Quality control analyst jobs in Green Oak, MI

V&S Galvanizing, LLC has over 100 years of experience in Hot Dip Galvanizing and we are the leader in the steel coating industry. Today we operate over 9 galvanizing plants in the U.S., featuring exceptional service to small fabricators as well as companies known worldwide. We are hiring for a Safety/Quality Control Coordinator at V&S Detroit Galvanizing, located in Redford, MI. Safety Responsibilities: Monitor and conduct safety trainings at facility. Verify and assist with inspections. Verify maintenance logs are complete. Verify equipment pre-op checks are complete. Assist with updating facility safety procedures. Conduct safety committee meetings at facility. Attend Corporate Safety Committee meetings. First point of contact for all online safety reporting at facility. Monitor and maintain a safe working environment. Answers directly to the General Manager and the Corporate Safety Manager. Act as Incident Manager to investigate all facility incidents, identify the root cause and create corrective actions current with company safety standards and report findings to the Corporate Safety Committee. Quality Control Responsibilities: Provide a piece count on all outgoing loads to verify the correct number of pieces. Verify the materials are loaded in a safe manor and ready for shipment. Provide random thickness sampling to verify zinc level are correct. Provide random quality checks on galvanized material on the floor and in the yard. Function as a back-up for material check-in to verify piece count and inspect the material. Compensation: Competitive Pay Paid Time Off Paid Holidays Health, FSA, dental, vision, life & disability benefits 401k program with company match V&S Galvanizing is proud to be an equal opportunity employer that values diversity and inclusion at every level.

Job Title : QC Records Analyst Department: Quality Control Reports To : QC Records Manager Shift : Full Time - 1st Shift ESSENTIAL DUTIES AND RESPONSIBILITIES Duties and responsibilities include, but are not limited to: Provides established repetitive and non-repetitive record reports. Provides reports or record copies when specifically requested by proper authority. Audit both physical and digital documents using AirVault, Microsoft Outlook, Adobe Acrobat, and other tools to ensure system entry directly reflects the work performed and compliance with FAA regulations and internal standards. Maintain clear and professional email correspondence with mechanics, maintenance stations, and other internal teams. Assist other departments by locating and providing required maintenance documentation upon request. Monitor the receipt of all maintenance-related documents and verify completeness and accuracy against work performed. Ensure proper digital archiving and secure handling of all records in compliance with regulatory and internal retention policies. Support ongoing audits and internal process improvements. Perform any other duties as assigned by the QC Records Manager. QUALIFICATIONS Have at least 1 year experience in office administration. Ability to work effectively in a high-volume, fast-paced, multitasking environment with shifting priorities. Strong working knowledge of Microsoft Outlook, Adobe Acrobat, and Microsoft Office Suite including Excel, Word, and Teams. Exceptional attention to detail with excellent data entry accuracy. Strong organizational and written and verbal communication skills. Ability to collaborate across departments and with maintenance personnel. Prior experience with AMOS or similar MRO database systems (preferred). Prior experience in aviation maintenance, technical records, or FAA documentation (preferred). EDUCATION and/or EXPERIENCE Fluent computer knowledge of MS Office Components (Word, Access, and Excel) and Adobe. Have at least 1 year experience in office administration. HS Diploma or GED. LANGUAGE SKILLS Ability to read, write and understand spoken and written English. Ability to write routine reports and correspondence. Ability to receive verbal and written direction. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is required to stand, walk, climb/descend stairs and maintenance stands, and be able to lift a minimum of 40 pounds. WORK ENVIRONMENT The work environment is in an office environment. Every employee has their own work station. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Qualified, interested internal candidates should submit to Human Resources an “Internal Application” form (found on ADP) that has been signed by their supervisor. *Must be authorized to work in the United States

Requirements Working knowledge of Fiserv core data system, including data specifications for deposit products, preferred. Knowledge of Banking regulations, including Regulatory requirements for IRA/HSA tax reporting of transactions, preferred. Demonstrate attention to detail and produce accurate, high-quality work. Demonstrate efficient and effective use of digital tools, including Fiserv core system, Director, Microsoft Word, Excel, Outlook, dual monitors, Microsoft Teams, and interest and ability to learn new applications. Ability to follow directions and apply proper policies, procedures, and guidelines. Excellent organizational and time management skills, with the ability to multi-task, maintain accuracy, and meet deadlines. Strong verbal and written communication skills with the ability to maintain confidentiality and professionalism while interacting with vendors, consumers, and internal team members. Customer service orientation with developed analytical and problem-solving skills. Possess the ability to work independently while supporting a team environment. Minimum Qualifications/Experience: 2 to 4 years' financial institution experience. Fiserv Premier experience preferred. Formal Education & Certification: High School Diploma or equivalent required. Physical Demands and 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 position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or finger, handle, or feel objects, tools or controls. The employee is occasionally required to stand; walk; sit; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, color vision, peripheral vision, and the ability to adjust focus. The noise level in the work environment is usually moderate.

