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Principal research scientist jobs in Norwalk, CT

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  • AD, Principal / Sr AD, Sr Principal Clinical Data Scientist

    Boehringer Ingelheim 4.6company rating

    Principal research scientist job in Ridgefield, CT

    As a Principal / Sr Principal Clinical Data Scientist, you would support the clinical drug research and development process by providing strategic planning and execution, including data transformation and all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data related to clinical projects like actual trial data, registries and real-world data bases. In particular this includes the provision of analytics tools, outputs and inference as necessary for the specific use case. May act as a BDS product owner up to Therapeutic Area/asset level. Represent BDS at a substance/asset level regarding data science related aspects. 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** **AD Responsibilities:** - Lead and oversee designing, transforming, analyzing and reporting complex phase I-IV clinical trials or projects with established BI experience and supporting complex international R&D projects. - Lead and oversee for designing, transforming, analyzing and reporting of other data from research and development like registries and real-world data bases with respect to a specific use case or project/asset. - Keep abreast of data science within and outside BI. Turn derived insights into new data science approaches relevant for clinical development, registration, and marketing of drugs. - Present compelling validated stories regarding complex data science aspects to BDS colleagues and other professionals within and outside of BI. - Ensure data transformation and analysis specifications to ensure completeness, correctness and adherence to department guidelines and SOPs as well as to applicable GxP requirements. - Guide and/or lead other colleagues, internal and external customer and external providers on data science related tasks. - Participate in cross-functional BI internal working-groups or lead cross-functional human pharma internal working-groups and drive/plan relevant data science aspects. Participate in external working groups. - If applicable, supports the clinical drug development process as a BDS Product Owner up to the level of substance/assets. - Ensures cross-functional and team-based working within BDS and with other units at BI. Fulfils tasks of other functions as needed and possible. Contributes to cross-functional- and team-based thinking. - Support fostering innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models. **Sr AD Responsibilities:** - Subject Matter Expert (SME) / Process Lead for designing as well as transforming, analyzing and reporting complex phase I-IV clinical trials that represent new challenges and for which project and therapeutic knowledge is not given, such as mega trials or new indications and for complex international R&D projects. - Identify trends in data science within and outside BI . Initiate and turn derived insights into new data science approaches relevant for clinical development, registration, and marketing of drugs. - Present compelling validated stories regarding complex data science aspects to BDS colleagues, other professionals within and outside of BI. - Ensure data transformation and analysis specifications to ensure completeness, correctness and adherence to department guidelines and SOPs as well as to applicable GxP requirements. - Lead/Guide other colleagues, internal and external customer and external providers on data science related tasks. - Lead cross-functional BI internal working-groups and drive/plan relevant data science aspects. Participate in external working groups. - If applicable, supports the clinical drug development process as a BDS Product Owner up to the level of Therapeutic Area/assets. - Facilitates and ensures cross-functional and team-based working within BDS and with the rest of the company. Fulfils tasks of other functions as needed and possible. Contributes to cross-functional- and team-based thinking. - Fosters innovative digital approaches to produce sophisticated, intelligent optimization solutions, innovative processes and predictive models. **Requirements** **AD Requirements:** + Bachelor of Science (BSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with a minimum seven (7) years of data science experience; Or + Master of Science (MSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; Or + Doctoral Degree (PhD) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with three (3) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions. + Working experience might be partially compensated by broad and deep topic-specific knowledge. + Broad knowledge and advanced experience in software languages relevant for business needs. + Broad knowledge and advanced experience in understanding of clinical trial development process required. + Advanced project lead experience required. + Understanding and applying key of principles of data science. + In-depth understanding of advanced statistical concepts related to Data Science. + Demonstrated broad knowledge in planning, transforming, analyzing, interpreting, and reporting data in complex clinical trials, in projects with established BI experience or data from other sources in clinical research and development. + Thorough knowledge of statistical methodology, design of clinical trials or clinical experiments, basic medical terminology and on processing clinical trial information. + Advanced working knowledge of broad variety of aspects of relevant software languages. + Mindful of local, global, internal and external cultures to ensure that messages are received positively and effectively. + Ability to lead and facilitate meetings. + Ability to develop and deliver training related to data science topics. + Evidence of strong teamwork, also in global and remote context. + Good interpersonal skills with the ability to interact effectively with people, internally and externally (e.g. CROs, experts, management). + Ability to pro-actively identify issues and solutions and to interact with internal and external bodies on routine data science issues. + Language skills: English: fluent (Read/Write/Speak). + Know, understand, and implement: + International regulations and guidelines for good clinical and statistical practice from all ICH regions, + The various international guidelines on clinical development, including statistical methodology, for TA-related disease areas, and + BI processes and SOPs that govern clinical development in particular with respect to strategic areas (e.g. Clinical Development Plan). **SR AD Requirements** ⦁ Bachelor of Science (BSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with a minimum of ten (10) years of data science experience; Or ⦁ Master of Science (MSc) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with ten (10) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions; Or ⦁ Doctoral Degree (PhD) from an accredited institution in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.), with six (6) years of experience within the pharmaceutical industry, CROs, regulatory authorities or academic institutions. **Compensation** This position offers a base salary typically between $140,000 and $222,000 for AD level and $170,000 and $269,000 for Sr AD level. 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.
    $170k-269k yearly 60d+ ago

