Production Team Member jobs in National City, CA

This position is responsible for setting up and operating CNC machining centers, mills, lathes, and router equipment. The Machine Operator produces quality product according to precise specifications within time constraints. At some locations, this position will also include general warehouse duties such as shipping and receiving. In this position, the employee will work with moderate supervision. Essential Functions: * Sets up and operates production machinery such as CNC saws, lathes, milling machines, drills, shapers, boring mills and grinders to fabricate and repair parts and products. Works with some guidance from supervision. * Reading and Interpreting Documentation and Product Quality - Reads and interprets blueprints, sketches, and parts lists. Studies and interprets assembly instructions, and verifies specifications. Conducts dimensional and visual part inspections to prints and specifications using standard quality assurance inspection equipment. * Responsible for maintenance of equipment - Completes preventative maintenance, troubleshoots malfunctions, and performs minor repairs as needed. Communicates errors in product, equipment, and other issues that may arise in fulfilling orders. * Performs general warehouse duties - Fills orders in a timely manner by operating warehouse equipment and machinery including operating a fork lift, computing and optimizing yields, and cutting material to size. Loads and unloads delivery trucks as needed, using SAP to receive and ship materials. Processes operational activities in SAP through work orders and prepares proper documentation including transfer orders, bills of lading, delivery notes, work orders, call tags for non-conforming material and others as required. * Problem solving and Communication - Resolves assembly and production issues and communicates errors in the product line, equipment and or issues in fulfilling orders. * Safety and Continuous Improvement - Participates actively in Continuous Improvement activities and submits ideas to help drive improvement. Ensures the workplace and environment are clean and safe. Follows Company Safety policies and procedures and looks for ways to improve safety. Performs other duties as assigned. Core Competencies: * Detail Orientation * Multi Tasking * Sense of Urgency & Work Ethic * Creativity & Innovation * Communication Skills * Process Improvement & Best Practices

Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics . Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 25 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. Our harmonized ISO15189 accredited and CLIA/CAP clinical laboratories offer a test menu focused on biomarkers which are clinically actionable to support therapeutic decisions, measurable residual disease (MRD) testing, patient stratification, and trial enrollment, all designed to accelerate approvals of new oncology drugs and treatments. For 25 years, we have been at forefront of precision diagnostics, and we're just getting started! We are looking to add a Manufacturing Associate II to support the daily activities of the Manufacturing Team in the production of reagents, master mixes, controls and/or assay cartridge/kits. Core Responsibilities Include: Performs production activities per schedule. Reviews and revises manufacturing documents (purchasing specifications, SOPs, manufacturing batch records, etc.). Implements/trains on the use of those documents as necessary. Manufactures master mixes and ASR, reconstitution of oligonucleotides, controls, cell cultures, reference standards and general-purpose reagents by following manufacturing batch records, work instructions, SOPs, forms and validated Excel spreadsheets. Executes validation for production processes and equipment. Verifies all materials necessary are available for manufacturing; prepares tubes/boxes/labels and formulation/fill. Maintains appropriate inventory levels of raw materials and supply items used in manufacturing. Ensures the production environment is maintained consistent with SOPs, operating practices and regulatory requirements. Maintains general lab cleanliness, lab equipment, monitors temperature/pressure in specified areas or equipment. Additional duties may include reagent testing and supportive administrative tasks as well as maintaining inventory and other as necessary. May contribute to training and observing other Associates as required; ensures Standard Operating Procedures are followed. You Bring: B.S. degree in a scientific discipline and, typically, 2+ years applicable experience in a GMP regulated industry; equivalent combination of education and experience may be considered. Applied working knowledge of a manufacturing environment, including use of SOPs, batch records, ERP systems and purchasing specifications is desired. Proficient working knowledge of PCR and molecular biology. Proficient with aseptic techniques and accurate pipetting skills. Proficient use of Microsoft Office Suite (Word, Outlook, Excel) and the ability to learn new software programs. We Bring: A beautiful modern facility centrally located in San Diego County, with many jobs conducive to flexible scheduling and telework options. A welcoming breakroom for gathering with hosted hot/cold beverages and healthy convenience foods, and an available micro-market to get you through the day. A positive workplace culture with an emphasis on support, respect and belonging. A diverse and inclusive work environment where you will learn, grow, and make new friends. Competitive pay, discretionary bonus program, incentive stock options, generous benefit options, 401k with a fully vested employer match, and generous time off benefits. Invivoscribe is an Equal Opportunity Employer.

