Scientist Jobs in Cudahy, WI

$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.

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

Our client is a is a leader in the development of sustainable and innovative biotechnological solutions. One of our competencies is as a manufacturer of flavors and ingredients for food and beverage manufacturers. We are looking to hire an experienced Fermentation Scientist who will be responsible for developing, optimizing, and scaling fermentation processes for the production of high-value bio-products. This position involves working collaboratively with the R&D team to design experiments, analyze data, and translate laboratory findings into commercial applications. The successful candidate will have a strong background in microbiology, fermentation, and bioprocess engineering, with a passion for innovation and problem-solving. This position requires a Master's Degree or a PhD in one of the natural sciences. This position is eligible for relocation assistance. (Key Words: yeast, bacteria, cloning, genetically modified natural products, probiotics, gene manipulation) Key Responsibilities: Fermentation Process Development • Design, execute, and optimize fermentation experiments to achieve target yields, productivity, and product quality. • Develop and refine protocols for microbial growth, metabolite production, and downstream processing. • Scale laboratory fermentation processes to pilot and production levels. Research and Innovation • Investigate and identify new microbial strains and fermentation technologies to enhance product development. • Stay current with advancements in fermentation science and propose innovative approaches to improve processes. • Collaborate with cross-functional teams to align fermentation projects with company goals. Data Analysis and Reporting • Monitor and analyze fermentation performance using analytical tools and techniques. • Maintain accurate and detailed records of experiments and results. • Prepare technical reports, presentations, and recommendations for internal and external stakeholders. Equipment Operation and Maintenance • Operate and maintain fermentation equipment, including bioreactors, pumps, and sensors. • Troubleshoot and resolve equipment or process-related issues. • Ensure laboratory equipment is calibrated and in compliance with quality and safety standards. Education and/or Experience: Master's degree in Microbiology, Biochemistry, Biotechnology, or related field (Ph.D. preferred). 2+ years of experience in fermentation process development or bioprocessing (industry experience is a plus). Lactic acid bacteria production / manufacturing know-how (R&D and scale-up) Cryopreservation and freeze-drying knowledge Yield optimization - media optimization, survivability optimization, process design Strong understanding of microbial physiology, metabolic pathways, and bioprocessing principles. Hands-on experience with bioreactors and fermentation equipment. Proficiency in analytical techniques, such as HPLC, GC, spectroscopy, or similar methods. Familiarity with process scale-up and technology transfer is preferred. Excellent problem-solving and critical-thinking abilities. Strong verbal and written communication skills for reporting and team collaboration. Ability to work independently and as part of a multidisciplinary team. We offer a competitive base salary, annual bonus, generous PTO, Medical and Dental Insurance, 401K, and relocation assistance for the successful candidate. You must currently live and work inside the USA in order to be qualified for this job. US Citizens or US Permanent Residents preferred. Sponsorship is NOT being offered for this role. Join a leader in the food industry. Apply for this job today!

CONTRACT MUST HAVES: Ph.D. in Biomedical Engineering or M.D. in a specialized area of Neuroscience/Neuro-Oncology and 5+ years experience Demonstrable experience with drug delivery to the Central Nervous System, including related surgical procedures and medical devices Role Description: The successful candidate will lead investigation of innovative device-based drug delivery solutions to improve tissue exposure when systemic delivery does not fully exploit the potential of our drugs. In close collaboration with partner functions in Discovery and Development Biological Sciences, the incumbent will develop a thorough understanding of delivery barriers and associated biology, and lead the search, evaluation, and assessment of relevant delivery technologies. This role offers the opportunity to shape strategy, develop and champion concepts, and assemble the data package to support translation into clinical development. The ideal candidate will also have strong writing and editorial skills to create peer-reviewed publications. Key Responsibilities: • Supplier Due Diligence: Execute due diligence on potential device suppliers, emphasizing those with capabilities to facilitate pathways to clinical trials and commercial launches. Partner with medical device suppliers throughout early development stages. • Preclinical Study Design: Collaborate in developing study protocols by providing expert insights to enhance device performance and achieve targeted endpoints effectively. • Data Analysis and Presentation: Analyze and interpret data from preclinical studies, focusing on drug biodistribution, efficacy, and toxicity. Co-author presentations designed to assist stakeholders in making informed project milestone decisions. • Publications: Co-author and co-edit white papers and external publications to share insights and findings with the broader scientific community. Qualifications: • Educational Background: Ph.D. in Biomedical Engineering or M.D. in a specialized area of Neuroscience/Neuro-Oncology. 5+ years experience • Drug Delivery to the CNS: Demonstrable experience with drug delivery to the Central Nervous System, including related surgical procedures and medical devices. • Research Publication Skills: Proven ability to independently draft peer-reviewed papers. Strong skills in editing, reviewing, and revising manuscripts to ensure clarity and coherence. Excellent communication abilities for collaborating with co-authors and editorial board members.

