Quality Technician Jobs in Stockton, CA

Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. Sanmina Corporation has facilities strategically located in key regions throughout the world. The Sanmina Fremont facility is a full-service enclosure systems solution manufacturing plant. Located in California's Silicon Valley, this facility produces low-to-mid volume New Product Introduction (NPI) runs to full-scale volume. The Fremont facility offers everything from small piece parts to fully integrated and tested systems. In addition, this location offers in-house painting capabilities and flexible logistics solutions in distribution, inventory management and hubbing, as well as repair services. Job Description As the Fremont Fabrication Quality Supervisor, you will be responsible for developing a world class quality department and driving plant wide continuous improvement that results in unparalleled quality performance. You will have the opportunity to reinforce foundational quality principals, as we develop innovative manufacturing and inspection processes at the leading edge of automation and fabrication technology. This position will be responsible for managing, coordinating and administering all functions of the site's Quality Management System, including receiving inspection activities, quality engineering, supplier quality management and the QC laboratory. Specific Responsibilites Develops, implements, and maintains policies, procedures in compliance to corporate procurement systems Lead and mentor QA Department, consisting of quality engineers, receiving inspection, and QC personnel Be an outspoken advocate for Quality First throughout the plant Expediently and effectively communicate with customers on quality escapes, visits, escalations, etc. Maintain and improve the site QMS (including NCR and CAPA system, internal audit, training, etc.) Maintain the site QMS compliance with ISO 9001:2015 and AS9100:2016 by coordinating and responded to site certification audits Responsible for ensuring effective quality planning (including PFMEAs, process flows and control plans) for NPI and production parts. Develop additionally sources of quality data and track and report key Quality-related performance indicators (KPIs), including first pass yield and scrap rates. Manage and improve supplier quality Be an advocate for lean and six sigma manufacturing principles and drive continuous Drive cross functional projects with manufacturing, supply chain, and engineering, to verify and validate existing manufacturing processes and capabilities Participate in Design for Manufacturability (DFM) reviews with engineering Address customer escapes by driving cross-functional teams to develop and implement corrective actions Supervisory Responsibilities Key focus is on leadership and motivation of staff, and contributing advanced quality engineering, supplier management, receiving inspection and quality control expertise. Responsible for all Quality functions to ensure that the individual and group's objectives and processes align with the overall business direction. Evaluates and supports employees to achieve their objectives, and removes barriers for success. Manage and lead cross functional teams. Education And Experience Bachelor's Degree required (Mechanical, Aerospace or Manufacturing Engineering preferred) Minimum of 6 years of experience in quality engineering or related area in a manufacturing environment with exposure to the following manufacturing processes: sheet metal fabrication, welding, painting, complex electromechanical integration, and clean room assembly Experience with reading and interpreting GD&T requirements required Detailed knowledge and hands on experience with quality tools including process flowcharts, FMEA's, control plans, CAPA, RCCA and 8D required Experience working in an ISO 9001 and AS9100 certified environment required. Experience implementing Lean Manufacturing and Six Sigma methodologies including statistical analysis techniques (Design of Experiments, Statistical Process Control (SPC), etc) preferred. Experience with machining and system integration/assembly preferred Experience with CMMs and laser inspection systems preferred Certified Green or Black belt a plus Internal audit experience a plus Oracle ( ERP ) experience desirable Experience using Microsoft Office product suite required Excellent verbal and written communication skills required This is an ITAR facility and applicant must be a US Citizen or a lawful permanent resident. Sanmina is an Equal Opportunity Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity Salary Range (annual): $80,000 - $110,000 In addition, Sanmina Provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.

Job Title: Process Technician III Duration: 12 Months RGDA - Regular, Mon-Fri shift hours: 8 AM - 5 PM Pay Range: $30-38/hour. Description: Performs technical tests and experiments for process engineering within R&D. Performs set up of processing equipment. Monitors, audits and provides guidance to line operators. Processes test runs and prepares records, charts, and graphs of results for presentation to engineering to identify yield problems or test new products. Provides technical assistance to process development and engineering personnel. Skills: Performs process engineering lab activities for customer demo and/or C&F process experiments. This includes sample preparation, sample chemical treatment and running waferflows on Lam tools. Performs measurement on metrology tools to collect experiment results including thin film measurement, CD measurement and SEM imaging. Understand process requirement and works with minimal supervision for execution of experiments. Creates process recipes from scratch and tunes process recipes for robustness. Provide suggestions for process recipe improvement Understands Lam tools operations, able to clear basic alarms and applies troubleshooting skills to reduce tool downtime Conducts statistical process control (SPC) and etch rates including measure, execution, analysis and reporting to ensure Lam chamber performance is under control and in-spec. Alert for any trend or out-of-spec issue and come up possible causes and troubleshooting actions Education: College graduate with associates or BS degree in electronics, material science, computer science, chemistry, physics

Quality Inspector - Rancho Cordova, CA Under limited supervision, performs product inspection and/or audits of quality control programs. Performs sampling and testing of incoming components and raw materials and packaging line and manufacturing inspections. Inspects and tests product manufactured or processed by suppliers to ensure conformance to requirements and specifications. Identifies material and processes as Conforming or Nonconforming. Writes reports of findings for review. Enters required data into system. Tasks may include complex and/or non-routine assignments. Responsibilities: Analyze and interpret drawings, data, manuals, and other materials to determine specifications, inspection and testing procedures, adjustment and certification methods, formulas, and measuring instruments required. Inspect, test, or measure materials, products, installations, or work for conformance to specifications which may include mechanical, electrical and/or chemical inspections. Notify supervisors and other personnel of production problems, and assist in identifying and correcting these problems. Discuss inspection results with those responsible for products, and recommend necessary corrective actions. Record inspection or test data, such as weights, temperatures, grades, or moisture content, and quantities inspected or graded. Mark items with details such as grade or acceptance-rejection status. Measure dimensions of products to verify conformance to specifications, using measuring instruments such as rulers, calipers, gauges, or micrometers. Compare colors, shapes, textures, or grades of products or materials with color charts, templates, or samples to verify conformance to standards. Write test or inspection reports describing results, recommendations, or needed repairs. Prepare first article reports and enter required data into computer Document inspection findings and complete rejection reports. Ensure raw materials, in-process and finished products meet company standards. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated. May assess draft and final label copy, utilizing knowledge of labeling regulations Minimize down time by reducing production rework and recalls. Follow established process/procedures for discarding or rejecting products, materials, or equipment not meeting specifications. Other duties as assigned. Education and/or Experience: Vocational or Technical Certificate, or college degree (Associates Degree) in related or specialized field 3-5 years of experience, and/or equivalent combination of education and experience in a directly related field.

Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. As a team, we've launched two satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $500 million from top global investors, and recruited a team of over 300 world-class engineers. We all work out of our (legendary) San Francisco office, which was once used to build ships during the World Wars. Our satellites, which operate from geostationary orbit (GEO), weigh only 400 kg and utilize a proprietary software-defined radio payload. Each satellite can connect over two million people, and we're very excited for the impact we'll soon have in the Philippines, Peru, Mexico, and more! Backed by substantial funding and a passionate, collaborative team, we offer a rewarding work environment where you'll learn and make a significant impact, no matter where you are in your career. Apply and join us on our journey towards global connectivity! Production Quality Inspector As a Production Quality Inspector, you are responsible for being the last line of defense in assuring mission success. You will work with the most cutting edge MicroGEO satellite technology and perform inspections in several workcenters to verify our hardware meets the highest level of quality. The ideal candidate is self-driven, extremely detail oriented, and seeks a highly cross functional dynamic environment. Responsibilities Perform in-process inspection and final verification of flight hardware to drawing, process specifications, and work order requirements supporting multiple work centers (assembly, integration, wire harnessing, or test) Identify, document, and verify resolution of production and test non-conformances in accordance with prescribed procedures and pursue corrective action as required Interface with engineering and production to communicate and help resolve nonconforming issues Independently perform verifications and document results in a clear, precise, and complete manner Support quality management system policies and procedure documentation, assess compliance to company and industry standards, initiate and lead continual improvement and lean manufacturing initiatives Perform other related duties, as assigned, for the purpose of ensuring an efficient and effective work environment Requirements 3+ years of inspection experience in an aerospace, military or manufacturing environment Substantial knowledge of the control of nonconforming hardware, failure/root cause analysis, corrective and preventive action processes Experience reading and interpreting design drawings and CAD models Experience with performing electronic testing and inspection using portable measuring devices and lab equipment (microscopes, testers, scopes, etc) Excellent communication (written and verbal) and teamwork skills Ability to work independently with a strong work ethic, be innovative, detail oriented, possess initiative, and team oriented Willing and able to work overtime and/or weekends as required Bonus Associate degree or higher in quality, engineering, or related field Knowledgeable with ISO 9001/AS9100 quality management systems Experience inspecting solder, crimping, conformal coating, staking, and surface mounted devices in accordance with IPC-J-STD-001 or IPC-A-610 standards Wire harness experience in accordance with IPC-A-620 standards Six Sigma Yellow/Green Belt certified What we offer: All our positions offer a compensation package that includes equity and robust benefits. Base pay is a single component of Astranis's total rewards package, which may also include equity in the form of incentive stock options, high quality company-subsidized healthcare, disability and life insurance benefits, flexible PTO, 401(K) retirement, and free on-site catered meals. Astranis pay ranges are informed and defined through professional-grade salary surveys and compensation data sources. The actual base salary offered to a successful candidate will additionally be influenced by a variety of factors including experience, credentials & certifications, educational attainment, skill level requirements, and the level and scope of the position. Base Hourly Pay $30 - $40 USD U.S. Citizenship, Lawful Permanent Residency, or Refugee/Asylee Status Required (To comply with U.S. Government space technology export regulations, applicant must be a U.S. citizen, lawful permanent resident of the United States, or other protected individual as defined by 8 U.S.C. 1324b(a)(3)) Our mission and our products are meant to connect the world and everyone in it, regardless of gender, race, creed, or any other distinction. We believe in a diverse and inclusive workplace, and we encourage all people to join our team and bring their unique perspective to help make us stronger.

