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What you'll do: Champion a positive safety culture; enforce OSHA standards Conduct daily safety checks and toolbox talk Direct and coordinate plant activities to meet production goals for crushed concrete and related material Monitor equipment performance and schedule maintenance as needed Ensure compliance with environmental and quality standards Maintain accurate time and production records Plan and schedule material processing to meet customer demand Inspect finished products for quality and consistency Complete required reports (production, safety, inventory) Communicate effectively with management and other departments Perform other duties as assigned or required What you'll need: High school diploma or equivalent; technical or vocational training preferred Minimum 3–5 years of experience in aggregate or concrete plant operations, with at least 2 years in a supervisory role Knowledge of crushing equipment, loaders, haul trucks, and pugmill operations Ability to read and interpret blueprints and production schedules Strong leadership, communication, and problem-solving skills Must pass drug screening, physical exam, and background check Ability to work outdoors in all weather conditions and lift up to 50 lbs Compensation: The Pay Range for this position is $36.45/hour to $40.00/hour with the midpoint at $38.22. Starting pay rate will be determined by the successful applicant's relevant experience and skill base. This position is non-exempt and eligible for overtime pay. Benefits Arcosa is proud to offer competitive benefits and programs to help you and your family meet your healthcare and retirement planning needs. The various benefits offered to employees based on eligibility may include: Medical, Dental, and Vision Insurance Paid vacation and sick time 401k with Employer Match 11 paid Company holidays Life Insurance Short-Term and Long-Term Disability Insurance Tuition reimbursement Health & Wellness Programs Flexible Spending Accounts Employee Discount Programs Professional Training and Development Programs Career Advancement Opportunities – We like to promote from within! California Applicants Please access our CPRA Notice for information concerning Arcosa’s California privacy policy, including how we collect and use the personal data of our candidates.
Are you a detail-oriented professional with a knack for precision and a passion for manufacturing? 74 Weld is looking for a 2nd shift CNC Operator to join our team. If you’re ready to take your skills to the next level and be part of a dedicated team, we want to hear from you! *Key Responsibilities:* * *Inspect Parts*: Use basic measuring tools to inspect parts and ensure they meet quality standards. * *Blueprint Interpretation*: Read and interpret blueprints and technical drawings. * Independently run CNC machines to produce high-quality components. * *Maintain Equipment:* Keep CNC machines and tools in clean, working order and report any issues. *Qualifications:* * *Experience:* Proven experience with CNC machines, including setup. * *Skills:* Proficiency with precision measuring instruments (e.g., calipers). * *Attention to Detail:* Strong focus on quality and precision. * *Communication:* Ability to communicate clearly and professionally. * *Work Ethic:* Reliable, detail-oriented, and committed to high standards. *Additional Information:* * 1+ years of experience * High school diploma or equivalent required; additional schooling in CNC operations is a plus. * Must maintain a safe and organized work environment. * Shift Schedule: 2:00pm-10:30pm *Why Join Us?* At 74 Weld, we value skill and dedication. If you’re ready to bring your expertise to a place where your contributions make a real impact, apply now! Job Type: Full-time Pay: $23.00 - $28.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Paid time off Experience: * Set up: 3 years (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Ability to Commute: * San Marcos, CA 92078 (Required) Work Location: In person
Manufacturing Sciences and Technology (MS&T) Engineer I Position Summary: Work Schedule: Monday-Friday, 8:00am-4:30pm 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Our purpose-built San Diego location provides comprehensive clinical supply services including clinical supply management, primary and secondary packaging, complex labeling services, clinical storage, distribution, and clinical returns and destruction, and will also include stability chambers. Located less than a mile from Catalent’s West Coast early-phase oral drug product development center of excellence, customers choosing this convenient Catalent location can now enjoy a fully integrated development, clinical supply manufacturing and distribution solution. The Manufacturing