Senior principal scientist jobs in White Plains, NY

Boehringer Ingelheim is currently seeking a Senior or Principal Scientist to support our Material and Analytical Sciences team to join our Ridgefield, CT facility. This role is part of Boehringer Ingelheim's Drug Substance-Drug Product Interface organization, driving innovation in small molecule development. The Principal Scientist/Sr. Scientist will lead efforts in solid-state chemistry and API engineering, focusing on phase-appropriate isolation processes and DS-DP co-processing technologies to ensure optimal material attributes-purity, crystal form, and physical properties. This position offers the opportunity to shape strategies for next-generation drug substance/drug product integration, collaborate across CMC Development and Operations, and implement cutting-edge solutions in manufacturing. 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** - Lead experimental design and hands-on execution for solid form, crystallization and isolation, and DS-DP co-processing development, applying QbD principles and appropriate engineering tools. - Champion DS-DP Co-processing as a platform technology; drive implementation across Boehringer's portfolio. - Develop scalable crystallization and isolation processes, identifying CPPs and establishing robust control strategies. - Conduct solid form screening (polymorphs, salts, co-crystals) and advanced characterization using XRD, DSC, TGA, DVS, Raman, and PAT tools. - Collaborate with cross-functional CMC teams to ensure process robustness, scalability, and tech transfer to GMP manufacturing. - Resolve scale-up challenges related to crystallization, particle engineering, and DS-DP integration; perform risk assessments and mitigation planning. - Author technical reports, regulatory documentation, and contribute to IND/NDA filings. - Serve as a scientific leader and mentor, fostering innovation and knowledge sharing within Material & Analytical Sciences. - Stay ahead of emerging technologies (AI/ML, automation, continuous crystallization) and regulatory trends. **Requirements** **Requirements for Both Levels:** - Strong expertise in solid-state chemistry, polymorphism, crystallization development, and Drug Substance (DS)-Drug Product (DP) interface. - Proven ability to design processes, generate and analyze data, and interpret results independently. - Hands-on development of cGMP isolation processes and scale-up principles. - Excellent communication and collaboration skills; ability to influence in a matrix environment. - Physical requirements: lift/carry up to 50 lbs.; respirator use may be required. - Appropriate level of understanding of applicable regulations **Requirements for Senior Scientist:** - Ph.D. Degree in Chemical Engineering, Organic Chemistry, Pharmaceutical Science, Polymer Science, or related field or equivalent with experience in a related field - Demonstrates a broad knowledge of field - Appropriate level of understanding of applicable regulations **Requirements for Principal Scientist:** - Ph.D. Degree in Chemical Engineering, Organic Chemistry, Pharmaceutical Science, Polymer Science or related fields or equivalent with five plus (5+) years related experience in a related field - At least 4 years post-graduation of pharmaceutical industry or relevant industrial experience in chemical engineering, process chemistry, physical chemistry or related fields. - One (1) to three (3) years project management/leadership experience - Has a proven track record of publication in peer-reviewed journals. **Desired Skills, Experience and Abilities:** - Experience in polymer science and DS-DP co-processing. - Familiarity with predictive modeling tools, PAT, and CFD. - Application of AI/ML for process optimization and digital development strategies. **Compensation Data** This position, Senior Scientist, MAS, offers a base salary typically between $140,000 and $222,000.00 USD. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here (***************************************************************** . **Eligibility Requirements** Must be legally authorized to work in the United States without restriction. Must be willing to take a drug test and post-offer physical (if required) Must be 18 years of age or older 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.

