Quality control analyst jobs in Battle Creek, MI

Quality Control Kalamazoo County, MI, NONE + Added - 28/10/2025 Apply for Job _Our client, a growing pharmaceutical company, is looking for a skilled QC Analyst to join their team in Kalamazoo County, MI!_ **Job Title:** QC Analyst **Department:** Quality Control **Pay rate:** $30/hr. - $34/hr. **Location:** Kalamazoo County, MI **Job Type:** Contract- hire **Job Purpose** The QC Analyst ensures the accurate and timely execution of laboratory analyses in accordance with cGMP standards. This role supports the development and validation of new analytical methods and is responsible for the proper scheduling and coordination of laboratory activities to ensure compliance and efficiency. **Key Responsibilities** + Maintain the Quality Control Laboratory in a state of compliance with current Good Manufacturing Practices (cGMP). + Perform QC testing for raw materials, in-process samples, intermediates, cleaning verification/validation, and final product release. + Participate in the development and validation of analytical methods. + Review laboratory data, documentation, and control records for accuracy and completeness. + Write, review, and revise Standard Operating Procedures (SOPs) and material specifications. + Support Quality Assurance during internal, customer, and regulatory audits. + Participate in Out-of-Specification (OOS) and deviation investigations, providing analytical support to QA. + Assist with execution of laboratory equipment qualification and calibration. + Manage and maintain inventory of reagents, standards, and reference materials. + Support the stability testing program, including performance of tests and evaluation of trends. + Issue Certificates of Analysis (CoAs) for tested materials/products. + Collaborate with cross-functional teams to resolve technical issues and improve laboratory processes. + Develop technical knowledge and independence through mentorship and hands-on training. **Qualifications** + Bachelor's degree in Chemistry or a related scientific discipline is required. + Minimum of 4 years in a GMP-regulated pharmaceutical or biopharmaceutical environment. + At least 2 years of experience in a Quality Control laboratory preferred. + Proficient in laboratory techniques with strong attention to detail. + Ability to perform testing independently and document results accurately. + Familiar with analytical instruments (e.g., HPLC, GC, UV-Vis) and troubleshooting techniques. + Understanding of cGMP, GLP, and other regulatory requirements. + Strong written and verbal communication skills. + Excellent organizational and time management abilities. + Capable of working both independently and as part of a team. **_Note:_** _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ \#INDBH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our ******************************** is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. Coinbase stores more digital currency than any company in the world, making us a top tier target on the internet. Security is core to our mission and has been a key competitive differentiator for us as we scale worldwide. Essential to scaling is building and running a security compliance program that reflects how we protect the data and assets in our care, to open the doors with customers, regulators, auditors, and other external stakeholders. Coinbase is looking for an Analyst, Tech Controls to support the second line of defense technology compliance initiatives. This role will play a critical part in assisting with the design, implementation, and monitoring of a technology control framework. The Analyst will work closely with cross-functional teams to ensure excellence in control ownership and contribute to the maturity of the Technology Risk and Controls program. *What you'll be doing (ie. job duties):* * Lead IT process and gap assessments against industry standards and technology regulatory requirements to evaluate control design and operating effectiveness * Design, review and validate processes and configurations across technology systems, including cloud environments, operating systems, databases, and network infrastructure, to ensure alignment with established standards, compliance requirements, and best practices * Assist in maintaining and providing oversight over the technology controls inventory to mitigate technology risks and meet regulatory requirements, technology policies, and frameworks * Collaborate with stakeholder teams including Security, Engineering, Technology Governance, IT, and Operational Risk to support technology requirements and ensure control ownership * Developing technology requirements for new products, updating existing controls, and providing subject matter expertise to product teams * Support Security Compliance, Information Security, Platform, and Engineering stakeholders in identifying and executing on continuous control monitoring opportunities * Provide guidance and leverage technical expertise to determine effectiveness of change management processes, i.e. unit testing, CI/CD, etc. * Define, draft and communicate identified issues and technology process improvement opportunities and assist in developing creative solutions to mitigate risks and address regulatory challenges * Provide reporting to stakeholders and management on progress, escalations, and control initiatives * Drive the creation of procedural documentation, including training materials that support first line of defense risk management, in the form of runbooks and narratives * Validate remediation efforts for identified gaps and issues to ensure resolution effectively aligns with regulatory requirements, industry standards, and internal policies * Drive creation of clear and concise technical documentation for control monitoring *What we look for in you (ie. job requirements):* * Minimum of 2+ years of experience in Security Engineering, Technology Compliance, IT audit, or equivalent roles * Strong knowledge and hands-on experience in technology frameworks such as COBIT, NIST, ISO 27001 * Hands on experience in security engineering, implementing security frameworks, or designing and managing technical controls * Proven technical understanding and operation within cloud technologies, AWS preferred * Strong understanding of control monitoring processes * Excellent oral and written communication skills * Ability to effectively and autonomously accomplish outcomes across cross-functional teams in ambiguous situations with limited supervision * Ability to multitask, prioritize work, and meet deadlines in a fast paced environment * Ability to communicate with technical and non-technical stakeholders to align on shared outcomes *Nice to haves:* * BA or BS in a technical field or equivalent experience * Cloud certifications such as AWS Certified Security Specialty, or equivalent certifications * Security certifications e.g. CISA, CISSP, COBIT or other relevant certifications * Technical understanding of fintech services and/or crypto space Position ID: P60079 \#LI-Remote *Pay Transparency Notice:* Depending on your work location, the target annual salary for this position can range as detailed below. Full time offers from Coinbase also include bonus eligibility + equity eligibility**+ benefits (including medical, dental, vision and 401(k)). Pay Range: $135,320-$159,200 USD Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the *********************************************** in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations*********************************** *Global Data Privacy Notice for Job Candidates and Applicants* Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available ********************************************************** By submitting your application, you are agreeing to our use and processing of your data as required. *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. The tool simulates realistic interview scenarios and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of a voice recording and/or transcript, to assess them against the qualifications and characteristics outlined in the job description. For select roles, Coinbase is also piloting an AI interview intelligence platform to transcribe and summarize interview notes, allowing our interviewers to fully focus on you as the candidate. *The above pilots are for testing purposes and Coinbase will not use AI to make decisions impacting employment*. To request a reasonable accommodation due to disability, please contact accommodations[at]coinbase.com

