Quality engineer jobs in Lansing, MI - 210 jobs

Leadership & Strategy Provide strategic direction, leadership, and consultative support for implementing and maintaining customer quality system requirements. Champion a culture of quality and continuous improvement across all departments. Act as the primary liaison for quality-related communication between customers, suppliers, and internal stakeholders. Quality Systems & Compliance Ensure compliance with IATF 16949, ISO 14001:2015, and other applicable industry standards. Develop, implement, and maintain policies, procedures, and methods to evaluate and improve product and process quality. Lead internal and external audits, ensuring corrective actions are implemented and sustained. Continuous Improvement Develop and implement programs to establish and maintain quality standards for existing and new products. Drive process control, error-proofing, and inspection methods to ensure products meet design intent and customer expectations. Analyze quality data, identify trends, and lead root cause investigations to reduce defects, scrap, and warranty claims. Partner with operations and engineering to implement lean manufacturing and Six Sigma methodologies. Team Management Supervise and mentor Quality Department personnel, fostering professional growth and accountability. Allocate resources effectively to support production, testing, and inspection needs. Provide training and guidance to employees on quality standards, tools, and best practices. Customer Focus Serve as the voice of the customer within the organization, ensuring quality requirements are met or exceeded. Lead customer complaint resolution, corrective action plans, and preventive measures. Support new product launches by validating quality systems and ensuring readiness for production. Documentation & Reporting Ensure system tests are completed, documented, and issues resolved in a timely manner. Maintain accurate records of quality metrics, audits, and certifications. Report regularly to senior leadership on quality performance, risks, and improvement initiatives. Other Duties Perform additional responsibilities as assigned to support organizational goals. Skills and Experience Requirements Minimum 5 years automotive Tier 1 management experience Bachelor's degree in engineering, business management or related field preferred IATF 16949 experience required and ISO 14001:2015 experience preferred. Strong interpersonal skills to build relationships with all levels across the organization and with customers. Strong analytical background with demonstrated ability to analyze, explain, and draw logical conclusions from complex operational, financial, regulatory and/or business data. Continuous Improvement / Kaizen / Lean facilitator