Job Details Division: Nucor Rebar Fabrication Southwest Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve. Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more. Compensation: * Hourly Rate: $20.00 - 33.29 (Experienced Rebar Fabricators encouraged to apply. Wage DOE) * Weekly Production Bonus * Profit Sharing: 20.43% 5 - Year Average * A chance to grow your career with a stable company owned by Nucor, North America's largest steel producer * A full benefits package, including Medical/Dental/Vision insurance; Vacation Days; Holidays; 401K; Nucor stock purchase program; Tuition reimbursement; Scholarship Program for dependents of employees Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times. What You'll Do: An entry level production worker at Nucor Rebar Fabrication will bend, cut, bundle and load reinforcing steel bars in accordance with customer's orders. You'll work with a mentor who will train you on safely using all machinery Responsibilities: * Unload trailers and store material in storage bins. * Operate a shearing machine or a power saw to cut reinforcing steel bars to specific lengths. * Operate a bending machine to bend reinforcing steel bars to specified shape. * Operate overhead crane to move, assemble and select material to be fabricated or shipped. * Assemble and load orders onto trailers for shipping. * Operate a spray gun in the application of epoxy touch up or reinforcing steel bars. * Maintain the shop or designated area in a clean and safe manner. Minimum Requirements: * Must be legally authorized to work in the United States without company sponsorship now or in the future * Must be age 18 or over * Due to the operating conditions of the position, this is a safety sensitive position, therefore you must pass a drug test, including THC * Must be able to work overtime when required Your Qualifications: * Able to read and comprehend basic safety and operational instructions * Able to perform basic math for accurate bar measurements Physical Demands: * Some heavy lifting may be necessary * Working conditions can be noisy/ dusty/ hot/ cold Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace

FLSA Status: Non-Exempt Job Summary: The Production Operator Level 1 is responsible for operating and maintaining production equipment to ensure efficient and safe manufacturing processes. This role involves performing routine tasks, monitoring equipment, and ensuring product quality. The Production Operator Level 1 will work closely with other team members to meet production goals and maintain a clean and safe work environment. Key Responsibilities: Operate and monitor production equipment to ensure efficient and safe manufacturing processes. Perform routine maintenance and cleaning of equipment. Conduct quality checks on products to ensure they meet specifications. Follow standard operating procedures and safety guidelines. Report any equipment malfunctions or safety concerns to the supervisor. Maintain accurate production records and logs. Assist with material handling and inventory management. Participate in continuous improvement initiatives to enhance productivity and efficiency. Collaborate with team members to achieve production targets. Qualifications: High school diploma or equivalent. Previous experience in a manufacturing or production environment preferred. Basic mechanical skills and ability to operate production equipment. Strong attention to detail and commitment to quality. Ability to follow instructions and work independently. Good communication and teamwork skills. Willingness to work flexible hours, including shifts and weekends. EEO Statement: [Company Name] is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. [Company Name] makes hiring decisions based solely on qualifications, merit, and business needs at the time.

