Research Scientist Jobs in Windsor, CT

Are you ready to join Connecticut Innovation's vibrant community of innovators? Connecticut Innovations (“CI”) is Connecticut's strategic venture capital arm, and we are passionate about serving our portfolio of 220+ companies across various industries, with strengths in life sciences, technology, and climate tech. Come join CellsBin, Home | CellsBin Inc.! Founded by Quantum-Si, Apple, and Nvidia alumni, CellsBin is building an ASIC-based cell-analysis platform enabling the exponential growth of cell therapies. CellsBin is a VC-backed startup that offers drug discovery, immunotherapy, and toxicity testing. It provides a 3D Cell Cartography that maps cell surface structures at scale. Its laboratory is in New Haven, CT. It serves as the center for their pioneering research and development endeavors. Senior Scientist - Cellular & Molecular Oncology We are seeking a Senior Scientist in cellular and molecular oncology with deep expertise in immunobiology and hematology to lead R&D efforts focused on cancer monitoring and cell therapy solutions. This role will drive the design and optimization of assays and technologies for rare-cell analysis and therapy response. The ideal candidate brings strong experience in immuno-oncology, rare-cell biology, and translational research, and will play a key role in shaping scientific strategy and innovation. In addition to R&D, the role involves close collaboration with the lab team to guide experimental execution, optimize protocols, and troubleshoot technical challenges. You will also engage directly with clients, serving as the technical lead to understand their needs, communicate scientific insights, and deliver tailored solutions-ensuring CellsBin's technologies address real-world challenges in oncology and cell therapy. Key Responsibilities Research & Assay Development Lead the design, development, and optimization of novel assays for rare-cell analysis (in cancer and cell therapy) Collaborate with the technology team to build and refine innovative tools addressing oncology challenges Data Analysis & Product Insight Analyze complex biological datasets to extract actionable insights Inform product refinement and contribute to the development of advanced capabilities in CellsBin's platforms Experimental Execution & Troubleshooting Partner with lab teams to implement protocols, optimize workflows, and troubleshoot technical issues Ensure experimental accuracy, reproducibility, and alignment with project goals Client Engagement & Technical Support Serve as the technical point of contact for customers, providing expert guidance on product applications Collaborate with clients to tailor solutions to their cancer and cell therapy monitoring needs Collaboration & Mentorship Mentor junior scientists and lab personnel, fostering a collaborative and knowledge-driven work environment Support cross-functional teams to accelerate research initiatives and translational impact We're Looking For PhD in Immuno-Oncology, Molecular Biology, Hematology, or related field 3+ years of postdoc or industry experience in cellular/molecular oncology, rare-cell biology, or cell therapy Proven R&D experience in assay development for cancer monitoring or therapeutic applications Proficient in flow cytometry, PCR, and other molecular biology techniques Strong background in immuno-oncology and hematology Effective collaborator with hands-on lab experience and protocol optimization Clear communicator, able to present complex science to diverse audiences Demonstrated leadership and mentoring ability with a focus on innovation At CellsBin, you'll: Join a fast-growing startup at the forefront of cancer research and cell therapy Collaborate with leading scientists, engineers, and innovators Contribute to breakthrough technologies in cancer diagnostics and precision medicine Help drive meaningful impact for patients worldwide. CellsBin is an Equal Opportunity Employer.