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**

We're not just a workplace - we're a Great Place to Work certified employer! Proudly certified as a Great Place to Work, we are dedicated to creating a supportive and inclusive environment. At Sonic Healthcare USA, we emphasize teamwork and innovation. Check out our job openings and advance your career with a company that values its team members! Location: Rye Brook, NY Days: Monday - Friday Salary range: $150K - $195K Hours: 8:00 AM - 5:00 PM Full-time: Benefit Eligible In this role, you will: Collaborate with senior leadership to align research and clinical validation priorities with organizational goals. Supervise and mentor a team of Molecular Technologists working under their supervision, fostering a culture of scientific excellence and continuous improvement. Oversee daily molecular R&D testing operations, ensuring accuracy, efficiency, and compliance with any regulatory agency at any level. Lead the design, optimization, and validation of high-throughput molecular assays for clinical and pharma applications. Conduct comprehensive validation studies, including precision, accuracy, sensitivity, and specificity assessments. Review the critical steps in developing new assays or technologies. Provide scientific and technical guidance for assay troubleshooting. Maintain robust quality assurance and quality control programs; implement corrective actions as needed. Develop, review, and update SOPs to ensure compliance with regulatory and accreditation standards. Collaborate with the QA Manager to prepare for inspections and audits; provide detailed reports and documentation. Identify emerging technologies and methodologies to enhance molecular testing capabilities. Collaborate with cross-functional teams to support research initiatives and pharma partnerships. Contribute to strategic planning for laboratory growth and integration of novel molecular platforms. Perform other job-related duties as assigned. Ensure adherence to CAP/CLIA/NYSDOH standards, other regulatory agencies, and internal SOPs. Manage and coordinate the procurement of laboratory supplies and equipment, as well as for special projects. Ensure all instrument maintenance is performed and documented; administer all established quality control procedures; and troubleshoot instruments effectively when appropriate. Maintain medical laboratory supplies inventory, determine inventory level, and anticipate needed supplies. We'll give you: Appreciation for your work A feeling of satisfaction that you've helped people Opportunity to grow in your profession Free lab services for you and your dependents Work-life balance, including Paid Time Off and Paid Holidays Competitive benefits including medical, dental, and vision insurance Help saving for retirement, with a 401(k) plus a company match A sense of belonging - we're a community! Scheduled Weekly Hours: 40 Work Shift: Job Category: Laboratory Operations Company: Sonic Healthcare USA, Inc Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. The R&D team is seeking an exceptionally talented and passionate individual to help us identify and implement innovative solutions to address current and future health care needs. Within BD Medication Delivery Solutions (MDS) Research & Development, the Staff Scientist, Microbiology will be part of the Materials Science team in Franklin Lakes NJ, reporting to the Associate Director, Materials Science. Our R&D Engineers and Scientists are responsible for developing and implementing new product materials and designs, product improvements, and critical component changes for disposable and durable medical devices. The preferred candidate will have strong technical skills, excellent written and oral skills, and leadership abilities. This candidate should possess a strong capability to interpret and ensure compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. The Staff Scientist, Microbiology plays a critical role in ensuring the microbiological integrity of products and processes throughout the development lifecycle. This position provides technical leadership in microbiology-related risk assessments, method development, and validation activities, supporting compliance with global regulatory requirements and internal quality standards. The role requires strong collaboration with cross-functional teams, including Platform Product R&D, Regulatory Affairs, and Manufacturing, to deliver safe, effective, and innovative medical devices. Key Responsibilities: * Microbiological Risk Management: * Lead microbiological risk assessments for new product development and sustaining projects. * Define and implement contamination control strategies aligned with ISO 11737, ISO 11135, and related standards. * Develop solutions to both unique and routine technical problems related to the assigned projects. * Method Development & Validation: * Provide technical leadership for key aspects of development projects requiring the design and performing of microbiology experiments in the laboratory that includes culture of pathogenic bacteria and fungi, and handling of blood and blood products. * Develop and validate microbiological test methods (bioburden, sterility, endotoxin, environmental monitoring). * Ensure robustness and compliance of methods with USP, EP, and ISO requirements. * Sterilization & Cleanliness Support: * Partner with sterilization engineers to establish and maintain validated sterilization processes. * Support packaging integrity and EO residual testing strategies. * Regulatory & Quality Compliance: * Author and review microbiology-related sections of regulatory submissions (510(k), CE marking, etc.). * Ensure adherence to GMP, ISO 13485, and FDA QSR requirements. * Cross-Functional Collaboration: * Provides experimental data and technical input to other scientists within R&D and provides support to other functional groups in pursuit of project objectives. * Serve as the microbiology SME in design reviews, hazard analyses, and CAPA investigations. * Provide guidance to project teams on microbiological considerations impacting design and manufacturing. * Continuous Improvement: * Identify opportunities to optimize microbiological testing efficiency and reliability. * Mentor junior associates and contribute to knowledge-sharing initiatives. * Leadership * Lead cross-functional technical governance for microbiology-related risk management and compliance, ensuring alignment with corporate and regulatory expectations. * Mentor and coach senior scientists and engineers, building organizational capability in microbiology evaluations. * Provide technical leadership for critical business decisions, including supplier qualification, material selection, and new technology adoption. * Engage with regulatory agencies and notified bodies as BD's microbiology subject matter expert during audits and inspections * Serve as global microbiology thought leader, representing BD in external technical forums, standards committees, and industry working groups. Qualifications: * Minimum bachelor's degree in microbiology or related field required, advanced degree preferred * Minimum 5 years of experience in microbiology within medical devices, pharmaceuticals, or related regulated industry. * Proven expertise in sterilization validation, bioburden control, and microbiological method development. * Research experience in microbiology, biochemistry or a related field that includes culturing and manipulation of microorganisms. * Experience in laboratory techniques in microbiology with demonstrated skills in adapting procedures to meet specific objectives and solve problems. * Strong knowledge of ISO 11737, ISO 11135, USP , , and related standards. * Understand and follow biosafety practices and use aseptic technique when working in microbiology labs. * Comprehensive knowledge of the medical device product development process under a quality management system in a regulated environment (ISO 13485, FDA cGMP/cGLP, etc) * Excellent analytical, problem-solving, and technical writing skills. * Ability to manage multiple priorities in a fast-paced environment. * Effective communicator and collaborator across functions and levels. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. At BD, we are committed to supporting our associates' well-being, development, and success through a performance-based culture. For this position, BD offers a competitive compensation package along with the following benefits specific to this role: * Annual Bonus Health and Well-being Benefits * Medical coverage * Health Savings Accounts * Flexible Spending Accounts * Dental coverage * Vision coverage * Hospital Care Insurance * Critical Illness Insurance * Accidental Injury Insurance * Life and AD&D insurance * Short-term disability coverage * Long-term disability insurance * Long-term care with life insurance Other Well-being Resources * Anxiety management program * Wellness incentives * Sleep improvement program * Diabetes management program * Virtual physical therapy * Emotional/mental health support programs * Weight management programs * Gastrointestinal health program * Substance use management program * Musculoskeletal surgery, cancer treatment, and bariatric surgery benefit Retirement and Financial Well-being * BD 401(k) Plan * BD Deferred Compensation and Restoration Plan * 529 College Savings Plan * Financial counseling * Baxter Credit Union (BCU) * Daily Pay * College financial aid and application guidance Life Balance Programs * Paid time off (PTO), including all required State leaves * Educational assistance/tuition reimbursement * MetLife Legal Plan * Group auto and home insurance * Pet insurance * Commuter benefits * Discounts on products and services * Academic Achievement Scholarship * Service Recognition Awards * Employer matching donation * Workplace accommodations Other Life Balance Programs * Adoption assistance * Backup day care and eldercare * Support for neurodivergent adults, children, and caregivers * Caregiving assistance for elderly and special needs individuals * Employee Assistance Program (EAP) * Paid Parental Leave * Support for fertility, birthing, postpartum, and age-related hormonal changes Leave Programs * Bereavement leaves * Military leave * Personal leave * Family and Medical Leave (FML) * Jury and Witness Duty Leave Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. Salary Range Information $130,400.00 - $215,200.00 USD Annual

