Scientist Jobs in Wilton, CT

W-2 Candidates only!! The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: Karl Fischer, Thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, particle size analysis are desirable. Job responsibilities may include analytical method development and validation; GMP stability and release testing; testing to support pharmaceutical development efforts; presentation of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. Working knowledge in analytical method development, validation, and testing in a cGMP environment. Experience with a wide-variety of software and information systems (e.g., Timao, TRIOS, Omnic, E-Workbook, LabWare LIMS). Experience in problem-solving skills and instrument trouble-shooting. Good oral and written communication skills and the ability to write technical reports. The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry.

Duration: 24+ Months We are seeking a highly skilled and motivated scientist at the Scientist II level to join our Immunology and Respiratory Disease Department located in Ridgefield, CT. The successful candidate, with a demonstrated ability to work in a matrix environment, will work within the Translational Biology group to develop in vitro cellular models relevant to fibrotic diseases. Candidate will work in a highly collaborative group and will support research projects that aim deliver innovative drug concepts for clinical development. Duties & Responsibilities: ● Work with lab managers and team members to plan and execute cellular assays using primary human cells. Experience with 2D and 3D cultures is a plus. ● Execute relevant cellular/molecule functional assays (ELISA, TaqMan qPCR, color-metric based assays etc.) and cell-based imaging with minimal supervision. ● Perform literature searches and extract relevant information from published protocols and implements them; demonstrate the ability to interpret outcome of experiments and to propose appropriate follow-up. ● Effectively communicate work orally and in writing; independently complete high quality work notebook and contribute to writing protocols and provide input for scientific reports; demonstrate agility in learning new techniques and adaptability to a matrixed work culture. ● Work in a collaborative manner with other members in the department; participate in cross departmental project teams when needed. ● Report and treat data with a high level of integrity and ethics; comply with applicable regulations, perform all work in a safe manner; maintain proper records in accordance with SOPs and policies. Skills: ● Previous hands-on experience in tissue culture is a must (primary human cell culture experience is a plus). ● Practical experience in basic molecular assays such as RNA isolation, qPCR, and/or ELISA is preferred. ● Practical experience or knowledge in imaging based cellular assay (i.e., immunofluorescence, live-cell imaging) is a plus. ● Proficient with basic analysis software such as Excel (must) and GraphPad Prism (preferred). ● Strong ability to work in a matrix environment. Requirements: ● Bachelor's Degree with 3+ years' experience or Master's Degree in immunology, molecular biology, biochemistry, or equivalent experience in related field.

12 Month Contract Onsite in New Haven, CT This is what you will do: The temporary Associate Scientist is responsible for performing assigned experimental tasks to support the development and optimization of cell line development and cell culture processes for the client's therapeutic protein candidates. The temporary Associate Scientist will work in collaboration with other members of Product Development and Clinical Supply, and with scientific staff in other Research & Development groups. The temporary Associate Scientist II will support and execute development studies for biologics lifecycle management and yield improvement with use of process intensification. You will be responsible for: • Perform routine upstream lab activities including medium preparation, seed train passages, bioreactor sampling, and analyzer maintainence in support of various upstream programs under supervision • Execute experimental studies to develop, optimize, and characterize upstream processes for therapeutic protein candidates under supervision • Executes experimental studies to support scale up of processes at pilot scale • Provide weekend support on critical upstream activities on rotation basis • Document study results in notebooks, and technical reports • Coordinate laboratory management including ordering and maintenance • Communicate scientific findings to colleagues within the group through informal presentations You will need to have: • BS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university, with minimal 2 years of relevant industrial experience, or MS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university • Understanding the fundamentals of biology, chemistry and chemical engineering • Strong learning agility to learn new techniques The duties of this role are generally conducted in an lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours. We would prefer for you to have: • Relevant experience working in a relevant laboratory setting • Excellent written and verbal skills and strong interpersonal skills • Collaborative and effective communication skills • Experience with various MS Office programs, including Word, Excel, Outlook, and PowerPoint