Forest River, Inc., the Nation's largest manufacturer of Recreational Vehicles, Cargo Trailers, Transit Buses and Boats has an immediate opening. Responsibilities * Help dealers and retail customers with technical issues * Work with R&D department testing new parts * Travel to dealers to assist in repairs & training purposes * Assist customer service with technical issues Qualifications * Boating experience recommended * Able to drive under DOT regulations - Forest River will assist getting eligible candidates approved for DOT driving * Proficient in communication skills * Able to use Microsoft Office proficiently Forest River offers a stable work environment that is fast paced. Our employees enjoy a highly competitive Wage and Benefit Package. We are looking for dedicated individuals with experience in the Industry as well as other Manufacturing Processes.

Be a part of a global team where what we do matters! At Epredia, we recognize that our talented employees are vital to our success. Our team is dedicated, our work is rewarding - both personally and professionally - because what we do matters. We seek talented individuals who will contribute to and thrive in our collaborative, diverse, fast-paced environment while demonstrating a commitment to our core values, People, Customer, Results, Continuous Learning, and Innovation. People - We win as a team. Customer - We deliver customer-centric solutions. Continuous Learning - We learn and always aim to be better. Innovation - We innovate every day. Results - Results matter for all of us. Job Title: Quality Control Chemist Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win. Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers. * You will perform routine testing and inspection of manufactured products, raw materials, in-process samples and finished products in our Quality Assurance Laboratory. This testing is is essential to ensure the quality of our products for customers' use in diagnosing cancer. * You will report directly to the QC Laboratory Manager and be a member of a top-notch team of highly-skilled, energetic analysts. Every phase of production depends on the accuracy and thoroughness of the testing and inspections performed by the QA Lab staff. Location: This is an on-site position based out of Kalamazoo, MI. What you will do: Performs routine testing on manufactured products, incoming raw materials, in-process products, and finished goods. Testing assays include: pH, water content (Karl Fischer titration), UV-Vis spectrophotometry, gas chromatography, formaldehyde titration, viscosity, refractive index, residue, and other routine chemical tests. Documents results with accuracy and adheres to current good manufacturing practices (cGMP, cGDP). Collaborates with Quality, Manufacturing, and R&D colleagues to troubleshoot issues, improve processes, assist with new instrument verification and validation, write work instructions, revise standard operating procedures, and develop/validate new testing assays. Works with colleagues in R&D, Regulatory, Marketing, and Manufacturing to review new raw materials, review product formulations, and adjust product formulations when necessary. * Inspect incoming products and raw materials for quality specifications. * Test samples for physical properties (pH, color, water content, residue, viscosity, specific gravity, RI, UV-Vis, FL-AA, GC assay, etc.). * Record data and test results following good manufacturing and documentation practices. * Calculate batch adjustments to meet specifications and approve batches for packaging. * Collaborate with Quality, Manufacturing and Engineering colleagues to troubleshoot issues, improve processes, validate equipment, write work instructions, and develop new tests. * Investigate non-conformances and write corrective action reports. Qualifications & Skills: * Bachelor's degree in Chemistry and a minimum of two years of experience in an analytical laboratory. * Experience with analytical equipment (pH, titrations, gravimetry, RI, FL-AA, GC, etc.). * Experience in proper data handling, documentation and recordkeeping (cGMP, cGDP). * Detailed-oriented, positive team attitude, able to handle a fast pace and shifting priorities. * Honesty, integrity, efficiency, punctuality, multitasking, and a good work ethic. The hiring range for this position is: $49,500 - $61,000, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. (Epredia Company) offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more. #LI-SJ1 TO ALL RECRUITMENT AGENCIES: Epredia does not accept unsolicited third-party resumes. Building an Inclusive Culture: We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information or any other protected classes which may exist under applicable federal, state or local law.

