Chemist Jobs in Madison, WI

Now Hiring: Lab Technician We are looking for a Lab Technician to join our team. This role is responsible for performing analytical testing, ensuring material quality, and supporting quality control efforts. If you have experience in laboratory testing, strong problem-solving skills, and a detail-oriented mindset, we encourage you to apply. Position Summary To determine mixed compound acceptance based on analytical tests including rheology, durometer, specific gravity, tensile, elongation, modulus and viscosity testing as defined on documented work instructions. Essential Duties/Responsibilities Run tests (rheology, durometer, specific gravity, tensile, elongation, modulus, and viscosity) to determine material properties and determine if passing according to customer requirements. Measure and add final batch chemicals to the test sample on the lab mill. Collect test results using a network of computers to generate a final test report for each batch. Document test failures, place on hold and communicate with the Quality Manager for final disposition. Responsible for product audits, as required. Support Strategic and Quality goals. Perform any other project/task as assigned by Management. Education, Skills, and Experience Requirements Associate Degree in related field, preferred. Experience may be considered in lieu of education. Two (2) years' laboratory testing experience, desired. Must have math analytical skills. Ability to work independently in support of shift priorities. Good written, verbal, and interpersonal communication skills to facilitate cross-functional results. Good computer/systems skills - MS Office (Excel/Word/PowerPoint/Outlook). Good cooperation and collaboration skills. Attention to detail, high energy, self-motivated and self-reliant. Organizational skills with the ability to handle multiple tasks and meet deadlines. Ability to interact well in a team environment with all personality types. Strong problem-solving skills. Physical Demands Physical demands for this position include the ability to sit, stand, and walk for most of the workday depending on the tasks at hand. The Associate may be required to lift up to 25 lbs. The physical demands described here are representative of those that must be met by an Associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work Environment This position will work in a lab environment, with potential for occasional visits to the production area as needed. This position has potential exposure to light dust, fumes, and noise from the production area. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Please note this job description is not designed to contain a comprehensive listing of all activities, duties, or responsibilities that are required of the Associate for this job. The employer has the right to modify essential job functions, physical demands of the job and job qualifications at any time.

OUR TEAM: The Genetic Analysis production team is a dynamic group of experts dedicated to solving problems with innovation and flexibility. We focus on maintaining the supply of nucleic acid products for forensic, academic, and clinical laboratories. Successful scientists on our team are motivated, outgoing, and enjoy working collaboratively to tackle complex challenges. We value strong communication, adaptability, and a passion for all areas of science. We are looking to build our team with scientists who share these values and who are inspired to embrace new opportunities! YOUR ROLE: As a Production Scientist on our master mix and buffer team, you will be responsible for the routine manufacturing of DNA purification and amplification solutions that support multiple product lines and customer needs. You will also collaborate with our R&D team to contribute to new product development, perform assays to ensure the quality and functionality of products, and work toward process improvements on existing products. YOUR EXPERIENCE: We are seeking a scientist with strong laboratory skills and a passion for continuous learning. The ideal candidate will be familiar with DNA purification and amplification techniques, have experience running agarose gels, handling RNA, and possess strong pipetting skills. Familiarity with PCR and an eagerness to work in a collaborative environment are key. If you are excited about science and enjoy working with others to achieve shared goals, this role is for you! CORE DUTIES: 1. Manufacture a variety of products to meet specifications and ensure timely delivery. 2. Perform assays to ensure product quality, including raw material evaluations. 3. Understand and follow quality requirements for the work area, maintaining proper documentation. 4. Assist with writing, reviewing, and revising manufacturing and QC protocols for clarity, improvements, or changes. 5. Design experiments to improve existing manufacturing and QC processes. 6. Support project plans and experimental design, providing data to others and assisting with implementation. 7. Contribute technical support to product improvement or development teams, interacting with Marketing, QA, and R&D as needed. 8. Promote inclusion, ensuring a safe and respectful workspace. 9. Embrace Promega's Emotional & Social Intelligence (ESI) principles in daily work. 10. Comply with all ethical, legal, and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. A.D., B.S., or M.S. in a scientific discipline (e.g. Biochemistry, Biotechnology, Molecular Biology, Microbiology) with 3+ years of postgraduate lab experience. 2. Documented record of experimental design and problem-solving relevant to this role. 3. Strong organizational, interpersonal, and communication skills. 4. Ability to interpret and communicate scientific results effectively within a team. 5. Proficiency with Microsoft Office applications. PREFERRED QUALIFICATIONS: 1. Industry experience. 2. Familiarity with ISO 9001 or cGMP Quality System requirements. 3. Experience with experimental data collection and analysis. 4. Self-starter with creativity and initiative to meet position requirements. PHYSICAL DEMANDS: 1. Ability to work at a laboratory bench for extended periods. 