Quality control analyst jobs in Kentwood, MI - 29 jobs

Join the leading beverage provider, Reyes Coca-Cola Bottling! Shift: Full-Time, Summer 2026 Hourly Pay Rate: $23 Targeted Graduation Date: Between December 2026 - May 2027 If you enjoy our products, you'll really enjoy being a part of our team! The Quality Internship is a full-time paid position for a current undergraduate or graduate student pursuing a degree in Food Science, Biology, Chemistry, Engineering, or related programs. This internship will support our Corporate Quality group at Reyes Coca-Cola Bottling for approximately 12 weeks during Summer 2026. This position will be based in Grand Rapids, MI but may also include significant travel to our manufacturing facilities across the Midwest. The Quality Intern will gain exposure to a variety of project-based work focused on improving corporate standardization and our plants' operational and financial performance. Ideal candidates will have an interest in pursuing a career in manufacturing quality or quality systems upon graduation. Candidates must have reliable automobile transportation, a valid driver's license, and auto insurance coverage at least to the minimum amount specified by the Company and state law. Position Responsibilities: + Perform and accomplish tasks, activities, and projects with guidance from Intern Manager + Meet and/or exceed project deliverables and deadlines + Develop technical expertise as needed for functional area + Develop business acumen by seizing opportunities to learn + Apply functional academic knowledge and skills to the specific internship position with a professional approach + Collaborates with members of their designated team and builds relationships with customers, leaders, and peers within the company + Other duties as assigned Required Education and Experience: + High School Diploma /General Education Diploma and currently pursuing a Bachelor's degree or Master's degree with 0 to 1 years of general work experience + Must be legally authorized to work in the United States. The Company will not sponsor applicants for work visas Benefits At the Reyes Family of Businesses, our Total Rewards Strategy prioritizes the holistic well-being of our employees. This position offers a comprehensive benefits package that includes Medical, Dental, Vision coverage, Paid Time Off, Retirement Benefits, and complimentary Health Screenings. Equal Opportunity Employee & Physical Demands Reyes Holdings and its businesses are equal opportunity employers. Company policy prohibits discrimination and harassment against any applicant or employee based on race, color, religion, sex, pregnancy or pregnancy-related medical conditions, marital status, sexual orientation, gender identity or expression, age, national origin, citizenship, disability, genetic information, military or veteran status, or any other basis protected by applicable law. In addition, the Company is committed to providing reasonable accommodation to applicants and employees in accordance with applicable law. Requests for accommodation should be directed to your point of contact in the Talent Acquisition or Human Resources departments. Background Check and Drug Screening Offers of employment are contingent upon successful completion of a background check and drug screening. Pay Transparency Our compensation philosophy embraces diverse factors for fair pay decisions, valuing skills, experience, and the needs of our business. Moreover, this role may have the opportunity to participate in a discretionary incentive program, subject to program rules. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and gender identity, national origin, disability, or protected veteran status. Drug Free Workplace.

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science-driven, risk-based quality culture is both flexible and innovative, always putting the customer first. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a culture that is not only compliant but also adaptable and forward-thinking, ensuring that we meet the highest standards in everything we do. What You Will Achieve This position is for a testing analyst in the Kalamazoo Raw Materials Laboratory working on first shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Raw Material Laboratory include titrations, wet chemistry, UV, Physical Testing (Specific Gravity, Melting Point, Refractive Index, pH, IR, etc), Atomic Absorption and ICP-MS testing. In this role, you will: Works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze in-process materials, raw materials, APIs, and/or finished product samples in direct support of the company's production units. Independently performs testing and documents results for qualitative or quantitative assays on samples using techniques that vary from use of standard laboratory equipment to highly modern and automated instrumentation. Troubleshoots test methods and analytical equipment. Participates in laboratory investigations as required. Here Is What You Need (Minimum Requirements) High School Diploma or GED and at least 3 years of relevant experience in quality or compliance required. Candidates with advanced science degrees and relevant experience may also be considered as follows: Associate's degree in Chemistry, Biochemistry or related science degree with at least 2 years experience in related field or Bachelor's degree in Chemistry, Biochemistry or related science with 0-1 years of experience in related field. Demonstrated proficiency in at least one high complexity technology (e.g. HPLC, uHPLC, GC, etc.) or, with two or more low to medium complexity technologies (e.g. TLC, titrations, wet chemistry/physical testing, water testing, etc.) as required by the business unit. The successful candidate must also have demonstrated the ability to quickly learn new skills/techniques. High productivity and the ability to multi-task coupled with a low error rate and attention to detail. Must demonstrate flexibility/agility and engagement in a changing environment. The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples. Experience troubleshooting test methods and analytical instrumentation. PHYSICAL/MENTAL REQUIREMENTS Laboratory and office work requiring walking, standing, and sitting throughout a shift. Lifting of items less than 25 kg. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS This position may require colleagues to work weekends and/or holidays to meet business or customer needs. All Laboratory colleagues adhere to safe work practices such as wearing appropriate personal protective equipment including lab coat, safety glasses, and gloves. There is no routine travel associated with this position. Work Location Assignment: On Premise The salary for this position ranges from $20.07 to $33.45 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company's policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Michigan - Kalamazoo location. Relocation assistance may be available based on business needs and/or eligibility. Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Pfizer endeavors to make ********************** accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Quality Assurance and Control

**QC Lab Assistant - Allegan MI - (flexible schedule)** Are you a passionate science student eager to gain hands-on laboratory experience in a dynamic pharmaceutical manufacturing environment? Kelly Science and Clinical is seeking a motivated, PT/flex schedule, contract QC Lab Assistant to support our client's QC Lab in the Allegan MI area. This is an exciting opportunity for a junior/senior in college pursuing a major in the sciences to apply your knowledge, develop practical skills, and potentially transition into a full-time Chemist role after graduation. **Responsibilities:** + Receiving and logging into samples as the enter the lab via a SAP system + Dispersing the samples through the lab + Performing checks in lab for inventory/quantities of reagents and chemicals + Ensuring glassware is cleaned and ready for use by other lab personnel/chemists + Utilizing industrial dishwashers for maintenance of glassware **Education/Skills:** + Enrolled as a junior/senior in an accredited college or university with a major in a science discipline (e.g., Chemistry, Biology, Chemical Engineering) + Strong attention to detail and organizational skills + Basic laboratory skills and familiarity with scientific procedures + Ability to adapt and work independently + Good communication skills + Previous laboratory internship or related experience + Knowledge of laboratory safety protocols + Familiarity with lab instrumentation and data recording + Basic proficiency in Microsoft Office Suite + Reliable transportation to the plant location **Pay** : $16/hr **Hours:** This part-time, one-year assignment offers flexibility with hours, targeting approximately 20 hours per week from Monday through Thursday, between 7AM - 6PMEST, allowing you to balance work and academic commitments. This is perfect for a student studying in the life sciences and wanting to move into a scientist or chemist position post graduation! For immediate consideration or more information, please contact me directly at ********************************** or at ************. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

