Process inspector jobs near me

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title DPI QA Inspector II Organization Name InvaGen Pharmaceuticals, Inc. Location Unit 1 - 7 Oser Avenue, Hauppauge, NY 11788 Employment Type Full Time Shift First Shift: 8:30 AM - 5:00 PM (May vary based on business needs) Salary Range (Base/salary) $18.72/hr - $26/hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, employee discounts, and other benefits. Responsibilities/ Accountabilities The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specifications. * Verification of raw materials during the dispensing process. * Dispensing printed packaging materials to packaging. * Perform in-process checks during batch manufacturing and packaging, as per manufacturing & batch packaging record instructions. * Collection of in-process blend, finished product, validation samples for analysis, sample collection as per protocols. Specifically, to perform blend uniformity (BU) sampling. * To clean and maintain the samplings rods/dies/sample boxes used for BU sampling. * Perform IPQA testing on the manufacturing floor specifically LOD, Bulk Density, Tapped Density, Leak Test, Weight Variation test. * Ensure cleaning of manufacturing and packaging equipment, area and provide line clearance. * To perform posting of dispensed materials and samples into SAP system (ERP system) and to perform other transactions in SAP. * Involve in investigation of Deviation, OOS, OOT, or any other non-conformances. * Ensure completion of individual training assigned and follow company policies, safety requirements, cGMP and SOP's. * Review of online batch records, area/equipment logbooks, calibration/PMP records etc. * Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record. * Review of engineering records (temperature and humidity data, calibration reports and PMP records). * To take daily Quality rounds at shop floor to ensure shop floor is maintained in state of compliance and per GMP requirement. * Report, escalate to Manager quality assurance about daily shop floor activities and any discrepancy during batch manufacturing and packing. * Other duties [additional support] that management may assign from time to time. Education Qualifications/Experience * Minimum Science Graduate * A minimum of 1-2 years of pharmaceutical experience (DPI, MDI or Injectables) preferred. * Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies * Knowledge of Good Manufacturing Practices and 21 CFR Part 820. * Ability to read, write and communicate effectively. * Basic computer skills (Microsoft Word, Power and Excel). * Self-motivated, with the ability to work in fast-paced manufacturing environment and handle multiple tasks simultaneously. * Excellent organization skills with strong attention to details skills. * Strong fundamental mathematical skills and knowledge. Physical Requirements * Work standing or walking unassisted for 75% or greater of an 8-hour period. * Unassisted lifting up-to 35 lbs., may be required. * Able to wear appropriate personal protective equipment at all times, when required. Other Information This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Remote work and relocation are note supported in this position. About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title DPI QA Inspector II Organization Name InvaGen Pharmaceuticals, Inc. Location Unit 1 - 7 Oser Avenue, Hauppauge, NY 11788 Employment Type Full Time Shift First Shift: 8:30 AM - 5:00 PM (May vary based on business needs) Salary Range (Base/salary) $18.72/hr - $26/hr Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, employee discounts, and other benefits. Responsibilities/ Accountabilities The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specifications. Verification of raw materials during the dispensing process. Dispensing printed packaging materials to packaging. Perform in-process checks during batch manufacturing and packaging, as per manufacturing & batch packaging record instructions. Collection of in-process blend, finished product, validation samples for analysis, sample collection as per protocols. Specifically, to perform blend uniformity (BU) sampling. To clean and maintain the samplings rods/dies/sample boxes used for BU sampling. Perform IPQA testing on the manufacturing floor specifically LOD, Bulk Density, Tapped Density, Leak Test, Weight Variation test. Ensure cleaning of manufacturing and packaging equipment, area and provide line clearance. To perform posting of dispensed materials and samples into SAP system (ERP system) and to perform other transactions in SAP. Involve in investigation of Deviation, OOS, OOT, or any other non-conformances. Ensure completion of individual training assigned and follow company policies, safety requirements, cGMP and SOP's. Review of online batch records, area/equipment logbooks, calibration/PMP records etc. Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record. Review of engineering records (temperature and humidity data, calibration reports and PMP records). To take daily Quality rounds at shop floor to ensure shop floor is maintained in state of compliance and per GMP requirement. Report, escalate to Manager quality assurance about daily shop floor activities and any discrepancy during batch manufacturing and packing. Other duties [additional support] that management may assign from time to time. Education Qualifications/Experience Minimum Science Graduate A minimum of 1-2 years of pharmaceutical experience (DPI, MDI or Injectables) preferred. Preference will be given to candidates with experience in generic pharmaceutical manufacturing. Skills/ Competencies Knowledge of Good Manufacturing Practices and 21 CFR Part 820. Ability to read, write and communicate effectively. Basic computer skills (Microsoft Word, Power and Excel). Self-motivated, with the ability to work in fast-paced manufacturing environment and handle multiple tasks simultaneously. Excellent organization skills with strong attention to details skills. Strong fundamental mathematical skills and knowledge. Physical Requirements Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to 35 lbs., may be required. Able to wear appropriate personal protective equipment at all times, when required. Other Information This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Remote work and relocation are note supported in this position. About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose ‘Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States. Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter. About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

