Postdoctoral scholar jobs in Smithtown, NY - 176 jobs

Join the Digital Ethics Center (DEC) at Yale University and contribute to advanced and innovative research on the human, societal, and environmental implications of digital technologies. We seek highly motivated Postdoctoral Associates to shape the future of digital ethics and policy in a collaborative and multidisciplinary academic environment. Responsibilities Under the direction and supervision of Prof. Luciano Floridi, the Postdoctoral Associates are encouraged and supported to: Conduct independent research aligned with the Center's focus on digital ethics, societal implications of digital technologies, and policy guidance. Publish high-quality, peer-reviewed articles in leading academic journals. Develop and refine innovative research questions for future exploration. Collaborate with DEC and Yale faculty and researchers on ongoing multidisciplinary projects. Contribute to the formulation of policy and legal debates on digital ethics issues at national and international levels. Present at academic workshops and conferences to disseminate research findings. Mentor graduate and undergraduate students, if applicable, fostering a vibrant intellectual environment. Postdoctoral Associates are expected to cultivate their own line of research while benefiting from Yale's and the DEC's collaborative and supportive academic community. Qualifications We are seeking candidates who meet the following criteria: A PhD or equivalent degree, already obtained, in a related field e.g., philosophy, law, computer science, social sciences, public policy, or a relevant interdisciplinary area. Interest in addressing the governance, ethical, legal, and societal implications (GELSI) posed by digital technologies such as AI, robotics, social media, and the Web. Interest in informing and steering policy and legal debates, nationally and internationally, on digital ethics broadly understood. Proven research experience in digital ethics, technology policy, or the societal implications of digital technologies. A strong publication record or evidence of potential for high-quality peer-reviewed publications relevant to digital ethics. Excellent communication skills, both written and verbal, to disseminate research findings effectively. A demonstrated ability to work both independently and collaboratively in a multidisciplinary academic environment. Additional Information The position is for up to four years, renewable annually based on performance. Competitive salary and benefits, including comprehensive health coverage, funding for conference travel, and much more are provided. Postdoctoral Associates are expected to work on campus full-time, following Yale University's postdoctoral policies. The Postdoctoral Associate position is expected to last up to four years, renewable on a yearly basis, subject to performance. Compensation is determined by experience All applications will be reviewed on a rolling basis through April 30, 2025. Visit **************************************** for more information on how to apply. We will not accept applications via LinkedIn. Questions? Reach out to Joanna Carmona, Program Manager (***********************)

Trexquant developed the Global Alpha Researcher Program (GAR) in 2015 with a mission to provide a platform for highly academically-talented and high achieving individuals who may not have traditional finance backgrounds but are interested in applying their skills in quantitative finance. Since inception, the GAR program has contracted more than 200 individuals and many of GARs have converted to full-time employment at Trexquant. We are seeking a Head of Global Alpha Researchers to lead and expand the GAR program. In this role you will be responsible for leading our GAR alpha research initiatives, fostering a collaborative environment for participants across multiple regions and defining the roadmap to further grow the program. The ideal candidate will have a strong background in quantitative research, excellent leadership skills, and a passion for mentoring emerging talent. Responsibilities Lead and mentor Global Alpha Researchers in developing Alpha Strategies Develop and execute the strategic vision for the GAR program, ensuring alignment with the company's goals and objectives. Oversee the implementation of research projects and ensure the program's curriculum are cutting-edge to the evolving landscape of quantitative finance Attract, recruit and retain high-caliber researchers Provide mentorship and professional development to support the GARs growth and integration to the finance industry Supervise and review research outputs, ensuring high standards of quality and innovation. Facilitate collaboration among GARs and proliferate GARs integration into Trexquant through the efficacy of their research and potential full-time employment. Present strategic vision of the GAR program, assessment of individual GARs, and GAR program milestones, to Trexquant management. Requirements Bachelor's, Master's and or PhD degree in Math, Engineering, Statistical Modeling Computers Science or other related STEM field Proven experience in quantitative finance, algorithmic trading, or a related field Demonstrate the ability to inspire and motivate researchers Strong analytical and problem-solving skills with a track record of developing successful Alpha Strategies Proficiency in Python programming and experience with machine learning techniques and data analysis tools Creative and forward thinking mindset with a commitment to drive research excellence and fostering an environment collaboration and innovation Previous leadership or managerial experience is a plus Benefits Competitive salary, plus bonus based on individual and company performance Collaborative, casual, and friendly work environment while solving the hardest problems in the financial markets PPO Health, dental and vision insurance premiums fully covered for you and your dependents Trexquant is an Equal Opportunity Employer

Job Description: Part-Time Research Assistant Department: CVM We are seeking a motivated part-time Research Assistant with hands-on experience in fundamental cell and molecular biology techniques. The ideal candidate should be reliable, detail-oriented, and comfortable working in a research laboratory environment. The position will involve working in BSL-2 laboratory space located in 225 Pell Hall. A positive attitude and the ability to perform laboratory tasks safely and efficiently are essential. Applicants are required to submit their Curriculum Vitae for consideration. Responsibilities: If you have expertise in any of the responsibilities listed below, please feel free to contact me. * Perform mammalian cell culture (maintenance, passaging, seeding, and sample preparation). * Conduct qPCR experiments, including RNA extraction, cDNA synthesis, and data analysis. * Run SDS-PAGE and assist with downstream protein analysis as needed. * Carry out functional assays using commercially available kits * Assist with flow cytometry sample preparation, staining, acquisition, and basic data handling. * Perform Scanning Electron Microscopy (SEM) sample preparation and imaging. * Conduct bacterial infection assays and any general bacterial work (e.g., culturing, plating, characterization, or sample preparation). Qualifications: * Bachelor of Science (BS) degree in a relevant field (e.g., Biology, Microbiology, or related discipline). * Strong attention to detail, ability to follow protocols, and capability to work independently. Expected salary: $20 per hour (up to 17 hours per week) LIU is an equal opportunity employer. LIU is committed to extending equal opportunity in employment to all qualified candidates who can contribute to the diversity and excellence of our academic community. LIU encourages applications from all qualified individuals without regard to race, color, religion, genetic information, sexual orientation, gender and/or gender identity or expression, marital or parental status, national origin, ethnicity, citizenship status, veteran or military status, age, disability or any other basis protected by applicable local, state or federal laws. Hiring is contingent on eligibility to work in the United States.

Overview Pepsi Lipton is a joint venture between Unilever and PepsiCo operating in the ready-to-drink Tea segment globally with three well-established brands Lipton, Brisk and Pure Leaf and Yachak. Our global business is worth 3.0 billion USD today, growing volume and with a double digit increase in net revenues. We operate across complex and diverse regions spanning Western Europe to Australia and New Zealand to the United States and Latin America with markets at different stages of development, with different consumer habits and different routes to market via a matrix of franchise, company-owned and third-party manufacturing operating models in which innovation delivery is key enable to accelerate growth. We have an established global R&D function based in two centres: Colworth UK, and Valhalla US. The centre at Valhalla is the primary `hub' from where the R&D team is focused on the North America and Latin America markets, whilst also supporting global programmes and some international markets. Our other R&D Site, Colworth, is our lead centre for tea expertise, bringing this to our product and process development to deliver products across our platforms to meet a wide range of consumer benefits and needs. A role in Pepsi Lipton is a unique experience in which to develop and add value to your career. Pepsi Lipton, although a Joint Venture between Unilever and PepsiCo, operates independently and has its own Board of Directors. Whilst we have the full backing and support of our two parent companies, our entrepreneurial set up gives us real autonomy. Our roles are broad, our responsibilities big and our experiences even bigger. We have high visibility and great exposure - to senior leadership and to talented colleagues all over the world. It means we need to be impactful, smart influencers. In order to support our ambitious growth agenda, we are looking for a Junior Product Developer (Associate Scientist) to join our team in Valhalla, NY. To learn more, visit ********************** Travel Requirements - Occasional short business trips within U.S. may be required (1-3 trips per year) Responsibilities The job holder will be a member of cross functional project teams providing product development capability across the Ready to Drink brand portfolio. This role will be focused on supporting North American Brisk and Pure Leaf development. In this role they will be responsible for owning and delivering product development activities within agreed projects with an onus on practical based activities in our food laboratory or pilot plant facility including: Designing and carrying out the practical & lab-based work program linked to assigned projects. Inputting into project timelines, risk analysis, resource loading associated with projects assigned. Ingredient sourcing including first point of contact with relevant suppliers, link in with parent company Material Expert Teams (METs) or specification team and ownership to drive quality integration into parent company systems and processes. This includes ingredient documentation, ingredient samples, ingredient ordering & ingredient specification builds. Generation of all prototypes to support project requirements including liaison with pilot plant for production of larger scale quantities & provision of key documentation & non-standard ingredient ordering for PP scheduling. Lead the provision of all relevant product related documentation linked to assigned project including documentation for consumer testing, requirements for registration, certification, or specific local BU-initiated requests. Ownership of functional specification delivery & utilization of digital tools (e.g. specification systems) to ensure technical output for artwork and labelling delivered at the agreed timescale including liaison with specification experts, concentrate teams, and QA Team members for specification parameter alignment where required. Ownership of any scale up trials required to confirm viability including ownership of trial briefing and point of contact with SC & Technical Contact Managers (TCM) and Quality along with suppliers. Liaison role with Consumer Technical Insights (CTI), Sensory Product Consumer Insights, and brand Insights to support relevant prototype, panel, or consumer tastings. Management of prototype sample shipment process to consumer test locations, stakeholders, teams, and event locations. Initiating and maintaining formal lab notes, trial reports, experimental write ups, handover documents and presentation cascades as required to capture key technical updates. Link in with Regulatory and local deploy partners where relevant to ensure prototype development and ingredient selection complies with local requirements; collate & cascade output to relevant stakeholders. Be the point of contact for product and ingredient related queries for formulations developed. Support wider technical activities, Business unite-initiated requests and broader R&D team requirements where required. Have awareness of competitor landscape, commercial produces, supply chain model and project management processes. Liaise with parent company groups to support any knowledge build or understanding. Adhere to safety and regulatory aspects throughout activities performed (traceability, allergen and consumer safety, microbiological clearance, food safety approvals) including ensuring Ensure compliance with all relevant Code of Business Principles, site, and company policies. Key Interfaces R&D Product Development Team Brand Marketing Insights Supply Chain Regional Marketing Teams Regional SC & Operations Team 3rd party contacts and supplier partners Sensory Parent company link ins (Safety/Regulatory) Compensation and Benefits: The expected compensation range for this position is between $70,700 - $118,400. Location, confirmed job-related skills, experience, and education will be considered in setting actual starting salary. Your recruiter can share more about the specific salary range during the hiring process. Paid time off subject to eligibility, including paid parental leave, vacation, sick, and bereavement. In addition to salary, PepsiCo offers a comprehensive benefits package to support our employees and their families, subject to elections and eligibility: Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts, Employee Assistance Program (EAP), Insurance (Accident, Group Legal, Life), Defined Contribution Retirement Plan. Qualifications Key Skills Passion to work in a practical & lab- based setting Proven track record of product development Creativity & flair with ability to innovate and translate product brief into winning launches Strong communication skills Attention to detail especially with experimentation, data recording, analysis & reporting Strong organisational skills Good time management and priority setting skills An ability to flex and multitask. Relevant Experience Degree (or equivalent) in Food Science, Chemical Science or Engineering and/or relevant experience in FMCG in fields related to product or process development/manufacturing in foods or beverages Experience of working cross-functionally and with external suppliers Experience of delivery of innovations from brief to market deployment Foundation training/qualification in food hygiene Leadership Behaviours Purpose & Service Personal Mastery Agility Business Acumen Talent Catalyst Consumer Love EEO Statement Our Company will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Fair Credit Reporting Act, and all other applicable laws, including but not limited to, San Francisco Police Code Sections 4901-4919, commonly referred to as the San Francisco Fair Chance Ordinance; and Chapter XVII, Article 9 of the Los Angeles Municipal Code, commonly referred to as the Fair Chance Initiative for Hiring Ordinance. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PepsiCo is an Equal Opportunity Employer: Female / Minority / Disability / Protected Veteran / Sexual Orientation / Gender Identity / Age If you'd like more information about your EEO rights as an applicant under the law, please download the available EEO is the Law & EEO is the Law Supplement documents. View PepsiCo EEO Policy. Please view our Pay Transparency Statement Key Skills Passion to work in a practical & lab- based setting Proven track record of product development Creativity & flair with ability to innovate and translate product brief into winning launches Strong communication skills Attention to detail especially with experimentation, data recording, analysis & reporting Strong organisational skills Good time management and priority setting skills An ability to flex and multitask. Relevant Experience Degree (or equivalent) in Food Science, Chemical Science or Engineering and/or relevant experience in FMCG in fields related to product or process development/manufacturing in foods or beverages Experience of working cross-functionally and with external suppliers Experience of delivery of innovations from brief to market deployment Foundation training/qualification in food hygiene Leadership Behaviours Purpose & Service Personal Mastery Agility Business Acumen Talent Catalyst Consumer Love The job holder will be a member of cross functional project teams providing product development capability across the Ready to Drink brand portfolio. This role will be focused on supporting North American Brisk and Pure Leaf development. In this role they will be responsible for owning and delivering product development activities within agreed projects with an onus on practical based activities in our food laboratory or pilot plant facility including: Designing and carrying out the practical & lab-based work program linked to assigned projects. Inputting into project timelines, risk analysis, resource loading associated with projects assigned. Ingredient sourcing including first point of contact with relevant suppliers, link in with parent company Material Expert Teams (METs) or specification team and ownership to drive quality integration into parent company systems and processes. This includes ingredient documentation, ingredient samples, ingredient ordering & ingredient specification builds. Generation of all prototypes to support project requirements including liaison with pilot plant for production of larger scale quantities & provision of key documentation & non-standard ingredient ordering for PP scheduling. Lead the provision of all relevant product related documentation linked to assigned project including documentation for consumer testing, requirements for registration, certification, or specific local BU-initiated requests. Ownership of functional specification delivery & utilization of digital tools (e.g. specification systems) to ensure technical output for artwork and labelling delivered at the agreed timescale including liaison with specification experts, concentrate teams, and QA Team members for specification parameter alignment where required. Ownership of any scale up trials required to confirm viability including ownership of trial briefing and point of contact with SC & Technical Contact Managers (TCM) and Quality along with suppliers. Liaison role with Consumer Technical Insights (CTI), Sensory Product Consumer Insights, and brand Insights to support relevant prototype, panel, or consumer tastings. Management of prototype sample shipment process to consumer test locations, stakeholders, teams, and event locations. Initiating and maintaining formal lab notes, trial reports, experimental write ups, handover documents and presentation cascades as required to capture key technical updates. Link in with Regulatory and local deploy partners where relevant to ensure prototype development and ingredient selection complies with local requirements; collate & cascade output to relevant stakeholders. Be the point of contact for product and ingredient related queries for formulations developed. Support wider technical activities, Business unite-initiated requests and broader R&D team requirements where required. Have awareness of competitor landscape, commercial produces, supply chain model and project management processes. Liaise with parent company groups to support any knowledge build or understanding. Adhere to safety and regulatory aspects throughout activities performed (traceability, allergen and consumer safety, microbiological clearance, food safety approvals) including ensuring Ensure compliance with all relevant Code of Business Principles, site, and company policies. Key Interfaces R&D Product Development Team Brand Marketing Insights Supply Chain Regional Marketing Teams Regional SC & Operations Team 3rd party contacts and supplier partners Sensory Parent company link ins (Safety/Regulatory) Compensation and Benefits: The expected compensation range for this position is between $70,700 - $118,400. Location, confirmed job-related skills, experience, and education will be considered in setting actual starting salary. Your recruiter can share more about the specific salary range during the hiring process. Paid time off subject to eligibility, including paid parental leave, vacation, sick, and bereavement. In addition to salary, PepsiCo offers a comprehensive benefits package to support our employees and their families, subject to elections and eligibility: Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts, Employee Assistance Program (EAP), Insurance (Accident, Group Legal, Life), Defined Contribution Retirement Plan.

Introduction to role This is a lab-based position, and the role requires the candidate to be present onsite in New Haven, CT. The candidate will follow the science by working in Alexion's state-of-the-art laboratories to help drive innovation and advance medicine to help improve patient lives. This position offers a unique opportunity to work in a dynamic and innovative research environment developing your career at the interface of research and clinical development. Contribute to Alexion's research and clinical development programs through the identification of suitable biomarkers for preclinical and clinical development of therapeutics, development of innovative platforms and omics technology for biomarker discovery and implementing AI systems to accelerate workstreams and precision medicine. Perform experiments at the bench to develop, optimize, and validate biomarker assays for monitoring disease pathogenesis and response to therapeutic treatment. Collaborate with external vendors and cross-functional teams including discovery, translational research, bioanalytics, diagnostics and data sciences to drive successful rare-disease drug development programs. Accountabilities Actively contribute to the biomarker support of multiple programs in multiple therapeutic areas through literature reviews and database searches to identify potential new biomarkers of disease activity and/or therapeutic efficacy (mechanism of disease, response/pharmacodynamic, predictive, exploratory, etc). Collaborate with colleagues and independently evaluate new technologies, design, develop, troubleshoot novel sample testing protocols, and follow existing protocols for the detection, quantitation and/or functional activity of target biomarkers in complex biological matrices including proteins and nucleic acids Develop and perform in vitro binding or functional assays using purified reagents, primary cells or cell lines (human, murine and/or primate) to evaluate target levels, functional activity or mechanism of action of candidate therapeutics Lead or support biomarker assay validation for clinical sample analysis and interact with cross-functional sub-teams and CROs supporting technical, operational and troubleshooting aspects of assays Provide support as required to other Translational Biomarker Research team members and groups within Research Analyze, summarize and present data in individual, group meetings, conferences or in written summary documents Essential Skills & Experience All candidates must have 5+ years of pharmaceutical industry experience. In addition, all candidates must have either a BA/BS in biochemistry or related field with 10+ years of total experience or a MS in biochemistry or related field with 7+ years of total experience Solid understanding of the principles of cell biology, disease pathogenesis and strategies for therapeutic intervention and application of these principles for understanding cellular responses and disease pathogenesis Proven track record of technical proficiency, creativity in experimental design and independent, critical thinking to identify novel methods or solutions/troubleshooting Ability to independently design, execute, analyze, and interpret experiments, as well as troubleshoot to overcome technical challenges in a high-tech, fast-paced environment Familiarity with clinical stage development programs, protocols, sample handling, data analysis and management according to GCPs Proven experience with protein and cell-based assays, examples include ELISA, MSD, Luminex, immunoprecipitation, proteomics (e.g. Olink), and/or flow cytometry Hands-on experience developing and optimizing single and multiplex assays; experience with assay validation in a GxP environment Excellent communication, record keeping and organizational skills and familiarity with electronic lab notebook procedures Strong interpersonal skills and ability to work well with cross-functional members Experience with Microsoft Office (e.g., Word, Excel, PowerPoint) and data graphing software (e.g. Graphpad Prism) for report writing, presentation and data analysis Desirable Skills & Experience Experience with exosome isolation and analysis Experience with nucleic acid purification and methodologies such as RT-PCR, RNAseq, micro RNA characterization and data analysis and interpretation Experience with SIMOA, spatial biology platforms (e.g., Nanostring CosMx) Experience with mammalian cell culture and aseptic techniques At AstraZeneca's Alexion division, we are driven by a pioneering spirit that pushes us to innovate and expand our reach. Our commitment to patients living with rare diseases brings us closer to our work and each other. Join us to grow in a rapidly expanding portfolio within a supportive culture that values connections, new ideas, and learning. You will be empowered with tailored development programs designed to enhance your skills and cultivate a deep understanding of our patient's journeys. Together, we inspire change with integrity, celebrating diversity, innovation, and the power of connection. Ready to make a difference? Apply today! Date Posted 15-Jan-2026 Closing Date 28-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Syensqo is all about chemistry. We're not just referring to chemical reactions here, but also to the magic that occurs when the brightest minds get to work together. This is where our true strength lies. In you. In your future colleagues and in all your differences. And of course, in your ideas to improve lives while preserving our planet's beauty for the generations to co We are looking for: We are seeking a motivated and detail-oriented Research Scientist to join our Polymer Additives team. We count on you for: * Hand-on technical lead on new NPI (New Product Introduction) product development meeting project's targeted technical performance * Lead cross-functional project teams to develop and commercialize new NPI products into core * and adjacent markets as Project Leader following the stage-gate process * Investigate and develop new additive formulations providing leading edge performance * Develop and analyze data, drawing sound conclusions and uncovering unexpected * performance benefits * Hands-on participation in lab operations including polymer processing, data acquisition, data * summary, data analysis, preparation of presentations and reports * Document, maintain and update laboratory project database * Identify IP potential for new technologies and file patent application as appropriate * Prepare and present presentation on new products at conferences * Write company reports and monthly reports * Develop high level of industry knowledge in all core market segments * Develop subject matter expertise (SME) in designated market segments * Engage in innovation dialogue with key customers * Maintain calibration and maintenance schedule for designated PA laboratory equipment You can count on us for: * We offer the opportunity to join an exciting growth company * A full range of benefits as expected of a successful company * Opportunities for growth and learning * Encouraging a diverse and inclusive workplace culture that values and respects individual differences and backgrounds * Long-lasting excellent customer relations, self-dependent working, and a variety of tasks in one of the world's leading chemical companies. You will bring: * Minimum B.S. degree in chemistry, polymer science & engineering, or relevant science or engineering field, advanced degree preferred * Minimum of 2+ years of relevant work experience in technical area * Practical polymer formulation and polymer processing experience preferred o Polymer Processing: extrusion, injection molding, rotomolding, etc. o Polymer Testing: MFI, color, gloss, physical properties, etc. o Testing Protocols: artificial weathering, thermal aging, etc. * Proven working knowledge of most additives used in polymers * Prior experience with rotational molding strongly preferred * Practical knowledge of polyolefin chemistry, production processes, properties, fabrication processes, and their use preferred * Practical knowledge and experience in intellectual Properties (IP) * Demonstrated Project Leadership skills in leading cross-functional project teams from product development to commercialization following the stage-gate (NPI) process * Strong track record of success in developing and launching new products * Understanding of application of AI / Machine Learning tools to new product and process development is a strong plus. Skills and competencies: * Project leadership skills * Analytical skills: This role requires special insightful analysis of data * Analytical data interpretation: TGA/DSC, SEM, HPLC/GC, FTIR, UV-Vis, etc. * Excellent problem solving and troubleshooting skills * Excellent communication and presentation skills * Ability to bring new ideas and concepts to a project * Ability to engage in innovation dialogues with customers * Work well in a team setting * High level of creativity and curiosity * Proactive, collaborative, entrepreneurial, dynamic, flexible, and able to multitask * Highly motivated with self-driven learning capacit * Customer focus - dedicated and sensitive to the customer needs You will get: * Competitive salary and benefits * The U.S. base salary range reasonably expected to be paid for this position is $85,000.00 to $140,000.00 per year. Since actual compensation packages are based on a variety of factors unique to each candidate we may ultimately pay more or less than the posted base salary range. Total compensation for this role also includes bonus and/or other incentives. * 16, or more, weeks of maternity/paternity and co-parenting leave, according to local regulations * Training platform for all employees * Free well-being sessions (physical and psychological) Additional Information: Travel up to 10% About us * Syensqo is a science company developing groundbreaking solutions that enhance the way we live, work, travel and play. Inspired by the scientific councils which Ernest Solvay initiated in 1911, we bring great minds together to push the limits of science and innovation for the benefit of our customers, with a diverse, global team of more than 13,000 associates. Our solutions contribute to safer, cleaner, and more sustainable products found in homes, food and consumer goods, planes, cars, batteries, smart devices and health care applications. Our innovation power enables us to deliver on the ambition of a circular economy and explore breakthrough technologies that advance humanity. * At Syensqo, we seek to promote unity and not uniformity. We value the diversity that individuals bring and we invite you to consider a future with us, regardless of background, age, gender, national origin, ethnicity, religion, sexual orientation, ability or identity. We encourage individuals who may require any assistance or accommodations to let us know to ensure a seamless application experience. We are here to support you throughout the application journey and want to ensure all candidates are treated equally. If you are unsure whether you meet all the criteria or qualifications listed in the job description, we still encourage you to apply. * Syensqo is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics. Nearest Major Market: Bridgeport Nearest Secondary Market: Danbury

Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience. This is a full-time position working daytime hours with weekend and holiday rotations. Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person. At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Holidays Monday to Friday Weekend availability Ability to commute/relocate: Norwalk, CT 06851 Experience: Embryology: 2 year Work Location: In person in Norwalk, CT

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 ************ ******************************

This role is central to the development of novel biologically active compounds within the Boehringer Ingelheim pipeline. We are seeking a highly skilled scientist to drive critical development work in Drug Substance-Drug Product (DS-DP) co-processing, solid form evaluation, and isolation development for early-stage compounds. The successful candidate will leverage a deep understanding of the drug development process integrating solid-state chemistry, process chemistry, and chemical engineering principles to lead the characterization and selection of process-suitable solid forms for both final APIs and synthetic intermediates. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees. **Duties & Responsibilities** - Solid Form Development: Independently design and execute phase-appropriate screenings for polymorphs, salts, and cocrystals. - Advanced Co-Processing: Support the development and optimization of DS-DP Co-processing processes to create amorphous solid dispersions. - Isolation & Scale-Up: Support activities to develop isolation processes for novel chemical entities (NCEs) and drug product intermediates. - Analytical Excellence: Perform routine and exploratory characterization using XRPD, DSC, TGA, DVS, PLM, and NMR, while integrating Process Analytical Technology (PAT) such as Raman and Blaze Metrics. - Cross-Functional Collaboration: Collaborate closely with CMC Development teams and pharmaceutical sponsors to ensure study compliance and project alignment. - Project Leadership: Manage multiple challenging projects simultaneously, drafting technical reports and communicating updates to multidisciplinary teams. **Requirements** - Master´s Degree with three plus (3+) years´ experience in Pharmaceutics/Chemistry or related scientific discipline or Bachelor´s Degree with seven plus (7+) years´ experience in Engineering or related scientific discipline or equivalent experience in related field - Supplemental technical courses in area of expertise - Ability to operate laboratory equipment and systems with independence - Ability to draft technical reports - Clear and effective written and verbal communication skills - Concise and accurate reporting of technical data and interpretation thereof - Proven problem solving ability - Solid knowledge and understanding of applicable regulations; able to act for supervisor in his/her absence - May require an ability to push, pull, lift and carry objects up to 50lbs. - May require ability to wear a Respirator. **Desired Skills and Experience:** - Sound knowledge and experience in solid-state chemistry, process chemistry. Previous experience with solid form studies, crystallization development and DS-DP co-processing development - Ability to independently perform hands-on activities for solid form screening and crystallization process development, data analysis and interpretation - Proficient in operating laboratory equipment and apparatuses, such as NMR, DSC, TGA, DVS, PLM, and PXRD techniques, along with HPLC method development and Process Analytical Tools (PAT), including IR, Blaze, EasyViewer, and Raman - Highly motivation to explore new technologies and concepts Key Competencies: - Strong problem-solving and analytical skills. - Excellent oral and written communication abilities. - Ability to work independently and collaboratively in a team environment. - Commitment to safety and compliance in laboratory operations. **Eligibility Requirements:** - Must be legally authorized to work in the United States without restriction. - Must be willing to take a drug test and post-offer physical (if required) - Must be 18 years of age or older **Compensation Data** This position offers a base salary typically between $90,000.00 and $147,000.00 USD. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here (***************************************************************** . All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

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 Studies the basic principles of plant and animal life and the effects of varying environmental and physical conditions such as radioactivity or pollution. Studies reactions of plants, animals, and marine species to parasites, bacteria, pharmaceuticals and chemicals. • Performing cell assay development and NTC studies on Client targets . • Skills: • Familiar with a variety of the fields concepts, practices, and procedures. • Education: • Bachelor's Degree • Cell biology and molecular biology skills a plus • Languages: • English Read Write Speak • Education: Bachelor's Degree • Skills: Familiar with a variety of the fields concepts, practices, and procedures.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. 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 • Perform general flow cytometry operation, including sample preparation and analysis. • Perform quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques • Operate, maintain, calibrate and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs • Maintain quality control and calibration logs of all Flow Cytometers • Analyze, summarize and document experimental results • Perform 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 required training. Qualifications • 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 • MS in Biology/Biochemistry/Medical Technology plus 1 year of relevant experience BS in Biology/Biochemistry/Medical Technology or 3 years of relevant experience • Experience in FACSCanto Flow Cytometer and FACSDiva software Additional Information Thanks Regards Ricky

Job Description Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience. This is a full-time position working daytime hours with weekend and holiday rotations. Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person. At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Holidays Monday to Friday Weekend availability Ability to commute/relocate: Norwalk, CT 06851 Experience: Embryology: 2 year Work Location: In person in Norwalk, CT

Postdoctoral Associate- Condensed Matter Required Qualifications: (as evidenced by an attached resume/cv) Ph. D. (or foreign equivalent) in Physics, Applied Physics, Materials Science, Electrical Engineering, or a closely related field in hand by the start of the appointment. Demonstrated experience in experimental condensed matter physics, nanophotonics, or quantum materials research. Strong background in experimental physics. Experience with cryogenic measurements and/or optical spectroscopy. Ability to design, execute, and analyze complex experiments. Preferred Qualifications: Experience with scanning probe techniques (e. g. , SNOM, AFM, STM). Experience with THz, infrared, or ultrafast optical systems. Familiarity with superconductivity, two-dimensional materials, or polariton physics. Record of first-author publications in peer-reviewed journals. Brief Description of Duties: The Postdoctoral Associate will assist the Principal Investigator Dr. Mengkun Liu in the department of Physics and Astronomy. The incumbent will conduct research and ensure that all experiments are appropriately conducted following the policies and procedures of Stony Brook University. The Postdoctoral Researcher will conduct independent and collaborative research using advanced THz and cryogenic near-field optical techniques to study superconductors and two-dimensional quantum materials. Responsibilities include the development and operation of THz-SNOM, Cryo-SNOM, and BOSON instrumentation; performing nanoscale measurements of polaritons, superconducting phase transitions, and light-matter interactions; analyzing experimental data; and disseminating results through publications and presentations. The incumbent will have strong written and oral communication and the ability to work independently and in a collaborative research environment. They will contribute to mentoring graduate and undergraduate students, maintaining experimental systems, supporting proposal preparation and collaborative research activities. The position emphasizes scientific creativity, technical excellence, and leadership in experimental research. ● Conduct independent and collaborative experimental research onsuperconductors and two-dimensional materials using THz-SNOM, Cryo-SNOM, and BOSON platforms; design and perform low-temperature, high-field measurements; analyze and interpret data; produce publishable scientific results. ● Develop, optimize, and maintain advanced experimental instrumentation, including cryogenic near-field optical systems and THz optical setups. ● Mentor graduate students, undergraduate students, and visiting researchers in experimental techniques, data analysis, and scientific communication. ● Prepare manuscripts, conference presentations, and research reports; present results at group meetings, conferences, and workshops. ● Other duties as assigned, which may include attending Scientific Conferences and Meetings. Assist the PI with proposal development, progress reports, and coordination of internal and external research collaborations. Applicants should submit the following materials through our online application system:• Curriculum Vitae• Research Statement Special Notes:The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption. Visit The Office of Postdoctoral Affairs to learn more about our postdoctoral community. Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at ************** or visit OEA. In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here. Visit our WHY WORK HERE page to learn about the total rewards we offer. SUNY Research Foundation: A Great Place to Work. The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. Job Number: 2600068Official Job Title: Postdoctoral AssociateJob Field: Post DoctoralPrimary Location: US-NY-Stony BrookDepartment/Hiring Area: Physics and AstronomySchedule: Full-time Shift :Day Shift Shift Hours: 9am-5pm Posting Start Date: Jan 20, 2026Posting End Date: Feb 20, 2026, 4:59:00 AMSalary:$60,000-$65,000Appointment Type: RegularSalary Grade:E89SBU Area:The Research Foundation for The State University of New York at Stony Brook

Postdoctoral AssociateRequired Qualifications: (as evidenced by an attached resume) Doctoral degree (or foreign equivalent) in Microbiology, Biochemistry, Cell Biology, or a closely related field in hand by the start of the appointment. Experience with bacterial cultures and aseptic technique. Experience with molecular approaches to study bacterial survival and antibiotic resistance. Preferred Qualifications: ● Experience with bacterial genetics. ● Experience with protein biochemistry and functional assays. ● Experience with mouse infection models. Brief Description of Duties: The Postdoctoral Associate will assist the Principal Investigator, Dr. Hwan Kim, in the department of Microbiology and Immunology. Please visit the Kim Laboratory to learn more about our department/research. The incumbent will conduct research and ensure that all experiments are appropriately conducted following the policies and procedures of Stony Brook University. ● Perform experiments with Staphylococcus aureus and study the underlying genetic and molecular mechanisms evading small molecules that are designed to neutralize essential biological and virulence functions. ● Conduct experiments with recombinant approaches to define mutations impacting Staphylococcus aureus biology and pathogenesis using in vitro and in vivo models. ● Document data generated in studies, analyze data with appropriate statistical methods, prepare manuscripts for publication in scientific journals and presentations for laboratory meetings and national conferences, assist with grant proposals, protocols, and compliance reports. ● General laboratory maintenance and assist laboratory manager. ● Other duties as assigned. Special Notes:The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption. Visit The Office of Postdoctoral Affairs to learn more about our postdoctoral community. Resume/CV and cover letter should be included with the online application. Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at ************** or visit OEA. In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here. Visit our WHY WORK HERE page to learn about the total rewards we offer. SUNY Research Foundation: A Great Place to Work. The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. Job Number: 2600013Official Job Title: Postdoctoral AssociateJob Field: Post DoctoralPrimary Location: US-NY-Stony BrookDepartment/Hiring Area: Microbiology and ImmunologySchedule: Full-time Shift :Day Shift Shift Hours: 8:30 am - 5:00 pm Posting Start Date: Jan 22, 2026Posting End Date: Feb 6, 2026, 4:59:00 AMSalary:$50,000-$65,000Appointment Type: RegularSalary Grade:E89SBU Area:The Research Foundation for The State University of New York at Stony Brook

**Duration: 24 Months Contract** + Initiates and completes routine in vitro studies in an independent, efficient, and timely manner, with minimal supervision. Interprets the outcome of those experiments and proposes appropriate follow-up; troubleshoots effectively. + Assists in the design and execution of non-routine cell-based in vitro and biochemical assays; conducts exploratory experiments with minimal supervision. + Performs literature searches and extracts relevant information from literature and published protocols. + Independently operates and is responsible for lab equipment; troubleshoots effectively. + Communicates their own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provides input for scientific reports. + Reports and treats data with a high level of integrity and ethics. Maintains accurate and up-to-date electronic lab notebooks. + Complies with applicable regulations, performing all work in a safe and compliant manner; maintains proper records in accordance with Standard Operating Procedures and policies. **Skills:** + Experience in aseptic animal tissue culture techniques and basic molecular biology techniques including nucleic acid extraction, RT-PCR, Western Blot, ELISA, transfection is required. Experimental design, execution, and interpretation in these areas will be required. + Proven problem-solving ability and eagerness to learn. Ability to evaluate new technologies and assist in incorporating them into our research. + Written and verbal communication skills: concise and accurate reporting of technical data and information. Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism. + Ability and willingness to work effectively in a highly collaborative environment. **Education:** + Master's Degree or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant 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.

Introduction to role This is a lab-based position, and the role requires the candidate to be present onsite in New Haven, CT. The candidate will follow the science by working in Alexion's state-of-the-art laboratories to help drive innovation and advance medicine to help improve patient lives. This position offers a unique opportunity to work in a dynamic and innovative research environment developing your career at the interface of research and clinical development. Contribute to Alexion's research and clinical development programs through the identification of suitable biomarkers for preclinical and clinical development of therapeutics, development of innovative platforms and omics technology for biomarker discovery and implementing AI systems to accelerate workstreams and precision medicine. Perform experiments at the bench to develop, optimize, and validate biomarker assays for monitoring disease pathogenesis and response to therapeutic treatment. Collaborate with external vendors and cross-functional teams including discovery, translational research, bioanalytics, diagnostics and data sciences to drive successful rare-disease drug development programs. Accountabilities Actively contribute to the biomarker support of multiple programs in multiple therapeutic areas through literature reviews and database searches to identify potential new biomarkers of disease activity and/or therapeutic efficacy (mechanism of disease, response/pharmacodynamic, predictive, exploratory, etc). Collaborate with colleagues and independently evaluate new technologies, design, develop, troubleshoot novel sample testing protocols, and follow existing protocols for the detection, quantitation and/or functional activity of target biomarkers in complex biological matrices including proteins and nucleic acids Develop and perform in vitro binding or functional assays using purified reagents, primary cells or cell lines (human, murine and/or primate) to evaluate target levels, functional activity or mechanism of action of candidate therapeutics Lead or support biomarker assay validation for clinical sample analysis and interact with cross-functional sub-teams and CROs supporting technical, operational and troubleshooting aspects of assays Provide support as required to other Translational Biomarker Research team members and groups within Research Analyze, summarize and present data in individual, group meetings, conferences or in written summary documents Essential Skills & Experience All candidates must have 5+ years of pharmaceutical industry experience. In addition, all candidates must have either a BA/BS in biochemistry or related field with 10+ years of total experience or a MS in biochemistry or related field with 7+ years of total experience Solid understanding of the principles of cell biology, disease pathogenesis and strategies for therapeutic intervention and application of these principles for understanding cellular responses and disease pathogenesis Proven track record of technical proficiency, creativity in experimental design and independent, critical thinking to identify novel methods or solutions/troubleshooting Ability to independently design, execute, analyze, and interpret experiments, as well as troubleshoot to overcome technical challenges in a high-tech, fast-paced environment Familiarity with clinical stage development programs, protocols, sample handling, data analysis and management according to GCPs Proven experience with protein and cell-based assays, examples include ELISA, MSD, Luminex, immunoprecipitation, proteomics (e.g. Olink), and/or flow cytometry Hands-on experience developing and optimizing single and multiplex assays; experience with assay validation in a GxP environment Excellent communication, record keeping and organizational skills and familiarity with electronic lab notebook procedures Strong interpersonal skills and ability to work well with cross-functional members Experience with Microsoft Office (e.g., Word, Excel, PowerPoint) and data graphing software (e.g. Graphpad Prism) for report writing, presentation and data analysis Desirable Skills & Experience Experience with exosome isolation and analysis Experience with nucleic acid purification and methodologies such as RT-PCR, RNAseq, micro RNA characterization and data analysis and interpretation Experience with SIMOA, spatial biology platforms (e.g., Nanostring CosMx) Experience with mammalian cell culture and aseptic techniques At AstraZeneca's Alexion division, we are driven by a pioneering spirit that pushes us to innovate and expand our reach. Our commitment to patients living with rare diseases brings us closer to our work and each other. Join us to grow in a rapidly expanding portfolio within a supportive culture that values connections, new ideas, and learning. You will be empowered with tailored development programs designed to enhance your skills and cultivate a deep understanding of our patient's journeys. Together, we inspire change with integrity, celebrating diversity, innovation, and the power of connection. Ready to make a difference? Apply today! Date Posted 15-Jan-2026 Closing Date 28-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Initiates and completes routine in vitro studies in an independent, efficient, and timely manner, with minimal supervision. Interprets the outcome of those experiments and proposes appropriate follow-up;troubleshoots effectively. Assists in the design and execution of non-routine cell-based in vitro and biochemical assays;conducts exploratory experiments with minimal supervision. Performs literature searches and extracts relevant information from literature and published protocols. Independently operates and is responsible for lab equipment;troubleshoots effectively. Communicates their own work effectively orally and in writing;contributes to writing protocols, procedures, and technical reports;provides input for scientific reports. Reports and treats data with a high level of integrity and ethics. Maintains accurate and up-to-date electronic lab notebooks. Complies with applicable regulations, performing all work in a safe and compliant manner;maintains proper records in accordance with Standard Operating Procedures and policies. Skills: Experience in aseptic animal tissue culture techniques and basic molecular biology techniques including nucleic acid extraction, RT-PCR, Western Blot, ELISA, transfection is required. Experimental design, execution, and interpretation in these areas will be required. Proven problem-solving ability and eagerness to learn. Ability to evaluate new technologies and assist in incorporating them into our research. Written and verbal communication skills: concise and accurate reporting of technical data and information Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism. Ability and willingness to work effectively in a highly collaborative environment. Education: Master s Degree or Bachelor s Degree with 3+ years experience in related scientific discipline;pharmaceutical, biotechnology or CRO experience is highly desirable;non-PhD applicant required. Skills and Experience The Skills and Experience match parameters for the candidate are parsed from the Duties, Skills, and Education. Required Skills ASEPTIC ANIMAL TISSUE CULTURE TECHNIQUES BASIC MOLECULAR BIOLOGY TECHNIQUES

Job Title: In Vitro Scientist II Type: Contract Global Pharma company looking to hire experienced Scientist to join their growing team. Must bring a Master's Degree or Bachelor's Degree with 3+ years experience in molecular biology. Pharmaceutical, biotechnology or CRO experience is highly desirable. Responsibilities + Initiates and completes routine in vitro studies in an independent, efficient, and timely manner, with minimal supervision. Interprets the outcome of those experiments and proposes appropriate follow-up; troubleshoots effectively. + Assists in the design and execution of non-routine cell-based in vitro and biochemical assays; conducts exploratory experiments with minimal supervision. + Performs literature searches and extracts relevant information from literature and published protocols. + Independently operates and is responsible for lab equipment; troubleshoots effectively. + Communicates their own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provides input for scientific reports. + Reports and treats data with a high level of integrity and ethics. + Maintains accurate and up-to-date electronic lab notebooks. + Complies with applicable regulations, performing all work in a safe and compliant manner; maintains proper records in accordance with Standard Operating Procedures and policies. Requirements + Master's Degree or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required. + Experience in aseptic animal tissue culture techniques and basic molecular biology techniques including nucleic acid extraction, RT-PCR, Western Blot, ELISA, transfection is required. Experimental design, execution, and interpretation in these areas will be required. + Proven problem-solving ability and eagerness to learn. Ability to evaluate new technologies and assist in incorporating them into our research. + Written and verbal communication skills: concise and accurate reporting of technical data and information + Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism. + Ability and willingness to work effectively in a highly collaborative environment. Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref: #558-Scientific System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Required Qualifications (as evidenced by an attached resume): Bachelor's degree (foreign equivalent or higher) in biology, biochemistry, physiology, biomedical sciences or a related field. Experience with research activities. Research experience in a laboratory setting. Preferred Qualifications: Proficient in wetlab (cell culture, bench assays), dry lab (computational analysis), and mouse work. Brief Description of Duties: The Yang Laboratory ************************************************** at Stony Brook University is seeking a motivated Research Technician to join our new and growing group. Research in the Yang Lab explores how mRNA translation drives dynamic cellular responses to nutritional and dietary inputs to reshape the proteome and metabolome in ways that influence health and disease. We use a multidisciplinary approach that integrates cellular and molecular biology, protein-metabolite interaction assays, and translational research to uncover how mRNA regulation contributes to metabolic disorders, cancer, and aging. Recent graduates with a background in the biological sciences, a history of academic productivity, and excellent references are encouraged to apply. The technician will receive comprehensive training in a broad range of experimental techniques, including cell culture, molecular and biochemical assays, metabolic analysis, imaging, and mouse handling and experimental work. This position offers an excellent opportunity to develop strong research skills, contribute to high-impact projects, and work closely with the PI in a collaborative and supportive environment. Under the direct supervision of Dr. Yang, the incumbent will perform the following duties: * Protein, RNA and DNA preparation and analyses; mammalian cell culture with sterile techniques. * Assist in ordering supplies and equipment to keep the lab inventory well stocked. * Maintain mouse colony, and mouse metabolic assays. * Data analysis and participate in manuscript writing for publication. * Maintain laboratory reagents and equipment. * Participate in weekly lab meetings, and other duties/projects as assigned. * Other Duties as assigned. Special Notes: The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Non-Exempt position, eligible for the overtime provisions of the FLSA. For this position, we are unable to sponsor candidates for work visas. Resume/CV and cover letter should be included with the online application. Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at ************** or visit OEA. In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here. Visit our WHY WORK HERE page to learn about the total rewards we offer. SUNY Research Foundation: A Great Place to Work. The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. '727943