The Manager, Global Product Quality - Controlled Substances is responsible for ensuring that all activities related to controlled substances across the product lifecycle meet Good Manufacturing Practices (GMP) and comply with global regulatory requirements, including DEA regulations. This role partners closely with R&D, Supply Chain, Product Development, and Warehousing & Distribution teams to ensure robust quality oversight and regulatory compliance in the handling, storage, manufacturing, and distribution of controlled substances. The role may also support day to day quality oversight of clinical and commercial products to ensure they are manufactured, tested, packaged, stored and distributed in compliance with Current Good Manufacturing Practices (CGMP) regulations, Otsuka Quality Standards and US/global (if applicable) regulatory requirements. **Key Responsibilities** + Product Oversight: Provide GMP oversight and guidance during the drug development process including review and approval of documentation and collaboration and oversight of suppliers/contract manufacturers.Act as a liaison with regulatory agencies and internal compliance teams regarding controlled substance matters. + Quality & Compliance:Serve as the quality and compliance lead for controlled substances, ensuring adherence to DEA regulations and other global controlled substance requirements (e.g., Health Canada, EMA, ANVISA). Develop, implement, and maintain global SOPs and standards for the compliant handling, storage, transportation, and distribution of controlled substances. Ensure warehousing and distribution operations meet all applicable regulatory and internal quality requirements, including security, inventory reconciliation, and chain-of-custody controls. + Audit & Inspection Readiness: Support DEA inspections, audits, and regulatory submissions, ensuring readiness and robust documentation. Participates in regulatory inspections and audits as required. + Process Optimization: Oversee and enhance quality systems related to product quality complaints, CAPA, deviations, and change control for controlled substances. + Data Analysis & Reporting: Monitor and analyze compliance metrics and trends to identify risks and drive continuous improvement initiatives. + Cross-functional Collaboration: Collaborate with R&D, Supply Chain, Product Development, and Manufacturing to ensure quality and compliance are integrated throughout the lifecycle of controlled substance products. + Training & Documentation: Provide training and guidance to global teams on controlled substance regulations, GMP expectations, and best practices. Authors and maintains SOPs, Work practices and Job Aids, related to assigned quality activities. **Qualifications** Required + Bachelor's degree in Chemistry, Engineering, Life Sciences, or a related field. + Minimum 5 - 7 years of experience in a regulated industry (pharmaceutical or medical device), with 3-5 years in pharmaceutical quality, with specific experience in controlled substances and commercial quality operations. + Demonstrated expertise in DEA regulations and compliance, including registration, quota management, recordkeeping, and reporting. + Working knowledge and understanding of FDA/ICH/USP requirements, including FDA 21 CFR Parts 210, 211, and Part 11 (and Part 820, if applicable), ICH Q7 + Strong understanding of GMP requirements and global regulatory expectations for controlled substances. + Experience managing quality systems (e.g., deviations, CAPA, change control, complaints) in a regulated environment. + Proven experience in warehousing and distribution controls, including security, inventory management, and transportation compliance for controlled substances. + Excellent communication, collaboration, and project management skills. + Must be detail oriented and able to write and/or review Technical Documents + Ability to work effectively in a global, cross-functional, and matrixed environment Preferred Experience + Experience with electronic Quality Management Systems (eQMS) such as Veeva, TrackWise, or similar. + Certification in DEA compliance, Quality Assurance, or Regulatory Affairs. **Disclaimer** This is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to their protected veteran or disabled status, or any protected status **Competencies** **Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change. **Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business. **Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders. **Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka. **Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals. **Empowered Development -** Play an active role in professional development as a business imperative. Minimum $104,640.00 - Maximum $156,400.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws. **Application Deadline** : This will be posted for a minimum of 5 business days. **Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits. Come discover more about Otsuka and our benefit offerings; ********************************************* . **Disclaimer:** This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) . **Statement Regarding Job Recruiting Fraud Scams** At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf. Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment. Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters. To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* . Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Howell, MI Who are we: Antolin is a leading global automotive supplier, we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and acoustic systems, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world's leading car brands, including JLR, BMW, Toyota, Volkswagen, Audi, Mercedes-Benz, and Ford. What can we offer you: You will be part of a highly engaged multinational Organization with international career opportunities. We offer you a learning journey adapted to your professional experience. You will work on international projects for world- renowned companies in Automotive sector. You can find an Open Environment to learn new technologies. We can offer you a competitive salary, benefits and valuable OEM discounts. Mission: The job mission of the Quality Manger is to ensure the quality management system is upheld and the products and processes meet customer, regulatory, and industry requirements throughout the product lifecycle. Responsibilities: Ensure compliance with IATF 16949, customer specific requirements, and applicable regulatory standards. Lead quality planning, assurance, and control activities from APQP to serial production. Drive zero defect strategy through preventative quality tools such as: FMEA, SPC, and Control Plans. Manage customer quality performance including PPAP submissions and audits. Monitor and improve supplier quality performance and development. Responsible for plant KPI's and lead continuous improvement initiatives. Direct Customer and Supplier liaisons for plant quality activities and concerns including scheduled visits. Establish and maintain all quality documents, samples, customer contact, supplier development, production start - up, product launch, and correction of production variances and warrant analysis. Manage Customer and Supplier quality scorecard and address any issues accordingly. Coordinate and lead all internal, external and Customer quality audits. What we are looking for: A Bachelor's degree in Engineering or Quality or equivalent work experience in the automotive industry with previous Management experience. 5+ years of prior Quality Management or Supervision. TS-16949 experience required. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Michigan Milk Producers Association (MMPA) is actively interviewing for a Quality Manager to join our team in our Ovid, MI dairy. The Quality Manager is responsible for managing Quality Assurance Programs establishing, implementing and monitoring Food safety and quality programs, including regulatory and customer audits. Ensuring food safety and quality of all products produced. Perform inspections of processes, employee training, compliance with applicable food laws and regulations and verify Food safety plans. Manage the QA laboratory. Actively participates in resolving customer complaints. Integral part of plant leadership team. Provides support to Sales and Operations on customer issues, questions and concerns Who are we? The Michigan Milk Producers Association is a dairy farmer owned cooperative and dairy processor. Founded in 1916, the MMPA serves dairy farmers in Michigan, Indiana, Ohio and Wisconsin. MMPA maintains a strong presence within the dairy industry with strategic business relationships through a variety of channels like processing shelf-stable, value-added dairy products. MMPA has four member owned processing plants in Michigan, Indiana and Ohio, including Superior Dairy and the Middlebury Cheese Company. Products made at MMPA's plants include fluid milk, sour cream, cheese, ultra-filtered milk, cottage cheese, ice cream, butter, nonfat dry milk, cream and condensed skim milk. We offer: Competitive salary Health and wellness benefits with medical coverage through Blue Cross Blue Shield, including mental health benefits Disability insurance Paid time off Retirement including 401k with employer contributions Personal and professional growth opportunities Employee appreciation events and recognition awards Employee wellness initiatives Employees feedback and suggestion forums Job Responsibilities: Leadership of Quality team at the Plant Oversee, implement and maintain quality programs related to vendor certification, raw materials, product mock recall, hold and release, food safety and quality programs Data analysis and trending to improve quality Work on customer complaint resolution (root cause analysis and development of corrective and preventive actions) Ability to work with cross functional teams (Operations, Maintenance, Sales, Supply Chain etc.) Development and maintenance of all food safety regulatory programs to meet FDA/USDA/State regulatory requirements Oversee employee training for Food safety and GMPs Responsible for disposition of all held product, with input from the Plant Manager and Director Quality (as needed) Act as a backup for Director of Quality Oversee product quality with regards to meeting the specifications, and identification of defects Leadership of Plant Laboratory Track, report, and review the Quality Performance Indicators on a regular basis to drive continuous improvement Manage cost of quality Conduct Effective Root Cause Analysis and implement corrective action and preventative action Direct management of quality assurance staff and testing laboratory Perform other duties, as assigned Qualifications and Skills BS Degree in Food Science, Biology, Microbiology, Chemistry or related field required 5-7 years in quality/manufacturing/sanitation management roles working in food manufacturing environments Equivalent combination of education and experience Leadership skills Good communication skills to share ideas/technical information in an easy to understand way Basic data analysis skills (collect data, establish facts, and draw valid conclusions) PCQI certified and SQF practitioner preferred, but not required Demonstrated initiative and desire to learn about the dairy industry Ability to ask questions and maintain accountability Be able to interact with employees at levels in the organization Shows interest to learn from and share the knowledge with other Essential Functions and Physical Requirements While performing the duties of this job, the employee is required to stand, walk, handle, reach above the shoulders, climb, balance, stoop, kneel, crouch and crawl. The employee is frequently required to sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. Join us in maintaining the highest standards in the dairy industry! Apply now and become part of our dynamic MMPA team! To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities. This job description is not designed to contain a comprehensive list of responsibilities that are required of the role. Responsibilities may change at any time with or without notice. MMPA provides the opportunity for meaningful work that makes a difference in the dairy industry and in our communities. The diverse talents and perspectives of our employees help us to meet the needs of our member farms and the customers we serve. We are interested in every qualified candidate who is eligible to work in the United States. MMPA is committed to maintaining a safe, healthy, and productive environment for all employees as one of our top priorities. As part of our commitment to your well-being and workplace safety, all applicants are required to undergo a drug screening and background check as part of the hiring process. We are not accepting unsolicited candidate introductions, referrals, or résumés from third-party recruiters or staffing agencies for this position. MMPA is an equal opportunity employer. #MMPAND1

