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*Job Overview* We are seeking a motivated and detail-oriented Assembler to join our dynamic manufacturing team. In this role, you will be responsible for assembling complex electronic and mechanical components with precision and efficiency. Your expertise will contribute to the production of high-quality products, ensuring they meet strict specifications and safety standards. This position offers an exciting opportunity to work with cutting-edge electro-mechanical components, develop your technical skills, and be part of a collaborative environment dedicated to excellence. *Duties* * Assemble printed circuit boards (PCBs) and electronic components using surface mount technology (SMT) and through-hole techniques. * Read and interpret electrical schematics, blueprints, and technical drawings to follow assembly instructions accurately. * Use hand tools, power tools, soldering equipment, and testing devices such as ohmmeters to complete electrical wiring and mechanical assembly tasks. * Build electrical panels and wiring harnesses in accordance with schematic diagrams and IPC 610 standards for electronic assemblies. * Troubleshoot assembly issues by analyzing schematics, schematics reading, and engineering troubleshooting methods to resolve problems efficiently. * Conduct quality inspections to ensure assemblies meet specifications for electrical assembly, surface mount technology, and electro-mechanical components. * Maintain a clean, organized workspace while adhering to safety protocols during all manufacturing processes. *Qualifications* * Proven experience in electronics assembly, electrical wiring, or mechanical assembly within a manufacturing environment. * Strong ability to read electrical schematics, blueprints, and technical drawings accurately. * Familiarity with PCB manufacturing processes, surface mount technology (SMT), and IPC 610 standards for electronic assemblies. * Proficiency with hand tools, power tools, soldering techniques, and testing instruments such as ohmmeters. * Knowledge of programmable logic controllers (PLCs), electrical blueprint reading, and engineering troubleshooting is highly desirable. * Ability to follow detailed blueprint specifications and schematics precisely while maintaining high-quality standards. * Excellent manual dexterity combined with the ability to work efficiently in a fast-paced production setting. Join our team as an Assembler to build innovative products that make a difference! We value precision, safety, teamwork, and continuous improvement — all while supporting your growth as a skilled manufacturing professional. Pay: $20.00 - $22.00 per hour Work Location: In person
*Job Summary* We are looking for a full-time MIG Welder/Fabricator to join our team in San Marcos, CA. This is an in-person shop position working primarily with steel. We are looking for someone who has a solid foundation in welding and fabrication, is dependable, takes pride in their work, and is interested in growing their skills. We are willing to train the right person. Your work won’t just stay in the shop—you’ll help fabricate the ramps, rails, and steel features that become skateparks and competition courses ridden by athletes across the world. *Duties* * MIG weld steel components and assemblies * Cut, fit, grind, and prepare steel for fabrication * Read measurements and basic fabrication drawings * Measure and fit components accurately * Operate common welding and fabrication tools * Inspect completed work for quality and accuracy * Maintain a clean and safe work area * Work with the fabrication team to complete projects on schedule * Be able to read plans *Experience* * Minimum 1 year of welding/fabrication experience preferred * MIG welding experience * Experience working with steel * Comfortable using grinders, saws, measuring tools, and other common shop equipment * Reliable and punctual * Strong attention to detail * Willingness to learn and take direction Position Details: * Full-time * In-person in San Marcos, CA * No travel required * Overtime opportunities available * On-the-job training available * Opportunity to grow your welding and fabrication skills We encourage applicants with a good foundation in MIG welding to apply even if they don't meet every qualification. We're willing to train someone who is dependable, motivated, and eager to learn. Pay: $30.00 - $45.00 per hour Expected hours: 40.0 per week Location: * San Marcos, CA 92069 (Required) Work Location: In person
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Pay Range The pay range for this position is $20.00 - $22.00 per hour. 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 participate in tasks related to the visual inspection of manufactured liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing as well as other types of visual inspection activities, as required. This role is 100% on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00 am - 9:30 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Perform visual inspection of pharmaceutical or medical products to identify defects or non-conformities. Ensure all inspected products meet established quality standards and regulatory requirements. Document results accurately in batch records or electronic systems. Maintain good documentation practices (GDP) and ensure inspection areas comply with aseptic and cleanliness standards. Operate and maintain inspection equipment and booths