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Description As a Quality Scientist at Thermo Fisher Scientific Inc., you will have a unique opportunity to support a world-class life science manufacturing facility in Detroit. You will play a crucial role in ensuring the flawless quality of our Peptone products used in critical Biopharmaceutical applications. With your exceptional skills and expertise, you will perform routine analytical, physical, and microbiological testing and support the timely disposition of raw materials and finished goods, helping us uphold rigorous quality standards and meet the needs of our global customers. Responsibilities: Perform Quality Control (QC) chemical and biological testing of raw materials and peptone finished products, including but not limited to product appearance, pH, bioburden, loss on drying, growth promotion, titration, and other physical and chemical assays. Set up, operate, and maintain laboratory equipment in accordance with established procedures, methods, and calibration/maintenance requirements. Accurately document test results, perform data analysis, and communicate findings to cross-functional partners in compliance with GMP and data integrity principles. Support laboratory test method and equipment qualifications/validations in accordance with ICH Q2(R1), FDA guidance, and internal quality system requirements. Draft, revise, and maintain standard operating procedures (SOPs), test methods, and other quality system documentation. Conduct environmental monitoring of production areas, including sampling, testing, trending, and reporting. Maintain an accurate and organized inventory of laboratory chemicals, reagents, standards, and consumables; procure supplies as needed to ensure uninterrupted testing activities. Support manufacturing through batch record review, in-process quality monitoring, and collaboration with operations personnel. Participate in internal and external audits and ensure ongoing compliance with site, regulatory, and industry standards. Perform Quality Assurance (QA) support activities as needed, including material release and documentation review. Requirements: Bachelor of Science (BS) degree in Chemistry, Biology, Chemical Engineering, or related scientific field. 1+ years of prior experience in a Quality Control Laboratory setting in the Pharmaceutical/Biotech/Life Science industry. Experience performing routine testing and supporting product disposition using analytical, physical, or microbiological methods. Strong analytical skills with the ability to conduct laboratory Out-of-Specification investigations using scientific knowledge and statistical methods. Knowledge of method qualification/validation principles and equipment qualification is preferred. Familiarity with standard analytical technologies (e.g., HPLC, FTIR, TLC, ICP-MS) is desired. Working knowledge of ISO 13485:2016, FDA cGMP regulations, and associated quality system expectations. Experience with batch record reviews and electronic Quality Management systems. In addition to the exciting responsibilities and requirements, Thermo Fisher Scientific Inc. offers a wide range of benefits and career advancement opportunities. We value our employees and provide: Medical, Dental, & Vision benefits from Day 1 Paid Time Off & Holidays 401K Company Match up to 6% Tuition Reimbursement available after 90 days Employee Referral Bonus Employee Discount Program Employee Recognition Program Charitable Gift Matching Company Paid Parental Leave

Responsive recruiter Benefits: Bonus based on performance Competitive salary Dental insurance Health insurance Opportunity for advancement Paid time off PEL Labs is looking for an environmental laboratory analyst to add to our rapidly growing firm. We are seeking an analyst ideally with experience in both flame AA lead paint analysis and PLM asbestos analysis, but will consider candidates with experience in one or the other who are willing to be cross-trained. Applicants must possess a minimum of 1-year of experience in lead paint analysis and/or PLM asbestos analysis in order to be considered. Primary duty will be as analyst in asbestos/lead, but will also be expected to assist with other general laboratory functions including sample accessioning, recordkeeping, supply ordering, phones, light janitorial, etc. Position is full time. Business hours are 9am - 5pm Monday to Friday, but there is some flexibility to work an earlier/later shift. Required weekend work is possible, although extremely rare. All full time employees are offered medical, dental, and vision insurance as well as a generous PTO plan. Benefits/Perks Flexible Scheduling Competitive Compensation Career Advancement Opportunities Job SummaryPreparing, identifying, and analyzing a variety of environmental samples. Responsibilities Preparation and analysis of bulk and paint chip samples for analysis using Atomic absorption spectrometry (AAS) and/or similar equipment. Preparation and analysis of bulk and solid materials for asbestos content using PLM (Polarized Light Microscopy) and all ancillary quality control procedures Determination of visual percentage and optical properties of asbestos and non-asbestos material Record data in a specified manner Sample and media preparation and inventory management Compensation: $45,000.00 - $60,000.00 per year PEL is a rapidly growing laboratory specializing in asbestos, mold, lead and smoke damage assessments. See our website, **************** for additional information on our growing company. We offer highly competitive pay, benefits, and room for anyone to grow within the company.

