Quality control analyst jobs in Yucaipa, CA

FirstCarbon Solutions (FCS), an ADEC Innovation, is focused on improving the world we live in. It's our goal to improve the lives of all the people we work with, whether they are clients, partners, or colleagues. Come join our team of amazing professionals dedicated to making the world a better place! FirstCarbon Solutions is searching for an Air Quality Scientist (CG06 - CG07) to join our team. The ideal candidate will be able to perform emission, air dispersion, and/or health risk modeling independently within minimal supervision. This role requires good knowledge of air quality and greenhouse gas emission regulations and legislative updates. The candidate needs to be a strong writer with extensive experience writing air quality, greenhouse gas, and energy sections pursuant to CEQA. The ideal candidate will also provide training and mentorship to junior staff and promote teamwork through interpersonal skills. This will report to the Senior Air Quality Scientist. This role is an evergreen position, meaning we are always looking for talented individuals to join our team. Applications for this position are continuously accepted and reviewed on a rolling basis. Duties and Responsibilities Review site plan and project information, coordinate with client on data needs, and gather all data necessary to conduct technically and legally defensible air quality/air dispersion/health risk modeling Author technically and legally defensible air quality, greenhouse gas, and energy analyses and technical appendices to be included in CEQA and NEPA environmental documents. Use approved software models, such as the California Emissions Estimation Model (CalEEMod) and EMFAC, to estimate a project's air pollutant emissions. Develop and quantify emission reduction potential of appropriate mitigation measures, if needed Use air dispersion models, such as AERMOD and HARP, to evaluate the project's construction-related and operational-related emission and health impacts. Strong knowledge of various Air District guidelines and latest greenhouse gas emission legislative updates Skills Ability to conduct air quality assessments. CalEEMod, AERMOD, and/or HARP experience Provide effective and quality communication through written and oral methods. Marketing and proposal preparation. Demonstrated proficiency in MS Office applications, especially Word and Excel, as well as internet usage. Education and Experience Bachelor's degree in environmental sciences or related field required, master's degree in environmental management or equivalent a plus. 5-7 years of experience in Environmental Services, air quality and/or greenhouse gas emission inventory quantification and modeling skills including AERMOD, CalEEMod, ArcGIS and other software models. Other air permitting or assessment/modeling experience highly desired. Work Environment The position operates in a dynamic and highly collaborative working environment. FCS provides our staff the opportunity to elect remote, hybrid home/office as well as as-needed field assignments (under COVID-19 safety regulations). This role routinely uses standard office equipment. This position may require some travel to attend meetings as well as fieldwork. Competitive, progressive benefits including Salary: $84,300 - $109,100 FCS offers competitive salaries and robust benefits with opportunities for personal and professional development. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply! Remote/Hybrid/in-office work location options Escalating PTO structure Up to 10 paid holidays (up to 4 are flexible holidays) Full health care package: Up to 100% employer-paid employee medical and 55% eligible dependent coverage* 80% employer-paid dental and vision Employer-paid Life and AD&D insurance Short- and long-term Disability insurance Employee Assistance & Wellness Program 401k & Roth Pet insurance discounts 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. While performing the duties of this job, the employee is regularly required to talk and hear; have hand/finger dexterity; and reach with hands and arms. The employee will spend extended periods of time in front of a computer/laptop. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus. Compliance with all ADECi & FCS Travel and Workspace Policies that align with the CDC, local, state, and federal guidelines must be followed and upheld. Information Security Adhering to all policies, guidelines, and procedures pertaining to the protection of information of the organization, employees must maintain confidentiality of all sensitive information to which they are given access. They are also responsible for reporting actual or suspected events or incidents, including vulnerabilities or breaches, that may affect the confidentiality, integrity, and availability of information to members of the Management Team. Mutual respect is fundamental. Fundamental to our teams. Fundamental to our clients. Fundamental to the communities we serve and live in. Fundamental to the landscapes we work within. We need you and your unique talents, history, and background to become the Company we aspire to be. We insist upon a culture of common respect, expect transparency, and celebrate the fundamental value and dignity of all individuals. Our mutual equality as humans is the path to diverse and innovative collaboration. We cultivate integrity, driving us to growth, and allowing us to achieve more together than we could ever hope to as individuals. FCS offers competitive salaries and robust benefits with opportunities for personal and professional development. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply!