Be a part of a global team where what we do matters! At Epredia, we recognize that our talented employees are vital to our success. Our team is dedicated, our work is rewarding - both personally and professionally - because what we do matters. We seek talented individuals who will contribute to and thrive in our collaborative, diverse, fast-paced environment while demonstrating a commitment to our core values, People, Customer, Results, Continuous Learning, and Innovation. People - We win as a team. Customer - We deliver customer-centric solutions. Continuous Learning - We learn and always aim to be better. Innovation - We innovate every day. Results - Results matter for all of us. Job Title: Quality Control Chemist Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win. Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers. + You will perform routine testing and inspection of manufactured products, raw materials, in-process samples and finished products in our Quality Assurance Laboratory. This testing is is essential to ensure the quality of our products for customers' use in diagnosing cancer. + You will report directly to the QC Laboratory Manager and be a member of a top-notch team of highly-skilled, energetic analysts. Every phase of production depends on the accuracy and thoroughness of the testing and inspections performed by the QA Lab staff. Location: This is an on-site position based out of Kalamazoo, MI. What you will do: Performs routine testing on manufactured products, incoming raw materials, in-process products, and finished goods. Testing assays include: pH, water content (Karl Fischer titration), UV-Vis spectrophotometry, gas chromatography, formaldehyde titration, viscosity, refractive index, residue, and other routine chemical tests. Documents results with accuracy and adheres to current good manufacturing practices (cGMP, cGDP). Collaborates with Quality, Manufacturing, and R&D colleagues to troubleshoot issues, improve processes, assist with new instrument verification and validation, write work instructions, revise standard operating procedures, and develop/validate new testing assays. Works with colleagues in R&D, Regulatory, Marketing, and Manufacturing to review new raw materials, review product formulations, and adjust product formulations when necessary. + Inspect incoming products and raw materials for quality specifications. + Test samples for physical properties (pH, color, water content, residue, viscosity, specific gravity, RI, UV-Vis, FL-AA, GC assay, etc.). + Record data and test results following good manufacturing and documentation practices. + Calculate batch adjustments to meet specifications and approve batches for packaging. + Collaborate with Quality, Manufacturing and Engineering colleagues to troubleshoot issues, improve processes, validate equipment, write work instructions, and develop new tests. + Investigate non-conformances and write corrective action reports. Qualifications & Skills: + Bachelor's degree in Chemistry and a minimum of two years of experience in an analytical laboratory. + Experience with analytical equipment (pH, titrations, gravimetry, RI, FL-AA, GC, etc.). + Experience in proper data handling, documentation and recordkeeping (cGMP, cGDP). + Detailed-oriented, positive team attitude, able to handle a fast pace and shifting priorities. + Honesty, integrity, efficiency, punctuality, multitasking, and a good work ethic. The hiring range for this position is : $49,500 - $61,000, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. (Epredia Company) offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more. #LI-SJ1 TO ALL RECRUITMENT AGENCIES: Epredia does not accept unsolicited third-party resumes. Building an Inclusive Culture: We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information or any other protected classes which may exist under applicable federal, state or local law. At Epredia, we improve lives by enabling better cancer diagnostics. We are a team of talented individuals with diverse backgrounds and expertise, working together to develop precision diagnostic solutions for our customers. We are a fast growing global company that drives innovation in diagnostics to create better outcomes for patients. Joining Epredia is much more than a job- it is an opportunity to be part of something with a purpose. Find out how you can improve lives while advancing your career.

