Chemist jobs in Kentwood, MI - 24 jobs

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve The Rapid Turn Lab (RTL) Chemist is responsible for scheduling prioritization, workload distribution, and laboratory process improvement for testing at the Kalamazoo site. This includes communicating priorities to the lab and following up with customers on testing status. The Chemist performs LIR supervisor duties for atypical, OOS, questionable, and invalidated data occurrences and will cover data integrity responsibilities. The Chemist represents the lab unit or the entire lab organization on moderate complexity projects and project teams both within and outside of Quality Operations. This role provides technical expertise to assist the laboratory with troubleshooting, investigations, computer validation and instrument qualifications. The chemist may be involved in second checking of data and will perform assays as needed. This role has the responsibility of serving as Management Designee and will have limited input into the OTE colleague performance assessment process. The chemist may defend QO Laboratory Quality Systems during audits and inspections. ROLE RESPONSIBILITIES Leads and documents laboratory investigations for procedural deviations, atypical, OOS, questionable, and invalidated data occurrences. Assures adherence to data integrity initiatives. As a Subject Matter Expert (SME), represents the lab unit or the entire lab organization on high complexity projects and project teams both within and outside of QO. Leads medium or high complexity project teams within QO tasked with improving laboratory or other quality systems. Assists QO Lab leadership in determining scheduling priorities and workload distribution to ensure customer needs are met. Performs data quality inspection through Quality audits and 2nd check of laboratory data packets Performs analytical assays during times of need. Demonstrates a technical mastery of one or more techniques in fields such as: wet chemistry, chromatography, physical chemistry, or spectroscopy as well as a complete knowledge of laboratory operations including both technical and compliance aspects. Applies knowledge of advanced techniques and procedures with recommendations and implementation of new or modified procedures or instrumentation for improved lab efficiency. Trains others in the theory and practice of both laboratory techniques and quality systems including investigations, instrument qualifications, etc. Independently writes SOPs, technical reports, project plans, instrument qualifications, etc. Supports and may lead implementation of various elements of IMEx. Performs analytical assays during times of need Serves as management designee and will have limited input into the OTE colleague performance assessment process. Here Is What You Need (Minimum Requirements) Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience Demonstrated technical skills in testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Laboratory Investigation Report Author Trained to execute and record check multiple Chemistry laboratory technologies Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Abilityto manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures PHYSICAL/MENTAL REQUIREMENTS Job requires sitting, standing, walking, ability to type, and dexterity for handling glassware/laboratory equipment. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS 2nd Shift 3:00pm -11:30pm Monday through Friday Work Location Assignment: On Premise OTHER JOB DETAILS Last Date to Apply for Job: February 3rd, 2026 The annual base salary for this position ranges from $68,600.00 to $110,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Relocation assistance may be available based on business needs and/or eligibility. Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Pfizer endeavors to make ********************** accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Quality Assurance and Control