12 Month Contract (May extend or convert to permanent) $33.10/hour W2 The Associate Scientist is responsible for performing assigned experimental tasks to support the development and optimization of cell line development and cell culture processes for the company's therapeutic protein candidates. The Associate Scientist will work in collaboration with other members of Product Development and Clinical Supply, and with scientific staff in other Research & Development groups. The Associate Scientist II will support and execute development studies for biologics lifecycle management and yield improvement with use of process intensification. Responsibilities: Perform routine upstream lab activities including medium preparation, seed train passages, bioreactor sampling, and analyzer maintenance in support of various upstream programs under supervision Execute experimental studies to develop, optimize, and characterize upstream processes for therapeutic protein candidates under supervision Executes experimental studies to support scale up of processes at pilot scale Provide weekend support on critical upstream activities on rotation basis Document study results in notebooks, and technical reports Coordinate laboratory management including ordering and maintenance Communicate scientific findings to colleagues within the group through informal presentations Requirements: BS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university, with minimal 2 years of relevant industrial experience, or MS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university Understanding the fundamentals of biology, chemistry and chemical engineering Strong learning agility to learn new techniques The duties of this role are generally conducted in an lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours. Preferred Skills: Relevant experience working in a relevant laboratory setting Excellent written and verbal skills and strong interpersonal skills Collaborative and effective communication skills Experience with various MS Office programs, including Word, Excel, Outlook, and PowerPoint

Temporary Assignment through 04/10/2026 This is what you will do: The temporary Associate Scientist is responsible for performing assigned experimental tasks to support the development and optimization of cell line development and cell culture processes for companies therapeutic protein candidates. The temporary Associate Scientist will work in collaboration with other members of Product Development and Clinical Supply, and with scientific staff in other Research & Development groups. The temporary Associate Scientist II will support and execute development studies for biologics lifecycle management and yield improvement with use of process intensification. You will be responsible for: Perform routine upstream lab activities including medium preparation, seed train passages, bioreactor sampling, and analzyer maintainence in support of various upstream programs under supervision Execute experimental studies to develop, optimize, and characterize upstream processes for therapeutic protein candidates under supervision Executes experimental studies to support scale up of processes at pilot scale Provide weekend support on critical upstream activities on rotation basis Document study results in notebooks, and technical reports Coordinate laboratory management including ordering and maintenance Communicate scientific findings to colleagues within the group through informal presentations You will need to have: BS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university, with minimal 2 years of relevant industrial experience, or MS degree in Biology, Chemistry, Chemical Engineering or related discipline from an accredited university Understanding the fundamentals of biology, chemistry and chemical engineering Strong learning agility to learn new techniques The duties of this role are generally conducted in an lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: Lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours. We would prefer for you to have: Relevant experience working in a relevant laboratory setting Associate Scientist II Excellent written and verbal skills and strong interpersonal skills Collaborative and effective communication skills Experience with various MS Office programs, including Word, Excel, Outlook, and PowerPoint Military experience equivalency may substitute for some requirements. We are an equal opportunity employer and will consider all applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, disability and/or other protected categories. We are also committed to providing reasonable accommodation(s) to qualified individuals with disabilities or needs, as required by law.

Duration: 12 Months Non-PHD candidates required Required Skills: DNA/RNA PURIFICATION CELLULAR IMMUNOLOGY TISSUE CULTURE CELL CULTURE We are seeking a highly skilled and motivated scientist at the Scientist II level to join our Immunology and Respiratory Disease Department. The successful candidate, with a demonstrated ability to work in a matrix environment, will work within the Translational Biology group to develop in vitro cellular models relevant to fibrotic diseases. Candidate will work in a highly collaborative group and will support research projects that aim deliver innovative drug concepts for clinical development. Duties & Responsibilities: ● Work with lab managers and team members to plan and execute cellular assays using primary human cells. Experience with 2D and 3D cultures is a plus. ● Execute relevant cellular/molecule functional assays (ELISA, TaqMan qPCR, color-metric based assays etc.) and cell-based imaging with minimal supervision. ● Perform literature searches and extract relevant information from published protocols and implements them; demonstrate the ability to interpret outcome of experiments and to propose appropriate follow-up. ● Effectively communicate work orally and in writing; independently complete high quality work notebook and contribute to writing protocols and provide input for scientific reports; demonstrate agility in learning new techniques and adaptability to a matrixed work culture. ● Work in a collaborative manner with other members in the department; participate in cross departmental project teams when needed. ● Report and treat data with a high level of integrity and ethics; comply with applicable regulations, perform all work in a safe manner; maintain proper records in accordance with SOPs and policies. Skills: ● Previous hands-on experience in tissue culture is a must (primary human cell culture experience is a plus). ● Practical experience in basic molecular assays such as RNA isolation, qPCR, and/or ELISA is preferred. ● Practical experience or knowledge in imaging based cellular assay (i.e., immunofluorescence, live-cell imaging) is a plus. ● Proficient with basic analysis software such as Excel (must) and GraphPad Prism (preferred). ● Strong ability to work in a matrix environment. Requirements: ● Bachelor's Degree with 3+ years' experience or Master's Degree in immunology, molecular biology, biochemistry, or equivalent experience in related field. (No PHD)

