Microbiologist jobs in Madison, WI

QC Technician 3rd Shift Tuesday - Saturday To accomplish daily Quality Control lab tasks through participation as a member of the Quality Control team. NATURE OF WORK To accomplish daily Quality Control lab tasks through participation as a member of the Quality Control team. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: * Adhere to all quality systems including, but not limited to, ISO 9001 and Food Safety, with an understanding of DuPont's Quality Policy and procedures. * Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. * Understand and follow procedures of the department for the proper calibration and use of the department's equipment. * Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products * Perform environmental sampling procedures. * Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES * Must have bachelor's degree in Chemistry, Microbiology, Biology or similar field, or associate degree with at least 2 years' relevant experience. * Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. * Must have the ability to work as an active team member as well as independently. * Must have strong math and good communication skills (both verbal and written). We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. • Perform routine Environmental Monitoring of the classified clean rooms • Monitor classified clean rooms during manufacturing operations, must gown qualify • Sample and test the Water for Injection System, USP Purified Water systems and Clean Steam systems; perform and document plate reads for all environmental and utility testing with minimal supervision • Write and execute protocols/experiments/SOPs under limited supervision • Reviews work of peers and SOP document changes under limited supervision • May assist senior staff in preparation of investigations, reports and execution of complex protocols • Visual inspection of media fill vials and plates • Perform general lab maintenance/housekeeping • Training of staff in routine processes • Other duties as assigned Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions. • Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear • Ability to sit or stand for prolonged periods of time • Must be able to walk and drive between locations • Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves • Must be able to occasionally lift and/or move up to 50 pounds • Must pass eye exam • Comfortable with working/handling of hazardous materials • Follow written instructions. Perform independent troubleshooting of common issues. • Able to work in a highly complex environment with competing demands and priorities Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear. • Ability to sit or stand for prolonged periods of time. • Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. • Must be able to occasionally lift and/or move up to 25 pounds. • Follow written instructions. Perform independent troubleshooting of common issues. Provide expertise for response to complex issues. • Able to work in a highly complex environment with competing demands and priorities. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • High School Diploma required. BS/BA degree in Microbiology or related scientific field preferred. • 3-5 years' experience in a cGMP environment. Two years of experience may be replaced by Associates/Non- Scientific Bachelor's degree. Four years of experience may be replaced with BS/BA degree in Microbiology or related scientific field. • Detail oriented • Ability to multi-task • Ability to gown to work in an ISO-5 environment • Ability to work varied hours as required by the production schedule #LI - LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. **Summary of Objective:** Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. **Essential Duties and Responsibilities:** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. - Perform routine Environmental Monitoring of the classified clean rooms - Monitor classified clean rooms during manufacturing operations, must gown qualify - Sample and test the Water for Injection System, USP Purified Water systems and Clean Steam systems; perform and document plate reads for all environmental and utility testing with minimal supervision - Write and execute protocols/experiments/SOPs under limited supervision - Reviews work of peers and SOP document changes under limited supervision - May assist senior staff in preparation of investigations, reports and execution of complex protocols - Visual inspection of media fill vials and plates - Perform general lab maintenance/housekeeping - Training of staff in routine processes - Other duties as assigned **Special Demands:** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions. - Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear - Ability to sit or stand for prolonged periods of time - Must be able to walk and drive between locations - Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves - Must be able to occasionally lift and/or move up to 50 pounds - Must pass eye exam - Comfortable with working/handling of hazardous materials - Follow written instructions. Perform independent troubleshooting of common issues. - Able to work in a highly complex environment with competing demands and priorities **Work Environment:** The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear. - Ability to sit or stand for prolonged periods of time. - Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. - Must be able to occasionally lift and/or move up to 25 pounds. - Follow written instructions. Perform independent troubleshooting of common issues. Provide expertise for response to complex issues. - Able to work in a highly complex environment with competing demands and priorities. **Qualifications:** The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - High School Diploma required. BS/BA degree in Microbiology or related scientific field preferred. - 3-5 years' experience in a cGMP environment. Two years of experience may be replaced by Associates/Non- Scientific Bachelor's degree. Four years of experience may be replaced with BS/BA degree in Microbiology or related scientific field. - Detail oriented - Ability to multi-task - Ability to gown to work in an ISO-5 environment - Ability to work varied hours as required by the production schedule **\#LI - LL1** Join us and be part of building the bridge between life changing therapies and patients. Let's talk future (***************** **Equal Employment Opportunity (EEO) Statement:** _PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._ _At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