Oversee all technical and formula development aspects for key projects, ensuring their progression through the product development process by collaborating cross-functionally with Engineers, Marketing, Consumer Insights, Procurement, Regulatory, Legal, and Operations teams. Responsibilities * Lead the technical and formula development for key projects. * Collaborate with cross-functional teams including Engineers, Marketing, Consumer Insights, Procurement, Regulatory, Legal, and Operations. * Ensure projects progress smoothly through the product development process. Essential Skills * 6+ years of experience in the consumer product industry, with a preference for knowledge in surface cleaning. * Experience and familiarity with analytical processes and stability processes. * Strong understanding of raw materials, preferably with surfactant systems. * Technical awareness of market trends. * Skills in chemistry, product development process, stability testing, analytical processes, innovation concept testing, formulation, polymers, and emulsions. Additional Skills & Qualifications * Experience with cold processing materials, surfactants, pH adjusters, chelants, and claim ingredients. * Familiarity with polymer emulsions. Work Environment The company fosters a deep, collaborative, and performance-driven culture, encouraging employees to support each other in a positive and productive work environment. It offers competitive pay, health, dental, and vision coverage, career growth and development opportunities, a 401K plan, and a company store. Employees can also participate in community volunteering and tuition assistance programs. Committed to sustainability, more than half of the company's products are 100% plant-based, with a goal to reduce Scope 1 and 2 carbon emissions by 42% by 2030. The company is dedicated to advancing social and environmental impact, supporting communities in times of need, and working with suppliers and customers to make a positive impact. Pay and Benefits The pay range for this position is $55.00 - $56.00/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 Montvale,NJ. Application Deadline This position is anticipated to close on May 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 for other accommodation options.