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

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

Job Description The Senior Vinyl Chemist is responsible for developing, formulating, and testing materials used in the manufacture of self-adhesive cast vinyl products targeting various applications, such as signage, vehicle wraps, and specialized coatings. This role involves designing and optimizing vinyl formulations, adhesives and coatings to meet performance, durability, and aesthetic requirements while ensuring compliance with industry standards and environmental regulations. The successful candidate will be a proactive leader that collaborates with cross-functional teams, including production, quality control, and sales/marketing, to innovate and optimize product performance. Key Responsibilities: Formulation Development: Design and develop cast vinyl formulations, including polymers, plasticizers, stabilizers, and additives, to achieve desired properties such as flexibility, adhesion, UV resistance, and color stability. Testing and Analysis: Conduct laboratory tests to evaluate the physical, chemical, and mechanical properties of vinyl materials, including tensile strength, elongation, and weatherability. Process Optimization: Collaborate with manufacturing teams to optimize casting processes, ensuring consistent product quality and scalability. Quality Control: Develop and implement quality assurance protocols to ensure products meet customer specifications and industry standards (e.g., ASTM, ISO). Research and Innovation: Stay updated on advancements in polymer chemistry and vinyl technology to innovate new products or improve existing formulations. Regulatory Compliance: Ensure formulations comply with environmental, health, and safety regulations, such as REACH, RoHS, and Environmental standards. Troubleshooting: Investigate and resolve issues related to product performance, manufacturing defects, or customer complaints. Documentation: Maintain detailed records of formulations, test results, and process parameters; prepare technical reports and presentations for internal and external stakeholders. Collaboration: Work with cross-functional teams, including product managers, engineers, and sales teams, to align formulations with market needs and customer requirements. Qualifications: Education: Bachelor's or master's degree in chemistry, Polymer Science, or a related field. Experience: 5+ years of experience in polymer chemistry, preferably with vinyl or related materials. Experience with cast vinyl production is a plus. Skills: Strong knowledge of polymer chemistry, formulation techniques (DOE), material science and statistical analysis of experimental metrics. Proficiency in physical testing and analytical techniques. Familiarity with casting processes and equipment. Problem-solving skills and attention to detail. Excellent communication and teamwork abilities. Certifications: Knowledge of Six Sigma or other process improvement methodologies is a plus. Software: Proficiency in laboratory information management systems (LIMS) and data analysis tools (e.g., Excel, Minitab). Work Environment: Primarily laboratory-based with occasional work in manufacturing facilities. May require handling of chemicals and adherence to safety protocols. Full-time position with occasional travel for supplier meetings or customer support.

is for Analytical /Technical I as part of our Business Planning division. is fully onsite. Responsibilities: * Safely perform tasks for scheduling the units per procedure(s) for scheduling or order entry * Able to prioritize inventory throughout to meet customer requirements for order specifications and warehouse dates * Able to review all unit inventories at the units to cover the turns required by the 13-week plan * Able to communicate with various departments within the company to ensure the customer requirements can be met (including, but not limited to, Operations, Quality Assurance, Logistics, Customer Service, and etc.) * Required to attend regularly scheduled meetings regarding job activities (i.e. morning line-up meetings with Operations, monthly safety meetings, continuous improvement, team projects and etc.) * Able to participate in Continuous Improvement project teams Preferred Skills: * Knowledge of the Mainframe systems, Microsoft Excel, and Microsoft Outlook Company Overview Since 1901, U. S. Steel has been a recognized leader in steel production. Today, as the first North American steel company to have declared a 2050 net-zero greenhouse gas emissions goal, we remain as innovative as ever, leading transformation across our industry while continuing to make products for everyday life - from industries as far ranging as automotive, construction, containers and packaging, appliances, and energy. Underneath it all is our Culture of Caring, which shows up in our community partnerships, charitable contributions, company-sponsored employee volunteer initiatives, scholarship programs, leadership training, and much more. And of course, it takes shape in a steadfast commitment to safety first in our workplaces and respect for our employees, who are United by Steel. We are honored to have earned accolades and awards from well-regarded organizations, including the following: * Ethisphere's World's Most Ethical Companies 2022, '23, '24 * Disability: IN's Best Places to Work for Disability Inclusion 2021, '22, '23, '24 * Human Rights Campaign Foundation's Equality 100 Award 2020, '21, '22, '23-24, '25 * Military Times' Best for Vets: Employers 2023, '24 Conducting business with integrity and with the highest ethical values has underpinned U. S. Steel's success for over 100 years, and it remains critical to our company's success in the future. U. S. Steel is an Equal Opportunity Employer. It is our policy to provide equal employment opportunity (EEO) according to job qualifications without discrimination on the basis of race, color, religion, ancestry, national origin, age, genetics, sexual orientation, sex, gender identity, disability status or status as a protected Veteran or any other legally protected group status. (California residents may visit ************************ regarding collection of personal information and U. S. Steel's privacy practices.)