Company Cox Automotive - USA Job Family Group Vehicle Operations Job Profile Quality Control Inspector II Management Level Individual Contributor Flexible Work Option No remote option; must work at a specified Cox location Travel % No Work Shift Day Compensation Hourly base pay rate is $17.79 - $26.63/hour. The hourly base rate may vary within the anticipated range based on factors such as the ultimate location of the position and the selected candidate's knowledge, skills, and abilities. Position may be eligible for additional compensation that may include commission (annual, monthly, etc.) and/or an incentive program. Job Description This position is considered a Utility. Detail QC, Inspector, Vehicle Photographer. Detail QC II- This position assists the Shop Manager in the daily operation of the shop, directing the work in an efficient and productive manner to meet required daily goals and Manheim's quality and service standards when preparing vehicles for sale. Inspector I - An Inspector I functions as a member of the Inspections team for an operating location with the primary responsibilities of providing accurate and complete documentation of overall vehicle condition. More specifically, the documentation provided by the Inspector is used to support the processing and sale of client/customer cosigned vehicles in lane and online. A basic understanding and delivery of the following is required: VIN recognition; proper notation of all options and equipment in vehicle; proper odometer reading and operable function; identification of damage, missing parts, and major mechanical problems; estimating repair cost pricing; recommending labor actions, severity, pricing; identifying value added options; identifying basic mechanical conditions; identifying common wear and tear; evaluating fluid levels; documenting vehicle condition in writing by completing appropriate Vehicle Condition Report; completing inspections process and data entry in appropriate time frames; collecting digital photos per specific criteria guidelines; test driving (when applicable); accurately determining grade using Manheim's Grading Scale (when applicable). Vehicle Photographer- This position is responsible for taking post recon, distribution center, InSight OVE/Simulcast, and TRA photographs of vehicles as defined by Image Standards. The Vehicle Photographer will include responsibility for Photo Booth processing if the location is so equipped. Additionally, this position supports uploading images captured during the inspection process. Qualifications: * High School Diploma or equivalent preferred. * Valid driver's license and safe driving record required. * Ability to drive vehicles with standard and automatic transmissions. * Basic computer skills required. * Regularly required to stand, walk, reach, talk, and hear. * Frequently required to stoop, kneel, crouch, bend, squat, and climb. * Ability to lift 1-15 pounds. * Vision abilities required include close, distance, and color vision, depth perception, and the ability to adjust focus. * Regularly required to stand, walk, reach, talk, and hear. Frequently required to stoop, kneel, crouch, bend, squat, and climb. Preferred * 1-3 years of experience in the automotive field, strongly preferred Work Environment: Exposure to outdoor weather conditions. Moderate noise level. May be exposed to fumes and odors. Drug Testing To be employed in this role, you'll need to clear a pre-employment drug test. Cox Automotive does not currently administer a pre-employment drug test for marijuana for this position. However, we are a drug-free workplace, so the possession, use or being under the influence of drugs illegal under federal or state law during work hours, on company property and/or in company vehicles is prohibited. Benefits Employees are eligible to receive a minimum of sixteen hours of paid time off every month and seven paid holidays throughout the calendar year. Employees are also eligible for additional paid time off in the form of bereavement leave, time off to vote, jury duty leave, volunteer time off, military leave, and parental leave. About Us Through groundbreaking technology and a commitment to stellar experiences for drivers and dealers alike, Cox Automotive employees are transforming the way the world buys, owns, sells - or simply uses - cars. Cox Automotive employees get to work on iconic consumer brands like Autotrader and Kelley Blue Book and industry-leading dealer-facing companies like vAuto and Manheim, all while enjoying the people-centered atmosphere that is central to our life at Cox. Benefits of working at Cox may include health care insurance (medical, dental, vision), retirement planning (401(k)), and paid days off (sick leave, parental leave, flexible vacation/wellness days, and/or PTO). For more details on what benefits you may be offered, visit our benefits page. Cox is an Equal Employment Opportunity employer - All qualified applicants/employees will receive consideration for employment without regard to that individual's age, race, color, religion or creed, national origin or ancestry, sex (including pregnancy), sexual orientation, gender, gender identity, physical or mental disability, veteran status, genetic information, ethnicity, citizenship, or any other characteristic protected by law. Cox provides reasonable accommodations when requested by a qualified applicant or employee with disability, unless such accommodations would cause an undue hardship. Applicants must currently be authorized to work in the United States for any employer without current or future sponsorship.