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)

**_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

Responsibilities Peraton Labs is looking for a self-motivated Adversarial AI Research Scientist with a passion for developing solutions for adversarial AI/ML (Artificial Intelligence/Machine Learning). Recent research has shown that AI-based systems are highly prone to error when presented with adversarially crafted inputs, such as imperceptible perturbations added to an image. Other sources of error arise from adversarial manipulation of training data. Such adversarial actions can be used to disrupt the performance of AI-enabled physical systems, such as autonomous ground vehicles and unmanned aerial vehicles. Such disruptions result in degraded performance (e.g., autonomous vehicles slowdown) or failure to accomplish a task (e.g., vehicle crashes). However, most of these effects have been demonstrated in simulation environments or assume unrestricted access to the model training pipeline, which is unrealistic. Peraton Labs is a leader in the field of Adversarial AI and we are seeking strong candidates to join our team and investigate challenging new problems in this space. You will work with a small team of research scientists to investigate the vulnerabilities of AI-enabled systems in real-world settings to attacks across multiple modalities and at different stages of the model training pipeline. You will devise physically realizable solutions to determine whether real-world systems like autonomous vehicles and unmanned aerial vehicles are vulnerable to attacks on their AI controls. Note that such vehicles will depend on sensors that span multiple modalities, such as visual, thermal, LiDAR, etc.; thus, for attacks to succeed, each of these modalities must be manipulated. Your work will involve research, design, and prototyping of software as well as field-testing to prove out technical concepts; you should therefore have strong software development skills and be willing to learn new skills and technologies as needed to develop cutting-edge solutions based on customer needs. The ideal candidate is one who is excited at the opportunity to work on cutting-edge research in an environment where they will continuously learn new concepts and innovate in collaboration with a strong team of individuals with diverse technical backgrounds. Qualifications Required Qualifications * A minimum of a MS with 3 years of experience, or a Ph.D. in Computer Science, Computer Engineering, or related field with a focus on machine learning research. * Hands-on experience with state-of-the-art machine learning software environments such as TensorFlow, PyTorch, scikit-learn. * Strong software development experience. * Excellent oral and written communication skills. * US citizenship is required for this position. * Candidates must be local to or willing to relocate to the immediate Basking Ridge, NJ area. Preferred Qualifications * A strong publication record in AI/ML. * Expertise and research experience specific to adversarial machine learning (AML) is desirable. Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range $86,000 - $138,000. This represents the typical salary range for this position. Salary is determined by various factors, including but not limited to, the scope and responsibilities of the position, the individual's experience, education, knowledge, skills, and competencies, as well as geographic location and business and contract considerations. Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Studies the basic principles of plant and animal life and the effects of varying environmental and physical conditions such as radioactivity or pollution. Studies reactions of plants, animals, and marine species to parasites, bacteria, pharmaceuticals and chemicals. • Performing cell assay development and NTC studies on Client targets . • Skills: • Familiar with a variety of the fields concepts, practices, and procedures. • Education: • Bachelor's Degree • Cell biology and molecular biology skills a plus • Languages: • English Read Write Speak • Education: Bachelor's Degree • Skills: Familiar with a variety of the fields concepts, practices, and procedures.

**PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best validated disease models and comprehensive preclinical capabilities to help companies discover the next generation of treatments for severely disabling CNS and orphan disorders and reduce the attrition rate in clinical development. We are known for our cutting-edge translational approach to research, our customized solutions, the breadth, and quality of our work, as well as for our ability to identify statistically relevant phenotypic changes that help our clients quantify the efficacy of their treatments before they move into the clinic. With an extensive portfolio of highly predictive disease models and unparalleled experience performing studies for biopharmaceutical companies of all sizes, we enable clients to deliver much needed superior clinical candidates to patients. PsychoGenics is seeking a Research Scientist (or Sr. Scientist, depending on experience) who will work closely with the VP, Translational Neuroscience and the Program Manager/Sr. Scientist to lead studies testing the efficacy of novel test articles and genetic manipulations for treating CNS diseases and disorders. We conduct studies that test new therapies for almost every CNS disorder. The ideal candidate will be an expert in pre-clinical (rodent) EEG with knowledge of basic sleep science. **THIS IS AN ONSITE POSITION.** **Responsibilities:** + Rapidly gain expertise in all procedures and techniques used by the EEG staff. + Work and manage all levels of personnel in a positive, respectful manner. + Ability to train staff and help nurture their careers. + In coordination with management, design and develop experiments to analyze EEG changes induced by pharmaceutical agents and/or genetic models for seizures, ERPs and sleep. + Perform, manage, and oversee studies, including surgeries, dosing, and EEG recordings. + Review and check the quality of analyzed EEG data, including sleep-scoring, seizure detection, evoked potentials, and spectral analysis. + Work with management to help write study plans and reports and be able to discuss the data collection and analyses processes in a clear, articulate manner. + Individual will have some client engagement on study design and reporting of data. + Maintenance and troubleshooting of EEG recording equipment. **Required Qualifications:** + Previous management/supervisory experience. + PhD in Neuroscience, Biomedical Engineering, or other related degree. + 3-10 years of demonstrated applicable experience in EEG. + Prior experience working with and handling rodents in a lab setting. + Ability to interact professionally with all levels of employees and work effectively as a member of a team. + Ability to simultaneously manage multiple responsibilities and priorities. + Ability to work in a fast-paced environment where priorities can change on a dime. + Demonstrated independent analytical and problem-solving abilities. + Knowledge of electronics and EEG recording systems (DSI, Spike2, Pinnacle/Sirenia). + Expertise in rodent EEG analyses including signal processing, sleep scoring, and seizure detection. **Preferred Experience/Qualifications:** + Prior experience working in a CRO and/or Drug Discovery environment. + Previous success as a team leader and motivator; excellent verbal and written communication and organizational skills. + Programming experience (i.e., Matlab, EEGLAB, Python, R and/or statistical software like SAS). The approximate base salary for this position is $100,000 - $120,000. Salary will be determined by factors including job-related skills, experience, education, and overall knowledge. **Total Rewards Plan** PsychoGenics offers competitive performance-based compensation, comprehensive benefits, and career development opportunities. This role is eligible for annual performance-based raise and discretionary bonus for both individual and PsychoGenics annual performance. Our benefits include: + Medical, dental, vision and life insurance plans + HSA, FSA and dependent FSA + Short- and long-term disability plans + Stock-based incentive plan + 401K with company contribution + Tuition reimbursement + Generous paid time off policy and paid parental leave policy + EAP + Additional voluntary benefits **PsychoGenics is a veteran/disability/equal opportunity employer.** We take pride in maintaining a diverse work environment. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, age, sex (including pregnancy, gender identity or expression and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), political affiliation, status as a protected veteran, or any other legally protected status. We strive to create a workplace that cultivates bold innovation through collaboration and allows our people to unleash their full potential. **Reasonable Accommodation** PsychoGenics provides qualified individuals with reasonable accommodation during the application and hiring process. If you require assistance or need reasonable accommodation due to disability, please contact Human Resources at: ************************ **Nearest Major Market:** New York City Apply now »