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Job Description: Quality Control Coordinator Company: Mobilize Michigan Job Type: Temporary, Full-Time, Non-Exempt position Schedule: Monday through Friday with occasional evenings/weekends Compensation: $54,080 annualized, equivalent to $26.00 per hour, with overtime paid in accordance with state and federal law. About Mobilize Michigan Mobilize Michigan is a grassroots organization dedicated to advancing progressive causes and empowering communities across the state. We believe in the power of direct democracy and grassroots organizing to create lasting change. Our work is driven by dedicated staff, passionate volunteers, and the fundamental belief that every voice matters. Position Summary Mobilize Michigan is seeking a detail oriented, highly organized Quality Control Coordinator to implement and manage the petition processing systems while maintaining the highest standard of accuracy and integrity.The role is responsible for the scanning, sorting, storing, striking of invalid signatures, and pulling and preparing pages for cure. The position will be entrusted with a vital role in the signature validation process and the secure storage, maintenance and rectification of legal documents The ideal candidate can work independently and efficiently, has strong problem solving skills, pays meticulous attention to detail and error reduction, excellent organizational skills, and is comfortable operating computer software and office equipment.This position would be great for someone who understands the importance of data hygiene and integrity, maintaining the highest standards of quality control and importance of strict adherence to organizational systems and processes. This role is temporary, full-time with an anticipated project end date May 30th. The position reports to the Senior Director of Data and Technology. Key Responsibilities Secure Handling: Ensure the secure and confidential handling of all petitions from the point of collection to the point of delivery. Maintain a clear chain of custody for all documents. Tracking: Accurately maintain logs of incoming and outgoing petition forms, track soft numbers, progress to batch completion, and petitions out for cure. Scanning: Timely, efficient and accurate scanning of petition forms in eQual platform with a high level of quality and accuracy. Re-scanning when errors occur. Sorting/Storing: Maintain a highly organized system of sorting and storing petitions for ease in locating individual petition forms when needed. Ensure the security of petition forms free from damage, theft, or loss. Striking/Curing: Locate and pull petition forms where striking or curing is necessary. Prepare petitions available for cure to return to collecting organization. Strike identified invalid petition signatures. Follow process for reporting back cured or struck signatures. Communication: Maintain clear, consistent, and professional verbal and written communication with courier, supervisor, eQual staff and campaign representatives. Coordination with Vendors: Work alongside vendors including those providing validation services to ensure proper adherence to systems, troubleshoot issues, problem solve and develop new processes. Other Duties as Needed: Perform other related duties as reasonably assigned in support of Mobilize Michigan's petition and compliance operations. Qualifications & Requirements Attention to detail and timelines; an ability to execute complicated sequential steps with rigor, precision, and efficiency. Ability to manage straightforward, effective systems and maintain databases and tracking reports.. Ability to communicate clearly and organize others to follow protocols Excellent time management and organizational skills with the ability to work independently and meet deadlines. A strong sense of integrity, responsibility, and discretion, especially when handling sensitive and confidential materials. Flexibility to accommodate occasional scheduling adjustments as campaign needs evolve. Basic computer competency and ability to operate and troubleshoot technology, online platforms, and office equipment including high speed scanners. Ability to lift and carry up to 30 pounds, including raising boxes above shoulder height, with or without reasonable accommodation. Additional Job Specifications Employment Period: Immediate start to April 31st, 2026 with the possibility of extension based on campaign needs and funding. Benefits: Medical, dental, and vision coverage, as well as participation in the 401(k) plan. Time off benefits including holiday pay, office closure pay, accrued sick and PTO time. Work Schedule: Primarily weekdays with occasional evenings and weekends. The daily schedule is flexible and will be determined by the needs of ongoing projects. How to Apply To apply for this critical role, please submit application here: **************************************** BOOM as the employer of record. Something like: Mobilize Michigan contracts with BOOM LLC for backend & operational support including hiring and employment. BOOM LLC is an equal opportunity, affirmative action employer. Those that identify as queer, trans, non-binary, Black, Indigenous, people of color, disabled, parents, are/have been system-impacted, are immigrants, and anyone who has experienced systemic oppression and/or gender-based violence are encouraged to apply. We consider qualified applicants with arrest and conviction records for employment.

Shape Your Future as a Product Quality Control Technician with Roskam Foods Picture yourself at Roskam Foods, where since 1923, we've been the pioneers in contract manufacturing, catering to renowned food brands with a diverse range of food and beverage solutions. Grand Rapids, Michigan is our home, but our influence spans across North America with extensive facilities and state-of-the-art production lines. Embrace our mission to harness potential in both our workforce and brand offerings. What You'll Do: Ensure product integrity by conducting meticulous inspections and fostering a culture of continuous improvement. Direct quality programs like HACCP, ingredient control, and allergen management to uphold our safety standards. Collaborate directly with production teams for seamless alignment to our quality policies. Enhance your understanding of manufacturing processes and contribute towards SQF certification. Investigate quality discrepancies and initiate corrective actions when needed. Qualities and Qualifications Needed: High school diploma or equivalent; advanced education in science disciplines is advantageous. Minimum of one year in quality assurance, with a deep understanding of food safety practices. Strong interpersonal capabilities and computer proficiency. Detail-orientation and multitasking prowess in a fast-paced environment. Roskam Foods rewards your dedication with a competitive compensation and benefits package. Medical, dental, vision insurance, along with life, disability coverage, and a 401K matching scheme, are part of our offerings. AAP/EEO Statement: Roskam Foods is a recognized veteran friendly and equal opportunity employer. Immerse yourself in a work environment that is supportive and growth-focused. You're more than welcome to become part of something great at Roskam. Roskam is an equal opportunity employer.