Michigan Milk Producers Association (MMPA) is actively interviewing for a Quality Manager to join our team in our Ovid, MI dairy. The Quality Manager is responsible for managing Quality Assurance Programs establishing, implementing and monitoring Food safety and quality programs, including regulatory and customer audits. Ensuring food safety and quality of all products produced. Perform inspections of processes, employee training, compliance with applicable food laws and regulations and verify Food safety plans. Manage the QA laboratory. Actively participates in resolving customer complaints. Integral part of plant leadership team. Provides support to Sales and Operations on customer issues, questions and concerns Who are we? The Michigan Milk Producers Association is a dairy farmer owned cooperative and dairy processor. Founded in 1916, the MMPA serves dairy farmers in Michigan, Indiana, Ohio and Wisconsin. MMPA maintains a strong presence within the dairy industry with strategic business relationships through a variety of channels like processing shelf-stable, value-added dairy products. MMPA has four member owned processing plants in Michigan, Indiana and Ohio, including Superior Dairy and the Middlebury Cheese Company. Products made at MMPA's plants include fluid milk, sour cream, cheese, ultra-filtered milk, cottage cheese, ice cream, butter, nonfat dry milk, cream and condensed skim milk. We offer: Competitive salary Health and wellness benefits with medical coverage through Blue Cross Blue Shield, including mental health benefits Disability insurance Paid time off Retirement including 401k with employer contributions Personal and professional growth opportunities Employee appreciation events and recognition awards Employee wellness initiatives Employees feedback and suggestion forums Job Responsibilities: Leadership of Quality team at the Plant Oversee, implement and maintain quality programs related to vendor certification, raw materials, product mock recall, hold and release, food safety and quality programs Data analysis and trending to improve quality Work on customer complaint resolution (root cause analysis and development of corrective and preventive actions) Ability to work with cross functional teams (Operations, Maintenance, Sales, Supply Chain etc.) Development and maintenance of all food safety regulatory programs to meet FDA/USDA/State regulatory requirements Oversee employee training for Food safety and GMPs Responsible for disposition of all held product, with input from the Plant Manager and Director Quality (as needed) Act as a backup for Director of Quality Oversee product quality with regards to meeting the specifications, and identification of defects Leadership of Plant Laboratory Track, report, and review the Quality Performance Indicators on a regular basis to drive continuous improvement Manage cost of quality Conduct Effective Root Cause Analysis and implement corrective action and preventative action Direct management of quality assurance staff and testing laboratory Perform other duties, as assigned Qualifications and Skills BS Degree in Food Science, Biology, Microbiology, Chemistry or related field required 5-7 years in quality/manufacturing/sanitation management roles working in food manufacturing environments Equivalent combination of education and experience Leadership skills Good communication skills to share ideas/technical information in an easy to understand way Basic data analysis skills (collect data, establish facts, and draw valid conclusions) PCQI certified and SQF practitioner preferred, but not required Demonstrated initiative and desire to learn about the dairy industry Ability to ask questions and maintain accountability Be able to interact with employees at levels in the organization Shows interest to learn from and share the knowledge with other Essential Functions and Physical Requirements While performing the duties of this job, the employee is required to stand, walk, handle, reach above the shoulders, climb, balance, stoop, kneel, crouch and crawl. The employee is frequently required to sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. Join us in maintaining the highest standards in the dairy industry! Apply now and become part of our dynamic MMPA team! To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities. This job description is not designed to contain a comprehensive list of responsibilities that are required of the role. Responsibilities may change at any time with or without notice. MMPA provides the opportunity for meaningful work that makes a difference in the dairy industry and in our communities. The diverse talents and perspectives of our employees help us to meet the needs of our member farms and the customers we serve. We are interested in every qualified candidate who is eligible to work in the United States. MMPA is committed to maintaining a safe, healthy, and productive environment for all employees as one of our top priorities. As part of our commitment to your well-being and workplace safety, all applicants are required to undergo a drug screening and background check as part of the hiring process. We are not accepting unsolicited candidate introductions, referrals, or résumés from third-party recruiters or staffing agencies for this position. MMPA is an equal opportunity employer. #MMPAND1

Job DescriptionDescription: Job title: Quality Manager Reports to: Managing Director Assures consistent quality of production by developing and enforcing good automated manufacturing practice (GAMP) systems; validating processes; providing documentation; managing staff. Key Responsibilities Communicate with customers as needed to resolve quality issues Work with engineering, manufacturing and other functional area to resolve customer, internal and/or supplier quality issues Support manufacturing to ensure conformance to the company's processes, as well as customer specific processes and requirements Manages APQP practices in support of new program launches including customer specific approval processes (PPAP, ISIR, etc) Manages in implementing QS, TS and IATF in the facility Manages the reading and interpretation of customer part and component drawings including GD&T, customer quality standards, and/or requirements Lead manufacturing facility in 8D Problem solving activities, in conjunction with collaborating with customer Demonstrate ability to initiate and accomplish assigned tasks in a manufacturing environment where priorities may change Responsible for performing sub supplier audits as needed Manages a team of quality techs to ensure process and quality standards are met Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements; implementing change. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Requirements: Required Qualifications Bachelor's degree in Engineering or equivalent in experience 3 -5 year of quality engineering experience Working knowledge of MS Windows/Office Excellent communication skills (verbal and written), organized and time management skills Ability to prioritize work load Establish and reach work goals in accordance to the direction established by customer and manufacturing Ability to travel nationally and internationally (25%) Physical Demands Required to stand for long periods of time and move about the facility Occasional lifting of items not to exceed 50 lbs Required to use safety glasses while performing specific tasks or while in specific areas of the plant Work Environment Works primarily in a plant environment Exposed to any number of elements. Other Perform other duties as assigned. Process Owner Process owners should ensure should ensure their processes: Describe its links and interactions with other processes Identify its documentation and training requirements Issue and maintain any procedures and instructions Implement processes consistent with the quality policy Make available necessary resources and information Operate and control an effective and efficient process Resolve any problems and prevent their recurrence Communicate process changes to the process users Define and manage interfaces with other processes Communicate input requirements to internal suppliers Meet the output requirements of internal customers Analyze performance data and set quality objectives Track progress against process performance targets Communicate with process users to identify issues Identify risks and opportunities with current process Investigate and propose process improvements Ensure all corrective action that are assigned to their process are completed in a timely manner