2. Comfortable handling hazardous materials while ensuring safety. 3. Use of standard laboratory protective equipment. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us. In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Responsibilities include, but are not limited to, the following: * Applies GMP/ GLP in all areas of responsibility, as appropriate * Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines * Learns how to document work and maintains study documentation and laboratory records * Learns how to use laboratory equipment and software appropriate for assigned tasks * Attends and participates in project meetings * Learns to perform peer review of data * Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments * Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members * Performs other related duties as assigned The ideal candidate would possess: * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team * Self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications * Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) * Authorization to work in the United States indefinitely without restriction or sponsorship * May work with potentially hazardous materials * Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) * Overtime and weekend work as required * Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top * Work requires use of PPE (personal protective equipment) Additional Information What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison, Inc is growing and we're looking for amazing team members to join us. We conduct food Chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation and analytical technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of instruments and techniques! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Analyzes samples and/or develops/validates methodologies for various compounds and components in compliance with SOPs and regulatory agency guidelines Principal Contacts and Scope of Communications Internal: Interacts with, internal clients and support groups, operational personnel, scientific personnel and department management External: Contact with external clients with guidance from scientific or management staff regarding experiment design and outcome. May contact vendors regarding troubleshooting and setup of equipment over the phone or on site Essential Duties and Responsibilities: Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Organizes, conducts and evaluates analytical results and testing independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines Documents work and maintains study documentation and laboratory records Independently uses and performs basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while performing routine and non-routine maintenance Provides input and participates in project meetings, plans, monitors and guides project work Performs peer review and QC review of data Performs assigned workload on a daily basis and effectively completes multiple assignments. Promotes and contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members. Maintains a clean and safe laboratory work environment Understands data generated, and history of methods. Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems. Identifies problems, determines appropriate actions, and implements solutions with support or independently as appropriate. Able to adapt to new procedures or particular needs as directed. Able to identify critical steps in an assay. Drives and implements process improvement initiatives Completes all required training courses. Trains and assists less experienced staff Assists in setting up and performing optimization and validation of various analytes in a variety of matrices Participates in client visits or calls as needed and assists in communicating technical information Assists in writing reports, methods, protocols and SOPs, and make suggestions for modifications in test methods and procedures. Knowledge of departmental procedures and policies Effectively plans and utilizes personnel and resources for timely completion of assigned projects May plan, monitor, or guide non-routine work within their team Viewed as a resource across multiple teams Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required 3+ years of related experience Bachelor's Degree in relevant field (Laboratory experience may be substituted for degree) Familiar with the use of standard laboratory equipment Experience with use and troubleshooting of analytical equipment is desired Basic knowledge of computers and software programs Bachelor's Degree in relevant field (Laboratory experience may be substituted for degree) Additional Information May work with potentially hazardous substances and/or radio labeled materials Mandatory immunizations and screening as required Expected to understand the process for handling hazardous wastes and receive on-the-job training for handling specific waste types in their job area. Will be exposed to food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.) Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top. Work requires use of PPE (personal protective equipment). Overtime and weekend work as required Will be exposed to potential food allergens. What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us. In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Responsibilities include, but are not limited to, the following: Applies GMP/ GLP in all areas of responsibility, as appropriate Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Learns how to document work and maintains study documentation and laboratory records Learns how to use laboratory equipment and software appropriate for assigned tasks Attends and participates in project meetings Learns to perform peer review of data Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members Performs other related duties as assigned The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Pay: 21/hr + 12% shift differential Qualifications Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) Authorization to work in the United States indefinitely without restriction or sponsorship May work with potentially hazardous materials Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) Overtime and weekend work as required Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top Work requires use of PPE (personal protective equipment) Additional Information What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Interested in contributing to improving and saving lives? Eurofins Food Microbiology is growing and we're looking for amazing team members to join us. We conduct food Microbology testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation and analytical technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of instruments and techniques! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Analyzes samples and/or develops/validates methodologies for various compounds and components in compliance with SOPs and regulatory agency guidelines Principal Contacts and Scope of Communications * Internal: Interacts with, internal clients and support groups, operational personnel, scientific personnel and department management * External: Contact with external clients with guidance from scientific or management staff regarding experiment design and outcome. May contact vendors regarding troubleshooting and setup of equipment over the phone or on site Essential Duties and Responsibilities: * Demonstrates and promotes the company vision * Regular attendance and punctuality * Applies GMP/GLP in all areas of responsibility, as appropriate * Organizes, conducts and evaluates analytical results and testing independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines * Documents work and maintains study documentation and laboratory records * Independently uses and performs basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while performing routine and non-routine maintenance * Provides input and participates in project meetings, plans, monitors and guides project work * Performs peer review and QC review of data * Performs assigned workload on a daily basis and effectively completes multiple assignments. * Promotes and contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members. * Maintains a clean and safe laboratory work environment * Understands data generated, and history of methods. * Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems. * Identifies problems, determines appropriate actions, and implements solutions with support or independently as appropriate. * Able to adapt to new procedures or particular needs as directed. * Able to identify critical steps in an assay. * Drives and implements process improvement initiatives * Completes all required training courses. * Trains and assists less experienced staff * Assists in setting up and performing optimization and validation of various analytes in a variety of matrices * Participates in client visits or calls as needed and assists in communicating technical information * Assists in writing reports, methods, protocols and SOPs, and make suggestions for modifications in test methods and procedures. * Knowledge of departmental procedures and policies * Effectively plans and utilizes personnel and resources for timely completion of assigned projects * May plan, monitor, or guide non-routine work within their team * Viewed as a resource across multiple teams * Conducts all activities in a safe and efficient manner * Performs other duties as assigned Qualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required * 3+ years of related experience * Bachelor's Degree in relevant field (Laboratory experience may be substituted for degree) * Familiar with the use of standard laboratory equipment * Experience with use and troubleshooting of analytical equipment is desired * Basic knowledge of computers and software programs * Bachelor's Degree in relevant field (Laboratory experience may be substituted for degree) Additional Information * May work with potentially hazardous substances and/or radio labeled materials * Mandatory immunizations and screening as required * Expected to understand the process for handling hazardous wastes and receive on-the-job training for handling specific waste types in their job area. * Will be exposed to food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.) * Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top. * Work requires use of PPE (personal protective equipment). * Overtime and weekend work as required * Will be exposed to potential food allergens. What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API's) according to current Good Manufacturing Practice (cGMP) requirements. The role of Production Scientist, Associate is a lab based role primarily focused on executing required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment. Essential Job Functions: * Function as a Primary Operator for a single group of GMP Production areas (i.e. Kilo Labs). * Draft preliminary reports detailing deviations from written procedures and potential contributing factors. * Utilize and provide minor updates to a variety of written procedures, including operating procedures with assistance from a supervisor or SME. * Help to identify and immediately correct equipment, process, and safety issues in the lab. * Mentor new employees by performing supplemental technical and on the job training. * Participate in a team-based, multi-shift manufacturing environment by actively engaging in inter-shift communication and maintaining high quality in-lab housekeeping. * Take independent ownership over a departmental support responsibility. * Engage in personal and professional career development through active participation in development objectives. * Provide departmental support through additional tasks as directed by department leadership. Who You Are Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science * Ability to read and understand written protocols * Effective oral and written communication skills * Able to stand for long periods of time * Must be able to lift and move up to 50 pounds with the assistance of equipment or teammates as necessary * Must be willing to work with highly potent / hazardous materials * Able to utilize proper personal protective equipment