Job DescriptionSalary: $23.79 - $29.08/HR Purpose The Production Technician under direct supervision, completes the manufacturing of collagen/final product in an FDA regulated aseptic and non-aseptic clean room environment (Class 100 to 10,000) and other production processes. This role requires strict adherence to FDA regulations, industry standards in accordance with cGMP's (current Good Manufacturing Practices). Duties and Responsibilities Follow written SOP's and batch records for bulk production, aseptic filling, assembly and final product labeling and packaging Print and inspect controlled labels for final product Perform inspection of finished Record process operations and data calculation entries into batch records and associated forms Qualify for aseptic gowning and operations (syringe filling) on a semi-annual qualification basis. Manually fill syringes in an aseptic environment for extended durations while being monitored for viable and non-viable microbial growth Perform line clearance prior to the commencement of each process by ensuring all related materials/components are released for use, and non-related materials/ components are not present; therefore removed Ability and knowledge to operate, calibrate, and standardize equipment released for cGMP use Process raw bovine in preparation for collagen extraction and Assemble pressurized tanks and process Formulate acidic and caustic dilutions from concentrated stock Process and sieve PMMA Clean and sterilize (autoclave) process equipment, vessels, and cleaning Perform room cleaning in aseptic and non-aseptic areas (ceilings, walls, floor, and biosafety cabinets) Neutralize waste using acidic or caustic solutions before Maintain production areas to cGMP compliance and inspection Participate in and support implementation of changes in processes and policies to maintain high professional Fill voids within the production Maintain acceptable attendance and punctuality for scheduled work hours and meetings Ensure completion of assigned tasks and responsibilities within defined times Flexibility to work overtime and or weekends to support operational needs when necessary Perform other duties as assigned Skills and Abilities Ability to work effectively in a team or independently Excellent attention to detail and organization Ability to cross-train Ability to work seated or stand for 6-8 hours Ability to lift, push, or pull objects weighing up to 25 lbs. as needed Excellent written and verbal communication Highest level of ethics and integrity Ability to lead and motivate the right behaviors Ability to multi-task and work in a demanding environment Strong technical writing Proficiency in Microsoft Office Qualifications/Requirements High school diploma or general education degree required A higher level of education may be considered, or equivalent combination of education and experience is preferred Experience in Biotechnology/Medical Device Associates degree (AA) in scientific discipline or equivalent from two-year college or technical school is preferred Clearance of favorable background investigation is required

Job Description 1. According to the requirements of workshop supervisor, complete the production task on time and in quantity, and complete the production task of the same day and month; 2. Production operation according to process requirements; 3. Obey the arrangement of leaders and complete the technical learning tasks outside the post; Requirements 1, education is not limited 2.1 years working experience in manufacturing enterprises; 3. Packaging experience, factory experience is preferred; 4. Hard-working and responsible. Benefits Medical insurance plan Retirement plan paid leave Training and development We are an equal opportunity employer that values diversity and recognizes that diversity of ideas and backgrounds builds stronger teams. We take diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, descent, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status or military service. Junior worker 17/ hour, senior 18/ hour, group leader 20/ hour, overtime 1.5 times. 5 days a week, 8 hours a day, 40 hours a week. Those who work overtime must be approved. Welcome interested friends to contact us, 联系电话********** **********

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. * This position is for 7th Shift - Wednesday 12AM Midnight - 6AM, Thursday - Saturday 6PM - 6AM. * Operate equipment to produce product that is in full compliance to required product specifications and any instructions appearing on the manufacturing order. * Pre-plate inspect all materials produced by the wiredraw dept. Alert wiredraw operators and supervisor of all non-conforming products to minimize scrap and production loss due to poor quality. * Must pass all quality audits of quality procedures and quality paperwork including product identification tags and grading. * Identify off-spec plated material as described in our operating procedures so the finishing operators can eliminate this material from the production run. * Required to operate the equipment above standard production rates consistently while meeting all quality and safety requirements. * Consistently meet production rates while meeting all quality and safety standards. * Responsible for the typical daily preventative maintenance (PM) duties of the machine. Works with maintenance group and team associates during scheduled weekly line PM's to maximize productivity. Responsible for the reject rate and scrap minimization generated by his/her machine. * Comply to and support all aspects of the ERICO quality system. * Actively participates in continuous improvement activities as requested. * Optimize production utilizing SPC techniques to reduce copper deposit thickness to lowest acceptable value. * Observe all prescribed safety rules and regulations and maintain work area in a neat and orderly condition. * Perform other related duties as assigned or directed which may require more than the normal shift hours or work week to meet company needs. YOU HAVE: * Academic background: High School Diploma or equivalent preferred. * Previous experience in or with: Over one year experience in a manufacturing facility required, preferably in plating. * Skills: Must have prior forklift training or be able to receive forklift training and maintain certification, Basic reading and writing skills, written and verbal communication skills, basic blue print reading skills (simple geometric parts, interpret dimensions), basic measuring tool skills (Calipers, Micrometers, Copper Thickness Gauge), basic math skills (addition, subtraction, multiplication, division), basic computer skills including Microsoft Office applications (Word, Excel, etc.). * Abilities to meet the physical and environmental demands: Ability to work in a chemical environment that it hot and humid wearing the appropriate PPE, ability to understand specifications as they relate to product produced, ability to lift up to 50 pounds. This position requires pulling, lifting, and pushing steel coil material. WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