Why Us? At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. Summary The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. Job Description Scope of Authority - span of control (work unit, site, department, division, etc.), monetary value of budget/spend authority ( capital, operating, etc.), P&L responsibility, etc. Typically supports one Par business, at a single site Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time Accountability Responsibilities % of Time Analysis & Testing Conducts routine laboratory analyses: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. Uses laboratory software for analyses 65% Lab Equipment Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping Cleans lab working surfaces and disposes of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals Under close supervision, learns to troubleshoot basic instrument problems 20% Investigations With guidance, participates in OOS/OOT/NOE and other investigations Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor May assist in drafting, editing, and reviewing SOPs and laboratory investigations 10% Training Maintains assigned training records current and in-compliance May assist in the training of less senior laboratory staff 5% Compliance Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs Follows internal processes related to controlled substances continuous Safety Follows EH&S procedures to ensure a safe work environment Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS continuous Total 100% Qualifications Education & Experience Minimal acceptable level of education, work experience and certifications required for the job Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. Some pharmaceutical laboratory experience preferred. Knowledge Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. Proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. Basic knowledge of wet chemistry techniques Knowledge of applicable safety and standards guidelines: SOP, cGMP, GLP, DEA regulations and/or MSDS Competency in Microsoft Office Suite Skills & Abilities Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. Ability to display and analyze data in a logical manner Good verbal and written communication skills as well as good computer skills Attention to details and accurate record keeping Establish and maintain cooperative working relationships with others Solid organizational skills Ability to take initiative, set priorities and follow through on assignments Physical Requirements Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals Must occasionally lift and/or move up to 15-25 lbs. Ability to wear personal protective equipment, including respirators, gloves, etc. Specific visions abilities are required by this job include close vision and color vision Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. EEO Statement: We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility, located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist II is responsible for providing analytical chemistry support for the facility. To perform this position 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: * Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices. * Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values. * Identify and protect the original technical information as part of the company property. Key responsibilities. * Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines. * Perform cleaning verifications on multi-use equipment using approved methods. * Test reference standards and stability samples. * Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance. * As required, test intermediates and final products to meet production timelines/client requirements. * Assist in the revision of documentation as required. * Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate. * Provide support in the maintenance and calibration of laboratory analytical instrumentation. * Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized. * As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed. Education/Experience. * Bachelor's degree in Chemistry or Biochemistry or equivalent. * One (1) year of experience in pharmaceutical quality control or equivalent is preferred * Familiarity with analytical testing and instrumentation. Job Competencies. * Excellent organizational and planning skills. * Strong written, verbal, and interpersonal communication skills. * High attention to detail. * Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines. Job Conditions. The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Physical Demands: * Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected. * Long periods of standing and walking can be expected in this position. * This position may require long periods of sitting, typing, computer entry or looking at a computer. * Work Environment: * Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes. * Potential limited exposure to hazardous chemicals. * Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.

Full-time Description Laboratory Analyst will be responsible for conducting accurate and timely analyses of environmental samples, ensuring compliance with regulatory standards and supporting the company's mission to promote environmental health and sustainability. Job Responsibilities: Perform chemical, physical, and microbiological analyses on environmental samples, including water, soil, air, and waste. Prepare, calibrate, and maintain laboratory instruments such as spectrometers, chromatographs, and other analytical equipment. Follow standardized procedures and methodologies to ensure precise and reproducible results. Record, interpret, and report test results in accordance with established protocols and regulatory requirements. Assist in the development and validation of new analytical methods. Maintain detailed and accurate laboratory records, including sample logs, chain of custody, and quality control documentation. Monitor laboratory quality assurance/quality control (QA/QC) procedures to ensure adherence to accreditation standards (e.g., ISO 17025, NELAC). Troubleshoot equipment malfunctions and participate in preventive maintenance schedules. Collaborate with team members to ensure timely project completion and client satisfaction. Adhere to all safety guidelines, maintaining a clean and organized workspace. Perform all other duties as assigned. Requirements Education: Bachelor's degree in Chemistry, Environmental Science, Biology, or a related field. Experience/Qualifications: 1-3 years of experience in an environmental or analytical laboratory setting required; TO-15 experience preferred. License/Certification: Must have a valid driver's license. Knowledge/Skills/Abilities: Familiarity with standard laboratory techniques, such as gas chromatography (GC), liquid chromatography (LC), and inductively coupled plasma (ICP). Strong understanding of environmental regulations and testing standards. Excellent analytical and problem-solving skills. Proficiency with laboratory information management systems (LIMS) and Microsoft Office Suite. Strong attention to detail, organizational skills, and the ability to manage multiple tasks. Effective communication and teamwork skills. Work Environment: Laboratory environment with exposure to chemicals and testing equipment. Requires adherence to safety protocols, including the use of personal protective equipment (PPE). May involve occasional lifting of heavy equipment or materials (up to 25 lbs). Equal Employment Opportunity: Metiri Analytical Group, Inc. is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Temp Required Qualifications for Employment: Quality Technician: - 3 Years practical or technical experience in quality control or CNC machining in a manufacturing environment. - Proficient in the use of hand-held calipers and micrometers as well as other measurement devices such as height gages, optical comparator, indicators, thread gages, pin gages, etc. - Good understanding of part drawing interpretation of English to metric conversions, dimensional tolerancing, revision blocks, etc. - At least 1 year experience with Excel, Word, PowerPoint, and Outlook. - Strong attention to detail. - Strong analytical and technical skills. - Record of job stability and good attendance history. Job Description: - Perform shop floor inspection of parts running on screw machines and CNC mills $ lathes. Ensure quality procedures relating to operator inspections, gage usage, non-conformances and process identification are being carried out correctly. Shop floor engagement comprises 40-60% of the day. - Perform incoming inspections of finished goods and WIP in the quality lab. - Recording of inspection results and generating new inspection templates in Excel. - Assisting quality lead on 1st piece approvals and gage calibration when needed. - From time-to-time, participate in defect soring and corrective actions.