  • Senior or Principal Scientist - Beverage & Flavor Applications

    Florida Food Products 4.1company rating

    Principal research scientist job in Melville, NY

    Founded in 1954, Vibrant Ingredients is committed to providing innovative clean label solutions that naturally provide exceptional food protection, flavor, color and texture for a variety of applications, including processed and cured meat, beverages, plant-based alternatives, health and wellness, culinary, and pet nutrition. Vibrant Ingredients believes in improving the food and beverages we eat and drink with ingredients from nature that work. About the role: We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, we are a true partner. We collaborate with our customers in ways that respect people and the environment. A commitment to Real. Simple. Better™ drives our innovation team to discover new, on trend solutions. As a Senior or Principal Scientist - Beverage & Flavor Applications, you will lead the development of innovative tea and beverage systems using cutting-edge flavor and botanical technologies. This is a visible, customer-facing role where you'll manage end-to-end project work-from benchtop formulation to commercialization-and collaborate cross-functionally with R&D, Sales, Marketing, and Operations to deliver impactful solutions. How will you contribute: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions. Essential job functions and duties include, but are not limited to: Lead formulation and development of beverage applications, especially tea, botanicals, functional drinks, flavored waters, syrups, and dairy alternatives. Develop and optimize extractions from botanicals, teas, and other plant-based materials to deliver targeted flavor, functionality, and performance. Design and run benchtop and pilot-scale trials using technologies such as MicroThermics and other beverage processing systems. Translate customer briefs into innovative, scalable beverage and flavor systems. Conduct sensory and analytical evaluations to ensure quality, taste, and consistency. Act as a technical expert during customer presentations, demo sessions, and plant trials. Work closely with internal stakeholders to ensure seamless handoff to commercialization and production. Stay informed on market trends, customer strategies, competitive landscapes, and new ingredient technologies. Support ongoing improvement of lab processes, documentation, and sample inventory systems. Minimum Requirements/Qualifications: Bachelor's degree in Food Science, Chemistry, Chemical Engineering, or related field. (Master's/PhD preferred for Principal Scientist level) 10+ years of beverage formulation and product development experience; at least 5 years with tea and botanical applications. Deep expertise in functional beverages and flavor system development. Experience with pilot-scale processing, sensory analysis, and customer interaction. Demonstrated ability to manage complex projects and deliver timely results. Work Environment: May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame. What Florida Food Products can offer you: Generous time off for vacations Paid Holidays 401(k) with company match Tuition reimbursement Medical/Dental/Vision Health & Wellness programs More about us: Vibrant Ingredients, headquartered in Lake Mary, FL, is one of the world's leading independent providers of natural ingredients. With a legacy spanning over 70 years, we deliver a diverse portfolio of clean label ingredients and innovative system solutions to the food and beverage industry. Our commitment to quality and performance is reflected in our American-made products, which enhance both taste and functionality. Backed by advanced manufacturing capabilities, we specialize in fermentation, patented cold brew extraction, custom flavor development, and a range of drying and blending technologies. Operating from four state-of-the-art facilities strategically located across the U.S., we ensure the accessibility of real, high-quality ingredients-helping our customers create better-for-you food and beverage for consumers. "Improving the food and beverages consumed by providing real ingredients from nature that work." This position is currently classified as on-site for our Indianapolis Facility. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Holidays, Vacation, Tuition Reimbursement Program. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. The Company reserves the right to modify, update, change and/or make corrections to this job description, at the sole discretion of senior management, at any time during the employee's employment term, at the sole discretion of management. EEO Statement Vibrant Ingredients is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Vibrant Ingredients will work with applicants to meet accommodation needs that are made known to Vibrant Ingredients in advance. **Please no external recruiters**
    $99k-127k yearly est. Auto-Apply 60d+ ago

  • Senior or Principal Scientist - Beverage & Flavor Applications

    Vibrant Ingredients

    Principal research scientist job in Melville, NY

    Founded in 1954, Vibrant Ingredients is committed to providing innovative clean label solutions that naturally provide exceptional food protection, flavor, color and texture for a variety of applications, including processed and cured meat, beverages, plant-based alternatives, health and wellness, culinary, and pet nutrition. Vibrant Ingredients believes in improving the food and beverages we eat and drink with ingredients from nature that work. About the role: We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, we are a true partner. We collaborate with our customers in ways that respect people and the environment. A commitment to Real. Simple. Better™ drives our innovation team to discover new, on trend solutions. As a Senior or Principal Scientist - Beverage & Flavor Applications, you will lead the development of innovative tea and beverage systems using cutting-edge flavor and botanical technologies. This is a visible, customer-facing role where you'll manage end-to-end project work-from benchtop formulation to commercialization-and collaborate cross-functionally with R&D, Sales, Marketing, and Operations to deliver impactful solutions. How will you contribute: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions. Essential job functions and duties include, but are not limited to: Lead formulation and development of beverage applications, especially tea, botanicals, functional drinks, flavored waters, syrups, and dairy alternatives. Develop and optimize extractions from botanicals, teas, and other plant-based materials to deliver targeted flavor, functionality, and performance. Design and run benchtop and pilot-scale trials using technologies such as MicroThermics and other beverage processing systems. Translate customer briefs into innovative, scalable beverage and flavor systems. Conduct sensory and analytical evaluations to ensure quality, taste, and consistency. Act as a technical expert during customer presentations, demo sessions, and plant trials. Work closely with internal stakeholders to ensure seamless handoff to commercialization and production. Stay informed on market trends, customer strategies, competitive landscapes, and new ingredient technologies. Support ongoing improvement of lab processes, documentation, and sample inventory systems. Minimum Requirements/Qualifications: Bachelor's degree in Food Science, Chemistry, Chemical Engineering, or related field. (Master's/PhD preferred for Principal Scientist level) 10+ years of beverage formulation and product development experience; at least 5 years with tea and botanical applications. Deep expertise in functional beverages and flavor system development. Experience with pilot-scale processing, sensory analysis, and customer interaction. Demonstrated ability to manage complex projects and deliver timely results. Work Environment: May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame. What Florida Food Products can offer you: Generous time off for vacations Paid Holidays 401(k) with company match Tuition reimbursement Medical/Dental/Vision Health & Wellness programs More about us: Vibrant Ingredients, headquartered in Lake Mary, FL, is one of the world's leading independent providers of natural ingredients. With a legacy spanning over 70 years, we deliver a diverse portfolio of clean label ingredients and innovative system solutions to the food and beverage industry. Our commitment to quality and performance is reflected in our American-made products, which enhance both taste and functionality. Backed by advanced manufacturing capabilities, we specialize in fermentation, patented cold brew extraction, custom flavor development, and a range of drying and blending technologies. Operating from four state-of-the-art facilities strategically located across the U.S., we ensure the accessibility of real, high-quality ingredients-helping our customers create better-for-you food and beverage for consumers. "Improving the food and beverages consumed by providing real ingredients from nature that work." This position is currently classified as on-site for our Indianapolis Facility. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Holidays, Vacation, Tuition Reimbursement Program. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. The Company reserves the right to modify, update, change and/or make corrections to this job description, at the sole discretion of senior management, at any time during the employee's employment term, at the sole discretion of management. EEO Statement Vibrant Ingredients is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Vibrant Ingredients will work with applicants to meet accommodation needs that are made known to Vibrant Ingredients in advance. **Please no external recruiters**
    $86k-123k yearly est. 16d ago

  • Principal Scientist, Translational Neuroscience

    Bexorg

    Principal research scientist job in New Haven, CT

    About Us Bexorg is a cutting-edge biotech startup focused on CNS drug discovery, leveraging its proprietary BrainEx platform to conduct preclinical studies on molecularly active, postmortem human brains. We combine advanced wet-lab experiments with AI/ML-driven drug discovery to revolutionize the understanding and treatment of brain disorders. We are seeking a Principal Scientist with deep expertise in translational biomarkers for neurological diseases, to contribute to our groundbreaking R&D efforts. The Role We are looking for a highly motivated and experienced Principal Scientist to lead efforts to identify and characterize translational biomarkers for our drug discovery programs. The ideal candidate will have extensive knowledge of preclinical and clinical biomarkers for Alzheimer's, Parkinson's or other neurodegenerative diseases. This is a full-time, on-site position requiring physical presence in our state-of-the-art facilities to conduct hands-on research and collaborate directly with cross-functional teams.We are looking for a highly motivated and experienced Principal Scientist to lead efforts to identify and characterize translational biomarkers for our drug discovery programs. The ideal candidate will have extensive knowledge of preclinical and clinical biomarkers for Alzheimer's, Parkinson's or other neurodegenerative disease biology. This is a full-time, on-site position requiring physical presence in our state-of-the-art facilities to conduct hands-on research and collaborate directly with cross-functional teams. Essential Duties/Tasks Lead translational biomarker efforts from target discovery through clinical development, ensuring each program has a fit-for-purpose biomarker plan that supports mechanism of action, patient selection, and pharmacodynamic readouts. Design and oversee biomarker assay development. Select, validate, and troubleshoot biofluid biomarker assays. Translate omics and pathways findings from preclinical studies into clinically actionable endpoints. Build quantitative PK/PD and exposure-response models linking biomarker changes to efficacy. Collaborate with cross-functional teams, including medicinal chemistry, pharmacology, and computational biology, to advance drug discovery projects. Coach scientists and research associates in assay development, study design, and data interpretation. Mentor junior scientists and provide technical guidance and leadership across the research team. Foster an inclusive, innovation-oriented culture. Manage external collaborations with academic institutions, CROs, and industry partners. Stay abreast of the latest scientific advancements and contribute to the company's overall strategy for neurodegenerative disease research. Present findings and progress to senior leadership, partners, and at scientific conferences. Preferred Education and Experience PhD in Neuroscience, Biology, Biochemistry, Pharmacology, or a related field with 5+ years of post-doctoral and/or industry experience. Deep expertise in translational biomarkers for neurodegenerative diseases such as Alzheimer's, Parkinson's, ALS, etc., with a strong track record of peer-reviewed publications. Hands-on experience with translational biomarkers for neurological disease. Proficiency with high-sensitivity biofluid platforms (Simoa, MSD, LC-MS/MS, SomaScan, O-link). Familiarity with spatial/transcriptomic, single-cell omics, proteomics, and metabolomics techniques. Experience building PK/PD and exposure-response models. Proven ability to lead projects and mentor scientific teams. Strong problem-solving and critical thinking skills, with the ability to design innovative experiments and troubleshoot complex issues. Excellent written and verbal communication skills, with experience presenting data to internal and external audiences. Experience managing collaborations with external research partners and CROs. Preferred Skills, Qualifications, or Technical Proficiencies Track record interacting with FDA/EMA on biomarker qualification or companion diagnostic paths. What We Offer Opportunity to work at the forefront of neuroscience and drug discovery. Collaborative work environment with a multidisciplinary team. Competitive compensation package including stock options. Career growth opportunities in a rapidly scaling company. Bexorg is an equal opportunity employer. We strive to create a supportive and inclusive workplace where contributions are valued and celebrated, and our employees thrive by being themselves and are inspired to do their best work. We seek applicants of all backgrounds and identities, across race, color, ethnicity, national origin or ancestry, citizenship, religion, sex, sexual orientation, gender identity or expression, veteran status, marital status, pregnancy or parental status, or disability. Applicants will not be discriminated against based on these or other protected categories or social identities. Bexorg will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. Please be advised that Bexorg operates a Biosafety Level 2 (BSL-2) laboratory. All laboratory personnel must adhere to strict safety protocols involving the handling, storage, and disposal of potentially hazardous biological agents. Regular participation in safety training and compliance with institutional safety policies are mandatory to ensure a safe work environment and to mitigate risks.
    $102k-145k yearly est. 60d+ ago