Ultimate Staffing is currently seeking Quality Control Inspectors to join a client in Rancho Cordova. These are temporary positions, but can potentially turn into temp to hire roles for the right candidate. The client operates a schedule of Monday - Friday 6:00 am - 2:30 pm with a starting pay of $23-$27 an hour based on experience. Overtime may be required as necessary. Job Duties: Analyze and interpret drawings, data, manuals, and other materials to determine specifications, inspection and testing procedures, adjustment and certification methods, formulas, and measuring instruments required. Inspect, test, or measure materials, products, installations, or work for conformance to specifications which may include mechanical, electrical and/or chemical inspections. Notify supervisors and other personnel of production problems, and assist in identifying and correcting these problems. Discuss inspection results with those responsible for products, and recommend necessary corrective actions. Record inspection or test data, such as weights, temperatures, grades, or moisture content, and quantities inspected or graded. Mark items with details such as grade or acceptance-rejection status. Measure dimensions of products to verify conformance to specifications, using measuring instruments such as rulers, calipers, gauges, or micrometers. Compare colors, shapes, textures, or grades of products or materials with color charts, templates, or samples to verify conformance to standards. Write test or inspection reports describing results, recommendations, or needed repairs. Prepare first article reports and enter required data into computer Document inspection findings and complete rejection reports. Ensure raw materials, in-process and finished products meet company standards. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated. May assess draft and final label copy, utilizing knowledge of labeling regulations Minimize down time by reducing production rework and recalls. Follow established process/procedures for discarding or rejecting products, materials, or equipment not meeting specifications. Requirements: 3-5 years of related experience. Associates Degree or related educational experience. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Reporting to the Senior Manager or Director of Quality, the Quality Engineer will have responsibility of ensuring that processes and products consistently meet established quality standards. While ensuring compliance to internal quality system and applicable regulations, the quality engineer will monitor and improve the quality of operational processes and outputs. His/her/their range of responsibilities will entail designing quality standards, inspecting materials, equipment, processes, and products, developing quality control systems, and determining corrective actions. Qualifications Bachelor's degree in engineering, biomedical engineering or related scientific discipline. 3-5 years' experience working in manufacturing of finished medical device or related industry. Working knowledge of the FDA Quality System Regulation, ISO 13485, ISO 14971, and the EUMedical Device Directive. Lead auditor credentials for QSR, ISO, or MDSAP are desired (ASQ Certification preferred). Responsibilities The range of responsibilities includes but not limited to developing and implementing quality standards, monitoring and analyzing quality performance, inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met; collaborating with cross-functional teams to develop and implement controls and drive improvements, ensuring that workflows, processes, and products comply with safety regulations, investigating and troubleshooting product or production issues, developing corrective actions, solutions, and improvements; reviewing specifications, and processes. The senior quality engineer may assume leadership role leading projects and teams, even strategizing, championing, motivating and ensuring all teams receive the appropriate information and guidance. Technical Develop and maintain quality systems and documentation in compliance with FDA, ISO, and EUMDR requirements. Lead and/or support on-time completion of design control deliverables for both new product introductions and design change projects. Support design verification/validation planning and execution, including any cross-functional investigation and resolution activities. Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps. Lead risk management activities from product concept through commercialization. Support Product development activities and design transfer into manufacturing. Support Manufacturing Engineering in the creation, release and maintenance of DHR/LHR, bills of material, and specifications for manufacturing. Assist in the selection, qualification, and assessment of new suppliers based on established procedures. Conduct supplier audits to evaluate their capabilities, processes, and quality management systems. Develop establish and maintain periodic reviews with suppliers on their performance(scorecards), and improvement or corrective action plan(s). Support nonconforming material investigation and disposition activity, participate in weekly MRB meetings, follow-up on supplier issues. Assist with maintenance of calibration system. Perform incoming inspection review and disposition of product components and subsystems. Assist in investigations of quality issues arising from product complaints, CAPAs, and non-conforming reports. Utilize problem solving tools to analyze and identify root causes and implement corrective actions. Actively participate in the Doc-Control process. Support the Environmental monitoring process. Initiate /approve validation protocols and reports (IQ, OQ, PQ). Initiate /approve process validation protocols and reports. Other duties and responsibilities as mutually agreed. Leadership/Communication/Compliance Be an advocate for quality and create a culture of quality. Be responsible in whole or in part for the effective manufacture of medical devices, compliance with internal policies/procedures and applicable regulations, and the efficient execution of related activities. Must be able to work under pressure and meet deadlines, while maintaining a positive attitude and providing exemplary customer service to both internal and external customers. Adhere to the Company's Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. Act as the QA representative in cross-functional team meetings, MRB, new product introductions, and supplier quality meetings. Make decisions and propose solutions based on calculated risks identified through data analysis.Process Customer Complaints and manage customer replies Champion continuous improvement through CAPA system, handling of complaints, analyzing key performance indicators. Support activities associated with Sterilization and Biocompatibility Assist in training personnel to processes associated with design and development and manufacturing. Attributes Attention to Detail and Cognitive Skills working on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Candidate must be highly motivated with excellent communication skills and proven ability to work as part of a team. Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers. Strong documentation capability for protocol and report generation and review. Ability to work ina rapidly changing and evolving environment. • Prior start-up experience is a plus. Physical Demands Business travel from 0% - 25%. Requires some lifting and moving of up to 40 pounds. Required to frequently stand, walk, sit, and use a computer for extended periods. Specific vision abilities required by this job include, close/distant vision and depth perception. Position also requires use of Personal Protective Equipment as needed

-6 month contract -Pay: $20.68/hr 2nd Shift: Sun-Wed-2:00PM-12:30AM Executes fundamental unit operations in Downstream manufacturing related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. Executes independently with adequate training non-complex fundamental operations as parts cleaning, weigh and dispense, equipment prep, kits assembly, and staging. Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies. Executes with oversight of qualified staff fundamental tasks as CIP and SIP of tanks, manufactruing equipment as well as buffer prep and transfer into tanks and bags Daily analytics and maintenance of analytical equipment. Cleaning and setup of equipment. Documents work according to cGMP and cGDP. Adheres to established regulations and follows cGMP established by site. Reports abnormalities and deviations in a timely and accurate manner. Adheres to safety standards and identifies unsafe situations / habits and escalates approriately. Maintains production areas according to predefined standards (5s). Skills: Working in a highly regulated environment following all applicable company and site SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies. Required to work according to given schedules in a 24/7 shift structure and flexibility to adapt working schedule upon prior given notice. Low to moderate - strong focus on execution of repeatable tasks with moderate technical complexity. Performing highly proceduralized tasks. Basic interactions Manufacturing Cell Culture, Manufacturing Purification, Manufacturing Compliance, Engineering & Technology, Supply Chain, Quality Assurance, Quality Control Does not require extensive technical knowledge of manufacturing operations. Low impact, repeatable, highly proceduralized. Ability to concentrate on detail oriented work in a complex technical setup with a Quality and Right the first time mindset. Strong written and verbal communication skills. Ability to work with computer-based systems. Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards. Ability to work as part of a high performing team and collaborate effectively with staff. Education: High school degree, entry level position. Associates/bachelors degree or biotechnology vocational training preferred. Preferable 1 or more years of experience in cGMP regulated industry