The Equipment and Process Technician I works with the Inspection and Packaging Supervisor in the activities associated with the inspection and packaging of sterile pharmaceuticals in accordance with company procedures and cGMPs. The incumbent meets inspection and packaging schedules while maintaining accurate records and professional behavior within the inspection/packaging areas. The Technician will perform manual inspection and train in the automatic inspection/packaging area for setup, of automated equipment and manual inspection processes, labeling and packaging equipment duties, line clearances and assist with inspection/packaging schedule. In conjunction with the Supervisor, the Technician plays a critical role in assuring safe, effective and compliant activities are performed in the manual inspection process while maintaining production schedules. The Equipment and Process Technician I will be proficient in all activities associated with the inspection process and be able to work with minimal supervision. The Technician will receive direction, training and mentorship from the Supervisor of Inspection and Packaging. ESSENTIAL DUTIES AND RESPONSIBILITIES Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. • Physically performs inspection and packaging activities as defined by established operating procedures and as directed by Manager/Supervisor. • Maintains accurate and complete records. • Maintains an accurate and complete Training Record. • Ability to set-up Manual Inspection process with little to no assistance. • Physically performs inspection, packaging, changeover, cleaning and provides documentation oversight for all such activities. • Physically performs inspection reconciliation and provides documentation oversight and acknowledgement for such activities. • Ability to review executed batch records and log books prior to submitting for final Production review. • Provides accurate and complete assistance to Quality Assurance as needed. • Works in a safe and effective manner. • Identifies and reports unsafe and non-compliant conditions. • Maintains work space in a clean and orderly manner. • Perform any other tasks/duties as assigned by management. • We all must embrace the QUALITY culture. QUALIFICATIONS AND REQUIREMENTS • High School diploma or GED preferred. Some college or technical training is a plus. • Minimum 1-year work experience in inspection, packaging, quality control and/or production preferred. • Must be able to work independently, completing assigned tasks with limited supervision. • Proven mathematical skills including addition, subtraction, multiplication, division, calculation of averages and percentages. • Excellent organizational, interpersonal and communication skills (oral and written). • Ability to take feedback constructively and consider the viewpoints of others. • Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. • Ability to work overtime as needed. PHYSICAL ENVIRONMENT AND PHYSICAL REQUIREMENTS • Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees. • Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. • Employee must be able to occasionally lift and/or move up to 50 pounds. • Must be able to sit for extended hours, focusing and concentrating on items being inspected. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. FMLA poster: ********************************************************** Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: · All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. · Our recruiting process includes multiple in person and/or video interviews and assessments. · If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. · We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. 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At Nouryon, our global team of Changemakers takes positive action every day to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society's needs - today and in the future. We are looking for team members who bring ideas forward, champion others, and work together to do better. Does that sound like you? About the job: The Process Technician ensures that the process operations assigned to him/her by direction or plant requirements operate continuously and efficiently, according to product and process specifications, with minimum production downtime. Also, ensure that safety, environmental, and good housekeeping standards are met at all times. In your future role as a Process Technician, you will: Assists the Chief Technician in his responsibility of operation and control of the plant. Operate the plant if the Chief Technician is outside of the control room by utilization of the Distributive Control System (DCS). In the absence of the Chief Technician, take necessary action in unforeseen situations such as shutdowns, equipment failures, emergencies, etc. so as to secure the plant, correct the situation, and inform the Chief Technician. Assist Production Supervision as requested. Work on a rotating shift schedule to man the seven-day continuous shift operations. Immediately correct all unsafe conditions if possible and immediately notify Production Supervision. Assists the operator in normal operating duties as deemed necessary by the Chief Technician. Ensure that the plant environmental standards are continuously maintained and in permit compliance by monitoring the operations of control equipment and verifying that emissions are within standards. Maintain cleanliness of plant. Will have proficient knowledge of all equipment in the plant in order to assist the Chief Technician in decision making. Will be able to operate mobile equipment. Will be able to perform the job duties of a Production Operator. Check critical equipment to be sure the equipment is functioning properly and notify the Chief Technician of any problems. Make corrections and adjustments in the plant as necessary to maintain process parameters and product specifications based on results from chemical testing. Performs monthly, weekly, and daily routines. Will learn the skills needed to become Chief Technician. Will be responsible for supporting a positive and professional working environment within his/her own shift and contributing to that of others. Will carry out directives and instructions in a safe, timely, efficient, and accurate manner. Will be responsible for maintaining proper flow of information to coworkers and supervisors, verbal and/or written reports during shift change, and entries in the daily log book or other reports as necessary. Will be required to perform basic mechanical operations. Responsible to report deviation from safety, quality, efficiency of operability standards to supervision in a timely manner. Required to maintain job certification by successfully completing a written exam and the demonstration of job skills as required by PSM regulation 29 CFR 1919, effective March 26, 1992. Will assist in the training of other personnel as requested. Will prepare work requests to repair equipment. Other duties can be added/deleted as deemed necessary. We believe you bring: High school diploma or GED equivalent or 2 year chemical industry experience Ability to read, analyze, and interpret general procedures Ability to write reports and present information to coworkers and peers. Ability to communicate with others on different job levels Ability to maintain communications with the Chief Technician through the various communication systems in the plant. Good to know: This is a full-time on-site position located in Columbus, MS. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ We look forward to receiving your application! We kindly ask our internal candidates to apply with your Nouryon email via Success Factors. About Nouryon: We're looking for tomorrow's Changemakers, today. If you're looking for your next career move, apply today and join Nouryon's worldwide team of Changemakers in providing essential solutions that our customers use to manufacture everyday products such as personal care, cleaning, paints and coatings, agriculture and food, pharmaceuticals, and building products. Our employees are driven by the wish to make an impact and actively drive positive change. If that describes you, we will gladly make way for your ambitions. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment. Visit our website and follow us on LinkedIn. #WeAreNouryon #Changemakers Nouryon 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, disability, veteran status, or any other characteristic protected under applicable federal, state, or local law. We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertisement agents, recruitment agencies or staffing companies.