Join our Phase I Clinical Research Unit and gain hands-on experience in clinical trials. Work closely with nurses and coordinators to support study procedures and ensure participant safety. Key Responsibilities: * Perform vital signs, ECGs, and venipuncture. * Collect, process, and distribute biological samples per protocol. * Monitor participant meals for dietary compliance. * Prepare rooms and equipment for study procedures. * Accurately document research data and maintain confidentiality. * Assist with screening and quality control of study documents. * Ensure participant safety and respond to inquiries promptly. Requirements * High School Diploma required; CNA, Medical Assistant, EMT, or Bachelor's in Science/Healthcare preferred. * 0-2 years of experience in healthcare, science, or research. * Phlebotomy experience strongly preferred. * Knowledge of FDA, ICH, and GCP guidelines is a plus. Job Type & Location This is a Contract to Hire position based out of Madison, WI. Pay and Benefits The pay range for this position is $23.00 - $23.00/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 Dec 16, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Our staff members are committed to making a difference in our organization, for our client partners and the patients we serve. We seek individuals with proven competencies and strong character to help lead our organization now and into the future. Our interns receive **professional** **mentorship** **and leadership** **development** **opportunities** to support future career growth with us. Whether you're looking to come back as a repeat intern, transition into one of our Leadership Development Programs, or pursue a full-time position post-graduation, our team is here to support your next step! **How** **will** **you** **make** **an** **impact?** Our interns are matched to projects based on their abilities and current business needs. All projects will have significant strategic and/or operating importance to the business to which they are assigned. Summer projects may include the following responsibilities: + Completes the formulation of reagents and solutions in a fast-paced manufacturing environment following controlled documents and procedures. + Apply specialized technical knowledge and skills to make detailed observations and analyze data within operating parameters. Actively participate in troubleshooting for specific processes or activities as assigned. + Maintain equipment, product inventory, and related records as assigned. Note variances on manufacturing documents; audit and evaluate process documents and propose revisions. + Identify manufacturing procedures intended to optimize existing processes and ensure compliance with regulatory requirements. + Inform the team lead/supervisor of factors that may affect quality of the product, initiate problem reports for deviations and non-conforming materials and suggest options and ideas for corrective actions and preventive actions (CAPA). + May support or assist in the review in the peer review of daily work orders to ensure compliance, accuracy and quality. + Satisfactorily complete Thermo Fisher Scientific training requirements on time and operate within all ISO, GMP, and FDA standards pertaining to Frederick Site Manufacturing Operations. + May be required to perform other related duties as required and/or assigned **Start Date:** This internship is set to begin on either May 11th or June 15th, 2026 for a duration of 10-12 weeks - dependent upon student availability per academic calendars. **Compensation & Relocation:** Our undergraduate Engineering internships offer an hourly rate between $21.50 - $28.75 dependent upon the location you are supporting (aligned to respective cost-of-living guidelines). Additionally, a relocation stipend is offered in the amount of $5,000 if necessary. Student must be located 50+ miles away from the physical location of the internship to be eligible for the relocation stipend. **How** **will** **you** **get** **here?** + Undergraduate student completing a Biology or Chemistry related degree between December 2026 and June 2027. + 0 years of work experience required; previous related internships preferred. + Consistenttrackrecord of results demonstrating integrity,innovation,involvement, and intensity. + Energized through championing change, driven in getting results, and savvy in navigating ambiguity. + Excellent interpersonalcommunicationskills with a high degree of emotionalintelligence. If this sounds like you, we'd love to hear from you! **To qualify, applicants must be legally authorized to work in the United States and should not require sponsorship (current or future) for employment visa status. Thermo Fisher does not offer employment in this position to holders of F-1, J-1, H-1, OPT, and CPT Visas for the** **purpose** **of** **obtaining** **practical experience.** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. * Perform routine Environmental Monitoring of the classified clean rooms * Monitor classified clean rooms during manufacturing operations, must gown qualify * Sample and test the Water for Injection System, USP Purified Water systems and Clean Steam systems; perform and document plate reads for all environmental and utility testing with minimal supervision * Write and execute protocols/experiments/SOPs under limited supervision * Reviews work of peers and SOP document changes under limited supervision * May assist senior staff in preparation of investigations, reports and execution of complex protocols * Visual inspection of media fill vials and plates * Perform general lab maintenance/housekeeping * Training of staff in routine processes * Other duties as assigned Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions. * Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear * Ability to sit or stand for prolonged periods of time * Must be able to walk and drive between locations * Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves * Must be able to occasionally lift and/or move up to 50 pounds * Must pass eye exam * Comfortable with working/handling of hazardous materials * Follow written instructions. Perform independent troubleshooting of common issues. * Able to work in a highly complex environment with competing demands and priorities Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear. * Ability to sit or stand for prolonged periods of time. * Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. * Must be able to occasionally lift and/or move up to 25 pounds. * Follow written instructions. Perform independent troubleshooting of common issues. Provide expertise for response to complex issues. * Able to work in a highly complex environment with competing demands and priorities. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * High School Diploma required. BS/BA degree in Microbiology or related scientific field preferred. * 3-5 years' experience in a cGMP environment. Two years of experience may be replaced by Associates/Non- Scientific Bachelor's degree. Four years of experience may be replaced with BS/BA degree in Microbiology or related scientific field. * Detail oriented * Ability to multi-task * Ability to gown to work in an ISO-5 environment * Ability to work varied hours as required by the production schedule #LI - LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Research Internships at Microsoft provide a dynamic environment for research careers with a network of world-class research labs led by globally-recognized scientists and engineers, who pursue innovation in a range of scientific and technical disciplines to help solve complex challenges in diverse fields, including computing, healthcare, economics, and the environment. Gray Systems Lab (GSL) is an applied research lab under Azure Data. We do research and development for databases, big-data, and cloud systems, working in close collaboration with product teams to design innovative solutions for real-world problems. We focus on a variety of exciting areas, including machine learning for systems, reinforcement learning finetuning and post-training techniques, natural language-to-query, agentic workflows, resource management, query optimization and execution. We also work on workload optimization, graph analytics, data storage formats and governance, modern/future hardware (e.g., GPU, NVM and FPGAs), program analysis, and data provenance. Our work covers both internal both Microsoft internal and open-source systems, such as Fabric, Spark, SQL Server, MySQL, Apache Iceberg, and more. We provide opportunities to work on ideas from internal collaborations, as well as external ones with partner universities, and to continue to be an active scholar in the research community. We are looking for highly motivated graduate students who are interested in cutting edge research in close collaboration with advanced industry product groups. Past Research Internships have resulted in a combination of impact on production systems and publications at top conferences. Applicants should demonstrate a track record in one or more systems, database, or data science topics and an aptitude for hands-on system building and design methodology to run and analyze experiments at scale. Responsibilities Research Interns put inquiry and theory into practice. Alongside fellow doctoral candidates and some of the world's best researchers, Research Interns learn, collaborate, and network for life. Research Interns not only advance their own careers, but they also contribute to exciting research and development strides. During the 12-week internship, Research Interns are paired with mentors and expected to collaborate with other Research Interns and researchers, present findings, and contribute to the vibrant life of the community. Research internships are available in all areas of research, and are offered year-round, though they typically begin in the summer. Qualifications Required Qualifications * Currently pursuing a PhD degree in computer science, statistics, mathematics, or related technical field. Other Requirements * Research Interns are expected to be physically located in their manager's Microsoft worksite location for the duration of their internship. * In addition to the qualifications below, you'll need to submit a minimum of two reference letters for this position as well as a cover letter and any relevant work or research samples. After you submit your application, a request for letters may be sent to your list of references on your behalf. Note that reference letters cannot be requested until after you have submitted your application, and furthermore, that they might not be automatically requested for all candidates. You may wish to alert your letter writers in advance, so they will be ready to submit your letter. Preferred Qualifications * Experience with one or more general purpose programming languages, such as Python, Java, C#, C++, Rust. * Experience with one of the following: PostgreSQL, MySQL, SQL Server, Spark, Apache Iceberg, CUDA, or other database or big data systems. * Experience contributing to research communities and/or efforts, including publishing papers (being listed as author) at academic conferences. * Take initiative but also follow a research/productization plan and work well as part of a team. * Critical thinking and communication skills. The base pay range for this internship is USD $6,710 - $13,270 per month. There is a different range applicable to specific work locations, within the San Francisco Bay area and New York City metropolitan area, and the base pay range for this role in those locations is USD $8,760 - $14,360 per month. Certain roles may be eligible for benefits and other compensation. Find additional benefits and pay information here: ************************************************* Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work. This position will be open for a minimum of 5 days, with applications accepted on an ongoing basis until the position is filled. Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance with religious accommodations and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations.