Major Responsibilities: Responsible for all aspects of assigned Program as Quality Engineer, including internal quality performance objectives, customer interface, program IPT (integrated product team), and program supplier quality support. Major Responsibilities: Schedules and maintains milestones and timeline tracking for key objectives. Performs Preliminary Reviews of DMRs and evaluates in-process rejections via QA Process procedures for Non-conforming Material and MRB Activity. Performs drawing control and CCB review activities for new and revised documents, ensuring customer notification of all changes. Performs Product Sell-Off included final work order test data package review prior to shipment to ensure product performance is within specified standards. Ensures Programs supplier quality issue resolution through coordination of resources and support of QC, Purchasing and Engineering groups. Interface with various company depart ments to assist in resolve quality problems and provide information to support ISO/AS9100 requirements Interfaces with customers, vendors, and various company depart ments to resolve quality problems and provide information and may perform internal and/or supplier surveys and audits. Performs analysis of manufacturing performance and prepares reports for management on quality trends and actions to improve. Ensures training of subordinate employees in quality or other required functions. Leads interdisciplinary teams to address quality problems via formal Customer, Internal or Supplier corrective and preventive actions. Presents oral and visual presentations during technical meetings Supports and implements added scope objectives and activities outlined by Quality Director. Education/Experience/Training: BS / MS degree, with a technical emphasis preferred, with 8 years of related QA experience... In lieu of a degree, 10-12 years consistent Quality Engineering "Hands-on" experience at a Senior Level. Preferred one or more certifications in Quality Sciences such as Lean, 5S, Six Sigma, ISO/AS9100, SPC, ASQ certified engineer/manager/auditor, or similar. Excellent communication skills and experience in oral and written presentations. Must have interfaced or performed as a liaison to the customer for QA - ie Experience in this role with DCMA or other government agencies preferred. Must be familiar with and have experience in design phase activities, manufacturing test and evaluation, working with electromechanical systems and mechanical hardware. Ability to develop and implement projects requiring interface with design engineers, quality engineers, and supplier and subcontract technical personnel. Should be familiar with government and commercial specification for Quality Assurance, and Test and Evaluation. Must be computer literate and have hands-on experience with current MS Office Software utilities and application programs. Additional Requirements: Must be able to obtain and maintain a Security Clearance, with potential to handle classified data. Flexible to work varied shifts, overtime, weekends and travel on occasion. Able to occasionally complete manual activities as part of job including stoop, bend, kneel, and squat and manual dexterity. Must have sufficient vision to see relative positions of small parts and able to discern symmetry and proper alignment. May be required to move items 25 pounds for distances of up to 25 feet. Must wear appropriate personal protective equipment as necessary. Based on job duties, and need to visit different areas within the company, may be exposed to fumes, dust, toxic or caustic chemicals (well below OSHA and ACGIH exposure guidelines), outdoor weather, moving mechanical parts and/or be part of a hearing conservation program due to noise levels around certain equipment. In compliance with pay transparency requirements, the salary range for this role is $76,500 - $142,500. This is not a guarantee of compensation or salary, as the final offer amount may vary based on factors including but not limited to experience and geographic location. Fisica Inc. also offers a variety of benefits, including relocation stipend, 401(k), PTO, EAP, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, and schedule type.

Must Have: 3+ years' experience as a Quality Control Inspector for Mechanical 3+ years of experience with ASME B31 piping codes, industrial and commercial construction, fabrication, welding, non-destructive testing Certification Requirement: AWS QC-1 as a Certified Welding Inspector (CWI) Plus: Mechanical - Commercial Certification AWS D1.1, D1.6, ASME Section IX, ASME B31 Piping Codes Experience Semiconductor or Biopharmaceutical Processing Equipment (BPE) and piping systems Day to day: A client of Insight Global is looking for a Quality Control Inspector to join their team. This individual will represent the company for pipe and equipment installation, welding inspection and oversight of subcontractor installation and quality. The QA QC Inspector will participate in the General Contractors project quality program documenting installation activities. Plans and conducts the analysis, inspection, design, test, and integration to assure the quality of assigned product or component. Performs quality engineering reviews of design documentation for compliance with stated requirements, including vendor quality manuals and company quality records. Reviews all purchased products or components and provides input to the decision of whether the product has been vetted for future purchases from the vendor. Documents data obtained during all quality assurance activities, consistent with company policies, codes and procedures. Communicates significant issues or developments identified during quality assurance activities and provides recommended process improvements to management. Prepares reports to communicate involvement and results of quality assurance activities. Maintains a working knowledge of codes and specifications for current industry quality standard Annual Compensation: $125,000 - $140,000 Exact compensation may vary based on several factors, including skills, experience, and education.

Quality Engineer (CNC high precision machining manufacturing) Our client is a global contract manufacturing company with multiple US locations, serving MedTech, Aerospace, and industrial end-market applications. This is an excellent direct hire career opportunity offering professional growth, competitive pay, and a generous benefits package. This position is onsite in Union City, CA. Responsibilities: Develop and implement quality systems focusing on product returns, complaint management, and root cause and corrective action measures to drive CAPA and optimize new product development within a manufacturing environment. Analyze system data to identify major contributors to poor-performing processes. Collaborate with cross-functional teams to develop and improve quality activities. Serve as a subject matter expert for data acquisition and quality software such as QC Gage and QC Calc. Perform other duties as assigned by the manager. Analyze production and supplier nonconformance data to determine causes. Investigate customer returns to identify underlying root causes promptly. Enhance QMS procedures and documents to align with ISO standards. Conduct root cause analysis of CAPA processes using DMAIC methodology and 8D/5 Why tools. Coordinate and create PFMEA, MSA, Control Plans, and Capability Studies for customer deliverables and to improve manufacturing processes. Compile PPAPs (Production Part Approval Process), implement defect containment measures, and conduct root cause analysis. Independently create PFMEA, Capability Studies, and PPAPs for customer deliverables and process improvements. Review and verify engineering/customer prints and ensure familiarity with REACH and RoHS requirements. Qualifications Must-Have: Bachelor's degree in a technical field or equivalent work experience. 5+ years of Quality Engineering experience. Proficiency with measuring tools and equipment. Strong problem-solving skills and the ability to multitask. Basic knowledge of quality systems, statistics, and sampling. Proficiency in Microsoft Office (Excel, Word, PowerPoint). Excellent interpersonal and communication skills, both written and verbal. Familiarity with high precision machining (± .0005). Nice to Have: Master's degree or equivalent work experience. Experience in a manufacturing environment. Knowledge of GD&T and engineering prints. Familiarity with ISO Quality Management Systems standards.

