Quality assurance technician jobs in Lansing, MI - 181 jobs

The Travel Cath Lab Technologist is a specialized allied health professional who operates advanced imaging equipment to assist physicians during cardiovascular procedures. This travel position, based in Flint, Michigan, involves 12-hour day shifts for 13 weeks and supports safe and effective patient care in surgical services. The role is provided through Malone Healthcare, a company focused on placing experienced healthcare professionals in rewarding assignments nationwide. Malone Healthcare - Nursing is seeking a travel Cath Lab Technologist for a travel job in Flint, Michigan. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel McLaren's Surgical Services provide a full spectrum of procedures and diagnostic tests across multiple specialties. From general elective surgeries to critical, life-saving interventions, McLaren consistently delivers high-quality surgical care. As a leader in innovation, McLaren was among the first to introduce numerous surgical techniques and technologies-and continues to advance its practices to improve patient outcomes. A skilled Cardiovascular Technician plays a vital role in supporting physicians and surgeons. This role involves operating specialized imaging equipment to evaluate patients before, during, and after cardiovascular and pulmonary procedures. The technician ensures accurate imaging, assists the care team throughout procedures, and contributes to safe, effective patient care. About Malone Healthcare - Nursing With a commitment to providing a higher standard of service and experience in patient care, Malone Healthcare places expert nurses and allied health professionals in rewarding careers throughout the United States. As a leading healthcare staffing agency, Malone's focus on compliance and integrity translates to a seamless experience for our team members and partner facilities. When you work with Malone Healthcare, you can rely on over 50 years of proven experience placing exceptional professionals in quality healthcare settings. Benefits Weekly pay Holiday Pay Guaranteed Hours Continuing Education 401k retirement plan Pet insurance Referral bonus Medical benefits Dental benefits Vision benefits License and certification reimbursement Life insurance Keywords: Cath Lab Technologist, Cardiovascular Technician, travel healthcare jobs, cardiovascular imaging, allied health professional, surgical services, Malone Healthcare, patient care, cardiac diagnostic procedures, temporary healthcare staffing

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Job Description We are looking for IVR QA Analyst & IVR Test Lead in Dimondale, MI Qualifications Position 1: The IVR Test Lead will lead a team of 2 - 3 people in utilizing Testing Center of Excellence (TCoE) processes, frameworks, templates & tools to perform all tasks within the Software Testing Life Cycle, including analyzing requirements, creating test scenarios, conditions and scripts, creating and managing test data, performing test execution and managing defect management processes. The IVR Test Lead is responsible for ensuring on time and on budget completion of all scheduled tasks and that all test artifacts for the project meet strenuous standards. Additionally, the IVR Test Lead will lead the implementation and utilization of web service test tools. Position 2: The IVR Test Analyst will align with the process & frameworks and leverage templates & tools to perform all aspects of the Software Testing Life Cycle, including analyzing requirements, creating test cases, conditions and scripts, creating and managing test data, test execution and defect management processes. The Test Analyst is responsible for ensuring on time and on budget completion of all scheduled tasks and that all test artifacts meet strenuous standards Additional Information Webcam interview is acceptable.

Job Description Quality Technician | Lansing, MI Salary Range: $42,000 - $65,000 depending on experience Are you a forward-thinking professional with a passion for inspection, testing, and ensuring product quality? The Pivot Group is committed to fostering meaningful relationships in the manufacturing community. We partner with companies in Lansing seeking skilled Quality Technicians. The Opportunity We are collaborating with manufacturing firms in Lansing that are seeking skilled Quality Technicians. These organizations are dedicated to maintaining high standards and are looking for professionals who can contribute effectively. By joining our network, you position yourself for opportunities aligned with your career goals. Key Responsibilities Perform in-process and final inspections of manufactured products. Utilize precision measurement tools (e.g., calipers, micrometers, CMM) to verify product specifications. Document inspection results accurately and maintain comprehensive quality records. Identify, isolate, and report non-conforming materials or products. Assist in root cause analysis and the implementation of corrective and preventive actions. Interpret engineering drawings, blueprints, and quality specifications. Calibrate and maintain inspection and test equipment according to established schedules. Recommended Qualifications Proficiency with precision measurement tools (e.g., calipers, micrometers) and ability to read blueprints/technical drawings. Understanding of quality control principles, basic Statistical Process Control (SPC), and familiarity with ISO 9001 standards. 1-3 years of experience in a manufacturing quality assurance or control environment. Strong attention to detail and accuracy in inspection and documentation. High School Diploma or GED; Associate's degree in a technical field preferred. Bonus Qualifications Experience operating CMMs or other automated metrology equipment. Proficiency with Statistical Process Control (SPC) software (e.g., Minitab). Lean Six Sigma Yellow Belt or Green Belt certification. Internal auditing experience for ISO 9001 or industry-specific standards. Job Titles That Should Apply Quality Technician, QA Technician, Quality Control Technician, QC Technician, Quality Inspector, QA Inspector, Quality Assurance Technician, Manufacturing Quality Technician, Production Quality Technician, Quality Assurance Associate, Quality Control Associate Why Pivot Group The Pivot Group was founded by manufacturing professionals who've been on both sides of the hiring process. Our clients are strategic-they partner with us because they want real insight into their roles and the people filling them, not a stack of resumes. We focus on match-driven placements built around what actually matters: Commute, Compensation, Culture, and Career trajectory. If you're ready to take the next step in your career and connect with a firm that values fit over speed, we invite you to reach out. The Pivot Group offers resources to support your search-market insights, resume feedback, and interview preparation. As our partnerships grow, we'll reach out with opportunities aligned with your goals. Thank you for considering this approach to career advancement.

Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities: 1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations, 2) QA on the floor during all manufacturing operations. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required, 2. Lead/represent QA on project teams in support of new product and manufacturing activities, 3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials, 4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.), 5. Perform review and approval of executed documents, 6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities, 7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance, 8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations, 9. Other duties as defined by Biovire. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision, 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture, 3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to communicate effectively, 5. Basic computer skills (proficient in Microsoft Office applications), 6. Excellent communication skills, both written and verbal, 7. Possess honesty and integrity with a commitment to the highest legal and ethical standards, 8. Treats every person with courtesy and respect, 9. Knowledge of CGMP and regulatory principles, 10. Commitment to quality in the manufacturing process, 11. Ability to independently analyze and resolve complex issues, 12. Strong sense of initiative, accountability, and responsibility WORK EXPERIENCE AND EDUCATION REQUIREMENTS · BS in scientific discipline · 3+ years experience in the biotech/pharmaceutical industry preferred · Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems

Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities: 1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations, 2) QA on the floor during all manufacturing operations. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required, 2. Lead/represent QA on project teams in support of new product and manufacturing activities, 3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials, 4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.), 5. Perform review and approval of executed documents, 6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities, 7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance, 8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations, 9. Other duties as defined by Biovire. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision, 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture, 3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to communicate effectively, 5. Basic computer skills (proficient in Microsoft Office applications), 6. Excellent communication skills, both written and verbal, 7. Possess honesty and integrity with a commitment to the highest legal and ethical standards, 8. Treats every person with courtesy and respect, 9. Knowledge of CGMP and regulatory principles, 10. Commitment to quality in the manufacturing process, 11. Ability to independently analyze and resolve complex issues, 12. Strong sense of initiative, accountability, and responsibility WORK EXPERIENCE AND EDUCATION REQUIREMENTS * BS in scientific discipline * 3+ years experience in the biotech/pharmaceutical industry preferred * Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems

**Discover a more connected career** At Ervin Cable Construction, LLC, as a Quality Control Field Technician, you'll ensure that construction or installation work meets specified standards by performing inspections, conducting tests, and monitoring compliance throughout projects. You'll address issues, document findings, and collaborate with teams to implement improvements and maintain high-quality outcomes **Connecting you to great benefits** + Weekly Paychecks + Paid Time Off, Parental Leave, and Holidays + Insurance (including medical, prescription drug, dental, vision, disability, life insurance) + 401(k) w/ Company Match + Stock Purchase Plan + Education Reimbursement + Legal Insurance + Discounts on gym memberships, pet insurance, and much more! **What you'll do** + Conduct quality inspections during the installation process to ensure work meets plans and specifications + Perform final inspections as requested by customers to ensure compliance with construction standards + Identify issues and report them to relevant team members for resolution + Record and follow up on non-compliance issues until they are resolved + Ensure all required testing is completed as specified and document the results + Follow installation milestones and support project activities as directed by management + Work overtime, travel, and handle on-call or after-hours responsibilities as needed, and perform duties in all weather conditions + Other duties as assigned **What you'll need** + To be 18 years of age or older + Authorization to work in the United States for this company + Valid State driver's license (cannot be Provisional), including an acceptable driving record + One year of relevant work experience Additional qualifications + Quality control experience preferred + Associates Degree in an industry related field or equivalent work experience + Knowledge and understanding of the telecommunication construction industry standard practices + Knowledge of Customer Installation Standards and Documentation **Physical abilities & exposures** + **Routinely** : work alone in remote locations, operate vehicle, squeeze, bend, stoop, stand, walking, climb stairs, use keyboard and mouse + **Occasionally** : work at heights, use ladder, life greater than 55 pounds **Why grow your career with us** Your career here is more than just a job - it's your pathway to opportunity. Our hands-on training, supportive environment, and responsive leadership connect you to work with purpose. Our commitment to you extends beyond professional development to a safety-first culture that ensures you can do what you do best, with peace of mind. **Building stronger solutions together** Our company is an equal-opportunity employer - we are committed to providing a work environment where everyone can thrive, grow, and feel connected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Summary/objective The Quality Technician III 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.