Job Description Astrophysics Inc. is a leading global designer and manufacturer of X-Ray security inspection systems. Since 2002, we have dedicated ourselves to ensuring a safer world through advanced X-Ray screening and imaging technology. Our systems are deployed in critical infrastructure, aviation, and ports and borders sites in more than 140 countries. Hotels, prisons, courthouses, embassies, airports, military bases, and government buildings around the world depend on us for their safety and security. Astrophysics is an expanding, dynamic and fast-paced company looking for individuals who want to grow with us and be a part of a meaningful security mission. We currently have an immediate full-time position opening for a Quality Control Inspector located in City of Ontario, California. Job Summary: The Quality Control Inspector I is responsible for the inspection of x-ray imagining systems and components based on established inspection criteria. Inspections consist of verifying software and hardware functionality. Inspections also include verifying and approving the visual aspects of each unit, paperwork, electrical and imaging inspections. All inspection activities will be recorded on appropriate forms. Essential Duties: • Perform in-line quality inspections to insure product is produced in accordance to documented procedures, work/assembly instructions, and/or drawings. • Perform Final QC inspections as per documented procedures. Properly fill out form F-82-03-06 Final Quality Control Report • Review final QC inspection paperwork and imaging with Quality Control Supervisor or Quality Control Inspector III before release to shipping. • Verify that all paperwork from previous operations are properly filled out before release of product. • Prepares reports of findings and report inspection and test data to the Quality Control Supervisor • Follow daily work assignments as delegated by the Quality Control Supervisor. • Upon successful completion of final inspections, release product to the shipping department. • Perform QC paperwork maintenance assignments such as sorting, filing and copying as determined by the Quality Supervisor. • Assists with QC line inspections, i.e.: Label Placement, QC report, Packaging • Identify the procedure required to conduct quality test and inspections. • Follow inspection procedures as outlined in SOP-82-03 Quality Control Inspections. Line Inspection • Perform line inspection by performing audits of paperwork, labels, and visual inspection of frame & panels. • Perform line inspections as per documented procedures • Operates independently from the production function, to assess and determine quality status of goods at each stage. • Follow up and maintain all documentation regarding incoming inspection Education and Experience: • Strong attention to details, highly organized • Computer literate to include experience in navigating and manipulating file systems • Ability to multi-task and work in a fast paced environment • Effectively deal with personnel from other departments • Ability to read and write in English • High school diploma or equivalent • 0-2 years similar work experience required • Very good understanding of measuring techniques and tolerance call-outs • Proficient in the use of measuring equipment such as rulers and micrometers. • Experienced in visual inspections to determine material defects and paint imperfections Excellent benefit package including 401K plan with Employer Match 11 Paid Holidays, 10 PTO Days, Free Donuts on Fridays, Company Luncheons and year end Party! PLEASE APPLY AT: ************************************************** Equal Opportunity Employer Astrophysics Inc. provides equal employment and advancement opportunities to all individuals. Employment decisions at Astrophysics Inc. are based on merit, qualifications and abilities. 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. If you need assistance or an accommodation while seeking employment, please call *************** and ask for Human Resources. Determinations on requests for reasonable accommodation will be made on a case-by-case basis. Powered by ExactHire:185618

Works to ensure that the quality of orthotics is up to standard for shipping and measurements for orders are within the bounds of reasonability. We would like to get to know you more. Using Loom.com, please record an introduction video (maximum of two minutes) and tell us more about your passion and experiences. You will be asked to paste the link to the video on the application form. This position is remote and on -site in Riverside, CA. Responsibilities: Ensures quality of materials in orthotics Ensures that finished orthotics meet physical standards Orthotics are not too wide/narrow, too short/long, or etc... Verifies the legitimacy of orders placed Double -checks the orders placed by order entry Verifies measurements for modifications that seem highly unusual, if not impossible Requirements Previous experience in an orthotics lab Understanding of human biomechanics and anatomy High School Graduate or GRE equivalent Ability to work as a team member Capability of communicating across departments for quality control Meticulous with an eye for details

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Nature and Scope Perform QC related work including, but not limited to, preparing/performing analysis samples from all phases of a manufacturing or other handling processes and creating/revising SOPs. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Perform QC testing in all phases of manufacturing including raw material, in-process, bulk, finished goods and stability testing. Conduct various laboratory procedures as per manufacturing/QC SOPs. Assist fundamental tasks for special projects on analytics and instruments. Prepare and maintain testing records. Involve in procedure review and propose modifications and updates. Support design and development of experimental protocols, SOP's, etc., consistent with cGMP/GLP. Under general supervision, manage own time effectively, maintains control over all current assignments and responsibilities. Perform any other tasks/duties as assigned by management. Additional Qualifications/Responsibilities Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. BS degree in Chemistry, Biology or equivalent combination of education and experience. Up to 2 years of related quality control and quality assurance in the pharmaceutical industry. Require/Preferred Experience with specific equipment/software/programs etc. Clean, organize and legible documentation. Knowledge of cGMP environment is a plus. Able to follow, create, maintain, and organize documents per established company guidance. Knowledge of workplace safety and safe materials handling as appropriate Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. Ability to work overtime as needed. Physical Environment and Requirements Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees. Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. Specific vision requirements include color vision. Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly. Employee must be able to occasionally lift and/or move up to 50 pounds. Expected Salary Range: $33.70-35.00

Who Are We? UniUni is a Canadian last-mile e-commerce logistics company that is one of the fastest-growing companies in Canada. As a platform that seamlessly integrates advanced technology with efficient delivery solutions, UniUni enables businesses to provide a superior online shopping experience, ensuring unparalleled efficiency and customer satisfaction. Catering to a diverse range of clients-from emerging e-commerce platforms to established online retailers and brands-UniUni offers exceptional service across North America. Recognized as the fourth fastest-growing company in Canada, UniUni continues to set industry standards, offering a robust, customer-centric approach to e-commerce logistics. What Do We Offer? At UniUni, we offer exciting opportunities to our employees to achieve their career goals. We believe all roles should develop your skills, broaden your experience, and help you build a rewarding career. If you are ready to join UniUni's dynamic team, while working hard and having fun doing it, we invite you to apply online and let us know how you can be part of our success story. Job Description： The Quality Control Assistant plays a crucial role in maintaining and improving delivery service standards. By ensuring POD accuracy and monitoring key logistics data, this role directly impacts customer satisfaction and operational efficiency. The assistant helps prevent delivery disputes, reduces errors in the supply chain, and contributes to overall service quality improvement. Additionally, the role requires collaboration with various departments to develop and enforce quality standards. The Quality Control Assistant is responsible for ensuring the accuracy and quality of last-mile delivery services by inspecting Proof of Delivery (POD) data and monitoring key performance metrics. This role involves managing a team to oversee delivery quality, identifying potential issues before customer complaints arise, and analyzing data to optimize logistics operations. Requirements Bachelor's degree or higher in Data Analysis, Computer Science, Logistics, or related fields. Experience with Tableau and Power BI for data visualization and reporting. Proficiency in Excel, Google Sheets, and other data management tools. Knowledge of Python or other programming languages for data processing is a plus. Strong time management and prioritization skills. Ability to multi-task and handle multiple responsibilities effectively. Detail-oriented, with a strong focus on data accuracy and quality. Proficient in written and verbal communication in both Mandarin and English. Previous experience in quality control, logistics, or data analysis is preferred but not required.