We are currently seeking a motivated Senior Principal Scientist to lead our AAV production team within Regeneron Genetic Medicines (RGM). You will oversee a talented team dedicated to supporting early-stage research for Regeneron's gene therapy portfolio and technology development through production and purification of research-grade AAV. As a Senior Principal Scientist, a typical day might include: Directly supervise and manage Regeneron's AAV Research Vector core, setting priorities and goals, facilitating cross-functional collaboration, forecasting demand, developing talent, and interfacing between RGM leadership, requestors, and team members. Identify new strategies, instruments, and technologies to improve process yield, turnaround time, efficiency, consistency, and quality. Collaborating with other Regeneron cores, technology centers, and therapeutic areas. Contributing to departmental, cross-functional, senior leadership, and external meetings by providing expertise and communicating timelines, expectations, and vision. Working closely with RGM teams to enable the next generation of gene therapies. Providing technical support and assisting teams within the lab. Overseeing lab activities and implementation of new technologies and processes. Coordinating production teams to maximize effectiveness and streamline workflows. This might be the right role for you if you: Are passionate about genetic medicines and supporting gene therapy development. Find yourself at home being close to the bench, but want additional leadership responsibilities. Enjoy problem solving and adapting to new technologies and challenges. Want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the RGM pipeline. Are excited to mentor and develop team members, providing growth opportunities, fostering a collaborative environment, and engaging the team with the impact of their work. In order to be considered for this role, you must have at least a Ph.D. and 8-10+ years or a BS/MS and 15+ years of relevant experience in either Chemical Engineering, Biochemical Engineering, Molecular Biology, Gene Therapy or related field. We need someone with a strong foundational understanding of AAV-based gene therapies, protein and/or virus purification, chromatography, process development, and analytical techniques. Must have experience with managing a team (5+ direct reports) and directing the growth and development of our processes and talent. Experience working within or managing a core function or support group is preferred. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. Salary Range (annually) $148,300.00 - $241,900.00 #J-18808-Ljbffr