FLSA Status: Non-Exempt Job Summary: The Production Operator Level 1 is responsible for operating and maintaining production equipment to ensure efficient and safe manufacturing processes. This role involves performing routine tasks, monitoring equipment, and ensuring product quality. The Production Operator Level 1 will work closely with other team members to meet production goals and maintain a clean and safe work environment. Key Responsibilities: Operate and monitor production equipment to ensure efficient and safe manufacturing processes. Perform routine maintenance and cleaning of equipment. Conduct quality checks on products to ensure they meet specifications. Follow standard operating procedures and safety guidelines. Report any equipment malfunctions or safety concerns to the supervisor. Maintain accurate production records and logs. Assist with material handling and inventory management. Participate in continuous improvement initiatives to enhance productivity and efficiency. Collaborate with team members to achieve production targets. Qualifications: High school diploma or equivalent. Previous experience in a manufacturing or production environment preferred. Basic mechanical skills and ability to operate production equipment. Strong attention to detail and commitment to quality. Ability to follow instructions and work independently. Good communication and teamwork skills. Willingness to work flexible hours, including shifts and weekends. EEO Statement: [Company Name] is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. [Company Name] makes hiring decisions based solely on qualifications, merit, and business needs at the time.

Job Description FLSA Status: Non-Exempt The Welder is responsible for welding and fabricating metal components per job specifications and blueprints. This position supports production requirements by producing quality welds, maintaining safety standards, and ensuring project timelines are met. Essential Job Responsibilities: Perform MIG welding based on material and project needs. Interpret blueprints, welding symbols, and work orders to determine welding requirements. Fabricate and assemble metal parts using tools, jigs, and fixtures. Inspect finished welds to ensure accuracy, strength, and compliance with quality standards. Maintain and clean welding equipment and ensure tools are in working condition. Follow company safety procedures including PPE usage and safe equipment handling. Participate in daily production tasks to meet scheduling requirements. Assist with material handling, receiving, and staging for weld projects. Work with other team members including fitters, fabricators, and engineers. Operate cranes, forklifts, and hoists to move large parts as necessary. Track work progress, log job data, and report any issues to supervisor. Work on any jobs in any department as required by company workload. Education/Experience: High school diploma or equivalent required. 1–5 years of welding experience in manufacturing, construction, or metalworking. Welding certification (AWS or equivalent) preferred. Experience with structural steel, stainless steel, or aluminum a plus. Ability to read a tape measure down to 1/16th Basic CNC knowledge a plus Communication Skills/Requirements: Able to communicate verbally and in writing regarding progress, safety, and quality issues. Will work cross-functionally with other departments to meet job specifications and delivery goals. Mathematical Ability: Able to add, subtract, multiply, and divide. Must be able to read and apply measurements using fractions, decimals, and basic geometry for layout and fitting. Reasoning Ability: Must be able to follow instructions, prioritize tasks, and troubleshoot problems with minimal supervision. Requires ability to interpret technical documents and adapt to production changes. Physical Demands: Must be able to lift up to 50 lbs. (required) Standing and walking for extended periods. Repetitive motions using hands and arms. Frequent bending, kneeling, and lifting (required). Must wear safety equipment including helmet, gloves, and protective clothing. Work Environment: Manufacturing plant with exposure to welding fumes, heat, noise, and sparks. Requires attention to safe work practices and use of all assigned PPE. Additional Information: Working hours: 6:30 am to 3:00 pm, however, working hours may vary depending on production demands. Overtime may be required. ***Attendance: Must be reliable with strong attendance and punctuality record. Safety: Steel toe boots and safety glasses required in all production areas. EEO Statement: [Company Name] is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. [Company Name] makes hiring decisions based solely on qualifications, merit, and business needs at the time.