**_About_** **_this_** **_position_** ** At Henkel, you can build on a strong legacy and leading positions in both industrial and consumer businesses to reimagine and improve life every day. If you love challenging the status quo, join our community of over 47.000 pioneers around the globe. Our teams at Henkel Adhesive Technologies help to transform entire industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop What makes you a good fit. Grow within our future-led businesses, our diverse and vibrant culture and find a place where you simply belong. All to leave your mark for more sustainable growth. Dare to make an impact? **What you´ll do** + Executes new product development projects + Develops new approaches, solutions, processes, products within an agreed timeframe + Executes and manages projects and resources to meet planned objectives + Ensures compliance with Henkel corporate SHE standards, policies and procedures and manages the lab and innovation process + Provides technical support services to Manufacturing and Quality as required + Assures all new products meet international chemical health and safety requirements and other regulations + Ensures that Henkel's new IP is protected through collaboration with internal and external partners + Provides guidance and recommendations on patents, trademarks and proprietary agreements + Approves technical readiness of raw materials and products as well as first production and quality specs + Tests or supervises tests on product stability and performance **What makes you a good fit** + Bachelor, Master or Ph.D. in Chemistry, Polymer Science, Materials Science, Chemical Engineering, or other relevant disciplines is preferred. + For a candidate with Ph.D. or MS, 2-3 year of relevant lab experience in an industrial setting is plus (especially, polymers, coatings, and adhesives). Otherwise, over 5 years of relevant experience preferred. + Prior knowledge of adhesive, coating, polymer technology and formulating is essential. + Broad based knowledge of polymer science, including polymer chemistry, structure property relationships, rheology, bulk and adhesive mechanics of soft materials. + Proven track record of on-time product development delivery from idea generation to completion is required. + Proven ability to invent and innovate, and strong ability to design and implement experiments are needed. + Ability to formulate and develop of your own with a minimal supervision + Ability to multi-task and handle multiple projects simultaneously + Strong teamwork skills with excellent interpersonal skills and proven ability to collaborate with others and independently on multi-task assignments + Technical writing and presentation skills **Some perks of joining Henkel** + Flexible work scheme with flexible hours, hybrid and work from anywhere policies + Diverse national and international growth opportunities + Globally wellbeing standards with health and preventive care programs + Gender-neutral parental leave for a minimum of 8 weeks + Employee Share Plan with voluntary investment and Henkel matching shares + Annual performance bonus + Comprehensive healthcare including mental health support and 401(k) plan matched by employer + Family benefits including fertility support, fully paid parental leave, caregiver services + Paid time off, sickness leave, holidays, volunteer time off, summer Fridays & more The salary for this role is $82,000.00 - $92,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future. Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral. Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories. **JOB ID:** 25075960 **Contact information for application-related questions:** ***************************** Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted. **Application Deadline:** As long as the vacancy is listed on our Career Site, we are happy to receive your application **Job-Center:** If you have an application already, you can create or log in to your accounthere (******************************************************************************************************************************************************** to check the status of your application. In case of new account creation, please use your email address that you applied with. Activate external content When clicking the button below external content will be loaded which involves transfer of personal data (e.g. IP address) to external servers. This may involve that cookies are set by the external content provider. Please see Data Protection Statement for further information. **Accept for all YouTube content** Deactivate loading external content from YouTube. How is work at Henkel

Clinical Research Investigator DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our sites in Hartford, CT. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical License (MD, DO) At least 2 years of experience as a Clinical Research Investigator. Spanish Bilingual a plus.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Position Description: The successful candidate will provide quantitative bioanalytical support using LC-MS/MS for a variety of high throughput in vitro ADME profiling assays. In this hands-on role, the candidate will perform sample analyses by mass spectrometry, and will review, interpret and report results. Instruments and software from various vendors including Sciex (Analyst) and Thermo (Excalibur) will be used along with custom internal data processing software to acquire data and process results. The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. Position Requirements: BS or MS in chemistry, with specialization in analytical chemistry preferred, along with 1 to 5 years of relevant pharmaceutical experience is required. Training or experience in mass spectrometry and separation science, as well as hands-on experience in quantitative LC-MS/MS analysis are desired. Proficiency in general computer software, including vendor specific instrument control and analysis tools, is required. Strong interpersonal and communication skills, both oral and written, are required as is commitment to working as a team player within a multifunctional organization. A working knowledge of allied disciplines such as computer science, lab automation, drug metabolism, pharmacokinetics and synthetic chemistry is helpful. Qualifications The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. LC-MS/MS analysis BS or MS in chemistry Additional Information Thanks & Regards Riya ************