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

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: ************

& Sons: Schweid & Sons is a family-owned and operated premium ground beef company with a proud heritage spanning four generations. We supply top-quality beef to Retail, Foodservice, and National Account customers across the U.S. and are committed to quality, customer service, and innovation in protein manufacturing. Summary: Are you a creative and driven professional with a passion for developing innovative premium protein products? Schweid and Sons is looking for a Food Scientist to add to our team. Reporting to the Director of Innovation, you will lead innovation and product development projects and initiatives, formulation, process improvement, ingredient, recipe and nutritional development, and provide food science strategy and guidance to take the company into the future. This role focuses on developing, improving, and ensuring the safety and quality of premium protein products, from fresh cuts to processed meats. The ideal candidate will have an understanding of meat science, food safety regulations, and product development processes within the beef and other protein industries. To be successful in this role, you must have strong food science, product development experience in protein, ability to improve and build repeatable processes, experience in meat operations, and knowledge of regulatory requirements. You should be comfortable leading key projects, working independently to ensure deadlines are met while balancing priorities. This is an incredible opportunity to join a well-established food manufacturing company that prides itself on putting its team members first by providing an incredible culture, amazing benefits, and commitment to innovation. Job Functions /Responsibilities: * Manage innovation projects, communicate, and coordinate with internal stakeholders as well as customers. Research and develop new products, including raw, fresh, cooked, cured, and value-added items. * Improve existing products in terms of taste, texture, shelf life, yield, and nutritional profile. * Design and conduct experiments on meat formulations, marination, cooking processes, and preservation techniques. * Organize sensory panels and conduct rigorous product testing to ensure we deliver a great tasting product. * Ensure all products comply with USDA, FDA, HACCP, and company food safety standards. * Conduct shelf-life testing and sensory evaluations of beef products. * Analyze raw materials and finished products for microbial, chemical, and physical properties. * Collaborate with procurement, QA, production, and marketing teams to bring new products to market. * Monitor trends in meat science, consumer preferences and processing technologies. * Prepare responses to customer inquiries with adequate scientific and technical evidence and provide solutions. * Complete the verification of the implementation of standard operating procedures for the laboratory or kitchen facilities. * Responsible for maintaining accurate records of formulations, procedures, and processes in appropriate software systems and platforms. Qualifications / Experience: * Bachelor's degree in Food Science or related field or equivalent experience. * USDA, FDA, HACCP and SQF experience. * 3 - 5 + years of Food Science in the protein category required. * 2 + years related protein experience required, preference for beef experience. * Food/nutrition manufacturing experience required. * Fundamental understanding of regulatory compliance and nutritional calculation software. * Understanding of daily lab and production processes. Expertise in raw material handling and stability. * Ability to independently formulate products based on consumer and customer requirements, identifying potential issues and promptly alerting managers or customers. Experience in food concept development and prototype improvement. * Some culinary and recipe development experience is a plus. * Able to effectively analyze data to develop presentations and reports. * Must be proficient in the use of Microsoft Office (Excel, Outlook, Word, and PowerPoint). What We Offer * The expected compensation for this role is $90,000 - $120,000 per year, depending on experience and qualifications. Final compensation will be discussed during the interview process. * Time Off: PTO, Safe & Sick Time, and Paid Holidays. * Health Benefits: Medical, vision, dental, HRA and voluntary disability benefits. * Financial Benefits: 401(k) + employer match and life insurance. * Location: This is an on-site role located in either East Rutherford, NJ or College Park, GA. * Environment: Office environment.

