Research Scientist Jobs in West Allis, WI

Duration: 12 Months Contract This position will contribute analytical and technical support for nitrosamines and impurities analysis. Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques. Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies. Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines. Operate, maintain, and troubleshoot MS instrumentation. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Independently plan and execute method development activities utilizing LC/MS/MS. Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs). Independently author and contribute to experimental protocols, summaries, and technical reports. Document and review laboratory work using an electronic laboratory notebook per Baxter's good documentation practices (GDP) and general good laboratory practices (GLP). Follow Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Provide support to maintain a compliant, safe, and clean working environment/laboratory. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. Qualifications: Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with MassHunter preferred. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis). Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills. Strong written and verbal communication skills in English. Provide and accept critical feedback from others in a constructive manner. Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables. Ability to objectively assess, organize, and clearly communicate information. Ability to plan and complete the assigned work to meet project deliverables in a timely manner. Proficient in Microsoft Office applications(Excel, Word, Outlook) Education and/or Experience: PhD with 0-3 years' experience, or a master's with 3-5 years' experience, or a bachelor's with 5-7 years' experience in a chemistry related field. Analytical or organic chemistry preferred. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Swati Email: *********************************** Internal Id: 25-36543

$42 - $45/hr based on if you choose to opt into medical benefits 1 year initial contract with possible 1 year extension Onsite in North Chicago M-F 8 am to 5 pm with some flexibility for schedule Orion Project Services and a market leading pharmaceutical company are teaming up for an exciting contract opportunity for Scientists in North Chicago, IL!! We are looking for a highly motivated person to support Developability and Formulation Development. The candidate will support early-stage assessment of candidates coming out of the Discovery pipeline, as well as the design and development of stable and robust drug product formulation for biologics used in clinical trials. In this role, the candidate will be part of a global team and will work closely with scientists from multiple functional areas, including Discovery, Analytical, and Process R&D. Job Description: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. Key Responsibilities Include: Support the biologics characterization and stability assessment activities of the assigned biologics, including candidate screening and selection for clinical studies and commercialization of monoclonal antibodies, antibody drug conjugates, bispecifics, and fusion proteins. Execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), and screen excipients (buffers, stabilizers, surfactants, etc.) to develop robust formulations for frozen, refrigerated liquid, and lyophilized dosage forms. Prepare concise and sound scientific presentations of experimental results to the management and assist in authoring detailed scientific technical reports. Stay current with the scientific literature and support new scientific initiatives. Qualifications needed to be successful in this role: BS or MS in a scientific field and typically 4 (BS) or 2 (MS) years of relevant experience. Extensive hands on expertise using analytical methods for chemical and structural characterization of biologics e.g. HPLC, UPLC, capillary electrophoresis, particle analysis, and other biophysical techniques (UV-vis, DLS, DSC, etc.) for protein characterization is a requirement. Scientific understanding of the structure & function of monoclonal antibodies, antibody constructs/conjugates, bispecifics, and fusion proteins and their modes of degradation/stabilization. Strong laboratory skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays) would be a plus. Solid understanding of the various unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling, and lyophilization for liquid and lyophilized NBEs. Key Leadership Competencies: Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Excellent oral communication skills in a scientific setting, as well as sound technical writing and documentation competencies are required. The candidate must be able to work independently, respond to changing priorities and short lead times for multiple tasks; able to identify problems and work toward solutions. Raises the bar and is never satisfied with the status quo. Creates a learning environment, open to suggestions and experimentation for improvement. Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Position Summary: The Scientist I performs testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, GLP Study work, product testing/development work. Authority: The Scientist receives sufficient authority from, and is accountable to, the Specialty Analysis Manager or Lab Director, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. Essential Duties and Responsibilities: Perform testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions. Instrumentation utilized will include a wide array including not limited to HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate). Perform and document method transfers, development work, validations/verifications. Maintain neat and accurate records. Ensuring that the client receives quality data by compiling and/or reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations or other internationally recognized standards (e.g., ISO/IEC 17025:2017). Interact with clients to assist in selection of test methods and interpretation of test data. Assist Sales and Business Team members on quote review if requested. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data. Enter testing data into LIMS and monitor for QC failures. Assist lab staff in determining corrective actions for QC failures. Review and approve laboratory analytical data including peer review Review and issue reports to clients. Maintain chemical/reagent traceability. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager. Maintain regular attendance and punctuality Conducts all activities in a safe and efficient manner Performs other duties as assigned Assist with case studies, white papers if requested by Sr. Management for marketing purposes. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments. Qualifications BS or greater in Chemistry or related field, 2+ years experience in a commercial laboratory in an autonomous environment Proficiency at HPLC, LCMS, GC, GCMS, and knowledge of all other major analytical instrument capabilities is imperative Knowledge of ISO 17025, CVM, FDA or other regulatory standards Additional Information Schedule: Monday-Friday 9:00am-5:00pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer. PandoLogic. Keywords: Chemist, Location: New Berlin, WI - 53151 , PL: 597425078

This position will contribute analytical and technical support for nitrosamines and impurities analysis. Specifically, this candidate will collaborate with subject matter experts (SMEs) by leading and executing laboratory experiments. This position requires daily in-person and on-site laboratory work. Responsibilities and Duties: Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques. Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies. Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines. Operate, maintain, and troubleshoot MS instrumentation. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Independently plan and execute method development activities utilizing LC/MS/MS. Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs). Independently author and contribute to experimental protocols, summaries, and technical reports. Document and review laboratory work using an electronic laboratory notebook per good documentation practices (GDP) and general good laboratory practices (GLP). Follow Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Provide support to maintain a compliant, safe, and clean working environment/laboratory. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The following knowledge, skills, and/or abilities are required: Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with MassHunter preferred. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis). Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills. Strong written and verbal communication skills in English. Provide and accept critical feedback from others in a constructive manner. Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables. Ability to objectively assess, organize, and clearly communicate information. Ability to plan and complete the assigned work to meet project deliverables in a timely manner. Proficient in Microsoft Office applications(Excel, Word, Outlook) Education and/or Experience: Educational and professional qualification: PhD with 0-3 years experience, or a masters with 3-5 years experience, or a bachelors with 5-7 years experience in a chemistry related field. Analytical or organic chemistry preferred.