Job Description BASIC PURPOSE OF POSITION: Assist in the set-up, run, and monitor any one of the machines used for the production of filament winding vessels. Ensures quality product is being produced in a timely fashion. ESSENTIAL FUNCTIONS OF THE POSITION: 1. Performs activities in the production of filament wound pressure vessels which may include assisting in the set-up winding, oven load, extraction, cutting, sanding, prep, milling, port install, troubleshoot, repair (as required), hydro-test, paint prep, paint and packaging. 2. Performs and ensures quality inspections of raw material and wound vessels. 3. Prepares and ensures production and department documents such as roll tickets, run log, maintenance log, utilization sheets, and sample work-up sheets are complete and accurate. 4. Follows Production Manager’s instructions, housekeeping policies, and standard operating procedures, written, oral, or diagram form that aid in the manufacturing of filament wound pressure vessels. 5. Acts in a safe manner at all times. Follows all company policies and procedures as they relate to safety reporting. Reports all safety incidents or hazards immediately upon occurrence. NON-ESSENTIAL FUNCTIONS: 1. Communicates with other plant personnel and supervisors regarding production issues. 2. Informs Manager of any parts or supplies needed. 3. Performs other duties as assigned and necessary. ESSENTIAL REQUIREMENTS OF THE POSITION: 1. High school diploma or GED required. One- or two-years' experience in a manufacturing plant. 2. Good mechanical ability, logical trouble-shooting skills and attention to detail. 3. Basic math skills and computer skills preferred. 4. Experience in a manufacturing environment desired. Physical Demands: 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of the job, the employee is regularly required to stand, walk, and use hands to finger, handle or feel objects, tools (such as a sander), or controls. The employee frequently is required to talk or hear. The employee is regularly required to reach with hands and arms, balance, stoop or kneel. The employee must regularly lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. 3rd Shift: Sunday through Friday from 10pm to 6:30am 1st Shift: Monday through Thursday from 6am to 2:30pm and Friday's from 4am to 12:30pm 2nd Shift: Monday through Thursday from 2pm to 10:30pm and Friday's from 12:30pm to 9:00pm

Job DescriptionSalary: $20-$21 Sublimation Operator Effectively manage the production line and help facilitate the printing, finishing, and packing of our garments Ability to work in a fast-paced, high-speed environment, follow standardized work, and adhere to safe work practices in a continuous improvement environment Perform necessary pre-operation activities to ensure proper equipment startup and operation on multiple pieces of equipment Operate/monitor multiple pieces of equipment during operation to ensure quality production and minimal unplanned stops Communicate with team members and support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials Start machines, monitor operation, and make adjustments as needed Notify supervisors or mechanics of equipment malfunctions Communicate effectively with off-going and on-coming shift personnel Maintain a clean and safe work area

Job Description Solatube (A Kingspan Company) is widely recognized as an industry innovator which has earned acclaim around the globe for its unrivaled ability to transform interior spaces with the power of daylight. Based in Vista, California, Solatube (A Kingspan Company) designs and manufactures a full line of daylighting systems and ventilation products. To help us continue to grow our offerings, we’re searching for a Production Operator who will perform any combination of repetitive machine operations and assembly functions to produce quality tubular daylighting devices and accessories safely and efficiently. Responsibilities: Operates work-cell stations (such as but not limited to): assembly, packaging, and soldering Follows written SOP and verbal job specifications and uses knowledge gained by experience May set stops or guides as indicated by prints, diagrams, and instructions Observes machine operation to detect workpiece defects or machine malfunction Positions workpiece against stops, or aligns layout marks Pushes buttons or depresses pedal to activate machine Bolts, clips, screws, cements, tapes, or otherwise fastens parts together using hand tools And/or power tools, riveter, elbow machine and hipot tester Assist with start-up and shut-down procedures Assist with color changeovers Hanging parts on the powder coat line Removing and packaging parts for delivery Ensuring paint booth and powder coating equipment is organized and clean Assist with quarterly maintenance Works in assigned work-cell station and within various rotations as production needs require including other departments Works on line where tasks vary as different model of same article moves along line Responsible for finished good to be shrink-wrapped and staged for delivery to distribution center Meets quality control standards Cleans up work area as required Communicate effectively with peers, supervisors, and management Completes accurately all daily summary, yield cards and scrap reports as required by the Company Performs all duties safely Attends meetings and classes as required Qualifications: High school diploma or equivalent degree and/or experience. Good communication skills. Ability to be a team player. At Solatube (A Kingspan Company), we believe our employees are our greatest resource. We offer a competitive salary, benefits, and vacation package for all full-time permanent positions. Kingspan is proud to be an equal opportunity workplace and is an affirmative-action employer.