Come join P2 Science, a Connecticut Innovations portfolio company! https:/p2science.com Founded in 2009, P2 Science was started by two scientists from Yale University, who were disheartened by the widespread use of non-sustainable, synthetic compounds found in everyday use. P2 Science started with a simple vision - develop high performance, innovative ingredients that align with planetary health. P2 Science has become a global leader in bringing naturally derived, sustainable ingredients to market; partnering with brands and manufacturers in 25 countries. Through a proprietary process called Process Intensified Continuous Etherification ("PICE"), P2 transforms renewable forest-derived feedstocks into high-performance ingredients for use in a variety of personal care, cosmetics, and beauty products. The company started up its first manufacturing plant in September 2018. In 2022, P2 won five industry awards, including the Innovation Best Breakthrough Supplier Award from BeautyMatter, one of the most trusted voices in beauty. In January 2023, Unilever's haircare brand, Living Proof, launched three new products built on P2's ingredients. In November 2023, P2 Science announced the appointment of Oihana Elizalde, PhD as Chief Executive Officer. Oihana joined P2 after having served as Head of Sales for BASF Personal Care North America, and VP / General Manager of the MIRUM business at Natural Fiber Welding. P2's investors include Advantage Capital, BASF, Chanel, Connecticut Innovations, Elm Street Ventures, HG Ventures, Lewis & Clark Agrifood, Safermade, and Xeraya. Quality Control Chemist Position Summary: Troubleshooting and testing batches using a variety of QC instruments, while ensuring strict adherence to regulatory standards and maintaining quality in a high-pressure environment. Responsibilities / Job Functions Responsible for overseeing manufacturing QC activities. Prepare, run, and analyze final product and in-process samples, ensuring QC testing is conducted using appropriate, established company methods (work instructions, standard operating procedures). Maintain accurate, complete, and traceable documentation related to analysis. Assist in completing and submitting lab documentation, including deviation investigations, OOS (Out of Specification) investigations, change controls, and their implementation. Perform calibration, troubleshooting, and maintenance of lab instrumentation; assist with scheduling annual Preventive Maintenance (PM). Prepare relevant documents, forms, and records related to QC in compliance with ISO 9001:2015 guidelines. Ensure successful, on-time completion of required training (both internal and external). Adhere to safety standards and regulations as per ISO 9001:2015, Food Safety 22000 requirements, and other company-established policies. Safety Responsibility Comply with all P2 safety policies and procedures. Qualifications B.S. in Chemistry or related field is required. 2-3 years of experience in: QC or raw material testing OOS (Out of Specification) or deviation reporting Experience in a GLP (Good Laboratory Practice) or GMP (Good Manufacturing Practice) environment is a plus Analytical instrumentation, such as GC, HPLC, DSC, viscometer, refractometer, NMR, UV-Vis, KF titration, and other titration methods. Strong attention to detail with excellent oral and written communication skills. Ability to multitask and collaborate effectively across departments. Flexibility to work overtime as needed or adjust schedule to meet manufacturing needs. Ability to lift up to 50 lbs. Why Join Us? Be part of a dynamic team that's leading the way in sustainable beauty innovation. Work in an environment that values creativity, sustainability, and inclusivity. Competitive salary and benefits package, including health, dental, and vision insurance, paid time off, and retirement savings plans. Opportunities for professional growth and development within the company. Make a positive impact on the planet and society through your work. P2 is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About Us Imagine the innovation and expertise behind the world's leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch. With 15 commercial offices and 15 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season. Position Summary The R&D Lab Technician works on different color cosmetic projects from batching formulas, to preparing samples and performing testing in Congers, NY. Essential Functions Make daily lab batches as assigned by chemist or lab manager Assist the color chemist to perform shades counter-matching Prepare samples for submission to clients (lipsticks, pressed powders, lip-glosses) Prepare paperwork for formula submissions and document specifications for various batches Perform testing on formulation (viscosity, volatiles, break points, drop tests…) Maintain detailed, organized records in formulation and project management databases Collaborate with formulators and lab manager to ensure inventory of raw materials are replenished and maintained appropriately Assist the chemists in the development of new shades and formulations Participate actively to the organization of laboratory Keep track of all raw materials and organize them in the most efficient way Maintain and organize the color library Job Qualifications Bachelor's Degree in any related science, such as chemistry, Biology, Physics, etc. 1 year relevant work experience in a lab environment (ideally cosmetics) Color perception and color matching skills, Formulation skills in all color cosmetics technologies, raw material knowledge (especially pigments), FDA guidelines Ability to follow instructions Able to use a computer and enter data in the system Ability to record and document critical batch process documents Attention to accuracy and detail Familiar with measurement scales, mixing, blending, chemical mills and other formulation manufacturing equipment Follow established formulas to create laboratory batches color cosmetics. Observe, record, investigate, duplicate and validate successful procedures. Perform calculations during shade matching under chemist supervision. Prepare and maintain accurate technical data and required documentation. Job Benefits Health Insurance: Comprehensive medical, dental, and vision coverage Retirement Plans: 401(k) plan, often with company matching Life Insurance: Coverage for employees in the event of death or disability Paid Time Off (PTO): Vacation days, sick leave, and personal days Holidays: Paid company holidays and floating holidays Professional Development: Training programs and opportunities for career advancement Performance Bonuses: Annual merit increase and/or bonus based on individual performance Company Events: Team-building activities, social events, and company outings Employee Assistance Programs (EAPs): Confidential counseling and support services for personal and professional issues. EEO Intercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.

We are seeking a skilled and experienced Data Analyst / Data Scientist with ~5 years of industry experience to develop reporting/tools as well as actively participation in the design and measurement of campaigns. End-product will be spreadsheets and/or dashboards that can take inputs (SKU participation, offer value, profitability) and estimate resulting volume. Secondary functions include assisting in media and consumption forecasting. The role is on-location in Stamford, CT, with the expectation of 4 days a week in the office to start, tapering to 3 days once EXPERIENCE • Managing business processes through reporting, analysis • ~5 Years in analytics/analyst roles • A/B Testing experience • CPG Experience is must • Regression modeling and similar experience a plus SKILLS • People skills - comfortable interacting with brand teams, retailer teams, and other stakeholders • Coordinate workstreams, and manage communication between internal business units and external agencies • Expert Excel skills • PowerBI development • Hands-on experience in building ETL/ELT pipelines for data ingestion • Expertise in Python or R for data manipulation, analysis, and model development

