Principal research scientist jobs in West Allis, WI - 73 jobs

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 investigators, 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 began, 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 Develops and elucidates scientific aims, experimental design and execution. A Research Scientist I is equivalent to the Research Assistant Professor position at many universities. The Zhu Lab is primarily focused on unraveling the mechanisms of receptor transmembrane signaling. Specifically, our attention is directed towards cell surface receptors featuring single transmembrane domains, such as integrins, receptor tyrosine kinases, and receptor-like tyrosine phosphatases. Through a multidisciplinary approach encompassing structural biology, protein engineering, biochemistry, and cell biology techniques, we aim to elucidate how these receptors transmit signals across the cell membrane. Our investigations center on understanding the conformational regulation triggered by ligand binding at the extracellular domain or cytoplasmic domain stimulations. Our goal is to illustrate the intricate mechanisms governing receptor-ligand interactions and the conformational changes necessary for transmembrane signaling, spanning the extracellular, transmembrane, and cytoplasmic domains. We are currently engaged in several projects, delving into the conformational requirements for bi-directional transmembrane signaling in integrins, elucidating the structural and functional basis of integrins as pathogen receptors, exploring integrin ligand interactions, and developing antibodies and small molecules that target or stabilize specific integrin conformations. Integrins, crucial cell surface receptors, play a pivotal role in regulating cell-cell and cell-matrix interactions across various biological processes, including development, hemostasis, antigen recognition, homing, and inflammation. Dysregulation of integrin activation is observed in pathological conditions such as autoimmune diseases and thrombosis. Our overarching goal is to uncover the intricate correlation between receptor conformational regulation and signal transduction, aiming to contribute to the design of more efficient and safer therapeutic agents. A new focus of our lab entails unraveling the mechanism behind coronavirus spike protein-mediated cell fusion and viral infection. We aim to apply the gained knowledge to develop inhibitors for antiviral treatment and diverse virus-based applications, including cell-specific gene delivery and oncolysis. 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 With direction from PI, assists in designing goal-oriented, hypothesis driven research program(s) Takes advantage of opportunities to apply for local or national grants as applicable to fund relevant research Experimental work and data analyses Maintains an active scientific publication and presentation record based on individual and PI's research. Minimum of one high impact in addition to multiple publications. Provides direction and/or supervise research technologists, pre- and postdoctoral trainees. Actively contributes to the scientific community in the Blood Research Institute Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification Understands and performs in accordance with all applicable regulatory and compliance requirements Complies with all standard operating policies and procedures Qualifications Education PhD PhD, MD, or equivalent degree in related scientific area required Experience 1-3 years postdoctoral experience required Knowledge, Skills and Abilities Demonstrated ability to independently apply understanding of scientific theory to the structure and execution of research experiments. required Demonstrated ability to interpret and explain the theoretical basis of the work performed. required Ability to perform research procedures independently. required Immediate proficiency in basic and sophisticated tests and procedures required in the scientific field. required Exceptional organizational, communication and problem solving skills. required Strong detail orientation and analytical ability. required Ability to prioritize and execute multiple tasks and meet deadlines. required Ability to supervise, coordinate and plan the work of several individuals involved in a project. required #LI-EH1 #VBRI

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Discover Impactful Work The Senior Process Development (Sr. PD) Scientist is responsible for developing, optimizing, and technology transfer of processes to the production area, while meeting specific quality, schedule, and cost requirements. The Sr. PD Scientist designs and carries out multiple, complex steps of chemical reactions and purifications of products independently and in accordance with established procedure. The Sr. PD Scientist also provides a high level of technical expertise and leadership across the company and must exercise judgment within broadly defined practices and policies. A Day in the life Follow established methods and standard operating procedures Work independently or lead a team to troubleshoot problems, recommend and execute improvements in laboratory operations and equipment use Analyze and simulate existing/new processes; design and execute experiments for characterization, isolation and purification of new product/processes using various techniques in process development/manufacturing Discover, develop and optimize reliable, robust and cost-efficient processes that are amenable to scale change. Evaluate processes for safety and reproducibility during development and scale up Write technical reports, critical experiment plan, item qualification and operating procedures for product manufacturing and equipment Provide product costing analysis. Evaluate equipment need, and provide selection and safety recommendation Provide technical leadership, coaching, and training to Manufacturing and Process Development staff on process optimization and scale up. Provide technical presentation to staff and Management team When needed, act as the project manager when working individually or with cross-functional teams to prepare for new product launches or other operational projects Participate/lead PPI projects The individual must understand and comply with RCRA Standards The position is also responsible for any other duties apparent or assigned. Keys to Success Education Ph.D. required, or an equivalent combination of degree and experience in nucleic acids or peptide chemistry. Experience 8+ years of demonstrated industrial experience in multistep organic synthesis, purification, process development/validation, scale up of heterocyclic compounds (Nucleic Acids/Peptide preferred), product analysis and instrumentation (HPLC, LC/MS, NMR) Demonstrated experience in process development techniques and application (process optimization, experimental design, and data analysis) Must possess expert analytical, troubleshooting, mathematical/data analysis, and technical writing skills, along with the ability to present information effectively to audiences of varying technical understanding Strong understanding of analytical data, troubleshooting, and method development Knowledge, Skills and Abilities Must be available to work overtime, including weekends as project schedule warrants Ability to regularly handle chemicals, solvents, and potentially hazardous substances Be mechanically adept and able to apply mechanical fundamentals to properly operate, the equipment within their area of responsibility Specific vision abilities required: close vision, distant vision, depth perception, ability to adjust focus, and differentiate colors The employee is occasionally required to walk, sit, stoop, bend, kneel, crouch, and crawl and frequently lift and/or move 50 pounds and occasionally lift and/or move more than 50 pounds with assistance 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!

AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. AbbVie employs approximately 28,000 people worldwide and markets medicines in more than 170 countries. Job Description APPLY HERE!!!! mygradjob.com/job/senior-scientist-8/ We are looking for a highly motivated person who drives new technologies and processes. The candidate will develop drug product formulations and scalable manufacturing processes for NBEs used in clinical trials through all phases of development. Working closely with analytical and formulation scientists in an integrated group the candidate will operate via multi-functional, global teams including API manufacturing, Process R&D, Pre-formulation and Pilot Plant Operations. Major Responsibilities The incumbent will participate in the development of parenteral formulation for monoclonal antibodies and antibody drug conjugates, Independently design and execute studies evaluating the stability (chemical & physical) of the monoclonal antibodies and antibody constructs/conjugates against solution conditions (pH, ionic strength, temperature, light e.tc) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, filtration and Lyophilization), and screen excipients (buffers, stabilizers, surfactants, tonicity & Tg' modifiers e.t.c) to develop robust formulations for frozen, refrigerated liquid and lyophilized dosage forms Perform upfront manufacturability assessment of the formulation candidates and recommend the best and back up formulation for both FIH and commercialization Make concise scientific presentations of experimental results to the management and author detailed scientific technical reports. Author CMC relevant sections of INDs/CTDs, as well as response questions scientific project lead, generating original technical ideas for formulation and analytical technologies of assigned NBE development projects Establishment and coordination of external development activities including supervision of technical, financial and regulatory requirements Qualifications Basic: BS and typically 10+ years of experience; MS or equivalent education with typically 8+ years of experience; PhD 0+ years of experience in formulation or analytical development of NBEs Scientific understanding of the structure & function of monoclonal antibodies and antibody constructs/conjugates, and their modes of degradation/stabilization An understanding of scientific approach to develop biologic protein formulations Strong lab skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays) Basic understanding of unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized NBEs Hands on expertise of bio analytical test methods for protein pharmaceuticals e.g. mass-spectrometry, HPLC and electrophoretic methods, particle imaging, ELISA, compendial tests Broad expertise around regulatory requirements for NBEs (mAbs, bispecifics, ADCs) and parenteral products is preferred (21 CFR parts 600 & 210, FDA cGMP-, ICH-, EU GMP-guidances). Statistical knowledge and experience is preferred e.g. capability analysis, gauge R&R and design of experiments (DOE) methodologies Additional Information All your information will be kept confidential according to EEO guidelines.

Salary: $65,000 - $70,000 annually, commensurate with experience The Center for Cancer Cell Biology, Immunology, and Infection (Department of Microbiology & Immunology) in the Chicago Medical School at Rosalind Franklin University of Medicine & Science is inviting applications for two Research Scientists positions. They will be involved in studying molecular virology, host-pathogen interaction, and substance use/abuse comorbidity. 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. RFU 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 The individuals will be expected to perform the following duties and responsibilities: (1) Design and conduct experiments; (2) Maintain detailed laboratory records; (3) Collect, analyze, and present data; (4) Work independently and as a team; (4) Prepare manuscripts. Conditions of Employment Must achieve satisfactory results from a background check Required Education & Experience PhD in biology, biomedical science, and related fields Required Knowledge, Skills, & Abilities A minimum of 3 years of wet laboratory research experience and skills broad biomedical knowledge and understanding well versed in main cell biology, biochemistry, and molecular biology techniques exceptional organization skills and adept with Microsoft Office tools, GraphPad Prism (or other data analysis software) Preferred Qualifications training or work experience in virology work experience with mice Typical Physical Demands & Working Conditions Selected candidates must have the mental and physical capabilities to perform the essential functions of the position with or without reasonable accommodations. EOE, Including Disability / Vets