Job Details San Diego Office - San Diego, CA $18.00 - $20.00 Hourly Day ManufacturingDescription DEPARTMENT: Manufacturing REPORTS TO: Manufacturing Manager STATUS: Non-Exempt LOCATION: San Diego, CA (Sorrento Valley) 92121 JOB SUMMARY: The Production Technician's responsibilities include assembling, testing, calibrating, inspecting, and packaging temperature sensors. Operating various machinery and equipment, interpreting work orders, and ensuring product quality are essential aspects of this role. This position contributes to the delivery of high-quality products to both internal and external stakeholders. RESPONSIBILITIES: Operating Machinery/Equipment: Operate various machinery and equipment, including a cutoff saw, sanding belts, buffing wheels, crimping machine, wire strippers, sand blaster, soldering iron, TIG welder, and measurement equipment (e.g., ruler, calipers, multimeter). Manual Fabrication & Assembly: Fabricate and assemble parts in accordance with Procedures and Work Instructions. Parts Management: Identify and pull parts as required. Interpret complex work orders to determine assembly requirements. Quality Control & Documentation: Conduct quality assessments with minimal training, ensuring product acceptability through process inspection sheets and workstation measuring and test equipment. Recognize and document quality issues and defects. Effectively communicate issues to co-workers and supervisors for potential process improvement. Accurately indicate acceptable products on work orders as per established procedures. Read and understand blueprints. Specific duties will vary on a daily basis. Qualifications MINIMUM QUALIFICATIONS: Proficiency in the English language (speaking, writing, and reading). Computer literacy (e.g., MS Word, Excel, internet) with a willingness to learn new programs. Reliable transportation to and from work (40-hour work week). Ability to stand for up to 8 hours. Strong manual dexterity and good eyesight (for reading blueprints). Ability to follow written instructions. Willingness to learn new skills. Strong work ethic, emphasizing efficiency on repetitive tasks and tackling technical problems. TIG welding skills and experience. PREFERRED SKILLS: Mechanical inclination, such as working on cars, building models, or having experience in final assembly. Soldering skills. Experience with calipers and multimeters. Ability to thrive in an environment with shifting priorities and prioritize work without direct supervision. Previous experience in a factory/production environment. Problem-solving abilities.