Responsibilities Provide strategic direction and hands-on leadership to implement and sustain customer quality system requirements. Champion a culture of quality, accountability, and continuous improvement across all functions. Serve as the primary point of contact for quality related communication with customers, suppliers, and internal teams. Ensure compliance with IATF 16949, ISO 14001:2015, and applicable customer and regulatory standards. Develop, implement, and maintain quality policies, procedures, and systems to improve product and process performance. Lead internal and external audits, ensuring timely and effective corrective and preventive actions. Establish and maintain quality standards for current and new products. Drive process control, error proofing, and inspection methods to meet design intent and customer expectations. Analyze quality data, identify trends, and lead root cause investigations to reduce defects, scrap, and warranty exposure. Partner with operations and engineering to implement Lean manufacturing, Six Sigma, and Kaizen initiatives. Lead, mentor, and develop quality team members while promoting accountability and professional growth. Allocate resources to support production, testing, and inspection requirements. Train and coach employees on quality tools, standards, and best practices. Act as the voice of the customer, ensuring requirements are met or exceeded. Lead customer complaint resolution, corrective action responses, and preventive actions. Support new product launches by validating quality systems and production readiness. Ensure quality system activities are completed, documented, and issues resolved in a timely manner. Maintain accurate records for audits, certifications, and key quality metrics. Report quality performance, risks, and improvement progress to senior leadership. Perform additional duties as needed to support business objectives. Qualifications Minimum five years of automotive Tier 1 management experience. Bachelor's degree in engineering, business, or a related field preferred. IATF 16949 experience required, ISO 14001:2015 experience preferred. Strong interpersonal skills with the ability to influence across all levels of the organization and with customers. Strong analytical background with the ability to interpret and draw conclusions from complex operational and business data. Experience leading continuous improvement, Lean, Kaizen, or Six Sigma initiatives. Centric Solutions Group places the world's best talent at industry leading companies. We specialize in hiring Technical, Professional, Mid-Management, and Executive employees. CSG and our client companies offer competitive wages and opportunities for growth and advancement for successful individuals. About this Opportunity: Responsibilities: Job Requirements/Qualifications: Centric Solutions Group Equal Employment Opportunity Statement: All qualified applicants will receive consideration for employment based on merit and will not be discriminated on the basis of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), political affiliation, military service or other non-merit based factors. These protections extend to all management practices and decisions, including recruitment and hiring, appraisal systems, promotions, training, and career development programs. Consistent with these obligations, CSG also provides reasonable accommodations to employees and applicants with disabilities and for sincerely held religious beliefs, observances, and practices.

DEPARTMENT: Quality Control SUPERVISED BY: Quality Director STATUS: Full time non-exempt Technique, Inc. is a Michigan-based stamping, tubing and welding facility offering the shortest lead-times and highest quality parts in the industry. We offer high-speed prototypes, ultra-low volume stampings, tubing and assemblies for production and emergency-based manufacturing for industries such as aerospace, automotive, medical and food processing. Technique, Inc. is a group of highly skilled technicians who consistently strive to improve the tools, technology and processes which allow us to continue growing at an incredible rate. The company is dedicated to the success of each team member in a culture that values safety, integrity, teamwork, learning opportunities and results. Position Summary: This position is responsible for inspecting components and finished products to determine compliance with engineering requirements. The employee will also create and maintain all documentation, as well as assist with dispositioning nonconforming product. The employee will develop procedures and coordinate efforts for quality system compliance. They will lead quality/continuous improvement projects in coordination with account managers and purchasing department, and work with setup technicians, customers and vendors on quality-related issues. Essential Job Functions: Use precision measuring tools to check parts against blueprints Assemble and submit PPAP, first piece inspection, source releases, and quality packages documentation. Use/write programs in PolyWorks to operate CMM machines Calibrate precision machinery Work with technicians to provide legible feedback per blueprint specifications and assist technicians with part development Create and complete customer documentation Reverse engineer to help with process improvement activities and corrective actions Professionally represent Technique when interacting with customer representatives Qualifications: EDUCATION: Associate's degree in engineering technology or related field preferred CREDENTIALS/LICENSURE: forklift operator's license preferred MINIMUM EXPERIENCE: 2-4 years of quality control in manufacturing/engineering environment Position Requirements (Skills & Abilities): Ability to multitask in a fast-paced environment Good understanding of GD&T and blueprints Strong communication, time management, and computer skills Experience in an ISO 9000 environment Experience using PolyWorks and SolidWorks Root cause analysis/problem solving skills Ability to use CAD and SolidWorks Ability to use precision measurement tools Travel No travel is required for this position. Other Duties Please note this job description is not designed to cover or contain a complete comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Minimum Physical Expectations: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk and hear. This position is very active and requires standing, walking, bending, kneeling, stooping, crouching, crawling, and climbing all day. The employee must frequently lift and/or move items over 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Position Type and Expected Hours: This is a full-time non-exempt position with a minimum of 40hrs / week with overtime as needed. Note: days and hours required may vary. Shifts include 1st - Monday-Friday - 7:00am-3:30pm Environmental Expectations: While performing the duties of this job, the employee is frequently exposed to manufacturing processes that include and are not limited to; fumes or airborne particles, hazardous chemicals, moving mechanical parts, industrial equipment, and vibration. The noise level in the work environment can be loud. EEO Statement Technique, Inc., is an equal employment opportunity employer. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work Authorization Employee must be eligible to work in the United States, either by means of U.S. Citizenship, Work Visa or H1B sponsorship. E-Verify partner employer. Powered by JazzHR zVN71MzHVG