COMPANY PROFILE Cedar Corporation is a professional service firm with disciplines in engineering, architecture, environmental, planning, landscape architecture, and land surveying. Founded in 1975, the company has grown to its present staff of 100. Our staff is dedicated to the principles on which the firm was developed: professionalism, state-of-the-art technology, and service to clients. We have continued to grow because of our commitment to providing comprehensive services and maintaining good communication with our clients. JOB OPPORTUNITY Cedar Corporation is a growing company that offers a professional, yet flexible work environment. We are seeking a Wetland Scientist with a keen interest in the natural sciences. The candidate will work closely with project managers, staff scientists, and senior scientists with development and delivery of environmental assessments for projects involving private industry, public infrastructure, and utilities. Join our Team where you can apply your passion in collaboration with other top-talent professionals! RESPONSIBILITIES Wetland delineation and assessment. Create mapping of wetland resources. Summarize findings in a comprehensive report. Record with WDNR under the Assured Delineator Program or wetland confirmation service. Developing concepts, monitoring and reporting on wetland mitigation and restoration projects. Prepare wetland mitigation bank design and assessment Assist with ecological restoration planning and site monitoring Conduct wildlife habitat and botanical surveys Coordinate construction and restoration activities with property owners and contractors. Build relationships with government agencies to create a streamlined authorization process. QUALIFICATIONS 5+ years of environmental/wetland field experience is preferred. Bachelor's degree in environmental science, geology, geography, soil science, or biology. Excellent computer skills with MS Office; GIS and/AutoCAD knowledge. Strong communication, technical writing, time management, and organization skills. Ability to work independently with direction from project team members. Ability and willingness to travel for short-term and long-term field assignments, as needed. Professional Wetland Assurance Certification is pre Valid driver's license Ability to walk up to five miles and lift up to 50 lbs. Understanding of regulatory compliance and permitting programs at the federal, state, and local levels. An equal opportunity employer.

Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry seeking an R&D Scientist to work at our Pleasant Prairie, WI location. We offer a wide range of products including decorative fashion paints, durable industrial roof repair coatings and, of course, our famous rust-fighting formula that started it all. R&D Scientist for Rust-Oleum Corporation to work at our Pleasant Prairie, WI loc. Summary and job description: Drive product [prod] development from concept to formula development, through prod launch. Test prod, document test data, generate + communicate test reports detailing project processes, results + conclusions, + recommend additional actions or research. Work closely w/ marketing, sales, + regulatory teams to develop competitive claims + prod demonstrations. Dev, improve, + customize prod, equipment, formulas, processes, + analytical methods. Conduct QC tests. Adhere to safety, quality, + housekeeping policies/guidelines. Work closely w/ peers + supervisors to analyze research projects, interpret test results, or develop nonstandard tests. Dev + maintain professional relationships w/ suppliers, technical experts, etc. Write technical papers + reports, + prepare standards + specifications for processes, prods, or tests. May undergo background checks incl drug screening. Must have Bachelors in Chemistry, Chemical Engineering, Plastics Engineering, Organic Chemistry or other rel sci field and 3 yrs related exp in formulating and testing water-borne and solvent-borne products. Required experience can be gained concurrent with academic studies. Candidates required to prepare a 30 min technical presentation during interview process. Apply at ********************************* Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Located in Milwaukee, Wisconsin, the Versiti Blood Research Institute (VBRI) is the largest blood-focused research institute in the United States. With over 30 basic, translational, and clinical researchers, the institute is dedicated to advancing scientific knowledge and developing innovative therapies related to blood and blood disorders. The institute's research interests encompass a wide range of topics, including transfusion medicine, cellular therapy, thrombosis/hemostasis, immunology, and hematologic malignancies. As a vital part of Versiti, a non-profit organization with a blood bank at its core, the VBRI strives to improve lives through innovative research and the development of novel diagnostics and treatments. VBRI is part of the Milwaukee Regional Medical Campus, a rapidly growing clinical-translational research hub. VBRI's proximity to the Medical College of Wisconsin, Childrens' Hospital of Wisconsin, and Froedtert Hospital facilitates seamless interdisciplinary collaborations. A range of exemplary core facilities support highly competitive research. In the summer of 2024, construction of a new research building will start, doubling existing VBRI research space to enable the recruitment of 10-15 new faculty. With its renowned researchers, strategic expansion plans and location in a highly collaborative environment, the VBRI is poised to maintain and expand its position as one of the leading hematology institutes in the world. Position Summary Transfusion Medicine Faculty Positions in Basic and/or Translational Research We seek to grow our Transfusion Medicine, Vascular Biology and Cell Therapy Program by recruiting innovative investigators with research interests in transfusion medicine and related fields such as cell therapy, gene therapy, glycobiology, and vascular biology. Applicants at all academic ranks with Ph.D., M.D., or equivalent degrees are encouraged to apply. Ideal candidates will develop or maintain independently funded basic and/or translational research programs. For physician-scientists, clinical transfusion medicine duties (up to 20% effort) may include blood bank oversight, transfusion consultations, therapeutic apheresis, and quality assurance activities. These