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.

Under the direction of the QC Manager, the QC Technician is responsible for performing QA/QC testing in compliance with all applicable ASTM, ACI, & Job Specific Standards and other associated tasks by direction Key Responsibilties: Working in safe professional manner Communication skills Performing proper plastic concrete testing at the plants and on jobsites in accordance with all applicable standards Ensure all materials meet or exceed all applicable state and job specifications Reporting: Ensure that all appropriate reports are properly filled out and recorded into the Command QC data base Monitor and test aggregate conditions for compliance with applicable standards at the plant level Properly logging in, breaking and recording results of concrete cylinders Acknowledge customer complaints/claims and take appropriate actions to resolve matter with reduction in liability whenever possible Attend pre-pour and other jobsite meetings as required Participate in Research and Development of new products Conduct and assist as needed with employee and customer training programs Participate in cross training of all departments at Shafer Redi-Mix / Shafer Bros Other related duties as required Job Requirements: Must have a valid driver's license Knowledge of and dedication to quality assurance / quality control principles and standards Completion of MCA/ACI Field Technician Level 1 or higher Attention to detail and ability to follow through without direction and constant supervision Operational knowledge of batch plants, mixers and related processes Good organizational and planning skills Excellent Customer service ability Basic knowledge of computers and Microsoft office Must be able to perform simple mathematical calculations Adaptability and flexibility to be able to adjust to continuous change Team player Physical Requirements: Work requires walking, climbing, bending, pushing, pulling, and lifting (50 lb minimum) objects Must be able to start work early mornings and work long hours according to seasonal and market demands Must be able to work in all weather conditions Benefits: Competitive Wages Health Insurance for employee and family with 75% premium contribution from employer and Health Savings Account matching program (available after 30 days) Employer paid Group Term Life Insurance for employee (available after 30 days) Employer paid Supplemental Accident, Disability and Critical Illness Insurance for employee (available after 90 days) Employee paid Dental and Vision Insurance Employer paid Sam's Club Card (sign up once a year) Holiday pay after 90 days of service Vacation Pay after 1 year of service 401(k) with Employer Match Contribution after 6 months