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

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Sterilization engineer/ Senior Microbiologist Location: Grand Rapids, MI Duration: 12+months (Possibility of extension) POSITION DESCRIPTION: Interfaces with diverse cross-functional team members to define and oversee environmental, sterilization and biocompatibility control policies to assure that Healthcare medical devices consistently comply with toxicological, microbiological and particulate contamination control requirements, standards, guidelines and industry practices, both domestic and international. POSITION RESPONSIBILITIES: · Provides microbial technical expertise during new product development activities, process modification studies and failure investigations regarding microbiological contamination control. · Serves as technical liaison with functional groups, manufacturing sites and sterilization sites. · Evaluates materials and products and recommends appropriate biocompatibility assessment to meet requirements. · Coordinates the biocompatibility testing of new products and materials. · Ensure compliance to Good Manufacturing Practices specific to Buildings, Environmental Control, Cleaning and Sanitation and Personnel Practices. · Assures compliance with all applicable international and domestic regulations and standards by defining policies and conducting regular training and assessments of all manufacturing sites. · Administers the Environmental Monitoring Program for manufacturing areas, in order to provide the necessary information (e.g., viable and non-viable particulate counts, product bio-burden, water and surface microbial levels, etc.) to ensure an appropriately controlled environment meeting regulatory expectations and industry standards. · Communicates detailed information regarding required policies and monitoring results to Manufacturing and Quality Assurance Managers. · Establishes trends; recommends revisions to monitoring program and/or manufacturing process controls. · Ensures effective corrective actions are implemented, where necessary. · Reviews and approves plant cleaning and pest/vermin control practices. · Provides microbiological technical expertise to the Facilities department regarding cleaning and contamination control. · Provides microbiological technical expertise to the Purchasing department in the selection and certification of component vendors. · Defines handling and test requirements for microbiological contamination control of vendor-supplied components as well as work-in-process inventory. · Assure timely, accurate and independent evaluation of product performance and compliance to sterilization and microbiology requirements prior to clinical studies or market release. · Support other business units' sterilization sites and microbiology labs, and act as an expert and advisor to drive improvements and changes. · Interface with validation teams and customers to determine sterilization needs. · Provides statistical support by leading creation of sterilization related metrics for improvement purposes. · Support Regulatory Affairs and other departments by providing reliability input in the evaluation of sterilization controls. · Manages EO Sterilization Validations, Out of Tolerance Investigations, Bacterial Endotoxin Testing. · Capable of working and leading cross functional team's providing microbiological and sterilization expertise. · Must have excellent knowledge of Microsoft word and excel. Statistical analysis a plus. Proficient report writing. Basic Qualifications: EDUCATION: · Bachelor of Science degree in Microbiology or related technical discipline. YEARS OF EXPERIENCE · 5+ year's industrial microbiology experience in the Medical Device or Pharmaceutical industry. SPECIALIZED KNOWLEDGE REQUIRED · thorough familiarity with FDA, EU and other international regulations, standards and guidelines covering sterilization and microbial contamination control in the manufacture of sterile medical devices. · Solid understanding of different types of sterilization methods (EtO, gamma, steam, etc.) including processes and equipment. · Proven leadership and knowledge in international and national standards such as AAMI/ANSI standards, E-Beam, ISO 17665 (Steam), 14160 (Liquid), 11137 (Radiation), 11135 (EtO) and others as applicable (i.e. EN). · Proven management and interpersonal skills. · Excellent organizational and judgment skills. · Ability to maintain and generate accurate records. Additional Information Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

**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.

Job DescriptionWhat if your lab work kept world‑class components moving? At Autocam/NN Inc., we craft high‑performance precision components and use inventive machining to push boundaries. We're looking for a Chemical Analysis Technologist who turns measurements into decisions that keep automotive production running smoothly. Why this role matters Your insight into process chemistry protects consistency, quality, and efficiency. You'll be the link between data, the Chemist's direction, and on-the-floor outcomes. How you'll contribute Continuously monitor, evaluate, and analyze chemicals that support automotive manufacturing processes. Establish and maintain required concentration levels; measure, record, and analyze results to hold operational control. Communicate findings with precise charts and graphs. Carry out project work and research assignments under the Chemist's guidance. Perform hands-on rework of parts when needed, including deburring and derusting. Test and compare cleaning chemicals to determine effectiveness. Your background Completion of at least 2 years of school toward a chemistry degree. If you enjoy applying chemistry in a production setting, collaborating across teams, and seeing immediate impact from your analysis, this is your next step.