positions provide attractive start-up packages and outstanding opportunities for collaboration with basic, translational, and clinical investigators. The VBRI is located on the same campus as the Medical College of Wisconsin (MCW), Children's Hospital of Wisconsin, and Froedtert Hospital, which facilitates collaboration, provides additional research breadth, and enables access to graduate students. VBRI faculty typically hold an appointment at MCW, including clinical departments, to facilitate translational research. Total Rewards Package Benefits Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others. Responsibilities Why Join the Versiti Blood Research Institute? The Versiti Blood Research Institute (VBRI), located in Milwaukee, Wisconsin, is focused on innovative blood and vascular research. The VBRI provides a unique academic environment, reflected by its long record of scientific excellence and innovation since its founding over seventy years ago. The VBRI is strategically strengthening its programs to promote both mechanistic and clinical-translational science. We are committed to impactful, rigorous science that can change lives. The VBRI currently houses 31 principal investigators in four Programs: Thrombosis and Hemostasis; Transfusion Medicine, Vascular Biology and Cell Therapy; Hematopoiesis; and Immunohematology. The VBRI has started a significant expansion of its research capacity with plans for adding 14 new principal investigators in the next 5 to 7 years. Designs for a new 60,000 - 80,000 ft 2 research building are under development with completion anticipated in 2026. The VBRI is part of Versiti, a not-for-profit organization focused on all aspects of hematology, including diagnostic testing, supply of blood products, and leading-edge basic, clinical, and translational research. A founding principle of Versiti is transfusion medicine research, and we have a long history of groundbreaking discoveries, including over 20 years of participation in the NHLBI-funded Recipient Epidemiology and Donor Evaluation Study (REDS) program. Qualifications Who are we looking for? Eligible candidates will have a Ph.D. and/or M.D. or equivalent doctoral degree. Successful candidates will have track records of creativity and productivity, a desire to integrate into our dynamic, collaborative, and rapidly expanding research community, and a commitment to our core values of equity, diversity, and inclusion. Successful candidates are expected to develop an innovative research program, obtain extramural funding, and participate actively in education, training, and mentorship. How do you apply? Qualified applicants should submit a single pdf containing a cover letter and CV, along with a summary of research accomplishments and future research plans (four pages maximum). Request up to four letters of recommendation be sent to *************************. Versiti is committed to increasing the diversity of its faculty and strongly encourages applications from individuals in groups that are underrepresented in the biomedical sciences such as candidates from rural areas. The VBRI will attract and retain a workforce and faculty that reflects the community we serve. Versiti is an equal opportunity employer. Milwaukee|milwaukee.org. Located on the west side of beautiful Lake Michigan in Wisconsin, Milwaukee is a well-kept secret of affordable quality of life. The city boasts a range of museums, some of the nation's largest summer festivals, a multi-cultural population rich in culinary and artistic tradition, a progressive downtown area, and many outdoor recreation opportunities, including plenty of parks, river walks, and public beaches. Housing is affordable, public and parochial schools are excellent, and traffic is a breeze. Milwaukee neighborhoods are known for variety, character, and unique architecture, offering superb quality of life and exceptional work-life balance in a city rife with history. With Chicago only 75 minutes away, world-class cultural and sporting venues and one of the world's busiest air travel hubs are within easy reach. #LI-EH1 #LI-Onsite #VBRI Not ready to apply? Connect with us for general consideration.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission. Your Role at Baxter This is where your work saves lives. The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate III at Baxter, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. As a key part of projects, our research and development team is responsible for delivering results to drive decisions and ensure safety of our existing and new products. We work on products that make a meaningful difference in others' lives. When you join Baxter, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure! Your Team While everyone at Baxter has a shared passion for our mission, the R&D teams play a meaningful role in our ability to save and sustain lives. Scientists and engineers in R&D work together to develop, test, sustain, and launch products that improve patient care. As a Research Associate III, you will be responsible for performing analytical testing with minimal assistance, demonstrating technical knowledge to troubleshoot problems and handle non-routine situations, assisting and mentor other team members, and embracing accountability for deliverables and leading team discussions/initiatives. While you will primarily support stability testing, you may also support new product development and/or sustaining product initiatives. What you'll be doing Develop analytical plan for new product development and sustaining product projects. Collaborate with other functions such as project management, regulatory, formulation, manufacturing and quality control in project teams. Act as a study director for thus design and execute method validation and transfer studies. Contribute to technical feasibility analysis of complex research and design concepts. Lead the analytical problem solving efforts to meet urgent business needs. Maintain knowledge of relevant QSR and other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. In addition to having an in-depth knowledge and understanding of cGxP and related regulations and guidance, is able to provide expert advice and/or is an active participant in the generation, review, adoption and interpretation of such regulations. Maintain focus on meeting both external and internal customer expectations. What you'll bring Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with at least 5+ years' experience or 3+ years' experience with a Masters degree. Analytical chemistry instrumentation experience (e.g. HPLC, UPLC, pH, KF, etc.) Must have HPLC/UPLC/UHPLC experience in a regulated environment and strong technical problem-solving skills. Electronic Lab Notebook experience is preferred Pharmaceutical GMP laboratory experience is desired. Empower experience required. Custom fields experience is desired. Stability study execution and/or method validation experience is desired Must demonstrate effectiveness in ability to train others, leadership, organization, teamwork/interpersonal skills, results orientation, and task completion. Must be able to handle multiple tasks concurrently and in a timely fashion. Possess relevant laboratory/technical, writing, and computer skills. Ability to organize and communicate complex information effectively with managers, peers, and subordinates. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $96,000 - $132,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry seeking an R&D Scientist to work at our Pleasant Prairie, WI location. We offer a wide range of products including decorative fashion paints, durable industrial roof repair coatings and, of course, our famous rust-fighting formula that started it all. R&D Scientist for Rust-Oleum Corporation to work at our Pleasant Prairie, WI loc. Summary and job description: Drive product [prod] development from concept to formula development, through prod launch. Test prod, document test data, generate + communicate test reports detailing project processes, results + conclusions, + recommend additional actions or research. Work closely w/ marketing, sales, + regulatory teams to develop competitive claims + prod demonstrations. Dev, improve, + customize prod, equipment, formulas, processes, + analytical methods. Conduct QC tests. Adhere to safety, quality, + housekeeping policies/guidelines. Work closely w/ peers + supervisors to analyze research projects, interpret test results, or develop nonstandard tests. Dev + maintain professional relationships w/ suppliers, technical experts, etc. Write technical papers + reports, + prepare standards + specifications for processes, prods, or tests. May undergo background checks incl drug screening. Must have Bachelors in Chemistry, Chemical Engineering, Plastics Engineering, Organic Chemistry or other rel sci field and 3 yrs related exp in formulating and testing water-borne and solvent-borne products. Required experience can be gained concurrent with academic studies. Candidates required to prepare a 30 min technical presentation during interview process. Apply at ********************************* Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry seeking an R&D Scientist to work at our Pleasant Prairie, WI location. We offer a wide range of products including decorative fashion paints, durable industrial roof repair coatings and, of course, our famous rust-fighting formula that started it all. R&D Scientist for Rust-Oleum Corporation to work at our Pleasant Prairie, WI loc. Summary and job description: Drive product [prod] development from concept to formula development, through prod launch. Test prod, document test data, generate + communicate test reports detailing project processes, results + conclusions, + recommend additional actions or research. Work closely w/ marketing, sales, + regulatory teams to develop competitive claims + prod demonstrations. Dev, improve, + customize prod, equipment, formulas, processes, + analytical methods. Conduct QC tests. Adhere to safety, quality, + housekeeping policies/guidelines. Work closely w/ peers + supervisors to analyze research projects, interpret test results, or develop nonstandard tests. Dev + maintain professional relationships w/ suppliers, technical experts, etc. Write technical papers + reports, + prepare standards + specifications for processes, prods, or tests. May undergo background checks incl drug screening. Must have Bachelors in Chemistry, Chemical Engineering, Plastics Engineering, Organic Chemistry or other rel sci field and 3 yrs related exp in formulating and testing water-borne and solvent-borne products. Required experience can be gained concurrent with academic studies. Candidates required to prepare a 30 min technical presentation during interview process. Apply at ********************************* Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Details: Stefanini Group is hiring! Stefanini is looking for Research Associate in Round Lake, IL (Onsite) For quick Apply, please reach out to Kamal Rawat - call: ********** / email: ************************* Work Hours: M-F (40 hours) Work Location: Round Lake, IL Shift: 1st Shift This position will contribute analytical and technical support for nitrosamines and impurities analysis. Specifically, this candidate will collaborate with subject matter experts (SMEs) by leading and executing laboratory experiments. This position requires daily in-person and on-site laboratory work at Round Lake site. Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques. Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies. Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines. Operate, maintain, and troubleshoot MS instrumentation. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Independently plan and execute method development activities utilizing LC/MS/MS. Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs). Independently author and contribute to experimental protocols, summaries, and technical reports. Document and review laboratory work using an electronic laboratory notebook per good documentation practices (GDP) and general good laboratory practices (GLP). Follow Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Provide support to maintain a compliant, safe, and clean working environment/laboratory. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. Details: PhD with 0-3 years' experience, or a master's with 3-5 years' experience, or a bachelor's with 5-7 years' experience in a chemistry related field. Analytical or organic chemistry preferred. Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with MassHunter preferred. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis). Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills. Strong written and verbal communication skills in English. Provide and accept critical feedback from others in a constructive manner. Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables. Ability to objectively assess, organize, and clearly communicate information. Ability to plan and complete the assigned work to meet project deliverables in a timely manner. Proficient in Microsoft Office applications(Excel, Word, Outlook) Listed salary ranges may vary based on experience, qualifications, and local market. Also, some positions may include bonuses or other incentives. Stefanini takes pride in hiring top talent and developing relationships with our future employees. Our talent acquisition teams will never make an offer of employment without having a phone conversation with you. Those face-to-face conversations will involve a description of the job for which you have applied. We also speak with you about the process including interviews and job offers. About Stefanini Group The Stefanini Group is a global provider of offshore, onshore, and near shore outsourcing, IT digital consulting, systems integration, application, and strategic staffing services to Fortune 1000 enterprises around the world. Our presence is in countries like the Americas, Europe, Africa, and Asia, and more than four hundred clients across a broad spectrum of markets, including financial services, manufacturing, telecommunications, chemical services, technology, public sector, and utilities. Stefanini is a CMM level 5, IT consulting company with a global presence. We are CMM Level 5 company. #LI-KR1 #LI-ONSITE

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. Job Title: Scientists Employer: Sigma-Aldrich Co LLC, 400 Summit Drive, Burlington, MA 01803 Job Location: Sigma-Aldrich Co LLC, 6000 N. Teutonia Avenue, Milwaukee, WI 53209 Responsibilities: * Design and execute experiments with the objective of optimizing chemical processes in a flow setting; * Conduct work following Safety and Ergonomic policies established by the company and with the highest regard for quality; * Maintain accurate documentary records and write reports when necessary; * Transfer the developed process technology to qualification and/or production groups via established protocol; * Lead technical projects when necessary and act as a coach-mentor-expert to help junior staff to develop to their fullest potential; * Plan, build, and maintain continuous reactor systems; * Evaluate potential chemical syntheses to determine if they are amenable to continuous manufacturing; * Assess the costs associated with competing chemical processes to determine the feasibility of synthetic routes; * Present development outcomes to peers and customers; and * Develop new continuous manufacturing technologies to enable novel chemical processes. Requirements: Employer requires a PhD in Chemistry, Chemical Engineering, or a related life science field. In addition, the employer requires the following: * Demonstrated ability assembling, maintaining, and understanding mechanical parts for laboratory devices, including pumps, pipes, fittings, regulators, and gauges, gained through three (3) years of work experience or through completion of a related doctorate-level thesis; * Demonstrated understanding of chemical synthesis and safe chemical handling gained through three (3) years of work experience or through completion of a related doctorate-level thesis; * Demonstrated understanding of purification techniques, including crystallization, distillation, and chromatography, gained through three (3) years of work experience or through completion of a related doctorate-level thesis; and * Demonstrated understanding of chemical analysis (GC, mp, HPLC, IR, UV, NMR) gained through three (3) years of work experience or through completion of a related doctorate-level thesis. All years of experience may be gained concurrently. In the alternative, the employer will accept a Master's degree in Chemistry, Chemical Engineering, or a related life science field and three (3) years of work experience as a Chemist or related occupation. In addition, the employer requires the following: * Demonstrated ability assembling, maintaining, and understanding mechanical parts for laboratory devices, including pumps, pipes, fittings, regulators, and gauges, gained through three (3) years of work experience or through completion of a related doctorate-level thesis; * Demonstrated understanding of chemical synthesis and safe chemical handling gained through three (3) years of work experience or through completion of a related doctorate-level thesis; * Demonstrated understanding of purification techniques, including crystallization, distillation, and chromatography, gained through three (3) years of work experience or through completion of a related doctorate-level thesis; and * Demonstrated understanding of chemical analysis (GC, mp, HPLC, IR, UV, NMR) gained through three (3) years of work experience or through completion of a related doctorate-level thesis. All years of experience may be gained concurrently. This position is eligible for the Sigma-Aldrich Co LLC's Employee Referral Program. Applicants can send resumes to Sigma-Aldrich Co LLC., 400 Summit Drive, Burlington, Massachusetts 01803 (Attn: Req #287374) or apply online at **************************** 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 ********************************************************

R&D Meat Food Scientist Salary: $73K and Up (Depending on Experience) Benefits: Full Benefits, Bonus, Health, 401K, Vacation & more. . Contact: *********************************** ******************************************************* Our client, a fast-growing premier food manufacturing company with products sold worldwide, is seeking an experienced R&D Meat Food Scientist for their Research Laboratory. This position will support multiple manufacturing plant facilities. Come join this team of fascinating R&D professionals who are leading the way to outstanding products & exciting innovation. Responsibilities: Create new food formulations and samples through R&D. Identify new ingredients to apply towards new innovative food products. Document product specifications & processes that will be consistent with the production of various manufactured food products. Conduct internal & external audits at multiple locations to measure product quality. Manage food product document control and records, specifications, attaining food safety, verification, product identification trace and incident management. Work with the R&D team to assure all specifications (ingredient specification, formula specification, making specifications, finished product specifications, trade specifications, labeling specification, proper handling specifications) are accurately developed before product launch. Requirements: BS. Degree in a related field of Food Science, Microbiology, Meat Science, Animal Science or Chemistry 2+ years or more experience in R&D or Food Technology from a food manufacturing or food development company. 