Full-time Description The Quality Technician supports the Quality Manager in planning, coordinating, and implementing quality control programs to ensure consistent production of products that meet customer and company standards. This role may require occasional overtime, including weekends. Essential Duties and Responsibilities Review and organize engineering prints; generate inspection documentation for drawing control and routing processes. Interpret technical drawings and specifications, including GD&T dimensional callouts. Perform full dimensional first-piece inspections and verify material certifications against parts. Conduct periodic gage verification; service and repair measuring equipment as needed and manage external repairs. Prepare documentation for rejected materials, scrap disposition, and print change/deviation requests. Compile production kits and maintain accurate records. Select and evaluate products at designated stages of production for dimensional accuracy, performance, and mechanical properties. Perform process audits to ensure compliance with QMS guidelines, policies, and procedures, review findings with process owners. Collaborate with production, engineering, and other departments to develop PPAP documentation, including Warrants, Control Plans, Flow Charts, PFMEA, Dimensional Results, MSA, and other AIAG-required documents. Communicate with customers regarding quality issues and assist with sorting suspect parts when necessary. Provide backup support to the Quality Manager and perform additional duties as assigned. Qualifications Education/Experience: Associate degree in a technical field or equivalent preferred; or 6-12 months of related experience/training; or a combination of education and experience. Technical Skills: Ability to read and interpret technical documents, safety rules, and procedures. Proficient in Microsoft Office. Mathematical Skills: Strong understanding of geometry and statistical concepts; ability to apply fractions, percentages, ratios, and proportions. Reasoning Ability: Capable of solving problems involving multiple variables and following written, oral, or diagram instructions. Basic understanding of measurement tools such as tape measure, calipers, micrometers. Physical Demands Regularly required to sit, use hands, and communicate effectively. Occasionally required to stand, walk, stoop, kneel, or lift to 25 lbs. The company will provide reasonable accommodation to enable individuals with disabilities to perform essential job functions. Work Environment Exposure to moving mechanical parts on occasion. Noise level is typically loud; appropriate PPE provided. SUPERVISORY RESPONSIBILITIES This job has no supervisory responsibilities. BENEFITS Comprehensive benefits offerings including but not limited to - Health, Dental, Vision, Life, & Disability Vacation time with automatic rollovers Minimum 7 Paid Holidays Weekly attendance bonus that pays an extra $25 for working at least 35 hours onsite! 401(k) Tuition Reimbursement up to $4,500 per year Shoe Reimbursement up to $50 on qualifying footwear with no waiting period! Requirements LANGUAGE SKILLS Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Write routine reports and correspondence. Speak effectively before groups of customers or employees. REASONING ABILITY Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations. COMPUTER Proficient in the use of computers and MS Office applications. Proficiency with ERP systems used for production planning, scheduling and inventory control to manage manufacturing processes; analyze and utilize data for decision making. MATHEMATICAL Work with math concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Apply concepts such as fractions, percentages, ratios, and proportions to practical situations. EDUCATION/EXPERIENCE Associate's degree (A. A.) or equivalent from two-year college or technical school; or six months to one year related experience and/or training; or equivalent combination of education and experience. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to sit; use hands to finger, handle, or feel and talk or hear. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually loud. Salary Description Starting at $20/hr and up to $25/hr

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 -- **********************

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

Job Description Analytical Technical Instructor For over 80 years, LECO has been a leader in the development and production of world class laboratory instruments delivering state of the art products nationwide and across the globe. Located in St. Joseph, Michigan, LECO continues to be a family-owned company that understands the value of shared interests, long-term stability, loyalty, and trust. Schedule: Full Time: 8:00am - 5:00pm, Monday - Friday and occasional weekend travel required Position Summary: A motivated, outgoing, independent person responsible for teaching technical classes of 20 people or less. Classes are typically 3 days per week, and some are 5 days covering both hardware and software supporting LECO analytical instrumentation. Courses taught at LECO headquarters located in St. Joseph, Michigan in addition to the remote offices in Henderson, Nevada and Ft. Myers, Florida.Travel will be required several times a year throughout the US. Position Responsibilities: Responsible for instructing technical courses to LECO customers Provide in-depth product knowledge to LECO Service personnel Assist with extensive training program for newly hired service department employees Develop and maintain accuracy in training material Must have good communication skills, and be comfortable with public speaking Possess good mechanical aptitude for product demonstrations during training course Help resolve customer concerns, and maintain professional customer relationships Position Requirements: Must have good communication skills, and be comfortable with public speaking Able to travel as needed (typically 4-6 days per trip) Willingness to travel domestically as required (less than 20% total per year) On-the-job training will be provided as necessary Strong written and verbal communication skills Ability to function independently as well as in a team environment Customer service-oriented personality is helpful Education/Certifications: Bachelor's Degree (chemistry or technical; others will be considered also),or related military training EOE M/F/VET/Disability You should be proficient in: Electrical Installation Service Experience in a Manufacturing Environment