  • R&D - Senior Researcher S&A

    Duracell 4.8company rating

    Principal research scientist job in Bethel, CT

    The primary functions of this role are to: 1) execute established Raw Material, In Process Materials, Finished Product, and Failure Analysis methods to enable R&D initiatives and resolve technical challenges. 2) recommend and contribute to the optimization/modification of existing methods and establishment of new ones to meet evolving R&D needs and 3) over time develop understanding of chemistries, materials and process transformations to create greater value and/or eliminate wasted effort/cost. The individual will be expected to use a variety of Battery Life Test Systems, Safety Test Systems, environmental chambers, shock and vibration testers, meters, gauges, power supplies, and various test lab management tools. Responsibilities/Duties: * Proficient in ability to perform high quality execution of established methods to achieve desired goals or results. * Methods and measurements will include but not limited to: * Battery internal gas measurements using a manometer or pressure transducer approach. * Leakage assessment visually and/or by using automated extraction method. * Pre and post-test battery electrical measurements. * ANSI and IEC standards for primary chemistry cells * Proficient in performing against multiple projects in parallel. * Mentor and train junior employees on established methods and new ways of thinking. * proficient in analyses (statistical, if needed) of data to uncover new findings from R&D work. * Use Lab Information Management system to execute daily scheduled tasks and enter method results. * Monitor environmental chambers and lab temperatures. * Comply with the lab's accreditation, operation, and EH&S requirements * Provide insights from "project level" R&D work. * ability to identify and improve (streamline or increase value) methods to create greater value and/or eliminate wasted effort/cost. Qualifications & Skill Requirements: * Degree in scientific discipline. Chemistry or engineering preferred. * Experience working in a lab environment and knowledge of safe lab practices. * Strong attention to detail and ability to follow procedures to maintain a safe working environment is required * Be able to lift 30 lbs. * Ability to work independently with a passion towards excellence and producing consistent quality and accurate results. Duracell is the world's leading manufacturer and marketer of high-performance alkaline batteries, complemented by a portfolio of high quality, market leading specialty, rechargeable and professional batteries. Duracell's products power numerous critical professional devices across the globe such as heart rate monitors, defibrillators, telemetry devices, smoke detectors, fire alarms, automated valves and security systems. As the leader in the professional power category, Duracell has a rich history of innovation, continuously introducing batteries that are smaller, thinner, with more energy and longer lasting than competitive brands. Since March 2016, Duracell has found its permanent home within Berkshire Hathaway (ranked #4 World's Most Admired Companies by Fortune Magazine and #3 in the Fortune 500), and will continue to focus on sustainable growth, industry-leading innovation while creating long-term value for our customers and consumers. At Duracell, integrity, end-to-end accountability across all levels, fast decision-making and a "can do" attitude is highly valued.
    $106k-131k yearly est. Auto-Apply 15d ago

  • Senior Scientist

    Integrated Resources 4.5company rating

    Principal research scientist job in Pearl River, NY

    A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty aretas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Our Client is looking for Senior Scientist-with good Protein related, UF/DF etc. experience…..!!!!! RESPONSIBILITIES: • The individual will perform complex synthesis and purification of biomolecules and derivatives as well as conduct characterization assays. • The individual is also expected to participate in team meetings, provide update and contribute to planning activities to achieve program deliverables. • Interaction with other groups/departments is expected. • Bench level experience with protein purification, synthetic organic chemistry and/or protein isolation, purification is expected. Qualifications QUALIFICATIONS AND SKILLS NEEDED: • Masters or Bachelor in Biology, Biochemistry, Immunology or other related field with laboratory research experience and specific expertise in antibody development and characterization. • Protein purification, UF/DF, chromatography. • 4-7 years of experience in Assay Studies. Additional Information Regards Pooja Mishra Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Tel: 732 429 1636 (W) 732-549-2030 x 214 | (F) 732-549-5549 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
    $94k-128k yearly est. 60d+ ago

  • Principal Scientist

    Henkel 4.7company rating

    Principal research scientist job in Darien, CT

    **_About_** **_this_** **_position_** At Henkel, you'll be part of an organization that's shaping the future through innovation, sustainability and collaboration. With our trusted brands like Persil , 'all , Loctite , Snuggle , and Schwarzkopf and our cutting-edge technologies, you'll have countless opportunities to explore new paths and grow. This position is with our Consumer Brands business unit - where we empower our employees to bring the best Laundry & Home Care and Hair products to people around the world. **Dare to learn new skills, advance in your career and make an impact at Henkel.** **What you´ll do** + Formulate innovative hair care products with minimal supervision, engaging in research to identify new technologies, application methods, and opportunities for breakthrough innovation. + Manage project timelines and cost objectives, developing estimates in collaboration with your supervisor and ensuring alignment with the new product development process. + Stay informed on industry regulations, applying foundational knowledge to current projects and proactively expanding expertise in global regulatory requirements. + Coordinate testing activities, including Test Salon, Biophysical, Microbiological, and Safety Testing, and document experimental procedures, results, and analyses. + Build strong relationships with raw material vendors and industry partners, leveraging external expertise to bring cutting-edge technologies in-house. + Translate product concepts into technical briefs, managing third-party innovation partners to ensure timely development and integration into Henkel's IT systems. + Support pilot and production batches, documenting procedures to ensure reproducibility and resolving formulation and manufacturing challenges. + Collaborate cross-functionally with teams across R&D, Marketing, Manufacturing, QA, and Salon Services. Conduct patent searches and review findings with your supervisor to inform project direction. + Maintain a well-organized lab environment, gaining proficiency with equipment used to assess product performance and physical attributes. Take ownership of assigned projects and contribute to a culture of excellence. **What makes you a good fit** + Education: Bachelor's or Master's degree in Chemistry, Biology, Engineering, or a related field + Minimum of 8+ years in the industry + Strong background in formulation lab work and quality testing procedures + Experience developing hair or skin care products is preferred + Project management experience is a plus + Technical Expertise:Solid understanding of hair care formulation science Ability to translate complex technical information into clear, non-technical language Skilled in balancing creativity with process discipline to drive innovation and execution + Professional Skills:Highly self-motivated, organized, and capable of managing multiple priorities Excellent verbal and written communication skills Strong presentation, interpersonal, and organizational abilities Proficient in relevant computer applications + Other Requirements:Willingness to travel up to 5% of the time **Some benefits of joining Henkel** + **Health Insurance:** affordable plans for medical, dental, vision and wellbeing starting on day 1 + **Work-Life Balance:** Paid time off including sick, vacation, holiday and volunteer time, flexible & hybrid work policies (depending on role), and vacation buy / sell program + **Financial:** 401k matching, employee share plan with voluntary investment and Henkel matching shares, annual performance bonus, service awards and student loan reimbursement + **Family Support:** 12-week gender neutral parental leave (up to 20 weeks for parents giving birth), fertility support, adoption & surrogacy reimbursement, discounted child and elderly care, and scholarships + **Career Growth:** diverse national and international growth opportunities, access to thousands of skills development courses, and tuition reimbursement The salary for this role is $105,000.00- $120,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future. Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral. Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories. **JOB ID:** 25087850 **Job Locations:** United States, CT, Darien, CT **Contact information for application-related questions:** ***************************** Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted. **Application Deadline:** As long as the vacancy is listed on our Career Site, we are happy to receive your application **Job-Center:** If you have an application already, you can create or log in to your accounthere (******************************************************************************************************************************************************** to check the status of your application. In case of new account creation, please use your email address that you applied with. Activate external content When clicking the button below external content will be loaded which involves transfer of personal data (e.g. IP address) to external servers. This may involve that cookies are set by the external content provider. Please see Data Protection Statement for further information. **Accept for all YouTube content** Deactivate loading external content from YouTube. How is work at Henkel
    $105k-120k yearly Easy Apply 36d ago

  • Senior Scientist

    Actalent

    Principal research scientist job in Tarrytown, NY

    In this role, you will develop antibody-based biologic drug products and assess their quality and stability. As a Senior Scientist, you will collaborate with various teams to move drug products from pre-clinical through commercial stages. Your responsibilities will include designing, executing, and documenting stability studies and other experiments to support formulation development and stability testing across various phases. Responsibilities + Design, write, execute, and document stability studies and other experiments to support formulation development and stability testing in various phases. + Characterize candidate molecules using various biophysical and biochemical analytical techniques. + Develop drug product formulations and support process development and manufacturing of clinical drug substances and drug products. + Develop fit-for-purpose analytical methods to support biophysical characterization, formulation and process development, and research stability testing. + Collect, process, and analyze data by following the organizational standard methodologies and policies. + Document experiments, results, and findings in electronic laboratory notebook. + Present work at group and department meetings; contribute to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication. + Contribute to general laboratory and equipment maintenance. Essential Skills + Protein characterization expertise + Experience with HPLC and UPLC + Background in chemistry + BS/MS with 5+ years of experience or PhD with 0+ years of experience in relevant fields Additional Skills & Qualifications + Knowledge about protein structure and function is required. + Expertise in protein chemistry/biochemistry and characterization. + Analytical and problem-solving skills are a must. + Experience with protein stability, structure, or biophysics is highly desirable. + Hands-on experience and trouble-shooting proficiency with chromatographic methods (HPLC, UPLC, column chromatography), capillary electrophoresis, and/or biophysical techniques. + Experience with statistical analysis software such as JMP is beneficial. + BS with 5+ years of exp OR MS with 3+ years of exp Work Environment This role operates within a laboratory environment, requiring onsite work five days a week. You will be part of the Formulation Development Group with a schedule from Monday to Friday, 8:00 am to 5:00 pm. The company is known for its excellent culture, recognized as a top employer, with significant growth expected over the next five years. Amenities include an onsite gym and cafeteria, with plans for a fully staffed daycare. Employees enjoy comprehensive packages including stock options, bonuses, and a 401k match, with contract employees accruing sick and vacation time alongside paid 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 Dec 13, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
    $45-60 hourly 7d ago

  • Scientist II

    Mindlance 4.6company rating

    Principal research scientist job in Ridgefield, CT

    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.
    $75k-107k yearly est. 1h ago

  • Technical Service Scientist

    Syensqo

    Principal research scientist job in Stamford, CT

    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 Technical Service Scientist to join our Polymer Additives team. This role is responsible for providing technical support to customers and internal teams, with a strong emphasis on hands-on polymer processing. The ideal candidate will have experience with polymer additives, laboratory testing, and polymer processing equipment such as extrusion, injection molding, and compression molding. We count on you for: * Prepare resin and additive formulations and produce test specimens using injection molding, compression molding, and other polymer processing techniques. * Conduct laboratory testing and analysis to support customer projects, product improvements, and new product development (NPI). * Troubleshoot and resolve technical issues related to polymer processing and additive performance. * Collaborate with customers, sales, R&D, and manufacturing teams to address technical inquiries and provide solutions. * Document experimental procedures, results, and technical reports in accordance with company standards. * Maintain and calibrate laboratory equipment to ensure accurate and reliable testing. * Support the development and optimization of new polymer additive products and applications. * Present technical findings and project updates to internal teams and customers. * Stay current with industry trends, technologies, and best practices in polymer additives and processing. 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: * Bachelor's degree in Chemistry, Chemical Engineering, Polymer Science, Materials Science, or a related field, with 3-5 years of relevant work experience. * Hands-on experience with polymer processing equipment (e.g., extrusion, injection molding, compression molding) is required. * Strong analytical and problem-solving skills. * Excellent communication and interpersonal skills. * Ability to manage multiple projects and work effectively in a team environment. * Experience with laboratory testing methods for polymers and additives is preferred. * Familiarity with polymer additive formulations and their applications preferred. * Experience in customer-facing technical service or support roles preferred. * Proficiency with laboratory instrumentation such as colorimeters, melt flow testers, and mechanical testing equipment preferred. You will get: * Competitive salary and benefits * The U.S. base salary range reasonably expected to be paid for this position is $89,000.00 to $116,000.00 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) 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
    $89k-116k yearly 35d ago

  • Bench Scientist

    Collabera 4.5company rating

    Principal research scientist job in New Haven, 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 ************ ******************************
    $75k-105k yearly est. Easy Apply 60d+ ago

  • Scientist IV

    Us Tech Solutions 4.4company rating

    Principal research scientist job in Ridgefield, CT

    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: ************
    $70k-108k yearly est. 60d+ ago

  • Scientist II; Analytical R&D

    Contract Pharmacal Corp 4.3company rating

    Principal research scientist job in Hauppauge, NY

    Job DescriptionDescription: Develop stability-indicating methods. Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. Generate method validation protocols. Execute methods validation and methods transfer. Generate method validation reports and analytical methods. Design and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. Identify and resolve problems with analytical methods and provide troubleshooting on instrumentation. Conduct Performance Qualification (PQ) on various instruments. Provide leadership, guidance and hands-on training to new employee and provide technical support to other departments. Effectively communicate information in concise reports. Other responsibilities as assigned by Senior Management. Requirements: Education and Experience: Bachelor's degree in chemistry or analytical chemistry with 4-5 years of pharmaceutical experience OR Master's degree or Ph.D. in chemistry or analytical chemistry with 3-4 years of pharmaceutical experience Instrumentation and Computer Experience Instrumentation: HPLC, UPLC, ICP, GC, FT-IR, UV, Dissolution, pH, TOC and Karl Fischer. Computer programs: Empower 1-3, EZ Chrome Elite, WindLab, ChemStation, Microsoft Word, Excel and Outlook. Work Conditions: Hours/Travel maybe subject to changed based on management/company discretion. Work location are subject to change as needed to meet business requirements. While performing the duties of this job, the employee is regularly required to stoop, kneel, crouch, stand, bend, sit, talk, hear or walk for long periods. The employee may lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: As needed Salary Range: $70,000 - $90,000 per year
    $70k-90k yearly 21d ago