2+ years of R&D experience with meat products. Knowledge of FDA & US Government regulations, including labeling & nutritional facts with use of Genesis Nutritional Software. Must be detailed oriented with excellent communication skills. Excellent technical writing skills. Experience with MS Office Suite and Excel. Ability to travel regionally with some overnight stays required. Some flexibility to work from home on occasion. Must be currently authorized to work in the USA without the need for visa sponsorship now or in the future. If you are interested, please send me your updated MS Word version of your resume and cover letter. Or if you know of someone that would be a great match, please have them contact - John Marino at *********************************** Or apply directly here online by clicking the “APPLY NOW” link: ******************************************************* #FoodTechnologist #R&D #ResearchAndDevelopment #Meat #MeatScience #SimplyHired #Monster.com #Indeed.com #LinkedIn #ZR #ZipRecuiter #Jobs #pork #poultry #beef #proteins

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Position Summary: The Scientist I performs testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, GLP Study work, product testing/development work. Authority: The Scientist receives sufficient authority from, and is accountable to, the Specialty Analysis Manager or Lab Director, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. Essential Duties and Responsibilities: Perform testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions. Instrumentation utilized will include a wide array including not limited to HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate). Perform and document method transfers, development work, validations/verifications. Maintain neat and accurate records. Ensuring that the client receives quality data by compiling and/or reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations or other internationally recognized standards (e.g., ISO/IEC 17025:2017). Interact with clients to assist in selection of test methods and interpretation of test data. Assist Sales and Business Team members on quote review if requested. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data. Enter testing data into LIMS and monitor for QC failures. Assist lab staff in determining corrective actions for QC failures. Review and approve laboratory analytical data including peer review Review and issue reports to clients. Maintain chemical/reagent traceability. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager. Maintain regular attendance and punctuality Conducts all activities in a safe and efficient manner Performs other duties as assigned Assist with case studies, white papers if requested by Sr. Management for marketing purposes. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments. Qualifications BS or greater in Chemistry or related field, 2+ years experience in a commercial laboratory in an autonomous environment Proficiency at HPLC, LCMS, GC, GCMS, and knowledge of all other major analytical instrument capabilities is imperative Knowledge of ISO 17025, CVM, FDA or other regulatory standards Additional Information Schedule: Monday-Friday 9:00am-5:00pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Position Summary: The Scientist I performs testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, GLP Study work, product testing/development work. Authority: The Scientist receives sufficient authority from, and is accountable to, the Specialty Analysis Manager or Lab Director, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. Essential Duties and Responsibilities: Perform testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions. Instrumentation utilized will include a wide array including not limited to HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate). Perform and document method transfers, development work, validations/verifications. Maintain neat and accurate records. Ensuring that the client receives quality data by compiling and/or reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations or other internationally recognized standards (e.g., ISO/IEC 17025:2017). Interact with clients to assist in selection of test methods and interpretation of test data. Assist Sales and Business Team members on quote review if requested. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data. Enter testing data into LIMS and monitor for QC failures. Assist lab staff in determining corrective actions for QC failures. Review and approve laboratory analytical data including peer review Review and issue reports to clients. Maintain chemical/reagent traceability. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager. Maintain regular attendance and punctuality Conducts all activities in a safe and efficient manner Performs other duties as assigned Assist with case studies, white papers if requested by Sr. Management for marketing purposes. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments. Qualifications BS or greater in Chemistry or related field, 2+ years experience in a commercial laboratory in an autonomous environment Proficiency at HPLC, LCMS, GC, GCMS, and knowledge of all other major analytical instrument capabilities is imperative Knowledge of ISO 17025, CVM, FDA or other regulatory standards Additional Information Schedule: Monday-Friday 9:00am-5:00pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