**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.

Join the MDP Diesel & Auto Team - Now Hiring a Quality Control Tech! Company: MDP Diesel & Auto - Independent, Fast-Growing Auto Repair Shop Quality Control (QC) Technician Type: Full-Time At MDP Diesel & Auto, we're more than just a repair shop-we're a tight-knit, happy team with a passion for cars and customer care. We're growing fast and looking to bring on a reliable QC Tech who thrives in a dynamic, high-energy environment. No two days are the same here. You'll be the go-to person for a variety of essential support tasks, including: Driving the customer shuttle Picking up parts and running shop errands Keeping the shop clean and organized Performing light vehicle cleaning (no detailing) Supporting the team in whatever way is needed-with a positive attitude and a smile If you're resourceful, motivated, and eager to learn the ropes in the auto industry, you'll love it here. Company-paid health benefits (yes, they're actually good ) Opportunities for career advancement (perfect if you're aiming to become a tech or apprentice) A supportive, upbeat team environment Competitive pay with potential to hustle and thrive What We're Looking For Our ideal candidate is someone who: Has 6+ months experience as a porter, lube tech, or tire technician Holds a clean driving record (no DUIs, max one moving violation in the last 3 years) Owns a dependable vehicle Can lift up to 75 lbs Has no felony record Is eligible to work in the U.S. Can pass a drug test and physical Lives within 40 minutes of our Jackson, MI location Ready to hustle, grow, and be part of a team that feels like family? Apply today and start your journey with MDP Diesel & Auto!

Summary/Objective The Quality Intern is responsible for the effective, efficient, and proactive execution of their activities on assisting with new product launches and sustaining existing products. Essential Functions • Uses quality tools to implement improvements including process flowcharting, Pareto analysis, correlation and regression analysis, significance tests, design of experiments, statistical process control, gauge repeatability and reproducibility (GR&R), and trend analysis techniques. • Monitors engineering processes and products for adherence to company and regulatory standards and practices. Participates in quality improvement initiatives and projects. • Performs quality reviews and assist with internal audits; evaluates data and writes reports to validate or indicate deviations from existing standards. • Assist or lead process and equipment validations. • May assist and process customer quality complaints. • Assists the development of essential QMS deliverables including, but not limited to complaint analysis, risk analysis, failure mode and effects analysis, CAPA, and process/equipment/software verification/validation. • Assist in the development, review and processing of change requests. • Work with production to document current process parameters and develop written instructions to eliminate unnecessary process variations. • Participates in pre- and post-production reviews providing engineering support. • Collects the required data and chart the quality goals established by the management team. • Supports measuring and analyzing key metrics to monitor performance. • Support productivity improvements by providing quality guidance. • Works with cross-functional teams to solve production and quality problems. • Support quality, engineering and compliance by complying with all Quality Management Systems (QMS or PQS) documentation requirements and establishing/supporting plan(s) to meet/exceed Niowave goals for Quality that support Safety, Compliance, Six Sigma Quality, On-Time Delivery (OTD) and financial objectives. • Support Y-90 production team or other internal NW teams as needed with various requests. Examples may be chemical experiments, resources needed for preparing production runs, radiation clean up, inventory assistance, etc. Job Title Quality Intern Reports To Director of Quality FLSA Classification Hourly Non-Exempt Competencies • Ability to apply logic and reasoning to solve complex problems, including identifying strengths/weaknesses, locating alternative solutions and conclusions, and approaches to problems; and making high-quality, timely decisions • Ability to proofread data • Excellent organizational skills • Strong computer skills • Strong interpersonal communication skills • Confident decision-making abilities Required Education and Experience • Bachelor's degree (in process) in Engineering or equivalent combination of work experience, certifications, and/or degree required Work Environment This job operates in a professional office environment. This role routinely uses standard office equipment. Physical Demands The position operates in a professional office and industrial environments which includes the use of standard office equipment and/or machinery related to the production of medical isotopes. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb stairs; talk or hear. The employee must occasionally lift or move office products and supplies, up to (20 - 50) pounds. Position Type/Expected Hours of Work This is a full-time position. Days of work are typically Monday through Friday, 8 a.m. to 5 p.m. Travel Travel is primarily local during the business day, although some out-of-area and overnight travel may be expected. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

