Quality Control Inspector Jobs in Manteca, CA

The Quality Control Technician will perform a variety of inspection and quality tasks in support of manufacturing operations and new product development activities. You will perform daily activities in the Incoming Quality Control lab including completion of inspections while meeting priorities. This is a 6-month contract; potential extension. Responsibilities Complete inspection of incoming materials including machined components, sheet metal parts, mechanical assemblies, printed circuit board assemblies, fasteners, and adhesives, per engineering drawings, specifications, and Quality Inspection Plans (QIP). Implement best measurement techniques for incoming inspection. Review supplier provided documentation including certificates of conformance, material certifications, and special process certifications. Complete material acceptance and rejection transactions in QAD ERP system. Coordinate MRB activities and initiate NCR's as required to ensure the proper disposition of non-conforming materials as required in the QMS. Complete and review First Article Inspections (FAI) as required. Create or assist in generating Quality Inspection Plan (QIP). Monitor performance of quality control systems to ensure effectiveness and efficiency. Perform manufacturing in-process and final inspections per inspection plans as required. Perform manufacturing in-process and final assembly traveler review for product release. Assist in calibration and preventive maintenance activities with outside suppliers. Perform and/or participate in quality system audits as assigned, report findings, and make suggestions for improvement. Support new product development activities as needed. Qualifications 3+ years of quality inspection experience in the medical device industry. Understanding of 21 CFR 820 Regulations and ISO 13485 Standards. Ability to read and interpret engineering drawings required. Solid proficiency in Geometric Dimensioning and Tolerancing required. Working knowledge in the use of standard metrology tools including surface plates, calipers, micrometers, height gages, bore gages, indicators, pin gages, and gage blocks. Experience programing and operating coordinate measuring machines (CMM) highly desired Familiar with vision systems and optical comparators. Working knowledge of gage R&R, test method validation & equipment qualification. Understanding of statistical process control (SPC). Computer skills including Microsoft Office (Word & Excel), email, and other common programs. Ability to lift up to 25 pounds required. Pay $35.00-$42.00/hr Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance - PPO, HMO & HSA Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

Ultimate Staffing is seeking a Swing Shift QC Inspector for our client in Hayward. This is a temp to perm role that starts at 2:30pm with a starting pay of $21 an hour. ESSENTIAL DUTIES AND RESPONSIBILITES Responsibilities include but are not limited to: * Monitoring operations to ensure that they meet production standards * Recommending adjustments to the assembly or production process * Inspecting, testing, or measuring materials or products being produced * Measuring products with rules, calipers, gauges, or micrometers * Operating electronic inspection equipment and software * Accepting and rejecting finished items * Removing all product and materials that fail to meet specification * Reporting inspection and testing data such as weights, temperatures, grades, moisture content, and quantities inspected ESSENTIAL EDUCATION AND TRAINING REQUIREMENTS * High School Diploma or GED * 1 year of quality control experience, preferred * Ability to verify the quantity of products * 1 year of shipping and receiving experience, preferred * Experience with quality management systems (QMS) * Math skills - data reporting, measuring, calibrating, and calculating specifications * Ability to stand for extended periods of time * A desire to achieve the best and ensure top-quality products 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.

: Vintage 99 Labels has been a trusted provider of premium wine labels for over 25 years. We take great pride in the quality and craftsmanship of every label we produce, treating it as an art form. Known for our exceptional service, quality, and value, we offer quick turnaround times and the latest print technology. Serving some of the most respected wineries in the industry, we operate out of Livermore, CA, and Santa Rosa, CA. Role Description: We are seeking a Quality Inspector to join our team in Livermore, CA. The Quality Inspector will be responsible for ensuring that labels meet predetermined specifications throughout the production process. This role requires a keen eye for detail, as well as the ability to communicate effectively with press operators and other departments to maintain the highest standards of quality. Key Responsibilities: Inspect labels on press prior to, during, and after production to ensure compliance with material, foil, colors, graphics, and text specifications. Collaborate with press operators to resolve any issues during production and notify the Quality Control (Q.C.) Manager of problems that cannot be resolved. Verify the accuracy of items on the Q.C. sheet and initial to indicate compliance. Attach appropriate samples to the Job Card and Q.C. sheet for documentation. Perform rub tests and bar code verification tests, attaching results to the Q.C. sheet. Verify roll change forms for consistency in labels and ensure all specifications are met. Operate rewind equipment to wind/unwind rolls of labels to specified lengths and counts, ensuring quality control at each stage. Perform final visual inspection of labels to ensure they meet company quality standards. Maintain a clean and organized workspace and adhere to safety procedures. Assist in other areas of the organization as needed to support production and quality efforts. Skills & Qualifications: Strong attention to detail and ability to spot quality issues during the production process. Excellent communication skills to collaborate effectively with press operators and customer service. Solid understanding of the printing process and troubleshooting in a print environment. Ability to handle multiple tasks efficiently and work under tight deadlines. Must be comfortable standing, walking, and lifting up to 75 pounds regularly. Strong organizational skills and ability to maintain accurate documentation. Basic computer skills with the ability to learn various software programs (e.g., MS Office, Labeltraxx software). Ability to read and interpret technical procedures and company policies. Strong math skills, including basic algebra and geometry, and ability to apply concepts in all units of measure. Ability to follow verbal and written instructions accurately. Education/Experience: High school diploma or general education degree (GED) required. 6 months of related experience or training, or an equivalent combination of education and experience. Previous experience in the printing industry or quality control is a plus. Other Skills and Abilities: Ability to work in a team-oriented environment and assist others across departments as needed. Strong troubleshooting and technical problem-solving skills. Willingness to work overtime and weekends when necessary. Ability to interact professionally and cooperatively with all levels of employees. Must be detail-oriented and possess strong proofreading skills. Physical Requirements: Regularly required to stand, walk, and use hands to operate machinery and handle materials. Must be able to lift and/or move more than 75 pounds of paper materials and rolls of labels. Specific vision abilities required include close vision, color vision, peripheral vision, and depth perception to assess material, quality, and color matching. Work Environment: The work environment involves exposure to moving mechanical parts, fumes, and airborne particles from inks and varnishes. The noise level is typically loud, and temperatures may range from 50°F to over 90°F in the production area. Safety protocols and protective equipment are provided. Why Vintage 99 Labels? Competitive salary: $20-$27/hr and benefits package. A dynamic and collaborative work environment focused on quality and customer satisfaction. Opportunities for growth and advancement within an established, family-owned company. If you're passionate about ensuring high-quality production and want to be part of a dedicated team producing top-tier labels, we'd love to hear from you!