KinkStore is seeking a passionate and knowledgeable production technician to join our content production team. The Kink Store production team is focused on the creation of compelling product videography and photography, as well as the creation of vlog, blog, and educational content in support of the store's product line and mission. This role requires the ability to work alongside our team and step into the roles of lighting technician, videographer, photographer, editor, production assistant and media management as needed. A solid understanding of the fundamentals of photography, video production & editing is required. A good understanding of the BDSM lifestyle is helpful. RESPONSIBILITIES: Assists the content production team in all production related tasks including lighting, still photography, videography, audio recording and editing Responsible for the capturing, storage and management of all media assets Shoots all white out product photography Edits content and works with our off-site editors to facilitate the flow of work, and ensure the delivery of completed edits in a timely manner Responsible for the proper operation, storage and maintenance of all production equipment. Responsible for all production assistant related duties including tracking, stocking, cleaning and maintaining all model related and other production related supplies, sets and props. Assists store Merchandiser with administrative duties as needed QUALIFICATIONS: Proven track record in photography / videography / editing Experience in lighting, sound, and camera equipment. Understands the fundamentals of photography and video editing Ability to work independently and meet deadlines consistently. Familiar with Google sheets, Adobe editing software, Adobe Photoshop ABOUT RED SYSTEM VENTURES LLC Red System Ventures was started in 2019 by Peter Acworth. Kink.com video production now happens in Las Vegas leaving Peter with time to oversee the San Francisco operation which consists of physical product R&D / sales and an educational/event center. Red System Ventures seeks to make sex toys that should exist but don't. We are investing heavily in new product development and aim to be the leader in innovative, internet connected toys, with a leaning towards ‘alternative sexuality' such as BDSM. Culture: we are fascinated by sex toys and work tirelessly, we are excited by the trajectory which includes remote control of toys and integration with our upcoming ‘fans' website, kink.com itself, and syncing of toys to movies. Here are examples of projects: ********************************************** HOW TO APPLY Please send a resume / portfolio / reels to *************. Please also send a note as to why you think you would be a good fit and what motivated you to apply. Thank you!

Job title:- Manufacturing GMP Cleaner Duration:- 6 months Pay rate: $23/hr • Performs and coordinates GMP cleaning and Sanitization of process areas on the manufacturing floor as assigned related to the manufacturing of bulk drug substance in a multi-product facility. • Responsible for cleaning, sanitization of small parts and hoses used in the manufacturing process. • Performs duties under limited supervision and according to standard operating and manufacturing procedures. • Documents work according to cGMP and cGDP. • Adheres to established regulations and follows cGMP established by site. • Reports abnormalities and deviations in a timely and accurate manner. • Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately. • Maintains production areas according to predefined standards (5s). • Prepares cleaning solution applicate to the area. • Cleans specified rooms on the manufacturing floor using approved cleaning solution, wearing appropriate PPE including respirator maybe required. • Perform other duties as assigned such as, trash removal, floor to ceiling cleaning, tidying up areas (5S), and potentially cleaning of small parts and equipment, performing real time documentation of cleaning in each area. • Responsible to be current with online training and qualifications. • Working in a highly regulated environment following all applicable client and client Fremont SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies. • Required to work according to given schedules in a 24/7 shift structure and flexibility to adapt working schedule upon prior given notice. • GMP room cleaning and trash removal. Skills: • 1 or more years of experience in cGMP regulated industry desired. • Physically demanding, requires great attention to details and thorough accurate ability to document activities real time. • Moderate to high - strong focus on execution of tasks with moderate technical complexity. • Performs moderate proceduralized tasks. • Identifies process anomalies and areas for improvement for operations. • Strong working knowledge of fundamental manufacturing concepts is required. • Moderate technical knowledge of biologics operations is preferred. • Ability to concentrate on detail-oriented work in a moderate technical setup with a Quality and Right the first-time mindset. • Strong written and verbal communication skills. • Ability to work with computer-based systems and ideally experience with process. • Must become familiar with cleaning chemical components and safety requirements. PHYSICAL DEMANDS: • Wear proper PPE that may include respirator to protect from cleaning agents, safety shoes, gloves. • Must be able to obtain full medical respiratory clearance and successfully complete respirator fit test. • Ability to perform repetitive motions and may require bending and reaching overhead, ability to lift up to 40 lbs. NOTE: • WORKERS MUST SUCCESSFULLY COMPLETE A RESPIRATOR FIT TEST AS WEARING A RESPIRATOR WILL BE REQUIRED FOR THIS POSITION. • SUCCESSFUL FITTING OF RESPIRATOR MUST BE COMPLETED PRIOR TO START OF ASSIGNMENT. Education: High School Degree, desired 1-2 years' work experience in GMP regulated industry. Skills Required CGMP VISUAL INSPECTION DETAIL-ORIENTED REAL TIME DOCUMENTATION