CMS At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. ZOLL Cardiac Management Solutions offers a unique portfolio of novel technologies designed to deliver better insights and better outcomes. On any given day, clinicians utilize these ZOLL products for tens of thousands of cardiac patients around the world: * LifeVest, the world's first wearable defibrillator, has been trusted to protect more than 1M patients at risk of sudden cardiac death. * HFMS (Heart Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been shown to reduce heart failure readmissions rates by 38 percent. * TherOx Super Saturated Oxygen (SSO2) Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the U.S. At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need. ZOLL has been Pittsburgh's Manufacturer of the Year, one of Western PA's Healthiest Employers, and even one of Pittsburgh's Coolest Offices. But it's our unique opportunity to impact people's lives that makes ZOLL the ideal place to build your career. Job Type On Site Job Summary Responsible for inspecting highly complex mechanical and electrical parts and providing technical responses and investigations. Essential Functions * Responsible for the generation of inspection reports. * Will read parts lists, manufacturing drawings, inspection instructions, wiring diagrams or schematics and engineering change notices. * Position involves basic measurement equipment (calipers, micrometers, pin gages, etc). * Must adhere to quality policies and procedures. * Perform other duties as assigned by Management * Responsible for the inspection of simple electrical and mechanical parts and assemblies * Responsible for performing simple MRP transactions as related to QA Required/Preferred Education and Experience * High School Diploma or equivalent required * A technical Associate's degree or equivalent experience preferred * Up to one year of related Quality Assurance experience required * Must be able to obtain a valid IPC-STD-001 or PC-A-610 certification upon hiring. Knowledge, Skills and Abilities * General working knowledge of using a computer PC (knowledge of Microsoft Office applications highly desirable). Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. * Standing - Constantly * Walking - Constantly * Sitting - Occasionally * Lifting - Constantly * Carrying - Constantly * Pushing - Constantly * Pulling - Constantly * Talking - Occasionally * Hearing - Frequently * Repetitive Motions - Constantly * Eye/Hand/Foot Coordination - Constantly Working Conditions * Extreme cold - Occasionally * Extreme heat - Occasionally * Humidity - Occasionally * Wet - Occasionally * Noise - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. #LI-KH1 The hourly pay rate for this position is: $18.00 to $22.00 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

As an essential business, Anomatic produces innovative and sustainable packaging for today's biggest brands. By leveraging over five decades of manufacturing expertise and employing an extensive technologies portfolio, we design, manufacture, and finish incomparable stock and customized solutions for numerous markets. Position: Quality Control Inspector Location: New Albany, Ohio Department: Assembly Reports to: Quality Manager Shift: Third Shift: Sunday - Thursday, 10:00pm - 6:00am _____________________________________________________ JOB SUMMARY The Quality Control Inspector is responsible for ensuring quality product is received and/or produced on the production floor. ESSENTIAL FUNCTIONS Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Sample products and components according to test plan. Inspect for defects; gauges for necessary dimensions and records as required. Process test parts through anodizing, assembly, deco, or metallizing and inspect for defects. Report any defects as appropriate (visual, functional and dimensional) and fills out final inspection report. Enter data into SyteLine ERP system. Perform quality control tests as required. Provide timely and complete communication with all appropriate departments and functions concerning the acceptability of raw products and components. Lead activities to ensure priorities are established and goals are achieved. Perform all other duties as needed. QUALIFICATIONS Basic mathematical skills, including addition, subtraction, multiplication and division. Understanding of quality control concepts and processes within a manufacturing environment. Self-motivated and able to work independently with minimal direction Able to work overtime as needed - sometimes on a short notice or on weekends Inspection background preferred. Minimum of two (2) years of quality control experience in a manufacturing environment preferred. Benefits you can expect from Anomatic: Competitive Pay Career Growth Health Coverage Starting Your First Day 401K with Company Match, to help save for the future Paid Time Off to Enjoy Family or Hobbies DailyPay, to get your money faster Training, to help hone skills Many more! Anomatic takes pride in creating a safe and inclusive environment that encourages, supports, and celebrates the diverse voices of our employees and the communities in which they live. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status.

The QA associate assures the implementation of quality control and performs the nondestructive examination of cryogenic components, vacuum jacketed piping and overall product quality as defined from blueprints and internal quality criteria specifications. The inspector plays a key position in the overall quality management system where process standardization and the reduction in performance variation are integral to the client's continuous improvement. Responsibilities: • Inspections of weld fit-ups, weld joints, and completed weldments. • Perform various NDT methods including visual, dye penetrant, hydrostatic, pneumatic, and helium mass spectrometer leak testing. • Complete required test records and assist with the document control as required. • Assist with the maintenance of measurement devices in the calibration program. • Handle multiple tasks and accept verbal direction with efficiency. • Maintain testing equipment and the work area. Skills and Abilities: • Ability to read blueprints/drawings. • Knowledge of proper usage methods for measurement equipment, i.e.: gages, calipers, micrometers and other standard devices. • Good mechanical background. • Basic technical problem-solving skills. • Good organizational skills and ability to handle administrative tasks. • Ability to interact with engineers and management. Qualifications: • Minimum HS diploma or GED required. • Experience with AWS, ASME VIII and B31 Codes and experience with NDT methods VT, MT & PT a huge plus. • Knowledge of welding a plus. • Ability to lift, carry, push, pull or otherwise move objects weighing up to 40 pounds. • Must demonstrate the ability to read the equivalent of the size and letters of the Jaeger II chart at a minimum distance of 12 inches and distinguish and differentiate the contrasts between colors illustrated on an Ishihara Test Chart. • U.S. CITIZENSHIP REQUIRED.

As a Data Center Quality Inspector I, you provide superb quality control services for our clients. The work includes performing essential inspections of electrical equipment and systems, such as switchgear and substations. Detailed knowledge of mechanical and instrumentation is critical to conduct inspections and interpret electrical drawings and specifications. Attentively, you ensure the equipment and technicians around you comply with company and site safety requirements. You prepare detailed daily reports about your findings, including time tracking and special inspection reports. Diligently, you approve and submit important documents such as Lockout/Tagout (LOTO) requests, team reports, and time tracking reports. You take pride in assuring that our clients receive safely installed and functional equipment every time. If you are an analytical and detail-oriented individual who communicates effectively and prioritizes safety, this could be the position for you! Travel may be required. Responsibilities Ability to read and interpret electrical drawings and specifications. Prepare written documentation such as daily narratives (work reports), special inspection reports, and daily time tracking. Perform inspections of switchgear, standby generators, protective relays, and other electrical distribution components. Submit LOTO requests, review and approve team reports, and time tracking. Ensure compliance with all company and site safety requirements. Benefits Competitive pay, depending on experience. Medical, dental, vision, 401(k) with company match, among other benefits. Holidays and paid vacation time. Extensive learning and development opportunities. Requirements: Requirements High school diploma or equivalent. Higher education degree preferred. Minimum of two years of experience inspecting, testing, commissioning, or operating electrical distribution systems. Commercial or naval nuclear experience is strongly desired. OSHA 10-hour Construction Safety training. Commitment to excellence and high standards.