Job Responsibilities: We are looking for an experienced quality control technician who can perform incoming inspections, handles supplier issues, scrap handling, sorting, and quality/procedure audits of production areas. • Assumes responsibility for incoming component quality inspection and related issues in production. • Assumes responsibility for finished product and sub-assembly inspection and auditing. • Use basic quality practices as well as interpret blue prints and drawings. • Handles parts with due care so as not to damage. • Processes scrap items internally as well as with outside suppliers. • Select and use appropriate gages and inspection tools. • Ability to read engineering drawings and standards. • Maintain gage calibration system. Skills and Requirements: • At least 1 year of experience in quality control. • Education Experience: A high school diploma or general education degree (GED) is required. • Mathematical Skills: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. • National background check required • Ability to read and comprehend complex instructions. • Frequently lift and/or move up to 45 pounds Benefits once hired in! • Health, Dental, Vision and Life Insurance • Short and Long Term Disability • 401K Retirement Plan • Flexible Spending Accounts • Paid Vacation & Holidays • Educational Assistance *This is a drug-free workplace. All candidates must be able to pass a pre-employment drug screen and be willing to submit to a national background check. If you're interested in this position, please apply with a complete resume and work history.*

Job DescriptionQuality Control $19.00/hour - 3rd Shift - Grand Haven, MI Are you a motivated and detail-oriented individual looking for a new opportunity? We're seeking a Quality Control to join our team in Grand Haven, MI. In this role, you'll be a vital part of our operations, helping support production by performing inspections, testing, and quality documentation for a leading powder coating manufacturer. What You'll Be DoingAs a Quality Control, your core responsibilities will include: Data Entry: Accurately record inspection and testing results into company systems. Sample Testing: Perform testing on product samples to ensure quality and compliance with specifications. Equipment Operation: Operate quality testing and lab equipment to support production needs. Lab Organization: Maintain a clean, safe, and orderly lab environment. Assist with additional quality checks and inspections as needed to support production flow. What We're Looking ForQualifications: High school diploma or GED Ability to perform confined space entry, work at heights, lift heavy objects, and complete manual labor Proficiency in Microsoft Word, Excel, and CMMS systems (such as MicroMain or SAP) Must be able to wear Personal Protective Equipment (PPE), including a respirator Skills: Technical Proficiency: Strong understanding of mechanical, electrical, and hydraulic systems to support testing and quality processes Problem Solving: Ability to identify issues and communicate findings to minimize production interruptions Attention to Detail: Ensures all work meets operational, safety, and quality standards while maintaining accurate records Why Join Us?This is an excellent opportunity for both short-term and long-term employment. We are committed to providing a supportive work environment and opportunities for growth. Workbox Staffing Benefits: Weekly Pay Hire-in Opportunities Comprehensive Benefits including Health, Life, and Dental Veteran-Friendly and Equal Opportunity Employer Ready to start? Apply online today and let's DO GOOD together!

The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally. · Performs, documents and record checks qualitative and quantitative assays on samples. · The primary technologies in this lab are HPLC and dissolution. · Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact. · Recommends and executes process improvements to continually improve laboratory performance. · High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position. · Demonstrates flexibility/agility and engagement in a changing environment. · The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples. · Ability to follow written procedures. · May train others as skills and knowledge allow. · Troubleshoot instrumentation as skills and knowledge allow. · Participates in laboratory investigations as required. · May participate in manufacturing QC support such as cleaning verification. · SHIFT HOURS: 2:00pm-10:30pm, nominally (some flexibility is allowed). Overtime may occasionally be required. EDUCATION AND EXPERIENCE · AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred. · Related experience in Quality Control is preferred but not required. · Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3 · Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail. · Job duties involve occasional lifting (less than 35 lbs). · Candidate must not be Cephalosporin/Penicillin sensitive. Full time 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.