Our company, Closet Factory, is the custom storage solution authority serving the worldwide need for custom space organization throughout the home. We design, sell and install custom closets, home offices, garages, home theaters, pantries, bookshelves and more. Our products are of the highest quality. We have been in business for over 22 years and have locations across the country. We have experienced substantial, long-term growth and as a result are searching for another member to add to our close-knit team of people to manufacture our products. Our factory produces all of the wood parts to our complete product line using the 32-millimeter system. Each team member will be trained on the latest machines designed to build and assemble custom cabinets. Members of our factory prepare each job and check it for accuracy and quality before it is sent to the client's home. Job Benefits: Full-time, permanent positions Year round work Best training in the industry Continual Support Room for advancement Specific requirements: q Experience with basic hand tools q Some woodworking experience a plus We recognize people as our most valuable asset and will train you to excel in your position. A future with Closet Factory has never been brighter. If you are thinking about taking the next big step in your career, this may be the opportunity you have been waiting for.

Job DescriptionJob Title: Quality Inspector Pay: $17/hour Shift: 1st shift We are seeking a Quality Inspector to join a 3rd party quality inspection company in Lansing. The successful candidate will ensure quality parts pass inspection and maintain accurate records.Responsibilities for the Quality Inspector: Inspect parts to ensure quality standards are met Maintain documentation and accurate records Ensure customers receive 100% certified parts Follow company work procedures for sorting, inspecting, reworking, and parts handling Review and understand job work instructions daily Requirements for the Quality Inspector: High school diploma or GED or history of successful work experience Experience in fieldwork and customer contact is valuable Highly developed organization skills Ability to communicate with team members and customers Ability to function in a stressful environment with time pressure Good eye for detail Work Environment: Quality inspection environment Physical demands not specified Benefits: Access to a personalized career consultant Healthcare Benefits Disability Insurance Advancement opportunities Opportunity for permanent hire How to Apply: Apply online or visit our office Equal Opportunity Employer.

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

Job DescriptionDescription: Perform quality testing on products manufactured by organization and incoming products as required to ensure quality standards for the products are met. Primary Functions and Responsibilities Self-organized control of raw materials and finished polyurethane resins Conduct analysis of the samples Compile data and interpret the results using standard procedures to determine compliance with specifications. Document and record data evaluate correctness of results Product certificates of conformance Organization and storage of test samples Block raw materials if properties don't meet specifications Block finished goods if properties don't meet specifications and/or quality standards Perform periodic preventive maintenance and calibration of lab equipment Ensure that supplies and equipment are maintained at an adequate level. Works following all safety policies and procedures in the lab Report inconsistencies, malfunctions and/or variations Performs other duties as assigned Requirements: Knowledge, Skills and Abilities Ability to plan, organize and take initiative Good oral and written communication skills Knowledge of basic statistics Neat and organized Chemical knowledge helpful Minimum Qualifications Microsoft office suite Attention to detail Experience working in a lab setting preferred Work Environment Lab setting