according to SOPs. Report defective products or process deviations to quality or production supervisors. Follow Good Manufacturing Practices (GMP) and safety protocols at all times. Participate in inspection and manufacturing readiness activities. Maintain cleanliness and organization of inspection areas, including gowning in all lab areas. This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs. Requirements and Qualifications High school diploma or equivalent required; 0-2 years of relevant experience. A Bachelor's degree in an engineering discipline or life science field is preferred. Must be able to effectively communicate within department and cross functionally with other divisions. High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction. Familiarity with GMP guidelines, including USP<790> and USP<1790>, and 21CFR 210/211 Proficiency in Microsoft Office; including Word, Excel, and Overlook 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 Overview:* We are looking for a responsible and professional team member to join our warehouse team. Ideal candidates will need to be self-reliant, reliable, and hard working. *Job Summary:* This position is for a department lead for Sculpt Nouveau and will be required to self-monitor and fulfill production needs. For this position, it may require sales by phone and in person, computer skills, knowledge of metal working and finishing. Shipping ground and freight. *Required Skills:* * Ability to listen and follow instructions * Desire to learn * *Ability to speak and read English* * Standing for a few hours at a time * Self-monitoring skills * Computer skills, Quickbooks * Shipping and receiving * *Education:High School DiplomaWork Hours:* Full Time - 40 hours a week 7 AM - 3:30 PM Monday through Friday No overtime or weekends. Job Type: Full-time Pay: $22.00 - $24.00 per hour Work Location: In person
Corporate Overview Argonaut Manufacturing Services Inc. is a leading contract development and manufacturing organization (CDMO) specializing in aseptic fill-finish services for pharmaceutical and biopharmaceutical products. Headquartered in Carlsbad, California, Argonaut supports clients from clinical development through commercial manufacturing, with a focus on product quality, yield optimization, and reliable delivery. Argonaut provides flexible drug product manufacturing solutions, including vial, syringe, and cartridge filling, as well as combination filling capabilities. The company also offers analytical services and short-term cGMP storage to support clients throughout the manufacturing process. With a commitment to quality standards and hands-on client support, Argonaut works closely with customers to help ensure consistent, compliant, and efficient manufacturing while meeting critical timelines and patient needs. 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 (Vacation Plan) 11 Paid Holidays Annually The pay range for this position is $175,000 - $210,000 annually. Actual compensation will be based on factors such as skills, education, experience, and other relevant qualifications. Position Overview The controller will handle high-level accounting and oversee all financial activities and reporting for the company. As head of the accounting department, the controller will manage and supervise all aspects of accounting including general ledger, payroll, tax compliance and external audits. Reports to the chief financial officer. Assists with development of internal control policies, procedures, and financial planning. This role is a primarily 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 Own the monthly, quarterly, and annual close and preparation of financial statements and management reports. Manage cost accounting, inventory accounting, revenue recognition, and financial reporting. Maintain and optimize NetSuite ERP system, including accounting processes, reporting, workflows, and controls. Support budgeting, forecasting, cash flow management, and financial analysis. Partner with Operations and leadership on manufacturing costs, pricing, customer profitability, capital expenditures, and business decisions. Maintain effective accounting policies, procedures, and internal controls. Coordinate audits, tax filings, and other financial compliance requirements. Provide timely financial reporting and analysis to the CFO, leadership team, and investors. Lead, mentor, and develop a small finance/accounting team. Identify opportunities to improve processes, systems, and financial controls as the company grows. Additional duties as needed Requirements and Qualifications Bachelor's degree in accounting, finance, business administration with an emphasis in Accounting, or a related field 5–10+ years of progressive accounting experience, including Controller, Assistant Controller, or Accounting Manager experience. Strong hands-on NetSuite experience a plus Biopharma, life sciences, CDMO, or regulated manufacturing experience preferred Excellent computer skills; experience in accounting software and Microsoft Office Suite Exceptional knowledge of finance, accounting, budgeting, cost accounting and cost control principles, and Generally Accepted Accounting Principles (GAAP) Excellent written and verbal communication skills Analytical ability to develop and implement improvements or recommendations Ability to work independently, prioritize effectively, and partner with senior leadership. 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.