Operate semiconductor and metrology equipment. Provide technical support and assistance. Set up process equipment for operation. Conduct technical tests and experiments for process engineering within research and development. Monitor and audit line operators, offering guidance as needed. Execute process test runs and compile records, charts, and graphs to present results to engineering teams, aimed at identifying yield issues or testing new products. Offer technical assistance to personnel in process development and engineering. Conduct laboratory activities for customer demonstrations and process experiments, including sample preparation, chemical treatments, and running wafer flows on company tools. Use metrology tools to perform measurements, including thin film measurements, CD measurements, and SEM imaging. Develop process recipes from scratch and fine-tune existing recipes for robustness, suggesting improvements as necessary. Implement statistical process control (SPC) and etch rate measurements, including evaluation and reporting to ensure that chamber performance remains in control and meets specifications; identify trends or out-of-spec conditions and propose troubleshooting actions. Follow customer instructions to determine target pattern features for first sample cleaving using microscopes, top-down SEMs, and micro-cleavers, and create or update PowerPoint instructions for others to follow. Train new process engineers, technicians, or field service engineers on lab equipment operation, sample preparation, and adherence to lab protocols. Serve as the first point of contact for alarm resolution, lab operations, and protocol inquiries. Collaborate with demo engineers and the metrology team to develop metrology recipes. Recommend enhancements to experiment execution for improved quality and efficiency. Operate computer interfaces and navigate diagnostic software as necessary. Work with the lab operations team to enhance lab safety, customer intellectual property, and lab protocols. Qualifications: Preferred experience in a clean room environment, with the ability to wear personal protective equipment (PPE) such as bunny suits, safety glasses, masks, shields, gloves, and safety footwear. 2-3 years of experience with silicon wafer handling is preferred. Ability to understand process requirements and execute experiments with minimal supervision. Familiarity with company tool operations, with skills to clear basic alarms and troubleshoot to minimize tool downtime. Degree in electronics, material science, chemistry, physics (Associates or BS) or equivalent work experience. At least 4 years of experience in the semiconductor industry, particularly in troubleshooting or operational roles. Demonstrates flexibility and responsiveness to changing priorities, including willingness to rework and work overtime. Able to install components from a height of 1 to 6 feet and reach into machinery for task completion. Proficient in using computer interfaces and diagnostic software. Basic proficiency in Microsoft Office applications (Excel, Word, PowerPoint). Strong communication skills to convey detailed pass-downs for seamless lab operations. Excellent attention to detail and organizational skills. Capacity to work independently as well as collaboratively in a team setting. Strong analytical and problem-solving abilities. Education: BS in Material Science preferred or equivalent relevant experience. Pay for this position is based on market location and may vary depending on job-related knowledge, skills, and experience. As a contractor, you may also be eligible for health benefits such as health, dental, and vision as well as access to a 401K plan. We are an equal-opportunity employer and value diversity at The Mice Groups Inc. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Pursuant to the San Francisco Fair Chance Ordinance, we will consider employment-qualified applicants with arrest and conviction records. Pursuant to the Los Angeles Fair Chance Ordinance, we will consider employment-qualified applicants with arrest and conviction records. The Mice Groups Inc. values your privacy. Please consult our Candidate Privacy Notice, for information about how we collect, use, and disclose the personal information of our candidates.

Come join an industry leader! Bellingham Marine is seeking a Concrete Quality Control Technician in Dixon, CA! Enjoy competitive wages, profit sharing, generous PTO and holiday schedule, 401k with employer contribution, and a full suite of health care benefits. You'll work in a team-oriented environment that puts safety first, including Covid-19 protocols. Location: Dixon, CA SUMMARY: Performs any combination of the essential duties and responsibilities of quality control at manufacturing facility in Dixon, CA. Successful candidates will be required to participate in a pre-employment drug screen and random drug screening per our Drug Free Workplace policy. Dependability for work schedule is crucial. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Inspects cast floats, float assemblies, and metal fabrications, hardware components, and lumber; * Inspects the casting process per drawing requirements; * Performs concrete tests per ACI / PCI and customer specifications; * Scans production and inspection documents; * Conducts safety tasks and inspections as required by The BMI Safety Program; and * Documents and records QC activities. * Performs other duties as assigned. COMPENSATION: Hourly wage between $22.00 - 25.00 dependent upon experience. Employee may receive Incentive Bonus Pay based on eligibility rules. * ?Competitive salary and benefits package including bonus programs * Opportunities for growth, development and career advancement * A supportive work environment where your expertise, work ethic and leadership is valued * Employer 3% contribution to your 401k account. Our 401k includes a ROTH deferral option. * A robust health benefit package including: medical, prescription, dental, vision, Employee Assistance Program, $1,000 annual contribution toward employee HSA account, basic life insurance, telemedicine, voluntary life insurance, long term disability, optional critical illness, accident and hospitalization policies. Benefits come with a customer care center for assistance with your health insurance questions. #SW

At Niagara, we're looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water. Consider applying here, if you want to: * Work in an entrepreneurial and dynamic environment with a chance to make an impact. * Develop lasting relationships with great people. * Have the opportunity to build a satisfying career. We offer competitive compensation and benefits packages for our Team Members. QA Technician Responsible for executing corporate and plant specific Food Safety, Quality and Laboratory requirements. The QA Technician reports to QA Manager. In the absence of the Quality Assurance Technician, the QA Manager or designate will assume the job duties. Essential Functions * Ensure all parameters of food safety and quality are being adhered to and maintained throughout the facility. * Assist with batching chemicals/ingredients for production. * Calibrate lab and line equipment for accurate results. * Collect in-process and finished product samples. * Conduct standardized qualitative and quantitative testing to ensure it meets specifications. * Perform aseptic testing for microbial contamination. * Follow protocols for documenting testing results. * Recognize deficiencies and initiate proper follow-up. * Identify and isolate product that does not meet standards. * Aid in troubleshooting deficiencies and non-conformances. * Review food safety and quality records. * Actively participate in plant teams (HACCP, Safety, etc.) * Conduct other duties as assigned by management. * Please note this job description is not designed to contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without prior notice. Qualifications * Minimum Qualifications: * 0 Years - Experience in Field or similar manufacturing environment * 0 Years - Experience in Position * 0 Years - Experience managing people/projects * experience may include a combination of work experience and education * Must read, write and communicate in English. * Must be able to work 12 hour shift (days or nights) on a rotating schedule * Must follow GMP Policy - wear company issued shirt, hat, safety glasses, earplugs and hairnet in production areas. * Able to lift up to 50 lbs. * Able to work under pressure in a very fast paced environment * Preferred Qualifications: * 2 Years- Experience in Field or similar manufacturing environment * 2 Years - Experience working in Position * 2 Years - Experience managing people/projects * experience may include a combination of work experience and education Competencies This position embodies the values of Niagara's LIFE competency model, focusing on the following key drivers of success: * Lead Like an Owner * Makes safety the number one priority * Keeps alert for safety issues and escalates immediately * Effectively prioritizes tasks based on department goals * Shows respect to others and confronts interpersonal issues directly * Prioritizes resolution of customer issues effectively * Responds promptly and honors commitments to internal and external customers * InnovACT * Makes recommendations to continuously improve policies, methods, procedures, and/or products * Demonstrates adaptability by reacting appropriately to unexpected changes in situations or circumstances * Increases performance through greater efficiency * Find a Way * Seeks to develop technical knowledge through learning from other experts * Understands interdepartmental impact of individual decisions and actions * Seeks solutions rather than placing blame * Empowered to be Great * Consistently looks for ways to improve one's self through growth and development opportunities * Communicates clearly and promptly up, down, and across * Communicates effectively to manage expectations Education * Minimum Required: * High School Diploma * Preferred: * Associate's Degree Certification/License: * Required: N/A * Preferred: HACCP Foreign Language * Required: Full Professional Proficiency * Preferred: None Required Typical Compensation Range Pay Rate Type: Hourly $22.95 - $30.41 / Hourly Benefits *********************************************** * *Los Angeles County applicants only Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable local and state laws. Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees. Niagara Plant Name STOCKTON 3