Join the best radiopharmaceutical company in the world! If you're looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer. At the forefront of NorthStar's technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission-advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package. Position The Senior Microbiologist, Product Development will be a technical leader, bringing the science of microbiology in a pharmaceutical application to the development and maintenance of equipment, cleanrooms, and processes used in the manufacture of radioisotopes. This includes gathering technical information about engineering system/set up and managing the implementation of novel radioisotope manufacturing technologies. The Senior QAPD Microbiologist will develop and execute microbiological methods and validations from concept phase through design, planning, and execution, as well as coordinating with other departments. This person is also responsible for working with cross functional teams, including RA/QA and Engineering, to apply efficient cGMP processes, to preserve data integrity and quality of the drug product, and to ensure the safety of all production and non-production personnel. Responsibilities Drive the development of overall microbial validation strategy for pharmaceutical application to development of equipment used in the delivery of radioisotopes. This would include developing and executing methods and validations from concept phase through design, planning, and execution as well as coaching other team members. Assist lab management. Be the primary point of contact for microbiology laboratory supplies, instrumentation, and environmental monitoring program activities. Develop, plan, implement, and support microbiological development projects in collaboration with cross-functional teams with an overall focus on microbiological safety. Maintain laboratory procedures in accordance with Good Laboratory/Manufacturing Practice standards of the US FDA, 21 CFR Part 210 & 211 Follow good laboratory practice, good documentation, and good manufacturing practice when creating and executing advanced protocols to verify and/or validate product conformance in the area of microbiological testing and control. Early Development After 3 months: You will have completed all required training for new employees; for job-specific duties, and safety; and for access to restricted areas relevant to your job duties. You will have integrated into the quality unit, project, operations, and other cross-functional teams. You will understand the function and responsibilities of each group within other areas of the Quality department. After 6 months: You will understand the Quality Management Processes that support Aseptic Process Controls, Environmental Monitoring, and other contamination control strategies. You will have become qualified to train, qualify, and maintain operator status in all aspects of Aseptic Process Controls including: Aseptic Techniques, Aseptic Gowning, and Aseptic Process Operator Qualification. You will have engaged a cross-functional team to qualify, and maintain the qualification status of the systems in-place to maintain room classifications, (ISO 5, ISO 7, and ISO 8). Qualifications Master's Degree in biological science and five (5) or more years of experience in the pharmaceutical/medical device industry or equivalent combination of education and experience. Experience developing clear, concise, and adequate protocols, procedures, and work instructions required. Must possess a working knowledge of lab controls and general scientific equipment and should strictly adhere to written procedures and enforce it in others. Master's degree in microbiology preferred. Experience with Radiopharmaceuticals would be a strong asset in this position. Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position. Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment. Under federal law, only truthful information may be provided on the Form I-9. Benefits Medical, dental, and vision insurance Healthcare Flex Spending Account (FSA) and Dependent Care FSA Company-paid short-term and long-term disability Company-paid life insurance & AD&D coverage Pet insurance 401(k) match Paid holidays and paid time off (PTO) Paid parental leave Bonus plan Equity Incentive Program Working Conditions This role may involve working in a controlled cleanroom environment, general office setting, or specific manufacturing areas. Conditions may include: Exposure to varying temperatures, both indoors (heated/air-conditioned spaces) and outdoors Noise levels range from quiet to loud, depending on the work area Specific vision abilities, including near vision, visual acuity, and color discrimination Personal Protective Equipment (PPE) is required and may include: Respirators, gloves, safety glasses, and full protective clothing Compliance with cleanroom gowning protocols (e.g., removal of all jewelry, including piercings) Prohibition of cosmetics, fragrances (perfume, aftershave), and nail products, including polish, artificial nails, or extensions As a radiopharmaceutical manufacturing site, radiation may be present in the laboratory and production areas. Employees in this role may be required to: Follow strict radiation safety procedures Participate in dosimetry monitoring and bioassay testing as part of the company protocol Inform leadership of any health conditions that may affect product integrity, by cleanroom standards Location NorthStar Medical Radioisotopes is proud to call Beloit, Wisconsin home. Our headquarters and primary manufacturing facility are located in this vibrant, growing community that combines the charm of a small city with the advantages of a central Midwest location. Beloit features a lively, revitalized downtown filled with local restaurants, shops, and cultural events, and is just a short drive from major metropolitan areas including Madison, Milwaukee, Chicago, and Rockford. Situated in the heart of the South Central Wisconsin and Northern Illinois region, Beloit offers a rare blend of urban amenities and scenic natural surroundings. Whether you're drawn to outdoor recreation, educational institutions, the arts, or historic landmarks, the area provides rich and diverse experiences for all interests. A variety of nearby communities, ranging from rural towns to suburban neighborhoods, offer flexible housing options and access to multiple school districts, making Beloit an excellent choice for individuals and families considering relocation. NorthStar Medical Radioisotopes is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Job Description Prairie Ridge Health is looking for a team member to join or Lab Department in the role of Certified Lab Scientist or Certified Lab Tech. This position is 0.2 FTE (8 hours per week) Day/PM shift Monday - Friday with an every 3rd weekend rotation. This position will be responsible for performing general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability...…. POSITION SUMMARY Lab Scientist The Medical Technologist performs general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability. The data obtained is used in the diagnosis and treatment of disease involving patient of all ages. The Medical Technologist develops and maintains test procedures and protocols, and troubleshoots both technology and sample related problems. (S)he exercises independent judgment and responsibility with minimal supervision. May supervise others in the absence of the Laboratory Supervisor. Makes decisions about the accuracy of test results, instrument operation, specimen suitability, and uses sound clinical judgment in setting the priority of tests/patients. OR Lab Tech I or II The Clinical Laboratory Technician I performs general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability. The data obtained is used in the diagnosis and treatment of disease involving patient of all ages. The Clinical Laboratory Technician II develops and maintains test procedures and protocols, and troubleshoots both technology and sample related problems. (S)he exercises independent judgment and responsibility with minimal supervision. Makes decisions about the accuracy of test results, instrument operation, specimen suitability, and uses sound clinical judgment in setting the priority of tests/patients. EDUCATION REQUIREMENTS/LICENSURE/CERTIFICATION/REGISTRATION Lab Scientist Bachelors' degree in Medical Technology and graduate of an accredited Medical Technology Program. Registered or eligible as a Medical Technologist (MT) or Clinical Laboratory Scientist (CLS) with a national accrediting agency (ASCP) or (AMT) or qualified as a MT/CLS having passed the Federal Equivalence Exam (HEW). Certification must be obtained within 9 months of employment. Meets the CLIA 88 requirements for individuals performing highly complex testing. CPR certification or obtained within 90 days of hire. OR Lab Tech I Associate degree and completion of a 2 year CLT / Medical Laboratory Technician (MLT) training program. Certified or eligible as a Clinical Laboratory Technician or Medical Laboratory Technician (MLT) with a national accrediting agency (ASCP) or (AMT). Certification must be obtained within 9 months of hire. Meets the CLIA 88 requirements for individuals performing highly complex testing. One year of experience in a clinical laboratory performing highly complex testing is preferred. CPR certification obtained within 90 days of hire. OR Lab Tech II Associate degree and completion of a 2 year CLT / Medical Laboratory Technician (MLT) training program. Certified or eligible as a Clinical Laboratory Technician or Medical Laboratory Technician (MLT) with a national accrediting agency (ASCP or AMT). Certification must be obtained within 9 months of hire. Meets the CLIA 88 requirements for individuals performing highly complex testing. A minimum of five years' experience as a CLT/MLT. CPR certification obtained within 90 days of hire FTE: 0.2 (8 hours per week) Shift: Monday-Friday Day/PM shift with every 3rd weekend rotation.

Our client, a leader in food chemistry testing, is seeking a Sample Prep Technician to join their team. As a Sample Prep Technician, you will be part of the Food Chemistry Testing Department supporting various teams. The ideal candidate will have attention to detail, strong communication skills, and a willingness to ask questions, which will align successfully in the organization. **Job Title:** Sample Prep Technician **Location:** Madison, WI **Pay Range: $18.50/hr plus shift differential ($20.17/hr)** **Shift:** 2pm - 10:30pm **What's the Job?** + Perform a variety of sample preparation tasks to ensure sample homogeneity, including labeling, transferring, and weighing samples. + Communicate sample information and discrepancies to appropriate personnel. + Handle internal customer inquiries and requests effectively. + Learn and apply critical thinking skills to solve problems quickly and efficiently. + Work collaboratively within a team to achieve departmental goals. **What's Needed?** + High School diploma or equivalent. + 1+ years working experience (not specific to industry) + Strong customer service skills, including attention to detail and effective communication. + Ability to learn new tasks and adapt to changing priorities. + Willingness to work in a fast-paced environment and maintain excellent attendance. **What's in it for me?** + Opportunity for growth and development within a reputable organization. + Engaging work environment with a focus on teamwork. + Hands-on experience in food chemistry testing. + Exposure to various sample preparation techniques and processes. + Potential for temp-to-hire transition based on performance. **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.

All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page.Job Posting Title:Research Assistant - visiting Position Type:VisitorDepartment:LSUAG PL1 - SPESS - Plant Environmental and Soil Sciences (Brenda Tubana (00000851)) Work Location:Madison B. Sturgis (New Agronomy Bldg) Pay Grade:: The scholar will research the evaluation of silicon fertilization and application of silica solubilizing bacteria in improving crop tolerance to stress and productivity. Additional Job Description:Competencies:NoneSpecial Instructions:Visiting ScholarPosting Date:July 29, 2024Closing Date (Open Until Filled if No Date Specified):Additional Position Information: Background Check - An offer of employment is contingent on a satisfactory pre-employment background check. Benefits - The LSU AgCenter has an attractive benefits package with a wide variety of benefit options. Benefits offered include retirement, multiple medical insurance options, supplemental insurances (dental, life, long-term disability, accident, vision, long-term care, etc.), Tax Saver Flexible Benefits Plan (saves tax dollars on some childcare and medical expenses), university holidays (14 per year), generous annual (vacation) and sick leave benefits, Employee Assistance Program, and possible educational leave and tuition exemption for coursework at campuses of the LSU System. Specific benefits depend on job category, percent effort and length of employment. Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, next Source Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement. Essential Position (Y/N):About the LSU Agricultural Center: The LSU AgCenter, is one of eight campuses within the broader LSU enterprise (LSU System). The LSU AgCenter includes the Louisiana Agricultural Experiment Station, which conducts agricultural-based research, and the Louisiana Cooperative Extension Service, which extends the knowledge derived from research to the people of the state. The AgCenter is headquartered in Baton Rouge and has 12 “on campus” academic departments and five regions which are made up of 15 branch research stations and an extension office in each parish. For more information, visit the AgCenter's website at ******************** The LSU Agricultural Center is an Equal Opportunity Employer and SAME Agency: The LSU Agricultural Center is a statewide campus of the LSU System and provides equal opportunities in programs and employment. The AgCenter is committed to fostering an environment of inclusion, respect, and appreciation of differences in individuals. The AgCenter is also designated as a State As a Model Employer (SAME) agency and provides assistance to persons needing accommodations or with the accessibility of materials. HCM Contact Information: Questions or concerns can be directed to the LSU AgCenter Human Resources Management Office at ************ or emailed ************************.