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $81,900.00 - $134,550.00 Position Summary: The successful candidate will join a rapidly growing company with a multidisciplinary high-tech team of Engineers, Biologists, and Scientists to sustain and rapidly impact ProteinSimple platforms. The Scientist will work in research and development area of Process Engineering team with a focus on polymer synthesis, surface modification and establishing chemical formulations for new polymeric coatings. The Scientist will apply ISO standards during product and process transfers into Manufacturing. Key Responsibilities: Provides hands-on leadership in the design, synthesis, and characterization of polymeric coatings and works independently in a lab environment Provides expertise in analytical chemistry with emphasis in polymer characterization Improves yield, stability and consistency of synthetic coating methods and troubleshoots chemical processes Performs biological assays on ProteinSimple platforms to assess performance of surface coatings, interprets results to determine next steps and iteratively improve processes Develops deposition technology and surface cleaning protocols Troubleshoots problematic reagents Establishes and validates methods and protocols for new product and new processes Analyses polymers and understands FTIR, DSC, TGA, DMA, GPC, GC, NMR, LC-MS, viscometry, rheology Works hands-on to solve challenging technical problems driving continuous improvement efforts Develops novel test methods to interrogate coating quality Develops robust and repeatable procedures, SOPs, and processes for new products Identifies process improvement opportunities and address documentation deficiencies Works according to EHS regulations, follows company policies and practices Must have the ability to manage multiple projects with minimal supervision Performs additional duties as assigned Education and Experience: PhD in polymer chemistry, material science, chemical engineering, or a closely related discipline; and up to 5 years of relevant experience OR, Master's in polymer chemistry, material science, chemical engineering, or a closely related discipline; and 8+ years of relevant experience Previous experience with polymer coatings, surface chemistry, polymer chemistry and characterization is a must Previous experience developing protein immobilization coatings is desirable Previous experience with biological assays utilizing proteins and antibodies is desirable Knowledge, Skills and Abilities: Able to design experiments, interpret data, and make conclusions from analytical instruments, DSC, TGA, DMA, FTIR, viscometry; must understand the theoretical applications and limitations of the instruments Have strong knowledge of the relationship between polymer structure and properties, familiarity with polymer synthesis and reactions Experience in SOP writing Good organization, planning, and critical thinking skills are required. Self-starter and can handle projects independently with ambiguous and incomplete information Meticulous and attention to details to troubleshoot and improve complex chemical processes In-depth knowledge with practices, concepts, and innovation in surface functionalization Must have strong organizational and communication skills, both verbal and in writing and possess working knowledge of analytical, process-equipment, quality control systems and statistical software The ability to work in a collaborative way Fluency in data analysis and presentation using R, JMP, Python, or PowerBI, etc is desirable Experience developing, writing, and releasing standard operating procedures Exhibit a high degree of flexibility, teamwork, and commitment to continuous improvement The Physical Demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Organic chemistry lab, work with chemical reagents Production Environment (Bio-Lab, Clean Room) Work with potentially biohazard samples Must be able to lift and handle items weighing 35 lbs Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. 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. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

About Us Cloverleaf Bio is an early-stage therapeutics company that is developing a new class of engineered tRNA therapeutics. Our tRNAs target an underappreciated vulnerability of cancer: addiction to high levels of tRNA modifying enzymes. Cloverleaf's approach to drugging tRNA modifying enzymes uses engineered “trojan horse” tRNAs to modulate translation in cancerous cells. The programmability, potency, and specificity of our tRNAs gives us the potential to dramatically improve cancer treatment. The Job We are seeking an experienced In Vivo Scientist to join our team. In this position, you will work in close conjunction with our founding team in the creation and development of a completely novel family of RNA therapeutics. Your responsibilities will include designing and executing in house animal experiments in mice, proposing, planning and coordinating toxicity, pharmacology and efficacy studies at CROs, performing cell culture experiments with lead candidate RNAs to predict in vivo outcomes, and providing in vivo pharmacology and physiology expertise to accelerate development of our tRNA therapeutics. About You Excited by the science. We are excited by how science can improve the world and are looking for people who are too. Flexible. We wear many different hats and are looking for people who are willing to do whatever it takes to pitch in and get the job done. Resilient. Working in an early-stage startup can be hard. Science is hard. We are looking for people who have a demonstrated track record of sticking with complex problems for the long haul. Cooperative. As a small team, communication and collaboration are key. We are looking for people who thrive working both independently and collaboratively. Qualifications: PhD in Cancer Biology, Molecular Biology, or related fields. Strong problem solving skills Demonstrated ability to independently plan and execute in-vivo studies, data analysis and interpretation. Experience with mouse models of disease (preferably oncology) Skilled in mammalian cell culture, passaging/seeding cells, etc. Nice to haves: Research experience in RNA biology and/or RNA modifications field. Experience with therapeutic development. Experience with design/development RNA therapeutics and lipid nanoparticles. Previous experience selecting and overseeing work at CROs. Benefits Competitive salary commensurate with experience and strong equity incentives. Medical, dental, and vision coverage. Brand new lab space in BioLabs New Haven in downtown New Haven, close to the Yale Shuttle, I-95/91 and Metro North. We will provide a stimulating, collegial, and fast-paced environment. If you are interested in joining our team, then we are excited to hear from you! Please submit resumes at cloverleafbio.com