**Duration: 6 months contract** **Purpose:** + The Genomics Research Center (GRC) is part of the Quantitative Medicine and Genomics (QM&G) functional area that promotes data-driven innovation in drug discovery by integrating diverse quantitative data and leveraging advanced computational models. + The GRC's goal is to develop world class genetics and genomics research focused on finding the right therapeutic targets and helping scientists better understand not only human disease biology but also the behavior and response to our drugs in clinical trials across all therapeutic areas. + Join our innovative Genomic Technologies (GTECH) lab team, where we are at the forefront of genomic research and discovery. + Our team is dedicated to advancing science through cutting-edge technologies and collaborative efforts. + We are seeking an experienced and highly organized **Sample Management** and Processing Scientist + (I) to support impactful **reverse translation** focused projects. In this role, daily responsibilities will center on supporting g **DNA isolation** from **clinical samples** across multiple therapeutic areas. + The Scientist (I) will execute manual and automated workflows for **high-quality nucleic acid** extraction, perform rigorous quality control assessments on isolated nucleic materials, maintain detailed and accurate **documentation in LIMS,** and interpret and report QC data. + In addition, effective cross-functional communication with researchers is essential to ensure the integrity and utility o **f isolated gDNA for downstream analyses** . + The successful candidate should have hands-on expertise with **diverse nucleic acid extraction methodologies** , meticulous adherence to SOPs, and a solid understanding of sample biology as it relates to clinical research. + Operational excellence, attention to detail, and organizational skills will be critical to deliver reliable support for reverse translation clinical initiatives. **Responsibilities:** + Adhere to department generated and company standard operating procedures for communication, lab operations, project reporting, and lab safety. + **Perform nucleic acid extraction, quality control,** and interpretation of data with minimal supervision and aligned to delivery within project timelines. + Attain operational proficiency for required daily functions within training schedules. + Perform troubleshooting for wet lab tasks independently and with collaboration. + Maintain clear and accurate documentation of all processes. + Formally and informally communicate project progress, completion, and data by delivering reports through collaborative meetings, and verbal or written presentations. + Timely recording and documentation of wet lab processes and progress in applicable **LIMS and project management** applications in accordance with policies and procedures. + Support the development and testing of LIMS workflows. + Maintain instrumentation as outlined by laboratory standards and manuals. **Qualifications** Experience required. BS degree in Genetics/genomic or related field or equivalent with 4+ years relevant experience, MS degree in Genetics/Genomics with 2+ years relevant experience. Theoretical and practical knowledge to carry out job function including but not limited to: o Experience with performing routine and or **complex nucleic acid workflows** from **source material such as cells, tissues, blood, other biofluids.** o Experience with performing routine and/or **complex nucleic acid quality control** and analyzing/interpreting data including but not limited to fluorescence quantification, absorbance, and integrity analysis. o Experience with **sample processing from source materials to nucleic acids** within a laboratory management system. o **Proficiency in micropipetting** and wet lab automation for multiple genomic laboratory techniques. o Ability to strictly adhere to SOPs and lab guidelines and thoroughly report deviations in a timely manner. o Strong computer skills, especially in Microsoft Office Suite. o Self-directed to deliver timely results both independently and collaboratively in a fast-paced and fluid environment with high attention to detail. o Strategic project planning and critical thinking to resolve routine and complex problems. **Preferred** - Experience with low and **high throughput sample tracking** and data management (LIMS). - Experience with performing and maintaining **workflows on automation platforms.** - Experience in a CLIA certified laboratory or other regulated laboratory environments. - Experience in clinical writing and editing documents/manuals. - Works well in a multidisciplinary team environment. - Capacity to learn new methodologies/techniques quickly and drives innovation to improve workflows. - Demonstrates effective and efficient communication. **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.

We are seeking an experienced and innovative Senior Chemist with deep expertise in aerosol coatings to join our R&D team in the Consumer Product Goods (CPG) sector. This role focuses on developing and optimizing aerosol coating products, ensuring they meet the highest standards of performance, safety, and regulatory compliance. The ideal candidate will possess a strong background in chemistry, particularly in the formulation and application of aerosol products. Technology Competency: The R&D Scientist candidate will demonstrate and apply the following skills to their work. Strong understanding of Scientific Methodology. Hypothesis driven research and problem-solving capability using experimental design, data analysis and documentation. Coating Chemistries: alkyd, acrylic, epoxy, urethane, phenolic, polyaspartics and sil(ox)anes etc. Coating Formulation Science: Lead the design, development, and optimization of aerosol coating formulations, including paints, sprays, and specialty coatings for various consumer applications both solvent borne and waterborne Utilize in-depth knowledge of aerosol technology, including propellant systems, valve systems, and spray mechanisms, to develop high-performance products. Analytical science and material science with an emphasis on structure-property relationship Technical Leadership: Ability to develop and implement project plans and timelines while managing multiple high level projects. Measuring progress and providing updates in alignment with marketing Demonstrated capability of becoming a vocal and influential voice in project planning and deliverables together in collaboration with a cross functional team Ability to make strategic decisions (technical and staff utilization) and influence leaders and scientist to execute those initiative while managing business strategy and value creation Outstanding technical skills, interpersonal communication, and presentation skills. The R&D Scientist must demonstrate and apply the following skills. Drive product innovation by researching and integrating new raw materials, technologies, and methodologies into aerosol formulations to enhance performance, durability, and user experience. Proven track record of identifying, researching and prototyping innovative ideas. Address and resolve complex formulation and application challenges, including issues related to stability, compatibility, and application efficacy Continuous learning and intimate awareness of open literature and competitive landscape The R&D Scientist works to assist in the allocation of resources towards initiatives by working with the leadership team to identify long term platform strategies The R&D Scientist demonstrates the ability to have influence in decision making and a demonstrated ability to communicate with project stakeholders and cross-functional teams, leadership and the external scientific community Organization Leadership: The R&D Scientist should exhibit the following attributes: Agility to respond to emerging business needs with strong management of change skills Builds strong partnerships internally within R&D, internal functions (marketing, manufacturing, sourcing, etc.) and externally (vendors, customers, etc.) Manage high stakes and challenging situations with all levels of the organization Assess the organizational processes and develop new processes to improve efficiency and quality Demonstrate strong career ambition - potential to become a top leader Strong business acumen Education Guidelines BS in Chemistry, Chemical Engineering, Materials, or other equivalent scientific field required MS or PhD strongly preferred 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.