Required Skills & Experience - 5+ years of experience coding in Python or R - Comfortable in Linux, Unix, or bash environment - Hands on experience analyzing data within a research environment - Experience developing automated pipelines - Understand how to productionize tools or software - Background in Biomedical / Life Science Industry Nice to Have Skills & Experience - More advance math skills - Implementing new statistics (using math to work with data in new ways) - Hematology and oncology research background - PhD Degree Job Description One of Insight Global's top clients within the biotechnology industry is looking for a computational scientist to sit on site once a week in Terrytown, NY. This person will be supporting hematology and oncology research within their genetics center. The computational scientist will be responsible for building automation and pipelines for semantic variant classification and analyses. They will apply new software and algorithms to create a process of identifying and categorizing somatic mutations based on their characteristics and potential impact. Doing so will allow the team to optimize current datasets and increase analytical capacity. Additional responsibilities include : - Developing version controlled code bases implementing algorithms for somatic calling from population scale genetic data - Leveraging previously generated in-house data assets to test which data types work best - using this to optimize algorithms and genetic data call sets - Developing new genetic phenotypes and datasets without having to perform additional sequencing or generate new experimental data - Returning results to translational and clinical colleagues that address biomedical requests and questions of interest - Improving reproducibility, scalability, and applicability across datasets - Reducing turn-around time to support multiple translation and clinical projects and requests

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 onX,Facebook,Instagram,YouTube,LinkedInandTik Tok. Job Description We are seeking a highly motivated and collaborative scientist with a background in immunology to join the si RNA therapeutics team at AbbVie. The candidate will be part of the newly formed si RNA team to build an internal si RNA platform for translational research to develop transformational therapeutics for immunology, neuroscience and oncology. The successful candidate will be part of a growing therapeutic si RNA group working with cross-disciplinary teams internally and externally. The candidate will serve as a lead scientist on their own project and contribute scientific insights into multiple other projects. Responsibilities: Function as a principal investigator to advance internal si RNA technology and programs related to immunology indications Independently responsible for project science within their area of expertise on one or more project teams Collaborate with therapeutic area colleagues to advance si RNA technology applied to internal programs Direct research and mentor a group of scientists within area of expertise Optimize internal si RNA platforms for functional tissue specific delivery Manage external CROs and internal resources to meet budget and timeline constraints Collaborate closely with internal colleagues to advance cross-functional collaborative experiments and projects Serve as a subject matter expert for si RNA delivery to target tissues and experimental design & execution Anticipate and critically evaluate scientific advanced or competitive threats and respond with appropriate new strategies Generate new scientific proposals and lead those efforts Clearly communicate technology achievements and needs with management and cross functional collaborators Qualifications Qualifications: BS with typically 14+ years, MS with typically 12+ years, or PhD with typically 6+ years of related work experience in biotech or pharma Previous experience with si RNA antibody conjugates and downstream assays to measure efficacy Experience with antisense oligonucleotides (ASOs) Deep experience in cell culture techniques and downstream assays to evaluate RNAi compounds Previous experience in animal study design and downstream assays to evaluate genetic medicines Experience with extrahepatic delivery of therapeutic si RNA is a plus Well versed with previous experience in the field of immunology (preferred) Excellent communication and interpersonal skills. Listens and understands others' point of view and articulates own perspective tacitly in order to clearly communicate scientific findings with key stakeholders 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. This job is eligible to participate in our long-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: ************************************************************* #J-18808-Ljbffr

The Scientific Team at Russell Tobin & Associates is supporting a family-owned scientific organization near Danbury, CT that has a direct hire opening for a Chemist. Responsibilities Support purification of organic chemicals using distillation techniques and related support systems/instruments. Setup equipment Use analytical equipment for assessing quality of distillation cuts and final products. Interpret results Requirements Bachelors degree in Chemistry Must understand principles of analytical and distillation lab equipment Must be able to evaluate materials by odor Additional Details: Position Type: DIRECT HIRE Onsite position Shifts are on a fixed scheduled of three, twelve hours shifts (3×12) a week. Straight days or straight nights. Current 12-hour fixed shifts: Pay rate range based on experience: $55K-$60K annually Must be authorized to work in the United States. APPLY NOW!