Overview Join our dynamic team in Escondido, CA, as a General Production team member! We are looking for motivated individuals who thrive in a fast-paced environment and are eager to contribute to our production processes. This is a fantastic opportunity to be part of a supportive team where your efforts will directly impact our success. If you’re ready to roll up your sleeves and make a difference, we want to hear from you! Position: General Production - Temp to Hire **Shift: **SWING Shift - 2 pm to 12:30 am (4/10 schedule) **Pay Rate: **$19/hr Location: Escondido, CA Responsibilities Assist in the production process by operating machinery and equipment. Perform quality checks to ensure products meet company standards. Maintain a clean and organized work area to promote safety and efficiency. Collaborate with team members to meet production goals and deadlines. Follow all safety protocols and guidelines to ensure a safe working environment. Report any equipment malfunctions or safety concerns to supervisors. Participate in training and development opportunities to enhance skills. Qualifications High school diploma or equivalent preferred. Previous experience in a production or manufacturing environment is a plus. Ability to work effectively in a team-oriented environment. Strong attention to detail and commitment to quality. Good communication skills, both verbal and written. Ability to lift up to 50 pounds and stand for extended periods. Willingness to work flexible hours, including overtime as needed.
Overview Join our dynamic team in Escondido, CA, as a CNC Set Up Operator! We are looking for a skilled and detail-oriented individual who thrives in a fast-paced manufacturing environment. As a CNC Set Up Operator, you will play a crucial role in ensuring our machinery operates efficiently and produces high-quality parts. If you have a passion for precision and a knack for problem-solving, we want to hear from you! Responsibilities Set up and operate CNC machines according to specifications and production schedules. Read and interpret blueprints, technical drawings, and work orders. Conduct quality checks on finished products to ensure they meet required standards. Troubleshoot and resolve any issues that arise during the machining process. Maintain and clean CNC machines to ensure optimal performance. Collaborate with team members to improve production processes and efficiency. Document production data and report any discrepancies to management. Qualifications High school diploma or equivalent; technical degree or certification in CNC operations preferred. Proven experience as a CNC Set Up Operator or similar role. Strong understanding of CNC machinery and programming. Ability to read and interpret technical documents and blueprints. Excellent attention to detail and problem-solving skills. Ability to work independently and as part of a team. Strong communication skills and a positive attitude.
Job Information Number ICIMS-2026-11069 Job function Other Job type Full-time Location Werfen - San Diego - AID - 9900 Old Grove Road San Diego, California 92131-1638 United States Country United States Shift 1st About the Position Introduction Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Job Summary Join Werfen's Autoimmunity business as a Manufacturing Associate I and play a key role in producing diagnostic products that help clinicians around the world detect autoimmune disorders. As a Manufacturing Associate within our ELISA Plates team, you'll operate and maintain specialized manufacturing equipment, support the production of ELISA plates, monitor quality throughout the process, and ensure products are stored and handled according to established procedures. You'll spend your day setting up equipment, overseeing production runs, inspecting materials, documenting work, and contributing ideas that improve efficiency and quality. Working alongside a supportive and collaborative team, you'll have the opportunity to develop expertise in regulated manufacturing environments while building skills in troubleshooting, equipment validation, and continuous improvement, creating a strong foundation for long-term career growth within Werfen. Responsibilities Key Accountabilities Under supervision follows standard operating procedures, work instructions, and other procedures for routine manufacturing and/or testing. Participates in the bulking and/or evaluation of in-process components and reagents according to procedures. Packages, fills, and operates equipment to ensure in-process components are completed (if applicable). Maintains detailed Device History Records and/or any other associated documentation for all manufacturing activities. Operates and cleans equipment and instrumentation for routine manufacturing and/or testing. Assists with evaluations of raw materials (if applicable). Follows established safety and environmental procedures. Maintains lab and work area in a clean and orderly manner. Complies with applicable Werfen standard operating procedures (SOPs), ISO, FDA and other Quality System regulations, as well as applicable Environmental Health & Safety (EHS), Human Resources and other regulatory and company policies. Reflects Werfen Values in the quality of work and in working relationships. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Networking/Key relationships Other Manufacturing teams Operations teams, including Equipment Engineering, Facilities & Environmental Health & Safety (EHS) Shared Services teams, including Filling and Packaging Product Testing team Manufacturing Technical Service Global Systems Support Qualifications Minimum Knowledge & Experience for the position Education: Bachelor’s degree in biologicial or related sciences required. Certificate program or A.S. degree with 3-4 years relevant experience in a life sciences laboratory may be substitued for a degree. Experience: 0-1 years of life sciences laboratory experience required. Experience in a regulated manufacturing environment in the healthcare sector strongly preferred. Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement. Skills & Capabilities Basic understanding of basic laboratory practices and procedures. Basic understanding of Good Manufacturing Practices. Strong attention to detail and commitment to quality. Attentiveness to details to spot flaws in products or problems with equipment to prevent quality issues. Problem-solving ability to troubleshoot and resolve issues. Time management skills to meet production goals without compromising quality. Ability to work collaboratively in a team environment. Curiosity and commitment to continuous learning. Compensation The annual base hourly pay range for this role is currently $23 to $29/hr. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs. This role is eligible for medical, dental, and vision insurance, 401k plan retirement benefits with an employer match, as well as paid vacation and sick leave. Our sales roles are eligible for participation in a commission plan and our management, and select professional roles, are eligible for a performance-based bonus. Travel requirements No routine travel required If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact [email protected] for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. www.werfen.com
At Boeing, we innovate and collaborate to make the world a better place. We’re committed to fostering an environment for every teammate that’s welcoming, respectful and inclusive, with great opportunity for professional growth. Find your future with us. Boeing Global Services (BGS) is seeking a Quality Assurance Representative to support V-22 modification efforts at MCAS Futenma, Okinawa, Japan. This is a Long-Term Assignment to MCAS FutenmaOkinawa, Japan for a minimum of 3.5 years. Relocation/assignment benefits to this international location will be provided. Ability to meet Int'l assignment health requirements required. If accompanied, family must also meet Int'l assignment health requirements. The individual will work closely with the V-22 Global Technical Operations Leadership to support the planning, execution and delivery of Quality products and services. This position will be100% on-site at MCAS Futenma, Okinawa, Japan. Position Responsibilities: Develops and motivates a team of diverse skills, capability, and experience to maximize individual and team performance. Performs inspections on aircraft for modification activities on the V-22 platform Maintains Quality directives, policies, processes, procedures and metrics to assure program, contract, customer, regulatory requirements, international standards and working agreements are deployed using established procedures Collects and verifies data to support the identification of root cause routine problems Performs internal audits to determine compliance with Quality Management System standards, configuration assurance, related business, regulatory and customer requirements Documents audit results in standard formats Works under general direction Basic Qualifications (Required Skills/Experience): 5+ years of experience in aircraft maintenance/modification 3+ years of V-22 aircraft experience 3+ years of Quality Assurance Inspector experience (CDI, CDQAR, QAR, 7-level) Experience in interpreting and utilizing aircraft technical data Willing to work variable shifts (shift 1, 2, or 3) Preferred Qualifications (Desired Skills/Experience): Experience in USN/USMC aviation maintenance/modification programs DCMA INST 8210.1 experience AS9100 Revision D experience Experience using or applying metrics to measure performance against projects to ensure high quality delivery Ex-Pat Information: Candidate must be able to obtain a work visa, depending on requirements of the country Candidate must be able to meet the cultural requirements of the country, as applicable Employment is contingent on the candidate’s ability to satisfy all labor and immigration formalities of the country Because the candidate selected will be expected to go on an international assignment, the offer will be contingent upon the candidate’s ability to obtain clearances from International Health Services and the receipt of a visa/work permit to the country in which he or she will be assigned. These contingencies also apply to any/all family members who may be relocating with the candidate. Relocation: Relocation benefits will be provided only to the international assignment. Conflict of Interest: Successful candidates for this job must satisfy the Company's Conflict of Interest (COI) assessment process. Drug Free Workplace: Boeing is a Drug Free Workplace where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies. Total Rewards and Pay Transparency: At Boeing, we strive to deliver a Total Rewards package that will attract, engage and retain the top talent. Elements of the Total Rewards package include competitive base pay and variable compensation opportunities. The Boeing Company also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including health insurance, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and a number of programs that provide for both paid and unpaid time away from work. The specific programs and options available to any given employee may vary depending on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements. Pay is based upon candidate experience and qualifications, as well as market and business considerations. Summary Pay Range: $83,300-$128,800/Annually Applications for this position will be accepted until Oct. 16, 2026 Export Control Requirements: This position must meet U.S. export control compliance requirements. To meet U.S. export control compliance requirements, a “U.S. Person” as defined by 22 C.F.R. §120.62 is required. “U.S. Person” includes U.S. Citizen, U.S. National, lawful permanent resident, refugee, or asylee. Export Control Details: US based job, US Person required Relocation Relocation assistance is not a negotiable benefit for this position. Security Clearance This position requires the ability to obtain a U.S. Security Clearance for which the U.S. Government