It's fun to work in a company where people truly believe in what they are doing! Essential Duties and Responsibilities: * The QC Lab Support role is fundamental to the successful, compliant operation of the QC Lab, ensuring technicians have the materials and environment needed for accurate testing. * Central responsibility for preparing, labeling, and quality documentation of all microbiological media, buffers, and cleaning solutions. This includes accurate weighing, pH adjustment, autoclaving, and log entries. * Responsible for daily lab cleaning and managing waste streams (regular, chemical, solid biohazard, and liquid biohazard). * Strict adherence to Good Documentation Practices (GDP), Good Laboratory Practices (GLP), and Aseptic Technique to maintain the integrity of the BSL-2 lab environment. * Perform daily temperature logging for critical equipment (incubators, refrigerators, freezers), assist with routine preventative maintenance (PM) tasks, perform pH meter calibration, and operate/document use of the autoclave and glassware dishwasher. * Assist other technicians with basic tasks, submit IT and Facilities support requests, and serve as a designated trainer for new hires on Lab Support core duties. Skills and Competencies: * Attention to Detail & Documentation: Exhibits strong attention to detail to ensure accurate log entries, clear labeling, and compliance with GDP standards. * Technical & Foundational Skills: Demonstrates a willingness to learn and execute fundamental laboratory support techniques, including aseptic practices, weighing materials, operating autoclaves/dishwashers, and managing waste. * Communication & Collaboration: Communicates clearly and effectively to coordinate lab supply needs and report immediate safety or quality concerns to the Supervisor or Manager. * Performance & Accountability: Highly dependable, consistently follows instructions and established procedures (SOPs), and takes responsibility for maintaining the lab's operational readiness. * Cultural Fit: Demonstrates and lives Neogen's Pillars of Trust (Openness, Honesty, Credibility, Respect, and Service) in all actions and behaviors. Understands their role and how it contributes to the organization's success. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: * High School Diploma/GED is required. * No prior experience is required as this is an entry-level position. Prior laboratory or commercial experience with material preparation, cleaning, or precise documentation is preferred. Language Skills: * Ability to read and comprehend documents such as safety rules, work instructions, and Standard Operating Procedures (SOPs) in English. * Ability to clearly and legibly record data and initials on logs and forms, which is critical for GDP compliance. * Ability to communicate clearly (orally and written) with team members and management. Mathematical Skills: * Ability to perform basic arithmetic (addition, subtraction, multiplication, division) for accurate weighing and dilution calculations when preparing media and cleaning solutions. Computer Skills: * Basic knowledge of computers and operating systems, including the ability to effectively communicate electronically and use portals for submitting support requests (IT, Facilities, Media). * Knowledge and experience with Microsoft Office Suite (Word, Excel) is preferred but not required. Physical Demands: * While performing the duties of this job, the employee is regularly required to see, talk, or hear. * Frequently required to stand, walk, and sit, especially when performing lab maintenance and preparation tasks. * Occasionally required to use hands to handle or feel, reach with hands and arms, climb or balance, and stoop, kneel, crouch, or crawl. * Must occasionally lift and/or move up to 25 pounds, such as media bottles or equipment. * Employee must pass a standardized color deficiency test with a score of > 80%. Work Environment: * Laboratory environment with potential exposure to moving mechanical parts and fumes or airborne particles. * Frequently exposed to biological agents and potentially pathogenic microorganisms. * Occasionally exposed to toxic or caustic agents used in laboratory procedures. * The noise level in the work environment is usually quiet to moderate, with occasional louder noises from equipment like autoclaves. Come Be Part Of A Mission that Matters! From inside the farm gate to our dinner plates, Neogen protects the world's food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there - and you can be too.