A Day in Your Life at MKS: As an Associate Chemist at MKS | Atotech in the GMF industry, your day begins by receiving and preparing samples for analysis, followed by conducting chemical tests using techniques like UV-Vis, FTIR, and HPLC. You'll spend most of your time at the lab bench or workstation, documenting results in digital systems and collaborating with production and quality teams to ensure materials meet specifications. You will be trained to safely operate a forklift, as part of your responsibilities will include moving chemical shipments and supplies within the facility. The work environment is fast-paced, safety-focused, and offers opportunities to contribute to process improvements and product quality. In this role, you will report to the Site Manager. You Will Make an Impact By: * Perform various laboratory tasks such as preparing chemical solutions, conducting experiments, and operating laboratory equipment safely and efficiently * Collect and analyze experimental data using various techniques and instrumentation. This may involve using software programs to process and interpret results accurately * Maintain detailed records of experiments, procedures, and results in laboratory notebooks or electronic databases. Ensuring that all documentation meets regulatory and quality standards * Assist in quality control procedures to ensure that products meet specifications and regulatory requirements. This may involve conducting tests on raw materials, intermediates, and finished products * Adhere to safety protocols and guidelines to ensure a safe working environment. Following standard operating procedures (SOPs) and regulatory requirements related to chemical handling, storage, and disposal * Perform warehouse functions - shipping and receiving chemical products Skills You Bring: * Bachelor of Science in Engineering degree or equivalent experience • Minimum of 0-1 year of related experience * Familiarity with instrumentation and chemical safety * Must either have hi-lo forklift experience or be willing to learn. This is a mandatory function of position. Physical Demands & Working Conditions: * Perform activities such as sitting, standing, for extended periods of time * Must be able to lift up to 50 lbs * Regularly requires good manual dexterity and coordination * Frequently positions self to perform tasks and positions objects below, at, and above shoulder level * Ability to remain in a stationary position for 60-80% of the time * Must be able to safely operate a forklift (training and certification within 30 days of hire) * Operates in a laboratory/manufacturing environment * Noise levels in the work environment are typically moderate * Occasional exposure to chemicals and fumes may occur; adherence to safety guidelines is mandatory #LI-AS1 Globally, our policy is to recruit individuals from wide and diverse backgrounds. However, certain positions require access to controlled goods and technologies subject to the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants for these positions may need to be "U.S. persons." "U.S. persons" are generally defined as U.S. citizens, noncitizen nationals, lawful permanent residents (or, green card holders), individuals granted asylum, and individuals admitted as refugees. MKS Inc. and its affiliates and subsidiaries ("MKS") is an affirmative action and equal opportunity employer: diverse candidates are encouraged to apply. We win as a team and are committed to recruiting and hiring qualified applicants regardless of race, color, national origin, sex (including pregnancy and pregnancy-related conditions), religion, age, ancestry, physical or mental disability or handicap, marital status, membership in the uniformed services, veteran status, sexual orientation, gender identity or expression, genetic information, or any other category protected by applicable law. Hiring decisions are based on merit, qualifications and business needs. We conduct background checks and drug screens, in accordance with applicable law and company policies. MKS is generally only hiring candidates who reside in states where we are registered to do business. MKS is committed to working with and providing reasonable accommodations to qualified individuals with disabilities. If you need a reasonable accommodation during the application or interview process due to a disability, please contact us at: accommodationsat *************** . If applying for a specific job, please include the requisition number (ex: RXXXX), the title and location of the role

Quality Inspector - Metal Parts (Tier 1 Automotive Stamping) Auburn Hills: 6:00am-4:30pm - $17/hr Lake Orion: 2:30pm-12:00am - $18/hr Job SummaryThe Quality Inspector is responsible for inspecting stamped metal automotive parts to ensure they meet customer specifications and company quality standards. This role supports production by identifying defects, documenting findings, and maintaining a safe and organized work environment. Key Responsibilities Perform visual and dimensional inspections of stamped metal parts Use gauges, calipers, check fixtures, and other measurement tools Follow quality standards, work instructions, and inspection criteria Record inspection results and complete required documentation Communicate defects or nonconformities to production and leadership Support containment, rework, and sorting activities as needed Maintain a clean, safe work area and follow all safety procedures Qualifications Previous manufacturing or quality experience preferred Ability to read and understand basic work instructions Comfortable standing for long periods and lifting up to 25 lbs Long term contract to hire #IND3