requires U.S. Citizenship. An interim U.S. Secret Clearance Pre-Start and final U.S. Secret Clearance Post-Start is required. Visa Sponsorship Employer will not sponsor applicants for employment visa status. Shift This position is for 1st shift Equal Opportunity Employer: Boeing is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law. Your Benefits No matter where you are in life, our benefits help prepare you for the present and the future. Generous company match to your 401(k). Industry-leading tuition assistance program pays your institution directly. Fertility, adoption, and surrogacy benefits. Up to $10,000 gift match when you support your favorite nonprofit organizations. These programs are subject to eligibility requirements and other conditions, which may differ for employees of certain subsidiaries or business units, or union-represented employees depending on bargaining agreement terms. If this information conflicts with the program documents, the latter shall control. This material is informational only.
Overview: Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger. We are seeking a Manufacturing Engineer II, NPI to support the introduction and industrialization of new life science manufacturing technologies within our Nitinol processing operations. This role is primarily focused on New Product Introduction (NPI) and the transition of processes from Process Development into Production, while supporting early-phase process characterization, optimization, and stabilization. The Manufacturing Engineer II, NPIserves as a technical liaison between Process Development, Quality, and Production, ensuring new products and processes are transferred efficiently, validated appropriately, and established with a strong foundation for long-term manufacturing success. This is a hands-on role, requiring active participation on the manufacturing floor to implement improvements, support validations, and train production personnel. Key Areas of Focus Introduction and establishment of Nitinol-based manufacturing technologies such as laser cutting, shape setting, electropolishing, cleaning, and dimensional inspection using CMM and OGP equipment Supporting New Product Introductions (NPI) through production readiness, validation execution, and early production ramp-up Applying statistical and data-driven methods to characterize processes, establish capability, and support robust process transfer Leading assigned NPI and process improvement activities through effective communication, cross-functional coordination, milestone tracking, and regular status reporting Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you. Responsibilities: Support the transfer of new products and processes from Process Development into Production, ensuring manufacturing readiness, quality awareness, and product integrity during NPI and early production phases. Introduce and establish manufacturing processes for Nitinol-based medical device components, including laser cutting, shape setting, electropolishing, and inspection operations. Execute and support process validation activities including IQs, OQs, PQs, and Test Method Validations (TMVs). Review, generate, and maintain process documentation including Work Instructions (WIs), routers, and supporting documentation to ensure alignment with process intent. Assist in establishing initial job cost baselines, cycle times, and ERP standards for new products and processes. Apply structured root cause analysis methodologies, including DMAIC, to investigate NPI issues, early yield losses, dimensional variation, and process instability. Utilize statistical tools and techniques such as Design of Experiments (DOE), process capability analysis (Cp, Cpk), ANOVA, regression analysis, and hypothesis testing to identify key drivers of variation and support data-based decisions. Support early production process optimization efforts including setup reduction, yield improvement, operator training, and process stability enhancements. Provide hands-on technical support during equipment setup, troubleshooting, and qualification activities. Collaborate with Quality and Production teams to support resolution of early-phase NCMRs, deviations, and process risks. Lead assigned NPI and process-related projects by defining scope, tracking actions and milestones, managing risks, and providing clear, data-driven status updates to stakeholders. Serve as a technical point of contact for internal stakeholders and, as needed, customers during NPI and continuation engineering activities. Required Qualifications: Minimum of 3 years of experience in an engineering role within a manufacturing environment, preferably supporting New Product Introduction or process transfer activities. Bachelor’s degree in Mechanical Engineering, Industrial Engineering, or a related technical discipline, or equivalent hands-on manufacturing experience. Strong technical writing skills with the ability to generate and maintain process documentation, validation protocols, and reports. Working knowledge of regulated manufacturing environments and quality system requirements. Preferred Qualifications: Experience within the medical device industry and familiarity with ISO 13485 and Quality System Regulations (QSR). Hands-on experience with Nitinol processing or other precision manufacturing technologies. Exposure to laser-based manufacturing processes or similar high-precision equipment. Experience applying statistical methods such as DOE, ANOVA, and process capability analysis in a manufacturing environment. Familiarity with Lean manufacturing principles and continuous improvement methodologies. Experience using data analysis or visualization tools (e.g., Excel, Power BI, Minitab). CAD or SolidWorks experience for basic fixture or tooling support. Compensation: The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $65,000–$102,000. For temp, temp-to-hire, and regular full-time positions, our company policy is that we are unable to provide visa or TN sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.