About Our Client: Our client is a well-established medical device manufacturer located in the Greater Grand Rapids area, specializing in the development and production of high-quality surgical products used by healthcare professionals worldwide. The organization is known for its strong commitment to patient safety, innovation, and operational excellence, and offers a collaborative, quality-driven environment focused on continuous improvement. Key Responsibilities: Ensuring products and processes meet quality, regulatory, and customer requirements. Investigating nonconforming product, leading root cause analysis, and implementing effective corrective and preventive actions (CAPA). Supporting manufacturing and engineering teams to resolve quality and technical issues while reducing scrap, downtime, and defects. Participating in new product introductions and process changes, including PFMEA/DFMEA, PPAP, validation, and risk build activities. Developing and maintaining inspection methods, gauging strategies, test procedures, and quality documentation Performing process capability studies, gauge R&R, and data analysis to identify trends and drive continuous improvement. Supporting customer complaint investigations, supplier quality issues, and product disposition decisions. Maintaining and improving the Quality Management System in compliance with FDA, ISO 13485, and other applicable regulations. Creating, updating, and training on quality procedures, work instructions, and quality alerts. Participating in internal, customer, and regulatory audits and supporting audit readiness. Using quality metrics and reporting to communicate findings and recommend improvements to management. Qualifications: Bachelor's degree in Engineering or a technical discipline preferred. 3+ years of experience leading or supporting quality improvement projects preferred. 2+ years of experience in a regulated industry (FDA and ISO environments preferred). ASQ certification a plus. Strong communication and interpersonal skills with the ability to work across all levels of the organization. Ability to adapt and remain effective in a fast-paced manufacturing environment. Strong teamwork mindset and positive attitude. Ability to read and interpret technical prints and drawings. Proven problem-solving skills, including root cause analysis and corrective action implementation. Project management skills with the ability to manage multiple priorities. Experience conducting PFMEA. Experience with 3D modeling; SolidWorks preferred. Proficiency with Microsoft Office and related computer tools. NO C2C CANDIDATES Interested Candidates please apply on our website at https://jobs.jblresources.com. For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com. JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be. **JBL is an Equal Opportunity Employer and E-Verify Company

**_What Industrial Engineering contributes to Cardinal Health_** Engineering is responsible for performing research and analyses to develop design options for components, products, systems and processes. Industrial Engineering is responsible for enhancing / developing processes, layout and associated tools. Identifies, analyzes and implements new or existing technology to optimize business processes. Designs process improvements to reduce cost, cycle time, improve quality and/or increase throughput. Directs external resources / contractors as required. The Principal Industrial Engineer supports Pharmaceutical Supply Chain Operations in the areas of capital project planning and management, capacity planning, operational process change, and overall distribution center operating layout optimization. The position will also support deployment of new process and automation solutions, facilitate new building designs and layouts changes. Additional responsibilities include partnering with Operations leaders, deploying capital project investments for Pharma Supply Chain Operations, and overseeing project implementation and adoption to realize improvements. **_Responsibilities_** + Drive process engineering initiatives including conceptual operational designs, layout-change scenarios, and innovative automation solutions. Work closely with business operations partners to iterate on solutioning to optimize results. Bring modernization concepts to Operations through material handling and engineering external partnerships. + Works closely with Pharmaceutical Supply Chain Operations Vice Presidents, and site leaders to manage capital projects planned within the buildings. Develops capital budget priorities, establishes preliminary budgets,business case justifications, and formalizes all capital requests for budgeted, approved, or newly scoped projects. + Leads multifunctional teams of stakeholders and contributors to deliver large complex projects on time and under budget.Coordinates with other functional groups including Corporate Real Estate,field operations, Security, Information Technology, Inventory, Quality & Regulatory, Sales,and EH&S to ensure efforts are aligned, and coordinated as projects are developed and analyzed. + Integrated team members supporting operations leadership teams to ensure that capital projects and infrastructure are deployed, coordinated, managed, and maintained to drive building performance expectations. This role also manages and executes small construction projects independent of Corporate Real Estate / Construction including all cage and vault construction resulting from expansion or relocation needs. **_Qualifications_** + Bachelor's Degree in related field or relevant work experience, preferred + 4-6 years of experience in Operations, project and budgetary management, capital investment analysis and deployment, leading complex projects with multi-functional teams, preferred + Experience with automation solutions, facility design, material handling systems, integrated warehouse controls and execution applications, preferred + Experience with AutoCAD and other software applications to drive warehouse design and concepting, preferred + Strong Leadership skills, Strong scheduling and organizational skills + Excellent technical problem-solving capability + High level of initiative - Team player + Willing and transparent communicator + Proficient with Microsoft Office Suite + Excellent written and verbal communication skills + Moderate travel to other facilities for projects and supervision of equipment installation (25%, up to 50% during specific deployment activities and project implementations) **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems + Solutions are innovative and consistent with organization objectives + Completes work; independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **Anticipated salary range:** $94,900 - $135,600 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 3/13/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

Essential Functions Monitor and maintain the state of inventory, quality, equipment, maintenance, calibration and facilities and ensure they comply with QS and cGMP requirements. Drive quality and compliance, adhering to all Quality Systems documentation requirements and establishing/supporting plans to exceed Niowave's goals for Quality, including Safety, Compliance, Six Sigma Quality, On-Time Delivery (OTD), and financial objectives. Support internal and external audits. Support validation of test methods, monitoring processes, and equipment. Support production teams in product/material hold, release, disposition, and traceability assessments, and implement improvements to reduce recurring deviations that lead to rework or scrap. Support new product introduction (NPI) quality activities including prototype testing, process validation, and technology transfer ensure successful product launches. Collaborate with cross-functional teams to support and solve production and quality challenges. Collect, monitor, analyze and communicate data to provide insight on quality metrics set by the management team.