Job SummaryInspect raw material and/or parts, audit production practices and processes, and report on non-conformances.Job Description Key Accountabilities: Accurately inspect raw materials and products visually, as well as with gauges, scales, or other measurement instruments as required and according to work instructions. Segregate non-conforming parts or material. Complete required documentation for work performed. Perform data entry of work results into appropriate databases. Perform final inspection to reconcile outgoing shipments, as required. May be required to identify causes of non-conformance. This is a position that works directly on the warehouse floor on or around heavy machinery. Meet TKMNA Employee Attributes / Competencies. The above is intended to describe the general content of and requirement for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or requirements. This position has been identified as “safety sensitive” by thyssenkrupp under applicable laws. Accordingly, any application for this position that is considered for employment with thyssenkrupp requires successful completion of pre-employment drug testing, which may include testing for marijuana in accordance with any applicable federal, state, and local laws. Qualifications: Minimum Requirements: High school diploma or equivalent Ability to read and write English and perform basic math problems Ability to learn correct use of basic measurement instruments (tape measure, scales, gauges) Basic computer knowledge to complete data entry Attention to detail and accuracy Ability to accurately inspect basic material, commodities, and/or processes Safety Mindset. Preferred requirements: Some college courses or certificates in Quality Assurance-related field of study Prior experience using basic measurement instruments Prior experience in a quality assurance inspection position Benefits Overview We offer competitive company benefits to eligible positions, such as : Medical, Dental, Vision Insurance Life Insurance and Disability Voluntary Wellness Programs 401(k) and RRSP programs with Company Match Paid Vacation and Holidays Tuition Reimbursement And more! Benefits may vary based on job, country, union role, and/or company segment. Please work with your recruiter or tk representative for applicable benefits information. Disclaimer This is to notify the general public that some individuals/entities are using the thyssenkrupp (“TK”) name, trademark, domain name, and logo without authorization. They are posing as employees, representatives, or agents of TK and its associated/group companies. These individuals/entities are fraudulently offering jobs online through texts, websites, telephone calls, emails, or by issuing fake offer letters. They are also soliciting jobseekers to deposit money in certain bank accounts or providing jobseekers with fraudulent checks to obtain banking information. TK does not ask, solicit, or accept any monies in any form from candidates, job applicants, or potential jobseekers, who have applied to or wish to apply to TK, whether online or otherwise as a pre-employment requirement. TK bears no responsibility for money being deposited/withdrawn therefrom in response to such fake offers. TK does not: 1. Send job offers from free email services like Gmail, Rediffmail, Yahoo mail, etc.; 2. Request payment of any kind from prospective jobseekers or candidates for employment; 3. Authorize anyone to collect money or agree to any monetary arrangement in return for a job at TK; 4. Send checks to job seekers; or 5. Make job offers through third parties. In the event TK uses professional recruitment services through a third party, offers are always made directly by TK and not by any third parties. PLEASE NOTE: 1. TK strongly recommends that potential jobseekers do not respond to such fake solicitations, in any manner; 2. TK will not be responsible to anyone acting on an employment offer that is not directly made by TK; 3. Anyone making an employment offer in return for money is not authorized by TK; and 4. TK reserves the right to take legal action, including criminal action, against such individuals/entities. TK follows a formal recruitment process through its own HR department and applications are evaluated by its HR department through pre-defined processes. Please visit our official careers website at ******************************** to view authentic job openings at TK. If you receive any unauthorized, suspicious, or fraudulent offers or interview calls, please email us at **********************************************. We shall not accept any liability towards the representation made in any fraudulent communication or its consequences, and such fraudulent communication shall not be treated as any kind of offer or representation by TK or its group companies and affiliates.

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. The Equipment and Process Technician I works with the Inspection and Packaging Supervisor in the activities associated with the inspection and packaging of sterile pharmaceuticals in accordance with company procedures and cGMPs. The incumbent meets inspection and packaging schedules while maintaining accurate records and professional behavior within the inspection/packaging areas. The Technician will perform manual inspection and train in the automatic inspection/packaging area for setup, of automated equipment and manual inspection processes, labeling and packaging equipment duties, line clearances and assist with inspection/packaging schedule. In conjunction with the Supervisor, the Technician plays a critical role in assuring safe, effective and compliant activities are performed in the manual inspection process while maintaining production schedules. The Equipment and Process Technician I will be proficient in all activities associated with the inspection process and be able to work with minimal supervision. The Technician will receive direction, training and mentorship from the Supervisor of Inspection and Packaging. ESSENTIAL DUTIES AND RESPONSIBILITIES Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. • Physically performs inspection and packaging activities as defined by established operating procedures and as directed by Manager/Supervisor. • Maintains accurate and complete records. • Maintains an accurate and complete Training Record. • Ability to set-up Manual Inspection process with little to no assistance. • Physically performs inspection, packaging, changeover, cleaning and provides documentation oversight for all such activities. • Physically performs inspection reconciliation and provides documentation oversight and acknowledgement for such activities. • Ability to review executed batch records and log books prior to submitting for final Production review. • Provides accurate and complete assistance to Quality Assurance as needed. • Works in a safe and effective manner. • Identifies and reports unsafe and non-compliant conditions. • Maintains work space in a clean and orderly manner. • Perform any other tasks/duties as assigned by management. • We all must embrace the QUALITY culture. Additional Qualifications/Responsibilities QUALIFICATIONS AND REQUIREMENTS • High School diploma or GED preferred. Some college or technical training is a plus. • Minimum 1-year work experience in inspection, packaging, quality control and/or production preferred. • Must be able to work independently, completing assigned tasks with limited supervision. • Proven mathematical skills including addition, subtraction, multiplication, division, calculation of averages and percentages. • Excellent organizational, interpersonal and communication skills (oral and written). • Ability to take feedback constructively and consider the viewpoints of others. • Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. • Ability to work overtime as needed. PHYSICAL ENVIRONMENT AND PHYSICAL REQUIREMENTS • Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees. • Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. • Employee must be able to occasionally lift and/or move up to 50 pounds. • Must be able to sit for extended hours, focusing and concentrating on items being inspected.