The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally. * Performs, documents and record checks qualitative and quantitative assays on samples. * The primary technologies in this lab are HPLC and dissolution. * Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact. * Recommends and executes process improvements to continually improve laboratory performance. * High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position. * Demonstrates flexibility/agility and engagement in a changing environment. * The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples. * Ability to follow written procedures. * May train others as skills and knowledge allow. * Troubleshoot instrumentation as skills and knowledge allow. * Participates in laboratory investigations as required. * May participate in manufacturing QC support such as cleaning verification. * SHIFT HOURS: 2:00pm-10:30pm, nominally (some flexibility is allowed). Overtime may occasionally be required. EDUCATION AND EXPERIENCE * AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred. * Related experience in Quality Control is preferred but not required. * Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3 * Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail. * Job duties involve occasional lifting (less than 35 lbs). * Candidate must not be Cephalosporin/Penicillin sensitive. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

The Quality Technician is responsible for completing projects/tasks assigned to them by the Quality Manager; the Quality Technician will also assist in guiding/reporting Production personnel with daily/weekly/monthly workflow and other tasks with direction by the Quality Manager - these tasks are critical in the Quality Control Plan. Responsibilities Perform quality control inspections, checks, and tests during the manufacture of Pregis products. Inspect materials, parts, and products at different stages of production. Record observations and may make recommendations for improving processes. Tests inspect and approve raw materials based on established quality specifications Perform auditing on incoming/receiving material, process/production, and outgoing parts Perform assigned, routine visual inspections, audits, and other specified tests on raw materials, goods in process, and finished products. Use statistical methods to test product samples to evaluate the quality of full production batch before delivery to clients or customers. Compare results of inspections and tests to the company's quality standards; report results to Quality Manager for final analysis and action steps. Coaches and helps train team members on Quality related issues as they arise. Develop, maintain, and post logs, charts, and forms detailing quality levels, inspection data, and results of special quality studies for review by line mechanics, supervisors, and other production staff. Consults with Quality Manager to determine appropriate recommendations and remedies for questionable products. Maintains gage calibrations and accurate records in the quality database. Competency (Knowledge, skills, and abilities) Strong organizational skills: ability to delegate, plan, and schedule accordingly. Ability to read a ruler, scale, and micrometer. Ability to work in a fast-paced environment with a focus on quality. Ability to communicate effectively verbally and in writing; ability to understand detailed written and/or oral instructions including basic mathematical skills. Works successfully independently and collaboratively across teams. Excellent data and computer skills. Problem Solving / Analytical thinking. Team leading/coaching in quality related scenarios. Organizational Skills. Time Management. Customer/Client Focus. Collaboration / Team Player. Report/Procedure Reading and Writing. Problem Solving. Education and Experience High School Diploma or equivalent required. 6 months to 1-year experience working in a manufacturing environment. Excellent organizational and problem-solving skills. Excellent written and verbal communication skills. Proficient in the use of various computer programs. Position Type Full time. Overtime expected per business demand. Physical Requirements This position will require a blend of sitting, walking, standing. May require the ability to bend, stoop, reach, lift up to 50lbs, and endure elevated temperature levels. #FLEX1

Job Description: Responsible for checking products at different stages of production to ensure they meet company quality standards.Key Responsibilities: Inspect and test products for accuracy, performance, and quality Record and analyze test data Report any defects or deviations from standards Recommend improvements to processes or standards Perform various tests (destructive/nondestructive) on materials or products Assist in training new team members Help coordinate team breaks and support supervisors as needed Perform other duties as assigned by management Requirements: Attention to detail and good record-keeping Basic understanding of measurement tools and inspection techniques Ability to work in a team and follow safety procedures