Senior Scientist - Research & Development PS Seasoning, our craft is flavor. A third-generation strong company, we believe that the best recipes are passed down from one generation to the next. From the award-winning food products we make to the customers we serve, our commitment to excellence is the foundation of everything we do. Just like the recipes we create, our team is only successful with a foundation of key ingredients: Customer Focus, Development, Family, Integrity, Teamwork, and Excellence. Since our inception in 1986, we've cultivated a culture of support, togetherness, respect, loyalty, and family values. When you join the PS team, you're part of a family and part of our recipe for success. Position Summary: As part of PS Seasonings' mission to build a world-class R&D organization, the Senior Scientist is a technical leader who will drive innovation in seasonings, sauces, and blends. This role combines hands-on formulation expertise with strategic influence, helping shape the future of flavor at PS. The Senior Scientist will lead complex projects from concept to commercialization, mentor Food Scientists, and partner cross-functionally to bring new ideas to life that delight customers, strengthen partnerships, and fuel business growth. What You'll Do: Lead development of new seasonings, sauces, and blends, including clean-label, functional, and encapsulated technologies. Translate culinary trends and customer requests into differentiated, scalable products. Manage high-complexity projects from concept through commercialization using the Stage Gate process. Conduct pilot trials, scale-ups, and plant validations while solving technical challenges. Partner with suppliers to identify innovative ingredients, technologies, and processes. Collaborate with Sales, Marketing, Operations, Supply Chain, and Quality to align on project goals. Ensure compliance with FDA/USDA regulations, HACCP, GFSI standards, and PS quality systems. Represent PS expertise during customer presentations, tastings, and innovation sessions. Mentor Food Scientists and Technicians, providing coaching and technical guidance. Drive cost-savings initiatives through ingredient optimization, yield improvement, and process efficiency. Maintain product specifications, nutritional documentation, and labeling accuracy. Stay current on food science trends, regulations, and emerging technologies. Other duties as assigned by manager. What We're Looking For: MS/PhD in Food Science, Food Chemistry, or related field; BS with extensive experience considered. 7-10+ years of product development experience, preferably in seasonings, sauces, condiments, or blends. Expertise in flavor systems, ingredient functionality, sensory science, and scale-up. Experience with encapsulation, clean-label strategies, or advanced flavor delivery preferred. Strong knowledge of FDA/USDA labeling, nutrition, and food safety requirements. Proven leadership in managing projects and cross-functional collaboration. Excellent communication skills with both technical and non-technical stakeholders. Hands-on problem-solving ability in plant environments. Highly organized, proactive, and growth-oriented mindset. Benefits of Working at PS Seasoning: When you join the PS family, you'll receive: Competitive Pay • Health, Dental, Vision & Life Insurance • 401K with Company Match • Paid Holidays & Vacation • 50% Off Employee Discount • Employee Appreciation Events • Outdoor Courtyard with Putting Green • Delicious Smells PS Seasoning is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. PS Seasoning participates in E-Verify and will verify employment eligibility for all new hires.

Job DescriptionSenior Scientist - Research & Development PS Seasoning, our craft is flavor. A third-generation strong company, we believe that the best recipes are passed down from one generation to the next. From the award-winning food products we make to the customers we serve, our commitment to excellence is the foundation of everything we do. Just like the recipes we create, our team is only successful with a foundation of key ingredients: Customer Focus, Development, Family, Integrity, Teamwork, and Excellence. Since our inception in 1986, we've cultivated a culture of support, togetherness, respect, loyalty, and family values. When you join the PS team, you're part of a family and part of our recipe for success. Position Summary: As part of PS Seasonings' mission to build a world-class R&D organization, the Senior Scientist is a technical leader who will drive innovation in seasonings, sauces, and blends. This role combines hands-on formulation expertise with strategic influence, helping shape the future of flavor at PS. The Senior Scientist will lead complex projects from concept to commercialization, mentor Food Scientists, and partner cross-functionally to bring new ideas to life that delight customers, strengthen partnerships, and fuel business growth. What You'll Do: Lead development of new seasonings, sauces, and blends, including clean-label, functional, and encapsulated technologies. Translate culinary trends and customer requests into differentiated, scalable products. Manage high-complexity projects from concept through commercialization using the Stage Gate process. Conduct pilot trials, scale-ups, and plant validations while solving technical challenges. Partner with suppliers to identify innovative ingredients, technologies, and processes. Collaborate with Sales, Marketing, Operations, Supply Chain, and Quality to align on project goals. Ensure compliance with FDA/USDA regulations, HACCP, GFSI standards, and PS quality systems. Represent PS expertise during customer presentations, tastings, and innovation sessions. Mentor Food Scientists and Technicians, providing coaching and technical guidance. Drive cost-savings initiatives through ingredient optimization, yield improvement, and process efficiency. Maintain product specifications, nutritional documentation, and labeling accuracy. Stay current on food science trends, regulations, and emerging technologies. Other duties as assigned by manager. What We're Looking For: MS/PhD in Food Science, Food Chemistry, or related field; BS with extensive experience considered. 7-10+ years of product development experience, preferably in seasonings, sauces, condiments, or blends. Expertise in flavor systems, ingredient functionality, sensory science, and scale-up. Experience with encapsulation, clean-label strategies, or advanced flavor delivery preferred. Strong knowledge of FDA/USDA labeling, nutrition, and food safety requirements. Proven leadership in managing projects and cross-functional collaboration. Excellent communication skills with both technical and non-technical stakeholders. Hands-on problem-solving ability in plant environments. Highly organized, proactive, and growth-oriented mindset. Benefits of Working at PS Seasoning: When you join the PS family, you'll receive: Competitive Pay • Health, Dental, Vision & Life Insurance • 401K with Company Match • Paid Holidays & Vacation • 50% Off Employee Discount • Employee Appreciation Events • Outdoor Courtyard with Putting Green • Delicious Smells PS Seasoning is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. PS Seasoning participates in E-Verify and will verify employment eligibility for all new hires.

In this role you will be a leading Scientist focused on defining and executing innovative strategies for biocompatibility evaluation and risk analysis of medical devices in the GE HealthCare Imaging/ X-ray/ CT family of businesses. This will include leading strategy for biocompatibility-related standards, acting as GE HealthCare's voice as policies develop, and overseeing programs to ensure successful implementation internally and with external bodies such as standard organizations and regulatory authorities. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job Description Roles and Responsibilities: * Design and execute medical device biocompatibility strategies to assure user and patient safety through the application of current biological evaluation and toxicological principles in support of new product development and sustaining activities. * Standardize test methods across multiple material and device types, leveraging common data to derive meaningful conclusions on the potential for biocompatibility concern. * Lead and author Biocompatibility deliverables - e.g., biological evaluation plan & reports, hazard analysis, white paper, technical memo, and other relevant activities in support of global programs. * Implement the use of ISO 10993 series, 21CFR58 GLP for non-clinical studies, and/ or other regulatory guidance documents to qualify GE Healthcare products. * Provide technical and strategic input to meet business objectives at the project team level while assuring compliance with GE Healthcare and external standards. * Interpret raw material, finished device data, and literature to assess overall risk to patient. * Develop justification to address ISO 10993 - 1 endpoints based on study data and literature. * Independently review literature and identify relevant information to support product development and registration. * As needed - engage in standards organization and/ or regulatory committees to ensure emerging regulations are based on well-established science and toxicological principles. * Keep upto date on regulatory requirements and assess the impact of new standards and/or regulations to enable the generation of appropriate strategies for biocompatibility work. Required Qualifications: * PhD in physical/organic/biochemistry, toxicology, material science, bioengineering, or an equivalent scientific field. * Expert knowledge in use and application of ISO 10993 series of standards * Experience (10+ years) in design and development of medical devices that are categorized as FDA Class I, II and Class III. * Experience conducting material and chemical characterization of medical devices, physicochemical analyses of polymeric materials, metals, and ceramics. * Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer's requirements. * Advanced experience and proficiency with MS Office word processing, spreadsheet, presentation, and collaboration applications. Desired Characteristics: * American Board of Toxicology Diplomate (DABT), or other national equivalent such as ERT. * Experience leading test lab operations that support medical device biocompatibility evaluations. * Experience in mechanical design (15+ years). * Experience as a lead convenor of a Technical Committee (TC) or Working Group (WG) of a Standards Development Organization (SDO) or National Standards Body (NSB) such as ISO, ANSI, or AAMI. * Experience preparing communications for and interacting with multiple regulatory bodies world-wide such as FDA, NMPA, TGA, MHLW, PMDA, CDSCO, BfArM, ANSM, etc. * Experience with high risk, life supporting, and life-sustaining products. * Demonstrated life-long learner; eagerness to obtain new skills and knowledge. * Humility in understanding, but assertive when needed; willing to make decisions and assign clear priorities. * Strong oral and written communication skills. Strong interpersonal and leadership skills. Demonstrated ability to analyze and resolve problems. Inclusion and Diversity GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. #LI-HOU1 Additional Information Relocation Assistance Provided: Yes

Job Title: Scientist 1, Sample Management and Sample ProcessingJob Description Join an innovative Genomic Technologies lab team at the forefront of genomic research and discovery. We seek an experienced and highly organized Sample Management and Processing Scientist to support impactful reverse translation projects. The role focuses on gDNA isolation from clinical samples across various therapeutic areas, executing manual and automated workflows for high-quality nucleic acid extraction, and maintaining detailed documentation in LIMS. Effective cross-functional communication with researchers is essential to ensure the integrity of isolated gDNA for downstream analyses. Responsibilities + Adhere to department and company standard operating procedures for communication, lab operations, project reporting, and lab safety. + Perform nucleic acid extraction, quality control, and data interpretation with minimal supervision, aligned to project timelines. + Achieve operational proficiency for required daily functions within training schedules. + Independently and collaboratively troubleshoot wet lab tasks. + Maintain clear and accurate documentation of all processes. + Communicate project progress, completion, and data through reports, meetings, and presentations. + Record and document wet lab processes and progress in LIMS and project management applications according to policies and procedures. + Support the development and testing of LIMS workflows. + Maintain instrumentation as outlined by laboratory standards and manuals. Essential Skills + Bachelor's degree in Genetics/Genomics or related field with 4+ years relevant experience, or Master's degree with 2+ years relevant experience. + Experience in performing routine and complex nucleic acid workflows from various source materials. + Proficiency in performing nucleic acid quality control and data analysis, including fluorescence quantification and integrity analysis. + Experience with sample processing from source materials to nucleic acids within a laboratory management system. + Skilled in micropipetting and wet lab automation for genomic laboratory techniques. + Ability to strictly adhere to SOPs and lab guidelines and report deviations promptly. + Proficient computer skills, especially in Microsoft Office Suite. + Self-directed in delivering timely results independently and collaboratively in a fast-paced environment. + Strategic project planning and critical thinking to resolve routine and complex problems. Additional Skills & Qualifications + Experience with low and high throughput sample tracking and data management (LIMS). + Experience with automation platforms and maintaining workflows. + Experience in a CLIA-certified or other regulated laboratory environments. + Experience in clinical writing and editing documents/manuals. + Ability to work well in a multidisciplinary team environment. + Capacity to learn new methodologies and drive innovation to improve workflows. + Demonstrates effective and efficient communication. Work Environment The work environment involves working in an advanced Genomic Technologies lab, utilizing cutting-edge technologies and equipment. The role requires adherence to lab safety standards and SOPs. The team fosters a collaborative and innovative atmosphere, encouraging strategic project planning and problem-solving. Job Type & Location This is a Contract position based out of North Chicago, IL. 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 Jan 26, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%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. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Position Summary The Scientist I performs testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor 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, unknown/material identification, failure analysis, simple de-formulations and select product testing/development work. Legal and Insurance work will typically be performed under the guidance of the Scientist II. Essential Duties and Responsibilities Perform testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor 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 FTIR, HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, FIA, LECO N2, Calorimetry, Physical and Thermal Analysis (includes DSC, TGA, DMA - outsourced) NMR interpretation 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. 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. Issue quotations for standard testing services where existing tests/methods are utilized. 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. Support the completion of unknown and failure investigations through testing performance and/or imparting chemical knowledge. 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 Education/Experience MS or PhD in Chemistry or related field or BS and 2+ years experience in a commercial laboratory. Experience as Expert Witness on Legal and Insurance Cases is highly desirable. Ability/Skills: Proficiency at GC, GCMS, HPLC, LCMS and knowledge of all other major analytical instrument capabilities is imperative. Additional Information 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. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Position Summary The Scientist I performs testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor 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, unknown/material identification, failure analysis, simple de-formulations and select product testing/development work. Legal and Insurance work will typically be performed under the guidance of the Scientist II. Essential Duties and Responsibilities Perform testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor 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 FTIR, HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, FIA, LECO N2, Calorimetry, Physical and Thermal Analysis (includes DSC, TGA, DMA - outsourced) NMR interpretation 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. 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. Issue quotations for standard testing services where existing tests/methods are utilized. 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. Support the completion of unknown and failure investigations through testing performance and/or imparting chemical knowledge. 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 Education/Experience MS or PhD in Chemistry or related field or BS and 2+ years experience in a commercial laboratory. Experience as Expert Witness on Legal and Insurance Cases is highly desirable. Ability/Skills: Proficiency at GC, GCMS, HPLC, LCMS and knowledge of all other major analytical instrument capabilities is imperative. Additional Information 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.

Salary: $65,000 - $70,000 annually, commensurate with experience The Center for Cancer Cell Biology, Immunology, and Infection (Department of Microbiology & Immunology) in the Chicago Medical School at Rosalind Franklin University of Medicine & Science is inviting applications for two Research Scientists positions. They will be involved in studying molecular virology, host-pathogen interaction, and substance use/abuse comorbidity. 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. RFU 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 The individuals will be expected to perform the following duties and responsibilities: (1) Design and conduct experiments; (2) Maintain detailed laboratory records; (3) Collect, analyze, and present data; (4) Work independently and as a team; (4) Prepare manuscripts. Conditions of Employment * Must achieve satisfactory results from a background check Required Education & Experience * PhD in biology, biomedical science, and related fields Required Knowledge, Skills, & Abilities * A minimum of 3 years of wet laboratory research experience and skills * broad biomedical knowledge and understanding * well versed in main cell biology, biochemistry, and molecular biology techniques * exceptional organization skills and adept with Microsoft Office tools, GraphPad Prism (or other data analysis software) Preferred Qualifications * training or work experience in virology * work experience with mice Typical Physical Demands & Working Conditions * Selected candidates must have the mental and physical capabilities to perform the essential functions of the position with or without reasonable accommodations. EOE, Including Disability / Vets

Job DescriptionDescription: At Curion, We Connect Brands to People. Our expertise and passionate pursuit of insights enable our clients to make informed decisions that drive meaningful impact. Our vision? Advancing the way brands connect to people to build a better future. Our core values: Integrity, Resiliency, Accountability, Curiosity, and Collaboration. Position Summary: As a member of the onsite team and under the supervision of the Account Manager, the Sensory Panel Leader has responsibility for supporting the sensory research programs and clients by coordinating Descriptive Analysis (DA), and other research as needed including test set-up, execution, and data analysis. Curion is looking for someone with a strong potential for growth into a leadership position. The ideal candidate would have a solid technical background in sensory testing methodology and the ability to effectively communicate with clients. Key Responsibilities: · Panel leadership and management, including but not limited to leading training and testing, communicating with panelists, managing panel dynamics, engagement, etc. · Support and execute panel performance measurement plan including but not limited to implementing calibration/validation exercises and providing panelists performance feedback. · Create and/or program ballots and questionnaires to support studies as needed. · Manage high quality, timely research in response to the client needs. · Interact with clients to ensure a clear understanding of project objectives, progress, product tracking, timelines, and deliverables. Receive project requests and communicate with client to schedule testing. Attend project meetings as needed. · Support study reporting with data entry, graphing, photographing samples, and editing presentations as needed. · Support special projects including, but not limited to, coordinating department meetings, setting up new procedures, and documenting protocols. · Actively participate on technical team offering suggestions, making recommendations, and assuming responsibility as needed. · Develop and enhance skills in sensory evaluation, consumer research, and data analysis. · Identify, develop, and execute new, novel approaches to research individually or as part of a team. · Perform other duties to ensure lab functions at high level such as procurement, sample preparation, etc. as needed. Physical Requirements: Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. · Standing, bending, walking, lifting/carrying, and reaching required to perform essential job functions in a laboratory environment including but not limited to preparation and storage of chemical dilutions, lab cleanup, test area setup and breakdown, etc. · Be able and willing to smell various fragrances and malodors and participate in odor evaluation training as needed · Be able and willing to apply and evaluate products on the skin. Qualifications: Education and Experience · Undergraduate degree in science or related major. · 1 or more years of experience in a research environment; experience with sensory testing or product research strongly preferred. Essential Skills · Ability to communicate effectively with others, both orally and in writing. · Assertiveness - Ability to act in a self-confident manner to facilitate completion of a work assignment or to defend a position or idea · Excellent organizational, planning and prioritization skills to meet challenging deadlines · Ability to effectively present information publicly · Ability to adapt to change in the workplace · Ability to accept responsibility and account for their actions. · Strong analytical skills · Excellent interpersonal skills - Ability to get along well with a variety of personalities and individuals, and to actively listen, and be approachable. · Motivation - Ability to inspire oneself and others to reach a goal and/or perform to the best of their ability. · Reliability - The trait of being dependable and trustworthy. · Ability to solve problems and manage conflict within a group setting. Computer Skills · Proficient in Office 365 including Microsoft Word, Excel, PowerPoint, Outlook, OneNote, and MS Project. · Sensory Data collections software experience preferred (e.g., RedJade, Compusense, FIZZ, EyeQuestion, etc.) For Curion's Associate Sensory Scientist position, we offer a starting hourly rate between $20.00-$23.00 per hour based on the qualifications and experience of each individual. Curion offers a benefits package for this position which includes: 401(k) retirement account with company match Health, dental, vision, basic life, short and long-term disability, accident insurance, critical insurance, pet insurance, flexible spending account (FSA), and more. Paid time off (PTO) Company paid holidays Curion is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. About Curion: Curion specializes in delivering impactful insights to the world's top CPG companies, helping them develop winning, repeatedly purchased products. Curion's deep data-driven product insights, sensory expertise, and state-of-the-art consumer centers enable them to uncover responses to critical client objectives. With over five decades of experience in the product testing industry, Curion is dedicated to guiding clients with their proprietary XP Xperience Performance platform, connecting brands to consumers at every step. An innovator in the industry, Curion recently developed a groundbreaking benchmarking product testing method, the Curion Score™, which has become a trusted and sought after tool within the industry. As one of the largest product and consumer insights companies in the U.S., Curion has built a reputation for excellence and trust among the world's leading consumer brands. Curion's commitment to innovation and expertise, coupled with a passion for delivering actionable insights, makes Curion a valuable partner for companies looking to develop and launch successful products. Requirements:

Our award-winning client is seeking a Senior Food Scientist to join their team.As a Senior Food Scientist / Culinologist, you will play a crucial role in developing and innovating new food products. You will be responsible for conducting research, formulating new products, and optimizing existing formulations. Your expertise in food science and culinary arts will be essential to driving product development and meeting customer needs. Responsibilities: Develop and formulate new food products, including dairy-based products, to meet customer requirements. Create and evaluate flavors to enhance the taste and aroma of food products. Conduct sensory and analytical testing to assess product quality and performance. Optimize production processes to improve efficiency and reduce costs. Provide technical support to customers and sales teams. Ensure compliance with food safety and regulatory standards. Maintain accurate and detailed documentation of research, development, and testing activities. Required Qualifications: Master's degree in Food Science or related field, or Bachelor's degree with 3-10 years of relevant experience. Strong understanding of food science principles, including chemistry, microbiology, and sensory evaluation. Experience in dairy science and fermentation chemistry is a plus. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Experience with laboratory equipment and techniques. Knowledge of food safety and regulatory requirements. Benefits: Competitive salary and bonus potential. Comprehensive benefits package including health, dental, and vision insurance. 401(k) with company match. Generous PTO and paid holidays. Relocation assistance.

AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. AbbVie employs approximately 28,000 people worldwide and markets medicines in more than 170 countries. Job DescriptionAPPLY HERE!!!! mygradjob.com/job/senior-scientist-8/ We are looking for a highly motivated person who drives new technologies and processes. The candidate will develop drug product formulations and scalable manufacturing processes for NBEs used in clinical trials through all phases of development. Working closely with analytical and formulation scientists in an integrated group the candidate will operate via multi-functional, global teams including API manufacturing, Process R&D, Pre-formulation and Pilot Plant Operations. Major Responsibilities The incumbent will participate in the development of parenteral formulation for monoclonal antibodies and antibody drug conjugates, Independently design and execute studies evaluating the stability (chemical & physical) of the monoclonal antibodies and antibody constructs/conjugates against solution conditions (pH, ionic strength, temperature, light e.tc) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, filtration and Lyophilization), and screen excipients (buffers, stabilizers, surfactants, tonicity & Tg' modifiers e.t.c) to develop robust formulations for frozen, refrigerated liquid and lyophilized dosage forms Perform upfront manufacturability assessment of the formulation candidates and recommend the best and back up formulation for both FIH and commercialization Make concise scientific presentations of experimental results to the management and author detailed scientific technical reports. Author CMC relevant sections of INDs/CTDs, as well as response questions scientific project lead, generating original technical ideas for formulation and analytical technologies of assigned NBE development projects Establishment and coordination of external development activities including supervision of technical, financial and regulatory requirements Qualifications Basic: BS and typically 10+ years of experience; MS or equivalent education with typically 8+ years of experience; PhD 0+ years of experience in formulation or analytical development of NBEs Scientific understanding of the structure & function of monoclonal antibodies and antibody constructs/conjugates, and their modes of degradation/stabilization An understanding of scientific approach to develop biologic protein formulations Strong lab skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays) Basic understanding of unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized NBEs Hands on expertise of bio analytical test methods for protein pharmaceuticals e.g. mass-spectrometry, HPLC and electrophoretic methods, particle imaging, ELISA, compendial tests Broad expertise around regulatory requirements for NBEs (mAbs, bispecifics, ADCs) and parenteral products is preferred (21 CFR parts 600 & 210, FDA cGMP-, ICH-, EU GMP-guidances). Statistical knowledge and experience is preferred e.g. capability analysis, gauge R&R and design of experiments (DOE) methodologies Additional Information All your information will be kept confidential according to EEO guidelines.