What You Will Achieve The Rapid Turn Lab Chemist is responsible for scheduling prioritization, workload distribution, and laboratory process improvement for Rapid Turn Lab testing at the Kalamazoo site. This includes communicating priorities to the lab and following up with customers on testing status. The Chemist performs LIR supervisor duties for atypical, OOS, questionable, and invalidated data occurrences and will cover data integrity responsibilities. The Chemist represents the lab unit or the entire lab organization on moderate complexity projects and project teams both within and outside of Quality Operations. This role provides technical expertise to assist the laboratory with troubleshooting, investigations, computer validation and instrument qualifications. The chemist may be involved in second checking of data and will perform assays as needed. This role has the responsibility of serving as Management Designee and will have limited input into the OTE colleague performance assessment process. The chemist may defend QO Laboratory Quality Systems during audits and inspections. How You Will Achieve It • Leads and documents laboratory investigations for procedural deviations, atypical, OOS, questionable, and invalidated data occurrences. • Assures adherence to data integrity initiatives. • As a Subject Matter Expert (SME), represents the lab unit or the entire lab organization on high complexity projects and project teams both within and outside of QO. Leads medium or high complexity project teams within QO tasked with improving laboratory or other quality systems. • Assists QO Lab leadership in determining scheduling priorities and workload distribution to ensure customer needs are met. • Performs data quality inspection through Quality audits and 2nd check of laboratory data packets • Performs analytical assays during times of need. • Demonstrates a technical mastery of one or more techniques in fields such as: wet chemistry, chromatography, physical chemistry, or spectroscopy as well as a complete knowledge of laboratory operations including both technical and compliance aspects. • Applies knowledge of advanced techniques and procedures with recommendations and implementation of new or modified procedures or instrumentation for improved lab efficiency. • Trains others in the theory and practice of both laboratory techniques and quality systems including investigations, instrument qualifications, etc. • Independently writes SOPs, technical reports, project plans, instrument qualifications, etc. • Supports and may lead implementation of various elements of IMEx. • Performs analytical assays during times of need • Serves as management designee and will have limited input into the OTE colleague performance assessment process. Here Is What You Need (Basic qualifications) Applicant must have HS Diploma with six years of relevant experience; OR an Associate's degree with four years of experience; OR a Bachelor's degree with 0-2 years of experience Bonus Points If You Have (Preferred qualifications) Laboratory Investigation Report Author Trained to execute and record check multiple Chemistry laboratory technologies PHYSICAL/MENTAL REQUIREMENTS Job requires sitting, standing, walking, ability to type, and dexterity for handling glassware/laboratory equipment. Work Location Assignment: On Premise Last Date To Apply: January 30, 2026 The annual base salary for this position ranges from $68,600.00 to $110,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Relocation assistance may be available based on business needs and/or eligibility. Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Pfizer endeavors to make ********************** accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Quality Assurance and Control

