendance required. Ability to read and follow detailed written instructions; strong verbal and written communication skills. Proficient in reading, writing, and conversing in English to understand cGMP manufacturing processes and SOPs. Knowledge of manufacturing production processes related to product integrity, including visual inspection of components and finished goods, manual and semi-automated packaging, and product labeling. Understanding of basic chemical and biological safety procedures. Basic knowledge of formulation, filling, and kitting operations and capabilities. 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.

Contract-to-Hire | $20-$26/hr DOE The Production Technician II supports hands-on manufacturing operations in a cGMP and ISO 13485 environment. This role executes production processes, maintains accurate documentation, and ensures compliance with quality and safety standards. Position is 100% on-site, Monday-Friday, 8-hour shifts (start time 6:00 AM or 12:00 PM). Overtime and weekends may be required. Responsibilities Execute production activities in compliance with cGMP, GDP, SOPs, and quality standards Complete and review manufacturing documentation Perform label printing, formulation, filling, and kitting Operate and monitor automated and semi-automated equipment Perform visual inspection of components and finished goods Clean and sanitize manufacturing and support areas Monitor equipment, report alarms, and ensure calibration compliance Perform basic math, unit conversions, and concentration calculations Handle hazardous waste per regulatory requirements Receive and distribute materials to production areas Perform NetSuite transactions including material issuance and work order completion Participate in continuous improvement and quality initiatives Perform other duties as assigned Requirements High school diploma or GED 3+ years of manufacturing experience in a cGMP environment Strong attention to detail and documentation skills Ability to read, write, and communicate effectively in English Knowledge of manufacturing processes, product integrity, and labeling Understanding of basic chemical and biological safety practices Experience with formulation, filling, and kitting operations #MS-CBMFG

Saronic Technologies is a leader in revolutionizing autonomy at sea, dedicated to developing state-of-the-art solutions that enhance maritime operations through autonomous and intelligent platforms. Job OverviewWe're seeking an Electromechanical Technician to ensure the operational readiness and reliability of our autonomous surface vessels for the DoD. You will be responsible for diagnosing, repairing, and maintaining ASVs and remain instrumental in sustaining mission-critical assets and ongoing operations.Responsibilities Conduct comprehensive diagnostic assessments of ASVs and their components to identify issues and malfunctions Perform timely and efficient repairs, replacements, and adjustments to restore ASVs to optimal functionality Collaborate closely with engineering and technical teams to troubleshoot complex problems and implement effective solutions Conduct thorough testing and quality assurance procedures to validate repairs and ensure compliance with performance standards Document all repair activities, including findings, procedures, and outcomes, adhering to company protocols and industry regulations Maintain an organized inventory of spare parts, tools, and equipment necessary for depot repair operations Assist in the development and optimization of repair procedures and protocols to enhance efficiency and effectiveness Provide technical support and training to field technicians and end-users as needed Qualifications Associate degree or technical certification in electronics, mechanical engineering, or a related field. Bachelor's degree preferred Experience in depot-level repair and maintenance of complex electronic and mechanical systems, preferably in the maritime or defense industry Proficiency in troubleshooting, diagnosing, and repairing electrical, electronic, and mechanical components and systems Familiarity with autonomous systems, marine navigation, and control systems is preferred Strong analytical and problem-solving skills with attention to detail Experience working with the DoD or government contracts is a plus Benefits Medical Insurance: Comprehensive health insurance plans covering a range of services Saronic pays 100% of the premium for employees and 80% for dependents Dental and Vision Insurance: Coverage for routine dental check-ups, orthodontics, and vision care Saronic pays 99% of the premium for employees and 80% for dependents Time Off: Generous PTO and Holidays Parental Leave: Paid maternity and paternity leave to support new parents Competitive Salary: Industry-standard salaries with opportunities for performance-based bonuses Retirement Plan: 401(k) plan Stock Options: Equity options to give employees a stake in the company's success Life and Disability Insurance: Basic life insurance and short- and long-term disability coverage Additional Perks: Free lunch benefit and unlimited free drinks and snacks in the office Physical Demands Ability to perform physically demanding work for extended periods of time, up to 12 hours/day Frequently and repetitively, lift, push and carry up to 20 lbs. The ability to carry 20 lbs. up and down stairs Ability to work outside for an extended period of time Frequently and repetitively, bend, lift and reach to install vehicle parts of varying size and weight overhead, accurately and in allotted timeframes Ability to stand and walk for up to 12 hours/day, including over varied and uneven terrain Stoop, lay, bend, reach, squat, kneel, crouch, twist and crawl for extended periods of time, including up to 12 hours/day Climb and maintain balance on ladders, platforms, or other high structures Ability to find issues in a work process and be alert to safety signals using sight, touch, and hearing Demonstrated ability to handle and manipulate tooling and mechanically fasten bolts within required cycle time Exposures to hazardous materials and ability to follow waste handling/disposal procedures Wearing Personal Protective Equipment, including but not limited to safety glasses, safety shoes, hearing protection, gloves and adhering to prescribed safety rules and guidelines This role requires access to export-controlled information or items that require “U.S. Person” status. As defined by U.S. law, individuals who are any one of the following are considered to be a “U.S. Person”: (1) U.S. citizens, (2) legal permanent residents (a.k.a. green card holders), and (3) certain protected classes of asylees and refugees, as defined in 8 U.S.C. 1324b(a)(3). Saronic does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits.