Quality control analyst jobs in Kentwood, MI

Quality Control Kalamazoo County, MI, NONE + Added - 28/10/2025 Apply for Job Pay Rate Low: 30 | Pay Rate High: 34 _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.

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The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze raw materials, packaging materials, in-process materials, APIs, utilities, and/or finished product samples in support of the company's quality program in the laboratory. * Performs, documents, record checks, and troubleshoots qualitative or quantitative assays on samples using techniques that vary from use of standard laboratory equipment to highly modern and automated instrumentation. May participate in manufacturing QC support such as cleaning verification. * Interprets and evaluates data in terms of accuracy, precision, trends, and potential GMP impact and recommends appropriate corrective action where necessary. * 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. * Able to comprehend and perform both routine and non-routine analyses from compendial and internal sources. * May train others as skills and knowledge allow. * Participates in laboratory investigations as required. * May be responsible for writing routine assay protocols or conducting assay, process, or instrument qualifications. * The successful candidate must also have demonstrated the ability to quickly learn new skills/techniques. EDUCATION AND EXPERIENCE * AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science. * A minimum of 2 years related experience in Quality Operations is preferred. * The successful candidate must have demonstrated proficiency in at least one high complexity technology (e.g. HPLC, uHPLC, GC, advanced spectroscopy, etc.) or at least 2 or more low to medium complexity technologies (e.g. TLC, titrations, wet chemistry/physical testing, water testing, etc.) as required by the business unit. * Job duties involve occasional lifting (less than 35 lbs), reaching, and sitting while working at computer terminal. * Candidate must not be Cephalosporin/Penicillin sensitive. SHIFT * 2:00pm to 10:30 pm 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.

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.

Hours: Full-time (Mon-Fri typical) This is an entry-level position built to turn someone who can hustle and learn into a productive automotive technician. You'll start in QC - doing final inspections, cleaning cars, running parts, and keeping the shop safe and stocked - but this role is explicitly a training track. We'll help you get your trainee permit, give you paid hands-on learning time during downtime, and promote from within when you're ready. What you'll do Run the shop's QC inspection on every completed repair order and perform a mini-clean before customer pickup. Verify repairs were completed to spec; document and report any rework. Keep shop floors, bathroom, and grounds clean and stocked. Drive company vehicle for parts runs and customer shuttles when needed. Help prep and maintain loaner cars when required. Use downtime to train on real vehicle work under supervision. Why this is different This is a real pathway into tech work, not just a janitor job. We pay you to learn on cars. We'll help you get your trainee permit and schedule training time. Strong performers get priority for technician openings and apprenticeships. Who we want Someone who wants to be a technician and is willing to do the work it takes to get there. Basic automotive familiarity - can identify under hood components, change a tire, check fluids. Valid US driver's license and ability to drive with passengers. Able to lift 50 lbs and do physical shop tasks (sweeping, bending, using floor machines). Good attitude, reliable, shows up on time, and can communicate with customers professionally. Able to read/write English and do basic math. What you'll get Paid, on-the-job training and supervised practice on cars. Trainee permit support (we'll help you through the paperwork/training). Clear path to technician role for people who learn fast and show up. Competitive pay and benefits.

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

**Analytical Chemistry Lab Analyst - $25 hr** Reckitt, formally Mead Johnson Nutrition, located in Zeeland Michigan, is looking for hardworking, motivated talent to join their team. This company is a major manufacturer of infant and child nutritional powders and the ZSP Analytical Chemistry Team is responsible for the analytical testing of finished products and in-process materials. ***This is a contract position through Manpower*** Don't wait... apply today! What's in it for you? + **$25** + **Day Shift - Sunday - Thursday or Monday - Friday** + Paid training + Full time hours + Clean and safe work environment What will you be doing? + Analysts are expected to follow established methods, utilize approved laboratory techniques, and perform complex calculations to ensure accurate results are delivered in a timely manner. In addition to release testing, analysts perform investigations and instrument/method optimization to support Operations and Quality objectives. Analysts are also expected to utilize a LIMS (Laboratory Information Management System) to maintain records in compliance with good manufacturing and regulatory practices What do you bring? + Positive, can-do attitude + High School Diploma or GED + Bachelor's Degree in science or technical subject desired. + Minimum of one year of analytical experience required. + Instrumentation experience with ICP-OES/ICP-MS, GC, NIR, and HPLC/UPLC/HPIC desired. + Strong critical thinking and problem-solving skills desired. + Proficiency with standard laboratory operations, equipment, and technique required. + Experience with the calibration and maintenance of lab equipment desired. + Familiarity with laboratory computer systems, including Chromeleon, Syngistix, and Sample Manager desired. + Experience in an FDA-regulated GMP environment required. Please send updated resumes to *************************. ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

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

PSG is the global pump, metering and dispensing-solution expert, enabling the safe and efficient transfer of critical and valuable fluids that require optimal performance and reliability in applications where it matters most. Additionally, PSG is a leading provider of flow meters designed to reduce waste and downtime while accurately measuring, monitoring and controlling the distribution of fluids. Headquartered in Downers Grove, IL, USA, PSG is comprised of several world-class brands, including Abaque , All-Flo™, Almatec , Blackmer , Ebsray , em-tec , Griswold , Hydro™, Malema™, Mouvex , Neptune , PSG Biotech, Quantex™, Quattroflow , and Wilden . PSG products are manufactured on three continents - North America, Europe, and Asia - in state-of-the-art facilities that practice lean manufacturing and are ISO-certified. PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional information on PSG, please visit psgdover.com. We thrive on winning and being number one; and are always looking to add the best and brightest to our talented team of professionals. PSG offers a unique combination of the both small company atmosphere: with an ownership mindset that allows you to make close-to-the-customer decisions; an innovative approach in seeing beyond what is possible today and entrepreneurial spirit in the pursuit of new opportunities; combined with benefits of a large company's scale, tools, expertise, and financial strength with Dover. Join PSG, a growing global company where your curiosity, hard work and ambition is rewarded with exceptional career opportunities in a friendly & fast paced environment. PSG is part of the Pumps and Process Solutions segment of the Dover Corporation (NYSE: DOV). Dover is a diversified global manufacturer and solutions provider with annual revenue of over $7 billion. We deliver innovative equipment and components, consumable supplies, aftermarket parts, software and digital solutions, and support services through five operating segments. Recognized for our entrepreneurial approach for over 65 years, our team of over 24,000 employees takes an ownership mindset, collaborating with customers to redefine what's possible. Quality Special - 2nd Shift Hours: 2:00 pm - 10:00 pm Hourly Rate: $30.28 Essential Duties and Responsibilities: Programs Coordinate Measuring Machines (CMMs) Performs 1st article inspections Calibrates measuring instruments Assists in capability studies Assists production in set-up measurements Performs shop floor inspections as required Trains as required Qualifications / Requirements: CMM Programming Basic machine math skills Understand and interpret GD&T (read blueprints) Proper use of precision measuring equipment Maintaining records must be complete Quality Special Training course and classes Basic computer/technology skills We consider several job-related, non-discriminatory factors when determining the pay rate for a position, including, but not limited to, the position's responsibilities, a candidate's work experience, a candidate's education/training, the position's location, and the key skills needed for the position. Pay is one of the Total Rewards that we provide to compensate and recognize employees for their work. Benefits: Our total rewards package for eligible team members also includes: a 401(k) savings plan with employer contributions; medical, dental and vision insurance; wellness programs; health savings account, health care and dependent care flexible spending accounts; company paid short-term disability and long-term disability; company paid employee basic life and AD&D insurance; supplemental employee and dependent life insurance; optional accident, hospital indemnity and critical illness insurance; adoption, surrogacy, and fertility benefits and assistance; commuter benefits; parental, military, jury duty, and bereavement leaves of absence; paid time off, including 13 paid holidays per calendar year, paid vacation days, employee discounts; and an employee assistance program that includes company paid counseling sessions and legal services. Eligibility for benefits is governed by applicable plan documents and policies. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law. Attention Applicants: If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please let us know. Likewise, if you are limited in the ability to access or use this online application process and need an alternative method for applying, we will determine an alternate way for you to apply. Please contact accommodations@psgdover.com for assistance with an accommodation. Kindly specify Job Requisition Number / Job Title and Location in response. #LI-LM1

**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.

As a family company, we serve people and communities. When you work at Meijer, you're provided with career and community opportunities centered around leadership, personal growth and development. Consider joining our family - take care of your career and your community! Meijer Rewards Weekly pay Scheduling flexibility Paid parental leave Paid education assistance Team member discount Development programs for advancement and career growth Please review the job profile below and apply today! Meijer offers an 11-week internship program that challenges interns to deliver innovative solutions to real projects that impact the business. Throughout the course of the internship experience, we deliver diverse personal and professional development opportunities that further develop skillsets that can be implemented both during and after the program. The internship program will allow for interaction with other interns and Meijer senior leaders. The internship program includes: Challenging and impactful projects Final presentations delivered to senior executives Executive speaker series Professional development and training opportunities Networking and community events Events highlighting key areas of the business What you will be doing as a Food Safety Intern: The projects that will be given to the Food Safety/Quality interns will be focused in key areas of the supply chain that will give a broad perspective of Food Safety/Quality in the supply chain, from procurement to manufacturing, as well as involvement in engaging projects where they can make a difference. In the Food Safety/Quality department, you will be exposed to several different aspects, such as procurement and merchandising strategies, product development, manufacturing QA, measuring own brand vendor quality standards, and customer service. Additionally, you'll gain experience in meeting and exceeding government standards regarding facility and product compliance. The intern may also get exposure to other activities of the function, including: Manufacturing Merchandising Store operations Legal Qualifications: Progress toward a Bachelor's degree in: Food Science Biological Sciences Chemistry Nutrition/Culinary Science Engineering (Agricultural, Biotechnology, Chemical) Other related/associated science degree Additional qualifications Proficiency in Microsoft Office applications, including Word, Excel, PowerPoint. Drive for results - has focus on the bottom line. Customer focus - dedicated to meeting expectations of internal and external customers. Relationship Skills - can create positive working relationships with customers, team members, leadership, and other internal and external constituencies. Communication Skills - conveys the right information in writing and verbally. Problem Solving - Probes all fruitful sources for answers and looks beyond the obvious to assemble and interpret data. Possible career path opportunities: Food Scientist Food Safety Specialist Manufacturing QA Distribution QA Regulatory Specialist Recall/Product Support Specialist Food Safety Training Specialist Data Analytics Program Governance

Job Title: Shipping Quality Control Technician Department: Shipping Supervisor: Greenhouse Shipping Coordinator Direct Reports: None FLSA Status: Non-Exempt Starting Rate: $21.50 PRIMARY PURPOSE AND FUNCTION The primary purpose of the Shipping Quality Control Technician is to demonstrate professional behavior with a team-based mentality to ensure that all products produced by Walters Gardens are shipped out with the highest standards for quality. ESSENTIAL DUTIES AND RESPONSIBILITIES Moisture Management Maintain proper moisture levels on all plants in shipping areas both on racks and on carts. Learn moisture requirements for each variety and plant size Check moisture levels on rack product in main building when orders are postponed Communicate with lead grower if moisture levels of incoming plants from contact growers are managed incorrectly Create watering notes for both S range and main building for the weekend watering crew to use as a guideline Participate and coordinate with weekend watering team as needed Plant Health Responsibilities Assist IPM manager by scouting and identifying insects, crown gall, diseases, or pathogens on items in S range Communicate with IPM team on crops in S range that need applications Additional Duties Daily shipping duties as directed by Greenhouse Shipping Coordinator Oversee the order-pulling work done by H2A staff Quality check carts after orders have been pulled When quality issues arise - oversee and correct order-pulling staff Twice daily quality checks of S range Replace missing plugs and fix any quality issues that may arise in a timely manner Organize staff to help clean product on larger jobs when needed Quality checks all product for boxing line Participate in meetings and educational events when directed by supervisor. Communicate with lead grower if there are constant quality issues in product from contract grower Off Season Duties Maintain high quality standards for material being sorted by production staff both in the greenhouse and in the processing room Asist staff in sorting/planting when needed Requirements KNOWLEDGE AND SKILLS REQUIRED 2 years of greenhouse experience preferred Bilingual in Spanish and English preferred Strong organizational and math skills Computer skills in Microsoft Office, Microsoft 360 and Microsoft Teams Desire to work in a collaborative environment Available to work weekends as needed Salary Description starting $21.50/hr

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

"Job Description: 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 " />

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.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's (*********************************** 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System (************************************************************ which makes everything possible. The Quality Control Scientist, Microbiology is responsible for supporting Cytiva's new plant for manufacturing of chromatographic resins. This exciting role will be part of the start-up of Laboratory Operations on the site to support all parts of manufacturing with product release testing and troubleshooting related to Laboratory and Manufacturing in the field of Life Science. Your duties vary from routine analyses to instrument maintenance, method and instruction updates, and cross-functional meetings and collaborations. This position reports to the Sr. Manager, Quality Control and is part of the Quality Control team located in Muskegon, MI and will be a fully on-site role. What you will do: + Set up quality routines for the new QC Laboratory according to Quality Management Systems. Including installation and commissioning of new equipment. + Review and develop all types of analytical methods and SOPs to be used for the start-up of the operations. + Perform investigations and deviation management according to Quality Management Systems. + Build expertise for analytical activities in the Laboratory to gain enough knowledge to train peers. + Lead and coordinate activities on site during the receiving and start-up of the laboratory. Who you are: + Bachelor, MBA or Advanced degree from an accredited University or College in Microbiology or applicable. + Minimum 4 years working experience within a Laboratory, preferably Quality Control Laboratory. + Strong and accurate documentation skills. + Ability to lead initiatives to improve ways of working in a laboratory through effective communication with local and international team. + Effective problem identification and solving skills. Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role + Overall travel is expected to be less that 5%. Some local and international travel is required during the project phase as several trips to Sweden may be required. + Ability to lift, move or carry equipment up to 20lbs frequently up to 35lbs occasionally, + Ability to stand or sit continuously for up to 3 hours at a time, + Ability to use hand fine motor skills to complete lab tests It would be a plus if you also possess previous experience in: + Water Testing + Use of Laboratory Information Management System (LIMS) Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info (**************************************************************************************** . Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

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.

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.