Senior scientist jobs in Norwalk, CT - 330 jobs

Job Title: Product Development Specialist Starting: 10/20/2025 Pay Comments: Minimum Pay (per hour): 55.00 Maximum Pay (per hour): 65.95 Duration: 6 months (may extend) Job Description: Responsibilities: The Product Development Scientist will: Be responsible for identifying technical solutions and delivering product formulation and scale up needs for the innovation and renovation project portfolio. Partner with Marketing to leverage and translate sensory and consumer insights into products from concept to launch. Lead overall product development initiatives from bench top formulation to scale up. Support associated industrialization trials in close collaboration with Quality. Represent the R&D team as subject matter expert for product development and product knowledge transfer to the factories. Collaborate internally and externally to build strong relationships to continuously improve technical capabilities and facilitate agile project management. Work closely with procurement team to ensure new suppliers/ingredients are qualified for use in current/future formulations. Qualifications: • Bachelor's degree required in Food Science, food engineering or related field • Minimum 7-10 years of relevant work experience in product development, process scale up, quality, or manufacturing in CPG setting (Beverage development highly preferred) • Strong project management experience with the ability to manage multiple projects concurrently and in matrix environments • Demonstrated competency in managing complexity and ambiguity • Communicates in a timely, concise, and effective manner, both written and verbally. • Strong interpersonal and leadership skills. Ability to effectively interface at all levels, with strong ability to influence with integrity, especially across functions. • Ability to facilitate meetings, conference calls and present effectively to groups at all levels • Strong computer skills, including the use of Microsoft Word, Excel, Project, and PowerPoint as well as SAP • Understanding of financials (COGs, basic P&L understanding) • Six Sigma Certification, GSTD/DMAIC, FI experience a plus. • Ability to travel, approximately 15% throughout the year. Key responsibilities for this position include, but are not limited to: • Lead consumer-focused new product/formula development projects for all domestic brands (Pure Life, Saratoga, Mountain Valley, Splash Refreshers Still & Sparkling, Poland Springs, Deer Park, Zephyrhills, Ozarka, Ice Mountain, Sparklettes, and Arrowhead). • Set and manage product development project plans and facilitate execution to ensure projects are completed on time and within budget • Hands on benchtop beverage development, scale up and industrialization • Collaborate cross-functionally with Marketing, Quality, Engineering, Purchasing, Regulatory and Legal while leveraging external resources from ingredient suppliers, co-manufacturers and other 3rd party resources to deliver project results and innovative new product formulations. • Lead the qualification of 3rd party flavor houses, develop RFP/Briefs for new flavor/ingredient opportunities. • Lead ingredient, product recipe and specification development deliverables through industrialization phase • Manage technical direction of projects; identify /communicate key deliverables and next steps. • Manage complex business relationships with ingredient, process technology partner companies, contract developers and manufacturers, consultants, vendors, cross-functional departments, and outside experts in support of achieving consumer needs and effective project execution. • Effectively prioritize and manage multiple projects concurrently varying in length. • Utilize the Primo Brands stage gate innovation framework to ensure full compliance with the Quality Management System and adhere to all relevant Primo Brands Technical Instructions for new product development initiatives. • Support on-going operations with recipe/ingredient specification changes and the qualification of new ingredients. The target hiring compensation range for this role is $55.00 to $65.95 an hour. Compensation is based on several factors including, but not limited to education, relevant work experience, relevant certifications, and location.

We're seeking a hands-on Scientist I / Formulation Technician to support a preclinical formulation team preparing dosing formulations for nonclinical studies. This is an execution-focused lab role ideal for someone who enjoys wet-lab work, structured processes, and working in a regulated environment. What You'll Do Prepare oral and parenteral dosing formulations for preclinical and toxicology studies Execute formulation prep for in-house studies and support early-stage programs Maintain batch records, formulation documentation, and study records Handle pharmaceutical materials, excipients, and test compounds per SOPs Support test item logistics, including inventory management and domestic/international shipments to CROs Coordinate with internal teams and external partners to meet study timelines Assist with GLP documentation, archiving, and lab compliance Support routine lab organization, inspections, and EHS compliance What We're Looking For Hands-on lab experience with formulation, chemistry, or pharmaceutical materials Comfortable working in a wet-lab environment Strong organization, documentation, and time-management skills Proficiency with MS Office (Excel, Word, PowerPoint, Teams) Team-oriented, proactive, and detail-focused Nice to Have Experience in a GLP or regulated lab environment (trainable) Exposure to preclinical or early-stage formulation Experience with LIMS systems (e.g., Pristima or similar) Prior CRO coordination or shipment logistics experience Education Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biology, or related field (Master's a plus)

Job Title: Biological/Chemical Scientist Pay rate: $44/hr.W2 Duration: 6 Months With possible Extension Shift timings: 9AM -5 PM Ensures analyses of materials and ingredients.* Ensures performing of prescribed chemical or biological procedures, in production environment.* Ensures adherence to established internal rules and guidelines, and to EHS standards. * Ensures taking protocols and storing in appropriate files. * Contributes to implement new testing, mixing procedures. Impacts: Needs professional technological, economical or scientific know how, methods, tools and principles, and applies to differing and variable situations. Needs to solve assigned, non-routine tasks, to contribute to projects or assignments, or to support development of guidelines, methods, tools or business processes. Key Responsibilities: "Experienced Professional" These positions are expected to contribute to and deliver business processes or detailed technology solutions, in a self-managed and target-oriented manner, and thus contributes to team results. Positions focusing on analysing, developing, testing or implementing processes, technologies and systems in their specific field of expertise, from first principles. Targets are short to medium term (best to be characterized as milestones), and achievements are monitored. They may provide functional advice to and integrate services of operational staff or semi-professional colleagues. Typically, these functions review to 2 to 5 years of relevant experience in their field of work and qualification. Experience: 2+ years or Master Entry. Knowledge: Good knowledge in a technical field or business method including the basic theoretical background. Recommended experience in pipetting, data analysis, and instrument/lab maintenance. Develops basic business understanding. Contributes to team effort, awareness of expected value add. May improve processes, business methods or technical components

Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions. Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you'll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better . We are seeking a Laboratory/Analytical Scientist for our First Quality Home Care Products, LLC facility located in Trumbull, CT. This role involves planning and practically performing laboratory assignments: testing formulations' physical characteristics, quantitative analysis of the key ingredients using written procedures, protocols or internal methods. Also, this role involves testing the Home Care formulations' stability and participating in their performance testing. The Laboratory/Analytical Scientist functions as part of an integrated cross functional R&D team. Laboratory/Analytical Scientist will successfully organize daily activities which are effective, efficient, and aligned to tasks priority. A self-driven professional, this position will help in searching and applying new and innovative testing methods, and/or sample preparations. He/she will actively help to drive R&D team performance, to stay engaged and committed. Primary responsibilities include: Manages the 3-rd party testing on competitive Home Care products: National Brand (NB) and National Brand Equivalent (NBE), including samples preparation Manages competitive Home Care products inventory and database Follows Stability Protocol requirements - pulls out samples at the designated time intervals and prepares them for physical characteristics testing Performs stability and analytical testing of lab batches, pilot batches, production batches and raw materials (if required) using traditional wet chemistry techniques and analytical instruments such as FTIR, HPLC/UV-Vis-ELSD, GC, HS-GC/MS, KF with Thermoven, Auto Titrator and other small instruments. Collects, calculates or evaluates raw data and reports results according to standard operating procedures (SOPs) or methods in the laboratory books and electronic e-files Ensures accurate data/results are generated during laboratory testing by performing laboratory equipment/instruments calibrations and/or settings according to the SOP Prepares all standard and/or solutions required for testing Participates in development of analytical and instrumental testing methods, methods transfer and methods validation Maintains inventory of all consumables required for the instrumental and analytical testing Maintains storage of standards and standard solutions in accordance with the internal protocols and safety guidelines Maintains storage of raw materials, lab batches and finished products, including stability samples, in accordance with internal protocols and safety guidelines Maintains inventory and storage of competitive products Follow all Standard Operating Procedures and Policies and participate in all training sessions including self-development, safety, Good Manufacturing Practices, Workplace Hazardous Materials Information System Helps perform cleaning performance testing of competitive National Brand and National Brand Equivalent products/formulations Initiates investigations for all out of specification results and reports findings Ensures the laboratory is kept in a clean, orderly, and safe manner and reports any deficiencies Performs Enzyme activity testing The ideal candidate should possess the following: Education - Bachelor's degree in Chemistry preferred Experience - 2+ years of relevant laboratory and industry experience Knowledge of testing methods and procedures used in the Microbiology Laboratory Strong communication skills, flexibility and adaptability to changing tasks' priorities, attention to details, understanding the importance of meeting communicated timelines Estimated annual base salary range for this position is $75,000- $85,000 Base pay is only part of our total compensation package, which also includes an attractive annual discretionary bonus and robust suite of employee benefits for which you are eligible to participate in starting on your first day of employment. Base pay offered will be determined on an individualized basis and we will consider your location, experience, and other job-related factors What We Offer You We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive: Competitive base salary and bonus opportunities Paid time off (three-week minimum) Medical, dental and vision starting day one 401(k) with employer match Paid parental leave Child and family care assistance (dependent care FSA with employer match up to $2500) Bundle of joy benefit (year's worth of free diapers to all team members with a new baby) Tuition assistance Wellness program with savings of up to $4,000 per year on insurance premiums ...and more! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

We are seeking a dedicated scientist to perform in vivo studies using mouse models of autoimmunity. You will be responsible for processing organs for immune cell isolation and analysis, maintaining, expanding, and/or modulating cells, and evaluating them using in vitro assays. Your role will include the analysis of data utilizing biological and statistical software such as FlowJo, Excel, and Prism. The position requires close collaborative interactions with various teams across the organization, along with meticulous documentation of experimental procedures and results. Responsibilities * Conduct in vivo studies with mouse models focusing on autoimmunity. * Process organs for immune cell isolation and analysis. * Maintain, expand, or modulate cells and evaluate using in vitro assays. * Analyze data using biological and statistical software like FlowJo, Excel, and Prism. * Collaborate closely with teams across the organization. * Document experimental procedures and results accurately. Essential Skills * Proficiency in in vivo assays, dosing, and injections. * Experience with in vitro techniques and flow cytometry. * Familiarity with biological and statistical software such as FlowJo, Excel, and Prism. Additional Skills & Qualifications * BS/MS degree with 5+ years of industry experience. * Training in the proper handling and care of mice, including blood and tissue sample collection, is strongly preferred. * Experience with tissue culture, cell-based assays, and flow cytometry is desirable. Work Environment Join a highly collaborative team focused on autoimmunity, immune cell biology, and tissue immunity within the Immunology & Inflammation Group. Engage in cutting-edge immunological research contributing to human health. Work in a vivarium and laboratory environment, onsite 5 days per week from 8am to 5pm. Enjoy a dynamic and supportive work culture with state-of-the-art facilities including a gym, cafeteria, and plans for a fully staffed daycare in five years. Benefit from opportunities for growth and comprehensive employee packages including stock options, bonuses, and 401k match. Contract employees receive accrued sick and vacation time, along with observed holidays. Job Type & Location This is a Contract position based out of Tarrytown, NY. Pay and Benefits The pay range for this position is $45.00 - $60.00/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 Tarrytown,NY. Application Deadline This position is anticipated to close on Jan 21, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Oncology Biotherapeutics is seeking an experienced scientist to support Flow Cytometry operations. Candidates should have a B.S./M.S. degree with 1-3 years hands-on experience working with flow cytometers. Job responsibilities include: 1. Develop standard protocols and supervise operation of cytometers. 2. Oversee daily operations of the cytometers, accessory instruments and calendars for cytometers and sorter. 3. Streamline sample submission, processing, data generation and analysis. 4. Run individual experiments on cytometers and sorter. Prepare and stain cells. Dissociate and prepare tumor tissues for flow analysis. 5. Supervise users who run their own studies. 6. Monitor and order supplies for cytometry use. 7. Oversee equipment maintenance and act as primary liaison with manufacturers/vendors. 8. Provide technical training on flow cytometry techniques and applications for users. Interact with researchers to identify cytometry support of their proposed projects and on project design. 9. Evaluates, optimizes and implements existing and emerging flow cytometry protocols, technologies and applications with colleagues. 10. Key point of contact for cytometry equipment Qualifications Candidates should have a B.S./M.S. degree with 1-3 years hands-on experience working with flow cytometers. Additional Information Akriti Gupta Associate Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Primary Responsibilities: 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. Experience in FACSCanto Flow Cytometer and FACSDiva software. 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/Client 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: Minimum of either 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 All your information will be kept confidential according to EEO guidelines.

The qualified candidate will join the Analytical R&D organization and will contribute to the development of biological therapeutics. Within Analytical R&D, the candidate will provide the analytical testing support for the Conjugation Process group. The qualified candidate will be responsible for general laboratory support. A knowledge and awareness of mechanism of action and the impact of structure on function for bio therapeutic products is desirable. Some experience in colorimetric assays and protein analytical and applying a broad range of analytical techniques (HPLC, CE, Spectroscopy, etc.) is required. A good understanding of chemistry/biochemistry and macromolecule analytics is required. Good communication and writing skills is required. Responsible for general laboratory and operational support. Including providing logistical support for samples and compounds management, ordering supplies and carrying out general bench work activities. Qualifications Only BS degree in Chemistry or Biochemistry Additional Information

Background & Purpose of the Job This position is on the North America Skin Cleansing BU team based in Trumbull. Driving market success of our key power brands daily is critical to overall business growth. This role will be responsible for the formulation of Horizon 1 Dove products, local jewel brands, as well as supporting ongoing factory issues for North America. The candidate will be responsible for activities related to the implementation of new product launches, including working with internal R&D teams, Marketing, CTI/Claims, Procurement, Supply Chain, external suppliers, and BG team counterparts. The candidate needs to be able to work in a safe, disciplined manner in a laboratory environment. The individual will take a hands-on approach to formula design and scale up activities. The position requires strong communication and team skills. This is an excellent opportunity to work in a very visible team, powering Skin Cleansing's top brands! Who You Are & What You'll Do This position will require you to: Workstream Leader of technical elements of Local Jewel brands, Dove Horizon 1 Cleansing bodywash, bar and format launches: Including formulation, stability, safety and performance testing, processing, specifications, regulatory, etc. Implement Horizon 1 Design Principles against technical briefs and be responsible for ensuring specifications of formulation, process, pack and quality assurance are correct and delivered against project timings. Develop and drive productive working relationships with a range of partners, including S&T, Packaging, Consumer Technical Insight & Claims, Specifications, Safety, Brand counterparts, Supply Chain, 3P manufacturers, RM Suppliers etc. You're a dot connector: Building strong relationships with all cross-functional teams is key to success in this role. Finding new and innovative ways of reaching the end goal with less resource, money and time requires all team members to function in unison and agree to take calculated risks. You love to win, and have fun doing it: A passion for success is a must. Detail orientated and able to manage multiple tasks. You're a storyteller: Have the ability to convey technical ideas/concepts to non-technical people in a simple and easy to understand way. You're a changemaker: You will bring new ideas and solutions to the table to deliver exciting innovations to the marketplace What You'll Need To Succeed B.S. in Chemistry, Chemical Engineering, or related science 1-3+ years of experience in Personal Care preferred Working knowledge of ingredients, formulation, process and product design principles Proficient in Microsoft office suite (Excel, Word, Power point) Excellent communication and presentation skills Working knowledge of root cause analysis, problem solving techniques and application to existing and new products Project and time management skills to coordinate multiple work streams and timelines for innovation projects. Ability to develop and maintain good working relationships What We Can Offer You Culture for Growth | Top Notch Employee Health & Well Being Benefits | Every Voice Matters | Global Reach | Life at Unilever | Careers with Purpose | World Class Career Development Programs | Check Out Our Space | Focus On Sustainability Pay: The pay range for this position is $69,360 to $104,040. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible. Benefits: Unilever employees are eligible to participate in our benefits plan. Should the employee choose to participate, they can choose from a range of benefits to include, but is not limited to, health insurance (including prescription drug, dental, and vision coverage), retirement savings benefits, life insurance and disability benefits, parental leave, sick leave, paid vacation and holidays, as well as access to numerous voluntary benefits. Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. ------------------------------------ At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee. Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities. For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.

Biophysical Assoc Scientist needs 2+ years experience Biophysical Assoc Scientist requires: College degree in science related field or equivalent laboratory experience. Proficient MS Excel, Word, PowerPoint and File Explorer Ability to learn and develop comfort with various instrumentation software. Careful adherence to established procedures and proposed experimental design. Detail oriented and manual dexterity when working with instruments and samples. Demonstrating integrity in performing tasks to produce repeatable data. Excellent organizational and communication skills. Biophysical Assoc Scientist duties: Collects samples and prepares hair swatches to perform methods adhering to a set procedure. Performs technical procedures to measure product performance on hair with variety of lab equipment. Analyzes data, performs statistical calculations, and draws conclusions to substantiate claims.

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

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

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

Job DescriptionR&D Sensory Scientist / Sensory Analyst Industry: Consumer Products Manufacturing Function: Research & Development - Sensory Science Employment Type: Full-Time Compensation: $90,000 - $100,000 base + full benefits Travel: Occasional Relocation: Possible for ideal candidate About the Opportunity: We are seeking a Sensory Scientist / Sensory Analyst to support a core R&D function within a global consumer products organization. This role is responsible for designing, executing, and interpreting robust sensory testing programs that substantiate consumer-relevant product claims and inform formulation and product development decisions. This position sits at the intersection of science, consumer insight, and innovation, partnering closely with R&D and Marketing teams to deliver high-quality sensory data that supports product performance, differentiation, and commercialization. What You'll Do: Design, execute, analyze, and report sensory testing to support consumer-relevant product claims Collaborate with R&D and Marketing partners to define project objectives and appropriate sensory methodologies Administer sensory panel activities, including test material preparation, assessor recruitment, panel execution, and data collation Ensure timely delivery of accurate, well-documented sensory results aligned with project timelines Investigate and apply advanced sensory methods and statistical approaches to uncover insights and trends Interpret sensory, consumer, and technical data to support product recommendations and claims substantiation Participate in cross-functional project meetings to align sensory strategy with business needs Maintain strong organization, documentation, and communication throughout the testing lifecycle What We're Looking For: Required Qualifications Bachelor's degree in Psychology, Food Science, Nutrition, Sensory Science, Chemistry, Market Research, or a related scientific discipline Coursework or training in sensory science, statistics, market research, or business Approximately 5 years of relevant professional experience, ideally with a focus on sensory testing Strong analytical, organizational, and communication skills Ability to partner effectively with cross-functional and external stakeholders Ability to read and interpret technical, sensory, and consumer research data Preferred Qualifications Sensory science certification or formal training (e.g., university-based sensory or market research programs) Experience supporting consumer product claims substantiation Background in consumer goods, food, home care, personal care, or related industries Comfort working in fast-paced, collaborative R&D environments What Success Looks Like: Sensory studies are executed accurately, efficiently, and on schedule Data and insights are clearly communicated and actionable Cross-functional partners trust and rely on sensory results for decision-making Product claims are supported by defensible, consumer-relevant evidence Sensory methodologies evolve to support innovation and continuous improvement Why This Role: High-impact R&D role supporting well-known consumer products (client confidential) Opportunity to influence product development and claims strategy Exposure to advanced sensory methodologies and cross-functional collaboration Strong compensation, benefits, and long-term growth potential If you are a detail-oriented sensory professional who enjoys blending science, data, and consumer insight to shape products people use every day, we encourage you to apply. Equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected characteristics.

About the Company: Acutis Diagnostics is a leading clinical laboratory committed to advancing precision medicine through accurate, timely, and innovative diagnostic testing. Specializing in toxicology, molecular diagnostics, and infectious disease testing, we empower healthcare providers with the data they need to make informed decisions. Our team is driven by a shared mission to improve patient outcomes and support the evolving needs of healthcare through science, service excellence, and cutting-edge technology. About the Role: The Research & Development Scientist - Toxicology Diagnostics will play a critical role in advancing Acutis' testing capabilities by refining existing toxicology assays for improved quality, sensitivity, and cost efficiency, while also developing new assays that meet emerging clinical and forensic needs. This role requires deep scientific knowledge, hands-on laboratory expertise, and the ability to translate research findings into validated, scalable diagnostic assays. Job Reponsibilities: Assay Optimization & Refinement Evaluate and optimize existing LC-MS/MS, immunoassay, and chromatographic assays used in toxicology diagnostics Enhance assay performance with respect to accuracy, precision, sensitivity, specificity, turnaround time, and cost Implement improvements that support operational efficiency and compliance with regulatory standards New Assay Development Design and develop new toxicology assays aligned with clinical demands, testing menus, and emerging drug trends Conduct feasibility studies, method development, method validation, and technology transfer to clinical operations Partner with cross-functional teams to support product launches and new diagnostic offerings Scientific & Technical Leadership Monitor advances in toxicology testing, emerging analytes of concern, and new diagnostic technologies Maintain deep technical expertise in mass spectrometry, molecular toxicology, and sample preparation techniques Provide troubleshooting support for complex assay-related challenges Regulatory & Quality Compliance Generate and maintain method SOPs, validation reports, and technical documentation Ensure all assay development and validation activities align with NYS DOH, CLIA, CAP, and other applicable standards Support internal audits, inspections, and ongoing quality initiatives Collaboration & Communication Partner with lab operations, QA/QC, and commercial teams to ensure successful implementation of assays Present scientific data and proposals to leadership and internal stakeholders Train laboratory staff on newly developed methods and workflows Salary Range: $65,000 - $75,000/year

Pfizer is a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Job Description Job Link: ********************************************************* APPLY HERE! ROLE DESCRIPTION This is a position within the Bacterial Vaccine Research and Technology group in Vaccines Research at Pfizer. The incumbent will be expected to apply bioinformatics methods to biological questions that occur during the vaccine discovery and development process. This will include, but not limited to, detailed analysis of whole genome sequence and transcript profiling from bacterial and viral pathogens, both laboratory and clinical invasive disease isolates. The individual needs to have a good publishing record, with a demonstrated ability to author well written and review external scientific publications and internal technical documents. The incumbent will be expected to prepare and present clear and concise oral presentations to both internal and external audiences. RESPONSIBILITIES • Analysis of whole genome sequence and transcript profiling data in support of all vaccine programs; includes isolates from both surveillance studies and clinical trials • Analyze/mine epidemiological and phylogenetic data - interpret/summarize comparative analysis of internal data with information accessed from external databases • Present data at internal and external meetings • Assist with document preparation for regulatory, patent and scientific presentations and submissions. Prepare written summary reports and presentations as required. Author manuscripts in peer-reviewed scientific journals. • Ongoing evaluation of commercial and web-based database tools designed to archive, search and analyze sequence diversity data; develop and implement alternatives to increase efficiencies • Develop best practices through interactions with colleagues in the Pfizer bioinformatics community • Maintain laboratory notebook in a detailed and descriptive manner • Satisfactorily complete all training in conformance with departmental requirements • Where applicable, perform job responsibilities in compliance with cGMP/GLP and all other regulatory agency requirements • Regular and efficient collaboration with colleagues in a matrixed environment is expected. In some instances, incumbent will also be asked to provide bioinformatic support for vaccine projects outside of the immediate group, both in Pearl River and at other Pfizer research sites. The individual is expected to be an effective team member and regularly communicate his/her commitments and project status to line management. Qualifications Advanced scientific degree (PhD) with minimum of 1 year of relevant post-graduate experience and demonstrated bioinformatics skill sets, preferably applied to infectious disease problems. Alternatively an individual trained in bioinformatics with a BS or MS plus 5 years of experience in a field of science relevant to the position (e.g., Microbiology, Immunology, Infectious Disease). Ability to create/develop programming code a plus. Additional Information All your information will be kept confidential according to EEO guidelines.

A global leader in food and beverage is interviewing for a contract Research and Development Scientist position in Valhalla, NY. The incumbent will conduct and support ingredient application programs. Qualifications: BS/MS Food Science & Technology / Food Chemistry or related field • 3-5 years of experience in the Food Industry or related area • Understanding of food chemistry, carbohydrates, product formulation and development, ingredient technology, and food safety • Functional knowledge of analytical test methodologies and data interpretation • Ability to make significant technical, and scientific advances utilizing internal and/or external resources. • Detail-oriented individual with proven ability to independently lead multiple projects and work streams simultaneously, leveraging project management tools. • Self-starter with good oral and written communication and presentation skills, the ability to work with various personalities and work styles, • Ability to travel when needed

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX work at Pfizer. Scope of work • The contingent worker will be responsible for mouse cancer model development. • This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts. • This work requires sterile technique and attention to detail • Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods). • The worker will also be required to participate in all of the preparation steps necessary for animal studies: surgical tool preparation, tool sterilization, and animal shaving and preparation. Qualifications Required skills / background • The worker should have a minimum 1-3 years' experience working with mice, preferably immune deficient mice. • The workers should also have experience in small animal surgery and sterile techniques. • The workers should preferably have knowledge of cancer research experimental designs and methods. Experience with dosing mice would be useful but is not a strict requirement. Additional Skills: • What are the most critical skills needed? Mouse handling (preferable immune deficient), mouse surgery, sterile technique, tissue culture, and database maintenance • What level candidate are you seeking? (i.e. 1-3yrs = Base/Entry; 4-7yrs = Intermediate; 7+ = Advanced) • Entry or intermediate dependent upon experience and skill sets Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-573-4748 ASAP! I look forward to hearing from you!