Quality control analyst jobs in Citrus Heights, CA - 47 jobs

Quality Control Technician: Sauna Want to join one of the hottest health and wellness startups in the country? Well, PLUNGE is looking for just the right person to take our team to the next level. Overview of Role The role will report to Quality Management and support all production and warehouse processes. This role will be involved in a variety of manufacturing, testing, kitting, and packaging operations in a dynamic and proactive work environment. This position will become an active part of a quickly growing team! This role will be located at our Lincoln, CA location. Key Responsibilities Inspect pre-cut/pre-assembled in coming raw materials (beams, frames, electrical wire, wood moisture content). Inspect individual sauna pieces during build for dimensional accuracy and aesthetic flaws. Test electronic heaters and lights for the sauna. Inspect completed sauna and verify that the fit and finish of all pieces together align with our quality standard. Inspect the crated sauna and verify all pieces are included, undamaged, and placed properly to prevent damage during shipment. Document wood shop products (saunas, showers, shipping crates) with photographs. Our Ideal Candidate Experience with woodworking and carpentry processes High attention to detail Experience working with a variety of different teams and departments Experience working in Quality or Manufacturing Operations Proposes new ideas and thoroughly investigates issues Proactively embraces changes and promotes continuous improvement Benefits, Perks, Time Off Comprehensive health insurance: Medical, dental, and vision. Shared cost. Life/ADD, STD, and LTD benefits. 401K plans with a 3% match after 6 months. Perks 1 free monthly float at Capical FLoats in Sacramento or Auburn Health reimbursement for gym, supplements or other health expenses Get Paid to Plunge bonus Monthly catered lunches with live DJ and raffle prizes. Reimbursement for participating in the Landmark Forum. *Conditions apply.

Job Description With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate I works to meet departmental and organizational goals. Job Responsibilities: Perform a broad variety of basic and moderately complex tests with documentation according to GMP. Review data and assess against established acceptance criteria. Perform technical review of peer-generated data. Evaluate data to identify trends and/or establish limits. Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed. Identify and troubleshoot technical problems. Identify gaps in systems and procedures. Receive and provide training. Participate in assay transfer and assay validation. Perform equipment qualification / maintenance. Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures. Support the maintenance and compliance of operational areas. Assure and apply GMP throughout operations. Coordinate with customers to support multi-site operational activities. Support internal and external audits and regulatory inspections. Works to meet schedules, timelines, deadlines. Participate in and/or lead group and project teamwork; project and process improvements. Write protocols and reports under limited supervision. Meets scheduled performance of 95% on time. Perform other duties as requested by managers to support Quality activities. Job Requirements: B.S./B.A. degree and 1-3 years experience or Master's Degree plus one year experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry. Strong verbal and written communication skills, ability to organize and present information both formally and informally. Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures. Routinely exercises sound judgment, reasoning and problem solving. Capable of working under limited supervision and determining own short term priorities. The hiring rate for this position is $27.50 per hour. The base pay actually offered will take into account internal equity, and may also vary depending on candidate's geographic region, job-related knowledge, skills, and experience amongst other factors. Harvest Technical Services is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, Sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or any other federal, state, or local protected class.

Job Description About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to the core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals Inc., Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Research Chemist (E&L) We are seeking an experienced Research Chemist (E&L) with a minimum of 3-5 years of pharmaceutical industry experience. Responsibilities: Maintain, operate, and troubleshoot LC-MS and GC-MS, GC-FID, and ICP-MS Systems. Perform extraction, analysis, and characterization of extractables and leachables from polymeric materials associated with container closure systems of pharmaceutical drug products as per USP, PQRI, ICH and other regulatory guidelines. Develop and optimize sample preparation techniques for analysis on GC-MS, LC-MS, and ICP-MS systems. Develop and validate LC-MS, GC-MS, and ICP-MS methods for finished product and raw material characterization as well as extractable/leachable testing. Unknown impurity identifications using GC-MS, LC-MS, and LC-MS/MS or other suitable techniques. Interpret complex spectral data and fragmentation patterns. Routine stability testing of API, finished product samples for assay and impurities using various instrumental techniques as suited, and prepare stability data summaries. Generate study designs, write protocols, methods, Datasheets and reports. Provide support in the critical review of analytical data, reports and protocols. Write Instrument-related SOPs and provide training on the instrument and related software. Train new recruits in the lab and support the team as needed. Participate in internal meetings and conferences. Provide support during technical transfer between R&D and QC. Whenever needed, attend SOP, Safety, and scientific trainings to remain current with cGMP regulations, safety standards, and development technologies. Preparation and review of analytical methods, method validation, and related study reports for ANDA/ NDA submissions and support, document preparation for ANDA/ NDA submissions. Any other activities as directed by the supervisor. Qualifications: Education/Experience: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. Knowledge, Skills, and Abilities: Familiarity with the characterization and isolation of impurities. Strong foundation in organic chemistry and structural elucidation, with expertise in small molecule pharmaceutical drug development and peptides, including computational techniques. Proficiency in using standard laboratory equipment, including pipettes, graduated cylinders, and balances. Skilled in laboratory techniques for measuring, weighing, and handling samples. Hands-on experience with HPLC (highly preferred). Knowledge of chemical handling procedures, including safety precautions and documentation such as Safety Data Sheets (SDS). Competency in Microsoft Office applications. Experience or familiarity with current Good Manufacturing Practices (cGMP) is preferred. Requirements: Must live or be willing to move to the Sacramento Metropolitan Region (Approximately 40 miles' radius) Benefits: Pay range $70,000 - $85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401 (k) savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment o retaliation based on any of these factors.