At HR Wallingford, we design smart, resilient solutions across the natural and built environments to help everyone live and work more sustainably with water. By harnessing research, data insights and the power of our collective expertise, we help the world to better understand the changing influence and impact of water. We are seeking a Scientist with knowledge and a keen interest in sediment transport and sediment transport modelling to join our Coasts and Oceans group. You will be involved in using numerical models and data to predict changes to the sediment regime in muddy or sandy coastal and estuarine environments caused by activities such as coastal developments, deepening of shipping berths and channels, or building port infrastructure. The models will be used to determine changes to beach elevations along sandy shorelines, assess port sedimentation rates and model plumes arising from dredging operations, and will be used to support Environment Impact Assessments and sustainable developments. Key qualifications and skills You will have a good scientific degree in a relevant subject and an MSc/MRes or PhD in oceanography or physical geography (or similar). It is expected that you will have some previous experience of using 2D and/or 3D numerical models of sediment transport (preferably TELEMAC, or similar software such as Delft3D or MIKE). Experience of modelling waves and hydrodynamics would be advantageous, as would experience of handling and processing data from field instrumentation used to measure hydrodynamics, suspended sediments and bed deposits from marine environments. Knowledge or expertise in the use of FORTRAN programming language would also be beneficial. Strong report writing skills are essential as is the ability to use scripting languages (such as Python or/and MATLAB) to process model results and data for incorporating informative graphical outputs into client reports. Further information Salary: £30,000 to £43,000 depending on experience Download a full job description Read the person specification Check our exceptional benefits at ***************************** The closing date for this role is 31 st May 2025 How to apply If you are excited about this role but unsure whether you're the right fit, we encourage you to apply. We're also happy to answer any questions by emailing ************************* Interested? Please apply providing your CV with covering letter. Additional information Our privacy notice for job applicants, available from our website, explains how we collect and process the personal data you may provide us when you apply for a job with us through our websites, or by any other means. This notice also explains how we'll store and handle that data and keep it. HR Wallingford are an equal opportunity employer and value diversity in our workplace. We do not discriminate, and work to create an inclusive culture across our business.

Position:Full-Time Total Rewards: Benefits/Incentive Information Gentex Optics is part of EssilorLuxottica, a global leader in the design, manufacture and distribution of world-class vision care products, including iconic eyewear, advanced lens technology and cutting-edge digital solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn! The Dudley, MA facility is home to Operations, Global Lens Engineering, and Research and Development teams that work together to develop, pilot and manufacture, semi-finished, polycarbonate lenses for premium markets. We also supply coatings, inks, inserts and other innovative products to customers throughout the world. Our team members bring our mission to life each and every day by helping people see a brighter world. GENERAL FUNCTION Essilor is seeking a dynamic Polymer Scientist to fill this entry level role to work on innovative processes, machines, and materials. This position will report to the Senior Manager and will have the opportunity to work within a rich and diverse resource team collaborating with others worldwide in R&D, Engineering, Operations, vendors, etc. Position is located in our Group Lens Innovation facility in Dudley, Massachusetts MAJOR DUTIES AND RESPONSIBILITIES Conduct 'hands-on' experimental, simulation, and modeling work on different optical elements Propose, modify, and optimize methodologies for characterization of textured plastic films and laminates * Conduct optical materials characterization, identify existing tools, and develop new fixtures & methodologies to quantify visual acuity, optical power, etc. Obtain meaningful instrumentation data on micro-textured samples prepared on films, laminates, and integrated into lenses. Integrate optical instrumentation, optical simulation software, and imaging analysis in a product development environment Develop optical metrology techniques for both off-line and in-line characterization of textured materials Provide data based evidence that developed processes meet product requirements through design of experiments and statistical process control Use optical modeling and simulation tools (Ansys Optics, Zemax, etc.) Participate as an active member of a research and product development team. Support innovation linked to active programs or studies Provide oral and written reports for new or improved analytical methodologies, process modifications, etc. Use appropriate data management and capitalization tools BASIC QUALIFICATIONS Degree requirements - A Masters/PhD in relevant field (e.g.: Engineering, Optics, Imaging, Materials, Physics, or related discipline) with 0-5 years of practical experience with relevant equipment and processes; equivalent education and experience in lieu of a doctorate degree will be considered Ability to document process and experimental results with proper lab notebook entries, technical memos, patent applications, and presentations Ability to work effectively with cross-functional working groups, skill levels and expertise in a global environment Demonstrate a spirit of innovation, a willingness to suggest and the ability to support the implementation of modifications of instrumentation, machinery, and processes using for developing new products. Flexibility in work assignments to accommodate group and personal goals Proactive in learning about many technologies Willingness and ability to travel domestically and internationally up to 10% annually PREFERRED QUALIFICATIONS Optical experience preferred ABO certification a plus Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. Upon request and consistent with applicable laws, EssilorLuxottica will provide reasonable accommodations to individuals with disabilities who need assistance in the application and hiring process. To request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Job Segment: Facilities, Supply, Social Media, Operations, Marketing