About Us Contemporary Amperex Technology Kentucky (CATK) is the US battery manufacturing subsidiary of Contemporary Amperex Technology Co., Limited (CATL). CATL is a global leader in research, development and manufacturing of battery energy storage system for vehicles, grid scale, and maritime applications. In 2024, CATL accounts for over 37% of global EV battery installed capacity. CATL has been the largest battery manufacturer in the world for the last 7 years. CATK is committed to providing cutting-edge solutions for global new energy applications. Our Vision Strive to be a global premier innovative technology corporation, deliver excellent contribution to green energy resolution for mankind, and provide a platform of pursuing the spiritual and material well-being for employees! Job Overview To better serve the global auto industry electric vehicle trend in the United States, CATL, through its U.S.-based subsidiary, CATK, is seeking multiple dedicated and experienced Production Quality Engineers to oversee the quality management and control of our production line processes. This role involves implementing quality assurance activities, managing process changes, addressing quality issues, and supporting continuous improvement initiatives. Essential Functions Oversee and ensure quality management and control of the production line processes. Implement and monitor quality control measures to maintain high standards. Ensure all quality-related activities are performed in compliance with company standards and requirements. Monitor and manage quality activities including SPC (Statistical Process Control), FAI (First Article Inspection), MES (Manufacturing Execution System) inspection, CTQ (Critical to Quality) management, FIFO (First In, First Out), error prevention, rework, and equipment qualification. Implement lessons learned and horizontal measures to prevent recurrence of quality issues. Support various process audits, including process audits and LPA (Layered Process Audit) audits. Conduct quality risk identification and initiate quality improvement activities. Manage changes in the production process and ensure effective implementation of process response plans. Coordinate with relevant teams to handle process changes smoothly. Provide training and support to enhance the team's overall competency. Minimum Qualifications Bachelors degree in Engineering, Quality Management, or a related field. 3+ years of experience in production quality control or quality assurance, particularly in the vehicle manufacturing industry. Strong knowledge of quality management systems and tools, including SPC, FAI, and MES. Proficient in using quality analysis and improvement tools such as FMEA (Failure Modes and Effects Analysis), FTA (Fault Tree Analysis), 8D (8 Disciplines Problem Solving), Six Sigma, and SPC (Statistical Process Control). Strong data analysis and processing abilities. Proficient in using office software (e.g., Microsoft Office Suite). Strong problem-solving skills and attention to detail. Excellent communication and interpersonal skills. Ability to maintain a full-time work schedule with regular in-person attendance is required for this position. Ability to interact professionally with individuals of varied backgrounds and skill level. Physical Requirements Ability to move around work sites, which may include walking, standing, and climbing ladders or stairs. Flexibility to bend, kneel, or crouch, particularly when inspecting installations or troubleshooting. Capability to lift and carry moderate weights, typically up to 25-50 pounds. Occasional lifting of heavier items may be required. Ability to work in various environments, including offices, construction sites, and manufacturing facilities. Willingness and ability to travel to various job sites, which may require driving or other forms of transportation Benefits Competitive salary commensurate with experience. Comprehensive benefits package including medical, dental, and vision coverage. 401(k) retirement savings plan with company match. Paid time off and holidays. Professional development opportunities. CATK is an Equal Opportunity Employer The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor is it intended to be an all-inclusive list of the skills and abilities required to do the job. The Company may, at its discretion, revise the job description at any time, and additional functions and requirements may be assigned by supervisors as deemed appropriate. Requirements, skills and abilities included have been determined to illustrate the minimal standards required to successfully perform the position.

Now Hiring Quality Technician Reports to: Quality Manager Middleby Refrigeration is seeking a motivated and dedicated Quality Technician to join our team in Greenville, MI. We are looking for someone who is passionate about maintaining high standards of product quality. This role requires a strong focus on conducting inspections, performing tests, and ensuring products meet established quality specifications. As a key contributor, you will support quality control processes, identify and report defects, and help ensure the ongoing success of our innovative product lines. As a Quality Technician, you will play a crucial role in ensuring that our products meet the highest quality standards. You will conduct product inspections, perform detailed tests, and work closely with the production team to identify and address any quality issues. If you are ready to be part of a team that values precision, innovation, and collaboration, this role is for you! Perks you can expect from us: A competitive benefits package including 401(k) matching Company provided life insurance, short and long-term disability insurance Paid time off at start Paid holidays Tuition reimbursement Employee referral program. Expected Hours of Work: This position is full-time. The general scheduled workdays are Monday through Thursday, plus overtime when required. Position Overview: Under the supervision of the Quality Manager, as a critical team member, the Quality Technician will ensure our products meet the highest quality standards. Conducting product inspections on finished product as well as inspecting in process product, raw material and components. Performing detailed tests and working closely with the engineering and production teams to identify and address any quality issues. Responsibilities: Perform daily product audits throughout the facility and issue quality inspection reports to the engineering/manufacturing/quality team. Perform quality process audits throughout the facility supporting all departments. Inspecting equipment or materials to identify the cause of errors, problems or defects coming up with solutions for permanent fix. Conduct quality testing of materials, components, and finished goods. Inspect incoming purchased materials, components, and first piece samples. Inspect in-house metal fabrication parts. Develop and Implement quality checks throughout the facility as required. Set-up, maintenance, and auditing of end-of-line product test software. Responsible for creating quality alerts, deviations, and standard work instructions for manufacturing. RMA/Warehouse testing and reporting required to send to appropriate team members. Analyze and interpret blueprints, data, manuals, and other materials to determine specifications, inspection and testing procedures, adjustment and certification methods, formulas, and measurement instruments required. Responsible for containment activities as they relate to supplied product or finished goods facilitating required sort and testing activity. Requirements Qualifications: High School Diploma or GED Minimum two (2) years working in manufacturing. Experience in a quality or leadership position (preferred). Working proficiency in Microsoft Word, Excel, and PowerPoint. Expected to perform mathematical and statistical calculations. Experience with blueprint reading Excellent communication and interpersonal skills. With the ability to work cross-functionally and train team members on quality alerts, deviations, and standard work. Expected to have exceptional time management skills, organizational efficiency, and the ability to balance priorities. Working Conditions: Office / production floor based. 8 hour shifts Monday-Thursday If interested in the position, Click here to Apply!

