Scientist Jobs in Derby, CT

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

BL Companies is growing! We're seeking a Project Scientist to join our team and support environmental and industrial hygiene assessments. A successful candidate will have 2-5 years of experience with industrial hygiene and hazardous building materials related projects. This role primarily focuses on hazardous building materials, industrial hygiene, and safety assessments. The role involves a combination of fieldwork, sample collection, regulatory compliance, and technical reporting. Job Responsibilities include but are not limited to: Supports and collaborates with all team members in conducting complex hazardous building material and/or industrial hygiene and safety assessments Assists in the preparation and collection of samples and data, including setting up equipment and documenting observations Analyzes previous building science and/or industrial hygiene and safety surveys to determine if additional sampling is needed or to develop scopes of work Independently performs field assessments where problems encountered are generally well-understood and easily identified Collects environmental and personal samples for analysis and prepares them for shipment to the laboratory Maintains, calibrates, and operates building science and industrial hygiene instruments and equipment Compiles and summarizes analytical data, organizes information for reports, creates sample location diagrams, and drafts reports with findings, conclusions, and recommendations Performs air sampling, project monitoring, and other environmental testing to measure concentrations of pollutants or hazardous agents and ensure compliance with applicable regulations and standards Contributes to educational and regulatory updates for colleagues and management on potential hazards, safe work practices, and the use of personal protective equipment (PPE) Collaborates with team members on various tasks May assist with basic management duties such as developing scopes of work and proposal budgets Studies reference materials and participates in training and professional development activities Maintains and tracks required annual training and licensing, as applicable Utilizes Microsoft Office and internal applications/software programs Maintains up-to-date knowledge of applicable state and federal regulations for various contaminants Stays current with regulatory updates and industry trends Travels to client sites, including occasional overnight stays Communicates effectively with team members, clients, and contractors Practices and maintains a safe working environment Always presents oneself in a professional and clean manner Requirements: 2-5 years of experience with industrial hygiene and/or hazardous building material projects. Valid driver's license and ability to pass drug and alcohol testing. Bachelor's degree in environmental science, industrial hygiene, occupational health, biology, geology, engineering, or a related field. Ability to wear PPE including a respirator and safety harness. Able to lift at least 25 lbs. Basic knowledge of construction materials and building systems. Ability to climb stairs and ladders. Reliable transportation. Experience with: Asbestos, lead-based paint, PCB, and radon surveys Indoor air quality assessments and building surveys Technical Requirements: Licenses (or willingness to obtain within specified timeframes): Asbestos Project Monitor (within 6 months) Asbestos Inspector (within 3 months) Lead Inspector (within 6 months) Strong technical writing and documentation skills. Proficiency in Microsoft Office and industry-related applications. Familiarity with sampling protocols, equipment, and hazardous material practices. Working knowledge of regulations related to asbestos, lead, PCBs, radon, IAQ, and related fields. Other Requirements: Local field work: up to 85% Occasional extended hours, nights, and weekends: up to 25% Regional or out-of-state travel: up to 25% Strong communication and interpersonal skills. 40-hour HAZWOPER certification preferred. BL Companies is 100% employee owned, giving us a competitive edge and a unique distinction from most other companies. We offer a competitive benefit package which includes 6 paid holidays plus the week from Christmas to New Years paid, generous PTO, Medical, Dental and Vision insurance, disability insurance, life insurance, 401k matching, and our Employee Stock Ownership Plan. We are an ENR Top 150 firm that provides engineering, architecture, land surveying, and environmental consulting services to the public and private sectors. BL has 18 offices and is expanding. Our employee owners are capable of being successful working in hybrid environments, and we offer opportunities to continue in this setting.