We are seeking a highly skilled and experienced Source Inspector to join our team on a freelance basis. The ideal candidate will have a strong background in monitoring fabrication work, with preferred knowledge and certifications in welding and non\-destructive examination (NDE). Responsibilities: Conduct inspections at supplier facilities to ensure compliance with specified requirements, including drawings, specifications, and industry standards. Perform visual inspections, measurements, and testing of fabricated components to verify quality and conformance to standards. Review supplier documentation, including inspection reports, material certificates, and test records, to ensure completeness and accuracy. Communicate effectively with suppliers to address any discrepancies or non\-conformances identified during inspections. Maintain detailed inspection records and documentation in accordance with company procedures and client requirements. Collaborate with project managers and engineering teams to provide timely and accurate feedback on inspection findings. Benefits Requirements Requirements Proven experience in monitoring fabrication work, preferably in industries such as manufacturing, aerospace, or oil and gas. Knowledge and certifications in welding and non\-destructive examination (NDE) techniques preferred. Strong attention to detail and ability to interpret technical drawings and specifications. Excellent communication and interpersonal skills, with the ability to communicate with suppliers effectively and internal stakeholders. Proficiency in Microsoft Office Suite and other relevant software applications. Ability to work independently and remotely, with access to necessary equipment and tools for inspections. Flexibility to travel to supplier locations as needed. BenefitsBenefits This is a remote freelance position, allowing the flexibility to work from home while providing valuable inspection services to our clients. If you meet the qualifications and are interested in joining our team, please submit your resume and cover letter outlining your relevant experience and qualifications. We look forward to hearing from you! "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"706730965","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Oil & Gas"},{"field Label":"Work Experience","uitype":2,"value":"5+ years"},{"field Label":"Salary","uitype":1,"value":"50"},{"field Label":"City","uitype":1,"value":"Iowa Park"},{"field Label":"State\/Province","uitype":1,"value":"Texas"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"76367"}],"header Name":"Source Inspector\-Iowa Park TX","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********01435003","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":false,"job Id":"**********04713066","FontSize":"12","location":"Iowa Park","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"iskfnff0418f820bf454495e86cc96b2cf14e"}

CMS At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. ZOLL Cardiac Management Solutions offers a unique portfolio of novel technologies designed to deliver better insights and better outcomes. On any given day, clinicians utilize these ZOLL products for tens of thousands of cardiac patients around the world: LifeVest, the world's first wearable defibrillator, has been trusted to protect more than 1M patients at risk of sudden cardiac death. HFMS (Heart Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been shown to reduce heart failure readmissions rates by 38 percent. TherOx Super Saturated Oxygen (SSO2) Therapy is the first FDA-approved therapy since the stent 20+ years ago to reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the U.S. At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need. ZOLL has been Pittsburgh's Manufacturer of the Year, one of Western PA's Healthiest Employers, and even one of Pittsburgh's Coolest Offices. But it's our unique opportunity to impact people's lives that makes ZOLL the ideal place to build your career. Job Type On Site Job Summary Responsible for inspecting highly complex mechanical and electrical parts and providing technical responses and investigations. Essential Functions Responsible for the generation of inspection reports. Will read parts lists, manufacturing drawings, inspection instructions, wiring diagrams or schematics and engineering change notices. Position involves basic measurement equipment (calipers, micrometers, pin gages, etc). Must adhere to quality policies and procedures. Perform other duties as assigned by Management Responsible for the inspection of simple electrical and mechanical parts and assemblies Responsible for performing simple MRP transactions as related to QA Required/Preferred Education and Experience High School Diploma or equivalent required A technical Associate's degree or equivalent experience preferred Up to one year of related Quality Assurance experience required Must be able to obtain a valid IPC-STD-001 or PC-A-610 certification upon hiring. Knowledge, Skills and Abilities General working knowledge of using a computer PC (knowledge of Microsoft Office applications highly desirable). Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Standing - Constantly Walking - Constantly Sitting - Occasionally Lifting - Constantly Carrying - Constantly Pushing - Constantly Pulling - Constantly Talking - Occasionally Hearing - Frequently Repetitive Motions - Constantly Eye/Hand/Foot Coordination - Constantly Working Conditions Extreme cold - Occasionally Extreme heat - Occasionally Humidity - Occasionally Wet - Occasionally Noise - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. #LI-KH1 The hourly pay rate for this position is: $17.00 to $20.00 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Location: East Liberty, OH Employment Type: 2nd Shift, Full-time, temp-to-hire Job Brief Kable Workforce Solutions is hiring a Quality Inspector for our client. This job involves inspecting parts using measuring and test equipment, sorting and documenting results, and completing production-related and administrative tasks. You'll follow written and verbal instructions, report issues to supervisors, maintain a clean work area, and provide accurate paperwork while meeting productivity and safety standards.What's a Typical Day Like? Use inspection, measuring and test equipment Perform a full range of varied sorting, inspection, production, and data entry Perform a full range of production-related tasks as well as administrative duties related to quality project work Read and follow written and verbal work instructions - all employee policies, work rules, and directions Identify problems and questions and report them to the appropriate supervisor Maintain organization and cleanliness work area Ability to use inspection and test equipment as required Provide accurate and complete information for paperwork Meet productivity standards after successfully completing training Comply with all safety, hazardous material and OSHA training, rules, and reporting, ensuring safe work environment. What Are the Requirements of the Job? 18 years old Previous experience in a distribution center environment helpful Ability to frequently lift cartons above (up to 8 feet overhead) or below shoulder level Ability to move or lift up to 50+ lbs. Walk, stand, and/or sit for an entire shift Ability to utilize hand/eye coordination and manual dexterity Maintain flexibility regarding job assignments including working scheduled hours, location changes (QA Inspectors go to the parts they are inspecting), or mandatory overtime Pass a background check and drug test Wear steel toes Capability to stand for prolonged periods of time Communication skills. Ability to reach, grasp, hold, push, pull, bend, twist, squat, climb, kneel. Why Choose Kable Workforce Solutions? Weekly Pay Exclusive Access Opportunities to V.I.P. Vault Day 1 Benefits Various Bonus Opportunities Eligibility for Employee of the Month Rewards How to Apply And Next Steps? Please submit your resume in our application by clicking “apply now.” We look forward to reviewing your application and you will hear from us within 1 business day.About Kable Workforce Solutions For over 50 years, Kable Workforce Solutions has been connecting skilled professionals with leading employers across the region. We're dedicated to helping people build lasting careers and helping companies grow through quality, integrity, and partnership.We believe in people first - empowering individuals to succeed and celebrating the work that drives our communities forward.Kable Workforce Solutions is proud to be an equal opportunity employer. We welcome and value diversity and are committed to creating an inclusive workplace where everyone can thrive. Read our full diversity statement here.This job description is not intended to be all-inclusive, and the employee will also perform other reasonably related business duties as assigned by the immediate supervisor and other management as required.