Description The City of San Clemente is excited to announce we are currently accepting applications for the position of: Distribution Operator I/II (Public Works, Utilities/Water) Distribution Operator I: $36.85-$44.79/hourly Distribution Operator II: $39.67-$48.20/hourly The City of San Clemente is looking for a dependable, safety-minded, and hardworking individual to join our Utilities team as a Distribution Operator I/II. This is an exciting opportunity to perform meaningful, hands-on work that directly supports public health, reliable water service, emergency readiness, and the daily operations of our community. Distribution Operators help maintain the City's water distribution system, water lines, valves, hydrants, meters, pump stations, reservoirs, and related facilities. If you enjoy working outdoors, operating equipment, solving problems, learning technical skills, and being part of a team that provides an essential public service, this may be a great opportunity for you. This position works a four (4) day workweek, 10 hours each day. Enjoy a 3-day weekend, every weekend! What You'll Do: As a Distribution Operator, you will help support the operation, maintenance, construction, and repair of the City's water distribution system. Duties may include: Maintaining and repairing water lines, valves, hydrants, meters, pump stations, reservoirs, and related facilities Reading, inspecting, repairing, and replacing water meters Performing leak detection surveys and utility mark-outs Supporting fire hydrant inspection, repair, and flushing activities Operating construction and maintenance equipment, vehicles, hand tools, and power tools Creating and updating work orders in the City's maintenance management system Assisting with capital improvement projects and field maintenance activities Responding to public inquiries and providing helpful, professional service Following safety procedures and supporting safe working conditions in the field At the Distribution Operator II level, employees may perform more advanced assignments, work more independently, operate specialized equipment, assist with training lower-level staff, explain work methods and procedures, and help support operational decisions to water system performance, water quality, flows, pressures, and system reliability. Essential Functions Essential and other important functions may include, but are not limited to, the following: Assist with the maintenance and repair of the City's the water distribution system and water filtration plant including water lines, valves, and hydrants; ensure safe working conditions of system; make recommendations for improvements. Read water consumption meters; turn on and off meters as needed; inspect meters to ensure accurate readings; repair and replace faulty meters. Assist with the maintenance and operation of pump stations; record data; generate work orders for maintenance and repairs. Operate various construction and maintenance equipment, including high velocity cleaning equipment, skid steer, front end loader and backhoe tractor equipment, dump trucks; use and maintain hand and power tools and assigned equipment; perform preventive maintenance on equipment. Maintain fire hydrant inspection program; inspect fire hydrants; ensure water quality and proper fire hydrant operation; make repairs as necessary. Utilize proper safety precautions related to all work performed. Assist in the construction of capital improvements projects. Perform leak detection surveys using various sound sensitive leak detection equipment. Perform Utility mark-outs related to water in accordance with Common Ground Alliance best practices and California law. Generate preventive and corrective work orders using the City’s CMMS-Lucity to document and track the work performed. Perform related duties and responsibilities as required. Participation in the City's on-call rotation is required, including responding to after-hours water system emergencies, nights, weekends, and holidays. Typical Qualifications The ideal candidate is someone who: Takes pride in providing reliable public service Enjoys hands-on field work and working outdoors Is dependable, safety-focused, and willing to learn Has experience with water systems, construction, maintenance, utilities, or related field work Can operate tools, vehicles, and equipment safety and effectively Communicates well with coworkers, supervisors, and members of the public Can stay organized, follow procedures, and document work accurately Is interested in building a career in water utilities and obtaining required certifications MINIMUM QUALIFICATIONS Distribution Operator I Experience: One (1) year of responsible experience performing field maintenance work, construction, plumbing or related work is desirable. License/Certification Requirements: Possession of, or ability to obtain within 12 months of employment, a valid Grade I Water Distribution Operator Certificate issue by the California State Water Resources Control Board. Possession of, or ability to obtain, a valid Class B Driver License within 18 months from date of