which could include but is not limited to: * Respiratory protection (dust masks, half/full face respirators, supplied air, etc) * MilliporeSigma issued work uniforms * Lab Coats * Full body protection (disposable coveralls, hazmat suits, etc.) Preferred Qualifications: * Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.) * Possess a high degree of internal motivation * Ability to multi-task while paying close attention to detail * Mechanical and technical aptitude * Strong mathematical skills * Able to operate hand tools, calculators, and weighing / measuring devices What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Your role: The Associate Production Scientist is a critical role in the safe and efficient manufacturing of APIs according to cGMP requirements. Kilo Lab and Pilot Plant manufacturing of APIs and intermediates Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines Working in a team environment, and being an effective member of a project team (PD through Production) Effectively operating production equipment Maintaining the safety and cleanliness of production areas and all related equipment during each shift, specifically potent compound handling techniques Providing support to the Managers and other team members, under a multi-shift manufacturing environment Authoring and utilizing a wide variety of written procedures, including batch records and OP's with assistance from a supervisor. Maintaining accurate and concise cGMP records as a primary or secondary operator Responsible for keeping inventory up to date during each shift, and purchasing raw materials for assigned projects Working on problems of limited scope in which analysis of a situation or data requires a review of identifiable factors Adhering to SAFC ethical and behavioral standards as outlined in the employee handbook Striving to be a role model for other employees through superb work habits and excellent occupational behavior May wear respirators, Saranex and/or Tyvek suits, and other personal protective equipment when handling highly potent/hazardous materials Who you are: Minimum Qualifications: Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science or, High School Diploma or GED equivalent 4+ years of pharmaceutical, chemical, or related production manufacturing experience Preferred Qualifications: Multi-tasking while paying close attention to detail Strong computer literacy Possess a high degree of motivation and are a self-starter

Our client, a leading organization in the food chemistry industry, is seeking an Associate Analytical Chemist to join their team. As an Associate Analytical Chemist, you will be part of a dynamic laboratory environment supporting innovative testing solutions. The ideal candidate will have strong computer skills, excellent communication abilities, and a keen attention to detail which will align successfully in the organization. **Job Title:** Associate Analytical Chemist **Location:** Madison, WI **Pay Range:** $21/hr **What's the Job?** + Applies GMP/GLP in all areas of responsibility, as appropriate. + Conducts routine analyses independently and in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. + Documents work and maintains study documentation and laboratory records. + Uses laboratory equipment and software appropriate for assigned tasks. + Participates in project meetings and performs peer review of data. **What's Needed?** + Bachelor's Degree in a relevant field (laboratory experience may be substituted for a degree). + Authorization to work in the United States indefinitely without restriction or sponsorship. + Ability to work with potentially hazardous materials and exposure to potential food allergens. + Strong organizational skills and ability to plan assigned workload effectively. + Self-motivation, adaptability, and a positive attitude. **What's in it for me?** + Opportunity to develop expertise on a wide variety of analytical instruments. + Innovative and collaborative team environment. + Exceptional career prospects in a growing company. + Training and development opportunities. + Potential for overtime and weekend work as required. **Upon completion of waiting period associates are eligible for:** + Medical and Prescription Drug Plans + Dental Plan + Supplemental Life Insurance + Short Term Disability Insurance + 401(k) If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! **About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells** _ManpowerGroup (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent. 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.

The Chemist will be responsible for executing existing validation and optimization efforts in the QC lab. The chemist will perform and document validation methods for both GC and LC instrumentation per SOPs, documenting per GDPs, and meeting all requirements of the QMS. While the focus will be on LC and GC, training will be provided on additional techniques like KF and ICPMS if needed. Responsibilities * Prepare samples and execute existing validation methods for existing compounds using LC and GC analysis. * Optimize existing methods where possible. * Capture and document all test method data in accordance with cGMPs. * Prepare technical reports consistent with QMS requirements. Required Qualifications * BS in Chemistry or Life Science Discipline * 2 years minimum experience running sample analysis via GC and/or LC in a GMP/FDA regulated environment. * Ability to articulate examples of performing LC and the process, including sample preparation and instrument use. * Understanding of basic instrument troubleshooting. * Sound understanding of validation parameters. * Comfortable working with a respirator, including PAPR. Pay and Benefits The pay range for this position is $23.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Apr 11, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our location in Madison, WI is currently looking to hire a full-time, entry-level Chemistry Technician. (40 hours/week plus benefits included) We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $20 - 22. D.O.E. plus a competitive benefits package. Monday - Friday 8am - 5pm w/rotating Saturdays Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of chemical analysis and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