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.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description We are hiring for multiple Scientist I positions in North Chicago, IL. Purpose: Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline. Responsibilities: + Independently design and conduct critical experiments that further project goals. + Implement and may innovate new experimental protocols/techniques. + Understand the goal and maintain a high proficiency in his/her projects as well as the overall program. + Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. + Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner. + Perform routine and complex tasks competently and independently and generate reliable and consistent results. + Impact projects mostly through lab and/or pilot plant based activities. + Responsible for compliance with all applicable Corporate and Divisional policies and procedures. + Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. Qualifications + Bachelor's Degree or equivalent education with typically 5 years of experience, or Master's Degree or equivalent education with typically two years of experience. + Theoretical and practical knowledge to carry out the job functions. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. + We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. + This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: ************************************************************* AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: ************************************************************* Salary: $35,000 - $172,500

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Key responsibilities: Assisting with method development for endogenous molecule/biomarker bioanalysis in supporting drug discovery and translational research for preclinical and clinical studies Performs and ensures analytical work in compliance with applicable regulations Perform method development and validations of bioanalytical assays Conduct assays utilizing automated pipetting extraction instruments, HPLC with LC/MS detection technique. Use computer skills to compile and analyze assay results Assume responsibility or assist in writing reports Review and approve data Drafts and reviews reports Reviews SOPs Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Associate Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-2 years) In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: General lab skills: lab safety, solution preparations, use of balances, pH meter, pipettes, and other instruments is a must Knowledge of bioanalytical extraction techniques and Instrumentation: PPT, LLE, SPE Experience with HPLC, LC/MS, Data Processing and Analysis (SCIEX Analyst) is a plus Good documentation skills Working Environment: Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Compensation and Benefits The hourly pay range estimated for this position based in Illinois is $27.41-$45.68. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description: Perform analytical testing of biologics products using HPLC and/or CE techniques. Author/review technical documents including eLN, protocols, and reports. Qualifications Education: B. S. Degree required in Analytical Sciences, Biochemistry or related field. Master or Ph. D. preferred Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus. Thank you. Kind Regards, Harris Kaushik Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO DIRECT # - (650)-399-0891 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Job Title: Scientist II - Immuno-oncology DiscoveryJob Description We are seeking a multidisciplinary Scientist II to join our Immuno-oncology Discovery team to perform proof of concept experiments that advance novel therapeutic modalities. The successful candidate will utilize skills in cellular and molecular biology, biochemistry, immunology, and/or cancer biology to conduct studies for novel oncology drugs. This role requires a strong desire to continue in a laboratory-focused environment to support the discovery and development of new cancer therapeutics. Responsibilities + Design and conduct critical experiments that further project goals. + Efficiently organize and present scientific plans/results at project team meetings. + Implement and innovate new experimental protocols/techniques. + Generate reliable data in a timely manner, interpret results, and draw conclusions from experiments. + Manage multiple research activities and possess a broad range of technical expertise. + Clearly and concisely communicate to internal and external stakeholders. + Exhibit strong teamwork and collaborative attitude within a fast-paced multi-disciplinary environment. Essential Skills + Broad and versatile technical expertise in cell/molecular biology (e.g., cell culture, gene editing, co-culture systems, flow cytometry, PCR, standard cellular assays). + Technical expertise in biochemical assays (e.g., Western blot, ELISA, MSD, FRET, additional cell and assay techniques). + Excellent oral and written communication skills. + Proficiency with software programs including MS Excel, PowerPoint, Word, GraphPad, and FloJo. + Masters Degree in cell/molecular biology, oncology/immuno-oncology, or a related field with 3-5 years of experience. Additional Skills & Qualifications + Experience in oncology drug discovery, small molecule PROTAC, or biologics is a plus. + A PhD scientist is preferred but not required. + Highly developed communication skills and ability to engage internal and external team members in collaborative research. + Enthusiasm and passion for executing innovative scientific research. + Impactful research experience demonstrated by high-quality publications, patents, and/or presentations at conferences. Work Environment The work environment is a multi-disciplinary setting. The role is full-time and on-site, requiring a collaborative attitude and a willingness to tackle new challenges in a fast-paced environment. Pay and Benefits The pay range for this position is $40.00 - $42.00/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 North Chicago,IL. Application Deadline This position is anticipated to close on Apr 18, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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.