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Job Description Run basic analytical instruments such as plate readers, microplate washers, automated workstations etc. Use low-volume laboratory liquid sample handling equipment (micropipettes) to prepare samples and solutions Prepare analytical samples and assay reagents according to established procedures Perform analytical techniques upon biological specimens such as qPCR, ELISAs, etc. Determine protein levels (host cell protein, protein A) in monoclonal antibody samples Run analytical methods, which may include HPLC, UPLC, SEC, gel electrophoresis, capillary electrophoresis, total protein analysis, amino acid analysis or similar methods Manage samples including ensuring proper storage and handling of samples Work with multiple scientists within the group to effectively schedule work Perform data analysis by using instrument computer software and office applications such as Word, PowerPoint, and Excel Analyze and interpret experimental data independently Contribute to writing of e.g. SOPs, study reports and protocols Write up laboratory notebooks regularly in compliance with guidelines Order, maintain and stock lab supplies such as common reagents, primary packaging materials, gloves, cleaning agents, safety glasses etc. Take care of general housekeeping activities such as cleaning bench spaces, processing equipment and glassware Apply lean 5S methods to laboratory operations Qualifications The ideal candidate would possess : Experience with SEC assays Experience in handling and analyzing proteins and other macromolecules Experience with low-volume liquid handling equipment strongly desired Highly computer literate. Capable of quickly learning and adapting to new computer programs Basic Minimum Qualifications : Bachelors in Chemistry or related field plus 2-3 years of industry experience OR Master's degree with academic research Technical laboratory experience involving analytical chemistry - academic research, internship or industrial HPLC experience Experience with Empower Software Candidates within a commutable distance of Kalamazoo, MI are encouraged to apply Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday-Friday, first shift 8AM-5PM. Candidates currently living in a commutable distance to Kalamazoo, MI are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Quality Control Coordinator (Roofing) CentiMark Corporation, the National leader in the commercial/industrial roofing industry, has an exceptional opportunity for a full time Quality Control Coordinator to support sale reps in the Kalamazoo MI area. Summary of :The QA Rep will be responsible for overseeing daily production of roofing projects. Monitor safety, quality of installation's, and daily customer communication. QA Rep will report directly to the field supervisor, customer and management. They will be responsible for paperwork, timesheets and ensuring that CentiMark Safety policies are followed. The QA Rep should be able to take their team and install a quality CentiMark roof with hours provided and in a safe and orderly manner Job Requirements: The successful candidate must show a positive work history and the ability to work within a team environment. Minimum experience in general roofing. Working knowledge of commercial/industrial roofing procedures and safety. Excellent communication, analytical, leadership, interpersonal, problem solving and organizational skills. Experience with: Single Ply, EPDM, PVC & TPO a plus. Previous Roofing and sales experience preferred. A valid driver's license (in good standing). Able to work Saturday and/or Sunday, if needed Premier Benefits: Health Insurance Plans: Free “Core Plan” - Free Medical & Dental “Buy Up Plan” - Features a lower deductible for Medical Vision Plan Free Life Insurance Traditional 401K with Company Match Roth IRA with Company Match Free Employee Stock Ownership Program (ESOP) Company Vehicle Flexible Spending Account (FSA) Paid Holidays and Vacation WHY WORK FOR CENTIMARK? >>>> CLICK HERE TO WATCH VIDEO! CentiMark provides a great work environment with challenging career opportunities. Drug Free Workplace - EOE (M/F/V/D) - E-Verify Employer For more information, please visit our website -- ********************** Quality Control Coordinator (Roofing) CentiMark Corporation, the National leader in the commercial/industrial roofing industry, has an exceptional opportunity for a full time Quality Control Coordinator to support sale reps in the Kalamazoo MI area. Summary of Job Description: The QA Rep will be responsible for overseeing daily production of roofing projects. Monitor safety, quality of installation's, and daily customer communication. QA Rep will report directly to the field supervisor, customer and management. They will be responsible for paperwork, timesheets and ensuring that CentiMark Safety policies are followed. The QA Rep should be able to take their team and install a quality CentiMark roof with hours provided and in a safe and orderly manner Job Requirements: The successful candidate must show a positive work history and the ability to work within a team environment. Minimum experience in general roofing. Working knowledge of commercial/industrial roofing procedures and safety. Excellent communication, analytical, leadership, interpersonal, problem solving and organizational skills. Experience with: Single Ply, EPDM, PVC & TPO a plus. Previous Roofing and sales experience preferred. A valid driver's license (in good standing). Able to work Saturday and/or Sunday, if needed Premier Benefits: Health Insurance Plans: Free “Core Plan” - Free Medical & Dental “Buy Up Plan” - Features a lower deductible for Medical Vision Plan Free Life Insurance Traditional 401K with Company Match Roth IRA with Company Match Free Employee Stock Ownership Program (ESOP) Company Vehicle Flexible Spending Account (FSA) Paid Holidays and Vacation WHY WORK FOR CENTIMARK? >>>> CLICK HERE TO WATCH VIDEO! CentiMark provides a great work environment with challenging career opportunities. Drug Free Workplace - EOE (M/F/V/D) - E-Verify Employer For more information, please visit our website -- ********************** Powered by JazzHR FWqD6VwbeY

Quality Student Intern. Intern will work as a member of a cross-functional team including Quality, Manufacturing, and Product Engineering to ensure product quality and customer satisfaction are achieved, by conducting data collection, analysis, and improvement actions for machining, assembly, and test operations. The Quality Intern will be involved in determining what and how improvements should be implemented and appropriate analysis to determine effectivity of changes. Work in a manufacturing environment with salary and union personnel Essential Functions: Work with a cross-functional team including Quality, Manufacturing, and Product Engineering to identify cause of non-conformances and implement appropriate corrective actions Work with cross-functional teams to meet company quality, cost and delivery metrics Prepare and distribute reports on Company Quality Metrics Assist the development of Quality Assurance work instructions, check sheets, final inspection records and provide approval Prepare performance charts on various quality indicators, coordinate continuous improvement efforts to improve product quality and resulting indicators Support metrology related activities, including risk assessments