* Ability to manage Quality on multiple projects * Supervise Quality staff * Train Quality activities and requirements at a divisional level * Assist Division Quality Manager as directed * Lead project team through engagement and processes * Ability to work with and report to senior management * Develop understanding/working knowledge of corporate quality control program, company standards, procedures, and building codes, required to perform assigned work * Develop Water+Min5 plan with project team * Review, comment, and work through Division Quality Manager for approval of trade partner project specific Quality Control Plans * Perform inspections and witness tests applicable to discipline to determine acceptability of work * Maintain work performance records, inspection records and other related items; assure correctness of all documents * Work with Project Manager and Site Superintendent to manage site quality program and assist in providing solutions to non-compliant items * Assist in preparation/implementation of quality control program, including but not limited to; procedures, inspection instructions, the control of measurement and testing equipment * Participate in internal/external quality control audits * Assist in reviewing purchase and submittal documents to ensure compliance with quality control requirements * Assist in resolution of reported project non-conformance issues * Monitor subcontractor work to ensure compliance with company standards, procedures and codes, when applicable * Ensure timely and successful implementation of corrective measures * Assist in and document commissioning processes * Complete other responsibilities as assigned Physical Demands and Environmental Conditions: * Occasional exposure to dust and fumes * Requires frequent stooping/bending/crouching, reaching, handling, finger dexterity, sitting, standing, walking, and lifting 20 or more lbs * Constant finger dexterity and ability to hear, and talk, and possess depth perception * Occasional climbing and carrying * The noise intensity level is moderate SUMMARY OF BENEFITS: This role is eligible for the following benefits: medical, dental, vision, 401(k) with company matching, Employee Stock Ownership Program (ESOP), individual stock ownership, paid vacation, paid sick leave, paid holidays, bereavement leave, employee assistance program, pre-tax flexible spending accounts, basic term life insurance and AD&D, business travel accident insurance, short and long term disability, financial wellness coaching, educational assistance, Care.com membership, ClassPass fitness membership, and DashPass delivery membership. Voluntary benefits include additional term life insurance, long term care insurance, critical illness and accidental injury insurance, pet insurance, legal plan, identity theft protection, and other voluntary benefit options. If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 98,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world. Our Rocklin, CA laboratory is looking for an entry-level Laboratory Analyst to join their team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. Job functions: After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies Performs routine operation, maintenance, calibration of laboratory instruments/equipment May assist with validation and MDL studies. Assists with investigation, and preparation of responses to client inquiries and CARs. Inputs and maintains technical information as needed to support the laboratory functions/operations. Maintains Laboratory Notebook where applicable. Adheres to internal standards, policies and procedures. Performs other duties as assigned. Qualifications Associate Degree in a Chemistry or similar scientific discipline and 0-2 years of experience in Analytical Chemistry Laboratories OR 3 years of relevant experience (i.e. Sample Prep) (Required) Bachelor's Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) Basic mathematical and reasoning skills (Required) Experience with Microsoft Office (Excel, Outlook, Word) (Required) Experience with LIMS (Preferred) Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required) The hourly pay for this position is $19-22/hr (dependent on experience). This position is eligible for overtime pay. In addition, your compensation package includes the following benefits: Participation in the Company's benefit programs coincident or following the first of the month in which you are hired. Immediate eligibility to participate in the Company's 401K Retirement Plan Paid vacation Four (4) floating holidays annually Seven (7) company observed holidays paid Sick time accrual Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

Full-time Description The Quality Control Inspector is responsible for maintaining quality standards by inspecting and approving machined, in-process production, purchased and finished products; recording quality results. The QC Inspector will work under limited supervision and directly with other inspectors and machinists to deliver a high quality product. Essential Duties & Functions: Completes all duties and responsibilities in adherence with Tri Tool's core values. Perform manual inspection of parts on surface plate using mechanical hand tools such as height gages, micrometers, and calipers. Inspects first article, in-process and final products by confirming product meets applicable drawings and specifications; conducting visual and measurement tests; documenting and communicating rejections of unacceptable items. Inspection of products for outside processes such as: heat treat, machining, plating/painting, engraving etc. Receiving inspection of purchased products and outside processes. Operate Manual and DCC bridge CMMs running CMM Manager. Write programs, fixture, and report for machined metal parts. Record and document inspection data in logs and computer tracking tools. Keep inspection and measurement equipment operating by following operating instructions; and notifying management when repairs are deemed necessary. Perform in-house calibrations on equipment such as micrometers, plug gages, thread gages, etc. Maintains a safe and healthy work environment by following standards and procedures; complying with State, Federal, and Company safety regulations. Effectively communicates with coworkers and managers to support efficient production. Performs other work in related duties as assigned to ensure a highly maintained and safe department. Work as part of the team to ensure productivity and cross train to other departments as needed. Requirements Requirements & Qualifications: High School Diploma or equivalent. A.A. degree in Machining/Inspection desirable; 2+ years of experience in field machining or manufacturing or technical training related to manufacturing; 1-2 years of full time inspection experience with previous machining experience. May consider machining experience only with directly related technical training; Proficient with inspecting multiple production processes including; turning, milling, grinding, fabricating, etc.; Ability to demonstrate a high level in reading and interpreting blueprints, specifications, and related documents; Familiar with ansi y14.5; Knowledge of ISO practices. Calculate figures using basic shop math; Reading of calipers, micrometers, bore gages, dial indicators, height gages, etc.; Operate manual and DCC CMM; Working knowledge of Tri Tool's product line preferred; Basic computer skills; MS Office applications and/or Inspection Software; Must have and demonstrate good decision making skills. Salary Description $25-$28 per hour depending on experience

Full-time Description The Quality Control Inspector I is responsible for routine (incoming, in-process, first article and final) QC inspection of raw materials, subassemblies and finished product. All receiving, in-process, first article and final inspections are performed in accordance with documented procedures and specifications. The QC Inspector I shall ensure that inspection equipment is properly calibrated, handled and maintained. The QC Inspector I documents inspection results and releases acceptable product for use. The QC Inspector I identifies and segregates nonconforming product/processes for disposition by the Material Review Board. The work schedule for this role is Monday through Friday, 6:00am to 2:30pm DUTIES/RESPONSIBILITIES The Quality Control Inspector I is responsible for performance of the following quality system functions in accordance with documented procedures: Inspection- Performing first article, receiving, in-process and final inspections in accordance with documented procedures. Assisting other personnel with inspection setups and questions. Process Control - Maintain product identification and traceability requirements throughout the inspection processes. Nonconformance Handling - Identification, documentation, evaluation, and segregation of nonconforming product pending review and disposition by the Material Review Board. Statistical Techniques - Employment of the appropriate statistical sampling techniques for inspection by attributes (ANSI/ASQ Z1.4). Requirements This position requires the following qualifications (at a minimum): Experience performing inspections in a regulated industry such as medical device, automotive, aerospace. Adequate knowledge and understanding of the applicable quality system requirements (ISO 13485:2016, 21 CFR Part 820, etc.); Adequate knowledge and understanding of industry-standards for the sampling (ANSI/ASQ Z1.4) and inspection of product; Excellent organizational and communication skills. The ability to follow directions and interpret engineering and inspection specifications, including GD&T. Experience with a variety of inspection instruments such as calipers, micrometers, go/no-go gauges with Optical Comparators and CMM operation being a plus. Experience with developing open inspection setups on surface plates using height gages, sine plates etc. Experience with the inspection of high polished, tumbled, sand blasted and satin brushed surface finishes is a plus. Good written and verbal communication skills and ability to solve problems. Basic computer skills using Windows operating system. Requires a high school diploma or its equivalent. One or more years of related experience preferred. Essential Functions Typical Working Conditions, Equipment Used, and Essential Physical Tasks: Depending on task assignment, the physical demands described here may be representative of those that must be met by an employee to successfully perform the essential functions of this job. Percentage of time in essential function may depend on assignment of tasks: Walking and standing on hard surface while using instrumentation. Working in a temperature controlled enclosed office area. Sitting for periods of up to 2 hours. Bending, kneeling, squatting, stooping, reaching, pulling, pushing, and lifting up-to 25 lbs. Must be able to stand for long periods of time - up to 50%. Some exposure to loud noises generated from manufacturing equipment. Use of magnification/visual assistance devices for inspection work. Typing using a keyboard and entering information into tracking systems. We offer company holidays, vacation and sick time off, medical, dental, vision, disability and life benefits as well as a 401(k) Plan. Shalby Advanced Technologies, Inc. provides equal employment opportunities to applicants and employees without regard to: age, genetic information/characteristics, marital status, medical condition, mental or physical disability, national origin and ancestry, pregnancy and perceived pregnancy, race and color, religion, sex/gender including pregnancy, breastfeeding, gender identity or gender expression, sexual stereotypes, sexual orientation, reproductive health decision-making and veteran or military status. The expected base salary range for this position is between $21.00-$22.00 per hour and the compensation offered will depend on the candidate's qualifications.

What makes us strong? Our employees in 50 countries worldwide - all working with passion to enable high-tech applications with our strong metals: tungsten and molybdenum. Our CERATIZIT site in Sacramento delivers precision cutting tools to a wide range of industries across North America-combining technical excellence with responsive local service. Join a highly motivated team in Sacramento, USA, where local expertise meets the global knowledge and values of the Plansee Group. Position type: Hourly Quality Control Inspector FULL-TIME/Swing Shift 3:15pm-11:45pm Your tasks: Responsible for performing visual and dimensional inspections of the products utilizing measuring instruments Responsible for filling out inspection documents; ensuring all sequences have been followed Logging returned materials and/or scrap materials Determines product acceptability based on company standards and consults with supervisor in unusual situations Performs extra duties or special projects when requested Your profile: Must be able to pay attention to detail and accurately follow instructions Experience in quality control (Preferably using equipment such as: micrometer, caliper, optical comparator, microscope) Experience with MS Excel, MS Word, and SAP preferred Ability to lift up to 40 lbs and stand for an 8-hour shift Ability to work in a team environment as well as independently Strong benefits: A stable job in an internationally established company Complete benefits package of employer contributions to Medical, Dental, Vision, 401K, Life Insurance, Sick and PTO, 11 paid Holidays per year Wages depend on experience and qualifications Alcohol and drug-free workplace. All qualified candidates must pass a pre-employment drug screening as a condition of employment Quality Control Inspector Equal Employment Opportunity We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class. Colleen Schneider | Recruiting Team | *********************************** CERATIZIT Sacramento LP

JOB DETAILS Base pay starts at $22.00 per hour plus $1.00 shift differential for 2nd shift Shift: 2nd - 3:00 pm - 11:30 pm, Monday-Friday (includes overtime) DUTIES AND RESPONSIBILITIES The Quality Technician conducts detailed inspections of fabricated parts, in process control inspections. Conducts audits of packaged, staged and loaded shipments to insure compliance with Ply Gem quality requirements and specifications. Knows and understands all safety rules and precautions necessary for working in and about a manufacturing environment Responsible for monitoring, inspecting, and reporting all assigned activities and finished goods to insure quality Ability to submit clear, concise, and accurate reports of inspections, audits, test results, job site visits and delivered goods Ability to conduct tests using a variety of tools and equipment Responsible for preparing daily quality control activity summaries Ability to assist in developing and implement objectives, plans and priorities to achieve quality control objectives in a timely manner to meet deadlines Communicates with Quality Manager on methods and problem-solving procedures to successfully meet deadlines Assists and periodically delivers internal external audits Maintains continuous improvement practices in work area May be assigned additional projects or duties as designated by Team Leader Ability to complete and present basic Root Cause analysis Inspect all incoming raw materials per inspection plan Record and maintain receiving inspection results Completes first article quality reports In-Process Verification of calibration tools for all inspection test equipment and tools Maintains gage calibration database and records Perform product test and records results during product manufacturing Ensures adherence to production practices and product quality standards Assists in the documentation of and resolution of nonconforming material and process discrepancy Evaluate product to determine if they are acceptable Perform start-up and changeover audits to verify that the product will meet specifications Proficient at using Microsoft office Qualifications To perform satisfactorily in this position, the employee must be able to perform each essential duty satisfactorily. The requirements listed below are representative of knowledge, skills, and/or ability required. Reasonable accommodations may be made for employees with certain disabilities to perform the essential functions. Language Skills: Ability to read and comprehend documents including but not limited to policy manuals, safety rules/programs, operating and maintenance instructions, procedure manuals, and simple correspondence, in addition, the ability to communicate information effectively one-on-one and in small group situations and settings is required Mathematical Skills: Ability to perform general mathematic calculations including but not limited to addition, subtraction, multiplication, fractions, percentages, and division Some positions may require advance mathematics Reasoning Ability: Ability to apply common sense understanding to perform work instructions furnished in written, oral or diagram form a must. In addition; the ability to solve problems, which involve multiple variables in a standard situation, is required Other Knowledge, Skills & Abilities: Must have a high degree of concentration Ability to work effectively to meet deadlines Ability to work with a diversified work force Ability to read different measuring devices (i.e. tape measure, protractor, micrometer) Physical Demands: While performing the duties of the job, the employee is regularly required to talk or hear The employee is frequently required to walk The employee is frequently required to stand; sit; bend; stoop; use hands and fingers to handle or feel objects; reach with hands and arms; lift; climb and/or balance essential tasks Specific vision abilities include close-up and distance vision, color vision, peripheral vision, and depth perception Work Environment: The employee may be required to enter areas that are near moving mechanical parts, with occasional exposure to hazardous chemicals, and extreme cold or heat The noise level in the work environment is considered moderate, and may require the use of hearing protection The employee will be required to utilize Personal Protective Equipment (PPE) when accessing certain manufacturing areas: hard hat, gloves, welding jacket or weld bibs, safety glasses, welding hood and earplugs Safety Responsibilities: Before initiating work at Ply Gem, the employee is required to read and understand the position's Job Safety Analysis The employee must wear appropriate Personal Protective Equipment (PPE) and perform tasks in a manner consistent with Ply Gem safety training, Ply Gem Employee Manual and OSHA regulations Additional Information Address: 3010 Ramco St # 100, West Sacramento, CA 95691 *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. All your information will be kept confidential according to EEO guidelines. The US pay for this full-time position is $22.00 per hour + $1.00 shift differential + medical, dental, vision benefits starting day 1 + 401k and PTO. (Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.) Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play . Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here . You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here . If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or [email protected] . If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or [email protected] . This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. All your information will be kept confidential according to EEO guidelines. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.

Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets. **If you are a current associate of Primo Brands, please apply** **here** **Factory Location:** Sacramento, CA **Compensation:** $23.50/hour _This position is_ **_seasonal_** _, with the possibility of direct hire and increased compensation upon transition to a permanent role, contingent on performance and other relevant factors._ **_Seasonal Benefits: Sick time Employee discounts 401K with a 5% match_** Responsibilities + Visually inspect and sign off product quality as it comes of the line during final point of control + Record all necessary activities on Zebra handheld computer accurately + Actively participate in the DOR, taking actions and coaching to gain results for manufacturing excellence + Operate, clean, and service water dispensers and equipment + Packaging parts, loading raw materials, equipment washing, quality control inspections and data recording + Maintain workstation in an organized and clean manner to ensure safety and Good Manufacturing Practices + Interact with production team members, quality control and maintenance technicians to maximize output and efficiency + Safely use and work around various chemicals and follow SOP's accordingly + Assemble, wash and sanitize various units as required using the established procedure + Effectively read and utilize instructional, mechanical, and electrical technical manuals + Capable of using a pneumatic drill and other hand tools + Considerable ability to follow oral and written instructions + Work in wet work areas, ensuring the use of proper chemicals and following all safety protocols + Perform other duties as assigned Qualifications + High School Diploma, GED, or equivalent work experience + Minimum (3) years' experience in related role, prior exposure to manufacturing in the food or beverage industry preferred + Ability to work independently or collaboratively, with strong communication skills + Able to lift and pull 50 lbs. as needed while performing work continuously throughout the shift + Ability to sit, stand, push, pull, climb ladders, walk all day with or without reasonable accommodation + Must be able to do physical inspections of equipment that will require climbing, reaching, and extending arms overhead Primo Brands' established portfolio includes billion-dollar brands Poland Spring and Pure Life , premium brands like Saratoga and Mountain Valley , regional leaders such as Arrowhead , Deer Park , Ice Mountain Ozarka , and Zephyrhills , purified brands, Primo Water and Sparkletts , and flavored and enhanced brands like Splash and AC+ION . Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come. Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law. Candidates must possess strong English language skills to effectively communicate with customers and provide exceptional service. Proficiency in English is essential for understanding customer needs, resolving inquiries, and collaborating with team members.

Quality Control Technician needs 2+ years of work experience in a professional, manufacturing, or laboratory setting Quality Control Technician requires: High school diploma or GED 2+ years of work experience in a professional, manufacturing, or laboratory setting Basic math skills Clear and effective oral and written communication with a small team within a large company Ability to work independently and to take directions based on circumstances Computer literacy in Microsoft Office Suite Be able to safely work with chemicals in a laboratory and manufacturing environment Preferred: Associates degree in sciences or some college coursework Knowledge of basic laboratory practices Physical Requirements: Must be able to lift up to 50 lbs. Must be able to stand for long periods of time Quality Control Technician duties: Operate analytical instruments to perform quality control testing of liquid 3D printing resin according to standard, including: o Digital Light Processing (DLP) 3D printing. Color and ultraviolet spectrophotometry. Rheology. ASTM methods D790, D412, D638, D7867 Calculate and report test results using Albert and SAP software for the completion of quality tasks Communicate with product development, engineering, and production personnel to make batch adjustments as needed Use good manufacturing practices to maintain clean working environments such as lab benches, fume hoods, and ovens. Monitor equipment performance by completing routine standards checks Perform incoming inspections of raw materials shipments and property data File, maintain, and appropriately dispose of raw material, quality retain, and finished product inventories Comply with weekly 5S standards including sweeping, mopping, organizing, and trash removal. Ensure end to end sample and product traceability Complete other miscellaneous responsibilities within the Quality Department as assigned by department manager

ABOUT OUR JOB The City of Vacaville - A beautiful place to live, a great place to work! With over 600 employees, the City of Vacaville is proud to serve a vibrant, growing community. We offer a supportive and engaging workplace with employee social and wellness events, casual dress days, flexible work schedules, every other Friday off and outstanding pay and benefits. Join us and help shape the future of Vacaville! The City of Vacaville invites applications for the position of Laboratory Analyst I/IIin the Utilities Department. Currently, one (1) vacancy exists. This recruitment will serve to establish an eligibility list for possible future use over the next 12-month period. Salary Information: Lab Analyst I $83,325 - $101,282/Annually Lab Analyst II $91,695 - $111,456/Annually A 2% COLA is scheduled for 11/1/2026 Working for the City of Vacaville comes with an excellent benefits package including: * Medical Insurance at affordable rates - City covers up to 85% of Kaiser premium, other plans are also available * Vision and Dental Insurancemonthly premiums covered 100% by the City * Healthcare double coverage opt-out incentive of $3,000 per year for eligible employees * Paid sick leave, vacation leave, thirteen holidays and two floating holidays a year * Tuition reimbursement and student loan repaymentup to $2,200 per fiscal year * Deferred compensation plan with City contribution, no employee match required * California Public Employees Retirement System (CalPERS) plan enrollment and Retiree Health Savings account * Please see our generous benefits packagehere.* The Laboratory Analyst I is the entry level class that receives training and performs routine laboratory work under the supervision of senior laboratory staff. Job duties include, but are not limited to: * Calculate and record laboratory test results * Perform inspections * Operate and maintain a variety of laboratory and operations equipment * Interpret test results and report them to operations personnel The Laboratory Analyst IIis the full journey level class that requires a significant level of analytical skills and functional expertise beyond that expected at the entry level. Job duties include, but are not limited to: * Develop and revise SOP, policies and forms * Train new analysts and college interns * Provide advanced reports * Run advanced analytical methods and instrumentation Applicants working in the Utilities Laboratory must be willing to potentially work any shift between the hours of 6:30am and 5:00pm, 365 days/year. Currently the department assigns a weekend rotation shift every 4-5 weeks. For more information, including the complete job description and benefits, please use the links below: Laboratory Analyst I Laboratory Analyst II ABOUT YOU The ideal candidate will possess: * Practical experience in a wide range of water and wastewater analysis * Microbiology knowledge, such as * MTF, HPC, substrate methodology, media preparation, autoclave use * Wet Chemistry analysis, such as: * TSS, TDS, BOD, pH, EC, Ammonia * Any experience analyzing samples and interpreting data with complex instruments such as: * Gas Chromatography (GC), Ion Chromatography (IC), High Pressure Liquid Chromatography (HPLC) and Mass Spectroscopy (MS) with any instrument * An understanding of the difference between quality assurance and quality control * Experience with Microsoft Excel and Word * Familiarity with EPA Water, Wastewater, and Environmental Compliance requirements and regulations * Familiarity with laboratory safety requirements and potential hazards and pitfalls * Detailed organizational skills * Training/experience with The NELAC Institute (TNI) regulations * Practical experience in dealing and communicating with individuals, groups and entities outside the laboratory * An AWWA or CWEA Lab Analyst Certificate Grade I or above LABORATORY ANALYST I Any combination of education and experience that would provide the required knowledge and abilities is qualifying. A typical way to obtain the knowledge and abilities would be in one of the following two ways: Education: Completion of two (2) years of college with major coursework in chemistry, biology, microbiology or other related laboratory science. Experience: One year of general laboratory analysis experience. License or Certificate: Must obtain the California Water Environment Association (CWEA) Laboratory Analyst Grade I certificate, or the American Water Works Association (AWWA) Water Quality Analyst Grade I certificate, plus any other State-mandated certifications, as a condition of passing probation. Must possess a valid California Class C driver's license and have a satisfactory driving record as conditions of initial and continued employment. OR Education: Possession of a Bachelor's Degree in chemistry, biology, microbiology or other related laboratory science. Experience: None Required. License or Certificate: Must obtain the California Water Environment Association (CWEA) Laboratory Analyst Grade I certificate, or the American Water Works Association (AWWA) Water Quality Analyst Grade I certificate, plus any other State-mandated certifications, as a condition of passing probation. Must possess a valid California Class C driver's license and have a satisfactory driving record as conditions of initial and continued employment. LABORATORY ANALYST II Any combination of education and experience that would provide the required knowledge and abilities is qualifying. A typical way to obtain the knowledge and abilities would be in one of the following two ways: Education: Completion of two years of college with major coursework in chemistry, biology, microbiology or other related laboratory sciences. Experience: Two years of water and/or wastewater laboratory analysis experience. License or Certificate: Possession of the California Water Environment Association (CWEA) Laboratory Analyst Grade III certificate, or the American Water Works Association (AWWA) Water Quality Analyst Grade III certificate, plus any other State-mandated certifications. Must possess a valid California Class C driver's license and have a satisfactory driving record as conditions of initial and continued employment. OR Education: Possession of a Bachelor's Degree in chemistry, biology, microbiology or other related laboratory science. Experience: One year of water and/or wastewater laboratory analysis experience. License or Certificate: Possession of the California Water Environment Association (CWEA) Laboratory Analyst Grade II certificate, or the American Water Works Association (AWWA) Water Quality Analyst Grade II certificate, plus any other State-mandated certifications. Must possess a valid California Class C driver's license and have a satisfactory driving record as conditions of initial and continued employment. ABOUT EVERYTHING ELSE This recruitment is open and continuous and may close at any time. The next review of applicants will take place on January 19, 2026. A completed City of Vacaville employment application and supplemental questionnaire must be received by the Human Resources Department at 650 Merchant Street, Vacaville, CA 95688bythe closing of this recruitment. Applicants are encouraged to apply online at************************ Application packets may also be requested in person at the Human Resources Department or by calling **************. Resumes will not be accepted in lieu of a completed application packet. IMPORTANT:Contact with applicants will primarily occur via email. Please ensure that your application indicates a valid email address which you check on a regular basis. For ADA information and other Frequently Asked Questions, please clickhere. Applicants receiving a conditional offer of employment must successfully complete the pre-placement process for this position before a final offer will be extended. Pre-placement assessments for this position include a Livescan (FBI/DOJ fingerprint review), employment verification, education review and DMV review.

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. Job Description Quality Control Utility - Arbuckle, CA This is an hourly position Position Summary: This position offers an exciting opportunity for Quality Control in Rough Rice department of Rice Mill. Job Responsibilities: Duties include but are not limited to: Duties include but are not limited to: Protect the product and make sure all quality control checks are being done Cross train and work in all departments Assist in development of SOP's and Work Instructions Train new hires Can work overtime each day Enforcement of all ADM policies and procedures Assist in completing JSA's Must have a demonstrated history of safe work behavior and a sincere desire to follow and improve upon safety policies and procedures. Promotes the ADM Way and Core Values Able to communicate with all levels of the organization All other duties assigned by management Qualifications Ability work under pressure, well with others Good attendance Must have a demonstrated history of safe work behavior and a sincere desire to follow and improve upon safety policies and procedures Basic Computer and Math skills Respectful, positive attitude Strong work ethic Must be self-motivated Must possess excellent leadership, team building, problem solving, time managing, and organizational skills Excellent written and verbal communication Bilingual is a plus Physical Requirements: Walking and/or standing for extended periods of time Working in environments at varying temperatures and noise levels Occasionally lifting, stooping and climbing Available to work occasional weekends and/or holidays as well as during off hours to address emergency conditions or other situations that may arise ADM requires the successful completion of a background check. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. The pay for this position is expected to be: $19.00-$21.00

About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to the core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals Inc., Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Research Chemist (E&L) We are seeking an experienced Research Chemist (E&L) with a minimum of 3-5 years of pharmaceutical industry experience. Responsibilities: Maintain, operate, and troubleshoot LC-MS and GC-MS, GC-FID, and ICP-MS Systems. Perform extraction, analysis, and characterization of extractables and leachables from polymeric materials associated with container closure systems of pharmaceutical drug products as per USP, PQRI, ICH and other regulatory guidelines. Develop and optimize sample preparation techniques for analysis on GC-MS, LC-MS, and ICP-MS systems. Develop and validate LC-MS, GC-MS, and ICP-MS methods for finished product and raw material characterization as well as extractable/leachable testing. Unknown impurity identifications using GC-MS, LC-MS, and LC-MS/MS or other suitable techniques. Interpret complex spectral data and fragmentation patterns. Routine stability testing of API, finished product samples for assay and impurities using various instrumental techniques as suited, and prepare stability data summaries. Generate study designs, write protocols, methods, Datasheets and reports. Provide support in the critical review of analytical data, reports and protocols. Write Instrument-related SOPs and provide training on the instrument and related software. Train new recruits in the lab and support the team as needed. Participate in internal meetings and conferences. Provide support during technical transfer between R&D and QC. Whenever needed, attend SOP, Safety, and scientific trainings to remain current with cGMP regulations, safety standards, and development technologies. Preparation and review of analytical methods, method validation, and related study reports for ANDA/ NDA submissions and support, document preparation for ANDA/ NDA submissions. Any other activities as directed by the supervisor. Qualifications: Education/Experience: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. Knowledge, Skills, and Abilities: Familiarity with the characterization and isolation of impurities. Strong foundation in organic chemistry and structural elucidation, with expertise in small molecule pharmaceutical drug development and peptides, including computational techniques. Proficiency in using standard laboratory equipment, including pipettes, graduated cylinders, and balances. Skilled in laboratory techniques for measuring, weighing, and handling samples. Hands-on experience with HPLC (highly preferred). Knowledge of chemical handling procedures, including safety precautions and documentation such as Safety Data Sheets (SDS). Competency in Microsoft Office applications. Experience or familiarity with current Good Manufacturing Practices (cGMP) is preferred. Requirements: Must live or be willing to move to the Sacramento Metropolitan Region (Approximately 40 miles' radius) Benefits: Pay range $70,000 - $85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401 (k) savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment o retaliation based on any of these factors.

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 98,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world. Our Rocklin, CA laboratory is looking for an entry-level Laboratory Analyst to join their team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. Job functions: * After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies * Performs routine operation, maintenance, calibration of laboratory instruments/equipment * May assist with validation and MDL studies. * Assists with investigation, and preparation of responses to client inquiries and CARs. * Inputs and maintains technical information as needed to support the laboratory functions/operations. * Maintains Laboratory Notebook where applicable. * Adheres to internal standards, policies and procedures. * Performs other duties as assigned. Qualifications * Associate Degree in a Chemistry or similar scientific discipline and 0-2 years of experience in Analytical Chemistry Laboratories OR 3 years of relevant experience (i.e. Sample Prep) (Required) * Bachelor's Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) * Basic mathematical and reasoning skills (Required) * Experience with Microsoft Office (Excel, Outlook, Word) (Required) * Experience with LIMS (Preferred) * Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required) The hourly pay for this position is $19-22/hr (dependent on experience). This position is eligible for overtime pay. In addition, your compensation package includes the following benefits: * Participation in the Company's benefit programs coincident or following the first of the month in which you are hired. * Immediate eligibility to participate in the Company's 401K Retirement Plan * Paid vacation * Four (4) floating holidays annually * Seven (7) company observed holidays paid * Sick time accrual Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

Job DescriptionDescription: The Quality Control Inspector I is responsible for routine (incoming, in-process, first article and final) QC inspection of raw materials, subassemblies and finished product. All receiving, in-process, first article and final inspections are performed in accordance with documented procedures and specifications. The QC Inspector I shall ensure that inspection equipment is properly calibrated, handled and maintained. The QC Inspector I documents inspection results and releases acceptable product for use. The QC Inspector I identifies and segregates nonconforming product/processes for disposition by the Material Review Board. The work schedule for this role is Monday through Friday, 6:00am to 2:30pm DUTIES/RESPONSIBILITIES The Quality Control Inspector I is responsible for performance of the following quality system functions in accordance with documented procedures: Inspection- Performing first article, receiving, in-process and final inspections in accordance with documented procedures. Assisting other personnel with inspection setups and questions. Process Control - Maintain product identification and traceability requirements throughout the inspection processes. Nonconformance Handling - Identification, documentation, evaluation, and segregation of nonconforming product pending review and disposition by the Material Review Board. Statistical Techniques - Employment of the appropriate statistical sampling techniques for inspection by attributes (ANSI/ASQ Z1.4). Requirements: This position requires the following qualifications (at a minimum): Experience performing inspections in a regulated industry such as medical device, automotive, aerospace. Adequate knowledge and understanding of the applicable quality system requirements (ISO 13485:2016, 21 CFR Part 820, etc.); Adequate knowledge and understanding of industry-standards for the sampling (ANSI/ASQ Z1.4) and inspection of product; Excellent organizational and communication skills. The ability to follow directions and interpret engineering and inspection specifications, including GD&T. Experience with a variety of inspection instruments such as calipers, micrometers, go/no-go gauges with Optical Comparators and CMM operation being a plus. Experience with developing open inspection setups on surface plates using height gages, sine plates etc. Experience with the inspection of high polished, tumbled, sand blasted and satin brushed surface finishes is a plus. Good written and verbal communication skills and ability to solve problems. Basic computer skills using Windows operating system. Requires a high school diploma or its equivalent. One or more years of related experience preferred. Essential Functions Typical Working Conditions, Equipment Used, and Essential Physical Tasks: Depending on task assignment, the physical demands described here may be representative of those that must be met by an employee to successfully perform the essential functions of this job. Percentage of time in essential function may depend on assignment of tasks: Walking and standing on hard surface while using instrumentation. Working in a temperature controlled enclosed office area. Sitting for periods of up to 2 hours. Bending, kneeling, squatting, stooping, reaching, pulling, pushing, and lifting up-to 25 lbs. Must be able to stand for long periods of time - up to 50%. Some exposure to loud noises generated from manufacturing equipment. Use of magnification/visual assistance devices for inspection work. Typing using a keyboard and entering information into tracking systems. We offer company holidays, vacation and sick time off, medical, dental, vision, disability and life benefits as well as a 401(k) Plan. Shalby Advanced Technologies, Inc. provides equal employment opportunities to applicants and employees without regard to: age, genetic information/characteristics, marital status, medical condition, mental or physical disability, national origin and ancestry, pregnancy and perceived pregnancy, race and color, religion, sex/gender including pregnancy, breastfeeding, gender identity or gender expression, sexual stereotypes, sexual orientation, reproductive health decision-making and veteran or military status. The expected base salary range for this position is between $21.00-$22.00 per hour and the compensation offered will depend on the candidate's qualifications.

The Quality Control Inspector is responsible for maintaining quality standards by inspecting and approving machined, in-process production, purchased and finished products; recording quality results. The QC Inspector will work under limited supervision and directly with other inspectors and machinists to deliver a high quality product. Essential Duties & Functions: Completes all duties and responsibilities in adherence with Tri Tool's core values. Perform manual inspection of parts on surface plate using mechanical hand tools such as height gages, micrometers, and calipers. Inspects first article, in-process and final products by confirming product meets applicable drawings and specifications; conducting visual and measurement tests; documenting and communicating rejections of unacceptable items. Inspection of products for outside processes such as: heat treat, machining, plating/painting, engraving etc. Receiving inspection of purchased products and outside processes. Operate Manual and DCC bridge CMMs running CMM Manager. Write programs, fixture, and report for machined metal parts. Record and document inspection data in logs and computer tracking tools. Keep inspection and measurement equipment operating by following operating instructions; and notifying management when repairs are deemed necessary. Perform in-house calibrations on equipment such as micrometers, plug gages, thread gages, etc. Maintains a safe and healthy work environment by following standards and procedures; complying with State, Federal, and Company safety regulations. Effectively communicates with coworkers and managers to support efficient production. Performs other work in related duties as assigned to ensure a highly maintained and safe department. Work as part of the team to ensure productivity and cross train to other departments as needed. Requirements Requirements & Qualifications: High School Diploma or equivalent. A.A. degree in Machining/Inspection desirable; 2+ years of experience in field machining or manufacturing or technical training related to manufacturing; 1-2 years of full time inspection experience with previous machining experience. May consider machining experience only with directly related technical training; Proficient with inspecting multiple production processes including; turning, milling, grinding, fabricating, etc.; Ability to demonstrate a high level in reading and interpreting blueprints, specifications, and related documents; Familiar with ansi y14.5; Knowledge of ISO practices. Calculate figures using basic shop math; Reading of calipers, micrometers, bore gages, dial indicators, height gages, etc.; Operate manual and DCC CMM; Working knowledge of Tri Tool's product line preferred; Basic computer skills; MS Office applications and/or Inspection Software; Must have and demonstrate good decision making skills. Salary Description $25-$28 per hour depending on experience