From smartphones to solar panels, innovative technology is needed to create the devices we use every day. Silfex's silicon components help make that technology a reality. Silfex Inc., A Lam Research Company is the leading provider of precision silicon components used to make and operate semiconductor tools, which enable the trillion-dollar global electronics industry. Our company's products are integral to the semiconductor equipment and optical markets. The outstanding team at Silfex makes that possible - through our people, we are advancing the world. The impact we have on the world is made possible by focusing on our people. So we recognize and celebrate our teams' achievements. We strive to create an inclusive and diverse culture where everyone's contribution and voice has value. We evaluate and evolve our offerings, so our people receive the support and empowerment to do meaningful things for their lives, careers, and communities. Our Perks and Benefits At Silfex, our people make amazing things possible. That's why we invest in you throughout the phases of your life with a comprehensive set of outstanding benefits that start on your first day of employment. Discover more at Lam Benefits Job Descriptions: Essential Function: Join Silfex as a Quality Inspector and be at the core of our mission for exceptional quality. In this role, you'll use your attention to detail and basic math and computer skills to ensure our products meet the highest standards. Working alongside experienced professionals, you'll learn inspection procedures and grow your expertise, all while making a direct impact on customer satisfaction. Essential Duties and Responsibilities: Know and understand specification criteria and perform inspections on parts to ensure they meet specifications. * Understand and be able to complete all documentation requirements for inspections as performed. * Read and understand work instructions to determine procedure for testing. * Commit to ongoing development and competence of job functions. * Perform tasks under direct supervision during the training cycle. * Effectively communicate information at shift change. * Perform daily check on the profilometer and check calibration date on all machines. * Must be able to shut down and restart all machines. * Ability to read and understand part drawings. * Develop and maintain a working knowledge of Silfex Quality Management System and properly apply Quality and Operating Procedures as appropriate. * Ensure the cleanliness and order of inspection and test stations. * Report any unsafe conditions to Silfex management, including the Manufacturing Manager, EHS Manager, and/or Director of Manufacturing. * Assist in applying lean manufacturing concepts and 5S. * Other duties as assigned. Culture: * Display a positive attitude and strong work ethic that reflects the Mission and Core Values of Silfex. * Create and maintain a culture where workplace safety is part of everything we do. Provide the safest possible workplace to our employees by modeling and following all company safety policies, reporting any incidents or unsafe conditions immediately to Silfex management. Wear all PPE as required by work area or job function. * Communication - Begin with the end in mind - Communicate boldly as well as effectively with empathy and respect to inspire teamwork and collaboration vertically and horizontally within Silfex. * Assist in applying lean manufacturing concepts and 5S. Demonstrate ownership of continuous improvement ideas and activities. Maintain organization and cleanliness, housekeeping and 5S within work area. Maintain these areas at the highest degree possible while responsibly escalating any maintenance issues. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. * High School Diploma or a General Education Degree (GED) required * Minimum of 1 year of previous manufacturing Quality Assurance experience or related experience * Ability to read and comprehend simple instructions, short correspondence, and memos * Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions * Must possess basic proficiency in operating computers, including navigating software and web-based platform * Work effectively as an individual and in a team environment * Strong attention to detail is required * Quality and safety minded * Good written and verbal communication skills. * Must be able to perform successfully under supervision Preferred Qualifications: * Knowledge and understanding of inspection criteria * Strong shop math skills * Microsoft Office experience (specifically Excel) * Knowledge of 5S and Lean manufacturing. D Shift: 6pm - 6am Our Commitment We believe it is important for every person to feel valued, included, and empowered to achieve their full potential. By bringing unique individuals and viewpoints together, we achieve extraordinary results. Silfex Inc., A Lam Research Company ("Silfex" or the "Company"), is an equal opportunity employer. Silfex is committed to and reaffirms support of equal opportunity in employment and non-discrimination in employment policies, practices and procedures on the basis of race, religious creed, color, national origin, ancestry, physical disability, mental disability, medical condition, genetic information, marital status, sex (including pregnancy, childbirth and related medical conditions), gender, gender identity, gender expression, age, sexual orientation, or military and veteran status or any other category protected by applicable federal, state, or local laws. It is the Company's intention to comply with all applicable laws and regulations. Company policy prohibits unlawful discrimination against applicants or employees.