The Senior Principal Scientist is responsible for spearheading the imaging biomarker strategy and implementation across cardiovascular and metabolic indications in early- and late-phase clinical trials. This role involves collaboration with cross-functional study teams where you will lead the design of complex imaging approaches to test the efficacy and safety of Regeneron products. In this role, you will be responsible for developing and validating novel imaging-based biomarkers to address the needs of the Regeneron experimental therapies. As a Senior Principal Scientist in Clinical Imaging you will: * Collaborate closely with Research and Global Development colleagues to formulate appropriate imaging biomarker strategies to inform and advance the Regeneron clinical pipeline. * Provide leadership during the strategy phase of study design, guiding the team on all imaging aspects of the study, presenting the imaging components of the integrated biomarker strategy to senior management for endorsement, and authoring of key study documents. * Work closely with Clinical Imaging Operations and Clinical Trial Management to ensure the delivery of high-quality imaging data in clinical studies. This includes drafting imaging manuals and other documents for the trial, supporting the clinical team during the study start-up phase, and monitoring data integrity throughout the trial. * Supervise imaging Clinical Research Organizations (CROs) to ensure execution of imaging components in the trial, timely address any image quality issues, and ensure flawless delivery of key study imaging data and achievements * Identify gaps in imaging assessments for particular indications and propose novel biomarkers, and spearhead validation through collaboration with other functions within Regeneron or external institutions. * Support regulatory submission packages as the imaging subject matter expert This role requires that you: * Work efficiently in a fast-paced, collaborative environment * Communicate extremely effectively across clinical teams and functions, and with senior management * Possess a broad knowledge of imaging and understand the challenges of image standardization across sites and countries * Have strong analytical and problem-solving skills * Thrive in addressing complex problems with innovative methods To be considered for this position, we expect you to have completed a PhD or MD/PhD program, with a minimum of 6 years of experience in clinical imaging, specifically within cardiovascular and/or metabolic domains. We believe you should have extensive expertise in the acquisition and analysis of various imaging modalities, including MRI, CT, ultrasound, and echocardiography. While experience in industry-sponsored clinical trials is preferred, it is not mandatory. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Salary Range (annually) $148,300.00 - $241,900.00

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

Job ID 33221 **Technical Service Scientist** Regular Stamford - CT, United States of America (****************************************** - CT,United States of America) My candidate profile **Important EEO information related to openings in the US** 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.Click here (************************************************************************************** to access the Know Your Rights poster. 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 come. **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. \#LI-RC1 \#Onsite

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.

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.

Department: Engineering About Us Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today. QCi products are designed to operate at room temperature and low power at an affordable cost. The Company's portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. Position Description We are seeking an experienced Quantum Application Research Scientist for research and development on utilizing QCi's entropy quantum computing hardware for solving computationally-hard optimization problems. This role involves close collaboration with the high-performance computing application team as well as the entropy computing hardware team. Duties and Responsibilities - Design, analyze, and implement algorithms for combinatorial optimization and related computationally challenging problems on entropy quantum computing hardware. - Collaborate with hardware engineers to map theoretical models and algorithms to physical implementations. - Benchmark entropy quantum computing approaches against classical and quantum alternatives, and publish results in peer-reviewed venues. - Develop simulation and modeling tools to characterize performance and scalability. - Contribute to interdisciplinary projects at the intersection of physics, computer science, and applied mathematics. - Work closely with the applications team to identify high-impact use cases in industry and government. - Communicate results and insights to both technical and non-technical audiences, including customers, collaborators, and leadership. Required Skills and Experience - PhD in Quantum Information Science, Physics, Computer Science, Applied Mathematics, or a related field. - Strong foundation in quantum algorithms, quantum information theory, or quantum statistical mechanics. - Demonstrated research experience in optimization methods, either quantum or classical. - Proficiency in scientific programming (Python, C++, or similar) and numerical methods. - Strong track record of publications or equivalent technical contributions. - Ability to work collaboratively across disciplines and communicate complex ideas clearly. Preferred Qualifications - Experience with NISQ (Noisy Intermediate-Scale Quantum) hardware, analog quantum devices, or non-traditional quantum computing paradigms. - Familiarity with entropy-based computing models or statistical physics approaches to optimization. - Background in high-performance computing, large-scale simulations, or hybrid classical-quantum workflows. - Experience with combinatorial optimization formulations such as Ising models, QUBO, or constraint satisfaction problems. - Industry or government R&D experience in applying quantum or advanced computational techniques to real-world problems. - Strong collaborative and leadership skills, including mentoring junior researchers. Incumbent(s) in this position may be required to perform other duties and special assignments not specifically stated above. Statements outlined in this section are designated as essential job functions in accordance with the Americans with Disabilities Act of 1990.