Job Title: Quality Control Inspector (Aerospace Job Shop) Department: Quality Assurance Reports To: Quality Manager Employment Type: Full-Time We are seeking an experienced Quality Control Inspector with a minimum of 5+ years in aerospace manufacturing to join our fast-paced job shop in Corona, CA. This role is responsible for performing in-process, first article, and final inspections using advanced measurement tools, including portable CMM equipment such as a Romer Arm. The ideal candidate must be highly proficient in GD&T, blueprint interpretation, and AS9100 requirements. Key ResponsibilitiesInspection & Measurement Perform first article, in-process, and final inspections on aerospace components in accordance with customer, engineering, and industry standards. Operate and program Romer Arm or similar portable CMM equipment to perform high-accuracy dimensional inspections. Use precision measurement tools including calipers, micrometers, height gauges, surface plates, bore gauges, and optical comparators. Interpret and apply Geometric Dimensioning & Tolerancing (GD&T) to inspect complex features and assemblies. Document inspection results and complete required forms, reports, and digital records. Quality Assurance Ensure products meet all customer specifications, engineering drawings, and AS9100/ISO quality standards. Identify, document, and report nonconformances; assist in root cause analysis and corrective actions. Support the creation and maintenance of First Article Inspection Reports (FAIRs) to AS9102 standards. Verify certifications, material traceability, and documentation packages for final release. Manufacturing Support Work closely with machinists, engineers, and production staff to resolve quality issues on the shop floor. Provide feedback on manufacturability, drawing interpretation, and potential process improvements. Assist in developing inspection methods and fixturing when required. QualificationsExperience 5+ years of Quality Control/Inspection experience in an aerospace or precision machining environment. Strong, hands-on experience with Romer Arm / portable CMM inspection tools. Proven expertise in GD&T (ASME Y14.5) and interpreting complex aerospace drawings. Education High school diploma or GED required; technical training or certifications in inspection, CMM, or aerospace manufacturing preferred. Technical Skills Proficiency with: Portable CMM systems (Romer, Faro, or equivalent) GD&T application and interpretation Reading complex blueprints and 3D models Standard inspection equipment (manual and digital) AS9100 & AS9102 First Article requirements Experience with ERP/MRP systems and digital inspection software a plus. KPG123

Job DescriptionFrom Engine Bay to Payload, we protect vital structures and systems. Hera Technologies is a premier contract manufacturer specializing in high-precision metallic and non-metallic solutions for the Aerospace, Defense, Space, and Commercial Airline sectors. Our commitment to quality, innovation, and customer satisfaction has positioned us as an industry leader in the design, manufacturing and maintenance of thermal support systems. Our team is driven by excellence, integrity, and a passion for advancing aerospace technology. Take the next step in your career with a company committed to excellence, where your contributions are recognized, and your potential is realized. Take the next step in your career with a company committed to excellence, where your contributions are recognized, and your potential is realized. Role OverviewThis is a full-time, on-site role for a Quality Control Inspector located in Ontario, CA. The Quality Control Inspector will be responsible for conducting inspections, ensuring quality control and quality assurance, and managing quality-related processes. The inspector will perform regular quality checks, document findings, analyze quality data, and maintain records. The role also involves collaborating with other team members to identify and address any quality issues and implementing corrective actions to ensure products meet the company's standards.Key Responsibilities Conduct in-process and final inspections of products to ensure conformance to standards. Perform regular quality checks, document findings, and analyze quality data. Maintain accurate and detailed records of inspections and test results. Collaborate with production teams to identify and address quality issues. Assist in implementing corrective actions to ensure products meet company standards. Ensure all processes and products adhere to industry standards and regulations. Required Qualifications Proven experience in Quality Control, Quality Assurance, and Inspection. Experience with Quality Management systems and processes. Strong communication skills. Excellent attention to detail and problem-solving abilities. Ability to work independently and as part of a team. Knowledge of industry standards and regulations. Associate degree or equivalent relevant experience. Preferred Qualifications Bachelor's Degree is preferred. Additional certifications in quality control or related fields are a plus. Previous experience in a manufacturing or fabrication environment is beneficial. Additional Requirements: Willingness to work long hours and weekends when needed to meet critical deadlines Willingness to travel to customers' locations or other Hera sites as needed Ability to use a computer and most common software programs to complete assignments Ability to communicate with individuals and groups in person, by phone and online Job DetailsType: Full TimeBusiness Hours: 7:00 AM - 3:30 PM or 2:00 PM - 12:30 AMHourly Range: $25 to $33Base Location: Ontario, CATravel: Up to 10% Your actual level and base salary will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, education, and experience. The base salary is just one part of your total compensation package at Hera. You will also have access to a comprehensive set of benefits like: Company paid employee medical, dental and vision insurance Retirement plan participation (eligibility required) Paid Sick LeavePaid VacationPaid holidays Discretionary bonuses Physical Requirements / Work Environments· Ability to work in office, lab, and manufacturing environments with occasional exposure to noise, dust, and temperature variations· Must be able to lift and carry up to 35 lbs and perform tasks involving standing, walking, bending, and manual assembly· Visual acuity required for reading technical drawings and digital media· Valid US driver's license and ability to operate motor vehicles The above statements are intended to describe the general nature and level of work performed. They are not intended to be an exhaustive list of all responsibilities, duties, or skills required. Management may modify or assign additional duties as needed. EXPORT CONTROL REQUIREMENTS:To conform to US Government export regulations, the applicant must be a (i) US Citizen, (ii) lawful permanent resident of the U.S. (aka green card holder), (iii) protected individual as defined by U.S.C. 1324b(a)(3), or (iv) eligible to obtain the required authorizations from the U.S. Department of State. Hera Technologies is an Equal Opportunity Employer, employment with Hera Technologies is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiologist I to work for a leading Orange County area biotechnology company. Pay Rate: $29-32/hour Summary:Perform microbiological testing of raw materials, intermediates, API, drug product release and stability samples, as well as collection and testing of environmental monitoring samples, in accordance with cGMP requirements, company policies and procedures as directed by laboratory management. Responsibilities Responsibilities: Perform routine microbiological laboratory analysis, such as Environmental Monitoring, Bioburden, Microbial Limits (preparatory & screening), Sterility, Endotoxin (Gel-Clot & Kinetic methods), operate autoclave, and prepare media in accordance with Customer, schedule and cGMP requirements. Read and understand test methodologies, study protocols, and Standard Operating Procedures in order to review or execute testing in compliance with necessary policies and procedures. Record/review data in controlled notebooks, data sheets, and electronic systems (i.e. LIMS, etc.) in accordance with cGMP requirements. Work on routine tasks where analysis of situations or data requires review and evaluation of limited factors, limited judgment is required in resolving problems and making routine recommendations. Exercise judgment within defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. Notify supervisor of any discrepancy in laboratory testing or general laboratory operations. In case of any observed discrepancies, initiate and follow through with the required quality exception documentation as needed. Assume ownership of assigned quality documentation, such as exceptions, change controls, and CAPAs, ensuring that documentation is initiated and closed on time, required actions are thorough and meet procedural requirements as well as customer needs. Obtain and maintain aseptic gowning qualification. Recommend equipment, facility and process improvements to your supervisor. Maintain clear, accurate and traceable manufacturing records to ensure compliance with Good Documentation Practices (GDP) Maintain laboratory and workspace cleanliness by adhering to the 5S method of organization. Abide by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor. This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary. Qualifications: Minimum of 1-2+ years industry experience. Bachelor's degree or equivalent in scientific discipline required. Knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to aseptic manufacturing operations. Knowledge of aseptic manufacturing regulations, aseptic technique, clean room behaviors, and environmental monitoring operations. Knowledge of USP, Pharm. Eur. and other compendial methods and procedures. Knowledge of microbiological practices, procedures, and common analyses, such as Environmental Monitoring, Bioburden, Microbial Limits (preparatory & screening), Sterility, Endotoxin (GelClot & Kinetic Chromogenic methods), validation - Inhibition/Enhancement Sterility Test Method Validation (Bacteriostasis/Fungistasis), and Preservative Efficacy Testing. Knowledge in the use of LIMS and electronic documentation systems (i.e. MasterControl). Please send resumes to *********************** and visit our website at ******************* for additional job opportunities!!!

Nature and Scope Perform QC related work including, but not limited to, preparing/performing analysis samples from all phases of a manufacturing or other handling processes and creating/revising SOPs. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Perform QC testing in all phases of manufacturing including raw material, in-process, bulk, finished goods and stability testing. Conduct various laboratory procedures as per manufacturing/QC SOPs. Assist fundamental tasks for special projects on analytics and instruments. Prepare and maintain testing records. Involve in procedure review and propose modifications and updates. Support design and development of experimental protocols, SOP's, etc., consistent with cGMP/GLP. Under general supervision, manage own time effectively, maintains control over all current assignments and responsibilities. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. BS degree in Chemistry, Biology or equivalent combination of education and experience. Up to 2 years of related quality control and quality assurance in the pharmaceutical industry. Require/Preferred Experience with specific equipment/software/programs etc. Clean, organize and legible documentation. Knowledge of cGMP environment is a plus. Able to follow, create, maintain, and organize documents per established company guidance. Knowledge of workplace safety and safe materials handling as appropriate Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. Ability to work overtime as needed. Physical Environment and Requirements Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees. Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. Specific vision requirements include color vision. Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly. Employee must be able to occasionally lift and/or move up to 50 pounds. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. FMLA poster: ********************************************************** Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: · All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. · Our recruiting process includes multiple in person and/or video interviews and assessments. · If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. · We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

Job Posting Start Date 11-04-2025 Job Posting End Date 12-05-2025 Crown Technical Systems, a Flex Company, is a leader in power distribution and protection systems concentrating on sophisticated, state-of-the-art relay and control panels, medium voltage switchgear, and enclosures (power/control buildings/ E-Houses). We specialize in customized, turn-key solutions that ensure safe, secure, and reliable power distribution. Working at Crown Technical Systems offers a dynamic and rewarding career path for individuals seeking to power the world. Through hands-on training, mentorship, and a culture of internal promotion, we empower you to reach your full potential and contribute to projects that truly matter. Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a/an Quality Control Inspector - Fabrication in USA, Fontana Ca. Reporting to the Production Manager the Quality Control Inspector - Fabrication is responsible for providing quality control and assurance throughout all phases of the production process including inspections of raw materials, in-process, and final products. What a typical day looks like: Performs visual inspections and other specified tests of incoming materials, in-process production, and finished products to confirm product meets drawings and specifications Uses observation and testing to identify faults in materials and manufacturing process Documents inspection results by completing inspection reports, logs, and checklists Communicates with supervisor to determine appropriate recommendations and remedies for questions regarding products Maintain quality records as needed Keeps inspection and measurement equipment operating by following operating instructions; and notifying management when repairs are necessary. Perform other related duties as assigned The experience we're looking to add to our team: High school diploma or equivalent 1-3 years' experience of quality inspections in a fabrication/manufacturing environment. Previous experience in an ISO 9001 Certified company Thorough understanding of the product and/or process being inspected Ability to read blueprints, specifications, and technical documents Excellent written and verbal communication skills Ability to handle multiple projects while maintaining attention to detail with the task at hand Proficient in Microsoft Office Suite or related software as needed to complete reports. What the physical requirements are: Prolonged periods standing and performing repetitive tasks. Must be able to lift up to 35 pounds at times. Dexterity and accuracy as needed to operate testing equipment or gauges. Must be able to bend, stretch, kneel, and squat to perform inspections Must be able to traverse production facility to conduct inspections Must wear PPE, such as gloves, safety glasses, hard hat, and ear protection, while working on the production floor #LI-GB1 What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Pay Range (Applicable to California)$18.33 USD - $24.75 USD HourlyJob CategoryQuality Is Sponsorship Available? No Crown is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Crown, you must complete the application process first).

Entry level laboratory analyst for work with GC-ECD samples. Duties include extraction/analysis of samples. Instrument maintenance, cleaning labware, preparation of reagents and standards. Following all laboratory protocol, following all standard operating procedures (SOPs) and adhering to any and all laboratory quality assurance protocols.Ideal Candidate will have experience with: Sample Analysis: Perform sample preparation, chemical analysis, and quantification of chemicals in accordance with EPA and standard methods Equipment Operation: Utilize advanced laboratory equipment such as Gas Chromatography (GC - FID, ECD, TCD), ICP, ICP-MS, CVAAS, GC-MS, UV-VIS analyses, balances, ovens, and more. Data Documentation: Maintain detailed records including laboratory notebooks, software data, standard preparations, and equipment logs. Equipment Maintenance: Conduct routine and in-depth maintenance, including troubleshooting laboratory equipment. Accreditation Support: Perform tasks required to maintain laboratory accreditation, such as running and reporting audit samples, completing MDL studies bi-annually, and updating documentation (e.g., SOPs, DOC forms). Quality Control: Perform and document standardizations, calibrations, and performance verifications daily. Safety & Compliance: Ensure proper sample custody, control, and hazardous waste disposal in compliance with safety protocols. Additional Duties: Assist with editing and reviewing SOPs, guidance documents, and other tasks as assigned. Essential Functions: Performs laboratory operations, including preparation, analysis, quantification of chemicals; prepares standards and samples for analysis, including quality control samples, and reports final results. Documents work performed; maintains laboratory notebooks, recordings, software data, etc. for raw data, standard preparations, and equipment Performs routine daily, weekly, and monthly maintenance of equipment Performs actions required to maintain accreditation; runs, reports, and passes audit samples bi-annually; completes MDL studies for each required method bi-annually, creates DOC forms for each quarter, and ensures all methods are run according to the requirements in each SOP Edits and reviews documents; reviews SOPs and guidance documents to ensure all procedures accurately reflect laboratory practices and meet NELAC and/or EPA requirements Maintains sample custody, control, and hazardous waste disposal Performs other job-related duties as assigned Required Qualifications: EDUCATION REQUIREMENT - Bachelor's degree in chemistry or science-related field Some experience in a laboratory setting Experience working with hazardous chemicals Familiarity with various sample methods STARTING PAY RATE: $20.00/hr.Knowledge, Skills & Abilities: General knowledge of chemistry and lab analysis operations and lab safety Proficiency in Microsoft Office programs, including MS Word and Excel Strong verbal and written communication skills Ability to lead a team and provide training and guidance to subordinates Professional demeanor and appearance; ability to serve as a representative of the company Ability to prioritize and multi-task Strong organizational skills and attention to detail Ability to read, count, and write to accurately complete all documentation Work Environment - While performing the duties of this job, the employee regularly works in a laboratory setting.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. Sitting or standing for extended periods and the use of hands to finger is common. Hearing and vision within normal ranges is helpful for normal conversations, to receive ordinary information and to prepare or inspect documents. Duties frequently involve repetitive motions and eye/hand/foot coordination. Testing priorities and timelines may serve as a source of emotional stress. Occasional heavy lifting is expected. Exertion of up to 30 lbs. of force may occasionally be required. While performing the duties of this job, good manual dexterity for the use of laboratory equipment is needed. The employee is occasionally required to walk, lift, carry, push, pull, climb, stoop, kneel, crouch, reach, handle, grasp, and feel. Use of applicable Personal Protective Equipment is mandatory. Other Duties Please note this job description is intended to describe the general nature and level of work performed by employees assigned to this position. It is not designed to contain or be interpreted as a comprehensive list of all duties, responsibilities, and qualifications. Additional job-related duties may be assigned. Alliance reserves the right to amend and change responsibilities to meet business and organizational needs as necessary with or without notice. KEY BENEFITS INCLUDE: Medical, Dental, and Vision Insurance Flexible Spending Accounts 401(K) Plan with Competitive Match Continuing Education and Tuition Assistance Employer-Sponsored Disability Benefits Life Insurance Employee Assistance Program (EAP) Paid Time Off (PTO), Paid Holidays, & Bonus Floating Holiday (if hired after July 1st) Profit Sharing or Individual Bonus Programs Referral Program Per Diem & Paid Travel Employee Discount Hub EEO Commitment We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, religion, disability, age, genetics, active military or veteran status, and any other characteristics protected under applicable federal or state law. #LABS