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Job Description •Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed. •Performed general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software. •Performed quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques. •Operated, maintained, calibrated and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs. •Maintained quality control and calibration logs of all Flow Cytometers. •Analyzed, summarized and document experimental results. •Performed data entry using laboratory information management system (LIMS) •Write experimental SOPs. •Update Biomarker Lead on the status, results and problems in method development and performance of the assays. •Complete all NHCRU/Pfizer required training. •Have a working knowledge of Microsoft office including Excel, Word and PowerPoint. •Possess multi-tasking and organizational skills. •Experience in ELISpot Assays and FlowJo software a plus. Qualifications MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience. Additional Information To schedule interview or get any further information feel free to contact: Sagar Rathore ************ ******************************

Conduct experiments to map cellular architecture in a wide range of tissue samples with our novel multi-omics spatial profiling platform. Contribute to the development and standardization of new SOPs for novel tissues and new omics chemistries. Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. Organize and communicate data with internal and external groups. Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Responsibilities * Conduct experiments to map cellular architecture in various tissue samples using our multi-omics spatial profiling platform. * Develop and standardize new SOPs for novel tissues and omics chemistries. * Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. * Organize and communicate data with internal and external groups. * Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Additional Skills & Qualifications * B.S. or M.S. in molecular biology, biochemistry, genetics, or related field with 1-3 years of industry experience. * Experience in tissue processing, histological slide preparation, and immunohistochemical and immunofluorescent staining in mammalian tissues. * Knowledge of a broad range of cellular, functional, IHC and/or pathology applications and imaging instrumentation. * Deep experience with molecular biology and microscopy techniques including qPCR and NGS library preparation. * Excellent communication skills, adaptive in interfacing between biologists, engineers, and other disciplines. * Ability to work full-time, on-site in New Haven, CT. Work Environment This position is based in a laboratory setting, working from 9am to 5pm on-site in New Haven, CT. The role involves collaborating closely with a multidisciplinary team of biologists, chemists, physicists, computer scientists, and engineers. Pay and Benefits The pay range for this position is $24.00 - $38.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in New Haven,CT. Application Deadline This position is anticipated to close on May 9, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Who We Are EvolveImmune Therapeutics is a next-generation immunotherapy company pioneering a new class of precision cancer medicines to transform patient outcomes, compared to current solid tumor therapies. Our first-in-category biotherapeutic EVOLVE platform utilizes integrated T cell co-stimulation to directly target tumor cells to deliver durable, tissue-localized anti-tumor adaptive immune responses. Our newly expanded, state-of-the-art 16,000+ square foot laboratory and office space located in the New Haven, CT biotechnology corridor and our laboratory footprint in Farmington, CT support in-house biologics, immunobiology, and translational activities, enabling our rapid pipeline progress. This includes EV-104, our lead solid tumor program rapidly advancing toward IND filing. The Role We are seeking a highly motivated and skilled Scientist to join our dynamic Biotherapeutics team and contribute to the characterization and development of our next-generation immuno-oncology pipeline. This role will focus on utilizing LC-MS, biochemical and biophysical methods to analyze and characterize the structural integrity, functionality, and stability of these innovative molecules. Key Responsibilities Develop and execute LC-MS workflows for biotherapeutics characterization, including intact and subunit mass analysis, peptide mapping, glycan profiling, and post-translational modification analysis. Perform analytical, biochemical, and biophysical assays using techniques such as SEC, HIC, DSC, ELISA, SPR, and BLI to assess purity, stability, aggregation propensity, and target binding kinetics and affinity. Collaborate effectively with cross-functional teams to ensure alignment of project goals and deliver accurate and timely results. Analyze and interpret experimental data to draw meaningful conclusions, present findings and recommendations to team and management. Address and resolve technical challenges related to LC-MS instrumentation and data analysis. Stay current with advancement in LC-MS and biophysical techniques, implementing innovative approaches where applicable, contribute to scientific publications. Qualifications PhD in Protein Biochemistry and Biophysics, or a related field with 2+ years of relevant experience; or MS with 5+ years, or BS with 8+ years of experience in industry settings. Strong expertise in LC-MS techniques for protein analysis, including hands-on experience with instruments and data analysis. Proficiency in biophysical methods for protein characterization, particularly in analyzing antibody stability and target interactions. Strong analytical and problem-solving skills with attention to detail. Effective communication skills for presenting complex data to diverse teams. Ability to work collaboratively in a cross-disciplinary environment. Preferred Qualifications Experience with protein expression in mammalian systems and purification techniques. Familiarity with the structure and function of T cell engagers and their unique analytical challenges. Experience in immune cell biology and functional cell-based assays relevant to T cell engagers. EvolveImmune Therapeutics requires all employees to be fully vaccinated against COVID-19. You may seek reasonable accommodations for medical and religious reasons. However, your application is no guarantee that such accommodations will be made available. EvolveImmune provides a competitive compensation and benefits package. EvolveImmune Therapeutics, Inc. is an equal opportunity employer.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS

The laboratory of Dr. Dan Mulkey in the Department of Physiology and Neurobiology at the University of Connecticut, Storrs is seeking a Postdoctoral Research Associate to explore the cellular and molecular basis of neuronal excitability in brainstem regions associated with respiratory control. Our studies use a combination of electrophysiology, fluorescent microscopy, and genetic approaches to identify cellular/molecular mechanisms contributing to control of breathing in health and disease. Highly motivated individuals holding a Ph.D. and a strong background in cellular neuroscience are encouraged to apply. The University of Connecticut, rated first among public universities in New England and in the top 20 nationwide, is located in northeastern Connecticut with easy access to Boston and New York City. The University has a vigorous molecular and cellular biology research environment with state of the art facilities. The web page of the Department of Physiology and Neurobiology and recent information on the laboratory of Daniel Mulkey can be found at ************************* DUTIES AND RESPONSIBILITIES I. Design and execute research experiments: * Perform slice-patch electrophysiological experiments * Assess respiratory function in vivo using whole-body plethysmography * Conduct molecular bench work II. Data analysis * Analyze and present data as part of lab meeting * Present results as posters or oral talks at national meetings * Draft manuscript for publication III. Mentor for Graduate Students * Serve as mentor and role model junior members of the lab. This role includes answering questions if the PI is not available, providing constructive feedback to graduate students during lab meeting and exhibiting a friendly disposition in the workplace. MINIMUM QUALIFICATIONS * Applicants must have a Ph.D. in the life sciences * Strong interest in understanding the cellular/molecular basis of disease * Strong communication skills * Ability to work independently PREFERRED QUALIFICATIONS * Experience maintaining mouse colonies * Background in cellular electrophysiology * Training in basic molecular biology techniques APPOINTMENT TERMS This is a 12-month appointment, end-date position, subject to renewal based on performance and funding. Salary will be commensurate with experience. TERMS AND CONDITIONS OF EMPLOYMENT Employment of the successful candidate is contingent upon the successful completion of a pre-employment criminal background check. TO APPLY Please apply online at ************************** Staff Positions, Search #495849 to upload a resume, cover letter, and contact information for three (3) professional references. This job posting will be open until filled. All employees are subject to adherence to the State Code of Ethics which may be found at ****************************************** All members of the University of Connecticut are expected to exhibit appreciation of, and contribute to, an inclusive, respectful, and diverse environment for the University community. The University of Connecticut aspires to create a community built on collaboration and belonging and has actively sought to create an inclusive culture within the workforce. The success of the University is dependent on the willingness of our diverse employee and student populations to share their rich perspectives and backgrounds in a respectful manner. This makes it essential for each member of our community to feel secure and welcomed and to thoroughly understand and believe that their ideas are respected by all. We strongly respect each individual employee's unique experiences and perspectives and encourage all members of the community to do the same. All 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. The University of Connecticut is an AA/EEO Employer.