Overview At MasTec Communications Group we build for the future. Yours and ours. As a Quality Control Inspector, you will develop new skills, work in a safety-minded environment, and join us in expanding technology for a better community. Join the MasTec family and help us provide the highest level of quality service to our customers and communities while maintaining our commitment to safety! Responsibilities As a Quality Control Inspector, you are responsible for performing the daily QC responsibilities associated with the establishment and monitoring of defined processes required in the delivery and execution of all project activities. You believe in doing the job right. Being the best. And you're up for the challenge. In addition, you will: Provide specialized technical expertise in support of the Quality program, including specialized inspection, testing techniques, quality training, statistical methods, audits, and quality tools for problem-solving and assessment Create inspection reports stating the conditions of a work area to ensure requirements are met Make recommendations for corrective action Apply knowledge of quality systems and tools to validate and verify contractually required standards for project execution Implement principles of performance evaluation and prediction methods to improve product systems' safety, reliability, and maintainability Generate reports of conditions found during inspection activities, notify operations and QC management of significant problems, and complete documentation necessary to attest to the satisfactory completion of inspection or test activities Under supervision, develop skills and knowledge to determine the degree of conformance of production and operations to specifications Assist in documentation to attest to the satisfactory completion of the inspection, corrective action, or test activities Qualifications About You: Safety is a part of your day-to-day You have a track record of completing work with a high level of quality You have a knack for figuring out hard problems and enjoy a hands-on approach to your work You are looking for long-term projects You enjoy getting your hands dirty with your team You have a High School diploma or equivalent You have 2+ years of verifiable experience in the telecommunications and/or construction field You have an understanding of drawings, permits, and specifications relevant to the Fiber, Cellular, and/or Cable industry You are computer literate, with knowledge of Windows and Microsoft Office (Word, Excel, and PowerPoint) Possess strong analytical and/or problem-solving skills Possess strong organizational skills Able to communicate effectively, verbally and in writing Hard work pays off. See what you'll get for your effort: Compensation: $42,000 to $50,000 a year. Financial Security 401(k) with company match Employee Stock Purchase Plan (ESPP) Life insurance Short-term and Long-term disability Health and Wellness Medical, dental, and vision insurance Dependent care and medical flexible spending accounts Employee Assistance Program (EAP) Work/Life Balance Paid time off Paid holidays Family and medical leave Paid sick time We meet your commitment with competitive pay and benefits. If this sounds like you, let's talk. Build your career with MasTec! MasTec, Inc. is an equal employment opportunity employer. The Company's policy is not to unlawfully discriminate against any applicant or employee on the basis of race, color, sex, sexual orientation, gender identity, religion, national origin, age, disability, genetic information, military status, or any other consideration made unlawful by applicable federal, state, or local laws. The Company also prohibits harassment of applicants and employees based on any of these protected categories. It is also MasTec's policy to comply with all applicable state, federal and local laws respecting consideration of unemployment status in making hiring decisions. #MasTecJobs #MasTecCareers #BeSuccessfulWithUs #IAmMasTec #WeAreMasTec #MasTecFamily #MasTecCommunicationsGroup #MasTecCommunicationsCareers About You: Safety is a part of your day-to-day You have a track record of completing work with a high level of quality You have a knack for figuring out hard problems and enjoy a hands-on approach to your work You are looking for long-term projects You enjoy getting your hands dirty with your team You have a High School diploma or equivalent You have 2+ years of verifiable experience in the telecommunications and/or construction field You have an understanding of drawings, permits, and specifications relevant to the Fiber, Cellular, and/or Cable industry You are computer literate, with knowledge of Windows and Microsoft Office (Word, Excel, and PowerPoint) Possess strong analytical and/or problem-solving skills Possess strong organizational skills Able to communicate effectively, verbally and in writing Hard work pays off. See what you'll get for your effort: Compensation: $42,000 to $50,000 a year. Financial Security 401(k) with company match Employee Stock Purchase Plan (ESPP) Life insurance Short-term and Long-term disability Health and Wellness Medical, dental, and vision insurance Dependent care and medical flexible spending accounts Employee Assistance Program (EAP) Work/Life Balance Paid time off Paid holidays Family and medical leave Paid sick time We meet your commitment with competitive pay and benefits. If this sounds like you, let's talk. Build your career with MasTec! MasTec, Inc. is an equal employment opportunity employer. The Company's policy is not to unlawfully discriminate against any applicant or employee on the basis of race, color, sex, sexual orientation, gender identity, religion, national origin, age, disability, genetic information, military status, or any other consideration made unlawful by applicable federal, state, or local laws. The Company also prohibits harassment of applicants and employees based on any of these protected categories. It is also MasTec's policy to comply with all applicable state, federal and local laws respecting consideration of unemployment status in making hiring decisions. #MasTecJobs #MasTecCareers #BeSuccessfulWithUs #IAmMasTec #WeAreMasTec #MasTecFamily #MasTecCommunicationsGroup #MasTecCommunicationsCareers As a Quality Control Inspector, you are responsible for performing the daily QC responsibilities associated with the establishment and monitoring of defined processes required in the delivery and execution of all project activities. You believe in doing the job right. Being the best. And you're up for the challenge. In addition, you will: Provide specialized technical expertise in support of the Quality program, including specialized inspection, testing techniques, quality training, statistical methods, audits, and quality tools for problem-solving and assessment Create inspection reports stating the conditions of a work area to ensure requirements are met Make recommendations for corrective action Apply knowledge of quality systems and tools to validate and verify contractually required standards for project execution Implement principles of performance evaluation and prediction methods to improve product systems' safety, reliability, and maintainability Generate reports of conditions found during inspection activities, notify operations and QC management of significant problems, and complete documentation necessary to attest to the satisfactory completion of inspection or test activities Under supervision, develop skills and knowledge to determine the degree of conformance of production and operations to specifications Assist in documentation to attest to the satisfactory completion of the inspection, corrective action, or test activities

Make a Difference in YOUR Career! Our vision is both simple and ambitious: to put our drinks on every table. We are the world's largest bottler for retailers and A-brands. Our products are distributed worldwide from our production sites in Europe and North America. Although our own branding may not appear on the labels of the beverages we produce, there is a good chance you are reading this while sipping one of our drinks. Our ambition is to continually improve and it's what keeps us at the top of our game. We are solutions-based. We are innovative. We seek out new challenges and conquer them. This is our company ethos, but it's our people's too: Refresco is at the cutting edge of a fast-moving industry because we have passionate people pushing the boundaries of what's best. Stop and think: how would YOU put our drinks on every table? Micro Tech Job Functions: Adhere to all company policies on health and safety policies/procedures, Current Good Manufacturing Practices (cGMPs) and personal protective equipment (PPE). Responsible to adhere to food quality and food safety regulations and standard(s) provided by corporate, customer, and/or governing bodies (ex. Global Foos Safety Initiative). Understands and maintains common microbiological test materials and instrumentation/equipment including calibration and troubleshooting. Ability to understand company and customer microbiological requirements. Evaluate micro-testing results for deviations and trends and make recommendations to supervisors and managers based on those results. Timely and accurately enters data into lab-based database (RealSPC) and SAP computer database. Preparation of standard solutions and materials required for Microbiological testing per the comp-nay or customer requirements. Always maintain microbiological lab in an organized, clean, and audit ready. Collaborate with quality and production leadership to follow up on problem areas and to assist with investigation. Understanding of beverages application of Current Good Manufacturing Practices, cleaning procedures and safe handling of chemicals/microbiological materials. Perform plating and/or other microbiological methods of samples per company or customer requirements. Responsible for further testing of micros if required. Follow up with quality department leadership for any out of specification micro results. Order/manage inventory and supplies for microbiology lab including proper rotation of materials to eliminate expired materials. Packs and ships samples to customers and/or 3rd party micro testing laboratories per customer specification or as required per quality management direction. Balances group and individual responsibilities. Exhibits objectivity and openness to others. Contributes to building a positive employee relations environment. Able to build morale and group commitments to goals and objectives. Able to train others in technical procedures and/or processes. Provide flexible work hours to support team initiatives. Perform other duties as requested by management including, but not limited to, participate in non-routine projects, validations, investigations, and method development to meet departmental and individual goals. Required Skills: Initiate and record actions to support the Food Safety Food Quality Management System. Report all Food Safety and quality issues to Quality Management team. Execution of Environmental (ATP Swabbing) program to meet corporate and customer policies. Execution of microbiological sampling, plating (maybe require other methods) and data interpretation for bulk ingredients, raw materials, raw water, treated water, intermediates and finished product. Operate effectively in a microbiological laboratory by demonstrating proficiency in safely handling microorganisms, and having no health conditions that would impede the ability to carry out these essential tasks. Execution of microbiological environmental tests including but not limited to Yeast, Mold, TPC, Pseudomonas and Lactobacillus. Able to effectively communicate with quality management team, corporate, and the customer. Creation/Revision of SOP's, and other documents required to support microbiological testing methods and specification that align with company and customer l requirements. Added value to obtain HACCP and PCQI Certification Able to read, understand, and document different units of measure. Able to work in a collaborative and flexible team environment while possessing a strong service mentality. The employee will be required to participate in an on-call schedule for various shift, holiday, or weekend work as needed. Working knowledge of Excel, Word and SAP preferred. Competencies: Technical: Skilled in maintaining accurate and detailed records of inspections and tests Integrity: Commitment to maintaining high ethical standards in all quality assurance activities. Adaptability: Flexibility to adapt to changing production environments and requirements. Communication: Clear and concise communication with production staff and management. Critical Thinking: Apply logical reasoning and problem-solving strategies. Independence: Working effectively without needing close supervision. Entrepreneurial: Thinking creatively and innovatively to develop new ideas or improve existing processes. Education and Experience: Preferred but not required degree in biology, microbiology, chemistry, food science or related discipline. Laboratory science technician program or related discipline preferred. 1-2 years' experience in a laboratory environment preferred. Knowledge of analytical techniques, chemistry, microbiology, math, basic computer skills Working Conditions: Work Schedule: Weekdays, weekends, afternoon, evening, and overnight may be required. Overtime scheduled as needed. Work Environment: Operating in a fast-paced production plant with numerous moving parts.  Noise levels require hearing protection and temperatures can get very hot and/or relatively cold (laboratory is temperature controlled). The environment is structured and supervised. Physical Requirements: R = Rarely (0-15%) O = Occasionally (16-45%) F = Frequently (46-100%) Physical Demand R O F Stand or Sit X Stoop, kneel, crouch, or crawl X Lifting 50 lbs. (minimum lbs lifted 5 lbs.) X Carry weight, lift X Walking X Driving X Climb (stairs/ladders) or balance X Visual/Sensory: This position requires attention to detail, requiring attention with one or two senses at a time. Mental Stress: There is pronounced pressure from deadlines, production quotas, accuracy, or similar demands. Other Duties: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. A Career with Refresco Refresco offers a competitive salary and comprehensive benefits, which include: Medical/dental/vision insurance Life insurance 401(k) savings plan with company match Paid holidays and vacation Well-being benefits Discount programs Join Refresco TODAY and enjoy a rewarding CAREER! Equal Opportunity Employer Refresco is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, ancestry, religion, sex, national orientation, sexual orientation, age, marital status, disability, gender identity, gender expression, Veteran status, or any other classification protected by federal, state, or local law.

General Definition and Scope of Job The Infection Control Coordinator is responsible for the surveillance, analysis, interpretation and reporting of hospital acquired infections (HAI's), educating health system staff about infection prevention, and development of health system policies and procedures to ensure rigorous infection control standards that meet OSHA, CMS, CDC, DNV and state regulatory requirements. Full Time, Exempt What are the job responsibilities? Assesses, plans, implements, monitors and evaluates a system-wide infection control program to assure a safe environment for patients, visitors and employees and meet all requirements of accrediting and regulatory agencies. Establishes and maintains systems and processes to ensure maximum compliance with related CMS, State of Michigan or other accreditation and regulatory standards. Conduct on-going surveillance using CDC infection criteria, documentation and investigation of hospital acquired infections. Actively participates/facilitates cross-functional teams to assess, monitor, improve and document compliance with various regulatory and accreditation agency standards. Participates with committees and task forces where his/her special expertise is needed. Consult on all construction renovation activities and provide ongoing monitoring and guidance. Aligns departmental, divisional and Medical Staff performance improvement activities with the Organization's plan for performance improvement. Provides Infection Control education and training to all levels and divisions of the organization, as needed. Designs, maintains, and monitors systems designed to identify problems, trends and patterns that present a threat to patient, staff or visitor safety. Prepares Infection Control reports for appropriate committees. Prepares new and updated in-services and programs related to Infection Control/ Health Services that are aligned with CDC and other regulatory guidelines. Participate in investigations of unusual infection outbreaks and collaborate as needed with laboratory staff, physicians, county/state health departments and CDC as necessary. Comply with mandatory reporting requirements related NHSN, MDHHS, and local health departments Oversee entire employee health program, with direct responsibility of the annual Influenza vaccine program, and the respiratory fit testing program Participate in various infection control organizations and committees to stay up to day on latest regulations and trends Perform Environment of Care (EOC)/Infection Control tours of all departments yearly and report results at EOC Committee. What Qualifications are needed? RN, BSN or higher degree in Nursing, or Masters in Public Health (MPH) and two or more years of experience as an employee health and/or infection control practitioner. Certification in Infection Control (CIC) desired upon hire, but required within 3 years of hire. Previous experience in Infection Control desired. Previous management responsibility is desirable. Basic Life Support (BLS) Certification Staff development, education and/or training experience preferred. Displays excellent customer service and communication skills. Able to formulate letters, memos, policies and procedures, and any other necessary correspondence independently and accurately. Proven history of managing multiple projects concurrently with successful outcomes. Excellent critical thinking and diagnostic skills. Proficiency with MS Word, Excel, and PowerPoint for windows or compatible word processing, spreadsheets and presentation graphics programs. Data base/statistical management experience is required. Ability to work with a wide variety of people with varying educational and cultural backgrounds. Ability to speak comfortably to small or large groups of people. Able to act as resource to the organization for performance improvement tools and techniques as well as data display and analysis. Able to understand, interpret and implement regulatory and accreditation requirements. Able to manage multiple demands, deadlines and projects simultaneously. Must have good communication skills and an ability to manage difficult situations and people with tact, respect and consideration. Must be organized and flexible. What Perks or Benefits Can You Look Forward to? Low cost benefits including medical, dental, and vision available to you and your dependents with no waiting period FSA/DCRA 401k/Roth, 403b, Financial Wellness benefit Education reimbursement Generous Paid Time Off (PTO) Paid Holidays Employee discount in the café, gift shop and pharmacy Great work environment with a family feel Critical Demands of the Job Ability to sit and/or stand for extended periods of time. Visual acuity, hearing acuity, and manual dexterity must be adequate to participate in meetings and proofread typed or written script, operate key pads, and other office machines. Working Conditions Majority of work is conducted in an office or meeting room setting. Stressful at times due to workload, competing deadlines and complex interpersonal situations involving a wide variety of functions and individuals throughout the hospital/system. Occasional lifting of books and equipment.