Job DescriptionOverview: Candidate will validate that components and product meet established standards and requirements. Perform basic measurements using measurement equipment. Duties and Responsibilities: Job Preparation and Set-up. Read Blue Prints & understands GD&T symbols. Accurately recognize datum scheme & function. Understands CMM machine operation and can program. Formatting Layout Reports in MS Excel Preparation of data and reports Perform basic analysis of specifications Review products for physical and technical acceptance Interprets engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards Recommends improvements to the system Preferred Qualifications: High school diploma combined with 2 years of CMM experience required Experience using software - CMM Manager 3.3SP1, Mcosmos 3.5, and Calypso 5.2 or higher Benefits: Health Insurance Dental Insurance Prescription Vision 401K + Company match Life Insurance Short Term Disability Long Term Disability Education Assistance Flex Spending Employee Assistance Programs 12 Paid Holidays Paid Time Off TAC Manufacturing, Inc. is a Japanese owned automotive parts supplier, serving the Japanese Transplants (Toyota, Nissan, Subaru, etc.) as well as the domestic OEMs (Ford and GM). Located in Jackson, MI, TAC Manufacturing, Inc. is a subsidiary company of Tokai-Rika Co. LTD, which is located in Nagoya, Japan. TAC was founded in 1991 and currently employs 700+ people at our Jackson, MI location. We manufacture security and safety-related products: shift levers, shift-by-wire, steering wheels, exterior mirrors, steering column locks, key cylinders, mechanical and remote keys, and more. Shift your career into drive and help TAC Manufacturing make the driving experience an intuitive connection between the human body and the vehicle. TAC Manufacturing, Inc. is an Equal Opportunity Employer. #tac

Summary/objective The Quality Technician II plays a pivotal role in ensuring the effective, efficient, compliant, and proactive support of new product launches and the continuous quality of existing products. The Quality Technician loves details and precision. This role finds standardized work in which deviation could cause an undesirable outcome to be invigorating. Analyzing processes and results to control variations and discussing when improvements would best be introduced is a desirable pastime. Words that describe the Quality Tech are dedicated, efficient, and someone who contributes to making the workday fly by with engaging conversation and team comradery.

Process Development & Program Management • Develop and maintain process parameters across all program phases (pre-prototype through service). • Own BOM creation and updates, ensuring accuracy and alignment with engineering changes. • Track and manage tooling and capital budgets, providing timely updates to leadership. Equipment & Tooling • Lead equipment installation, certification, and run-off activities; escalate issues proactively. • Ensure tooling meets safety, ergonomics, and quality standards; oversee tool design reviews and builds. • Modify equipment/tooling as required to support engineering changes and production improvements. Quality & Continuous Improvement • Collaborate with Quality Engineers to integrate PFMEA, Control Plans, and error-proofing into robust manufacturing systems. • Drive scrap reduction, OEE improvements, and corrective actions through root cause analysis and continuous improvement initiatives. • Ensure compliance with APQP documentation standards and customer requirements. Training & Support • Develop operator training programs, reference materials, and support resources to prepare teams for launch. • Ensure successful execution of Run at Rates, PSOs, HVPTs, and related launch milestones. Cross-functional Collaboration • Act as central communication point between plant, corporate, and customer stakeholders. • Support other programs during critical stages or issue resolution. • Develop optimized cell layouts for material flow and ergonomics. Documentation & Tracking • Maintain equipment records and databases; track material usage during trials and prototypes. • Document and update process flows and operator standard work instructions. Requirements/ Qualifications: • Bachelor's degree in engineering or related discipline • 3 to 5 years' experience in Manufacturing/Process Engineering related to an automotive industry • Interior Components/Assembly/Injection Molding preferred • Strong written and verbal communications skills • Proficient PC skills - MS Office, MS Project, and WEB based software. • Strong analytical and problem-solving skills

Now Hiring Quality Technician Reports to: Quality Manager Middleby Refrigeration is seeking a motivated and dedicated Quality Technician to join our team in Greenville, MI. We are looking for someone who is passionate about maintaining high standards of product quality. This role requires a strong focus on conducting inspections, performing tests, and ensuring products meet established quality specifications. As a key contributor, you will support quality control processes, identify and report defects, and help ensure the ongoing success of our innovative product lines. As a Quality Technician, you will play a crucial role in ensuring that our products meet the highest quality standards. You will conduct product inspections, perform detailed tests, and work closely with the production team to identify and address any quality issues. If you are ready to be part of a team that values precision, innovation, and collaboration, this role is for you! Perks you can expect from us: * A competitive benefits package including 401(k) matching * Company provided life insurance, short and long-term disability insurance * Paid time off at start * Paid holidays * Tuition reimbursement * Employee referral program. Expected Hours of Work: This position is full-time. The general scheduled workdays are Monday through Thursday, plus overtime when required. Position Overview: Under the supervision of the Quality Manager, as a critical team member, the Quality Technician will ensure our products meet the highest quality standards. Conducting product inspections on finished product as well as inspecting in process product, raw material and components. Performing detailed tests and working closely with the engineering and production teams to identify and address any quality issues. Responsibilities: * Perform daily product audits throughout the facility and issue quality inspection reports to the engineering/manufacturing/quality team. * Perform quality process audits throughout the facility supporting all departments. * Inspecting equipment or materials to identify the cause of errors, problems or defects coming up with solutions for permanent fix. * Conduct quality testing of materials, components, and finished goods. * Inspect incoming purchased materials, components, and first piece samples. * Inspect in-house metal fabrication parts. * Develop and Implement quality checks throughout the facility as required. * Set-up, maintenance, and auditing of end-of-line product test software. * Responsible for creating quality alerts, deviations, and standard work instructions for manufacturing. * RMA/Warehouse testing and reporting required to send to appropriate team members. * Analyze and interpret blueprints, data, manuals, and other materials to determine specifications, inspection and testing procedures, adjustment and certification methods, formulas, and measurement instruments required. * Responsible for containment activities as they relate to supplied product or finished goods facilitating required sort and testing activity. Qualifications: * High School Diploma or GED * Minimum two (2) years working in manufacturing. Experience in a quality or leadership position (preferred). * Working proficiency in Microsoft Word, Excel, and PowerPoint. * Expected to perform mathematical and statistical calculations. * Experience with blueprint reading * Excellent communication and interpersonal skills. With the ability to work cross-functionally and train team members on quality alerts, deviations, and standard work. * Expected to have exceptional time management skills, organizational efficiency, and the ability to balance priorities. Working Conditions: * Office / production floor based. * 8 hour shifts * Monday-Thursday If interested in the position, Click here to Apply!