z/OS Systems Programmer, with ISV and DR testing- Remote no on call Remote - United StatesJR011237 At Ensono, our **Purpose is to be a relentless ally, disrupting the status quo and unleashing our clients to Do Great Things** **_!_** We enable our clients to achieve key business outcomes that reshape how our world runs. As an expert technology adviser and managed service provider with cross-platform certifications, Ensono empowers our clients to keep up with continuous change and embrace innovation. **Role** **Summary** As the z/OS Systems Programmer, you will be engaged on the transition from client's in-house IT into Ensono's support. You will participate in Knowledge Transfer with clients and assist in documentation creation. The focus is on the ISV software and license key procedures for those products. You will identify which software products require a license key, document procedures for applying, and then apply keys for the products during migration. Your primary job responsibility will be to shadow the client engineers and assist in the transition of services to Ensono engineers. You will support mainframe disaster recovery team during disaster recovery drills and exercises. While supporting ISV and z/OS for the Disaster Recovery Team, you may be engaged in more than one DR drill simultaneously. You will also install and support ISV software on a z/OS system and attend project meetings to understand scope of planned disaster recovery drills, address issues as they arise during the drill as well as review and correct any procedures as necessary. **What You Will Need:** + 8-10 years of experience working within a z/OS environment + 3-5 years ISV licensing experience + Familiarity with mainframe functional areas such as z/OS, Storage, VTAM + Understanding of JCL + Successful associates should be familiar with installation or support of mainframe ISV products such as SAS, CA/Broadcom, McKinney Systems, BMC, PRECISELY and others + This includes experience with SMP/E, base installation and maintenance application + Must be self-motivated and able to manage multiple projects simultaneously + Proficient in Microsoft Word and Excel to a level of creating documents which can be shared with clients. **Why Ensono?** Ensono is a place where we unleash Associates to Do Great Things - for our clients and for your career. This could mean achieving a professional goal, collaborating with your team on an innovative idea, learning a new skill, reaching a wellness milestone, or engaging in your community through volunteer programs. Whatever it means to you, we want Ensono to be the place where you can do great things. We value flexibility and work-life balance. Positions that are not required to be onsite to support a client may offer the ability to work remotely or hybrid at an Ensono office location. + Unlimited Paid Day Off (PDO) Plan + Two robust health plan options through Blue Cross Blue Shield + 401(k) with a generous company match + Eligibility for dental, vision, short and long-term disability, life and AD&D coverage, and flexible spending accounts + Depending on location, ability to take advantage of fitness centers + Wellness program + Flexible work schedule As of the date of this posting, a good faith estimate of the current pay scale for this role is $80,000 to $148,000 annually based on a full-time schedule. Please note that placement in the range may vary based on numerous factors including but not limited to skills, experience, internal equity, and business needs. In addition to base salary, other compensation programs, depending on eligibility, include an annual bonus plan based on company and individual performance, and an equity grant under our Associate Equity Appreciation Program. Ensono is an Equal Opportunity/Affirmative Action employer. We are committed to providing equal employment to our Associates and building a diverse and inclusive workforce. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or other legally protected basis, in accordance with applicable law. Pay transparency nondiscrimination statement/posting OFCCP's pay transparency policy can be found on OFCCP's website (*********************************************************************************************** . If you need accommodation at any point during the application or interview process, please let your recruiter know or email ****************************** . JR011237

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Our staff members are committed to making a difference in our organization, for our client partners and the patients we serve. We seek individuals with proven competencies and strong character to help lead our organization now and into the future.Our interns receive professional mentorship and leadership development opportunities to support future career growth with us. Whether you're looking to come back as a repeat intern, transition into one of our Leadership Development Programs, or pursue a full-time position post-graduation, our team is here to support your next step!How will you make an impact?Our interns are matched to projects based on their abilities and current business needs. All projects will have significant strategic and/or operating importance to the business to which they are assigned.Summer projects may include the following responsibilities: Completes the formulation of reagents and solutions in a fast-paced manufacturing environment following controlled documents and procedures. Apply specialized technical knowledge and skills to make detailed observations and analyze data within operating parameters. Actively participate in troubleshooting for specific processes