Responsibilities: Perform visual and dimensional checks various incoming products (sheet metal, PCBAs or CCAs, Printed Boards or PCBs, Conformal Coating, Labels or markings, Cables, Harnesses; COTS items, and etc.) at various stages (Incoming, RMA, In-process, Final, Shipping, etc.) Test and or verify products for a variety of characteristics such as functional performance mechanically or electrically, or chemical properties or composition. Perform First Article Inspection and prepare FAIRs as needed. Record Inspection findings and generate NCMR's, DCRs' and ERRs' as needed. Communicate with the Project Mangers or QA for any possible delays and/or resolutions of any urgent and high priority jobs. Required: Extensive working knowledge of IPC-A-600, J-STD-001 and IPC-A-610, and IPC-A-620. Prior or current IPC training and/or certification is preferred. Ability to read, comprehend and interpret engineering drawings and documentation such as electrical schematic diagrams, mechanical and assembly drawings, BOM, and assembly instructions, and etc. Ability to adjust in fast-paced dynamic operations. Ability to apply concepts of basic algebra and geometry such as decimals, fractions, length, proportions, percentages, area, circumference, and volume. Ability to confer with management or engineering staff to determine quality and reliability standards or applicable requirements. Ability to use mechanical measurement tools such as calipers, micrometers, and electrical measurement tools, etc. Ability to operate computers and able to use computer applications and files such Microsoft Word and Excel, Adobe PDF, Outlook emails, and other databased platforms. Detail oriented, dedicated and self-motivated. Ability to work under minimum supervision. Work well in a team environment. Must have good interpersonal skills.

Job Details Irvine, CA Full Time High School $25.00 - $25.00 HourlyDescription Job Title: Inspector, Quality Control Supervisor/Manager Title: Staff Engineer, Quality (Production Support) Job Description Summary: Responsible for supporting the Quality department with quality control activities related to the manufacture of the THV within the Leeds and Irvine production facilities. To include in-process and final inspection, labelling/packaging, documentation, and environmental monitoring. The role holder will also provide routine reports and communications to provide timely updates on inspection status. Job Responsibilities: Conduct routine testing on THV, to include functional, visual, and final inspection processes, along with supporting sterilization preparation. Perform Microbiological monitoring on ViVitro (Leeds) or BDC (Irvine) when required. Conduct Preventative Maintenance and calibration of the ViVitro (Leeds) or BDC (Irvine) equipment. Conduct audits on the in-process paperwork associated with the manufacturing process including, but not limited to: manufactured valve DHRs, Jasmine preparation and ancillary logs. Provide support to the Engineering staff by gathering data on clinical product to allow decisions to be made on functionality. Adhere to Quality System and record retention requirements. Comply with all site Health & Safety requirements. Contribute to continuous improvement efforts related to valve manufacture and inspection processes. Inspect final packaging labels and confirm they are applied correctly per the relevant standards and Work Instructions. Support other areas of the business as necessary and applicable to the role. Qualifications Required Education and Experience: A-Levels, or equivalent and substantial relevant practical experience, in science related subjects are required. Bachelor's degree in a division of Biology, Chemistry or a Biomedical related discipline is desired (Leeds). Minimum of 3-5 years' experience in Quality within the medical devices or pharmaceutical industries is desirable. Must be familiar with 21CFR820 and ISO 13485 requirements. Hands on experience with these requirements is preferred. Experience assessing products for compliance and final release is desirable. Skills and Abilities Required for This Job: Must be able to work effectively and collaborate within cross-functional teams. Must possess the ability to handle multiple tasks, with high attention to detail. Ability to file and organize records in a compliant, easily retrievable manner. Must be able to effectively articulate (verbally and in writing) results and conclusions. Must have good documentation skills. Must be able to take initiative and work autonomously with the ability to prioritize a workload.

Job Description This position is responsible for performing in-process, component and finished goods visual and dimensional inspections using SPC/AQL sampling plans to support production, incoming receiving inspection and Quality investigations as needed. These inspections utilize industry standard metrology and gaging methods to identify defects and ensure product meets customer requirements. This position works on the production floor sampling, performing visual inspections and assessing quality of the parts and process. Attention to detail and the ability to work with minimal amount of supervision and understanding of quality inspection tools and equipment is required. Essential Job Functions and Responsibilities: Perform dimensional and visual In-process and finished good inspection on parts/boxes per approved control plans, test methods and customer drawings. Quality / SPC evaluation when required per site documentation. Communicate with Machine Technicians, Operators and Production Supervisors inspections/SPC results to operation when defects are detected to ensure process adjustments are made and in an effort to run a consistent quality product. Review daily NCR reports, SPC charts and quality system documentation. Enforce and maintain our Quality System and provide suggestions to maintain our continuous improvement system. Visually and dimensionally evaluate product and packaging in accordance with established acceptance criteria and standards. Follow all Safety rules and guidelines. Report any unsafe condition or practice. Maintain a clean work area throughout the shift. Evaluate product documentation for adequacy and completeness. Visually and dimensionally evaluate product and packaging in accordance with established acceptance criteria and standards. Measure process performance against established acceptance criteria and standards. Record real time data and prepare formal reports. Other assignments as may be given by the Quality Engineer or Managers. Support maintenance and calibration requirements for Quality Lab and production floor Place non-conforming product on hold and create non-conforming records and assist with Quality inspections of rework product as needed. Partner with Quality Control department for the management of product retains. Update Quality Inspection requirements Assist in the creation, closure review and verification of completion of batch records and release products and issuance of certificates of compliance to ensure product produced meet the customer and regulatory requirements Assist with New Product validation as required. Participate in Gage Repeatability and Reproducibility (GR&R), Geometric Dimensioning and Tolerancing (GD&T or GD and T) Intermedium studies and product/process validations Review and release product for shipping though issuance of COC ensuring all Customer requested documents are provided at the time of shipment Maintain cleanliness of QC lab, implement and sustain 6S, Quality boards and speak to status of site Quality metrics Able to generate and reconcile Labels (as needed) Perform Environmental monitoring activities according to site procedures. Train Quality personal on environmental monitoring activities and clean room requirements. Other assignments as may be given by the Quality Supervisor or Plant leadership team. Core Competencies: Statistical Process Control Knowledge Cosmetic, visual and dimensional Inspection Housekeeping General Safety Communication & Teamwork Skills Computer literate. Good verbal and written communication skills. Ability to perform standard measurement and test equipment. Attendance-dependability Time Management IQMS Knowledge Inspection Skills Organizational Skills Basic math skills Metrology Blueprint Reading Data Entry Skills Knowledge, Skills, and Abilities Read and write in the English language. Must be able to perform basic math such as addition, subtraction, multiplication, division, fractions, and decimals. Ability to read and interpret basic engineering drawings and product specifications. Proficiency with utilizing ANSI Sampling Plans Proficient in utilizing hand measurement tools (Caliper, Micrometer, Ruler, Gage Blocks, etc.) Experience with PCDMIS and Measuremind 3D automated inspection software usage (CMM, OGP, Smart scope, etc.) and programming a plus Knowledge of Medical device standards and Regulations (ISO 13485) Ability to read and decipher blueprints Knowledge of GD&T Experience with handling non-conforming material Experience with device history record creation and review Knowledge of ERP and quality system elements Proficiency in using Microsoft Excel, Access Database and Word Experience in supporting process validation activities including testing and Gage R&R Knowledge of sample plans creation is a plus Understanding of risk management is a plus Education and/or Experience: High School Diploma or GED. Minimum 6 months factory related experience in a regulated industry. Minimum of one year experience in visual and dimensional evaluation of molded products; or minimum three years experience in plastic injection molding and assembly processes Experience with calipers and micrometers is required; Other inspection equipment such as indicators, height gage, & pin gauges are a plus. Should have prior experience in a manufacturing environment to understand normal safety requirements. Certified Quality Inspector or Technician a plus

Full-time Description Shift: 2:30pm - 11:00pm Scope: Inspect and evaluate final products to ensure compliance to customer requirements prior to delivery. Essential Job Function: Perform Final Inspection on finished product to ensure compliance to customer requirements. Read customer drawings Perform measurements with measurement tools such as calipers, micrometers, and pin gages. Perform rework as appropriate, which may include mask touch-up, material removal with an x-acto knife, burnishing, soldering irons, final finish brush plating, sanding Verify acceptability of rework after completion Identify and mark non-conforming product to ensure it is not delivered Prepare standard and AS9102 First Article Reports as needed Verify certifications and reports are complete and accurate and can be used for final acceptance and certification of product Complete Deliverables for Customers and ensure they are complete and accurate Complete department logs and record yield data as required Perform preventative maintenance as defined by department maintenance schedule Support other work areas or departments as required by production or management. Ability to work overtime as requested Keep work area clean and organized Requirements Essential Qualifications, Education and Experience: High school diploma or equivalent One year of PCB manufacturing experience Knowledge of IPC-6012, or IPC-6013 Knowledge of IPC-600 Strong work ethic Ability to work effectively in a team environment Physical Requirements: Prolonged periods sitting and performing visual and manual tasks. Fine motor skills Ability to use microscopes for long periods of time performing job duties ITAR Compliance Requirement: This position requires access to controlled technical data and/or participation in activities subject to the International Traffic in Arms Regulations (ITAR). As such, all applicants must be U.S. persons, as defined by ITAR (U.S. citizens, U.S. lawful permanent residents, or individuals with refugee/asylee status). Candidates who do not meet ITAR eligibility requirements will not be considered for this position. AdvancedPCB is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, status as a protected veteran, marital status, genetic information, medical condition, or any other characteristic protected by law (EEOC). Compensation: Exact compensation may vary based on skills, experience, and location. About AdvancedPCB AdvancedPCB is a leading manufacturer of high-reliability printed circuit boards. The company features 6 total manufacturing sites: Santa Clara, our headquarters in the heart of the Silicon Valley; 2 in Southern California, 1 in Maple Grove, Minnesota, Aurora, Colorado and Chandler Arizona. Currently, the company is viewed as over $100 Million; 180,000 sq. ft. of manufacturing space with over 480 employees, making AdvancedPCB one of the largest privately held printed circuit board manufacturers in North America. Visit us! ********************************** Salary Description $18.00- $24.00

MK Magnetics (******************** specializes in the production of custom and standard tape wound soft magnetic cores for transformers and inductors. All the cores we sell are manufactured on site in Adelanto, California in a modern 75,000 sqft facility specially designed and built for manufacturing tape wound magnetic cores. We recognize and appreciate the value and contribution of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Working in accordance with the established policies and procedures, the Lab Inspector is responsible for inspection of parts produced by MK Magnetics for quality before they are shipped to the customer, often to customer inspection specifications and when needed during the production process. Responsibilities: Inspects electrical properties of unfinished product for pretest. Inspects electrical, mechanical and cosmetic properties of finished tape wound cores for conformance to specifications. Measures dimensions of product to verify conformance to specifications, using measuring instruments such as calipers and micrometers. Works with low and high voltage equipment. Sets controls and observes test equipment and records test data. Visually inspects product for defects and correct core identification. Reads process sheet to determine inspection criteria and verify identification markings. Operates various electrical test equipment to measure electrical and magnetic properties of product and document results of test. Completes Test Data reports as needed. Inspects coated material for proper coverage and color, using coated material samples, when necessary. Inspects incoming raw material for physical and cosmetic qualities. Completes Material Review Board (MRB) document for non-conforming product. Completes Discrepancy Material Report (DMR) for non-conforming product. Trains and oversees quality of work of new employees when requested by Lab Supervisor. Labels secondary containers per Hazards Communication Plan. Monitors equipment to ensure safe and efficient operation and reports any concerns to Lab Supervisor. Qualifications: Associates' Degree in electronics or electromagnetic industry preferred or two years minimum experience in electronics or electromagnetic. Experienced in analog electronic test equipment and test processes. Knowledge in basic electronic theory, algebra, metric and standard measurement. Experience in conducting tests and inspections of products to evaluate quality or performance. Experience in operation of electronic and magnetic test equipment is preferred. Able to read basic blueprints and schematics. Knowledge of basic computer skills to include Microsoft Word and Excel. Capable of matching or detecting differences between colors, including shades of color and brightness. Able to perform the job accurately with attention to detail. English/Spanish language is a plus. Other duties as assigned. MK Magnetics, Inc. is an Equal Opportunity Employer.