Overview: Candidate will validate that components and product meet established standards and requirements. Perform basic measurements using measurement equipment. Duties and Responsibilities: Job Preparation and Set-up. Read Blue Prints & understands GD&T symbols. Accurately recognize datum scheme & function. Understands CMM machine operation and can program. Formatting Layout Reports in MS Excel Preparation of data and reports Perform basic analysis of specifications Review products for physical and technical acceptance Interprets engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards Recommends improvements to the system Preferred Qualifications: High school diploma combined with 2 years of CMM experience required Experience using software - CMM Manager 3.3SP1, Mcosmos 3.5, and Calypso 5.2 or higher Benefits: Health Insurance Dental Insurance Prescription Vision 401K + Company match Life Insurance Short Term Disability Long Term Disability Education Assistance Flex Spending Employee Assistance Programs 12 Paid Holidays Paid Time Off TAC Manufacturing, Inc. is a Japanese owned automotive parts supplier, serving the Japanese Transplants (Toyota, Nissan, Subaru, etc.) as well as the domestic OEMs (Ford and GM). Located in Jackson, MI, TAC Manufacturing, Inc. is a subsidiary company of Tokai-Rika Co. LTD, which is located in Nagoya, Japan. TAC was founded in 1991 and currently employs 700+ people at our Jackson, MI location. We manufacture security and safety-related products: shift levers, shift-by-wire, steering wheels, exterior mirrors, steering column locks, key cylinders, mechanical and remote keys, and more. Shift your career into drive and help TAC Manufacturing make the driving experience an intuitive connection between the human body and the vehicle. TAC Manufacturing, Inc. is an Equal Opportunity Employer. #tac

About Us Contemporary Amperex Technology Kentucky (CATK) is the US battery manufacturing subsidiary of Contemporary Amperex Technology Co., Limited (CATL). CATL is a global leader in research, development and manufacturing of battery energy storage system for vehicles, grid scale, and maritime applications. In 2024, CATL accounts for over 37% of global EV battery installed capacity. CATL has been the largest battery manufacturer in the world for the last 7 years. The Company is committed to providing cutting-edge solutions for global new energy applications. Our Vision Strive to be a global premier innovative technology corporation, deliver excellent contribution to green energy resolution for mankind, and provide a platform of pursuing the spiritual and material well-being for employees! Job Overview To better serve the global auto industry electric vehicle trend in the United States, CATL, through its U.S.-based subsidiary Contemporary Amperex Technology Kentucky, LLC (CATK) is seeking multiple full-time and dedicated Manufacturing Process Engineers to join our local team. The ideal candidates will be responsible for enhancing product quality, optimizing production processes, and supporting the introduction of new products and materials. These roles require a proactive approach to identifying and solving production issues, maintaining high standards, and ensuring customer satisfaction. Essential Functions Analyze and enhance the yield and utilization rates of quality products. Strive to improve the First Time Yield (FTY) rate, ensuring products meet quality standards on the first attempt. Develop and implement effective monitoring systems for mass production processes. Conduct thorough analysis to detect and address anomalies promptly. Evaluate risks associated with the introduction of new products, materials, processes, and equipment. Develop and implement strategies to mitigate these risks, ensuring smooth integration. Implement corrective measures to address and resolve batch quality issues. Analyze customer complaints thoroughly to identify root causes. Develop and implement improvement plans to address and prevent recurrence of issues. Provide on-site support for mass production customers. Ensure compliance with quality standards and address any issues that arise during audits. Maintain an organized file system for all relevant documentation. Ensure all records are up-to-date and accessible for reference and audit purposes. Minimum Qualifications Bachelor's degree or higher in electrochemical engineering, engineering, materials science, or related fields. experience within a automotive manufacturing environment preferred. Strong analytical skills with the ability to identify and resolve issues effectively. Proficient in various engineering techniques including Six Sigma, Design of Experiments (DOE), Measurement System Analysis (MSA), Statistical Process Control (SPC), Failure Modes and Effects Analysis (FMEA), and the 8D problem-solving process. Skilled in using Microsoft Office Suite, as well as data analysis tools like Minitab and JMP. Excellent communication and interpersonal skills for customer interaction and support. Proficiency in documentation and maintaining organized records. Ability to maintain a full-time work schedule with regular in-person attendance is required for this position. Ability to interact professionally with individuals of varied backgrounds and skill levels. Physical Requirements Ability to move around work sites, which may include walking, standing, and climbing ladders or stairs. Flexibility to bend, kneel, or crouch, particularly when inspecting installations or troubleshooting. Capability to lift and carry moderate weights, typically up to 25-50 pounds. Occasional lifting of heavier items may be required. Ability to work in various environments, including offices, construction sites, and manufacturing facilities. Willingness and ability to travel to various job sites, which may require driving or other forms of transportation. Benefits Competitive salary commensurate with experience. Comprehensive benefits package including medical, dental, and vision coverage. 401(k) retirement savings plan with company match. Paid time off and holidays. Professional development opportunities. CATK is an Equal Opportunity Employer The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor is it intended to be an all-inclusive list of the skills and abilities required to do the job. The Company may, at its discretion, revise the job description at any time, and additional functions and requirements may be assigned by supervisors as deemed appropriate. Requirements, skills and abilities included have been determined to illustrate the minimal standards required to successfully perform the position.