appointment. Distribution Operator II Experience: Two (2) years of responsible experience performing field maintenance work, construction, or related work on water distribution facilities or similar systems is desirable License/Certification Requirements: Possession of a valid Grade II Water Distribution Operator Certificate issued by the California State Water Resources Control Board. Possession of a valid Grade I Water Treatment Certificate issued by the California State Water Resources Control Board. Possession of, or ability to obtain, a valid Class B Driver License within 18 months from date of appointment. (Both Distribution Operator I and II) Education/Training: High School Diploma, or equivalent, supplemented by specialized training in maintenance, construction, water distribution, utilities, or a related field. For more information, you can review the full Classification Specification: here. Supplemental Information All applicants must submit a completed City of San Clemente application form and supplemental questionnaire in order to be considered. Applications will not be accepted by fax or email. Applications must be submitted via the City's web site at https://www.governmentjobs.com/careers/sanclemente. Prior to employment, the prospective candidate must successfully complete a background review, medical examination, including drug screen, and be fingerprinted, all at City expense. If selected, acceptable identification showing entitlement to legally work in the United States will be required. SELECTION PROCESS Applications and Supplemental Questions will be reviewed and evaluated for relevant education and experience. Candidates considered to have the best qualifications will be invited to participate in the selection process. The selection process will consist of an Oral Interview weighted at 100%. An eligibility list will be established and may be used to fill future vacancies. WORKING CONDITIONS Work Environment: Work involves working within an indoor office, laboratory environment, water treatment plants, and water operations facilities. Work involves exposure to water, mud, sewage, noise, dust, grease, smoke, fumes, gases, traffic, chemicals, machinery, dirt, vibration head, cold and dampness; exposure to biological hazardous environments. Work may take place in inclement weather conditions; at elevated heights on scaffolding and/or ladders; within confined spaces, underground, on slippery or uneven surfaces; and/or around heavy construction equipment. Physical Requirements: Essential functions require: Strenuous and manual tasks for prolonged periods of time Operating motorized vehicles and heavy equipment Frequent lifting, carrying, pushing, and/or pulling of heavy items Standing, walking, or sitting for prolonged periods of time Stooping, kneeling, crouching and/or crawling Manual dexterity to operate a computer keyboard and other office equipment, handle files and documents. Hearing and speaking to exchange information in person or on the telephone Visual acuity to see/read documents and computer screen and to read instrumentation dials, measures devices, or other related components For more information regarding this recruitment, please contact Cara Morin at (949) 361-8203 or [email protected]. As an equal opportunity employer, the City strongly encourages people with disabilities and people from historically marginalized communities to apply. The City of San Clemente provides excellent benefits which include: FLEXIBLE WORK SCHEDULE – Most positions work a 9/80 work schedule. HOLIDAYS – The City presently recognizes 12 regular holidays, plus two floating holidays. VACATION – Employees accumulate vacation at the rate of 104 hours per year increasing to a maximum of 176 hours based on years of service. SICK LEAVE - Accrual of 8 hours per month. INSURANCE – The City provides a comprehensive benefit package including employee medical, dental, vision. LIFE INSURANCE – Value equal to two times annual earnings up to a maximum of $100,000. DEFERRED COMPENSATION – Employees may elect to enroll in a voluntary plan and defer up to the IRS permitted annual maximum. Employees may defer up to a maximum of $24,500 annually in 2026. Individuals aged 50 and older can contribute up to $8,000 in catch-up contributions to these plans. FLEXIBLE SPENDING ACCOUNT – Employees may participate in either or both of the Health Care or Dependent Care programs. EMPLOYEE ASSISTANCE PROGRAM – The City offers full-time employees and their dependents an EAP program which provides a variety of professional services. ON-SITE FITNESS CENTER - The City provides a no fee on-site fitness center with state of the art equipment located in City Hall. RETIREMENT – The City of San Clemente is a member of the California Public Employees' Retirement System (CalPERS), and is subject to the Public Employees' Pension Reform Act (PEPRA). The retirement formula for new employees is based on the category below that the new employee falls under. Employee contribution rates will be determined by the employee's classification and requirements under PEPRA. NOTE: The City is also a member