We invite you to join Takasago, where you can be innovative and contribute to society through technology. The management of Takasago aims to create a company where each employee can experience a sense of fulfillment and happiness at an elevated level. Specifically, we strive to establish an environment where people from diverse backgrounds can work with joy and a sense of purpose, create a system that supports individual growth, and above all, implement management practices that enable employees to achieve a healthy work-life balance. Takasago is a major global leader and producer of flavors, fragrances, aroma ingredients and fine chemicals. Takasago is headquartered in Japan and operates in 28 countries and regions, with manufacturing facilities, research and development centers, and sales offices worldwide. Takasago ranked 8th overall and 1st in Asia on the Global Top Food Flavors and Fragrances Companies. We currently have an opportunity for an Associate Innovation Scientist - Candle Lab position located in Rockleigh, NJ. The key role of this Associate Innovation Scientist position is to provide hands-on product development support to all projects in the Fragrance Delivery Systems group, with a focus on candles. This includes the design, testing, and validation of candle fragrances and, most notably, operation of the candle burn lab. Responsibilities: Assist in the design and crafting of fragrance technologies and candles for testing proof of principle. Formulate products to deliver breakthrough performance in for candles, which includes candle wax formula development, solvents for candle fragrances, additives, etc. Coordinate activities with project stakeholders, internal and external. Prepare test candles based on project requirements. Maintain familiarity with candle market - particularly product launch activities, IP landscape, consumer understanding/trends, customers' brand & innovation strategies. Develop and perform investigational laboratory testing, procedures, calculations, etc. Conduct and document burn studies for various candles and waxes. Maintain familiarity with relevant laboratory techniques, equipment & processes. Manage a portfolio of projects. Prepare technical presentations for internal and external customers. Maintain accurate records and prepare technical reports. Responsible for operation of the candle burn laboratory, including safety, quality, equipment calibration, and maintenance. Adhere to all applicable regulatory requirements (e.g., good manufacturing practices, good laboratory practices, occupational safety and health, etc.) Some degree of lifting and heavy work is common with the daily moving of equipment, machinery, samples, and supplies. Knowledge and Skills: Must be a ‘hands on' person, highly competent in a laboratory environment. Exceptional communication skills, both verbal and written, are needed. The role will require the ability to effectively communicate with a variety of audiences. Must have ability planning and to work with minimal supervision Ability to work under pressure without compromising on deliverables. A self-starter, with good interpersonal skills and a results-driven attitude. Attention to detail. Must be highly organized and possess accurate record keeping abilities. Knowledge of basic engineering concepts and principles is preferred. Working knowledge of MS Office (Word, Excel, PowerPoint, etc.) Desire to learn, apply and enhance skill set while seeing new opportunities. Education Requires an undergraduate degree in chemistry or another scientific or engineering discipline. Work Experience: BA/BS degree in a related field 0-2 years relevant experience in Fragrance Fragrance industry experience preferred. Competencies: Physical Demands: Must be physically able to operate a variety of machines which include a computer, printer, typewriter, facsimile machine, copy machine, calculator, telephone, laboratory equipment, etc. While performing the duties of this job, the employee may handle hazardous chemicals in the laboratory. The employee will be required to wear all appropriate Personal Protective Equipment (PPE) including but not limited to eye protection, gloves, and lab coat. The noise level in the work environment is moderate. Physical demands vary from sedentary to moderately active work to include standing, walking, and reaching for prolonged periods of time, not to exceed 8 hours for any given activity. Invitation to apply Interested candidates will be prompted to complete an application and submit a resume letter ************************************************************************************************************************ Id=19000101_000001&type=JS&lang=en_US Any questions regarding the application process, please contact ****************************** . Takasago's Employee Benefits and Perks: Takasago offers flexible work arrangements, tuition assistance, health benefits, employee discounts to various services and products, and life insurance 1.5 times your salary. When we think about employee success and financial security, we think long-term. Takasago provides robust retirement savings plans, as well as an employee assistance program. We hope you will join us and achieve professional growth and enrichment. EEO Statement Takasago is dedicated to providing equal opportunities and equal access to all individuals regardless of race or ethnicity, sex/gender (including pregnancy), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, civil union status, familial status, religion, national origin or citizenship, military service status, or any other category protected by law.