or activities as assigned. Maintain equipment, product inventory, and related records as assigned. Note variances on manufacturing documents; audit and evaluate process documents and propose revisions. Identify manufacturing procedures intended to optimize existing processes and ensure compliance with regulatory requirements. Inform the team lead/supervisor of factors that may affect quality of the product, initiate problem reports for deviations and non-conforming materials and suggest options and ideas for corrective actions and preventive actions (CAPA). May support or assist in the review in the peer review of daily work orders to ensure compliance, accuracy and quality. Satisfactorily complete Thermo Fisher Scientific training requirements on time and operate within all ISO, GMP, and FDA standards pertaining to Frederick Site Manufacturing Operations. May be required to perform other related duties as required and/or assigned Start Date: This internship is set to begin on either May 11th or June 15th, 2026 for a duration of 10-12 weeks - dependent upon student availability per academic calendars. Compensation & Relocation: Our undergraduate Engineering internships offer an hourly rate between $21.50 - $28.75 dependent upon the location you are supporting (aligned to respective cost-of-living guidelines). Additionally, a relocation stipend is offered in the amount of $5,000 if necessary. Student must be located 50+ miles away from the physical location of the internship to be eligible for the relocation stipend.How will you get here? Undergraduate student completing a Biology or Chemistry related degree between December 2026 and June 2027. 0 years of work experience required; previous related internships preferred. Consistent track record of results demonstrating integrity, innovation, involvement, and intensity. Energized through championing change, driven in getting results, and savvy in navigating ambiguity. Excellent interpersonal communication skills with a high degree of emotional intelligence. If this sounds like you, we'd love to hear from you!To qualify, applicants must be legally authorized to work in the United States and should not require sponsorship (current or future) for employment visa status. Thermo Fisher does not offer employment in this position to holders of F-1, J-1, H-1, OPT, and CPT Visas for the purpose of obtaining practical experience.

PEAK is seeking 1 Production Laboratory Intern to perform research projects within our Watertown Production laboratory. This is a hands-on internship that will include learning and performing laboratory procedures, compiling research data, and presenting back to company leaders. The intern will step foot into all facets of PEAK Production while developing a network and gaining an understanding of the semen production process. Major Areas of Accountability: Perform processing duties in the production laboratory as outlined by company protocols and SOPs Evaluate samples for motility, concentration, volume, and quality Keep records on bull registration and enter in appropriate databases Conduct detailed research trial(s) designed to optimize current lab practices Summarize research and present recommendations for the future based on the research trial outcomes Attend company intern orientation and networking events Explore career opportunities within PEAK and the other URUS Operating Companies Qualifications: Students pursuing an education within agriculture, biology, genetics or data science Applicants currently attend a 2-year technical college or 4-year university Passionate about agriculture and innovation Willingness to learn and experience new things Detail-oriented individual with an interest in completing an independent research project Internship applications will close on October 31 st , 2025, please note you may not be contacted until after this date.

Since 1997, Truckstar has been an independent, family-owned and operated, heavy duty collision repair shop, helping to get our customers' vehicles back on the road. We pride ourselves in always doing the job right and work on all makes and models, so you never know what kind of vehicle is pulling in next! Truckstar takes pride in providing a fun and fulfilling environment for our employees. BENEFITS: Monthly incentives for work produced Weekly pay period Fun and family-like work environment Free coffee, donuts and pizza Company sponsored health insurance Company paid life insurance and group plan rates Company sponsored short term disability Paid vacation, holidays, and sick time 401k with up to 4% company match Dental and vision insurance Long-term disability, accident, and critical illness insurance Company sponsored and paid on-the-job training Company outings, potlucks, holiday parties, and a turkey or ham for Thanksgiving Overtime available ROLE AND RESPONSIBILITIES: Disassemble and assemble vehicles as needed Move and setup vehicles and equipment for blasting & painting Use hand and power tools to sand, prime and block Mask adjacent panels Wiping down and preparing for paint application Physical ability to work at a variety of heights and positions Read and understand work orders Wash vehicles and perform light detailing REQUIREMENTS: Work experience in collision repair industry Positive attitude Ability to read and understand work orders Ability to problem solve Willingness to learn Strong attention to detail Ability to work independently Be able to multitask Provide your own tools Be reliable We are an equal opportunity employer and prohibit discrimination/harassment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by federal, state or local laws.