This position requires a self-driven, well organized, experienced Food Scientist who can exercise decision making skills and time management. This position supports the company's production facility with the responsibilities that are included below. Primary Responsibilities: Work with cross functional teams in the development of new high complexity product formulations and/or reformulations of existing products, including commercialization. Manage a portfolio of assigned high-level product development projects through the various stages of the product development life cycle. Duplicate competitive seasonings for flavor, texture, color, nutritional content, and adherence to FDA and USDA standards and regulations. Facilitate product development by working with suppliers as well as marketing, quality and production. Utilizes knowledge of current regulations, product formulation, supplier specifications, customer requirements and Company standards to develop and update finished product ingredient statements and nutritional documents as defined by FDA and USDA, in addition to product specifications and processing procedures. Independently initiates, investigates, and implements significant new process improvements, and cost savings projects. Working with sourcing, assess raw material substitutions for usage and formulation consistency Coordinate with the Quality Department to comply with HACCP and all Food Safety Programs Support operations through project handoff and during production with formulation issues Stay up-to-date on new regulations and current events regarding food science by reviewing FDA and USDA regulations. Provide guidance to other Food Scientist(s) Comply with GMP, personal hygiene, HACCP and other quality and employee safety programs Other duties as assigned Skills & Qualifications: Bachelor's in Food Science/ Biology/ Chemistry or related field with relevant 5+ years' work experience in seasonings, spices, sauces, processed foods, sausage or meat snacks industry preferred Knowledge of product specifications, nutrition and labeling for finished products and ingredients Demonstrated experience in high-level product development and formulation from concept to completion Proven ability to apply food science and food engineering principles to solve problems Strong computer skills, especially Excel Ability to effectively communicate and interact when working with cross-functional teams Well organized with the ability to prioritize projects and adapt to changing deadlines Ability to take initiative and work independently Willingness to cultivate career-growth opportunities and advancement within a progressive, forward-thinking firm with a proven record of steady growth

Salary : $54,000 - $56,000, depending on experience and qualifications The Center for Cancer Cell Biology, Immunology, and Infection in the Department of Microbiology & Immunology at the Chicago Medical School, Rosalind Franklin University of Medicine & Science, is seeking applications for a full-time Research Associate (Postdoctoral Level) in the laboratory of Dr. Rahul Vijay. This position will focus on investigating the dynamics of immune responses during various pathogenic insults and identifying potential immunomodulatory interventions to enhance adaptive immunity . Our generous benefits package includes medical, dental, and vision plans; paid parental leave; short term and long term disability plans; life insurance; flexible spending accounts; and a 403(b) retirement plan which includes a 8% employer contribution after 2 years of service. RFUMS is committed to employee wellbeing and work-life balance. Full time staff are eligible for 3 weeks of vacation/ paid leave, 15 sick days, and 13 holidays plus two floating holidays. Who We Are Rosalind Franklin University of Medicine and Science (RFU) is a graduate health sciences university committed to serving the population through the interprofessional education of health and biomedical professionals and the discovery of knowledge dedicated to improving wellness. The university embodies the spirit of inquiry and excellence modeled by its namesake Dr. Rosalind Franklin, whose Photo 51 was crucial to solving the structure of DNA. Today, the university's 6 colleges continue Dr Franklin's legacy through rigorous academics, pioneering research, and innovative community service. Our unique interprofessional education model allows students to learn from and with each other in a variety of settings, including our simulation labs, the student-led Interprofessional Community Clinic, and through partnerships with area hospitals and clinics. RFU is a national leader in interprofessional research and practices, and is nationally recognized for its research in areas including neuroscience, brain-related diseases, inherited disorders, proteomics, cancer cell biology and immunology, cardiac resuscitation, and gait and balance. Essential Duties & Responsibilities As a member of the Vijay Lab and in collaboration with other research groups at RFUMS and beyond, the candidate will be expected to: Lead independent research projects , including planning, execution, data collection, analysis, and manuscript preparation. Train and mentor graduate students , fostering their growth toward research independence. Work independently and collaboratively within a team-oriented research environment. Demonstrate strong English communication skills (written and verbal). Foster an inclusive and diverse research environment. Conduct the following specific research activities: Flow cytometry (multicolor analysis) Mouse handling and colony management Nucleic acid extraction and preparation for PCR-based assays Western blotting and molecular biology techniques (including cloning) Mammalian and bacterial cell culture maintenance Expression and purification of recombinant proteins and plasmids Immunofluorescence microscopy Mass spectrometry Data analysis using Microsoft Office, GraphPad Prism, and other relevant software Conditions of Employment Must achieve satisfactory results from a background check Compliance with the current COVID19 vaccination policy Required Education & Experience Ph.D. in Microbiology, Immunology, or a related field Expertise in multicolor flow cytometry Research experience in vaccination strategies and immune modulation A strong record of peer-reviewed publications Required Knowledge, Skills, & Abilities Expertise in multicolor flow cytometry Research experience in vaccination strategies and immune modulation A strong record of peer-reviewed publication Preferred Qualifications Ph.D. in Microbiology or Immunology. Typical Physical Demands & Working Conditions Selected candidate must have the mental and physical capabilities to perform the essential functions of the position with or without reasonable accommodations. EOE, Including Disability / Vets