  • Fault-tolerant Quantum Algorithm Resource Estimation Research Scientist

    IBM 4.7company rating

    Principal research scientist job in Yorktown Heights, NY

    **Introduction** Research Scientists at IBM drive the leading edge of quantum computing technologies with the industry's most advanced hardware and software. Join an elite team of engineers and scientists building a path towards scalable fault tolerant quantum computation. **Your role and responsibilities** A successful candidate will * identify feasible quantum algorithms and application areas for early fault tolerant quantum devices, * benchmark resource requirements depending on problem parameters, implementation details, and circuit synthesis strategies, * develop understanding in relevant application domains such as physics, chemistry, etc., develop estimates of relevant problem parameters, and characterize performance and accuracy of quantum algorithms in practice, * and compare quantum methods to the classical state of the art. **Required technical and professional expertise** * Doctorate degree in Engineering, Physics, or Computer Science, or related software experience * Experience with quantum algorithm design, analysis, and resource estimation * Familiarity with programming languages for scientific computing (Python, or equivalent) **Preferred technical and professional experience** * Familiarity with programming languages for high-performance computing (Rust, C++, or equivalent) * Experience with large-scale software engineering projects involving multiple contributors and programming languages IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
    $76k-104k yearly est. 3d ago

  • Bench Scientist

    Artech Information System 4.8company rating

    Principal research scientist job in Pearl River, NY

    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 The individual will perform complex synthesis and purification of biomolecules and derivatives as well as conduct characterization assays. The individual is also expected to participate in team meetings, provide update and contribute to planning activities to achieve program deliverables. Interaction with other groups/departments is expected. Bench level experience with protein purification, synthetic organic chemistry and/or protein isolation, purification is desirable but not expected. Qualifications BS OR MS Additional Information Best Regards, Anuj Mehta ************
    $73k-105k yearly est. 60d+ ago

  • Biophysical Assoc Scientist

    Global Channel Management

    Principal research scientist job in Darien, CT

    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.
    $73k-106k yearly est. 60d+ ago

  • Senior Research Associate

    ARGA Investment Management

    Principal research scientist job in Stamford, CT

    ARGA Investment Management, LP seeks motivated professionals excited by global business analysis. You will develop insights into how businesses work and their normalized earnings power. You are brilliant and enjoy multicultural interaction and teamwork. Members of our research team typically cover sectors globally. This role would provide that opportunity, along with emphasis on China or Japan. We are seeking uniquely talented and entrepreneurial candidates who can help develop future offices in Asia. JOB DESCRIPTION * Understand key drivers at company and industry levels * Build detailed global industry models and forecasts * Forecast company financial statements by business segment * Identify issues and conduct company management meetings * Present conclusions through models, written reports and presentations QUALIFICATIONS * Demonstrated academic excellence in a top graduate program * Excellent oral/written communication in Mandarin Chinese or Japanese * Unquestionable integrity * Strong financial statement analysis and modeling background * Ability to understand and forecast business fundamentals * Entrepreneurial * Flexibility in international travel (at an appropriate time) Send your resume to ********************** FIRM DESCRIPTION ARGA Investment Management is a leading global value manager. ARGA manages global equity portfolios on behalf of institutional clients. We use a sophisticated process combining research and technology to identify businesses that are underpriced. ARGA is based in Stamford, CT, with offices in Chennai and Mumbai, India, Hongkong and London, UK. For more information, visit
    $70k-104k yearly est. Easy Apply 60d+ ago

  • Senior Scientist - Bioinformatics

    Mygradjob

    Principal research scientist job in Pearl River, NY

    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.
    $77k-129k yearly est. 60d+ ago

  • R&D Scientist

    Noor Staffing Group

    Principal research scientist job in Valhalla, NY

    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
    $69k-97k yearly est. 60d+ ago

  • Bench Scientist/ HPLC

    Pioneer Data

    Principal research scientist job in Pearl River, NY

    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
    $67k-97k yearly est. 60d+ ago

Learn more about principal research scientist jobs

How much does a principal research scientist earn in Norwalk, CT?

The average principal research scientist in Norwalk, CT earns between $82,000 and $165,000 annually. This compares to the national average principal research scientist range of $87,000 to $184,000.

Average principal research scientist salary in Norwalk, CT

$117,000
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