Band Level 2 At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy (RLT) to cancer patients. We are looking for dedicated and enthusiastic professionals to join our new manufacturing site in Carlsbad! Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. Shift: Shift schedule will be phased in as the site approaches go-live. We are planning for 12-hour rotating shifts which will include at least one weekend day. Key Responsibilities: Executes all activities related to the manufacturing of RLT products. Responsibilities include operating and maintaining grade A isolators, focusing on KPI goals as well as ensuring adherence to all state, federal and Novartis radiation safety guidelines. Responsible for successful on-time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including Health, Safety & Environment (HSE) for the specific role. Supports all technical aspects related to production readiness including manually cleaning the cell and performing sterilization of the isolators. Conducts routine and dynamic environmental monitoring as required. Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure. Facilitates a culture of “speaking up” and ensuring all cGMP compliance activities are followed. Prepares applicable documents and records such as batch records, shipping documents, and training materials. Given the time sensitive nature of the product, this position will require unplanned overtime to ensure process continuity and completion. Essential Requirements: Bachelor of Science strongly preferred. If the applicant does not have a degree, a minimum of 2 years of experience in a cGMP or aseptic environment is required. External candidates: 2+ years of experience in aseptic pharmaceutical manufacturing. Preferably in drug product filling operations. Current Novartis Associates: Must be a Production Technician for a minimum of 12 months including prior RLT experience and be qualified in at least two critical production isolator tasks Knowledge of cGMP regulations and FDA guidance applicable to aseptic manufacturing. Proficient in MS Office applications. Flexibility to don clean room garments and personal protective equipment (PPE). Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted. Makeup, jewelry, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas. Ability to lift or carry up to 35 pounds. #LI-Onsite Benefits and rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally: ************************************************* The pay range for this position at commencement of employment is expected to be between $27.78 to $51.58 per hour; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to ************************ call **************** and let us know the nature of your request and your contact information. Please include the job requisition number in your message. *************************************************************************************** Salary Range $57,800.00 - $107,300.00 Skills Desired Assembly Language, Cooperation, Efficiency, Electronic Components, Flexibility, General Hse Knowledge , Good Documentation Practice, Installations (Computer Programs), Iso (International Organization For Standardization), Job Description, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Nuclear Medicine, Physics, Product Distribution, Production Line, Scheduler

Tests and calibrates parts Uses hand tools and power tools Identifies units that do not meet product specifications Repair units that fail testing Qualifications Some experience in the field MUST have high school diploma OR equivalent (and able to provide a copy of diploma) Able to lift 10-15 pounds Able to pass background screening AND drug screening Additional Information Pay Rate: $8.00/hr Shift: Monday-Friday, 7AM-3:30PM 8+/- Month Contract

We are a Fortune 500 Aerospace company seeking entry level production workers to assist in the daily functions of the facility. Job Description Tests and calibrates parts Uses hand tools and power tools Identifies units that do not meet product specifications Repair units that fail testing Qualifications Some experience in the field MUST have high school diploma OR equivalent (and able to provide a copy of diploma) Able to lift 10-15 pounds Able to pass background screening AND drug screening Additional Information Pay Rate: $8.00/hr Shift: Monday-Friday, 7AM-3:30PM 8+/- Month Contract

Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics . Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 25 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. Our harmonized ISO15189 accredited and CLIA/CAP clinical laboratories offer a test menu focused on biomarkers which are clinically actionable to support therapeutic decisions, measurable residual disease (MRD) testing, patient stratification, and trial enrollment, all designed to accelerate approvals of new oncology drugs and treatments. For 25 years, we have been at forefront of precision diagnostics, and we're just getting started! We are looking to add a Manufacturing Associate II to support the daily activities of the Manufacturing Team in the production of reagents, master mixes, controls and/or assay cartridge/kits. Core Responsibilities Include: Performs production activities per schedule. Reviews and revises manufacturing documents (purchasing specifications, SOPs, manufacturing batch records, etc.). Implements/trains on the use of those documents as necessary. Manufactures master mixes and ASR, reconstitution of oligonucleotides, controls, cell cultures, reference standards and general-purpose reagents by following manufacturing batch records, work instructions, SOPs, forms and validated Excel spreadsheets. Executes validation for production processes and equipment. Verifies all materials necessary are available for manufacturing; prepares tubes/boxes/labels and formulation/fill. Maintains appropriate inventory levels of raw materials and supply items used in manufacturing. Ensures the production environment is maintained consistent with SOPs, operating practices and regulatory requirements. Maintains general lab cleanliness, lab equipment, monitors temperature/pressure in specified areas or equipment. Additional duties may include reagent testing and supportive administrative tasks as well as maintaining inventory and other as necessary. May contribute to training and observing other Associates as required; ensures Standard Operating Procedures are followed. You Bring: B.S. degree in a scientific discipline and, typically, 2+ years applicable experience in a GMP regulated industry; equivalent combination of education and experience may be considered. Applied working knowledge of a manufacturing environment, including use of SOPs, batch records, ERP systems and purchasing specifications is desired. Proficient working knowledge of PCR and molecular biology. Proficient with aseptic techniques and accurate pipetting skills. Proficient use of Microsoft Office Suite (Word, Outlook, Excel) and the ability to learn new software programs. We Bring: A beautiful modern facility centrally located in San Diego County, with many jobs conducive to flexible scheduling and telework options. A welcoming breakroom for gathering with hosted hot/cold beverages and healthy convenience foods, and an available micro-market to get you through the day. A positive workplace culture with an emphasis on support, respect and belonging. A diverse and inclusive work environment where you will learn, grow, and make new friends. Competitive pay, discretionary bonus program, incentive stock options, generous benefit options, 401k with a fully vested employer match, and generous time off benefits. Invivoscribe is an Equal Opportunity Employer.