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.

Be a part of a global team where what we do matters! At Epredia, we recognize that our talented employees are vital to our success. Our team is dedicated, our work is rewarding - both personally and professionally - because what we do matters. We seek talented individuals who will contribute to and thrive in our collaborative, diverse, fast-paced environment while demonstrating a commitment to our core values, People, Customer, Results, Continuous Learning, and Innovation. People - We win as a team. Customer - We deliver customer-centric solutions. Continuous Learning - We learn and always aim to be better. Innovation - We innovate every day. Results - Results matter for all of us. Job Title: Quality Control Chemist Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win. Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers. You will perform routine testing and inspection of manufactured products, raw materials, in-process samples and finished products in our Quality Assurance Laboratory. This testing is is essential to ensure the quality of our products for customers' use in diagnosing cancer. You will report directly to the QC Laboratory Manager and be a member of a top-notch team of highly-skilled, energetic analysts. Every phase of production depends on the accuracy and thoroughness of the testing and inspections performed by the QA Lab staff. Location: This is an on-site position based out of Kalamazoo, MI. What you will do: Performs routine testing on manufactured products, incoming raw materials, in-process products, and finished goods. Testing assays include: pH, water content (Karl Fischer titration), UV-Vis spectrophotometry, gas chromatography, formaldehyde titration, viscosity, refractive index, residue, and other routine chemical tests. Documents results with accuracy and adheres to current good manufacturing practices (cGMP, cGDP). Collaborates with Quality, Manufacturing, and R&D colleagues to troubleshoot issues, improve processes, assist with new instrument verification and validation, write work instructions, revise standard operating procedures, and develop/validate new testing assays. Works with colleagues in R&D, Regulatory, Marketing, and Manufacturing to review new raw materials, review product formulations, and adjust product formulations when necessary. Inspect incoming products and raw materials for quality specifications. Test samples for physical properties (pH, color, water content, residue, viscosity, specific gravity, RI, UV-Vis, FL-AA, GC assay, etc.). Record data and test results following good manufacturing and documentation practices. Calculate batch adjustments to meet specifications and approve batches for packaging. Collaborate with Quality, Manufacturing and Engineering colleagues to troubleshoot issues, improve processes, validate equipment, write work instructions, and develop new tests. Investigate non-conformances and write corrective action reports. Qualifications & Skills: Bachelor's degree in Chemistry and a minimum of two years of experience in an analytical laboratory. Experience with analytical equipment (pH, titrations, gravimetry, RI, FL-AA, GC, etc.). Experience in proper data handling, documentation and recordkeeping (cGMP, cGDP). Detailed-oriented, positive team attitude, able to handle a fast pace and shifting priorities. Honesty, integrity, efficiency, punctuality, multitasking, and a good work ethic. The hiring range for this position is: $49,500 - $61,000, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. (Epredia Company) offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more. #LI-SJ1 TO ALL RECRUITMENT AGENCIES: Epredia does not accept unsolicited third-party resumes. Building an Inclusive Culture: We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information or any other protected classes which may exist under applicable federal, state or local law.

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 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. 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 RegularColleague 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.

Forest River, Inc., the Nation's largest manufacturer of Recreational Vehicles, Cargo Trailers, Transit Buses and Boats has an immediate opening. Responsibilities * Full Inspection of Inside and Outside of Units Qualifications * Experience in the RV Industry * Strong People Skills * Code Knowledge is a Plus * Excellent Attendance a must Forest River offers a stable work environment that is fast paced. Our employees enjoy a highly competitive Wage and Benefit Package. We are looking for dedicated individuals with experience in the Industry as well as other Manufacturing Processes.