Job Description: Quality Control Coordinator Company: Mobilize Michigan Job Type: Temporary, Full-Time, Non-Exempt position Schedule: Monday through Friday with occasional evenings/weekends Compensation: $54,080 annualized, equivalent to $26.00 per hour, with overtime paid in accordance with state and federal law. About Mobilize Michigan Mobilize Michigan is a grassroots organization dedicated to advancing progressive causes and empowering communities across the state. We believe in the power of direct democracy and grassroots organizing to create lasting change. Our work is driven by dedicated staff, passionate volunteers, and the fundamental belief that every voice matters. Position Summary Mobilize Michigan is seeking a detail oriented, highly organized Quality Control Coordinator to implement and manage the petition processing systems while maintaining the highest standard of accuracy and integrity.The role is responsible for the scanning, sorting, storing, striking of invalid signatures, and pulling and preparing pages for cure. The position will be entrusted with a vital role in the signature validation process and the secure storage, maintenance and rectification of legal documents The ideal candidate can work independently and efficiently, has strong problem solving skills, pays meticulous attention to detail and error reduction, excellent organizational skills, and is comfortable operating computer software and office equipment.This position would be great for someone who understands the importance of data hygiene and integrity, maintaining the highest standards of quality control and importance of strict adherence to organizational systems and processes. This role is temporary, full-time with an anticipated project end date May 30th. The position reports to the Senior Director of Data and Technology. Key Responsibilities Secure Handling: Ensure the secure and confidential handling of all petitions from the point of collection to the point of delivery. Maintain a clear chain of custody for all documents. Tracking: Accurately maintain logs of incoming and outgoing petition forms, track soft numbers, progress to batch completion, and petitions out for cure. Scanning: Timely, efficient and accurate scanning of petition forms in eQual platform with a high level of quality and accuracy. Re-scanning when errors occur. Sorting/Storing: Maintain a highly organized system of sorting and storing petitions for ease in locating individual petition forms when needed. Ensure the security of petition forms free from damage, theft, or loss. Striking/Curing: Locate and pull petition forms where striking or curing is necessary. Prepare petitions available for cure to return to collecting organization. Strike identified invalid petition signatures. Follow process for reporting back cured or struck signatures. Communication: Maintain clear, consistent, and professional verbal and written communication with courier, supervisor, eQual staff and campaign representatives. Coordination with Vendors: Work alongside vendors including those providing validation services to ensure proper adherence to systems, troubleshoot issues, problem solve and develop new processes. Other Duties as Needed: Perform other related duties as reasonably assigned in support of Mobilize Michigan's petition and compliance operations. Qualifications & Requirements Attention to detail and timelines; an ability to execute complicated sequential steps with rigor, precision, and efficiency. Ability to manage straightforward, effective systems and maintain databases and tracking reports.. Ability to communicate clearly and organize others to follow protocols Excellent time management and organizational skills with the ability to work independently and meet deadlines. A strong sense of integrity, responsibility, and discretion, especially when handling sensitive and confidential materials. Flexibility to accommodate occasional scheduling adjustments as campaign needs evolve. Basic computer competency and ability to operate and troubleshoot technology, online platforms, and office equipment including high speed scanners. Ability to lift and carry up to 30 pounds, including raising boxes above shoulder height, with or without reasonable accommodation. Additional Job Specifications Employment Period: Immediate start to April 31st, 2026 with the possibility of extension based on campaign needs and funding. Benefits: Medical, dental, and vision coverage, as well as participation in the 401(k) plan. Time off benefits including holiday pay, office closure pay, accrued sick and PTO time. Work Schedule: Primarily weekdays with occasional evenings and weekends. The daily schedule is flexible and will be determined by the needs of ongoing projects. How to Apply To apply for this critical role, please submit application here: **************************************** BOOM as the employer of record. Something like: Mobilize Michigan contracts with BOOM LLC for backend & operational support including hiring and employment. BOOM LLC is an equal opportunity, affirmative action employer. Those that identify as queer, trans, non-binary, Black, Indigenous, people of color, disabled, parents, are/have been system-impacted, are immigrants, and anyone who has experienced systemic oppression and/or gender-based violence are encouraged to apply. We consider qualified applicants with arrest and conviction records for employment. Powered by JazzHR tf EoNPqBHK

States considered: Michigan Role Description The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally. * Performs, documents and record checks qualitative and quantitative assays on samples. * The primary technologies in this lab are HPLC, Dissolution and KF. * Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact. * Recommends and executes process improvements to continually improve laboratory performance. * High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position. * Demonstrates flexibility/agility and engagement in a changing environment. * The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples. * Ability to follow written procedures. * May train others. * Troubleshoot instrumentation. * Review documentation of other analysts. * Participates in laboratory investigations as required. * As a Level VI or VII analyst, the selected candidate will be expected to contribute to the success in multiple ways including, process and method improvements, training, and demonstration of efficient work practices. * May participate in manufacturing QC support such as cleaning verification. * SHIFT HOURS: 8:00pm-4:30pm, nominally (some flexibility is allowed). Overtime may occasionally be required. EDUCATION AND EXPERIENCE * AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred. * 5 years minimum related experience in Quality Control. * Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3 * Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail. * Job duties involve occasional lifting (less than 35 lbs). Candidate must not be Cephalosporin/Penicillin sensitive. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