of the Social Security system. As such, Full Time employees make contributions to Social Security in addition to their CalPERS contributions. Classic Member: Retirement Formula: 2% @ 55 Definition: CalPERS refers to all members that do not fit within the PEPRA definition of a "new member" as "classic members" who are subject to the Public Employees' Retirement Law (PERL). PEPRA allows a member after January 1, 2013, to retain his/her classic member retirement benefit status if the member continues his/her membership in all previous California Public Retirement System(s) by leaving his/her service credit and contributions (if any) on deposit, and the member enters into employment that results in CalPERS membership within six months of separating from the most recent California Public Retirement System. Classic member status also requires the membership date to be on or before December 31, 2012, in a California Public Retirement System in which reciprocity is established. New Member: Retirement Formula: 2% @ 62 Definition: A new member is defined in PEPRA as any of the following: A new hire who is brought into CalPERS membership for the first time on or after January 1, 2013, who has no prior membership in any California Public Retirement System. A new hire who is brought into CalPERS membership for the first time on or after January 1, 2013, who has a break in service of greater than six months with another California Public Retirement System that is subject to Reciprocity. A member who first established CalPERS membership prior to January 1, 2013, who is rehired by a different CalPERS employer after a break in service of greater than six months.
MAST Biosurgery is a growing medical device company dedicated to developing and delivering innovative solutions that enhance patient outcomes. Specializing in advanced biomaterials and surgical products, MAST supports healthcare professionals with high-quality devices used in a range of surgical applications. With a strong commitment to quality, performance, and patient care, we’re on a mission to become the most trusted provider of medical device molding and assembly services. Ready to ditch the cubicle and make a real impact? Join MAST Biosurgery as a Quality Engineer and help support the quality and reliability of our medical devices. You’ll work closely with quality, manufacturing, and engineering teams to investigate issues, improve processes, and maintain our Quality Management System. *What You’ll Do* * Support investigations into product complaints, nonconforming materials, and other quality issues. * Help identify root causes and implement corrective and preventive actions (CAPA). * Support supplier quality, equipment calibration, and environmental monitoring activities. * Review quality documentation and track data to identify trends and improvement opportunities. * Assist with audits and regulatory inspections. * Work with other departments to maintain quality standards and accurate records. * Perform other duties as assigned. *What You’ll Bring* * Bachelor’s degree in Engineering, Life Sciences, or a related technical field. * Two or more years of quality engineering or quality assurance experience in medical devices, pharmaceuticals, or a similarly regulated industry. * Familiarity with FDA quality requirements and ISO 13485. * Experience supporting quality investigations, root cause analysis, or CAPA activities. * Strong attention to detail, problem-solving, and communication skills. * Ability to manage priorities and work collaboratively. * Proficiency with Microsoft Office; experience with electronic quality management systems is a plus. *Preferred Experience* Experience with sterile or implantable medical devices, equipment calibration, environmental monitoring, or audit support. *What We Offer:* * We offer competitive medical, dental, and vision insurance. * Company sponsored life and disability Insurance * Paid holidays * Flexible Time Off * Pleasant non-corporate environment *Work Environment & Physical Demands* *Office* While performing the duties of this job, the employee regularly works in an office setting. Occasional exposure to a warehouse environment. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. This is not necessarily an all-inclusive list of job-related responsibilities, duties, skills, efforts, requirements or working conditions. While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed as assigned. While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. Must be able to sit or stand at computer for a reasonable length of time typing and reading. Regularly required to walk or stand. Job Type: Full-time Pay: $90,000.00 - $110,000.00 per year Benefits: * 401(k) * Dental insurance * Flexible schedule * Health insurance * Life insurance * Paid time off * Vision insurance Application Question(s): * What is your salary requirement? * Do you have at least two years of quality engineering or quality assurance experience in the medical device, pharmaceutical, or another regulated industry? Experience: * Quality assurance: 2 years (Required) Work Location: In person