Become a key player in aviation innovation as a Quality Inspector with A+P! Join a leading aviation manufacturer in San Jose for a long-term contract role. This is a fully onsite position with a rapidly growing team. Are you passionate about ensuring the highest standards of quality in aerospace? Do you thrive in a hands-on environment where your skills directly contribute to the success of cutting-edge projects? We're looking for a Quality Inspector to join a rapidly growing, forward-thinking aviation manufacturer. In this role, you'll be at the heart of ensuring the excellence and safety of aircraft systems and components. If you're ready to make an impact, we want you on our team! What You'll Be Doing: Ensure Quality Excellence: Perform daily inspections for receiving, in-process, and final inspections to identify defects and deviations from design specifications. You'll play a crucial role in maintaining top-tier product quality throughout the entire manufacturing process. Collaborate with the Best: Document defects or nonconformances accurately and clearly, and collaborate with engineering or manufacturing teams to quickly resolve any issues. Your attention to detail will be key in identifying potential problems and making sure solutions are implemented swiftly. Ensure Compliance: Review completed manufacturing operations to ensure compliance with company requirements, maintaining the highest standards for every part of the process. Innovate Inspection Processes: Provide valuable input in the creation of an aircraft inspection plan, using cutting-edge tools such as CMMs, laser trackers, and other advanced inspection equipment to ensure precision and accuracy. Support FAA Certification: Play an essential role in the planning and execution of FAA conformity inspections, directly contributing to the certification process and helping the company meet critical regulatory requirements. Drive Continuous Improvement: Contribute to the roll-out of Advanced Product Quality Planning (APQP) techniques, including PFMEAs, control plans, and SPC, helping to elevate the company's quality assurance practices. What You Need: Solid Foundation: A High School Diploma or equivalent is required. A passion for quality and precision is key. Hands-On Experience: 5+ years of experience using basic inspection tools such as surface plates, thread gauges, micrometers, calipers, height masters, and more. You'll bring your hands-on expertise to the table in ensuring every detail is accounted for. Precision and Accuracy: Strong experience with tolerance and drawing reviews, including assessing the ability to verify dimensional requirements. You'll be integral in making sure all specifications are met with uncompromising accuracy. Expert Measurement Skills: An in-depth understanding of surface plate layouts and the ability to read and interpret quality control specifications and engineering drawings. You'll be skilled at recognizing critical characteristics and ensuring compliance with them. AS9102 First Article Inspections: Experience completing AS9102 compliant First Article Inspections (FAI) with proficiency in the tools and processes involved. Tech-Savvy: Experience with MES systems like SAP and using electronic inspection plans. Your ability to work with digital tools will enhance inspection efficiency and accuracy. Measurement Terminology: A strong grasp of measurement terminology, types of measurements, and the principles behind them.

The Quality Control Engineer will maintain ARIA's quality system and ensure the quality of products being shipped to ARIA's customers. The Quality Control Engineer is responsible for corrective action, internal audits, process improvements, RMA testing and analysis, and maintaining vendor performance metrics. Duties/ResponsibiIities: Develop, implement, and improve production processes, with the goal of reducing cost and maximizing efficiency. Monitor the quality of employee training and safety standards in the manufacturing process. Analyze workflow, space requirements and equipment layout. Develop and update Work Instructions for products using Adobe InDesign. o Conduct training for Production Technicians on any updates. Work directly with suppliers on all aspects of quality control. Accept or reject incoming and in-process products. Oversee customer RMA processing, analysis, and root cause identification. o Analyze customer feedback to identify potential flaws in product or process. Conduct ARIA's weekly quality meeting. Create and manage quality cases in Epicor as needed. o Present quality KPIs and initiatives. Create and maintain supplier quality/corrective action metrics and reports. o Involved with supplier quarterly business reviews. Conduct internal audits of the Quality Management System. Work directly with suppliers to provide Failure Analysis reporting in a timely manner. Check production output for quality. Enforce strict safety guidelines and company standards. Perform other related duties as assigned by management. Qualifications and Experience: Bachelor's degree (B. A.) from four-year college or university; or one to two years related experience and/or training; or equivalent combination of education and experience. Experience with software such as Epicor, Power Bl, Excel, and Adobe Creative Cloud is preferred. Highly organized, efficient, with exceptional attention to detail. Experience working with and development of a Quality Management System. Competencies: Analytical - Synthesizes complex or diverse information; collects and researches data; uses intuition and experience to complement data; designs workflows and procedures. Problem Solving - Identifies and resolves problems in a timely manner; gathers and analyzes information skillfully; develops alternative solutions; works well in group problem solving situations; uses reason even when dealing with emotional topics. Technical Skills - Assesses own strengths and weaknesses; pursues training and development opportunities; strives to continuously build knowledge and skills; shares expertise with others. Communication - Speaks clearly and persuasively in positive or negative situations; listens and gets clarification; responds well to questions; demonstrates group presentation skills; participates in meetings; writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information. Quality Management - Looks for ways to improve and promote quality; demonstrates accuracy and thoroughness. Professionalism - Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; Follows through on commitments. Physical Requirements and Work Environment: Regularly required to stand, walk, and sit. Regularly required to utilize hand and finger dexterity. Regularly required to climb, balance, bend, stoop, kneel or crawl. Regularly required to talk or hear. While performing the duties of this job, the noise level in the work environment is usually moderate, depending on the area. The employee must occasionally lift and/or move up to 45 pounds. The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or physical requirements. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Halo Technology provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. ARIA Technologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Pay Transparency: The starting annual salary for this opportunity ranges from $75,000-$90,000. Other rewards may include annual bonus eligibility, which is based on company and individual performance. Company provides a variety of benefits to employees, including medical, dental and vision insurance coverage, life and disability insurance, retirement savings plan, paid holidays, and paid time off (PTO). Please note that the compensation information is a good faith estimate for this position. It assumes a rate based on location and experience. Location Type: On-site