**Why People choose to work at Labcorp:** At Labcorp, it is our people that make us great - it's what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends. **We have an excellent career opportunity for a 3rd Shift Study Technician to join our Dose Formulation team in Madison, WI.** **Position Summary:** As part of the Dose Formulations team you will learn to perform and document techniques used in preparing materials for dose administration in compliance with appropriate SOPs, GLPs, and regulatory guidelines. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions and capsules according to study protocols. **Education/Experience:** + Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field + No experience required **Essential Duties:** + Collect and record applicable hand and computer generated data in accordance with protocol, SOPs, and GLPs. + Perform study calculations and specific techniques for test material formulation. + Learns study set up and management, data organization, QA audit response, internal and external client communication skills, and quality check procedures. + Learns the process of disposition of samples from prepared dose materials + Learns the process of formulation verification and storage of prepared test materials. + Learns procedures for safe handling of test materials. + Maintains a clean and safe work environment. + Learns to recognize deviations from normal results and informs Study Director, Principal Investigator, Formulations Coordinator and/or management of any problems and/or deviations that may affect the integrity of the data. + Reports all animal care concerns and becomes involved in the resolution and appropriate corrective action, when necessary. + Learns to plan assigned workload on a daily basis and effectively schedules multiple assignments. **How you will be rewarded:** + **Pay rate:** $23/hr. plus 12% shift differential + **Shift:** 3rd (3:00am-11:45am) **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here (************************************************************** . **Labcorp is proud to be an Equal Opportunity Employer:** As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site (**************************************************** or contact us at Labcorp Accessibility (Disability_*****************) . For more information about how we collect and store your personal data, please see our Privacy Statement (************************************************* .

Why People choose to work at Labcorp: At Labcorp, it is our people that make us great - it's what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends. We have an excellent career opportunity for a 3rd Shift Study Technician to join our Dose Formulation team in Madison, WI. Position Summary: As part of the Dose Formulations team you will learn to perform and document techniques used in preparing materials for dose administration in compliance with appropriate SOPs, GLPs, and regulatory guidelines. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions and capsules according to study protocols. Education/Experience: Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field No experience required Essential Duties: Collect and record applicable hand and computer generated data in accordance with protocol, SOPs, and GLPs. Perform study calculations and specific techniques for test material formulation. Learns study set up and management, data organization, QA audit response, internal and external client communication skills, and quality check procedures. Learns the process of disposition of samples from prepared dose materials Learns the process of formulation verification and storage of prepared test materials. Learns procedures for safe handling of test materials. Maintains a clean and safe work environment. Learns to recognize deviations from normal results and informs Study Director, Principal Investigator, Formulations Coordinator and/or management of any problems and/or deviations that may affect the integrity of the data. Reports all animal care concerns and becomes involved in the resolution and appropriate corrective action, when necessary. Learns to plan assigned workload on a daily basis and effectively schedules multiple assignments. How you will be rewarded: Pay rate: $23/hr. plus 12% shift differential Shift: 3rd (3:00am-11:45am) Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

OUR TEAM: The Protein Purification Team at Promega is dedicated to manufacturing proteins critical to our life science products, which are instrumental in enhancing global health. Our team thrives in a state-of-the-art facility that supports cutting-edge research and development. We foster an inclusive and supportive environment where every team member's contributions are valued. We are committed to maintaining a healthy work-life balance, understanding that our team's well-being is essential to our success. If you are a highly motivated scientist, attentive to detail, enjoy facing challenges, and thrive in a collaborative team setting, you could be an excellent fit for our dynamic production environment. YOUR ROLE: As a vital member of our Protein Purification Team, you will engage in the manufacture of a diverse array of proteins essential to Promega's broad product portfolio. Your role will involve conducting meticulous QC assays to verify that these proteins adhere to stringent quality specifications and perform effectively. In addition to your core manufacturing duties, you will collaborate with multidisciplinary teams to identify and resolve production challenges, drive process enhancements, and contribute to the launch of innovative new products. This role offers a unique opportunity to directly impact both the quality of our products and the efficiency of our processes, ensuring that we continue to meet the evolving needs of the communities we serve. CORE DUTIES: 1. Manufactures a variety of products to meet product specifications. Follows production schedules to ensure on-time delivery of finished product. 