JOB DETAILS Base pay starts at $23.00 per hour + $1.00 Shift Differential Shift: 2nd - 3:00 pm - 11:30 pm, Monday-Friday (includes overtime) DUTIES AND RESPONSIBILITIES The Quality Technician conducts detailed inspections of fabricated parts, in process control inspections. Conducts audits of packaged, staged and loaded shipments to ensure compliance with Ply Gem quality requirements and specifications. * Knows and understands all safety rules and precautions necessary for working in and about a manufacturing environment * Responsible for monitoring, inspecting, and reporting all assigned activities and finished goods to ensure quality * Ability to submit clear, concise, and accurate reports of inspections, audits, test results, job site visits and delivered goods * Ability to conduct tests using a variety of tools and equipment * Responsible for preparing daily quality control activity summaries * Ability to assist in developing and implement objectives, plans and priorities to achieve quality control objectives in a timely manner to meet deadlines * Communicates with Quality Manager on methods and problem-solving procedures to successfully meet deadlines * Assists and periodically delivers internal external audits * Maintains continuous improvement practices in work area * May be assigned additional projects or duties as designated by Team Leader * Ability to complete and present basic Root Cause analysis * Inspect all incoming raw materials per inspection plan * Record and maintain receiving inspection results * Completes first article quality reports * In-Process Verification of calibration tools for all inspection test equipment and tools * Maintains gage calibration database and records * Perform product test and records results during product manufacturing * Ensures adherence to production practices and product quality standards * Assists in the documentation of and resolution of nonconforming material and process discrepancy * Evaluate product to determine if they are acceptable * Perform start-up and changeover audits to verify that the product will meet specifications * Proficient at using Microsoft office Qualifications To perform satisfactorily in this position, the employee must be able to perform each essential duty satisfactorily. The requirements listed below are representative of knowledge, skills, and/or ability required. Reasonable accommodations may be made for employees with certain disabilities to perform the essential functions. Language Skills: * Ability to read and comprehend documents including but not limited to policy manuals, safety rules/programs, operating and maintenance instructions, procedure manuals, and simple correspondence, in addition, the ability to communicate information effectively one-on-one and in small group situations and settings is required Mathematical Skills: * Ability to perform general mathematic calculations including but not limited to addition, subtraction, multiplication, fractions, percentages, and division * Some positions may require advance mathematics Reasoning Ability: * Ability to apply common sense understanding to perform work instructions furnished in written, oral or diagram form a must. In addition; the ability to solve problems, which involve multiple variables in a standard situation, is required Other Knowledge, Skills & Abilities: * Must have a high degree of concentration * Ability to work effectively to meet deadlines * Ability to work with a diversified work force * Ability to read different measuring devices (i.e. tape measure, protractor, micrometer) Physical Demands: * While performing the duties of the job, the employee is regularly required to talk or hear * The employee is frequently required to walk * The employee is frequently required to stand; sit; bend; stoop; use hands and fingers to handle or feel objects; reach with hands and arms; lift; climb and/or balance essential tasks * Specific vision abilities include close-up and distance vision, color vision, peripheral vision, and depth perception Work Environment: * The employee may be required to enter areas that are near moving mechanical parts, with occasional exposure to hazardous chemicals, and extreme cold or heat * The noise level in the work environment is considered moderate, and may require the use of hearing protection * The employee will be required to utilize Personal Protective Equipment (PPE) when accessing certain manufacturing areas: hard hat, gloves, welding jacket or weld bibs, safety glasses, welding hood and earplugs Safety Responsibilities: * Before initiating work at Simenton, the employee is required to read and understand the position's Job Safety Analysis * The employee must wear appropriate Personal Protective Equipment (PPE) and perform tasks in a manner consistent with Ply Gem safety training, Ply Gem Employee Manual and OSHA regulations Additional Information Address: 2019 E Monte Vista Ave, Vacaville, CA 95688 Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play. Full-time* team members receive medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. You can also join one of our Employee Resource Groups which help support our commitment to providing a diverse and inclusive work environment. * Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement. All your information will be kept confidential according to EEO guidelines. The US pay for this full-time position is $23.00 per hour + medical, dental, vision benefits starting day 1 + 401k and PTO. (Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.) Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. You can find the Equal Employment Opportunity Poster here. You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here. If you'd like to view a copy of the company's affirmative action plan or policy statement, please contact Human Resources at ************ or *******************************. If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or *******************************. This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.