Laboratory bench work individually or in a team setting to accomplish daily Quality Control lab tasks. Active participation as a member of the Quality Control team in testing and release of production materials. Working in a lab setting to supporting fermentation facility that produces probiotics and dairy cultures. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: · Adhere to all quality systems including, but not limited to, ISO 22000, NSF, and GLP guide-lines, with an understanding of IFF's Quality Policy and procedures. · Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. · Understand and follow procedures of the department for the proper calibration and use of the department's equipment. · Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products. · Perform environmental sampling procedures. · Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES · Must have bachelor's degree in chemistry, Microbiology, Biology or similar field, or associate degree with at least 1 year relevant experience. · Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. · Must have the ability to work as an active team member as well as independently. · Must have strong math and good communication skills (both verbal and written). WORKING CONDITIONS This position operates in a laboratory environment 95-100% of the time. Exposure to hazardous materials training is required. Must wear Personal Protective Equipment (PPE) as appropriate in accordance with plant policy. SCOPE OF POSITION This position reports directly to the Quality Control Supervisor and has no direct supervisory responsibilities. Must be able to work overtime as needed. Management retains the discretion to add or change the duties and responsibilities of this position at any time. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Laboratory bench work individually or in a team setting to accomplish daily Quality Control lab tasks. Active participation as a member of the Quality Control team in testing and release of production materials. Working in a lab setting to supporting fermentation facility that produces probiotics and dairy cultures. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: * Adhere to all quality systems including, but not limited to, ISO 22000, NSF, and GLP guide-lines, with an understanding of IFF's Quality Policy and procedures. * Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. * Understand and follow procedures of the department for the proper calibration and use of the department's equipment. * Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products. * Perform environmental sampling procedures. * Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES * Must have bachelor's degree in chemistry, Microbiology, Biology or similar field, or associate degree with at least 1 year relevant experience. * Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. * Must have the ability to work as an active team member as well as independently. * Must have strong math and good communication skills (both verbal and written). WORKING CONDITIONS This position operates in a laboratory environment 95-100% of the time. Exposure to hazardous materials training is required. Must wear Personal Protective Equipment (PPE) as appropriate in accordance with plant policy. SCOPE OF POSITION This position reports directly to the Quality Control Supervisor and has no direct supervisory responsibilities. Must be able to work overtime as needed. Management retains the discretion to add or change the duties and responsibilities of this position at any time. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page.Job Posting Title:Research Assistant - visiting Position Type:VisitorDepartment:LSUAG PL1 - SPESS - Plant Environmental and Soil Sciences (Brenda Tubana (00000851)) Work Location:Madison B. Sturgis (New Agronomy Bldg) Pay Grade:: The scholar will research the evaluation of silicon fertilization and application of silica solubilizing bacteria in improving crop tolerance to stress and productivity. Additional Job Description:Competencies:NoneSpecial Instructions:Visiting ScholarPosting Date:January 4, 2024Closing Date (Open Until Filled if No Date Specified):Additional Position Information: Background Check - An offer of employment is contingent on a satisfactory pre-employment background check. Benefits - The LSU AgCenter has an attractive benefits package with a wide variety of benefit options. Benefits offered include retirement, multiple medical insurance options, supplemental insurances (dental, life, long-term disability, accident, vision, long-term care, etc.), Tax Saver Flexible Benefits Plan (saves tax dollars on some childcare and medical expenses), university holidays (14 per year), generous annual (vacation) and sick leave benefits, Employee Assistance Program, and possible educational leave and tuition exemption for coursework at campuses of the LSU System. Specific benefits depend on job category, percent effort and length of employment. Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, next Source Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement. Essential Position (Y/N):About the LSU Agricultural Center: The LSU AgCenter, is one of eight campuses within the broader LSU enterprise (LSU System). The LSU AgCenter includes the Louisiana Agricultural Experiment Station, which conducts agricultural-based research, and the Louisiana Cooperative Extension Service, which extends the knowledge derived from research to the people of the state. The AgCenter is headquartered in Baton Rouge and has 12 “on campus” academic departments and five regions which are made up of 15 branch research stations and an extension office in each parish. For more information, visit the AgCenter's website at ******************** The LSU Agricultural Center is an Equal Opportunity Employer and SAME Agency: The LSU Agricultural Center is a statewide campus of the LSU System and provides equal opportunities in programs and employment. The AgCenter is an Equal Opportunity/Affirmative Action Employer and is committed to fostering an environment of inclusion, respect, and appreciation of differences in individuals. To learn more, visit The AgCenter's Diversity, Inclusion and Opportunity site. The AgCenter is also designated as a State As a Model Employer (SAME) agency and provides assistance to persons needing accommodations or with the accessibility of materials. HCM Contact Information: Questions or concerns can be directed to the LSU AgCenter Human Resources Management Office at ************ or emailed ************************.

QC Technician 3rd Shift Tuesday - Saturday To accomplish daily Quality Control lab tasks through participation as a member of the Quality Control team. NATURE OF WORK To accomplish daily Quality Control lab tasks through participation as a member of the Quality Control team. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: • Adhere to all quality systems including, but not limited to, ISO 9001 and Food Safety, with an understanding of DuPont's Quality Policy and procedures. • Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. • Understand and follow procedures of the department for the proper calibration and use of the department's equipment. • Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products • Perform environmental sampling procedures. • Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES • Must have bachelor's degree in Chemistry, Microbiology, Biology or similar field, or associate degree with at least 2 years' relevant experience. • Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. • Must have the ability to work as an active team member as well as independently. • Must have strong math and good communication skills (both verbal and written). We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more