Quality Control Technician needs 2+ years of work experience in a professional, manufacturing, or laboratory setting Quality Control Technician requires: High school diploma or GED 2+ years of work experience in a professional, manufacturing, or laboratory setting Basic math skills Clear and effective oral and written communication with a small team within a large company Ability to work independently and to take directions based on circumstances Computer literacy in Microsoft Office Suite Be able to safely work with chemicals in a laboratory and manufacturing environment Preferred: Associates degree in sciences or some college coursework Knowledge of basic laboratory practices Physical Requirements: Must be able to lift up to 50 lbs. Must be able to stand for long periods of time Quality Control Technician duties: Operate analytical instruments to perform quality control testing of liquid 3D printing resin according to standard, including: o Digital Light Processing (DLP) 3D printing. Color and ultraviolet spectrophotometry. Rheology. ASTM methods D790, D412, D638, D7867 Calculate and report test results using Albert and SAP software for the completion of quality tasks Communicate with product development, engineering, and production personnel to make batch adjustments as needed Use good manufacturing practices to maintain clean working environments such as lab benches, fume hoods, and ovens. Monitor equipment performance by completing routine standards checks Perform incoming inspections of raw materials shipments and property data File, maintain, and appropriately dispose of raw material, quality retain, and finished product inventories Comply with weekly 5S standards including sweeping, mopping, organizing, and trash removal. Ensure end to end sample and product traceability Complete other miscellaneous responsibilities within the Quality Department as assigned by department manager

JOB DETAILS Base pay starts at $22.00 per hour Shift: 1st shift, 6:00 am - 2:30 pm, Monday-Friday, overtime as designated DUTIES AND RESPONSIBILITIES The Quality Technician conducts detailed inspections of fabricated parts, in process control inspections. Conducts audits of packaged, staged and loaded shipments to ensure compliance with Ply Gem quality requirements and specifications. Knows and understands all safety rules and precautions necessary for working in and about a manufacturing environment Responsible for monitoring, inspecting, and reporting all assigned activities and finished goods to ensure quality Ability to submit clear, concise, and accurate reports of inspections, audits, test results, job site visits and delivered goods Ability to conduct tests using a variety of tools and equipment Responsible for preparing daily quality control activity summaries Ability to assist in developing and implement objectives, plans and priorities to achieve quality control objectives in a timely manner to meet deadlines Communicates with Quality Manager on methods and problem-solving procedures to successfully meet deadlines Assists and periodically delivers internal external audits Maintains continuous improvement practices in work area May be assigned additional projects or duties as designated by Team Leader Ability to complete and present basic Root Cause analysis Inspect all incoming raw materials per inspection plan Record and maintain receiving inspection results Completes first article quality reports In-Process Verification of calibration tools for all inspection test equipment and tools Maintains gage calibration database and records Perform product test and records results during product manufacturing Ensures adherence to production practices and product quality standards Assists in the documentation of and resolution of nonconforming material and process discrepancy Evaluate product to determine if they are acceptable Perform start-up and changeover audits to verify that the product will meet specifications Proficient at using Microsoft office Qualifications To perform satisfactorily in this position, the employee must be able to perform each essential duty satisfactorily. The requirements listed below are representative of knowledge, skills, and/or ability required. Reasonable accommodations may be made for employees with certain disabilities to perform the essential functions. Language Skills: Ability to read and comprehend documents including but not limited to policy manuals, safety rules/programs, operating and maintenance instructions, procedure manuals, and simple correspondence, in addition, the ability to communicate information effectively one-on-one and in small group situations and settings is required Mathematical Skills: Ability to perform general mathematic calculations including but not limited to addition, subtraction, multiplication, fractions, percentages, and division Some positions may require advance mathematics Reasoning Ability: Ability to apply common sense understanding to perform work instructions furnished in written, oral or diagram form a must. In addition; the ability to solve problems, which involve multiple variables in a standard situation, is required Other Knowledge, Skills & Abilities: Must have a high degree of concentration Ability to work effectively to meet deadlines Ability to work with a diversified work force Ability to read different measuring devices (i.e. tape measure, protractor, micrometer) Physical Demands: While performing the duties of the job, the employee is regularly required to talk or hear The employee is frequently required to walk The employee is frequently required to stand; sit; bend; stoop; use hands and fingers to handle or feel objects; reach with hands and arms; lift; climb and/or balance essential tasks Specific vision abilities include close-up and distance vision, color vision, peripheral vision, and depth perception Work Environment: The employee may be required to enter areas that are near moving mechanical parts, with occasional exposure to hazardous chemicals, and extreme cold or heat The noise level in the work environment is considered moderate, and may require the use of hearing protection The employee will be required to utilize Personal Protective Equipment (PPE) when accessing certain manufacturing areas: hard hat, gloves, welding jacket or weld bibs, safety glasses, welding hood and earplugs Safety Responsibilities: Before initiating work at Simonton, the employee is required to read and understand the position's Job Safety Analysis The employee must wear appropriate Personal Protective Equipment (PPE) and perform tasks in a manner consistent with Ply Gem safety training, Ply Gem Employee Manual and OSHA regulations Additional Information Address: 2019 E Monte Vista Ave, Vacaville, CA 95688 Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play . Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. You can also join one of our Employee Resource Groups which help support our commitment to providing a diverse and inclusive work environment. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. All your information will be kept confidential according to EEO guidelines. The US pay for this full-time position is $22.00 per hour + medical, dental, vision benefits starting day 1 + 401k and PTO. (Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.) Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play . Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here . You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here . If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or [email protected] . If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or [email protected] . This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. All your information will be kept confidential according to EEO guidelines. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.