Job DescriptionBenefits: Dental insurance Employee discounts Health insurance Paid time off Training & development Vision insurance Company Information Arch Environmental Group, Inc. is an environmental consulting and hazardous materials services company serving clients throughout Michigan and the Midwest. We are looking for a candidate for the safe EARTH team of our company, the team which is responsible for hazardous waste management, emergency spill response, lab packs, industrial cleaning, and waste consulting services. Arch Environmental Group, Inc. is headquartered in Farmington Hills, Michigan, with a satellite office in Cedar Springs, Michigan (greater Grand Rapids area). This position will report to the Farmington Hills location. Job Title Chemical Technician / Driver Farmington Hills, MI Location We are looking for a candidate with a valid Class A or Class B Commercial Drivers License (CDL). Existing hazardous materials CDL endorsement is preferred, but not required for hiring. This position will include assisting project managers and field chemists with consolidation/packaging of hazardous wastes, industrial cleaning, spill response and clean-up, recycling activities, and transportation (driving) of hazardous and regulated wastes. This position is based out of our Farmington Hills office with work primarily centered around southeastern Michigan, but will include occasional overnight travel throughout Michigan and the surrounding states. This is a field position, NOT a laboratory position. Work Activities Day-to-day work activities for this position will include, but are not limited to: Packaging, labeling, manifesting, and transport of universal wastes, liquid industrial by-products, medical wastes, and hazardous wastes. Perform consolidation of hazardous materials/wastes (including bulk packaging and repackaging). Properly complete regulatory documents for compliant transport and disposal of waste materials. Assist in preparation of chemical inventories for proper waste handling and/or disposal. Assist in the safe, compliant, and timely clean-up of chemical spills. Assist in industrial cleaning projects. Operate a commercial motor vehicle transporting hazardous materials and wastes for recycling and/or disposal. Hours This is a full time position. Anticipated full-time work hours will be Monday - Friday, typically 7:00 a.m. - 4:00 p.m. or 8:00 a.m. - 5:00 p.m. depending on project commitments. Additional overtime and weekend work may be needed from time to time to support specific project deadlines. This position is also required to have weekend on-call commitments two weekends per month. Job Requirements Self-starter, efficient, productive, works well with a team. Valid Commercial Drivers License (CDL) Class A or Class B. Due to insurance requirements, the candidate must be at least 23 years of age and have a clean driving record. Successful completion of OSHA/DOT physical examination and drug test. Clean criminal/security history required to obtain TSA Threat Assessment clearance for CDL Hazardous Materials endorsement. Must be able to frequently move/lift equipment and supplies weighing 50-100 pounds. Basic computer experience to handle day-to-day project assignments, use of MS Office. Preferred Experience/Qualifications Current CDL endorsements for Hazardous Materials (H) Current DOT Medical Examiners (ME) card Experience in the hazardous waste or emergency response industries 1-3 years' experience preferred Schedule: 8 hour shift Day shift Monday to Friday

Primary Responsibilities: * Ensure that all product meets or exceeds customer specifications. * Ensure allocation is followed, validate correct product is pulled and shipped to customer. * Assist Quality Control Inspection Supervisor to ensure that all product inspections are being performed, labeling specification are adhered to, and non-conformance product is pulled and corrected. * Flex Between the shipping dock, receiving dock and production to assist Quality Control Inspection Supervisor with Quality issues and/or inspections. * Report any exceptions to the customer specifications to Quality Control Inspection Supervisor. * Send out Quality Issues Emails for Non-Compliant Product. * Oversee floor operations when the Quality Control Inspection Supervisor is unavailable. * Remember recent rejections and rejection trends. * Ensure Product packaging is in presentable condition for our customers. * Ensure Presentation is of highest standards. * Performs any other Quality Control related tasks or special projects as assigned. * Provide training when required. FULL TIME Night Shift - Thursday- Saturday, alternating Wednesdays. 6:00 p.m. - 6:00 a.m. Training will be on our B1 shift Thursday-Saturday alternating Wednesday 6:00 a.m. - 6:00 p.m. Education/Background Requirements: * 1 Year College degree or 6 Months year of experience in a related field required. * Previous experience in produce industry preferred. Specific Knowledge, Skills and Abilities Required * Must pass Background Check and pre-employment Skills Testing. * Must sign a confidentiality agreement upon hire. * Must be a self-starter and willing to work flexible hours. * Proficiency in use of English language with the ability to communicate effectively and professionally. * Proficient in computer-use skills (MS Office: Word, Excel and PowerPoint). * Strong organizational, analytical and problem-solving skills. Need to be creative, adaptable and able to accurately work with a sense of urgency. * Spanish as a second language would be an asset. * Inspection/audit experiences, working in software applications are considered assets. * Proficient in basic computer skills, JDA or NAV experience preferred. * Ability to use and read measuring devices such as scales, calipers, ruler. * Excellent communication and interpersonal skills. Working Conditions: * Environment includes an expansive refrigerated warehouse, where the temperatures range is 45-55 degrees (except office areas). The background noise approaches 70 dcbs. * Must be capable of lifting up to 35 lbs.

Job Description Steel Tool & Engineering is looking for a highly analytical, precise, and detail-oriented person to join our team as a full-time Quality Control Inspector. You'll play a critical part in our manufacturing processes, making sure every product we create meets client needs and our company's standards. Keep reading to learn just a few of the perks of joining us! PAY & BENEFITS Competitive wage of $19.25 - $20.25/hour 100% paid medical - if you already have coverage and want to opt out of our plan, you could receive a waiver of $300/month Dental and vision for you and your dependents 401(k) Paid Vacation Paid life insurance Holiday pay Pet insurance THE QUALITY CONTROL INSPECTOR WE'RE LOOKING FOR Ability to work the 1st shift from 6:00 am to 4:30 pm Ability to read and interpret blueprints, specifications, and technical drawings Physical ability to stand for extended periods, lift 50 lbs., and perform repetitive tasks with few breaks Strong knowledge of measurement tools Excellent problem-solving skills Clear and effective communication skills Ideally, we'd prefer a candidate familiar with ISO standards/industry regulations and who has quality inspection experience in an industry like steel, tooling, or engineering. WHAT WE DO At Steel Tool & Engineering, we don't just build precision aerospace components-we build careers. Specializing in brazed honeycomb assemblies for turbine engines in both commercial and military markets, we're proud to be a one-stop shop where innovation meets craftsmanship. What makes us different? Our commitment to system-driven, data-backed processes that ensure top-tier quality, productivity, and delivery. We support our customers through every stage of new product development, and we do it with a team that feels more like family. If you're looking for a workplace where your skills are valued, your growth is supported, and your contributions truly matter, Steel Tool & Engineering is the place to be. WHAT YOU'LL DO Our Quality Control Inspector ensures our products meet our high standards while actively seeking out ways to improve processes and increase efficiency. Using measuring tools like calipers and micrometers, you'll inspect finished steel tools, components, and engineering materials to make sure they check all the boxes. You'll maintain detailed product records for audits and quality tracking, making note of any defects or problems in the products. If you notice a recurring issue, you'll work with quality, production, and engineering teams to solve the problem and optimize our manufacturing processes. You'll play a big part in our day-to-day success and long-term growth. Think you have what it takes to succeed in this quality inspection role? Make your move and apply now using our short initial form! Job Posted by ApplicantPro