0 0 **About** Applied Aerospace Structures Corp is located in Stockton CA. We specialize in design, fabrication and testing of lightweight Aerospace Structural Assemblies. Our Quality Inspectors work closely with program teams throughout the manufacturing process. They collect data, as well as, inspect parts and materials. Inspectors must know AMSE Y14.5 (GD&T).Inspectors must have sufficient computer skills and be able to read and understand blue prints and customer specifications. They also must be able to communicate well with others. Laser Trackers or 3D experience is a plus. Inspectors should have experience with calipers, micrometers, etc. Applied Aerospace pays competitive wages and benefits. We offer Medical, Dental, Vision, 401K plan, and life insurance. The company has 9 paid holidays per year. AASC is a EOE/M/F/D/V. **Contact** P.O. Box 6189 Stockton, California 95206 United States Fax: ************

* Posted 16-Dec-2024 (CST) * 942 South Stockton Avenue, Ripon, CA, USA * 22.45-24.45 per hour * Hourly * Full Time * *Paid Medical, 401k, Profit Sharing* Email Me This Job **JOB SCOPE** : The Quality Control Technician's overall responsibility, and objective, is to ensure that all aspects of the SQF, Quality, and Food Safety Programs are followed by all employees, vendors, visitors, etc. **Work Environment: Graveyard Schedule 6pm - 6:25am 12hr** **Shifts** (Alternative Work Schedule Including Weekends) **ESSENTIAL DUTIES AND RESPONSIBILITIES:** • Routinely check operator paperwork for accuracy and completeness. • Assure checks are documented clearly, cross referenced and traceable. Communicate results of routine QA tests to production personnel. Notify supervisory personnel and Quality Control and Food Safety Manager of product quality or plant conditions which may have a negative impact on product quality and work together to correct the situation. • In the case of finished product, perform follow-up testing until situation is corrected and product disposition is resolved in a quality conscious manner. • As directed and trained, conduct various tests for incoming ingredients, including sieve, NIR, moisture, and mycotoxin testing. • Maintain and report hold/reject product and assure its proper disposition. • Collect routine ingredient and finished product samples, as required (detailed in QA Manual). • Train and educate all personnel on quality and food safety practices. • Promptly respond to calls for assistance clearly communicating and ETA of arrival. • Promptly respond to quality/food safety concerns, following up as needed. • Follow First In First Out (FIFO) and enforcing other departments to follow the same process. • Continuously work with and/or assist production, maintenance, and sanitation personnel as needed throughout the shift. • Maintain a clean work environment and stock supplies as needed for next shift. • Ensure, and hold accountable, all personnel, visitors, vendors, etc. comply with all Standard Operating Procedures (SOPs) in addition to all SQF, Quality, and Food Safety Programs. • Maintain accurate, complete, and legible paperwork. **QUALIFICATIONS, EDUCATION & EXPERIENCE REQUIRED:** • Must successfully pass a pre-employment drug test, physical (physical, lifting, hearing, and vision), and background check. • Minimum of 2-year experience in a Quality Control position preferred. • AA Degree in a related field would be accepted in lieu of experience. • Skilled in computer work involving Microsoft Office. You must select a location. You must select an education status answer. You must select a seeking status answer.

Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. As a team, we've launched two satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $500 million from top global investors, and recruited a team of over 300 world-class engineers. We all work out of our (legendary) San Francisco office, which was once used to build ships during the World Wars. Our satellites, which operate from geostationary orbit (GEO), weigh only 400 kg and utilize a proprietary software-defined radio payload. Each satellite can connect over two million people, and we're very excited for the impact we'll soon have in the Philippines, Peru, Mexico, and more! Backed by substantial funding and a passionate, collaborative team, we offer a rewarding work environment where you'll learn and make a significant impact, no matter where you are in your career. Apply and join us on our journey towards global connectivity! Production Quality Inspector As a Production Quality Inspector, you are responsible for being the last line of defense in assuring mission success. You will work with the most cutting edge MicroGEO satellite technology and perform inspections in several workcenters to verify our hardware meets the highest level of quality. The ideal candidate is self-driven, extremely detail oriented, and seeks a highly cross functional dynamic environment. Responsibilities Perform in-process inspection and final verification of flight hardware to drawing, process specifications, and work order requirements supporting multiple work centers (assembly, integration, wire harnessing, or test) Identify, document, and verify resolution of production and test non-conformances in accordance with prescribed procedures and pursue corrective action as required Interface with engineering and production to communicate and help resolve nonconforming issues Independently perform verifications and document results in a clear, precise, and complete manner Support quality management system policies and procedure documentation, assess compliance to company and industry standards, initiate and lead continual improvement and lean manufacturing initiatives Perform other related duties, as assigned, for the purpose of ensuring an efficient and effective work environment Requirements 3+ years of inspection experience in an aerospace, military or manufacturing environment Substantial knowledge of the control of nonconforming hardware, failure/root cause analysis, corrective and preventive action processes Experience reading and interpreting design drawings and CAD models Experience with performing electronic testing and inspection using portable measuring devices and lab equipment (microscopes, testers, scopes, etc) Excellent communication (written and verbal) and teamwork skills Ability to work independently with a strong work ethic, be innovative, detail oriented, possess initiative, and team oriented Willing and able to work overtime and/or weekends as required Bonus Associate degree or higher in quality, engineering, or related field Knowledgeable with ISO 9001/AS9100 quality management systems Experience inspecting solder, crimping, conformal coating, staking, and surface mounted devices in accordance with IPC-J-STD-001 or IPC-A-610 standards Wire harness experience in accordance with IPC-A-620 standards Six Sigma Yellow/Green Belt certified What we offer: All our positions offer a compensation package that includes equity and robust benefits. Base pay is a single component of Astranis's total rewards package, which may also include equity in the form of incentive stock options, high quality company-subsidized healthcare, disability and life insurance benefits, flexible PTO, 401(K) retirement, and free on-site catered meals. Astranis pay ranges are informed and defined through professional-grade salary surveys and compensation data sources. The actual base salary offered to a successful candidate will additionally be influenced by a variety of factors including experience, credentials & certifications, educational attainment, skill level requirements, and the level and scope of the position. Base Hourly Pay $30 - $40 USD U.S. Citizenship, Lawful Permanent Residency, or Refugee/Asylee Status Required (To comply with U.S. Government space technology export regulations, applicant must be a U.S. citizen, lawful permanent resident of the United States, or other protected individual as defined by 8 U.S.C. 1324b(a)(3)) Our mission and our products are meant to connect the world and everyone in it, regardless of gender, race, creed, or any other distinction. We believe in a diverse and inclusive workplace, and we encourage all people to join our team and bring their unique perspective to help make us stronger.