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 our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Perform dose formulation analysis under FDA GLPs for nonclinical studies. Provide dose formulation stability testing for GLP studies. Develop and validated analytical methods for doser formulation analysis. Assume responsibility for analytical support of nonclinical studies as contributing scientist/principal investigator working with BI nonclinical drug safety study directors and CRO scientists/study directors. Review laboratory notebooks and chromatographic data. Write analytical reports for inclusion in nonclinical study reports. Write dose formulation stability reports for GLP study support. Skills: Expertise in HPLC and analytical method development. Preferred experience in GLPs, Microsoft Office, Empower chromatographic data system. Qualifications Education: Bachelor's Degree and 7-10 years' experience in analytical chemistry/chromatography Additional Information Richha Saini Senior Clinical/Pharmaceutical Recruiter Tel: ************** Ext 7179 Direct: ************

W-2 Candidates only!! Our client is in need of a Scientist who will be responsible for performing experimental work in the Spatial Biology Lab including sectioning of FFPE tissue blocks, IHC and ISH in single and multiplex assays, imaging and support with analysis. All laboratory experiments will be documented in a laboratory notebook. Duties include preparing reagents and keeping the lab clean and organized. histotechnology experience, IHC, ISH, communicate effectively both orally and in writing Bachelors' Degree in relevant scientific discipline or equivalent experience in a related field

• Reporting to the Principal Scientist, Operations Lead, to execute the laboratory-based clinical research strategy and program at GSSI's research hub in Valhalla, NY. • Lead Clinical Exercise Physiologist working with the Medical Director to ensure research program safety standards and development/execution of related SOPs. • Conducting medical screenings (e.g., stress tests with ECG, blood pressure auscultation) to determine participant eligibility for entry into GSSI clinical research trials. • Laboratory operations, including preventative maintenance/calibration of laboratory equipment • Assisting in the day-to-day execution of research projects including data collection, data entry, and writing of internal reports. • Collaborating across the wider GSSI team (US and Internationally based colleagues) and some additional opportunities outside of main research role, including Product Innovation, Elite Athlete Service, and Education initiatives. Qualifications/Requirements • M.S. required in Exercise Physiology/Kinesiology or related discipline. • ACSM Clinical Exercise Physiology certification highly preferred. • Demonstrable knowledge of and following of good clinical practice (GCP) guidelines. • Demonstrable knowledge of exercise physiology. • Two or more years of experience in clinical research (can include experience gained during M.S. thesis work). • Excellent graded-exercise stress/VO2max testing and ECG interpretation skills. • Must have a pro-active work style, able to multitask, and be flexible to work in a high-performance and ever-changing environment. • Self-starter with good interpersonal communication skills and ability to work with various personalities and work styles. • Flexibility and willingness for occasional domestic travel (approximately 5-10%) for field research, to attend scientific conferences and visit/collaborate with colleagues at GSSI satellite laboratories, and for other GSSI or PepsiCo offsite meetings. • Flexibility and willingness to work during non-traditional hours (e.g., start time before 8:00am or finish time after 5:00pm) as needed depending upon research schedule.

We are seeking a skilled and driven Principal Scientist with a proven background in tumor immunology, autoimmunity, or both to join our Immunology and Inflammation team. Our team contributes to the discovery and development of novel therapeutics in the Cancer Immunology group at Regeneron. You will join a fast-paced growing team that develops the next generation of combination immunotherapies, including but not limited to CD3x and co-stimulatory bispecific antibodies, checkpoint inhibitors, ADC, chemotherapy, vaccine and/or radiation-based combinations. We hope you are excited to have a central role in identifying and developing the right preclinical models necessary not only to understand the way our drugs are working but also to inform and influence clinical trial study design. As a Principal Scientist in the Cancer Immunology team, a typical day might include the following: Leading the development of in vivo animal (syngeneic and xenogeneic) models relevant to our IO and autoimmune portfolio. Independently planning and executing in vivo studies including treatments with injections through various routes (IP, IV, SC), blood and tissue collection for downstream analysis of immune responses. Analyzing data using biological and statistical software such as OMIQ, Prism, Excel, etc. Collaborating with cross-functional scientists to drive target validation and therapeutic antibody development. Delivering impactful presentations to colleagues across our business (preclinical, clinical, and translation), including senior leadership. Writing protocols and study reports, as well as maintaining accurate electronic records. Routinely reviewing relevant literature, attending scientific meetings, and improving expertise in the field of Immunology and Immuno-Oncology. Training and managing research associates as needed. This role might be for you if you: Get excited about developing immunotherapies that promote a tumor-specific and durable immune response to eradicate cancer for patients. Have a passion for innovation and desire to lead new scientific directions. Are a team player with a collaborative spirit. Possess excellent communication, organization, and time management skills. Independently design and execute experiments, analyze data, and interpret results. Are experienced with animal model development and experimental design. Are confident with multitasking and managing multiple projects simultaneously. In order to be considered for this role, you must have at least a Ph.D. in immunology, immuno-oncology, or a related field and 5+ years of relevant experience or a BS/MS and 15+ years of relevant experience. Must have a strong record of innovation and publication. Proven expertise in T cell biology with experience using mouse tumor and autoimmune models, including high-dimensional immunophenotyping, is required. Proficiency with fluorescence microscopy and advanced imaging techniques is a plus. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. Salary Range (annually) $126,700.00 - $206,900.00 #J-18808-Ljbffr

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 X, Facebook, Instagram, YouTube, LinkedIn, and Tik Tok. Job Description AbbVie Precision Medicine Pathology organization is committed to driving tissue based translational and biomarker efforts for our pre-clinical and clinical stage programs. We are seeking a highly motivated ML/AI scientist to join our expanding computational pathology group to revolutionize digital pathology and precision medicine. Candidates for this senior position should have several years of experience in the field, a passion for research, and a track record of productivity and accomplishments. They should enjoy working in a fast-paced, dynamic and highly interactive environment. Their scientific leadership will enable them to independently and expertly guide teams in their approaches to quantitative image derived data generation and interpretation. The ideal candidate will apply their expertise in computer vision and AI to analyze complex microscopy image and spatial-omics datasets, enabling breakthroughs in companion diagnostics, biomarker discovery, and personalized treatment strategies. As a computational pathology scientist, you will be embedded in our small but evolving organization that works closely with colleagues in the various pathology laboratories as well as with the research pathologists. You will provide scientific leadership to our team as you interface with investigators in discovery and late-stage research across our spectrum of disease areas which ranges from oncology, cancer immunotherapy, immunology, to neuroscience. Key Responsibilities: Lead the design, development, and deployment of state-of-the-art machine learning algorithms such as deep learning, representation learning, and self-supervised learning to solve key challenges in tissue image analysis, segmentation, and classification. Develop interpretable AI approaches by integrating attention mechanisms or explainable AI (XAI) techniques for clinical validation and adoption. Evaluate large-scale histopathology and spatial omics datasets to identify biomarkers that inform patient stratification and companion diagnostics. Collaborate cross-functionally with pathologists, biologists, statisticians, data analysts, and fellow scientists to ensure seamless integration of ML/AI solutions into workflows and pipelines. Manage external collaborations with research partners to enhance project outcomes and foster innovation. Mentor and guide junior AI scientists and engineers in the team, fostering a collaborative and innovative environment. Publish research findings in top-tier journals and conferences and present your work to internal and external stakeholders. Stay at the forefront of advancements in AI, computer vision, and digital pathology to continuously refine and expand the impact of your work. Qualifications Required Qualifications: Ph.D. in Computer Science, Electrical Engineering, Computational Biology, Bioinformatics, or related field with an emphasis on computer vision or machine learning with 5+ years of relevant industry experience; OR M.S. with 10+ years of relevant industry experience. Demonstrated expertise in developing, validating, and deploying advanced computer vision and deep learning algorithms, evidenced by the successful release of products. Proficiency in programming with Python, C++, and experience using computer vision libraries such as OpenCV and ML frameworks like TensorFlow and PyTorch. Strong experience in image analysis and techniques such as segmentation, object detection, and classification, preferably in the field of digital pathology (e.g., histopathology or tissue imaging) and/or spatial omics. Experience with MLOps practices, including deployment, monitoring, and lifecycle management of machine learning models in production environments. Knowledge of cloud computing platforms and scalable AI/ML pipelines (e.g., AWS, Azure, GCP). Excellent communication skills, with the ability to convey complex technical concepts to non-technical stakeholders. Proven ability in scientific writing. Strong problem-solving skills and demonstrated creative approaches to overcoming challenges. Excellent organizational skills and the capability to manage multiple projects simultaneously. Preferred Qualifications: Experience handling large-scale heterogeneous biomedical data with a focus on image processing and associated clinical data integration. Experience with spatial omics datasets and integration of molecular data with image analysis. Understanding of precision medicine applications, including biomarker discovery, patient stratification, and personalized treatment strategies. Demonstrated desire and ability to learn, understand and master new techniques or technologies. Familiarity with cell and molecular biology concepts relevant to immunology, cancer immunotherapy, or oncology, or a strong willingness to learn about these areas. 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. This job is eligible to participate in our long-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: ************************************************************* #J-18808-Ljbffr