TRIGO Global Quality Solutions has several immediate openings for Quality Inspectors in Marion, OH. MUST HAVE YOUR OWN RELIABLE TRANSPORTATION TO TRAVEL BETWEEN PLANT AND WAREHOUSES DURNING THE WORKDAY AS NEEDED. Day & Night shift. ($0.75 shift diff. pay.) Payrate is $16.00. Overall Purpose of the Quality Inspector Provide Quality services and support for all missions assigned to a manufacturing or warehouse site while ensuring a healthy and safe work environment. Reports to Site Supervisor/Site Leaders Responsibilities (To include but not limited to the following) Client Relationship & Business Development * Act as an impartial third party between the production source and the customer facility to ensure the product meets set criteria Operations * Check/inspect manufactured parts or products for defects * Read and follow work instructions and general processes * Use measuring or testing equipment as needed * Ensure products meet quality standards * Display excellent customer service * Must comply with local and company Health & Safety legislation, laws, and policies Organization & Management * Collect and record data Technical * Utilize company portal for time recording and policy acknowledgements Other * Any other duties as assigned Knowledge, skills, abilities Hard skills * Must be able to speak and read in the English language * Good communications skills * Must be able to multi-task * Ability to work in a fast-paced environment * Ability to handle sensitive and confidential material * Ability to walk and stand for long periods of time * Ability to bend, lift, twist and move freely * Ability to periodically lift/move up to 50 pounds * Must have reliable transportation Values & attitudes Global team spirit * Team player * Caring for people * Open-minded Excellence * Reactive * Resilient to pressure * Rigorous Customer focus * Client oriented * Reliable & trustworthy * Flexible Initiative * Autonomous * Innovative * Daring Work experience Overall recommendations * No experience necessary * Ability to read blueprints a plus Education background Overall recommendations * High School Diploma or Equivalent recommended or comparable work experience About TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and aerospace industries. With a team of more than ten thousand professionals present in 20+ countries across 4 continents, TRIGO offers a comprehensive portfolio of Quality Assurance services ranging from inspection to expert auditing, consulting and training. The unrivaled expertise, industrial mindset and extensive global footprint that TRIGO has built up over the last 3 decades has made TRIGO the leading quality solutions provider using the latest innovative and reliable digital systems and standard processes, delivering results in the most demanding industries. TRIGO has recently started to expand its clientele by offering quality services to the medical, chemical and food industries. TRIGO Global Quality Solutions is committed to the core values of equal employment opportunity. We are committed to treating people fairly, and with respect and dignity. We offer employment opportunities based upon an individual's qualifications and performance, free from discrimination or harassment because of race, ancestry, place of origin, ethnic origin, color, citizenship, creed, sex, sexual orientation, age, marital status, family status, and disability.

Job Description ***********PLEASE READ BELOW***************** The Immediate Pay, Quality Inspector position offers individuals the opportunity to receive payment for their work on the same day they perform their duties. This position is designed to provide a quick and fair compensation system for workers who are seeking immediate income. Upon starting the job, workers will be paid for their first day of work (ONLY) at the end of that day. However, it is important to note that if a worker does not show up for their second day of work without prior notice or valid reason, they will be terminated from the position. This is a W2 position. You will not be considered if you do not perform video screen. Overall Purpose of the Quality Inspector Provide Quality services and support for all missions assigned to a manufacturing or warehouse site while ensuring a healthy and safe work environment. Reports to Site Supervisor/Site Leaders Responsibilities (To include but not limited to the following) Client Relationship & Business Development Act as an impartial third party between the production source and the customer facility to ensure the product meets set criteria Operations Check/inspect manufactured parts or products for defects Read and follow work instructions and general processes Use measuring or testing equipment as needed Ensure products meet quality standards Display excellent customer service Must comply with local and company Health & Safety legislation, laws, and policies Organization & Management Collect and record data Technical Utilize company portal for time recording and policy acknowledgements Other Any other duties as assigned Knowledge, skills, abilities Hard skills Requirements Must be able to speak and read in the English language Good communications skills Must be able to multi-task Ability to work in a fast-paced environment Ability to handle sensitive and confidential material Ability lift /move 50 pounds Must have reliable transportation

Rittal is a leading global provider of solutions for industrial enclosures, power distribution, climate control, and IT infrastructure, as well as software and services. The company is a member of the Friedhelm Loh Group, a successful international player with 18 production plants, 80 subsidiaries, and 12,000 employees. Rittal LLC has built a strong tradition of innovation and takes pride in a progressive approach to engineering. We design and manufacture the world's leading industrial and IT enclosures, racks, and accessories, including high-efficiency, high-density power management, and climate control systems for industrial, data center, outdoor, and hybrid applications. Primary Activities/Duties Visually inspect parts for compliance with quality requirements. Verify documentation and paperwork for accuracy. Read blueprints to determine specifications and tolerances for machined components and assemblies. Use inspection tools to complete dimensional reports. Initiate containment activities when discrepancies are identified. Review and refine data collection requirements based on customer drawings, models, work orders, purchase orders, sketches, and PPAP standards. Participate in Gage R&R studies. Act as an impartial third party between production and customer to ensure product quality. Perform a variety of inspection tasks with minimal supervision. Communicate inspection findings and non-conformances to relevant stakeholders. Read and follow work instructions and general processes. Use measuring and testing equipment as needed. Ensure products meet quality standards and comply with health and safety policies. Collect and record inspection data. Utilize company portal for time tracking and policy acknowledgements. Perform other duties as assigned. Safety Requirements Wear safety-toed footwear. Safety glasses with side shields. Hearing protection. Additional personal protective equipment as required. Follow all safety procedures including Lock Out Tag Out when applicable. Physical Requirements Stand, walk, bend, twist, and reach frequently throughout the shift. Lift 25-50 pounds to waist level and up to 25 pounds above shoulder level. Stand for extended periods and occasionally work at a computer. Work Environment Manufacturing and warehouse areas with exposure to moving mechanical parts, dust, and high noise levels. May be required to work outdoors in various weather conditions. Regular use of cleaning solvents, oils, lubricants, and other substances. Knowledge & Experience High school diploma or GED required. One year of related experience or training preferred; equivalent combinations of education and experience considered. Ability to read engineering drawings and blueprints. Knowledge of GD&T and experience with measurement tools such as calipers, micrometers, and indicators. Strong communication skills and attention to detail. Ability to multi-task and work in a fast-paced environment. Familiarity with Microsoft Office and SAP is a plus. Basic understanding of ISO 9001:2015 standards. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may contact the company's Human Resources Department at **************. This option is reserved for individuals who require accommodation due to a disability. Rittal LLC and Eplan are proud to be an affirmative action/equal opportunity employer. EEO, including Disability/Vets.