**Posting Title:** Instrumentation & Controls Coordinator **Reports To:** Project Executive **Salary Range:** $130,000 to $160,000 Final determination of a successful candidate's starting pay will vary based on a number of factors, including market location and may vary depending on job-related knowledge, skills, education and experience. The pay scale listed for this position is generally for candidates that meet the specified qualifications and requirements listed on this specific job description. We provide a competitive compensation package that recognizes your experience, credentials, and education alongside a robust benefits program to meet your needs. Our compensation reflects the cost of labor across several US geographic markets. **WHO WE ARE** For nearly 70 years, Cupertino Electric, Inc. (CEI) has been powered by people who've built a reputation for delivering high-profile, complex projects. Real, tangible things that alter the landscape and improve lives. But even more than that, we've built a reputation for integrity. We're problem solvers and innovation seekers. We're team players and safety fanatics. And we always-always-do the right thing. Even when no one is looking. Because what we do here is important, but how we do it is everything. **THE COMMERCIAL TEAM** Our strong project management teams, dedicated in-house engineering resources and skilled union field staff work together seamlessly to deliver commercial projects that are as innovative and unique as the clients who build them. **ABOUT THE ROLE** The Instrumentation and Controls Coordinator plays a pivotal role in overseeing the planning, coordination, and implementation of instrumentation and control systems for water and wastewater facilities. This role involves working closely with project teams, technicians, and electricians to ensure that control systems are designed, installed, calibrated, and tested to meet project requirements. The coordinator will be responsible for coordinating the day-to-day operations related to instrumentation and controls, ensuring that project timelines, quality standards, and safety protocols are adhered to. The ideal candidate will have a proven background in instrumentation and control systems, with the ability to coordinate activities across multiple teams and stakeholders. They will be the key point of contact for troubleshooting, providing technical direction, and ensuring that all systems are integrated and operational within the scope of the project. + Develop, update, and maintain procedures for instrumentation and control system checkout, integrated system test, calibration, and operation. + Provide technical direction to site teams in the installation, checkout, calibration, troubleshooting, and operation of the respective systems. + Review design and construction documents for I&C and create and maintain consolidated and fully coordinated block diagrams and interconnect diagrams for all projects. + Collaborate with engineers, process system vendors, project managers, and technicians to ensure that control systems meet all functional, safety, and regulatory requirements. + Maintain and update controls schematics related to instrumentation and control systems. + Provide technical direction and support to field technicians and electricians during the installation and commissioning phases of the project. + Review and evaluate vendor proposals for control systems & instruments, ensuring compliance with project specifications. + Coordinate and manage the procurement, installation, and maintenance of instrumentation and control hardware/software. + Ensure that all control systems are documented, and that training materials are developed for operations and maintenance staff. + Provide ongoing support for system troubleshooting, maintenance, and upgrades. **Knowledge:** Having broad expertise or unique knowledge, uses skills to contribute to development of company objectives and principles and to achieve goals in creative and effective ways. Barriers to entry such as technical committee review exist at this level. **Job Complexity:** Works on significant and unique issues where analysis of situations or data requires an evaluation of intangibles. Exercises independent judgment in methods, techniques and evaluation criteria for obtaining results. Creates formal networks involving coordination among groups. **Supervision:** Acts independently to determine methods and procedures on new or special assignments. May supervise the activities of others. **WORK ENVIRONMENT** Visual and physical contact of test system hardware and installed test articles. Multiple workstation assignments (office, test facility, control room, laboratory, shops, etc.). Transportation of notebooks, drawings, forms, etc. required. Work is accomplished in an office, control room, and in and around project facilities Some work areas are high in noise. Work assignments are usually during normal work hours, but overtime is frequently necessary to support meetings, test schedules, and test operations. Testing may occur any day or time of day, depending on the schedule and test requirements. Regular daily attendance to a CEI Office is required to maintain team effectiveness. Travel to the different project sites will be required. **ABOUT YOU** + Exceptional communication and interpersonal skills, with the ability to work collaboratively with cross-functional teams. + Demonstrated experience in producing system documentation, procedures, and training materials. + In-depth knowledge of instrumentation and control systems, including signal conditioning, data acquisition, and Programmable lLogic Controllers (PLC). + Familiarity with Human-Machine Interface (HMI) systems, instrumentation calibration and testing, and specialized measurement equipment. + Strong organizational skills with the ability to manage multiple tasks and prioritize effectively. + Ability to identify, examine, and resolve complex issues related to instrumentation and controls. + Good communication and interpersonal skills are highly desirable as the Controls Engineer will interface with Engineers and Technicians. + Produce system documentation and procedures and train personnel. + Strong knowledge and understanding of water and wastewater treatment testing and facility operations. + Direct working knowledge of the following types of equipment: + PC computer operations (MS Windows [XP, 7] and Macintosh OSX, MS Office). + Signal conditioning and data acquisition and processing hardware and programming (National Instruments LabVIEW). + Programmable logic controller hardware and programming (GE Proficy, Rockwell RSLogix, Emerson Ovation). + Human-Machine (i.e., User) Interface hardware and design. + Test instrumentation (multimeter, oscilloscope, pressure / temperature / electrical calibrators). + Specialized measurement instrumentation (position, pressure, temperature, and flow transducers and switches). **MINIMUM QUALIFICATIONS** _Any combination of education and experience that would likely provide the required knowledge, skills and abilities as well as possession of any required licenses or certifications is qualifying._ **Education:** High School Diploma or GED required. Bachelor's Degree or higher in Electrical or related engineering discipline is preferred. _*Applicants must be authorized to work in the United States. This position is not eligible for sponsorship._ \#LI-JJ1 **PLEASE NOTE:** CEI will never ask for any money or financial information from applicants during the hiring process. To learn more about "job scams" how to avoid them, click here. (******************************************** CEI is a place where every single person can-and does-have an impact on the work we do and the communities we serve. Here, you can build your own story and grow to your full potential. You can collaborate and celebrate with amazing people. And you'll go home every day knowing you helped contribute to important work that shapes people's lives. Our commercial, data center and energy projects may be complex, but our approach is simple. We build great things and we do it with great people. The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department, program or project needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned. Cupertino Electric, Inc. (CEI) is proud to be an Equal Employment Opportunity and affirmative action employer. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. Cupertino Electric Inc. aims to make cei.com accessible to any and all users. If you have a disability or special need that requires accommodation to navigate our website or complete the application process, please contact us at *************** or 1-(877)-747-4CEI. Cupertino Electric, Inc. (CEI) is proud to be an Equal Employment Opportunity and affirmative action employer. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $25.20 - $34.65 Job Purpose The Quality Control Inspector receives raw materials and performs product inspection and/or audits in accordance with established quality control program. This role involves sampling and testing of incoming raw materials to ensure that they, along with in-process and finished products meet the company's quality standards Responsibilities · Receive and perform inspection of incoming raw material/components to ensure compliance with company quality standards · Perform visual inspections on sub-assemblies and finished good products to identify defects and non-conformances · Maintain product quality by adhering to data management protocols · Support efficient supply chain operations by complying with and maintaining inventory control procedures · Ensure compliance with internal quality control standards and external regulations, and continuously improve quality control processes · Assist in the development and implementation of quality control procedures. · Collaborate with production teams to address quality issues and recommend corrective actions Qualifications Education: · High School Diploma · A.A Degree a plus Skills and Experience: · Life Sciences industry experience preferred. · Experience working in a Quality Control environment is strongly desired. · Previous experience performing incoming inspections is strongly desired. · Detail-oriented, efficient, and excellent organization skills. · Excellent verbal and written communication skills · Strong team player with the ability to work independently. · Able to multi-task and prioritize. · Proficiency in Microsoft Office and other relevant software · ISO and GMP experience preferred Working Conditions: · Significant amount of time on the production floor, in a laboratory setting · Some time in an office setting documenting inspection result, analyzing data, and communicating with team members Physical Requirements: · Standing and walking · Lifting and moving materials up to 50 pounds · Use of hands for precises tasks such as handling samples and testing equipment Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $25.20 - $34.65 Job Purpose The Quality Control Inspector receives raw materials and performs product inspection and/or audits in accordance with established quality control program. This role involves sampling and testing of incoming raw materials to ensure that they, along with in-process and finished products meet the company's quality standards Responsibilities · Receive and perform inspection of incoming raw material/components to ensure compliance with company quality standards · Perform visual inspections on sub-assemblies and finished good products to identify defects and non-conformances · Maintain product quality by adhering to data management protocols · Support efficient supply chain operations by complying with and maintaining inventory control procedures · Ensure compliance with internal quality control standards and external regulations, and continuously improve quality control processes · Assist in the development and implementation of quality control procedures. · Collaborate with production teams to address quality issues and recommend corrective actions Qualifications Education: · High School Diploma · A.A Degree a plus Skills and Experience: · Life Sciences industry experience preferred. · Experience working in a Quality Control environment is strongly desired. · Previous experience performing incoming inspections is strongly desired. · Detail-oriented, efficient, and excellent organization skills. · Excellent verbal and written communication skills · Strong team player with the ability to work independently. · Able to multi-task and prioritize. · Proficiency in Microsoft Office and other relevant software · ISO and GMP experience preferred Working Conditions: · Significant amount of time on the production floor, in a laboratory setting · Some time in an office setting documenting inspection result, analyzing data, and communicating with team members Physical Requirements: · Standing and walking · Lifting and moving materials up to 50 pounds · Use of hands for precises tasks such as handling samples and testing equipment Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Quality Inspector Level I and II Full-time / Permanent Hourly $18.00 - $35.00 Shifts Available: * Day Shift * Weekend Shift * We are not accepting candidates from third party agencies. About Us: Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do - and have a lot of fun doing it. About this Opportunity: This position is responsible for building mechanical products in accordance with customer supplied assembly documentation and Vantedge Medical standards in addition to providing your team with leadership & guidance. It requires the ability to advise operators of deviations found upon inspection. This position may train and advise the Inspector Trainee position. Responsibilities: * Prioritizes which inspections to perform based upon workload and job priorities. * Inspect product at receiving and incoming inspection from suppliers, specifically plating and custom made parts using applicable measuring tools and test equipment. * Inspect product In-Process (1st Piece) supplied by the operator. Inspector checks the product against the print, work order (notes) and other pertinent documentation using applicable measuring tools and test equipment. * Advises operator of deviations found upon inspection. * Performs "Lot" inspection on product "ready to" move to the next operation. Will check the product against the print, work order (notes) and other pertinent documentation using applicable measuring tools and test equipment. * Create and compile quality records as defined by the Quality Management System and/or by Customer specific requirements. * Record inspection results into the "Kebrite" Software, which is linked to Visual Manufacturing. * Undertake additional responsibilities or activities as required by the Quality Manager - Metals. * Assist the Director of Quality in maintaining of ISO 13485:2003 and 9001:2008 certifications. Requirements / Skills: * 1 year of manufacturing fabrication or inspection experience minimum. * Knowledge of measuring tools: Caliper, Micrometer, etc. * A good understanding of mathematics. * Read and interpret blueprints. * Familiar with quality management systems and calibration. * General Inspection knowledge, methodology, metrology, plating and painting. * Proficient with Microsoft Word and Excel and able to manipulate documents using Adobe Acrobat or Fox it. * Read, write and communicate in English.

Quality Control Inspector Job Location: 4245 Technology Drive, Fremont, CA 94538 Department: Quality Assurance Worker Category: Full-Time/Non-Exempt Industry: Neurovascular / Medical Devices About Q'Apel: At Q'Apel, we are passionate about revolutionizing neurovascular access. In the simplest sense, we're a company that creates solutions. We design novel access device technology for vascular interventions and unmet clinical needs. Because in the precious seconds that surround a stroke emergency, clinicians need technology that delivers. That's where Q'Apel comes in. Successful Q'Apel team members step up to the plate and work together to achieve our goals every single day. We are a fast paced, high growth company with a startup philosophy which requires an all-hands-on-deck attitude, taking on all changes with excitement and a great attitude. Who We Want: Q'Apel Is looking for a Quality Control Inspector who thrives in a fast-paced startup environment. As a pivotal member of our team, you will wear multiple hats, contributing not only to quality assurance but also to the overall growth and success of our company. You are a proactive problem-solver, excellent communicator, and enthusiastic about learning and adapting to new challenges. If you are passionate about delivering high-quality products and have a keen eye for detail, we want you to join us on our exciting journey. What You'll Work On: Performs QC inspections to work in progress (WIP) product and incoming components. Perform inspection and testing activities pertaining to manufacturing in process, IQA, First Article Inspections (FAI), final packaging. Generate detailed and accurate inspection data sheets in accordance with current Good Manufacturing Practices (cGMP) and Q'Apel's Quality Management System (QMS) requirements. Generate NCMRs and assist in the investigations of nonconformances. Work with engineering and operations staff to resolve issues in a timely and effective manner. Assure equipment used for inspection activities are qualitied prior to use. Identify potential improvements for inspection systems and processes. Assure that the company's QMS is compliant with current FDA QSR, ISO 13485:2016, and other standards as applicable. Support the Q'Apel's Quality Policy and Quality System. Be aware of QS procedures and requirements, including regulatory requirements, and training requirements for the position. Inform responsible personnel of concerns involving product quality. Perform job functions in a safe and effective manner. Adhere to the safety procedures of the company. Other duties as assigned. What You Bring: Education: High School Diploma AA degree, or equivalent experience, in a technical discipline preferred. Experience & Skills: 1+ years minimum experience working in a regulated industry (medical device experience preferred, along with a solid working knowledge of FDA Quality System Regulations and ISO 13485). Experience performing QA inspection / testing activities pertaining to IQA and in process. Familiar with testing equipment such as, but not limited to, Microscope, Instron, video inspection systems, borescope, etc. Ability to interpret and read technical specification and mechanical drawings. Experience working in a controlled environment room (CER) Good manual dexterity and visual acuity. Strong interpersonal skills. Effective communication skills (both written and verbal) required. Experience in a small company environment is a plus. Knowledge and exposure to applicable regulations (QSR, and ISO). Ability to work and independently or in in a team setting. Works well under pressure, organized, and self-motivated. Shift: QC Inspector (#1) hours will be 6:00 am - 2:30 pm Our compensation ranges are calculated by role and level. Your position within that range will be determined by your job-related knowledge, skills, experience, relevant education, and training/certifications. In addition to those factors, we also examine internal equity as well as consider the current market rate, and the title may be assessed one level lower or higher accordingly. After you join the company your performance, contributions, and results along with business and organizational needs will affect your compensation. The compensation range for this full-time, non-exempt position is between $28/hr to $30/hr + equity + benefits. This document contains confidential, proprietary information of Q'Apel Medical, Inc. It may not be copied or reproduced without prior written permission from Q'Apel Medical, Inc.

Build an Aviation Career You're Proud Of Build your career with integrity by working at a company that doesn't just treat you like a number. You'll get the tools to do things right in a clean and safe work environment and the trust to fix any issue that comes your way. Our on-the-job training and team of experts mean you'll be set up for success. StandardAero is looking for a seasoned Chief Inspector to assign, assist, and oversee our quality inspectors in the inspection of components, subassemblies, and finished products. As a Chief Inspector, you'll * Train our beginner-senior level inspectors on engine overhaul inspection process * Write non-conforming materials reports when required and be familiar with the process of quarantining products that have been rejected by QA * Lead quality and engineering in investigations of process related quality issues * Read, understand, interpret, and follow maintenance manuals, illustrated parts catalogs, service bulletins and technical orders to carry out tasks * Strong leadership and communication skills to effectively mentor team members as their resident inspection expert on components and subassemblies * Detail oriented, ability to stay on task, and self-motivated * Be compliant with safety procedures and policies Basic Qualifications: * Highschool diploma or GED with 2 years of related experience * Knowledge of MISTR components * Ability to possess Repairman's Certificate * Familiarity with government technical orders Preferred Qualifications * Certification in precision inspection, GD&T and other related discipline * Familiarity ISO or AS 9100 QMS Salary Range: $ 78,540 - $108,834 per year. The above salary range represents a general guideline; however, StandardAero considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions. Benefits that make life better: * Comprehensive Healthcare * 401(k) with 100% company match; up to 5% vested * Paid Time Off starting on day one * Bonus opportunities * Health- & Dependent Care Flexible Spending Accounts * Short- & Long-Term Disability * Life & AD&D Insurance * Learning & Training opportunities Raising the Standard of Excellence since 1911 With over a century of proven excellence, StandardAero has become an industry leader in MRO services and customized solutions in the aerospace field. Our shared values and learning-based culture inspire our team to exceed their potential and power our customers' missions worldwide. With on-the-job training, advancement opportunities, and excellent benefits, StandardAero invites you to experience a fulfilling and meaningful career with us. Inclusivity Is Our Standard StandardAero offers equal employment opportunities for all. Our supportive environment celebrates diversity with no room for harassment or discrimination of any kind. We invite you to bring your authentic self to our team and experience our welcoming culture.

Build an Aviation Career You're Proud Of Build your career with integrity by working at a company that doesn't just treat you like a number. You'll get the tools to do things right in a clean and safe work environment and the trust to fix any issue that comes your way. Our on-the-job training and team of experts mean you'll be set up for success. StandardAero is looking for a seasoned Chief Inspector to assign, assist, and oversee our quality inspectors in the inspection of components, subassemblies, and finished products. As a Chief Inspector, you'll Train our beginner-senior level inspectors on engine overhaul inspection process Write non-conforming materials reports when required and be familiar with the process of quarantining products that have been rejected by QA Lead quality and engineering in investigations of process related quality issues Read, understand, interpret, and follow maintenance manuals, illustrated parts catalogs, service bulletins and technical orders to carry out tasks Strong leadership and communication skills to effectively mentor team members as their resident inspection expert on components and subassemblies Detail oriented, ability to stay on task, and self-motivated Be compliant with safety procedures and policies Basic Qualifications: Highschool diploma or GED with 2 years of related experience Knowledge of MISTR components Ability to possess Repairman's Certificate Familiarity with government technical orders Preferred Qualifications Certification in precision inspection, GD&T and other related discipline Familiarity ISO or AS 9100 QMS Salary Range: $ 78,540 - $108,834 per year. The above salary range represents a general guideline; however, StandardAero considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions. Benefits that make life better: Comprehensive Healthcare 401(k) with 100% company match; up to 5% vested Paid Time Off starting on day one Bonus opportunities Health- & Dependent Care Flexible Spending Accounts Short- & Long-Term Disability Life & AD&D Insurance Learning & Training opportunities Raising the Standard of Excellence since 1911 With over a century of proven excellence, StandardAero has become an industry leader in MRO services and customized solutions in the aerospace field. Our shared values and learning-based culture inspire our team to exceed their potential and power our customers' missions worldwide. With on-the-job training, advancement opportunities, and excellent benefits, StandardAero invites you to experience a fulfilling and meaningful career with us. Inclusivity Is Our Standard StandardAero offers equal employment opportunities for all. Our supportive environment celebrates diversity with no room for harassment or discrimination of any kind. We invite you to bring your authentic self to our team and experience our welcoming culture.

Temporary Description Quality Control Inspector DEPARTMENT: Inspection and Compliance REPORTS TO: District Supervisor FLSA STATUS: Non-Exempt COMPENSATION: $20.00 (New Inspectors) - $21.00 (Licensed) Hourly Rate CHERRY SEASON ONLY The Cooperative Agricultural Support Services (CASS) is a Joint Powers Authority established as a partnership between the California Department of Food and Agriculture (CDFA) and the Counties of Yolo and Trinity. Over time, CASS has significantly expanded its reach across California, delivering essential support to the agricultural industry and its consumers. CASS specializes in providing comprehensive human resources and administrative support services to enhance the efficiency and effectiveness of agricultural programs. Its diverse program activities include agricultural inspections, pest prevention, and other critical initiatives administered by CDFA, county agricultural commissioners, and various public agencies. By fostering collaboration and leveraging expertise, CASS continues to play a vital role in supporting California's agricultural industry and safeguarding the quality and safety of its products. Our current work includes: Agricultural Commodity Grading Program Grading using County, State, and Federal standards. Emergency Pest Detection Trapping and Survey program Professional Develop and Educational Training We are seeking enthusiastic Quality Control Inspector - Commodity Inspectors to join our Inspection and Compliance Department. This position reports directly to the District Supervisor. Requirements Select and evaluate samples of various commodities. Grading, sorting, counting, and sampling work in connection with agricultural commodities. Prepare samples for titration (sugar/acid ratio) testing and pressure testing to determine degree of ripeness. Ripe or ripeness indicates readiness or fitness for use (Condition factor). Examine the quality, size and/or condition of selected samples using state, federal or industry standards and language. Language to understand include, but not limited to: Defects Damage - “Serious and Very Serious” Insect damage Scars Healed cuts Discoloration Accurately and carefully maintain daily reports of work including, but not limited to: Inspection Field Notes Inspection Certificates Inspector's Daily Report Ensure provided equipment is available, in working order, and always secured. Participate in safety and commodity inspection training as required. SKILLS & QUALIFICATIONS: High School Diploma or GED Required Valid driver's license with safe driving record Demonstrate the basic knowledge of the following: Federal/State/Industry relations Licensee responsibilities/authority. Proper use of inspection equipment. Sampling procedures: Harvesting, packing, and/or processing methods. Product grading for size, quality, and condition defects. Application of tolerances in the applicable standard. Note sheet and certificate preparation. Must be available to travel throughout the state as required. Attendance, punctuality, and dependability are essential to the proper operation of CASS's program. Must demonstrate the ability to interpret, understand, and conform to written and oral instructions; and contact appropriate supervision for assistance and/or guidance in performing the duties of their position. Excellent Oral and Written Communication skills Excellent Time Management and Organizational skills Ability to maintain confidentiality and handle conflict in a tactful and professional manner COMPENSATION: Non-Exempt $20.00 (New Inspectors) - $21.00 (Licensed) per hour - CHERRY SEASON ONLY Benefits package including medical benefits, matching retirement contributions, and annual and holiday leave. Travel and mileage reimbursement and advances provided. Qualified applicants with arrest and/or conviction records will be considered for employment in a manner consistent with federal and state laws. PHYSICAL REQUIREMENTS: The incumbent in this position will be required, with or without reasonable accommodation, to stand and walk constantly. The role also demands the ability to lift 30 pounds frequently and up to 50 pounds on an occasionally. The position involves repetitive arm and wrist motions, as well as bending, stooping, twisting, reaching. The incumbent must maintain visual acuity and possess normal color vision to differentiate color correctly. Additionally, the position requires driving and enter and exit the vehicle numerous times throughout the workday. WORK ENVIRONMENT: Duties for the job are performed inside or outside of buildings. Weather, temperature, lighting, and noise levels may constantly vary. Terrain may vary from smooth and stable to irregular and unstable. The incumbent may continually work with or around machinery or motorized equipment, work in a noisy environment and be exposed to dust, pollen, moisture, and temperature extremes. Driving a vehicle, as well as entering and exiting the vehicle numerous times throughout the workday, is required. Recruitment Process Applicants are advised that as part of CASS's recruiting process, only Human Resources personnel are authorized to extend conditional or official employment offers. Individuals involved in the interview process are not authorized to discuss or negotiate salary, benefits, or other terms of employment. All compensation and employment-related discussions will be handled exclusively by Human Resources personnel to ensure consistency and compliance with agency policies. We appreciate your understanding and look forward to your application!

Job Details Fremont 0NK54 - Fremont, CA High School $22.00 - $26.00 Hourly ManufacturingDescription Perform in-process inspection on product being processed through the work cell, specifically at SMT, Wave and Selective Soldering operations. Essential Duties and Responsibilities: Adhere to all ESD requirements and Board Handling. Use of Moisture Sensitive Device (MSD) handling requirements based on component moisture sensitive levels (MSL). Verify process compliance to document control process and procedures. Examine product to verify conformance to workmanship standards. Inspects and approves incoming materials by confirming specifications, conducting visual and measurement tests, and rejecting unacceptable materials through the designated ERP system. Inspect product being processed through work cell according to specific in-process inspector training and procedure, along with IPC-A-610 & J-STD-001 workmanship standards. Documents inspection results by completing reports and logs as applicable. Resolve quality-related issues in a timely matter. Approves finished material and/or product by confirming specifications, conducting visual measurement tests, returning products for re-work and confirming re-work. Responsible for stopping processes, with communication to Production Supervisor, lead and/or engineering, to control manufacture of non-conforming assemblies. Support and follow all ISO standards related to various Quality Management Systems. These systems may include, but are not limited to, quality, the environment, health, safety and security. Maintains safe and healthy work environment by following standards and procedures, and complying with legal regulations. Perform all other duties, as assigned. Qualifications Job Knowledge, Skills & Abilities: Ability to apply IPC-A-610 standard requirements Ability to apply J-STD-001 standard requirements Ability to apply IPC-600 standard requirements Written and verbal communication skills Basic computer skills Knowledge of interpretation of designated specifications High attention to detail. Sense of urgency, successful at meeting deadlines. Ability to work effectively as part of a team. Monitor processes, materials, or surroundings. Experience/Education: High School Diploma or equivalent. 2+ year minimum, Electronics manufacturing experience preferred. Experience with measuring devices such as calipers, pin gauges, feeler gauges, height gauges and other measuring instruments Experience with automated measuring equipment is a plus: SmartScope, CMM, etc. Certification to IPC-600, IPC-610 & J-STD-001 is a plus Experience with GD & T is a plus Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Sick Leave, Vacation Time, and company-paid Holidays are also provided as paid time off. NEOTech also provides a 401(k) Retirement Savings Plan option with a company match. NEOTech is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran status, or any other characteristic protected by applicable federal, state, or local law. NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company's equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana. NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company's equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana.

Job purpose Perform inspection activities in the following areas; Incoming Inspection electrical and mechanical, In-process and Final areas of product. Inspect, audit, and report the quality level of incoming and outgoing products, ensuring that all customer quality requirements are being met such as: appearance, fit, form, function; including on time delivery of shipments. Reject and isolate defective part/s and accurately complete all associated paperwork and data entry with non-conforming reports. Perform duties according to IPC 600, IPC 610 and or J-Std-001 and J-Std-001 Space addendum (latest revisions) and our Quality System work instructions. Properly interpret customer documentation, drawings/blue prints, Bills of Material (BOM), datasheets and specifications and other documents necessary to perform inspection duties. Must be available to work over-time. Cross-train in other areas or perform other duties as required, by the Quality Supervisor. Duties and responsibilities Perform first article/piece inspection of parts at the beginning of each production run and verify requirements are met. Report discrepancies of material, process or design issues. Interface with Production, Inside Sales, Engineering, Program Management and Customer Representative. Perform roving sample inspection and quality audits in designated areas per documentation package to include; drawings, BOM, and other procedures to ensure continuous flow of acceptable products to our customers. Ensure conformity to customers documentation and report in-process concerns and discrepancies using IPC workmanship criteria. Interface with Production and Engineering personnel. Perform 100% final inspection to ensure the quality of materials, processes and overall quality performance has been achieved prior to shipping to Customers. Ensure that all acceptance and/or discrepancies have been documented. Interface with Production, Inside Sales, Engineering, Program Management and Customer Representatives. Perform mechanical and visual inspections in Receiving Inspection and mechanical areas to ensure the quality of incoming Turn-Key material and other services. Maintain quality records for evaluation of performance outside Vendors and throughout internal processes. Research customer history and use experience to determine part acceptance when a decision is needed based on judgment. Act independently and resolve problems by exercising initiative and discretion outside the sphere of specifically described job duties and responsibilities. Qualifications Must have 3-5 years experience as a Quality Inspector in one of the following areas: In Process, Final, or Source Inspection High school diploma or general education degree (GED) Prior manufacturing experience, knowledge of soldering and component recognition Basic reading, writing, and mathematical skills with the ability to write correspondence. Ability to read, write and understand written and verbal instructions. Capable of accurately charting inspection and test data. Physical ability to repetitively lift, stand, climb, and bend etc., within a manufacturing environment. Knowledge of using small hand measuring tools, test lights, capable of working under a microscope. Familiar with ISO9001, AS9100, or ISO13485 processes preferred. Comply with company policies and procedures. Website: **************** EEO / ACCOMMODATIONS Naprotek is an Equal Employment/Affirmative Action employer including Disability/Vets . We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state, or local law. If you need a reasonable accommodation for any part of the employment process, please respond to this email and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Perform in-process inspection on product being processed through the work cell, specifically at SMT, Wave and Selective Soldering operations. Essential Duties and Responsibilities: * Adhere to all ESD requirements and Board Handling. * Use of Moisture Sensitive Device (MSD) handling requirements based on component moisture sensitive levels (MSL). * Verify process compliance to document control process and procedures. * Examine product to verify conformance to workmanship standards. * Inspects and approves incoming materials by confirming specifications, conducting visual and measurement tests, and rejecting unacceptable materials through the designated ERP system. * Inspect product being processed through work cell according to specific in-process inspector training and procedure, along with IPC-A-610 & J-STD-001 workmanship standards. * Documents inspection results by completing reports and logs as applicable. * Resolve quality-related issues in a timely matter. * Approves finished material and/or product by confirming specifications, conducting visual measurement tests, returning products for re-work and confirming re-work. * Responsible for stopping processes, with communication to Production Supervisor, lead and/or engineering, to control manufacture of non-conforming assemblies. * Support and follow all ISO standards related to various Quality Management Systems. These systems may include, but are not limited to, quality, the environment, health, safety and security. * Maintains safe and healthy work environment by following standards and procedures, and complying with legal regulations. * Perform all other duties, as assigned. Qualifications Job Knowledge, Skills & Abilities: * Ability to apply IPC-A-610 standard requirements * Ability to apply J-STD-001 standard requirements * Ability to apply IPC-600 standard requirements * Written and verbal communication skills * Basic computer skills * Knowledge of interpretation of designated specifications * High attention to detail. * Sense of urgency, successful at meeting deadlines. * Ability to work effectively as part of a team. * Monitor processes, materials, or surroundings. Experience/Education: * High School Diploma or equivalent. * 2+ year minimum, Electronics manufacturing experience preferred. * Experience with measuring devices such as calipers, pin gauges, feeler gauges, height gauges and other measuring instruments * Experience with automated measuring equipment is a plus: SmartScope, CMM, etc. * Certification to IPC-600, IPC-610 & J-STD-001 is a plus * Experience with GD & T is a plus Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Sick Leave, Vacation Time, and company-paid Holidays are also provided as paid time off. NEOTech also provides a 401(k) Retirement Savings Plan option with a company match. NEOTech is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran status, or any other characteristic protected by applicable federal, state, or local law. NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company's equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana. NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company's equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: Lilly is designing and building a new state of the art Parenteral, Device, and Packaging Assembly Facility in Concord, North Carolina. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The Quality Control Laboratory assures patients worldwide receive safe and efficacious drug and drug/device combination products through effective execution of product testing. Position Description: The QC Expert Environmental Monitoring Technician will provide support for Parenteral Operations by performing environmental monitoring of the classified manufacturing areas and by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings. The QC Expert Environmental Monitoring Technician will assist the QC Environmental Monitoring management with training QC Environmental Monitoring Technicians and providing support in the manufacturing areas during routine environmental monitoring and utility sampling. Key Objectives/Deliverables: * Adhere to and promote compliance with all cGMP procedures, Quality Systems, and Good Documentation Practices. * Provide support for Parenteral Operations activities by performing environmental monitoring of classified manufacturing areas. * Provide support for manufacturing and laboratory activities by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings. * Assist with technical training and mentoring of QC Environmental Monitoring Technicians through formal process/program. * Participate in department/company continuous improvement projects and initiatives. * Assist with authoring Standard Operating Procedures and Work Instruction documentation. * Adhere to and promote compliance of all safety standards. Minimum Requirements: * Education * High School Diploma or equivalent, Associate Degree is preferred. * * Experience * 3+ years of demonstrated relevant experience in performing Environmental Monitoring in a GMP Pharmaceutical Manufacturing facility, preferably associated with aseptic production. * Demonstrated ability in performing environmental monitoring techniques including, but not limited to viable surface monitoring, viable and non-viable air monitoring, compressed air monitoring, and water (potable, purified water, water for injection, clean steam) collection and analysis. * Previous experience with Laboratory IT systems such as LIMs, LES, and MODA. Additional Preferences: * Experience with cGMP requirements and regulatory compliance associated with a cGMP Manufacturing facility. * Strong interpersonal skills and ability to train/mentor QC Environmental Monitoring Technicians. * Strong oral and written communication skills for communicating to colleagues, management, and other departments. * Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations. * Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Other Information: * The role will be phased from a project support role to a routine support role as the development facility and processes progress. * Tasks may require repetitive motion and standing or walking for long periods of time. * Tasks may require lifting of up to 30 pounds and may require the ability to pass, push, and pull to execute specific aspects of the job role. * Ability to work 12-hour shifts.Ability to have a flexible schedule as the position may require training or working on day/night shift for a short duration prior to transitioning to designated day/night shift. * Travel will be required during the project phase for training and implementation of the Environmental Monitoring Program for the Concord site. The job specification is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job specification. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 - $39.06 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Maintain South Bay Solution quality standards by measuring and testing incoming materials, in-process production, and finished products and analyzing, and recording the inspection results. Number of positions : 3 Schedules Day shift Mid shift Swing shift Required Skills ASQ's CQI Certified Quality Inspector is a plus. Complete knowledge of application and interpretation of ASM Y14.5M, GD&T. Complete knowledge and application of GD&T symbols. Ability to set-up, apply mathematical concepts, fundamentals of datum structure plane, geometry and trigonometry to achieve actual dimensions. Able to perform inspections using video CMM (Keyence). Ability to perform inspection using Optical Comparator using Quadra-Chek 200. Knowledgeable in performing mechanical inspection on manual Mitutoyo CMM, and in running Zeiss CMM programs. Ability to discuss inspection methods and inspection results with those responsible for products. Able to input and trend inspection data and Key Process Indicators. Ability to setup unproved CMM programs effectively. Ability to troubleshoot CMM programs. Ability to validate parts using multiple inspection methods. Responsibilities Read blueprints and specifications. Inspect parts on surface plates. Measure and test product using all the inspection equipment being employed at SBS. Perform Visual Inspection to SBS and customer specifications. Perform product identification and traceability activities. Accept or reject product, document information, reports, inspection data, and issue NCR's into ERP databases. Education / Experience High School diploma or equivalent must have basic math, geometry, trigonometry, knowledge and application. Up to 2 years of on the job-experience in mechanical inspection in manufacturing environment. MS-Office suite experience, up to two years' experience generating spreadsheets, data entry. Benefits: Health Insurance (Medical/Dental/Vision) paid 100% for employees Life insurance policy Safe Harbor 401(K) plan 401(K) match Paid time off (vacation/sick/holidays/floating holiday) Referral program The employee may be required to perform other job-related duties.

About Summit Steel Works Corporation With over 23 years' experience as a total service steel trade partner, Summit Steel Works specializes in design, fabrication, and installation. We take pride in professionalism, responsiveness, and quality. Together, we tackle complex projects everyday. Make an impact! Work at a place where you can hone your craft and experience structural steel. QUALITY CONTROL INSPECTOR About The Role The Quality Control Inspector (QCI) is responsible for the accuracy of all items fabricated within the shop. As the QCI, you will act as the gate keeper for all items fabricated. As the QCI you will use a combination of code knowledge (AWS, AISC, RCSC, etc.) and technical expertise to verify that the final product is free of defects and meets the requirements in the contract documents and company fabrication drawings. Responsibilities Candidate Requirements • Conduct inspections for dimensions, fit-up, welds, bolts, and paint. Ensure all aspects meet contract and code requirements. • Scheduling, communicating, and coordinating with 3rd party (QAI) inspectors. • Ensure received materials, parts, and consumables meet all quality requirements. • Conduct welder qualification testing. • Develop company WPS and PQRs as required. • Maintain and ensure fabrication adheres to company quality management system and AISC standards • Certified welding inspector (CWI) with current certification preferred. At minimum, Associate welding inspector (AWI) with current certification is required. • Extensive knowledge of welding code, including AWS D1.1. • Knowledge of RCSC bolt inspection and testing requirements. • Experience with AISC audits preferred • Knowledge of NOMMA and AESS finish requirements preferred. • Experience working in fabrication or erection environment. Compensation & Benefits • $35hr - $55hr. Potential for bonus. • Full-time non-exempt. Occasional overtime • PTO and Holiday Pay • Medical (we pay 100% for the employee) • 401K after one year of service Please send a cover letter and resume to ****************************