Kalamazoo, MI, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. **Job Description** + Run basic analytical instruments such as plate readers, microplate washers, automated workstations etc. + Use low-volume laboratory liquid sample handling equipment (micropipettes) to prepare samples and solutions + Prepare analytical samples and assay reagents according to established procedures + Perform analytical techniques upon biological specimens such as qPCR, ELISAs, etc. + Determine protein levels (host cell protein, protein A) in monoclonal antibody samples + Run analytical methods, which may include HPLC, UPLC, SEC, gel electrophoresis, capillary electrophoresis, total protein analysis, amino acid analysis or similar methods + Manage samples including ensuring proper storage and handling of samples + Work with multiple scientists within the group to effectively schedule work + Perform data analysis by using instrument computer software and office applications such as Word, PowerPoint, and Excel + Analyze and interpret experimental data independently + Contribute to writing of e.g. SOPs, study reports and protocols + Write up laboratory notebooks regularly in compliance with guidelines + Order, maintain and stock lab supplies such as common reagents, primary packaging materials, gloves, cleaning agents, safety glasses etc. + Take care of general housekeeping activities such as cleaning bench spaces, processing equipment and glassware + Apply lean 5S methods to laboratory operations **Qualifications** The ideal candidate would possess: + Experience with SEC assays + Experience in handling and analyzing proteins and other macromolecules + Experience with low-volume liquid handling equipment strongly desired + Highly computer literate. Capable of quickly learning and adapting to new computer programs Basic Minimum Qualifications: + Bachelors in Chemistry or related field plus 2-3 years of industry experience OR Master's degree with academic research + **Technical laboratory experience involving analytical chemistry - academic research, internship or industrial** + **HPLC experience** + **Experience with Empower Software** + Candidates within a commutable distance of Kalamazoo, MI are encouraged to apply + Authorization to work in the United States indefinitely without restriction or sponsorship **Additional Information** + Position is full-time, Monday-Friday, first shift 8AM-5PM. Candidates currently living in a commutable distance to Kalamazoo, MI are encouraged to apply. + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays + _\#LI-EB1_ **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Sterilization engineer/ Senior Microbiologist Location: Grand Rapids, MI Duration: 12+months (Possibility of extension) POSITION DESCRIPTION: Interfaces with diverse cross-functional team members to define and oversee environmental, sterilization and biocompatibility control policies to assure that Healthcare medical devices consistently comply with toxicological, microbiological and particulate contamination control requirements, standards, guidelines and industry practices, both domestic and international. POSITION RESPONSIBILITIES: · Provides microbial technical expertise during new product development activities, process modification studies and failure investigations regarding microbiological contamination control. · Serves as technical liaison with functional groups, manufacturing sites and sterilization sites. · Evaluates materials and products and recommends appropriate biocompatibility assessment to meet requirements. · Coordinates the biocompatibility testing of new products and materials. · Ensure compliance to Good Manufacturing Practices specific to Buildings, Environmental Control, Cleaning and Sanitation and Personnel Practices. · Assures compliance with all applicable international and domestic regulations and standards by defining policies and conducting regular training and assessments of all manufacturing sites. · Administers the Environmental Monitoring Program for manufacturing areas, in order to provide the necessary information (e.g., viable and non-viable particulate counts, product bio-burden, water and surface microbial levels, etc.) to ensure an appropriately controlled environment meeting regulatory expectations and industry standards. · Communicates detailed information regarding required policies and monitoring results to Manufacturing and Quality Assurance Managers. · Establishes trends; recommends revisions to monitoring program and/or manufacturing process controls. · Ensures effective corrective actions are implemented, where necessary. · Reviews and approves plant cleaning and pest/vermin control practices. · Provides microbiological technical expertise to the Facilities department regarding cleaning and contamination control. · Provides microbiological technical expertise to the Purchasing department in the selection and certification of component vendors. · Defines handling and test requirements for microbiological contamination control of vendor-supplied components as well as work-in-process inventory. · Assure timely, accurate and independent evaluation of product performance and compliance to sterilization and microbiology requirements prior to clinical studies or market release. · Support other business units' sterilization sites and microbiology labs, and act as an expert and advisor to drive improvements and changes. · Interface with validation teams and customers to determine sterilization needs. · Provides statistical support by leading creation of sterilization related metrics for improvement purposes. · Support Regulatory Affairs and other departments by providing reliability input in the evaluation of sterilization controls. · Manages EO Sterilization Validations, Out of Tolerance Investigations, Bacterial Endotoxin Testing. · Capable of working and leading cross functional team's providing microbiological and sterilization expertise. · Must have excellent knowledge of Microsoft word and excel. Statistical analysis a plus. Proficient report writing. Basic Qualifications: EDUCATION: · Bachelor of Science degree in Microbiology or related technical discipline. YEARS OF EXPERIENCE · 5+ year's industrial microbiology experience in the Medical Device or Pharmaceutical industry. SPECIALIZED KNOWLEDGE REQUIRED · thorough familiarity with FDA, EU and other international regulations, standards and guidelines covering sterilization and microbial contamination control in the manufacture of sterile medical devices. · Solid understanding of different types of sterilization methods (EtO, gamma, steam, etc.) including processes and equipment. · Proven leadership and knowledge in international and national standards such as AAMI/ANSI standards, E-Beam, ISO 17665 (Steam), 14160 (Liquid), 11137 (Radiation), 11135 (EtO) and others as applicable (i.e. EN). · Proven management and interpersonal skills. · Excellent organizational and judgment skills. · Ability to maintain and generate accurate records. Additional Information Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Provides support in the preparation and/or manufacture of common dosage forms such as tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids; Assist in preparation of pharmaceutical dosage units, including filling, capping, labeling, and inventory Perform general laboratory unit operations such as weighing, mixing/blending, milling, compressing, dissolution testing, etc.; Run simple analytical tools such as pH measurement, osmolarity, moisture content determination, viscosity, syringeability, turbidity and/or opalescence, particle size determination, etc.; Assists with the cleaning and minor repair/adjustment of parts and equipment; Take care of general housekeeping activities and laboratory safety, such as cleaning bench space and equipment, safety walk-throughs, executing equipment calibrations, and stocking supplies such as glass ware, packaging materials, and other disposables. Qualifications Basic Minimum Qualifications: Bachelor's or Master's degree in biological sciences, chemistry or related discipline preferably with 1 to 5 years of industrial/laboratory experience Ability to work with beta-lactams including cephalosporins and penicillins Ability to develop and maintain effective, trusting work and customer relationship Experience running analytical tools such as pH measurement, osmolarity, moisture content determination, viscosity, syringeability, turbidity and/or opalescence, particle size determination, dissolution, etc Knowledge of drug degradation pathways and stabilization techniques Familiarity with scale-up and technology transfer of Pharmaceutical dosage forms. Experience preparing and/or manufacture of common dosage forms such as tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Kalamazoo, MI are encouraged to apply Excellent full-time benefits include: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holiday Yearly goal-based bonus & eligibility for merit-based increases Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Provides support in the preparation and/or manufacture of common dosage forms such as tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids; Assist in preparation of pharmaceutical dosage units, including filling, capping, labeling, and inventory Perform general laboratory unit operations such as weighing, mixing/blending, milling, compressing, dissolution testing, etc.; Run simple analytical tools such as pH measurement, osmolarity, moisture content determination, viscosity, syringeability, turbidity and/or opalescence, particle size determination, etc.; Assists with the cleaning and minor repair/adjustment of parts and equipment; Take care of general housekeeping activities and laboratory safety, such as cleaning bench space and equipment, safety walk-throughs, executing equipment calibrations, and stocking supplies such as glass ware, packaging materials, and other disposables. Qualifications Basic Minimum Qualifications: Bachelor's or Master's degree in biological sciences, chemistry or related discipline preferably with 1 to 5 years of industrial/laboratory experience Ability to work with beta-lactams including cephalosporins and penicillins Ability to develop and maintain effective, trusting work and customer relationship Experience running analytical tools such as pH measurement, osmolarity, moisture content determination, viscosity, syringeability, turbidity and/or opalescence, particle size determination, dissolution, etc Knowledge of drug degradation pathways and stabilization techniques Familiarity with scale-up and technology transfer of Pharmaceutical dosage forms. Experience preparing and/or manufacture of common dosage forms such as tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Kalamazoo , MI are encouraged to apply Excellent full-time benefits include: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holiday Yearly goal-based bonus & eligibility for merit-based increases Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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