Quantitative, Translational & ADME Sciences Department has an open position for a Scientist II position. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including extraction, data analysis and interpretation. Responsibilities: • Perform high throughput quantitative in vivo and in vitro LC-MS/MS analysis, troubleshooting and problem solving of small molecule compounds from various bio-matrices. • Operate, perform routine maintenance, and hands-on troubleshooting of AB Sciex LC-MS/MS systems. • Train and mentor junior scientists. • Maintain excellent documentation of all work including LIMS, electronic notebooks, test methods, and protocols. • Work closely with multiple teams across Discovery and QTAS to support bioanalysis. • Write or contribute to study reports for regulatory submissions. Skills: • Proven method development experience using various extraction, chromatographic and analytical methodologies. • Proven experience with quantitative bioanalysis of small molecules. • Proven experience operating and troubleshooting Agilent HPLCs, Leap/CTC PAL autosamplers and AB Sciex Mass Spectrometers. • Detail oriented and committed to generating high-quality results within tight deadlines and across different projects. • Proven ability to work independently or under minimal supervision in a high-throughput environment to design and conduct experiments, interpret, document, and communicate results, as well as in a team environment to collaborate successfully across other groups within R&D. • Communication, interpersonal, and presentation skills. • Work experience in regulated bioanalysis and/or CRO Facility settings is a plus. Education and experience: • M.S. (2+ years preferred), or B.S. (3-6+ years preferred) in analytical chemistry or related field with relevant academic/pharmaceutical industry experience. Leadership Competencies: • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance. • Learns fast, grasps the "essence" and can change course quickly where indicated. • Raises the bar and is never satisfied with the status quo. • Creates a learning environment, open to suggestions and experimentation for improvement. • Embraces the ideas of others, nurtures innovation and manages innovation to reality. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Shivangi Email: ********************************* Internal Id: 25-35903

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission. Job Description Your Role at Baxter This is where your work saves lives. The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate II at Baxter, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. As a key part of projects, our research and development team is responsible for delivering results to drive decisions and ensure safety of our existing and new products. We work on products that make a meaningful difference in others' lives. When you join Baxter, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure! Your Team While everyone at Baxter has a shared passion for our mission, the R&D teams play a meaningful role in our ability to save and sustain lives. Scientists and engineers in R&D work together to develop, test, sustain, and launch products that improve patient care. As a Research Associate II, you will be responsible for performing analytical testing with minimal assistance, demonstrating technical knowledge to troubleshoot problems and handle non-routine situations, assisting and mentor other team members, and embracing accountability for deliverables and leading team discussions/initiatives. While you will primarily support stability testing, you may also support new product development and/or sustaining product initiatives. What you'll be doing Conduct critical chemical and physical analyses on finished product stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or department projects. Work under minimum supervision. May act as a study director for studies, supervisor for testing exceptions and owner for laboratory investigations. Independently evaluate results and impact to studies/laboratory. May provide training and supervision to junior members within the laboratory. Routinely provide advice and assistance to team members regarding unique problems. Perform review of test data, which includes overall documentation practices. Perform review functions in LIMS or other computerized systems. Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to be a system owner or conduct validations. Perform advanced chemical assays requiring precise analytical skills and understanding of chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations. Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support. Support project teams and lead initiatives. Embrace accountability for critical decisions and deliverables within area of responsibility. Influence program, project and/or functional leadership and cross-functional teams. Proposes and drives solutions to complex technical problems in area of expertise. Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation. What you'll bring Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with at least 2+ years of experience. Analytical chemistry instrumentation experience (e.g. HPLC, UPLC, pH, KF, etc.) Must have HPLC/UPLC/UHPLC experience in a regulated environment and strong technical problem-solving skills. Must have good oral and written communication skills, strong analytical skills and be detail oriented. Electronic Lab Notebook experience is preferred. Pharmaceutical GMP laboratory experience is desired. Empower experience is preferred. Stability study execution and/or method validation experience is desired. Must be able to handle multiple tasks concurrently and in a timely fashion. Possess relevant laboratory/technical, writing, and computer skills. Ability to organize and communicate complex information effectively with managers and peers. Physical Activities and Requirements: Must be able to hand write and use computers for the majority of the work day. Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing. May require standing for extended periods. Must be able to lift up to 10 pounds routinely. This work is subject to hazards including exposure to chemicals, drug products, and bacteria. This includes Penicillin, Cephalosporin, their related products and/or materials. The individual must not be allergic to Penicillin, Cephalosporin, or their related products and/or materials. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $80,000 - $110,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.