2. Performs assays to ensure that products meet existing quality control requirements. This includes evaluation of raw materials when necessary. 3. Understands quality requirements that relate to work area. Demonstrates good documentation practices and consistently produces quality products and documentation. Follows existing policies for data recording and record keeping. 4. Assists with writing, reviewing, and revising manufacturing and QC protocols for clarity, appropriate technical content, process improvements, scale-up, and/or raw material changes. 5. Designs experiments to problem solve and improve existing manufacturing and QC processes. 6. Assists with and follows project plans and experimental design with assistance. Provides data or information to others in work area and assists in implementation activities for own products. 7. May assist on multidisciplinary product improvement or development teams by providing information and technical support to meet team goals. Interacts as needed with Marketing, QA, and R&D personnel to identify customer requirements for new products and process improvements. 8. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 9. Embraces and is open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 10. Understands and complies with ethical, legal, and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. A.D., B.S., or M.S. degree in a scientific discipline (e.g. Biochemistry, Biotechnology, Molecular Biology, Microbiology). Degree and 3+ years of postgraduate lab experience in industrial manufacturing operations as reflected in a proven record of accomplishment in the Core Duties of this position are used to determine qualification. 2. Documented record of accomplishment in experimental design and problem solving relevant to this position. 3. Documented record of organizational and multi-tasking skills; ability to effectively work on several projects and/or products. 4. Ability to interpret and communicate scientific results and interact productively with others on the team. 5. Strong organizational, interpersonal, written, and verbal communication skills. 6. Ability to use a computer/Microsoft Office applications. PREFERRED QUALIFICATIONS: 1. Prior industry experience. 2. Experience with ISO 9001 or cGMP Quality System requirements (e.g. complaint investigation, nonconformance, change control). 3. Experience with use of computers for collection and analysis of experimental data. 4. Is a self-starter, creative, and capable of initiating and implementing methods to accomplish the requirements of this position. PHYSICAL DEMANDS: 1. Ability to work at a laboratory bench for extended periods of time. 2. Ability to work with hazardous materials (e.g. chemicals, radioactivity, electrical equipment) so as not to endanger oneself or others. 3. Ability to use standard laboratory protective equipment. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us. In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Responsibilities include, but are not limited to, the following: Applies GMP/ GLP in all areas of responsibility, as appropriate Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Learns how to document work and maintains study documentation and laboratory records Learns how to use laboratory equipment and software appropriate for assigned tasks Attends and participates in project meetings Learns to perform peer review of data Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members Performs other related duties as assigned The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) Authorization to work in the United States indefinitely without restriction or sponsorship May work with potentially hazardous materials Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) Overtime and weekend work as required Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top Work requires use of PPE (personal protective equipment) Additional Information What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us. In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Responsibilities include, but are not limited to, the following: * Applies GMP/ GLP in all areas of responsibility, as appropriate * Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines * Learns how to document work and maintains study documentation and laboratory records * Learns how to use laboratory equipment and software appropriate for assigned tasks * Attends and participates in project meetings * Learns to perform peer review of data * Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments * Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members * Performs other related duties as assigned The ideal candidate would possess: * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team * Self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Pay: 21/hr + 12% shift differential Qualifications * Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) * Authorization to work in the United States indefinitely without restriction or sponsorship * May work with potentially hazardous materials * Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) * Overtime and weekend work as required * Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top * Work requires use of PPE (personal protective equipment) Additional Information What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Associate Production Scientist- Weekend Night Shift in Madison, WI is primarily focused on safe and efficient manufacturing of active pharmaceutical ingredients (API's) according to current Good Manufacturing Practice (cGMP) requirements. This role is lab-based and primarily focused on executing required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment. Additional responsibilities include: * B Shift: Rotating shift, Thursday - Sunday 6:30am - 7:00pm, then Friday - Sunday 6:30am - 7:00pm * Demonstrating proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. * Functioning as a Primary Operator for a single group of GMP Production areas (i.e. Kilo Labs). * Draft preliminary reports detailing deviations from written procedures and potential contributing factors. * Utilize and provide minor