We are seeking a Scientist III to join our team and support laboratory work for pharmaceutical projects. This role involves performing analytical testing, developing and validating methods, and ensuring product quality in a cGMP environment. The ideal candidate will have hands-on experience with analytical techniques such as Karl Fischer, thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, and particle size analysis. You will also assist in pharmaceutical development efforts, conduct stability and release testing, and generate technical reports for data presentation. Responsibilities: Perform laboratory tests to support analytical testing for pharmaceutical products. Use and apply a variety of analytical techniques, including Karl Fischer, thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, and particle size analysis. Develop and validate analytical methods to support GMP stability, release testing, and pharmaceutical development. Conduct testing to evaluate product stability and ensure compliance with regulatory standards. Present data and prepare clear, concise technical reports documenting test results. Troubleshoot instrumentation issues and provide problem-solving support in the lab. Evaluate and recommend new instrumentation or analytical techniques for implementation in the lab. Qualifications: B.S. or M.S. in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or related field. Relevant working experience in the pharmaceutical industry with a focus on analytical method development, validation, and testing in a cGMP environment. Hands-on experience with analytical methods such as Karl Fischer, TGA/DSC, IR/Raman spectroscopy, X-ray powder diffractometry, and particle size analysis. Familiarity with lab software and information systems (e.g., Timao, TRIOS, Omnic, E-Workbook, LabWare LIMS). Strong troubleshooting skills with laboratory instruments and equipment.

Job Title: Scientist II Duration: 12+ months contract. Key Responsibilities: Plan and execute cellular assays using primary human cells cultures. Perform cellular/molecular functional assays (ELISA, qPCR, assays) and cell-based imaging. Communicate findings orally and in writing; maintain detailed work notebooks and contribute to scientific reports. Required Skills: Hands-on experience in cell or tissue culture. Experience in biochemical assays development, enzymology research methods, and enzyme inhibition studies via techniques including spectroscopy (absorbance, fluorescence, and luminescence), and mass- spectroscopy. Demonstrated ability with cell-based assays and molecular biology techniques including, but not limited to, immunoassays (ELISA, Western Blots), PCR, qPCR, and flow cytometry. Education: Bachelor's Degree with 3+ years' experience OR master's degree in immunology, molecular biology, biochemistry, or a related field.

VARITE is looking for a qualified Scientist II in Ridgefield, CT WHAT THE CLIENT DOES? An American biopharmaceutical company that focuses on researching and developing antiviral drugs used in the treatment of HIV/AIDS, hepatitis B, hepatitis C, influenza, and COVID-19. WHAT WE DO? Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. Job Title: Scientist II Location: Ridgefield, CT Contract Duration: 24 months HERE'S WHAT YOU'LL DO: Summary: 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. If this opportunity interests you, please respond by clicking on EasyApply. Know someone who would be perfect for this role? Refer them to us and if they are hired, you could be eligible for our employee referral bonus! Help us grow our team with top talent from your network. VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Top skills: analytical skills: Karl Fischer, spectroscopic techniques, x-ray, etc. 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. Skills: 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. Education: The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry. Pay rate range: $30-44/hr depending on experience

Duration: 12 Months Contract Design, plan and execute experiments in an independent manner leveraging scientific and technical expertise to achieve defined objectives. Independently initiates and carries out the process for assay development, optimization and validation in a timely manner as required. Utilizes various biochemical, molecular, cellular, and functional techniques to develop and validate complex assays using mammalian cells, tissues, and recombinant proteins to interrogate biological pathways of interest and support emerging biological concepts. Communicates own work effectively orally and in writing; Contributes to writing protocols, procedures, technical reports, and publications; Collaborate efficiently with other team members. Complies with applicable regulations, performing all work in a safe manner while maintaining proper records in accordance with SOPs and policies. Skills: Experience in biochemical assays development, enzymology research methods, and enzyme inhibition studies via techniques including spectroscopy (absorbance, fluorescence, and luminescence), and mass- spectroscopy. Hands on experience with culturing primary cells and cell lines, and experience processing tissues or samples for cell isolation or other downstream applications Demonstrated ability with cell-based assays and molecular biology techniques including, but not limited to, immunoassays (ELISA, Western Blots), PCR, qPCR, and flow cytometry. Strong written and oral communication skills with the ability to prepare and present data to project teams and research management as needed. Reports and treats data with a high level of integrity and ethics. Excellent multitasking and time management skills. Ability to function in multi-disciplinary teams. Education: Scientist II: Bachelor's Degree with over 3 years of experience in a related scientific discipline, or a Master's Degree in a related scientific discipline, or equivalent experience in the field. Previous industry experience is a plus. Scientist III: Master's Degree from an accredited institution with three-plus (3+) years of experience in related scientific discipline, OR Bachelor's Degree from an accredited institution with seven-plus (7+) years of experience in related scientific discipline or equivalent experience in related field. Industry experience required. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Swati Email: *********************************** Internal Id: 25-33853

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)

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.

BYK Additives & Instruments is one of the world's leading suppliers in the field of additives and measuring instruments. Around the world, the additives of BYK ensure that coatings and plastics precisely obtain the desired properties and the correct quality. We're looking for a highly motivated, experienced Chemist to join our production team! Excellent Medical, Dental, and Vision Benefit plans eligible to enroll within 30 days of hire Annual Merit increases, Bonuses, and 401K Discretionary company match up to 5%! Opportunity for advancement and training opportunities for all employees. KNOWLEDGE: Knowledge about BYK additives and their purpose for applications in graphic arts Understanding formulation ingredients, application techniques and substrates for Graphic Arts applications Understanding of how formulations and application methods for Graphic Arts are different from other markets Basic knowledge of laboratory equipment applicable to Graphic Arts Understand the safety considerations and labeling procedures of chemicals in the laboratories Knowledge of which products are unique and not easily replaced in customer formulations, leading to a more secure position. Basic knowledge of physical and health hazards associated with Graphic Arts coating chemistries. Knowledge of computer programs necessary for generating reports and presentations (e.g. Microsoft Word, PowerPoint, Excel, etc.). Ability to design experiments, analyze the data, and interpret the results. SKILLS: Problem solving skills and the ability to correct flaws in the customer's process and formulations with BYK additives. Ability to design and conduct laboratory experiments while determining the long-term implications of our additives in customer's formulations, both to increase our position (for the additives) and decrease potential liability of changing customers' formulations. Ability to speak and understand the “language” used in the Graphic Arts markets (including application equipment) increasing communication and building teams to understand the customer's needs and capitalize on opportunities. Ability to develop presentations and present them in a professional and interesting way at sales meetings or in front of customers. Common sense awareness of safety and quality (ISO standards) in the lab and in the company Customer service skills for both written and telecommunication to relate and serve the customer. ATTITUDE: Must be team oriented and be able to interface positively and supportively with other members of the laboratory staff, sales team, and other internal/external departments. Eager to bring a technical service experiment or project to completion. Flexibility and Multitasking - Must be able to manage multiple projects at one time, while setting priorities. Maintains good technical contact with agents, reps and suppliers. Must be a self-starter and initiate experiments and projects with a minimum of supervision. On occasion, must be willing to work additional hours, as necessary, to meet deadlines. DUTIES AND RESPONSIBILITIES: Perform Technical Service Request (TSR) and Laboratory Projects Perform TSR on behalf of BYK USA Inc. Create report(s) of TSR performed Evaluate new additives in Graphic Arts systems Reply to customer technical inquiries received by telephone/email Evaluation of competitive additive products Evaluation of new coatings, raw materials, binders, solvents, pigments, etc., as directed by the Regional End Use Manager Assist in preparation of sales meetings and trade shows (preparation of demonstration material, etc.) or other events Assist in product training and lectures preparation Interact with Wesel (Germany) personnel Occasionally work on-site at customer's lab, as required Organize and keep operational the Industrial Applications Laboratory Maintain laboratory equipment in good working condition Order and maintain stock of raw materials Maintain contact with raw materials and equipment suppliers Specify and order new equipment as needed Handle hazardous waste according to procedure Follow emergency response procedures Perform routine daily maintenance functions (such as compliance, clean up, etc.) Other duties and responsibilities: Up to 20% travel to present to customers and technical events around the country International travel required for onboarding and technical training - generally 6-8 weeks abroad (in Germany) within the first year of hire Prepare monthly reports of activities performed Other duties as assigned by management Must successfully complete various training according to job function and regulations (such as DOT, RCRA, ISO, etc.) Participates in emergency response as defined in the program and training capability ESSENTIAL FUNCTIONS: Must be capable of lifting 70 lbs. Ability to drive a car Good telephone skills Data entry skills Ability to travel by ground and by air Be able to work with chemicals Be able to cope with conditions of international travel Must be able to wear SCBA QUALIFICATIONS: Four-year technical degree and/or approximately 5 years practical experience. Good problem-solving abilities. Good communication skills. Able to work independently without constant supervision This role is not eligible for sponsorship. In the ALTANA Group, you will work in a unique culture of innovation where the utmost importance is attached to promoting individual ideas and abilities as well as open, trusting interaction. ALTANA AG and its subsidiaries is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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

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 Operation PDST Biological Development and Lunch at AbbVie is seeking a highly motivated Principal Scientist with a strong understanding of early and late stage Biological pipeline cell line development and genetic characterization to lead the Molecular Biology team at the AbbVie Bioresearch Center (ABC). The ABC site, based in Worcester, MA, offers a unique setting where Biologics drug discovery, development and manufacturing coexist in one location. In this position, the leader will be responsible for asset transition from Discovery into development, vector construct development, cell line development, cell bank genetic characterization and qualification, as well as modernizing traditional molecular biology methods through innovation and developing next generation genetic characterization platform processes. Experience with cutting edge technologies such as NGS, Omics, AI/ML, HT automation and digitalization for process optimization are preferred. Responsibilities: Develops and achieves discipline strategy in alignment with functional goals and key scientific objectives. Ensure the successful transition of AbbVie biological assets from Discovery into development. Executes and guides the development and genetic characterization of cell lines, cell banks empowering all stages of pipeline development. Identify and implement advanced technologies strategically to support accelerated biological pipeline programs. Provide strategic, operational, and scientific guidance to the molecular biology team. Conduct general laboratory research proficiently and independently, adapting and troubleshooting experimental designs and equipment to meet research requirements. Apply creative thinking to solve complex problems and promote new technologies, while effectively communicating mission and ideas to diverse audiences. The ideal candidate should be able to manage multiple projects across therapeutic disciplines within a dynamic and fast-paced team setting. Presents scientific concepts and results for functional scientific and non-scientific leaders as well as potential and existing partners. Maximize impact and value of expertise. Advances scientific expertise within function. Proactively advises and shares knowledge and expert opinions with subordinates, peers, and senior management. Mentors and trains functional colleagues and assesses current and emerging business challenges enabling functional goal achievement. Qualifications BS with 14+ years of experience or MS with 12+ years of experience or PhD +6 years of experience in Biology, Molecular and Cellular Biology, or related field. Interact well with diverse groups within function and maintain strong working relationships with internal and external collaborators. Broad experience in cell line development across diverse cell types, with a proven track record of contributing to drug candidate development. Expertise in molecular biology for plasmid construction and genetic characterization. Proven ability to innovate with a history of new or improved methods or workflows. Demonstrates strong attention to quality and detail in organizational, documentation, and communication to work effectively within a collaborative work environment. 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 Skill in the operation of distillation and support equipment. -Knowledge of piping and valve operations to control processes. Additional Details: Position Type: DIRECT HIRE Onsite position Shifts available: Sun - Tue, 6:00pm - 6:30 am (Wed) (Additional shift differential included) Pay rate range based on experience: $55K-$60K annually

W-2 Candidates only!! Our client is in need of a Scientist with Two+ years of experience in related scientific discipline is desired. - Experience with cell culture techniques and molecular biology techniques including but not limited to Western blot, qRT-PCR, ELISA, FACS, enzyme inhibition assays, viability assays, functional screening assays of biologics, 2D & 3D culture systems of primary mouse and/or human cells - Strong understanding of basic biology and immunology, preferentially with emphasis on tumor and tumor-immune biology. - Ability and willingness to work effectively in a highly collaborative research environment. - Excellent verbal and written communication skills, with the ability to propose, articulate and evaluate scientific ideas and data. - The ability to prioritize responsibilities and be comfortable with ambiguity, changing direction and priorities. - Complies with all applicable regulations and ensures that work performed in the area(s) of responsibility is conducted in a safe and compliant manner. - Design, plan, and execute in vitro experiments in an independent manner to achieve defined objectives. Independently initiate and carry out the studies as a team player under manager's direction. - Draw conclusions from experiments and apply knowledge to interrogate target biology. - Operate in a highly organized fashion in terms of goal setting and delivery for multiple simultaneous experiments/tasks. - Independent execution of routine experiments and independent application of basic scientific principles. - Collaborate within the lab/group and work together with the team for larger experiments requiring assistance. - Communicate experimental results and present data at cross-functional meetings. May give oral presentations at external meetings. - Efficient, organized, and meticulous record keeping and tracking of experiments in accordance with SOPs, policies, and electronic workbook rules. Bachelor's degree with three+ years of experience in related scientific discipline, preferably in the Biopharmaceutical/Biotech industry, or Master's degree. PhD applicants will not be considered.

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.

Duration: 12 Months Contact 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 About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Swati Email: *********************************** Internal Id: 25-35644

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. Skills: 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. Education: The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry.

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

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!