DEPARTMENT: AbilityOne- Detroit Arsenal SUPERVISOR: Director, Contracts Gesher Human Services is a bridge to hope and opportunity for people at work, at home, and in the community. Gesher's workforce development, behavioral health, and inclusion programming serves all Metro Detroiters while meeting the needs of the Jewish community. GENERAL Perform daily quality inspections of contracted areas inside the Detroit Arsenal as well as identify potential and actual problem areas in the provided contracted services. Measures and updates quality standards as needed to ensure compliance with current contract. Required: * High school diploma or equivalent. Other: * Three to four years of janitorial experience with a documented work history performing custodial services preferred. * Demonstrated experience in the performance of quality control * Ability to work with individuals with disabilities * Interpersonal skills sufficient to establish and maintain productive relationships that emphasize a customer focus as well as communicate effectively with participants, staff, government officials and public. * Composition skills sufficient to prepare required reports * Basic proficiency in Microsoft Word. * Must be able to obit Department of Defense Security Clearance. * Must be able to provide immunization records for Mumps, Measles, Rubella (MMR vaccine); Tetanus, Diphtheria, Polio (Tdap Vaccine) Hepatitis B; Varicella (Chicken Pox); and TB Skin test. * Valid Michigan Drive License and a driving record must meet safe standards as established by Agency insurance carrier. DUTIES AND RESPONSIBILITIES * Develop, implement and maintain complete quality control program (QCP) to assure the requirements of the contract as specified, including a documentation system of the inspections, results and actions. * Identifies potential and actual problem areas in providing and contracted services. * Perform daily quality inspections of contracted areas. * Measures and updates quality standards as needed to ensure compliance with contracts * Meets with government officials as deemed appropriate by the officials to discuss quality inspections and discrepancies. WORKING CONDITIONS * Ability to work flexible hours, including early morning shift (5:30am-9:30am) * Work involves the ability to obtain clearance to work on work on federal government contracts * Ability to push and lift equipment, office furniture, and accessories weighing up to 50 pounds * Work involves the ability to stoop and bend for up to four hours a day. NON-EXEMPT This position is non-exempt and eligible for overtime pay in accordance with the Federal Fair Labor Standards Act. The above is for general informational purposes only and is not intended to be all inclusive or limiting as to specific duties. The Agency reserves the right to modify, interpret, or apply this in any way the Agency desires and in no way implies that these are the only duties, including essential duties, to be performed by the employee occupying the position. The described job requirements are subject to change to reasonably accommodate qualified individuals with a disability. This job description is not an employment contract, implied or otherwise and any employment relationship remains "at-will." Gesher is proud to be an equal employment opportunity and affirmative action employer. We celebrate diversity and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran or disability status, or any other applicable characteristics protected by law.

VQQ Inc is looking for QC inspector for each shift: days, afternoon and the night shift at its project site/s in MI and/or MO state.. The candidate should be: Responsible to do sorting/ inspection of automotive parts as a third party as per work instructions. Unpack the parts and repack the parts after inspection into its original packaging. Be familiar with automotive inspection/sorting methods and handheld measuring devices e.g., Ruler, tape, vernier caliper. micrometer etc. Rework parts as directed with handheld shop tools /devices/ machines (e.g. cutting, drilling, sanding, trimming, grinding, gluing, etc.); Be able to stand, work on production line, move, work in vehicles shipping yard, bend, lift (part weight varies) Able to read/speak and write in English language and follow all work instructions, visual aids/pictures, procedures, and policies as applicable. Be able to use handheld computer PC devices, tablets, scanners etc.