updates to a variety of written procedures, including operating procedures with assistance from a supervisor or SME. * Help to identify and immediately correct equipment, process, and safety issues in the lab. * Mentor new employees by performing supplemental technical and on the job training. * Participate in a team-based, multi-shift manufacturing environment by actively engaging in inter-shift communication and maintaining high quality in-lab housekeeping. * Take independent ownership over a departmental support responsibility. * Engage in personal and professional career development through active participation in development objectives. * Provide departmental support through additional tasks as directed by department leadership. Physical Attributes: * Working with highly potent / hazardous materials * Standing for long periods of time * Lifting and moving up to 50 pounds with the assistance of equipment or teammates * Utilizing proper personal protective equipment which could include but is not limited to; respiratory protection such as dust masks, half/full face respirators, supplied air, etc., and full body protection such as disposable coveralls, hazmat suits, etc., MilliporeSigma issued work uniforms and Lab Coats Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering, or other Life Science discipline Preferred Qualifications: * Ability to read and understand written protocols. * Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.) * Effective oral and written communication skills * Mechanical and technical aptitude * Able to operate hand tools, calculators, and weighing / measuring devices * Strong mathematical skills * Possess a high degree of internal motivation * Ability to multi-task while paying close attention to detail What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our location in Madison, WI is currently looking to hire a full-time, entry-level Chemistry Technician. (40 hours/week plus benefits included) We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website to learn more about what we do at ******************* Compensation: Starting hourly rates $20 - 22. D.O.E. plus a competitive benefits package. Monday - Friday 8am - 5pm w/rotating Saturdays Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of chemical analysis and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences. SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

OUR TEAM: The Fermentation Team at Promega is responsible for cultivating microbial systems that drive the production of essential biomolecules for our life science products. We work in a well-equipped facility designed to support reliable, scalable fermentation processes that ensure high-quality output. Our team values collaboration, precision, and continuous improvement, striving to optimize fermentation techniques and maintain robust production workflows. We foster an inclusive and supportive environment where every team member's contributions are valued. Understanding the importance of work-life balance, we encourage a healthy and sustainable approach to success. If you are a detail-oriented scientist who thrives in a hands-on, team-based setting, we invite you to join us in driving fermentation excellence. YOUR ROLE: As a key member of our Fermentation Team, you will be responsible for executing fermentation production runs to support Promega's diverse product portfolio. Your primary focus will be on operating and monitoring bioreactors, preparing media, inoculating cultures, and maintaining strict process controls to ensure consistent, high-quality yields. You will perform in-process sampling and analytical assays to verify fermentation performance and product quality. Additionally, you will assist with troubleshooting production challenges and work closely with cross-functional teams to ensure smooth handoffs between fermentation and downstream processing. This role offers an excellent opportunity to develop hands-on experience in microbial fermentation while contributing to the reliable supply of critical biomolecules. CORE DUTIES: 1. Manufactures a variety of products to meet product specifications. Follows production schedules to ensure on-time delivery of finished product. Understands basic laboratory concepts and performs basic laboratory techniques. 2. Performs assays to ensure that products meet existing quality control requirements. May require supervision to determine +/- passing results. 3. Follows the quality requirements that relate to work area. Demonstrates good documentation practices and consistently produces quality products and documentation. Follows existing policies for data recording and record keeping. 4. Participates in and follows project plans and experimental design with assistance. Provides data or information to others in work area and assists in implementation activities for own products. 5. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 6. Embraces and is open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 7. Understands and complies with ethical, legal, and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. A.D. or B.S. degree in a scientific discipline (e.g. Biochemistry, Biotechnology, Molecular Biology, Microbiology). May have 0-3 years of related experience. 2. Familiar with basic principles of documentation using either laboratory notebook or batch record. 3. Ability to use a computer/Microsoft Office applications. PREFERRED QUALIFICATIONS: 1. Prior industry experience. 2. Familiarity with ISO 9001 or cGMP Quality System requirements (e.g. complaint investigation, nonconformance, change control). 3. Experience with use of computers for collection and analysis of experimental data. 4. Is a self-starter, creative, and capable of initiating and implementing methods to accomplish the requirements of this position. PHYSICAL DEMANDS: 1. Ability to work at a laboratory bench for extended periods of time. 2. Ability to work with hazardous materials (e.g. chemicals, radioactivity, electrical equipment) so as not to endanger oneself or others. 3. Ability to use standard laboratory protective equipment. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.