A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your role At MilliporeSigma, the Associate Flow Production Scientist will manufacture products according to established flow protocols, provide technical support to others and perform operations in support of the group and department. Safely perform operations to meet quality expectations Perform routine assays, processes and/or unit operations Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) Communicate the status of operations and bring deviations to the attention of the Supervisor Provide complete and accurate records consistent with quality guidelines Ensure all applicable logbooks have been filled out completely as required by current procedures Interact with other departments as needed Participate as needed in quality audits Accurately perform procedures independently Improve processes through application of scientific knowledge, experience, and principles in compliance with change control procedures Participate in process improvements under the guidance of a Supervisor or Scientist Train personnel and act as a technical consultant as needed Perform and interpret analytical evaluations of products and intermediates Perform preventative maintenance on flow equipment Physical Attributes: Wear personal protective equipment such as respirator or chemical protective clothing Lift and or push up to 50 pounds Work second shift - 3:30pm - 12:00am Who you Are: Basic Qualifications: Bachelor's Degree in Chemistry, Biochemistry, Biology, Chemical Engineering or related Life Science OR Associates Degree in Chemistry, Biochemistry, Biology, Chemical Engineering or related Life Science with 2+ years of laboratory experience OR High School Diploma or GED Equivalent with 4+ years of laboratory experience Preferred Qualifications: Independent lab research experience. Aptitude for building and repairing flow equipment. Knowledge in chemistry or biochemistry, math and general science. Knowledge of continuous flow production and flow equipment. Familiarity with laboratory instruments and production equipment. Knowledge of process techniques and unit operations. Experience with analytical techniques and equipment. Safe chemical handling methods experience. Proficient with communication (both oral and written), computers, mechanical ability, troubleshooting, interpersonal, laboratory and analytical skills. Knowledge of ISO Quality standards. RSRMS What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious? Apply and find more information at ************************* The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

We Are Accenture is helping companies use generative AI to reinvent their enterprise and optimize business functions for breakthrough innovation and competitive advantage. With over 1,600 professionals dedicated to generative AI, leveraging the depth and experience of more than 40,000 AI and data professionals across the company our Generative AI and LLM Center of Excellence brings together our Experienced Innovation, Strategic Investment, Exceptional Talent, and Power Ecosystem. You Are As an Advanced AI Research Scientist, you formulate real-world problems into practical, efficient, and scalable AI and Machine Learning problems. * You lead a team and provide guidance to explore and implement new methodologies, model building techniques, and cutting-edge algorithms, and applying these techniques with the right architecture to solve real-world problems. * You have a deep understanding and ability to remain at the forefront of generative AI, LLM, and multi-modal models (with a focus on driving innovation by applying these techniques to new business problems, use cases, and scenarios). * As needed by the specific problem, you train and/or fine-tune generative AI models and evaluate on the specific problem. * As a significant part of this role, you will be justifying the value of innovative generative AI or traditional Machine Learning approaches (or a combination of both) in the business problems, and you'll be expected to construct methodologies that clearly demonstrate their value. * You'll also work collaboratively with teams from both the business and technical side, including users, use case representatives, business owners, engineers, architects, and UI designers, to achieve end-to-end project development goals. The Work * Participate internal and external discussions to gather business use case requirements, provide on the spot AI expertise and AI solution options for business problems. * Design, develop and implement advanced AI/ML models, especially LLM and other Gen AI models from scratch or existing foundation models via self-supervised learning, transferred-learning, and fine-tuning techniques. * Design, develop and implement highly sophisticated Gen AI based applications including generative agent and similar architectures which support multiple Gen AI models to work together for complex tasks. * Lead technical teams and grow true AI expertise within broader team including offshore * Collaborate seamlessly with diverse, cross-functional teams to accurately identify and prioritize requirements, ensuring that the AI solutions meets the needs and expectations of various stakeholders. * Develop and execute an AI solution project plan with team, timeline, and infrastructure dependency. * Define and implement a value justification approach to the AI solutions; estimate solution cost with right technological choices; and calculate ROI. * Create and maintain comprehensive technical documentation that comprehensibly captures the intricate details of the solution, capture IP, facilitating seamless understanding, knowledge transfer and future development. * Collaborate with academia partners to stay on the cutting edge of AI, especially Gen AI technologies, provide through leadership on AI trend, AI use case innovation trend, new AI opportunities, or foreseeable limitation, risks, and concerns. Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements. This is a hybrid role based in Mountain View, California. Qualification Here's What You Need * Minimum of 4 years of experience in designing and developing neural network models, especially deep learning model, and Foundation models. * Minimum of 4 years of experience of experience in building, fine-tuning Foundation models including LLMs and multi-modal models. * Minimum of 4 years of strong working knowledge of the different technologies, their differences, modalities in the Generate AI space. * Minimum of 4 years of working knowledge and familiarity with different LLM driven application architecture patterns. * Minimum of 4 years of experience in deep learning and neural networks, in particular training and large language models with popular libraries and GPUs. * Minimum of 4 years of working knowledge of computer architecture, and familiarity with the fundamentals of GPU architecture. * Minimum of 4 years of proven experience with processor and system-level performance modelling. * Minimum of 2 years of experience of technical team management or team mentoring. * Bachelor's degree or equivalent (minimum 12 years) work experience. (If Associate's Degree, must have minimum 6 years' work experience) Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired in California, Colorado, District of Columbia, Illinois, Maryland, Minnesota, New York or Washington as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Annual Salary Range California $73,800 to $220,400 Colorado $73,800 to $190,400 District of Columbia $78,500 to $202,700 Illinois $68,300 to $190,400 Minnesota $73,800 to $190,400 Maryland $68,300 to $176,300 New York $68,300 to $220,400 Washington $78,500 to $202,700 #LI-NA-FY25 Locations

Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners. Job description: Quantitative, Translational & ADME Sciences Department has an open position for a Scientist II position in North Chicago, IL. 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. Requirements: M.S. (2+ years), or B.S. (6+ years) in analytical chemistry or related field years of relevant academic/pharmaceutical industry experience. 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. The ideal candidate is 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. Strong communication, interpersonal, and presentation skills. Work experience in regulated bioanalysis and/or CRO Facility settings is a plus. Key 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. Additional Information All your information will be kept confidential according to EEO guidelines.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma in Milwaukee, WI we are seeking a Scientist - Analytical Development to develop, execute and evaluate new analytical methods, technologies, and experimental plans in support of chemical process development and manufacturing. * Develop, improve, or optimize analytical laboratory methods supporting ongoing research, process development and custom chemical manufacturing * Design and execute experiments with the goal to assess reaction conditions, raw material quality and final product purity * Support process development with rapid - response analytics * Transfer the developed analytical platforms to quality control operations via departmentally supported procedures * Maintain databases, document work and results accurately and generate technical reports * Establish credibility as individual contributor and work as a team to achieve goals, including meeting deadlines and productivity markers * Execute appropriate on-line and literature searches in support of assigned work and/or troubleshooting * Interpret spectral and other analytical data for structural elucidation and chemical understanding * Problem solving and troubleshooting in support of departmental or plant operations * Present scientific rationales for unexpected experimental outcomes including out-of-specification products * Participate in the development of new technologies with applications in laboratory, in - line or at - line testing * Assist process development team in establishing specifications for intermediates and final products Who You Are: Minimum Qualifications: * PhD in Chemistry, Chemical Engineering or other Scientific discipline OR * Master's Degree in Chemistry, Chemical Engineering or other Scientific discipline * 2+ years' experience in an industrial process development or QC environment OR * Bachelor's degree in Chemistry, Chemical Engineering or other Scientific discipline * 5+ years' experience in an industrial process or QC development environment Preferred Qualifications: * Knowledge of chemical synthesis and safe chemical handling * Basic chemical analysis skills (GC, mp, HPLC, IR, UV, NMR). Knowledge of spectra interpretation and mathematics * Experience with techniques such as ICP-MS, GC-MS, LC-MS, IC, and wet chemical analysis * Effective oral and written communication skills * Technical writing (experimental procedures, reports, etc.) Computer literate (SAP, Word, Excel, PowerPoint, Lotus Notes, etc.) * Organizational and time management skills. Interpersonal skills and knowledge of ISO Quality standards 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 ********************************************************

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. The VBRI will attract and retain a diverse workforce and faculty body that reflects the community we serve. We believe that societal change requires actions, not words, and are deeply committed to diversity of backgrounds, experiences, and thought to advance excellence in science and medicine. Versiti is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment based on age, sex, race, color, religion, national origin, veteran status, disability, or sexual orientation. 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.

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.