Concorde Battery Corporation is a manufacturer of specialty lead-acid batteries and is the leading producer of lead-acid batteries for aircraft. Our other products include batteries for Marine, RV, and Photovoltaic Systems. We've been in business for over 45 years and continue to grow to meet the needs of our customers. People are the most important component to the success of a company and Concorde is fortunate to have a staff with over 150 years of battery manufacturing, designing and aircraft system experience. If you think you might be a good match, we encourage you to apply. Concorde Battery Corporation is currently looking for a driven candidate to start a career working in the Quality Department as a Quality Control Inspector. The successful candidate will be responsible for in-process and final inspections. The Quality Control Inspector is part of the QA team and is also responsible for general quality related tasks. The Quality Control Inspector reports directly to the Quality Production Supervisor. Position Responsibilities: * Perform inspection of materials, processes and final product, per business need. * Generates inspection reports according to AS9100 requirements. * Enter inspection data into systems. * Utilizes inspection tools including calipers, gauges and testing equipment (CMM). * Reads and interprets drawings, procedures and work instructions. * Identifies areas for improvement in inspection processes and coordinates implementation. * Comply with all safety requirements; participate in safety training/practices. Qualifications: * 1+ years QA inspection experience using standard inspection tools including calipers, gages, etc. in a manufacturing environment. * Understanding of QA requirements, processes, practices and systems. * Demonstrated ability to work in team-based environments. * Ability to read engineering drawings to determine and measure features and tolerances. * Strong written and verbal communication skills in English. * Software experience; Excel, Word, Power Point, etc. * Bilingual - English/Spanish Perks and Benefits: * Desired first shift schedule * Premium Health Insurance - $0 employee premium & $0 deductible * Company provided life insurance for all employees with $0 employee contribution * Dental * 10 paid holidays * 5 paid sick days * Accrued vacation * 401(k) * Profit Sharing * Frequent overtime availability based on customer demand This position description reflects the general level and nature of the job, and is not to be considered as all inclusive. Concorde Battery Corporation offers a competitive salary and outstanding benefits. For more information about Concorde Battery Corporation please visit our website at *********************** CONCORDE BATTERY CORPORATION IS AN AFFIRMATIVE ACTION/EQUAL OPPORTUNITY EMPLOYER.

SPT Labtech is a global supplier of innovative lab automation products for the life science markets. Our solutions save time and material costs and simplify complex operations. We are natural innovators. We create, design and manufacture high quality, robust and innovative automated laboratory equipment for academic, pharmaceutical and biotechnology research. We are looking for a talented Quality Control Inspector to join our growing team. You must have the ability to work on complex products and to work collaboratively and flexibly across several inter-disciplinary teams. Inspector Job Responsibilities: Inspect and approve incoming materials by confirming specifications, conducting visual and measurement tests, and rejecting and returning unacceptable materials. Inspect in-process production by confirming specifications, conducting visual and measurement tests, communicating required adjustments to production supervisor. Approves finished products by confirming specifications, conducting visual and measurement tests, returning products for re-work, and confirming re-work. Reject all in-coming materials, in-process production, and finished goods products that fail to meet quality standards by specifications or quality criteria through non-conformance process. Assists Quality team members or management with failure and nonconformance data recording and reporting Prioritizes schedules based on product introduction and manufacturing schedules, maintaining a minimum turnaround time. Accomplishes quality and organization mission by completing tasks and responsibilities as needed. Keeps measurement equipment operating by following operating instructions and calibration requirements and calling for repairs. Maintains safe and healthy work environment by following standards and procedures and complying with legal regulations. Support the engineering manager or take ownership in resolving quality-related issues in a timely manner Recommend improvements to the production and quality control inspection process to ensure quality control. Be a team member of the quality department and support Production, Engineering and other internal departments to further the interests of the company as a whole. Requirements Written and verbal communication skills Experience with inspecting electromechanical assemblies, machined and metal fabrication highly desired. CMM experience a plus Basic math skills Excellent computer skills to include use of MS Office Attention to detail Analytic skills Documentation skills Time management skills Flexibility and able to change priorities on short notice based on production demands Hand/eye coordination Reporting skills Blueprint reading Education and Experience Requirements: High school diploma Experience with measuring devices such as meters, gauges, computers, calipers, and other measuring instruments One to two years' quality inspector experience Knowledge of ISO and QMS is highly desired Benefits 401(k) Health insurance Dental insurance Vision insurance Paid time off SPT Labtech is committed to a diverse and inclusive workplace. SPT Labtech is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status.

The Quality Control Inspector is responsible for verifying that Solar PV, BESS, and EV projects are installed in compliance with design drawings, codes, standards, and client requirements. This role ensures quality assurance through inspection, documentation, and enforcement of corrective actions.