1. According to the requirements of workshop supervisor, complete the production task on time and in quantity, and complete the production task of the same day and month; 2. Production operation according to process requirements; 3. Obey the arrangement of leaders and complete the technical learning tasks outside the post; Requirements 1, education is not limited 2.1 years working experience in manufacturing enterprises; 3. Packaging experience, factory experience is preferred; 4. Hard-working and responsible. Benefits Medical insurance plan Retirement plan paid leave Training and development We are an equal opportunity employer that values diversity and recognizes that diversity of ideas and backgrounds builds stronger teams. We take diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, descent, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status or military service. Junior worker 17/ hour, senior 18/ hour, group leader 20/ hour, overtime 1.5 times. 5 days a week, 8 hours a day, 40 hours a week. Those who work overtime must be approved. Welcome interested friends to contact us, 联系电话********** **********

Purpose The Production Technician under direct supervision, completes the manufacturing of collagen/final product in an FDA regulated aseptic and non-aseptic clean room environment (Class 100 to 10,000) and other production processes. This role requires strict adherence to FDA regulations, industry standards in accordance with cGMP's (current Good Manufacturing Practices). Duties and Responsibilities Follow written SOP's and batch records for bulk production, aseptic filling, assembly and final product labeling and packaging Print and inspect controlled labels for final product Perform inspection of finished Record process operations and data calculation entries into batch records and associated forms Qualify for aseptic gowning and operations (syringe filling) on a semi-annual qualification basis. Manually fill syringes in an aseptic environment for extended durations while being monitored for viable and non-viable microbial growth Perform line clearance prior to the commencement of each process by ensuring all related materials/components are released for use, and non-related materials/ components are not present; therefore removed Ability and knowledge to operate, calibrate, and standardize equipment released for cGMP use Process raw bovine in preparation for collagen extraction and Assemble pressurized tanks and process Formulate acidic and caustic dilutions from concentrated stock Process and sieve PMMA Clean and sterilize (autoclave) process equipment, vessels, and cleaning Perform room cleaning in aseptic and non-aseptic areas (ceilings, walls, floor, and biosafety cabinets) Neutralize waste using acidic or caustic solutions before Maintain production areas to cGMP compliance and inspection Participate in and support implementation of changes in processes and policies to maintain high professional Fill voids within the production Maintain acceptable attendance and punctuality for scheduled work hours and meetings Ensure completion of assigned tasks and responsibilities within defined times Flexibility to work overtime and or weekends to support operational needs when necessary Perform other duties as assigned Skills and Abilities Ability to work effectively in a team or independently Excellent attention to detail and organization Ability to cross-train Ability to work seated or stand for 6-8 hours Ability to lift, push, or pull objects weighing up to 25 lbs. as needed Excellent written and verbal communication Highest level of ethics and integrity Ability to lead and motivate the right behaviors Ability to multi-task and work in a demanding environment Strong technical writing Proficiency in Microsoft Office Qualifications/Requirements High school diploma or general education degree required A higher level of education may be considered, or equivalent combination of education and experience is preferred Experience in Biotechnology/Medical Device Associate's degree (AA) in scientific discipline or equivalent from two-year college or technical school is preferred Clearance of favorable background investigation is required