Sciences and Technology (MS&T) team provides technical process support for San Diego Ware operations, leading package and process development and acting as the technology transfer owner for assigned projects. This role supports internal and external technology transfers, packaging component design, and technical documentation in compliance with cGMP and change control requirements. The position partners cross‑functionally with project management, manufacturing, quality, supply chain, labeling, and facilities teams to implement and sustain processes, while promoting continuous improvement, professionalism, strong communication, and customer service excellence as a Catalent Operations advocate. The Role: Under leadership of MS&T, coordinate projects ensuring correct technical requirements documentation generated, monitored and assist to ensure successful adherence and completion. Attend and produce minutes and actions for internal client meetings to support MS&T team and understand full scope requirements to generate required project requirements documentation. Support authoring technical reports, source documents, SupplyFlex records, legacy records, master batch records, product and equipment specifications, protocols and any other technical documents not listed in support of tech transfer and cGMP activities. Assist with departmental training and completion of training documentation. Assist in the preparation and regular review of Standing Operating Procedures relating to your own areas of responsibility. Support Complaint & Deviation investigations and root cause analysis. Stay appraised of development within the healthcare packaging industry. Any other duties which may properly be assigned to this post. May be requested to perform any role/level within the CSE team if trained to do so. All other duties as assigned. The Candidate: Bachelor’s degree in Engineering, or Science required; Packaging Engineering or Packaging Sciences preferred. Minimum of 1 years of experience with GMP equipment, manufacturing, healthcare, and/or pharmaceutical preferred Minimum of 1 years of experience in a customer service or appropriate business-related area Project management experience and skills preferred Demonstrated knowledge of manufacturing equipment and GMP processes, with the ability to manage multiple tasks effectively while maintaining a strong customer service focus. Strong communication, teamwork, and professionalism, including excellent written, verbal, and interpersonal skills, a positive attitude, and the ability to meet commitments with a right‑first‑time approach. Proficient in Microsoft Office (Word, PowerPoint, Excel, Visio); ArtiosCAD experience preferred.Physical Requirements: able to perform duties which include standing, walking, sitting, kneeling, push/pulling frequently and significant amount of use of office equipment; Must be able to lift up to 35lbs and work in temperature-controlled freezers/fridges occasionally. The anticipated salary range for this role in California is $90,000 - $100,000. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why you should join Catalent: Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, on-site yoga classes, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment. Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean-up activities for community engagement. Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. Several Employee Resource Groups focusing on Diversity and Inclusion. Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment. 152 hours of PTO + 10 paid holidays. Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic. Tuition Reimbursement – Let us help you finish your degree or earn a new one! WellHub program to promote overall physical wellness. Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.
Hydranautics is a part of the Nitto Group of companies and a global leader in the field of integrated membrane solutions which includes reverse osmosis, nanofiltration, ultrafiltration and microfiltration for water, wastewater and process treatment and applications. Currently used on seven continents throughout the world for diverse applications such as seawater desalination, industrial high-purity water, surface water treatment, wastewater treatment and specialty process applications. Here at Hydranautics, we believe that diversity is key to our competitive advantage. All qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, ancestry, sex, sexual orientation, age, disability, marital status, domestic partner status or medical condition. We are proud to be a Drug-free, E-Verify and EEO employer. We are proud to offer a generous compensation and robust benefits package to include medical, dental, vision, life insurance plans, F.S.A. and H.S.A plans, Retirement plans (401k and ROTH), (12) Paid company holidays, generous PTO, tuition reimbursement and career development, Employee Assistance Plan, and more. This is an onsite position in our Oceanside, CA facility. We presently have the following Production Operator II and III positions available for 2nd and 3rd shifts. *JOB SUMMARY* Under direct supervision, performs machine operator tasks as setting-up or shutting-down machines, prepares material for production loading and unloading on to machine or production equipment; maintains required level of output; monitors output by completing detailed quality inspections to ensure product meets customer requirements. Keeps accurate records and logs associated with production, measuring, quality, quantity and any other necessary record-keeping activities. *ESSENTIAL DUTIES and/or RESPONSIBILITIES:* *Finishing Operator:* 1. Confirms product does not exceed outer diameter dimensional requirements. 2. Verifies trim measurements using calibrated tools such as ring gauges, trim gauges, etc 3. Places seal carriers at both ends of the element using calibrated tools such as ring gauges, core tube extension gauges, etc. 4. Performs product inspections using air lines, leaf adhesives and visual spot-checking for bubbles on product; makes necessary repairs. *Rolling Operator: * 1. Operates element rolling table to assemble components into a spiral configuration, changing membrane leaf adhesive drums as required. 2. Ensures all glue lines, side and end seals are applied during manufacturing process. 3. Some positions may verify glue ratio, including proper placing, accuracy, consistency, and diameter of glue lines in accordance to Manufacturing Standard Operating Procedures. *Caging Operator:* 1. Operates machine to seal the cage outerwrap to process separation products, conducting a visual inspection of elements for damage. 2. Seals cage outerwrap to feed spacer on the end seal glue lines. 3. Trims leaves manually using scissors eliminating flaps and exposing proper placement of serial number. *APPLIES TO ALL:* 1. Loads/unloads product from manufacturing transport equipment on to appropriate machine or production equipment for tasks. 2. Maintains daily, weekly and monthly productivity goals set by production management, including clean-up, rework, core tube preparation or other production activities. 3. Documents product data information such as serial number, defects, rejects, scarp etc. on production logs, reports or summaries as well as any other record keeping activities as it pertains to products throughout shift. 4. Follows all quality, safety and lean manufacturing policies, processes or procedures including sustaining work station and area in cleanliness in accordance to 5S standards. 5. Informs Production Supervisor and/or Production Lead of increased pattern of defects in products. 6. Other duties as assigned. *MINIMUM EDUCATION and/or EXPERIENCE:* 1. Minimum 0-6 months manufacturing experience; high school diploma or GED; or an equivalent combination of education and experience. *KNOWLEDGE, SKILLS and/or ABILITIES:* 1. Set-up, operate and make minor adjustments to machines. 2. Basic to intermediate language skills, including verbal and written proficiency in English; ability to read work instructions in English. 3. Work independently and foster a cooperative spirit within a large and/or small team while maintaining flexibility to changing priorities. 4. Ability to work in a detailed-oriented atmosphere with accurate record-keeping, outstanding follow-through to meet production requirements and in a fast-pace manufacturing environment. 5. Recognize numbers and millimeters and perform basic mathematical calculations with the aid of a basic hand-held calculator. 6. Deal with standard and basic non-complex issues; basic problem-solving ability; carry out simple verbal work instructions. *PHYSICAL DEMANDS and/or WORK ENVIRONMENT:* (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) 1. Will be required to stand for the duration of the shift. As with most production positions, long periods of standing (app. 6 to 8 hours) and walking are necessary to run the assigned equipment. 2. Some lifting and material maneuvering is required to set up and during material change over. Average lifting weights may reach 20 to 50 lbs. Typical lifting techniques in the prep area are 2-person. The average times lifting is required is app. 2 to 3 times per shift (5 to 10 minute increments). 3. Repetitive light grasping is required to transfer prepped material (element packs) onto prepped membrane carts. 4. Typical pushing requirement is equivalent to approximately 20 lbs. Carts will need to be transferred to the Rolling area app. 6 times per shift. 5. Waist high lifting for membrane and overhead for brine spacer material is required. 6. Hand light grasping is required for handling membrane and brine spacer material. 7. Follows all quality and safety policies. 8. Maintains work station and area cleanliness according to 5S standards. 9. Participation in daily exercise activities is expected. 10. Safety shoes and safety glasses must be worn. 11. Other Personal Protective equipment such as hearing protection may also be required depending on the position being performed. 12. Must be able to work extended hours per the demands of the business specifically for month-end closing. *PLEASE NOTE:* Employment is contingent on successfully clearing pre-employment references, criminal background check, drug screen and physical. *NO AGENCIES, PLEASE* Pay: $20.67 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Health savings account * Life insurance * On-the-job training * Paid time off * Professional development assistance * Referral program * Retirement plan * Tuition reimbursement * Vision insurance Work Location: In person
About Axillon Aerospace: Axillon Aerospace is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. We are comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. Learn more at axillonaerospace.com. Job Summary: The Quality Engineer 2 provides a wide range of engineering expertise to ensure that Axillon products meet established quality standards and perform as designed. The Quality Engineer 2’s primary focus is on ensuring high product reliability and functionality in line with design specifications and customer requirements. Job Core Responsibilities: Promotes compliance with internal and external requirements on the assigned program(s) by means of addressing quality issues Works with customers to request approval of products deviating from approved processes and requirements Leads APQP/PPAP package generation, including orchestrating the development and update of the package items Reviews and approves changes to planning, work instructions, procedures and product acceptance Reviews and creates inspection forms, records, techniques and procedures for accuracy and relevance and provide changes when necessary Defines and conducts both systematic/methodical and random/arbitrary tests to ensure proper performance of products Leads MRB team to assess defect severity and occurrence, providing input on internal product disposition Leads analyses of data using Statistical Process Capability (SPC) to either confirm compliance with established standards or identify deviations from standards to support yield improvements Analyzes causes for defects and provides opportunities for improvement activities while monitoring process capabilities Leads and performs root cause analysis initiatives for process related concerns Provides technical and regulatory expertise for a range of quality assurance testing and inspection activities associated with product development and manufacturing Performs internal audits of the operation process using inspection results and statistical techniques to provide timely, accurate process and product analysis Analyzes audit results and determines proper corrective and preventive action Performs review and release of products, engaging customer representatives as required, and completing the shipping paperwork Performs First Article Inspections for initial qualifications or changes to fit, form, or function to the products using AS9102 Consistently exercises independent judgment and discretion in matters of significance Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary Job Requirements: Education : Post-secondary degree in Engineering or equivalent combination of relevant education and work experience that will allow successful performance of job expectations. Experience: 3 - 5 years of relevant quality engineering experience Skills Knowledge of complex Quality Engineering processes and regulatory requirements Demonstrated ability to apply a systematic and analytical approach to problem solving Advanced knowledge and ability to apply core concepts of engineering and statistical process control Ability to interpret internal/external business challenges and make recommendations for improvements to products, processes or services Ability to explain a range of complex technical information and options to overcome challenges Demonstrated analytical skills to proactively identify and solve problems: 6 sigma certification and applied experience a plus Effective interpersonal, verbal and written communication skills to drive tasks to completion Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $100k-$110k/yr. Axillon is an Equal Opportunity Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position is subject to meeting export compliance eligibility requirements. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee.
AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. Job Summary The Manufacturing Engineer 2 oversees the activities associated with the planning, development, implementation and maintenance of manufacturing methods, processes and operations for new and existing products. This includes ensuring the effective use of materials, equipment, and personnel in producing quality products at minimum costs. The ME2 will develop, implement and maintain methods, operation sequences and processes in the manufacture and fabrication of parts which will include the estimation of manufacturing costs, time standards and the ability to recommend tooling and process requirements for new and existing products. They will act as a liaison with internal and external customer in releasing new products, participate in the selection, development and evaluation of personnel to ensure the efficient operation of the function. Additionally, the Manufacturing Engineer 2 will provide high level technical expertise to a project or program planning, task layouts, technical calculations, design and analysis functions, technical report writing, presentations and other engineering functions as required. Job Core Responsibilities Provides significant expertise in developing a range of engineering solutions to improve the manufacture of new and existing Axillon products Improves current production processes to manufacture products, using applicable methods and procedures Transfers new products into production from a “design for manufacturability” approach Participates in developing and maintaining documentation for processes and designs Understands key business drivers; uses this understanding to accomplish own work Solves problems in straightforward situations; analyzes possible solutions using technical experience, judgment and precedents Other responsibilities as assigned Consistent exercise of independent judgment and discretion in matters of significance Regular, consistent and punctual attendance is required. May need to work variable schedules and additional hours as necessary Job Specifications Education: B.S. degree in Mechanical, Aerospace or Industrial engineering. Experience : 5+ years of manufacturing engineering experience in a manufacturing environment required. 2+ years of experience with composite materials and processing techniques such as autoclave, RTM, and compression molding preferred. Skills : Experience with AS9100 quality management system Excellent working knowledge of GD&T Self-starter with excellent time management skills and ability to establish objectives and specify the strategies and actions to achieve these objectives Experience with marketing support (meetings, presentations, customer interface) and proposals (excellent technical writing skills, cost estimating) experience is required Comfortable working in teams, yet also able to function independently Be able to make technical, data-driven decisions and execute with limited management support Use logic to analyze or identify underlying principles, reasons or facts from data to draw conclusions Understand, follow and adhere to corporate Quality Management System on a daily basis Experienced with machine shop floor practices Mechanically able to assemble and disassemble parts and assemblies Experienced with composite material testing Experienced with contact and noncontact inspection methods Experienced with data acquisition systems to record temperature, position and pressure Organized, 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 Familiarity with processing techniques such as wet lay-up, mold and fixture design, inspection methods, and infusion preferred Experience with NADCAP quality management system preferred Computer software skills: SolidWorks, NX Experience with Minitab, Made to Manage (or other ERP systems), and nesting software preferred Ability to work 9/80 work schedule with flexibility to support additional demand when necessary Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $95K-$110K Axillon is an Equal Opportunity Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position is subject to meeting export compliance eligibility requirements. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee.
Summary We are seeking a hands-on Quality Engineer (Level II) to play a critical role in product quality and compliance across both instruments and consumables. This role requires a self-starter who can operate independently, think critically, and uphold high-quality standards. You will be deeply involved in product release, quality systems, and continuous improvement initiatives while partnering closely with engineering, manufacturing, and supply chain. Primary Duties and Responsibilities Review and verify product release documentation, including Device History Records (DHRs), manufacturing batch records, Certificates of Analysis (COAs), and other quality system records, to ensure accuracy, completeness, and compliance with specifications and procedures (20%). Manage CAPA and non conformance program effectively by partnering with internal technical teams to investigate, identify root causes and implement effective corrective actions (20%). Manage equipment calibration and preventive maintenance program, ensuring all equipment remains compliant, and support validation activities (IQ, OQ, PQ, PV) (20%). Support design control and risk management activities using standard Quality Improvement tools, prepare fishbone diagrams, perform root-cause analysis and provide recommendations to management (20%). Support critical supplier quality oversight and performance monitoring. Collaborate with contract manufacturers to ensure product quality and adherence to specifications and build records (10%) Other duties as assigned (10%). Required Skills and Abilities Self-motivated individual who can work in a multidisciplinary team Strong troubleshooting, communication, teamwork skills Excellent at multitasking and prioritization of tasks Strong interpersonal skills to lead and collaborate with other cross functional partners Strong technical writing ability Knowledge of ISO 9001,ISO 13485,QSR (21 CFR Part 820), GLP, GCP, and GMP Preferred Skills and Abilities Experience with complex life science systems and assays, including automated sample prep systems Experience workingwith engineers, chemists,techniciansand analysts to ensure smooth laboratory and plant operations Product release,CAPA, Deviation and Non-conformance reporting, internal auditing, complaints, and supplier management experience Able to lead investigations and root cause analyses Proficiencyin MS Office software applications and statistical analysis Education, Certifications, Licenses Bachelor’s degree in Science, Engineering, or other relevant field required. At least3years of experiencerequiredworking in a GMP regulated environment with a good understanding of ISO 9001,ISO 13485, IVD/IVDR/MDR regulations, and 21 CFR Part 820 requirements Certifications required/ preferred: Lead Auditor and Lead Six Sigma certification preferred Leadership Responsibility (Direct/ Indirect): N/A Additional Requirements Work Location: Onsite–San Diego Travel Requirements: Up to 10%of travel time expected Physical Requirements and Work Environment: Sit and stand for prolonged periods Repeating motions that may include the hands,wristsand/or fingers Use of hands to finger, handle, or feel, and reach with hands and arms Stand and/or move about the office or in various environments (including tight and confined spaces), or from one worksite to another Specific visual abilities, including close vision and ability to adjust focus, read, review, and assess the accuracy and thoroughness of the work assigned Verbal abilities require communicating with others to exchange information Occasionally adjusting or moving objects up to 20 pounds in all directions Work environment involving low/high temperatures; hazardous conditions, low ventilation, noisy environments, small/enclosed spaces In-person interaction with others indoors and outdoors Use standard computer, telephone and related equipment for communication, and record keeping Able to travel, including international travel, without personal assistance The above physical requirements and work environment characteristics generally reflect those of this position but is not an exhaustive list. Reasonable accommodations may be made to enable individuals with qualified disabilities to perform the essential functions of the position, provided that such accommodation does not impose an undue hardship on the Company. Disclaimer Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. This description generally reflects management’s assignment of essential functions but is not intended to be a comprehensive list of the duties and responsibilities of the position, and it does not limit or restrict the duties and responsibilities that may be assigned from time to time. The duties, responsibilities and job description of this role are subject to change at any time without notice.
Company Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description NO Experience Needed AM Shift: Monday - Friday 7:00AM - 3:30PM Pay: $17.00 - $18.00 an hour depending on experience Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a KanBan Operator you will: Processing parts through the Kanban production area including cutting of material to specific lengths using horizontal band saws and chop saws as well as facing and deburring of tubes. What will my responsibilities include? Cutting material to length with horizontal/chop saws based off start dates on the daily cut list. Responsible for setting the length using the saw length guide and cut the amount of tubes needed for the job as specified on the job traveler. Facing of tube ends using 2CP/3CP end finish machines. This includes picking up the tube, placing it in the dies located inside the jaws of the machine, closing the jaws around the tube and cycling the facing arbor to square the end of the tube Deburring of tube ends using deburr machine that uses an arbor with sharp edges. This includes picking up the tube and positioning the tube inside diameter (ID) on the ID deburr tool and then on outside diameter (OD) deburr tool within the machine Trimming straight tubes to customer required length using calipers to measure for accuracy Logging of jobs that are completed in the KPI/ERP systems Bundle and load jobs to Bend staging racks sorted by job number, material type, quantity and center line radius Performing equipment preventative maintenance. This includes, but is not limited to, checking of the belts on 2CP/3CP end finish machine for wear, adding lubrication to machines, inspecting and replacing saw blades, if needed Maintaining 5’s + Safety of department Meeting goals established in department for productivity Using required PPE required for the department Other reasonable duties as business and operational needs dictate Qualifications What key skills and experience do I need? Requires the ability communicate verbally and in writing in a clear, easily understood manner Requires English verbal and written skills Ability to wear special PPE required to do the job (respirators and safety glasses) Education: High School diploma or equivalent NO Experience Needed Basic math skills to perform basic calculations such as addition and subtraction General understanding of manufacturing processes and use of hand tools Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor
*Overview* Join our dynamic manufacturing team as an Assembly Production Operator, where your hands-on skills and mechanical expertise will drive the creation of high-quality products. This role offers an energetic environment focused on precision, teamwork, and continuous improvement. As an integral part of our production line, you will be responsible for assembling components, operating tools and machinery, and ensuring every product meets strict quality standards. If you thrive in a fast-paced setting and take pride in your craftsmanship, this is the perfect opportunity to grow your career in manufacturing. *Responsibilities* * Assemble mechanical components using equipment, hand tools, and power tools * Utilize visual inspection equipment and precision measuring instruments such as calipers, micrometers, and other tools to verify dimensions and quality standards * Conduct quality checks throughout the assembly process to identify defects or discrepancies * Maintain a clean and organized work area in compliance with safety regulations * Assist with warehouse tasks including material handling using forklifts or other equipment as needed Pay: $17.50 - $21.00 per hour Work Location: In person
Carpentry & Framing Apprentice - Looking for North County San Diego Applicants Compensation: $25 per hour Employment type: Full-time Compensation will be based on experience and skill level. Medical Benefits *waiting time applicable Retirement savings option available upon hire We are a residential remodeling and new construction contractor seeking to hire a motivated Carpentry & Framing Apprentice who takes pride in the work that they do. An ideal candidate for this position is someone who has some baseline training in the construction field and who desires to work their way up the construction career path and advance in their skills and knowledge. As a construction professional, you’ll play a vital role in building the structures and environments people depend on. It’s gratifying work, and every day is a little bit different! Requirements: Must have at least 1 year of work experience in construction carpentry & framing. Must have reliable transportation and have your own hand tools. Must have a good work ethic Be on time & reliable Follow directions Work well with others Experience in foundation, framing, windows, and door installation Job duties include: Assist the foreman and other workers in accomplishing the tasks outlined for the day. Tasks can include but are not limited to demolition or construction of residential materials, heavy lifting, excavation, and use of assorted hand tools and/or power tools. Framing, foundation, windows, and doors installation labor Specific duties responsible for, but not limited to: All main cleaning duties (including assorted chores in the field and shop areas) Morning Prep: Loading tools, materials, and site protection materials. Site Clean-up. Tools put away and accounted for. Over time, you can advance by: Learn the Musick Construction Inc daily processes and workflow. * Learn the tools necessary for each type of construction project as well as the time necessary to complete it. Owning your own tools. Learn job site safety procedures Staying on time Staying organized Low error margin: fixes, tool loss, repeat work Please include your construction experience in your resumé. *All work processes and procedures are according to the standards of Musick Construction Inc. About Musick Construction Inc: Musick Construction Inc. is a family-owned and operated remodeling company in Oceanside. Quality craftsmanship and happy clients are our top priorities. www.constructionbymusick.com E04JI800sr9640963ec
Minimum qualifications: Bachelor’s degree in Electronic Material Science, Polymer Engineering, Electrical engineering, Computer Aided Design, Semiconductor Physics, Manufacturing Statistical Process Control or a related field and 10 years of progressive post-baccalaureate experience in the job offered or in a Silicon Product Engineering-related occupation. Alternatively, will accept a Master’s degree in Electronic Material Science, Polymer Engineering, Electrical engineering, Computer Aided Design, Semiconductor Physics, Manufacturing Statistical Process Control or a related field, and 8 years of experience in the job offered or in a Silicon Product Engineering-related occupation. Position requires 8 years of experience in the following: Advanced Packaging Process Development & HVM Qualification such as for Mobile SOC or SiP (System in Package) IC Packaging Failure Mode and Effects Analysis (FMEA), Design of Experiment techniques (DOE) and Statistical Process Control (SPC) Chip-Package Interaction(CPI) evaluation, Electromigration (EM) Analysis, Package component & board level reliability testing Failure Analysis and Root Cause Corrective Action for IC Packaging Technical engagement and program execution with all packaging ecosystem partners including OSATs, substrate manufacturers, and material/machine suppliers. About the job Google's mission is to organize the world's information and make it universally accessible and useful. Our Devices & Services team combines the best of Google AI, Software, and Hardware to create radically helpful experiences for users. We research, design, and develop new technologies and hardware to make our user's interaction with computing faster, seamless, and more powerful. Whether finding new ways to capture and sense the world around us, advancing form factors, or improving interaction methods, the Devices & Services team is making people's lives better through technology. The US base salary range for this full-time position is $176,150 - $237,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. Learn more about benefits at Google. The Platforms and Devices team encompasses Google's various computing software platforms across environments (desktop, mobile, applications), as well as our first party devices and services that combine the best of Google AI, software, and hardware. Teams across this area research, design, and develop new technologies to make our user's interaction with computing faster and more seamless, building innovative experiences for our users around the world. Responsibilities Define, develop, and optimize high-volume manufacturing (HVM) processes for advanced semiconductor packaging technologies for consumer devices, ensuring compliance with electrical, thermal, mechanical, environmental, and cost requirements, especially mobile SOC SIP for on-device AI. Drive process optimization and yield improvement using Design of Experiments (DOE) methodology, and establish rigorous process monitoring and control systems to ensure robust manufacturing. Establish and evaluate the effects of package assembly and bumping processes, specifically assessing Chip Package Interaction (CPI) effects such as Silicon ELK stress and impact on board-level reliability. Lead Electromigration (EM) evaluations for fine-pitch package solutions, defining material and process requirements to meet long-term package development and reliability roadmaps. Perform comprehensive failure analysis and root cause resolution for manufacturing and field issues encountered during both the technology development and mass production phases. Collaborate and manage key suppliers, including OSATs, substrate vendors, and packaging ecosystem partners, to drive technology roadmap execution and establish internal packaging. Domestic and International travel required. Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also Google's EEO Policy and EEO is the Law. If you have a disability or special need that requires accommodation, please let us know by completing our Accommodations for Applicants form.
Monday – Friday, 7:00 am - 3:30 pm About the Opportunity Maintains and improves the quality systems in accordance with the requirements of MDSAP, ISO, FDA, QSR, and Argen policies. Executes activities concerned with development, implementation, maintenance, and continuous improvement of Argen’s quality system. In this role, the successful candidate will: Aids in the preparation of regulatory documentation for domestic and international product registrations and secures appropriate regulatory documentation including device licenses, device listings, permits, and import/export certificates. Ensures compliance to applicable regulatory standards and internal procedures. Supports design and development activities for new product development, including regulatory submissions. Test Method Documents (TMs, TM Validation Protocols, TM Validation Reports) pFMEAs. Performs ongoing quality activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations, supplier activities and actions as necessary. Assists in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities. Assists Engineering in the preparation and execution of verification and validation protocols and verification and validation test reports for new products and changes to current products. Participates in Hazard Assessment, Failure Mode and Effect Analysis, and risk management analysis, as required, for new and current products. Plans and participates in internal and external audits as required. Aids in the evaluation of customer complaints for regulatory compliance and adherence to product claims. Assists in manufacturing NPI activities. Creates SOP’s and update exiting SOP’s. Reviews and approves Device History Records for finished device release as required. Serves as a technical resource for technicians, assemblers, and other Argen personnel. Other duties as assigned. What does it take to be successful? Bachelor’s degree in Quality Engineering, Quality Assurance, Biomedical Engineering or an equivalent degree from an accredited institution is required or equivalent experience in quality system such as ISO 13485, 21CFR820 Preferred working knowledge of ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3. Demonstrated understanding of required standards / regulations impacting medical devices Team-oriented professional with good interpersonal skills who is hands-on with a high energy approach to work Ability to communicate ideas and information clearly, effectively, and frequently (verbal and written) · Ability to prioritize and execute tasks in a timely manner without direct supervision Knowledge of PFM, Crown and Bridge applications and their use in the dental lab is a plus Our Awesome Benefits! Working for a growing innovative company like Argen means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, Argen is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes: Health Plans Dental Plans Vision Plan 401k with Employer Match Paid Time Off and Paid Holidays Employee Events Wellness Programs Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more! EOE/M/F/Vet/Disabled VEVRAA Federal Contractor