We're Not Just in the Packaging Business-We're in the "Wow" Business Pregis is Hiring! Why Join Pregis? Pregis is in the packaging business to protect what matters. We are committed to providing our customers and employees sustainable growth through purpose-driven innovation and customer-centric packaging solutions. If you are looking for a company that is thriving across various high growth industries and is innovative, customer focused, high integrity, believes in strong teamwork and collaboration, Pregis is the company for you. Check out the Pregis Purpose to learn how sustainability and social responsibility is at the very core of our company DNA. Job Title: Converting Quality Technician (2nd Shift) Schedule: 2:45PM - 11:00PM Mon-Fri Location: Grand Rapids, MI Job Description The Quality Technician is responsible for completing projects/tasks assigned to them by the Quality Manager; the Quality Technician will also assist in guiding/reporting Production personnel with daily/weekly/monthly workflow and other tasks with direction by the Quality Manager - these tasks are critical in the Quality Control Plan. Responsibilities * Perform quality control inspections, checks, and tests during the manufacture of Pregis products. * Inspect materials, parts, and products at different stages of production. * Record observations and may make recommendations for improving processes. * Tests inspect and approve raw materials based on established quality specifications * Perform auditing on incoming/receiving material, process/production, and outgoing parts * Perform assigned, routine visual inspections, audits, and other specified tests on raw materials, goods in process, and finished products. * Use statistical methods to test product samples to evaluate the quality of full production batch before delivery to clients or customers. * Compare results of inspections and tests to the company's quality standards; report results to Quality Manager for final analysis and action steps. * Coaches and helps train team members on Quality related issues as they arise. * Develop, maintain, and post logs, charts, and forms detailing quality levels, inspection data, and results of special quality studies for review by line mechanics, supervisors, and other production staff. * Consults with Quality Manager to determine appropriate recommendations and remedies for questionable products. * Maintains gage calibrations and accurate records in the quality database. Competency (Knowledge, skills, and abilities) * Strong organizational skills: ability to delegate, plan, and schedule accordingly. * Ability to read a ruler, scale, and micrometer. * Ability to work in a fast-paced environment with a focus on quality. * Ability to communicate effectively verbally and in writing; ability to understand detailed written and/or oral instructions including basic mathematical skills. * Works successfully independently and collaboratively across teams. * Excellent data and computer skills. * Problem Solving / Analytical thinking. * Team leading/coaching in quality related scenarios. * Organizational Skills. * Time Management. * Customer/Client Focus. * Collaboration / Team Player. * Report/Procedure Reading and Writing. * Problem Solving. Education and Experience * High School Diploma or equivalent required. * 6 months to 1-year experience working in a manufacturing environment. * Excellent organizational and problem-solving skills. * Excellent written and verbal communication skills. * Proficient in the use of various computer programs. Position Type * Full time. * Overtime expected per business demand. Physical Requirements This position will require a blend of sitting, walking, standing. May require the ability to bend, stoop, reach, lift up to 50lbs, and endure elevated temperature levels. #FLEX1

Quality Control Coordinator (Roofing) CentiMark Corporation, the National leader in the commercial/industrial roofing industry, has an exceptional opportunity for a full time Quality Control Coordinator to support sale reps in the Kalamazoo MI area. Summary of :The QA Rep will be responsible for overseeing daily production of roofing projects. Monitor safety, quality of installation's, and daily customer communication. QA Rep will report directly to the field supervisor, customer and management. They will be responsible for paperwork, timesheets and ensuring that CentiMark Safety policies are followed. The QA Rep should be able to take their team and install a quality CentiMark roof with hours provided and in a safe and orderly manner Job Requirements: The successful candidate must show a positive work history and the ability to work within a team environment. Minimum experience in general roofing. Working knowledge of commercial/industrial roofing procedures and safety. Excellent communication, analytical, leadership, interpersonal, problem solving and organizational skills. Experience with: Single Ply, EPDM, PVC & TPO a plus. Previous Roofing and sales experience preferred. A valid driver's license (in good standing). Able to work Saturday and/or Sunday, if needed Premier Benefits: Health Insurance Plans: Free “Core Plan” - Free Medical & Dental “Buy Up Plan” - Features a lower deductible for Medical Vision Plan Free Life Insurance Traditional 401K with Company Match Roth IRA with Company Match Free Employee Stock Ownership Program (ESOP) Company Vehicle Flexible Spending Account (FSA) Paid Holidays and Vacation WHY WORK FOR CENTIMARK? >>>> CLICK HERE TO WATCH VIDEO! CentiMark provides a great work environment with challenging career opportunities. Drug Free Workplace - EOE (M/F/V/D) - E-Verify Employer For more information, please visit our website -- ********************** Quality Control Coordinator (Roofing) CentiMark Corporation, the National leader in the commercial/industrial roofing industry, has an exceptional opportunity for a full time Quality Control Coordinator to support sale reps in the Kalamazoo MI area. Summary of Job Description: The QA Rep will be responsible for overseeing daily production of roofing projects. Monitor safety, quality of installation's, and daily customer communication. QA Rep will report directly to the field supervisor, customer and management. They will be responsible for paperwork, timesheets and ensuring that CentiMark Safety policies are followed. The QA Rep should be able to take their team and install a quality CentiMark roof with hours provided and in a safe and orderly manner Job Requirements: The successful candidate must show a positive work history and the ability to work within a team environment. Minimum experience in general roofing. Working knowledge of commercial/industrial roofing procedures and safety. Excellent communication, analytical, leadership, interpersonal, problem solving and organizational skills. Experience with: Single Ply, EPDM, PVC & TPO a plus. Previous Roofing and sales experience preferred. A valid driver's license (in good standing). Able to work Saturday and/or Sunday, if needed Premier Benefits: Health Insurance Plans: Free “Core Plan” - Free Medical & Dental “Buy Up Plan” - Features a lower deductible for Medical Vision Plan Free Life Insurance Traditional 401K with Company Match Roth IRA with Company Match Free Employee Stock Ownership Program (ESOP) Company Vehicle Flexible Spending Account (FSA) Paid Holidays and Vacation WHY WORK FOR CENTIMARK? >>>> CLICK HERE TO WATCH VIDEO! CentiMark provides a great work environment with challenging career opportunities. Drug Free Workplace - EOE (M/F/V/D) - E-Verify Employer For more information, please visit our website -- **********************