We go where others won't, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect and enhance life. I. JOB SUMMARY The role of a Laboratory Resources Associate Technician is to provide the support work, care and daily observation of animals as required to assure continued accreditation through the Association for the Assessment and Accreditation of Laboratory Animal Care, International (AAALAC), and the continued availability of Emergent's unique stock of guinea pig for use in product related testing. This position is a non-traditional position, meaning weekend, holiday, and as needed overtime is required. II. ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Animal Care & Facility Support * Operation of autoclaves/cage washers/rack washers, including manual cleaning of caging and facilities as required. May operate a forklift as needed. * Daily care of animals (feeding, watering, observing) cleaning cages, maintaining a high level of cleanliness and sanitation in the animal area including documentation of completed tasks * Performance of technical assignments in care of animals such as weighing animals, recording weights, performing identification technique, and euthanasia * Perform basic document review * Assist in training of routine activities based on department needs Behavior/Cultural Responsibilities: * Ownership - Actively participate in self-development (SLII, IPMP) * Accountability - Follow through on commitments * Detail oriented - Able to complete required tasks and associated documentation with minimal error * Adaptability - Maintain positive attitude in a changing work environment Communication - Effectively communicate with all levels of management, support staff and supporting departments * Escalate issues through the proper channels * Effectively build and maintain working relationships between Lab Resources and supporting departments The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions. III. MINIMUM EDUCATION, EXPERIENCE, SKILLS Education * HS Diploma or equivalent Skills & Experience Required * Good verbal and written communication skills Skills & Experience Preferred * Experience with Microsoft Word, Excel, Teams, Outlook, and PowerPoint is preferred * Experience working with animals, particularly in a laboratory animal environment preferred If the hiring manager expresses an interest in interviewing you for the open position, you must discuss your interest in the open position with your current manager prior to an interview being scheduled. U.S. Base Pay Ranges and Benefits Information The estimated annual base salary as a new hire for this position ranges from $34,000 to $41,200. Individual base pay depends on various factors such as applicant's education, experience, skills, and abilities, as well as internal equity and alignment with market data. The salary may also be adjusted based on applicant's geographic location. Certain roles are eligible for additional incentive compensation, including merit increases, annual bonus, [and/or long-term incentives in the form of stock options.] Additionally, Emergent offers a comprehensive benefits package*. Information regarding additional benefits can be found here: ************************************************************* (*Eligibility for benefits is governed by the applicable plan documents and policies). If you are selected for an interview, please feel welcome to speak to a Human Resources Partner about our compensation philosophy and available benefits. ABOUT EMERGENT Protecting and Enhancing 1 billion lives by 2030 focuses our energy to improve the quality of life for individuals around the world, giving them the opportunity to experience the fullness of life. Our drive towards this vision informs all of our actions-whether it is our approach to product development, manufacturing, encouraging employee health and wellness or giving back to the community-we strive every day to achieve this shared goal. WE BELIEVE IN OUR VALUES * Lead with Integrity * We gain trust and confidence through ethics, quality, and compliance excellence * Stand shoulder to shoulder no matter what * We combine our best thinking and communicate openly to support each other. * Own it always * Every person at Emergent is engaged and accountable for delivering on our commitments. * Break through thinking * We take smart risks, pursue innovation and challenge ourselves to constantly improve. * Compete where it counts * We set the right goals and respect each other as we conquer them together.

Job Description Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities: 1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations, 2) QA on the floor during all manufacturing operations. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required, 2. Lead/represent QA on project teams in support of new product and manufacturing activities, 3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials, 4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.), 5. Perform review and approval of executed documents, 6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities, 7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance, 8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations, 9. Other duties as defined by Biovire. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision, 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture, 3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to communicate effectively, 5. Basic computer skills (proficient in Microsoft Office applications), 6. Excellent communication skills, both written and verbal, 7. Possess honesty and integrity with a commitment to the highest legal and ethical standards, 8. Treats every person with courtesy and respect, 9. Knowledge of CGMP and regulatory principles, 10. Commitment to quality in the manufacturing process, 11. Ability to independently analyze and resolve complex issues, 12. Strong sense of initiative, accountability, and responsibility WORK EXPERIENCE AND EDUCATION REQUIREMENTS · BS in scientific discipline · 3+ years experience in the biotech/pharmaceutical industry preferred · Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems

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.