Are you ready to join Connecticut Innovation's vibrant community of innovators? Connecticut Innovations (“CI”) is Connecticut's strategic venture capital arm, and we are passionate about serving our portfolio of 220+ companies across various industries, with strengths in life sciences, technology, and climate tech. Come join encapsulate.bio | as a Cancer Research Scientist, Microfluidics & Organoid Specialist Encapsulate Overview Encapsulate is a venture-backed MedTech pioneer transforming precision diagnostics for personalized cancer therapy. Our proprietary tumor-on-a-chip platform leverages advanced microfluidics and patient-derived organoid technologies to rapidly deliver precise, actionable treatment insights to oncologists. We screen patient-specific microtumors against clinical treatment regimens within days, dramatically improving patient outcomes and reducing unnecessary treatment side effects. Every cancer patient's tumor is unique-our solutions are tailored to match that uniqueness. Technology initially developed at UConn, with ongoing headquarters at UConn's Technology Incubator in Farmington, CT. Recently completed oversubscribed seed funding led by Blackwood Healthcare Breakthroughs, Ambit Health Ventures, and Connecticut Innovations. Why Join Encapsulate? Addressing the $4 billion precision diagnostics market, initially targeting colorectal and pancreatic cancers. Tackling unmet needs such as ineffective chemotherapy cycles, escalating treatment costs, and chemotherapy-associated toxicities. Internationally recognized: 2nd place at the 2024 Entrepreneurship World Cup Global Finals. Named “Innovator of the Month” by U.S. Senator Chris Murphy (D-Conn.), July 2024. Successfully launched our tumor-on-a-chip technology to the International Space Station in March 2024. Funded by a Small Business Innovation Research (SBIR) award from the U.S. National Science Foundation and NASA. Cancer Research Scientist, Microfluidics & Organoid Specialist We seek a highly skilled and innovative Cancer Research Scientist specializing in microfluidics, biochips, and organoid-on-a-chip technologies. Join our team to pioneer groundbreaking advancements in precision diagnostics, directly impacting cancer patient care. If you have substantial experience in microfluidic system development, biochip engineering, and patient-derived organoid models, this role provides an ideal opportunity to advance your career and significantly improve patient outcomes. Key Responsibilities: Lead the development, optimization, and application of advanced microfluidic devices and biochips for cancer diagnostics. Process and culture patient-derived biopsies into 3D organoid systems within microfluidic environments. Design and execute precise, reproducible experimental protocols focused on organoid-on-a-chip assays. Analyze experimental data meticulously and present detailed, publication-quality reports. Innovate and continuously improve our tumor-on-a-chip technologies through novel microfabrication approaches. Collaborate closely with multidisciplinary teams of engineers, biologists, and bioinformaticians. Maintain cutting-edge laboratory equipment, troubleshoot experimental setups, and uphold rigorous quality standards. Stay informed about emerging microfluidic and organoid technologies, contributing strategic insights to Encapsulate's technological roadmap. Minimum Qualifications: PhD degree in Biomedical Engineering, Bioengineering, Mechanical Engineering, or related fields with emphasis on microfluidics and biochip technologies. Extensive hands-on experience in microfluidic device design, fabrication, and characterization. Proven expertise in 3D mammalian cell culture, particularly patient-derived tumor organoid models. Proficient in microscopy techniques, especially fluorescence microscopy and advanced imaging analysis. Strong analytical and data interpretation skills, with proven ability to document and communicate scientific results. Demonstrated excellence in problem-solving, attention to detail, and experimental rigor. Proactive, innovative mindset capable of independently driving projects forward in a collaborative team environment. Preferred Qualifications: Advanced experience with biofabrication techniques and microfabrication tools (soft lithography, photolithography, rapid prototyping). Familiarity with AI-driven biochip analytics, sequencing technologies, bioinformatics, and biostatistics. Experience in assay automation and integration of microfluidic systems for clinical applications. Equal Opportunity Employer Encapsulate is an equal-opportunity employers committed to fostering an inclusive, diverse work environment. We provide competitive compensation, generous benefits, and robust personal leave policies, ensuring a rewarding and empowering professional environment.

Position Description: The successful candidate will provide quantitative bioanalytical support using LC-MS/MS for a variety of high throughput in vitro ADME profiling assays. In this hands-on role, the candidate will perform sample analyses by mass spectrometry, and will review, interpret and report results. Instruments and software from various vendors including Sciex (Analyst) and Thermo (Excalibur) will be used along with custom internal data processing software to acquire data and process results. The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. Position Requirements: BS or MS in chemistry, with specialization in analytical chemistry preferred, along with 1 to 5 years of relevant pharmaceutical experience is required. Training or experience in mass spectrometry and separation science, as well as hands-on experience in quantitative LC-MS/MS analysis are desired. Proficiency in general computer software, including vendor specific instrument control and analysis tools, is required. Strong interpersonal and communication skills, both oral and written, are required as is commitment to working as a team player within a multifunctional organization. A working knowledge of allied disciplines such as computer science, lab automation, drug metabolism, pharmacokinetics and synthetic chemistry is helpful. Qualifications The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. LC-MS/MS analysis BS or MS in chemistry Additional Information Thanks & Regards Riya ************

About Us Cloverleaf Bio is an early-stage therapeutics company that is developing a new class of engineered tRNA therapeutics. Our tRNAs target an underappreciated vulnerability of cancer: addiction to high levels of tRNA modifying enzymes. Cloverleaf's approach to drugging tRNA modifying enzymes uses engineered “trojan horse” tRNAs to modulate translation in cancerous cells. The programmability, potency, and specificity of our tRNAs gives us the potential to dramatically improve cancer treatment. The Job We are seeking a Research Associate to join our team. In this position, you will work in close conjunction with our founding team in the creation and development of a completely novel family of RNA therapeutics. Your responsibilities will range from designing and executing experiments independently and in collaboration with team members, preparation, and handling of RNAs and cell cultures, performing advanced laboratory techniques and methodologies, analyzing data and maintaining excellent written documentation of experiments (e.g. electronic lab notebook). About You Excited by the science. We are excited by how science can improve the world and are looking for people who are too. Flexible. We wear many different hats and are looking for people who are willing to do whatever it takes to pitch in and get the job done. Resilient. Working in an early-stage startup can be hard. Science is hard. We are looking for people who have a demonstrated track record of sticking with complex problems for the long haul. Cooperative. As a small team, communication and collaboration are key. We are looking for people who thrive working both independently and collaboratively. Qualifications: BS/BA in biology or related field. Strong problem-solving skills. Ability to work independently. Experience with standard molecular biology techniques, including but not limited to, RNA/DNA extraction, PCR, RT-PCR, qPCR, western blotting, etc. Skilled in mammalian cell culture, passaging/seeding cells, etc. Nice to haves: 1+ years of post-degree wet lab experience Research experience in tRNA, RNA biology and/or RNA modifications field. Prior experience with data analysis software (e.g. Prism) and statistics. Experience with mammalian cell line engineering (e.g. lentivirus, CRISPR-CAS) Benefits Competitive salary commensurate with experience and strong equity incentives. Medical, dental, and vision coverage. Brand new lab space in BioLabs New Haven in downtown New Haven, close to the Yale Shuttle, I-95/91 and Metro North. We will provide a stimulating, collegial, and fast-paced environment. If you are interested in joining our team, then we are excited to hear from you! Please submit resumes at cloverleafbio.com