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: Analytical characterization and assessment of clinical trial supplies (e.g. GMP compliant stability and release testing for both drug substances and drug products) Understand corporate standards regarding code of conduct, safety, and GxP compliance. Responsible for compliance with all applicable Client policies and procedures. Document experimental data appropriately in laboratory documentation systems. Maintains laboratory equipment and optimize laboratory operations for safe and efficient use of time and resources. Troubleshoots equipment and experimental problems. Laboratory operational support for the group's experimental development and testing activities Complex solution preparation in a GxP environment Laboratory balance checks and pH meter standardizations Inventory/resource management (e.g. ordering supplies, stockkeeping, etc.) Laboratory hygiene including waste disposal management and safety checks Document experimental data appropriately in an electronic laboratory notebook Problem solving, either independently or with assistance, pertaining to experiment and/or instrumentation issues Identify areas for improvement in laboratory operations to improve efficiency and resource usage and assist in continuous improvement activities Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2-4 years' experience) OR Masters degree with 0-2 years' experience 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: Experience in a regulated cGMP Lab Experience in analytical methodology, such as chromatography (HPLC/GC/IC), KF, UV and common compendial methods required. Experience in some specialty techniques required (LCMS, GCMS, PXRD, ICP, Dissolution, Disintegration). Experienced in laboratory systems (LIMS, CDS, ELN) required. Full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance Proven problem solving and troubleshooting abilities 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! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. *This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. 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: *****************************************************

Sensory Scientist Application works under the guidance of the Applications Manager and collaborates cross-functionally with Sales, R&D, and Management. This role combines benchwork and sensory science responsibilities to support the development and presentation of innovative ingredient solutions. This position operates within FDA, FSMA, and Global Food Safety Initiative (GFSI) requirements defining food safety standards for the safe production of food in the plant and offices, within the standards of defined risk levels by area. ESSENTIAL FUNCTIONS Reasonable Accommodations Statement To perform this job successfully, an individual must be able to satisfactorily perform each essential function. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Essential Functions Statement(s) Apply deep knowledge of Butter Buds' products to develop innovative applications and demos. Conduct benchwork and maintain accurate records of formulas, batch sheets, and results. Design, execute, and improve sensory testing (e.g., triangle, preference), ensuring reliable data. Develop and maintain a standardized sensory lexicon for internal and customer-facing use. Present sensory and application data to Sales, R&D, and leadership to support decision-making. Coordinate and lead internal tastings and sensory panels. Support training efforts and provide technical guidance to Applications, Sales, and Marketing. Stay current with food and sensory science trends to drive innovation. Prepare samples and technical presentations for trade shows and customer visits. Maintain a safe, clean, and organized lab workspace. Collaborate cross-functionally on sensory initiatives. POSITION QUALIFICATIONS Competency Statement(s) Communication, Oral - Ability to communicate effectively with others using the spoken word. Problem Solving - Ability to find a solution for or to deal proactively with work-related problems. Communication, Written - Ability to communicate in writing clearly and concisely. Accountability - Ability to accept responsibility and account for his/her actions. Commitment Ability to work within companys policies of customer satisfaction and teamwork within a collaborative environment. SKILLS & ABILITIES Education: Advanced degree in sensory, food science or related field of study. Experience: 4-8 years technical experience in a food laboratory. Working knowledge of food chemistry: protein, carbohydrates, fats and their interactions. Computer Skills: Proficient with Microsoft Word and Excel.

Job Title: Scientist 1, Sample Management and Sample ProcessingJob Description Join an innovative Genomic Technologies lab team at the forefront of genomic research and discovery. We seek an experienced and highly organized Sample Management and Processing Scientist to support impactful reverse translation projects. The role focuses on gDNA isolation from clinical samples across various therapeutic areas, executing manual and automated workflows for high-quality nucleic acid extraction, and maintaining detailed documentation in LIMS. Effective cross-functional communication with researchers is essential to ensure the integrity of isolated gDNA for downstream analyses. Responsibilities + Adhere to department and company standard operating procedures for communication, lab operations, project reporting, and lab safety. + Perform nucleic acid extraction, quality control, and data interpretation with minimal supervision, aligned to project timelines. + Achieve operational proficiency for required daily functions within training schedules. + Independently and collaboratively troubleshoot wet lab tasks. + Maintain clear and accurate documentation of all processes. + Communicate project progress, completion, and data through reports, meetings, and presentations. + Record and document wet lab processes and progress in LIMS and project management applications according to policies and procedures. + Support the development and testing of LIMS workflows. + Maintain instrumentation as outlined by laboratory standards and manuals. Essential Skills + Bachelor's degree in Genetics/Genomics or related field with 4+ years relevant experience, or Master's degree with 2+ years relevant experience. + Experience in performing routine and complex nucleic acid workflows from various source materials. + Proficiency in performing nucleic acid quality control and data analysis, including fluorescence quantification and integrity analysis. + Experience with sample processing from source materials to nucleic acids within a laboratory management system. + Skilled in micropipetting and wet lab automation for genomic laboratory techniques. + Ability to strictly adhere to SOPs and lab guidelines and report deviations promptly. + Proficient computer skills, especially in Microsoft Office Suite. + Self-directed in delivering timely results independently and collaboratively in a fast-paced environment. + Strategic project planning and critical thinking to resolve routine and complex problems. Additional Skills & Qualifications + Experience with low and high throughput sample tracking and data management (LIMS). + Experience with automation platforms and maintaining workflows. + Experience in a CLIA-certified or other regulated laboratory environments. + Experience in clinical writing and editing documents/manuals. + Ability to work well in a multidisciplinary team environment. + Capacity to learn new methodologies and drive innovation to improve workflows. + Demonstrates effective and efficient communication. Work Environment The work environment involves working in an advanced Genomic Technologies lab, utilizing cutting-edge technologies and equipment. The role requires adherence to lab safety standards and SOPs. The team fosters a collaborative and innovative atmosphere, encouraging strategic project planning and problem-solving. Job Type & Location This is a Contract to Hire position based out of North Chicago, IL. 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 Jan 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.