Job Description Quality Technician | Caledonia, MI Salary Range: $47,000 - $70,000 depending on experience Are you a dedicated professional with a passion for inspection, testing, and ensuring product quality? The Pivot Group is committed to fostering meaningful relationships and supporting career growth. We partner with leading manufacturing companies in Caledonia, seeking experienced Quality Technicians to strengthen their teams. The Opportunity We are collaborating with manufacturing firms in Caledonia that are seeking skilled Quality Technicians. These organizations are dedicated to maintaining high standards and are looking for professionals who can contribute effectively. By joining our network, you position yourself for opportunities aligned with your career goals. Key Responsibilities Perform visual and dimensional inspections of raw materials, in-process components, and finished products. Document inspection results, non-conformances, and corrective actions in quality reports and systems. Operate and maintain various inspection equipment, including calipers, micrometers, CMMs, and optical comparators. Assist in the investigation of root causes for quality issues and support the implementation of corrective and preventive actions. Conduct routine calibration of measurement tools and gauges according to established schedules and procedures. Collaborate with production and engineering teams to ensure adherence to quality standards and specifications. Collect and analyze quality data to identify trends, support continuous improvement initiatives, and prepare summary reports. Recommended Qualifications Experience using precision measurement tools (calipers, micrometers, gauges). Ability to read and interpret blueprints, schematics, and GD&T symbols. Knowledge of quality management systems (e.g., ISO 9001) and quality methodologies (e.g., SPC, Root Cause Analysis). Proficiency in performing various types of inspections (e.g., First Article, In-process, Final). Strong computer skills for data entry, report generation, and quality software. Bonus Qualifications Experience with CMM programming software (e.g., PC-DMIS, Calypso). ASQ Certification (e.g., CQT, CQI) or Lean Six Sigma Yellow Belt. Proficiency with statistical analysis software (e.g., Minitab, JMP). Familiarity with problem-solving methodologies (e.g., 8D, 5 Whys). Advanced Geometric Dimensioning and Tolerancing (GD&T) interpretation skills. Job Titles That Should Apply Quality Technician, QA Technician, Quality Control Technician, QC Technician, Quality Inspector, QA Inspector, Quality Assurance Technician, Manufacturing Quality Technician, Production Quality Technician, Quality Tester Why Pivot Group The Pivot Group was founded by manufacturing professionals who've been on both sides of the hiring process. Our clients are strategic-they partner with us because they want real insight into their roles and the people filling them, not a stack of resumes. We focus on match-driven placements built around what actually matters: Commute, Compensation, Culture, and Career trajectory. If you're ready to take the next step in your career and connect with a firm that values fit over speed, we invite you to reach out. The Pivot Group offers resources to support your search-market insights, resume feedback, and interview preparation. As our partnerships grow, we'll reach out with opportunities aligned with your goals. Thank you for considering this approach to career advancement.

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

We go where others won't, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect and enhance life. I. JOB SUMMARY The role of a Laboratory Resources Associate Technician is to provide the support work, care and daily observation of animals as required to assure continued accreditation through the Association for the Assessment and Accreditation of Laboratory Animal Care, International (AAALAC), and the continued availability of Emergent's unique stock of guinea pig for use in product related testing. This position is a non-traditional position, meaning weekend, holiday, and as needed overtime is required. II. ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Animal Care & Facility Support • Operation of autoclaves/cage washers/rack washers, including manual cleaning of caging and facilities as required. May operate a forklift as needed. • Daily care of animals (feeding, watering, observing) cleaning cages, maintaining a high level of cleanliness and sanitation in the animal area including documentation of completed tasks • Performance of technical assignments in care of animals such as weighing animals, recording weights, performing identification technique, and euthanasia • Perform basic document review • Assist in training of routine activities based on department needs Behavior/Cultural Responsibilities: • Ownership - Actively participate in self-development (SLII, IPMP) • Accountability - Follow through on commitments • Detail oriented - Able to complete required tasks and associated documentation with minimal error • Adaptability - Maintain positive attitude in a changing work environment Communication - Effectively communicate with all levels of management, support staff and supporting departments • Escalate issues through the proper channels • Effectively build and maintain working relationships between Lab Resources and supporting departments The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions. III. MINIMUM EDUCATION, EXPERIENCE, SKILLS Education • HS Diploma or equivalent Skills & Experience Required • Good verbal and written communication skills Skills & Experience Preferred • Experience with Microsoft Word, Excel, Teams, Outlook, and PowerPoint is preferred • Experience working with animals, particularly in a laboratory animal environment preferred If the hiring manager expresses an interest in interviewing you for the open position, you must discuss your interest in the open position with your current manager prior to an interview being scheduled. U.S. Base Pay Ranges and Benefits Information The estimated annual base salary as a new hire for this position ranges from $34,000 to $41,200. Individual base pay depends on various factors such as applicant's education, experience, skills, and abilities, as well as internal equity and alignment with market data. The salary may also be adjusted based on applicant's geographic location. Certain roles are eligible for additional incentive compensation, including merit increases, annual bonus, [and/or long-term incentives in the form of stock options.] Additionally, Emergent offers a comprehensive benefits package*. Information regarding additional benefits can be found here: ************************************************************* (*Eligibility for benefits is governed by the applicable plan documents and policies). If you are selected for an interview, please feel welcome to speak to a Human Resources Partner about our compensation philosophy and available benefits.