Job Details Bremen, OH $24.00 - $29.00 HourlyDescription Westerman, Inc., an employee-owned company, is a multiple site manufacturer of production and storage equipment within the oil, gas, and nuclear industries. Our equipment helps optimize well pad design, improve separation efficiency and lower overall equipment spend through high-performance surface separation and processing technology. Our equipment is setting new standards for performance and economics nationwide. SUMMARY The Quality Inspector is responsible for inspecting parts of Pressure Vessels and process piping for stress and failure using multiple methods per regulatory, customer, and internal requirements. Candidates for this role should have a working knowledge of all inspection roles/ processes such as visual inspection, hydrostatic and various NDE methods. The Quality Inspector will be responsible for helping to detect the root cause of Quality issues as well as keeping track of Quality documentation through Westerman's document control software. The Quality Inspector must have applicable knowledge of all ASME codes that pertain to pressure vessels. The Quality Inspector will be required to have the ability to train, coordinate, and communicate effectively and professionally with all departments and personnel. SALARY $24 - $29 per hour - Depends on experience. BENEFITS 401(k) matching Health insurance Health Savings Account Vision insurance Dental insurance Life insurance Short Term/Long Term Disability Paid time off Parental leave Referral program Employee Assistance Program Employee-Owned Company Qualifications QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty or responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. RESPONSIBILITIES Regular and punctual attendance at work is an essential job function of each position and is necessary to your individual effectiveness and that of your work group. Regular and punctual attendance is required of all employees. Performs internal testing, internal checks, and cosmetic inspections. Performs inspections on material and product throughout production process Performs relevant non-destructive examinations using varying methods Completes all documentation required for tracking and record keeping Completes data entry and evaluates results of data entered Performs root cause analysis on non-conformities found Other duties as required and assigned. REQUIREMENTS 2 years' experience as Code Welder, Quality Inspector or equivalent knowledge required. Previous Quality Inspector experience strongly preferred. Associate's or Bachelor's degree in a related field preferred ASME Section VIII and B31.3 code knowledge required Candidate should have at least LVL 1 training in VT/PT/UT/MT and RT Film Interpretation Must be meticulous about capturing and retaining information Must have basic computer skills (Word, Excel, Record-keeping software, etc.) Must be able to work in a team environment and be able to explain issues in a professional manner Must be analytical and detail oriented Must have working knowledge of mathematical and measurement principles Must have a positive attitude and a desire to continually improve OSHA safety training and HazMat training preferred An understanding of Lean principles and practices is strongly preferred. PHYSICAL DEMANDS/ WORK ENVIRONMENT The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Must be able to stand for extended periods of time, up to entire length of shift (10 - 12 hours). Must be able to handle physical repetitive work. Must be able to exert moderate to heavy physical effort with lifting requirement up to 50 pounds. Must have strong range of motion. Must be able to sit, stand, reach, stoop, kneel, crouch, climb, and bend repetitively. Must be able to see, speak, read, and hear. Must be able to read instructions and all measuring devices. Must use fingers and hands to manipulate tools and small parts. Must be able to walk over both even and uneven surfaces. Must be able to work in extreme temperatures, both hot and cold. Must be able to wear appropriate PPE. Must be physically able to access all areas of the plant and grounds. Some aspects of this position may require working in tight quarters (inside vessels). Some aspects of this position may require close vision, depth perception, the ability to see small detail, and the ability to adjust focus.

TRIGO Global Quality Solutions has several immediate openings for Quality Inspectors in Bellefontaine, OH. 1st shift only. Sit Down job. Payrate is $14.00. Overall Purpose of the Quality Inspector Provide Quality services and support for all missions assigned to a manufacturing or warehouse site while ensuring a healthy and safe work environment. Reports to Site Supervisor/Site Leaders Responsibilities (To include but not limited to the following) Client Relationship & Business Development Act as an impartial third party between the production source and the customer facility to ensure the product meets set criteria Operations Check/inspect manufactured parts or products for defects Read and follow work instructions and general processes Use measuring or testing equipment as needed Ensure products meet quality standards Display excellent customer service Must comply with local and company Health & Safety legislation, laws, and policies Organization & Management Collect and record data Technical Utilize company portal for time recording and policy acknowledgements Other Any other duties as assigned Knowledge, skills, abilities Hard skills Must be able to speak and read in the English language Good communications skills Must be able to multi-task Ability to work in a fast-paced environment Ability to handle sensitive and confidential material Ability to walk and stand for long periods of time Ability to bend, lift, twist and move freely Ability to periodically lift/move up to 50 pounds Must have reliable transportation Values & attitudes Global team spirit Team player Caring for people Open-minded Excellence Reactive Resilient to pressure Rigorous Customer focus Client oriented Reliable & trustworthy Flexible Initiative Autonomous Innovative Daring Work experience Overall recommendations No experience necessary Ability to read blueprints a plus Education background Overall recommendations High School Diploma or Equivalent recommended or comparable work experience About TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and aerospace industries. With a team of more than ten thousand professionals present in 20+ countries across 4 continents, TRIGO offers a comprehensive portfolio of Quality Assurance services ranging from inspection to expert auditing, consulting and training. The unrivaled expertise, industrial mindset and extensive global footprint that TRIGO has built up over the last 3 decades has made TRIGO the leading quality solutions provider using the latest innovative and reliable digital systems and standard processes, delivering results in the most demanding industries. TRIGO has recently started to expand its clientele by offering quality services to the medical, chemical and food industries. TRIGO Global Quality Solutions is committed to the core values of equal employment opportunity. We are committed to treating people fairly, and with respect and dignity. We offer employment opportunities based upon an individual's qualifications and performance, free from discrimination or harassment because of race, ancestry, place of origin, ethnic origin, color, citizenship, creed, sex, sexual orientation, age, marital status, family status, and disability.