Temp Quality lead Assistant - 5 years minimum practical or technical experience in quality control or CNC machining in a manufacturing environment. - Proficient in the use of hand-held calipers and micrometers as well as other measurement devices such as height gages, optical comparator, indicators, thread gages, pin gages, etc. - Good understanding of part drawing interpretation of English to metric conversions, dimensional tolerancing, revision blocks, etc. - At least 1 year experience with Excel, Word, PowerPoint, and Outlook. - Strong attention to detail. - Strong analytical and technical skills. - Record of job stability and good attendance history. - General understanding of Geometric Dimensioning & Tolerancing (GD&T) - Familiar with statistical process control (SPC) and process capability (CpK). - Proficient with creating and editing forms in Excel and PowerPoint presentations. - Thorough understanding of thread specifications and measurements. - Performed gage calibration and recording of results. - Experience with Cause & Corrective Actions. - Involved with ISO 9001 or IATF 6949 procedures and auditing. - Performed 1st & Last piece inspections. - Some familiarity with Production Part Approval Process (PPAP). Job Description: Perform shop floor inspection of parts running on screw machines and CNC mills $ lathes. Ensure quality procedures relating to operator inspections, gage usage, non-conformances and process identification are being carried out correctly. Shop floor vs. lab time skews more and more toward lab time involvement over time. - Perform incoming inspections of finished goods and WIP in the quality lab. - Recording of inspection results and generating new inspection templates in Excel. - Assisting quality lead on 1st piece approvals and gage calibration when needed. - From time-to-time, participate in defect soring and corrective actions. - Learn and operate Keyence optical measurement equipment. - Perform 1st piece inspection approvals independently. - Perform new tooling verification records & results. - Sole responsibility for scheduling and logging gage calibration records. - Assist Quality Manager in PPAP preparation. - Assist Quality Manager in internal auditing. - Generate SCARS and internal CARS for root cause and corrective actions. - Perform SPC and Cpk studies and interpretations for process improvements. - Engage in supplier interactions for process improvements. Engage in supplier interactions for quality concerns and non-conformances.

A Day in Your Life at MKS: As an Associate Chemist at MKS | Atotech in the GMF industry, your day begins by receiving and preparing samples for analysis, followed by conducting chemical tests using techniques like UV-Vis, FTIR, and HPLC. You'll spend most of your time at the lab bench or workstation, documenting results in digital systems and collaborating with production and quality teams to ensure materials meet specifications. You will be trained to safely operate a forklift, as part of your responsibilities will include moving chemical shipments and supplies within the facility. The work environment is fast-paced, safety-focused, and offers opportunities to contribute to process improvements and product quality. In this role, you will report to the Site Manager. You Will Make an Impact By: • Perform various laboratory tasks such as preparing chemical solutions, conducting experiments, and operating laboratory equipment safely and efficiently • Collect and analyze experimental data using various techniques and instrumentation. This may involve using software programs to process and interpret results accurately • Maintain detailed records of experiments, procedures, and results in laboratory notebooks or electronic databases. Ensuring that all documentation meets regulatory and quality standards • Assist in quality control procedures to ensure that products meet specifications and regulatory requirements. This may involve conducting tests on raw materials, intermediates, and finished products • Adhere to safety protocols and guidelines to ensure a safe working environment. Following standard operating procedures (SOPs) and regulatory requirements related to chemical handling, storage, and disposal • Perform warehouse functions - shipping and receiving chemical products Skills You Bring: • Bachelor of Science in Engineering degree or equivalent experience • Minimum of 0-1 year of related experience * Familiarity with instrumentation and chemical safety * Must either have hi-lo forklift experience or be willing to learn. This is a mandatory function of position. Physical Demands & Working Conditions: • Perform activities such as sitting, standing, for extended periods of time • Must be able to lift up to 50 lbs • Regularly requires good manual dexterity and coordination • Frequently positions self to perform tasks and positions objects below, at, and above shoulder level • Ability to remain in a stationary position for 60-80% of the time * Must be able to safely operate a forklift (training and certification within 30 days of hire) • Operates in a laboratory/manufacturing environment • Noise levels in the work environment are typically moderate • Occasional exposure to chemicals and fumes may occur; adherence to safety guidelines is mandatory #LI-AS1 Globally, our policy is to recruit individuals from wide and diverse backgrounds. However, certain positions require access to controlled goods and technologies subject to the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants for these positions may need to be “U.S. persons.” “U.S. persons” are generally defined as U.S. citizens, noncitizen nationals, lawful permanent residents (or, green card holders), individuals granted asylum, and individuals admitted as refugees. MKS Inc. and its affiliates and subsidiaries (“MKS”) is an affirmative action and equal opportunity employer: diverse candidates are encouraged to apply. We win as a team and are committed to recruiting and hiring qualified applicants regardless of race, color, national origin, sex (including pregnancy and pregnancy-related conditions), religion, age, ancestry, physical or mental disability or handicap, marital status, membership in the uniformed services, veteran status, sexual orientation, gender identity or expression, genetic information, or any other category protected by applicable law. Hiring decisions are based on merit, qualifications and business needs. We conduct background checks and drug screens, in accordance with applicable law and company policies. MKS is generally only hiring candidates who reside in states where we are registered to do business. MKS is committed to working with and providing reasonable accommodations to qualified individuals with disabilities. If you need a reasonable accommodation during the application or interview process due to a disability, please contact us at: accommodationsat *************** . If applying for a specific job, please include the requisition number (ex: RXXXX), the title and location of the role