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Job Description •Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed. •Performed general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software. •Performed quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques. •Operated, maintained, calibrated and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs. •Maintained quality control and calibration logs of all Flow Cytometers. •Analyzed, summarized and document experimental results. •Performed data entry using laboratory information management system (LIMS) •Write experimental SOPs. •Update Biomarker Lead on the status, results and problems in method development and performance of the assays. •Complete all NHCRU/Pfizer required training. •Have a working knowledge of Microsoft office including Excel, Word and PowerPoint. •Possess multi-tasking and organizational skills. •Experience in ELISpot Assays and FlowJo software a plus. Qualifications MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience. Additional Information To schedule interview or get any further information feel free to contact: Sagar Rathore ************ ******************************

Who We Are EvolveImmune Therapeutics is a next-generation immunotherapy company pioneering a new class of precision cancer medicines to transform patient outcomes, compared to current solid tumor therapies. Our first-in-category biotherapeutic EVOLVE platform utilizes integrated T cell co-stimulation to directly target tumor cells to deliver durable, tissue-localized anti-tumor adaptive immune responses. Our newly expanded, state-of-the-art 16,000+ square foot laboratory and office space located in the New Haven, CT biotechnology corridor and our laboratory footprint in Farmington, CT support in-house biologics, immunobiology, and translational activities, enabling our rapid pipeline progress. This includes EV-104, our lead solid tumor program rapidly advancing toward IND filing. The Role We are seeking a highly motivated and skilled Scientist to join our dynamic Biotherapeutics team and contribute to the characterization and development of our next-generation immuno-oncology pipeline. This role will focus on utilizing LC-MS, biochemical and biophysical methods to analyze and characterize the structural integrity, functionality, and stability of these innovative molecules. Key Responsibilities Develop and execute LC-MS workflows for biotherapeutics characterization, including intact and subunit mass analysis, peptide mapping, glycan profiling, and post-translational modification analysis. Perform analytical, biochemical, and biophysical assays using techniques such as SEC, HIC, DSC, ELISA, SPR, and BLI to assess purity, stability, aggregation propensity, and target binding kinetics and affinity. Collaborate effectively with cross-functional teams to ensure alignment of project goals and deliver accurate and timely results. Analyze and interpret experimental data to draw meaningful conclusions, present findings and recommendations to team and management. Address and resolve technical challenges related to LC-MS instrumentation and data analysis. Stay current with advancement in LC-MS and biophysical techniques, implementing innovative approaches where applicable, contribute to scientific publications. Qualifications PhD in Protein Biochemistry and Biophysics, or a related field with 2+ years of relevant experience; or MS with 5+ years, or BS with 8+ years of experience in industry settings. Strong expertise in LC-MS techniques for protein analysis, including hands-on experience with instruments and data analysis. Proficiency in biophysical methods for protein characterization, particularly in analyzing antibody stability and target interactions. Strong analytical and problem-solving skills with attention to detail. Effective communication skills for presenting complex data to diverse teams. Ability to work collaboratively in a cross-disciplinary environment. Preferred Qualifications Experience with protein expression in mammalian systems and purification techniques. Familiarity with the structure and function of T cell engagers and their unique analytical challenges. Experience in immune cell biology and functional cell-based assays relevant to T cell engagers. EvolveImmune Therapeutics requires all employees to be fully vaccinated against COVID-19. You may seek reasonable accommodations for medical and religious reasons. However, your application is no guarantee that such accommodations will be made available. EvolveImmune provides a competitive compensation and benefits package. EvolveImmune Therapeutics, Inc. is an equal opportunity employer.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS