Trabajos scientist en Clifton, New JerseyCrear alertas

Company Description: Stira Pharmaceuticals is a Sterile Injectable CDMO specializing in pharmaceutical product development and the manufacturing of small molecules and peptides. Our expert scientific team utilizes advanced in-house technology platforms combined with extensive industry experience to tackle challenging product developments. We offer comprehensive services including Analytical R&D, Preformulation, Formulation Development, Manufacturing, and Regulatory Support. Job Overview: Stira Pharmaceuticals, LLC, located in Fairfield, NJ, seeks a motivated and detail-oriented Analytical Scientist for a full-time, on-site role. The successful candidate will develop, validate, and transfer analytical methods for drug substance and drug products with a specific focus on related substances. This role requires adherence to cGMP guidelines and collaboration across multiple functional teams. Responsibilities: • Develop, validate, and transfer analytical methods for drug substances, drug products, related substances, and raw materials., • Perform both routine and complex analyses utilizing analytical techniques such as H/UPLC, GC-HS, Ion Chromatography, Atomic Absorption Spectroscopy, and related instrumentation., • Collaborate with R&D, Quality Control, and Regulatory Affairs teams to ensure product compliance with industry standards., • Interpret analytical data and prepare comprehensive reports for regulatory documentation and submissions., • Troubleshoot analytical methods and optimize procedures to enhance accuracy, precision, and efficiency., • Stay informed on the latest developments in analytical techniques, specifically related to small molecules, peptides, and sterile injectables, integrating relevant innovations into projects., • Train, mentor, and guide junior analytical staff in method execution and best laboratory practices. Qualifications: • Ph.D., Master’s, or Bachelor’s degree in Analytical Chemistry or a related discipline with emphasis on small molecule analysis., • Minimum of 6-10 years of relevant laboratory experience, ideally within the pharmaceutical or biotechnology sectors., • Solid understanding of advanced analytical chemistry theories and proven method development skills., • Proficiency with analytical instrumentation such as H/UPLC, GC-HS, Ion Chromatography, and Atomic Absorption Spectroscopy., • Familiarity with regulatory requirements (FDA, ICH guidelines) pertinent to analytical method development and validation., • Strong ability to independently manage projects, meet deadlines, and prioritize tasks effectively., • Exceptional problem-solving capabilities and experience in leading analytical investigations., • Excellent written and verbal communication skills for clear and concise presentation of complex data., • Proven ability to work collaboratively in a dynamic, multidisciplinary environment., • Demonstrated experience in GMP settings and practical knowledge of their application to pharmaceutical development. Location: Fairfield, NJ Position Type: Full-Time, On-Site • We invite talented individuals committed to scientific excellence and innovation to join our dynamic team at Stira Pharmaceuticals.

Lead Data Scientist Location: Hybrid — Newark, NJ (3 days/week onsite) Employment Type: Contract-to-Hire Pay Rate: $70-$85 per hour, based on experience. No C2C/1099. W2 only. About the Role • Join a leading investment firm as a Lead Data Scientist, partnering with Machine Learning Engineers, Data Engineers, Data Analysts, and cross-functional teams to build AI and Machine Learning products, • Implement Machine Learning, AI, and agentic capabilities that deliver stability, scalability, and integration across products and services, • Solve sophisticated business problems and deploy innovative products and experiences What You'll Do • Provide deep technical leadership across a portfolio of high-impact data science initiatives, • Identify optimal data, models, and training/testing techniques for successful product delivery, • Manage team members across data analysis, model development (traditional ML and statistical models), GenAI and agent development, testing, training, and tuning, • Write production-grade code and partner with ML engineers to push models into production, including traditional ML, statistical models, GenAI, and agentic solutions, • Work hands-on with Agentic AI systems, fine-tuning techniques (e.g., LoRA), LLM deployment, RAG, Agentic RAG, Strands, Claude Agents SDK, and related agentic concepts, • Communicate model design and development clearly to technical and non-technical audiences, • Leverage CI/CD best practices, including test automation and monitoring, for ML model and application deployment, • Stay current on emerging technologies and embed learning/innovation into the team's daily work, • Program primarily in Python and SQL What You Bring • Advanced degree (Master's or Ph.D.) in Mathematics, Statistics, Engineering, Econometrics, Physics, Computer Science, Actuarial Science, Data Science, or a related quantitative field, • Experience leading a small team with minimal guidance, • Demonstrated ability to mentor team members and manage operations based on project and resourcing needs, • Ability to influence business stakeholders and drive adoption of AI/ML solutions, • Experience with Agile methodologies and Test-Driven Development (TDD), • Strong business acumen to support sound, context-driven decision-making, • Excellent problem-solving, communication, and collaboration skills, • Experience with cloud-based AI platforms such as Bedrock and SageMaker Preferred Technical Expertise (several of the following) • Data acquisition and transformation using APIs, semantic data models, SQL, and Python, • Database management across relational (SQL), unstructured (NoSQL), and graph/ontology (Graph DB) systems, • Data analysis using visualization, manipulation, and statistical methods to identify trends and anomalies, • Strong foundation in multivariable calculus, linear algebra, differential equations, applied probability, and applied statistics, • Deep understanding of machine learning theory, including supervised and unsupervised models, • Experience with Generative AI and NLP, including RAG, LangChain, LangGraph, vector databases, LangFuse, and AgentCore, • Understanding of the model deployment lifecycle, A/B testing, CI/CD pipelines, and frameworks such as AWS SageMaker and Azure Agentic AI tools

Our client, a hugely successful, innovative, and well established bakery products company is experiencing enormous growth and now seeking a Director, Innovation & R&D as an addition to staff: Job Title: Director, Innovation & R&D Department: R&D/Innovation; ‘Bake Excellence’ Reports to: Ownership Collaborates with: Baking Direct Reports: Food Scientists/Technologists; Application Chefs/Bakers; Lab Techs. Overview: ‘Imagineer’ and oversee all aspects of Research and Development activities related to the creation and betterment of our company’s bread and baked goods products. Collaborate with Baking, Quality, Operations, Engineering and other Departments to qualify, optimize, and commercialize these new products and their processing, always with the goal to meet and exceed our customers' demands and expectations. This position requires a resourceful background in food science, baking technologies, and project management, along with exceptional leadership and collaboration skills. Presence Expectations: • Presence in the Facility, spanning five work days per week;, • ‘On the R&D/Production Floor’ Presence during trials, troubleshooting, initial commercializing;, • ‘In the Lab’ during Reviews and Meetings;, • ‘On the Road’ for Food and/or Ingredient Shows and Conferences; occasional Presentational or Technical visits to Customers; at will to seek new ideas. _ Essential Company-Wide Duties: • Be a ‘Bake Excellence’ Steward who supports and protects the Mission and Culture of our Company., • Exemplify Transformative Leadership., • Maintain a Safe and Sanitary Working Environment for all employees., • Support highest level Food Safety Program and Culture. Infuse Purpose, Clarity, Energy, and Opportunity to your Department and Workforce. • Promote and Support Training and Growth of Personnel, inclusive direct training by you to those who directly report to you; while, equally, showing those directly under you the foundations to train those directly under them; etc., • Create a Platform of Walk-Throughs, Meetings, Huddles and Reviews that are efficient, informative, and preliminary for ensuing follow up actions; you shall moderate those meetings that need your direct involvement., • Support your departments with measured and sensible Metrics, which will become consolidated into accurate and detailed Reporting, presented daily, weekly, monthly, quarterly, etc. Departmental and Positional Responsibilities: Intimately Know Our Products, Our Equipment’s Capabilities, Our Markets, Our Customers- and their needs; • Structure a 3 Year Plan for New Products, engaging Marketing and Consumer Trends;, • Create and exercise a Stage-Gate Process that will collaborate with supporting personnel and departments to ideate and imagineer the development and subsequent commercialization of new bakery products, including, but not limited to, new breads, bread-based snacks, filled / folded handheld breads, par baked breads, frozen dough, non-flour based baked goods and sweet goods;, • Develop and maintain quality control procedures for test raw materials, ingredients, and finished products to ensure consistent product quality and food safety during testing and development., • Establish proper laboratory and kitchen procedures to ensure the proper testing of products, use of equipment, delivery of samples to customers and preparation of presentations for visiting customers and clients., • Manage sensory evaluations and laboratory testing to monitor and improve product attributes and shelf life., • Stay updated with food safety regulations and industry standards to ensure products meet all necessary requirements., • Work with Baking, Processing and continuous Improvement to provide improvements and/or savings to products and production;, • Attend, present and represent the company at food shows, supplier/customer events, Customer presentation and/or ‘pilot’ runs;, • Travel to different markets, both domestic and global, to keep abreast with changing Consumer trends; QUALIFICATIONS • College educated, though no specification as to major;, • Baking or Culinary Scientist or Equivalence, • ‘Foodie’ Friendly, • Project-Management highly skilled, • Minimum 15 years of experience working within the Food Industry; minimum 10 years of those years involved in R&D/Innovation; vast experience working with ‘Bakery’ _ COMPENSATION • $165K to $200K Base Annual Salary, pending Qualifications, • Incentives based on Scorecard and/or mutually agreed Goals and Timelines, • Medical, 401K Programs, • 20 PTO Days annually, • Major Holidays This is a growth opportunity with an industry leader!

Job Title-: Data Scientist Duration: 6-month contract with potential for full-time conversion Location-: Newark, NJ (Hybrid) Department: Data Science Team – Long-Term Care (Fraud, Waste, and Abuse Detection) Description-: The team is seeking a Data Scientist with strong MLOps and full-stack data experience, capable of both developing models and supporting production deployment within an AWS environment. Key Focus Areas: • Fraud, Waste, and Abuse (FWA) detection in long-term care, • Strong understanding of business processes and ability to translate data insights into business logic, • Emphasis on candidates who can learn and adapt to new business contexts Technical Requirements Core Skills: • Programming: Python (required), • MLOps / Full-Stack Data Science:, • Experience in deploying machine learning models to production, • Proficiency in containerization (Docker, etc.), • Working knowledge of AWS (specifically SageMaker, pipelines, access management), • Understanding of machine learning pipeline orchestration Preferred Tools/Platforms: • AWS ecosystem (SageMaker, Bedrock, etc.), • Exposure to LLMs (Large Language Models) or generative AI is a plus Nice-to-Have: • Background or understanding of insurance or healthcare data, • Hands-on experience with fraud detection systems Experience & Education • Education:, • Bachelor’s degree acceptable with strong professional experience, • Master’s or PhD preferred but not a hard requirement, • Experience Level:, • Approx. 6 years of relevant data science experience Day-to-Day Responsibilities • Focus primarily on model development (core function), • Collaborate closely with machine learning engineers for production deployment, • Engage in end-to-end data science processes:, • Data exploration and modeling, • Model validation and tuning, • Assisting with model deployment and monitoring, • Work closely with business stakeholders to understand fraud patterns and operational nuances Team Structure • Reports to Hiring Manager, • Collaborates with:, • Senior Data Scientists (peer mentors and project leads), • Machine Learning Engineers (for deployment/product ionization), • Business partners (for domain understanding and data interpretation) Key Insights • Preference for candidates who are strong in MLOps even if slightly less advanced in pure data science theory., • The ability to grasp new business models quickly is critical, especially for FWA detection., • Ideal candidate demonstrates hands-on experience with both model building and AWS-based deployment., • Someone with experience using large language models or recent GenAI technologies would stand out., • Environment/Tools: AWS (SageMaker, Bedrock, etc.), • Programming Languages: Python required

About the Role Join our expanding AR&D team as an AR&D Scientist II. This role is responsible for method development, validation, and analytical support activities for both drug substances and drug products in a dynamic, fast-paced environment. This role requires strong technical proficiency in chromatographic and spectroscopic techniques, combined with a solid grasp of regulatory requirements. Mentor and guide junior scientists while collaborating closely with cross-functional teams in Formulation, QC, Regulatory, and Manufacturing. Responsibilities • Develop and optimize analytical methods (HPLC, UPLC, GC, Dissolution, UV, FTIR, KF, ICP, PSD, IVRT/IVPT etc.) for APIs and finished dosage forms., • Perform and document method validation per USP and ICH guidelines., • Design and execute stability-indicating methods; support stability protocol creation and data review., • Maintain and troubleshoot analytical instruments; ensure calibration and qualification compliance., • Review and approve analytical data, notebooks, and reports under GMP/GLP expectations., • Provide analytical support to formulation development, scale up, and tech transfer., • Perform other duties assigned commensurate with position. Qualifications • Master’s or Ph.D. in Chemistry, Pharmaceutics, or a related scientific discipline., • 5+ years of analytical development experience, with a proven track record in the pharmaceutical industry., • Deep understanding of cGMP with hands-on experience writing quality investigations., • Proficient in using Empower Chromatography software including custom field calculations., • Strong math skills, clear communication, and proven capability to work productively both independently and within collaborative teams.

AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more.AI systems learn, reason, and perform.Our platform identifies and vets top talent through an AI recruiter

You'll need a deep background in immunology, thymic biology and iPSCs.Lead a cutting-edge team developing iPSC-derived thymic epithelial cells (iTECs) and thymic organoids to rejuvenate the aging immune system.Contribute highly practical and readily translatable thymic regeneration, immune reconstit

We're using machine learning to predict cancer signatures to enable early intervention when cancer is most treatable.Lead a cutting-edge cancer biomarkers group to detect cancer at its earliest stages.Contribute highly practical and readily translatable pan-cancer screening/early detection, diagnost

We're hiring an exceptionally talented.You'll need extensive bench skills, and the ability to emphasize practical, innovative research approaches to tinnitus and age-related hearing dysfunction in a personalized medicine paradigm.Successful integration of audiology knowledge at the molecular, cellul

InVitro Cell Research (ICR) is dedicated to solving some of the most challenging problems in aging and age-related disease. We're hiring Associate Research Scientists to join our dynamic, team-oriented environment engage in cutting-edge, high-impact biomedical research. With us, you'll get to: • Research and develop cell-derived interventions for aging and age-related disease, • Explore iPSC-derived extracellular vesicles and organoids for regenerative medicine potential, • Collaborate with other ICR scientists in cutting-edge preventive and regenerative medicine research projects Please apply if you have: • A BS or MS in a biomedical field, • A solid grasp of modern molecular and cell biology, • Mammalian cell culture experience (required), preferably with iPSCs or other stem cells, • Experience with extracellular vesicles, qPCR and cell-based assays, • Even if you don't meet all of these criteria, please apply And you'll need: • An easygoing, friendly personality, • The ability to work in the United States without sponsorship If you don't combine your cover letter with your CV or resume when you apply through LinkedIn, after you apply please send your cover letter only to: with "Cover [Your name]" as the Subject line. Position title and compensation are commensurate with experience. The compensation ranges listed below are starting ranges. Starting base pay range: $70,000/yr - $90,000/yr Starting bonus range: $5,000/yr - $12,000/yr Why join ICR? • EXERCISE your intellect in challenging and rewarding science, • ENTER an career dedicated to a mission that matters to everyone, • ENGAGE in cutting-edge regenerative medicine research, • EXCELLENT research environment, salaries and relocation expenses (fully covered!)

AI & LLM Applications Scientists.ICR scientists’ workloads, improving both quality and productivity across the organization.The ideal candidate has a deep, practical understanding of modern AI and large language models, including how they work, what they can and cannot do, and how to most wisely i

An MS or PhD in a Biomedical Science and extensive experience with computational biology, bioinformatics and data science. Experience incorporating AI tools into bioinformatics workflows. Conduct complex bioinformatics analyses on large genomics, transcriptomic, proteomic, metabolomic, and lipidomic

We're looking for talented scientists to join our Functional Genomics group. Tasked with going "from SNP to phenotype," our Functional Genomics scientists connect genomic variants with organismic-level symptoms through molecular, cellular, tissue and animal models. Collaborate with other ICR scien

Bachelor’s Degree in Physical/Environmental Sciences or a similarly related field. Collecting and interpreting environmental sampling data, and providing field consultations as required. Lead teams performing project tasks, both in the office and field locations.

Absci is looking for a Senior/Staff AI Scientist to advance and deploy protein design models for antibody drug design. Provide our AI Scientists with access to industry-leading compute resources, enabling large-scale experimentation for model training and deployment. Maintain our own Wet Lab, enabli

Deep theoretical and practical expertise in computer vision, with strong foundations in areas such as representation learning, visual recognition, image or video generation, multimodal learning, and large-scale model training. We’re looking for a Senior Staff Machine Learning Scientist to help us

As a Technical Support Scientist, you’ll play a key role in delivering a world-class customer experience for 10x Genomics products. You will be part of the Global Support Team, providing scientific expertise, troubleshooting guidance, and technical content development that empowers our customers��

Job Description Overview Join a leading healthcare laboratory as a Medical Laboratory Scientist, where your expertise will directly impact patient care through precise and accurate laboratory testing. This role offers the opportunity to work in a dynamic environment, utilizing your technical skills to analyze specimens, review test results, and ensure quality standards are met all while contributing to a team committed to excellence in diagnostic services. Responsibilities Follow established procedures for specimen handling, test analysis, reporting, and record keeping of patient test results. Maintain records demonstrating proficiency testing samples are processed similarly to patient specimens. Analyze specimens using approved testing techniques in accordance with department SOPs. Review and release test results accurately while adhering to quality control policies. Document and perform instrument calibrations, maintenance, and any corrective actions taken during testing. Follow safety guidelines outlined by CLIA, HIPAA, OSHA, and other relevant standards to ensure a safe working environment. Identify and resolve issues affecting test performance or reporting, escalating when necessary. Report STAT or critical results promptly to clients following departmental procedures. Maintain comprehensive records of all testing performed and ensure reagents/test kits are properly labeled with received, opened, and expiration dates. Participate in ongoing training, safety sessions, and departmental meetings to stay current with procedures and regulations. Assist in inspections and participate in quality assurance activities as needed. Maintain the general appearance of the laboratory workspace, ensuring cleanliness and organization. Required Skills Solid understanding of basic and high-complexity laboratory testing procedures. Strong computer skills with the ability to work across multiple laboratory information systems. Knowledge of quality control (QC) and quality assurance (QA) practices. Ability to review, interpret, and accurately report laboratory test results. Excellent attention to detail and problem-solving skills to identify and address testing issues. Additional Skills & Requirements Bachelor’s degree in Medical Technology, Chemistry, Biology, or a related field preferred; or an Associate degree in Laboratory Science or Medical Technology. Certification as a Medical Technologist (MT) or Medical Laboratory Technician (MLT) from recognized organizations such as ASCP or AMT is highly desirable. Minimum of one year of clinical laboratory experience, preferably in high-complexity testing. Strong interpersonal skills with the ability to interact professionally with team members and clients. Ability to prioritize multiple procedures and handle shifting demands efficiently. Must be able to work in a clinical laboratory setting and comply with safety regulations. Perform your role with precision and professionalism to support accurate diagnostics and quality patient care. Embrace this opportunity to advance your career in a reputable clinical laboratory environment. About Us: All Medical Personnel streamlines hiring to get you back to the work you love. Established in 1990, our staffing business lines place locum tenens, travel nursing, allied health, and clinical laboratory professionals from coast-to-coast. We believe in focusing and uplifting the hiring process, with a deep understanding of the unique challenges you face. We are here to ensure each experience with us is simplified, elevated, and impactful, for you and your patient. Please reference Job number: 301626

Shift: Monday through Friday, 10:30 AM - 7:00 PM\n \n Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. \n \n This is a full-time, onsite, Scientist 1 position located in Fairfield, NJ, Monday through Friday, 10:30 a.m. - 7:00 p.m. \n \n Compensation: $21.00 per hour \n \n The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate’s geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer. \n \n Make an Impact. Build a Career. \n \n At Pace®, everything we do is built upon an unwavering commitment to making the world a safer, healthier place. Since 1978, we’ve continued developing innovative practices that drive sustainability and empower our partners with accurate quality data at every critical moment and milestone. \n \n That's why we need you -- your curiosity, your talents, and your drive -- to help us advance this important work, and your career. \n \n We’re seeking curious, motivated individuals who are passionate about protecting our environment and the communities we serve. If you’re looking to develop your skills, contribute to meaningful scientific work, and build a long-term career in environmental science, Pace® could be the perfect place for you. \n \n Find Your Place at Pace® \n \n Join us as a Scientist and put your passion for science to work in our environmental testing laboratory. In this role, you’ll conduct hands-on analysis within our laboratories, helping ensure the integrity and quality of environmental data that impacts communities and ecosystems. \n \n What You’ll Do \n\n • Work with instruments such as GC, HPLC, ICP and more \n\n\n, • Analyze air, water, and soil samples using established chemistry and biochemistry methods looking for environmental contaminants \n\n\n, • Review and interpret the results from the sample analysis \n\n\n, • Accurately document procedures, observations, and results to maintain high-quality, organized laboratory records \n\n\n, • Clean, maintain, and calibrate laboratory instruments and equipment \n\n \n What You’ll Bring \n\n • Bachelor’s degree in Chemistry, Biochemistry, or other science related degrees — or an equivalent combination of education, training, and experience. We are happy to provide training! \n\n\n, • Ability to work effectively in a laboratory environment, including standing for extended periods, working around strong odors, and wearing required PPE (lab coat, safety glasses, gloves—all provided by Pace®) \n\n \n PHYSICAL/MENTAL REQUIREMENTS: The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. \n \n Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone. \n \n WORKING ENVIRONMENT: \n Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gases, noxious odors, and related items in a lab and sample setting. \n \n Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. \n \n Benefits \n When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. \n \n Equal Opportunity Employer \n Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Job DescriptionQuality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle. • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients., • Support routine GMP testing as assigned. Mentor and train team members, • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements., • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports., • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data., • Identify, evaluate, and implement continuous business process improvements., • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS)., • Provide support during laboratory investigations., • Train QC personnel during method transfer and validation. Provide support during equipment qualification., • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices., • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures., • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.REQUIREMENT, • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products., • 8-10 years of experience in the areas of method development, validation, and transfer., • Direct GMP Experience., • Proficiency in project management skills and tools., • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc., • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs., • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required., • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution., • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team., • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction., • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external., • Must be familiar with GMP lab environment and Aseptic techniques.Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Proven fluency with AI-native developer and analyst tooling — Claude, Claude Code, Cursor, Hex AI Agent, Omni AI, or equivalent — used in production analytical workflows.

Collaborate closely with cross-functional teams comprising Disease Biologists, Structural Biologists, Computational Biologists, and Wet Lab scientists to define and address the problem space within specific indications. Actively develop organizational talent through coaching and mentoring other Scie

As a Principal Applied Scientist at Upstart, you will help define the long-term technical direction for some of Upstart’s most important offer optimization and conversion modeling systems. Partner with scientists, engineers, and cross-functional stakeholders to translate analytical insights into d

Perform large-scale data processing and analysis using Python, SQL, Databricks, Spark, and distributed computing across structured and unstructured datasets. Mentor other data scientists and analysts, and contribute to technical standards, data governance, and MLOps best practices. We're looking for

We are looking for a data scientist who will bring a deep understanding of our sportswriting, our in-game experience, and the way our subscribers use The Athletic to help us make our best-in-class product even better.In this role, you will work closely with our data, product, growth, and engineering

We are seeking a Principal Clinical Scientist to lead execution of key components of clinical development for our early cancer detection (ECD) program. You will serve as a clinical science lead within cross-functional teams – partnering with Clinical Operations, Biostatistics, Medical Affairs, and

At Rad AI, we’re on a mission to transform healthcare with artificial intelligence.Founded by a radiologist, our AI-driven solutions are revolutionizing radiology—saving time, reducing burnout, and improving patient care.With one of the largest proprietary radiology report datasets in the world,

Job Description T&M Associates is seeking a highly motivated and experienced Environmental Scientist or Engineer to join our NJ Environmental Market. The successful candidate will serve as a senior technical specialist within the remediation practice, providing advanced technical expertise and independent decision-making on complex environmental projects. This position will include leading technical execution, developing solutions to challenging environmental issues, and supporting project teams in delivering high-quality, compliant remediation services. Key Responsibilities • Serve as a senior technical specialist for environmental remediation projects involving site investigation, remedial design, environmental data evaluation, regulatory compliance, permitting, and long-term site management., • Independently evaluate environmental conditions, analyze technical data, and develop recommendations and solutions for complex remediation challenges., • Lead technical execution of projects, including preparation and review of work plans, technical reports, permit applications, and regulatory submittals., • Provide technical guidance and mentorship to engineers and scientists in support of project delivery and professional development., • Serve as Project Manager on a variety of environmental investigation projects with a focus on those requiring compliance with the NJDEP’s Site Remediation Program., • Collaborate with other Project Managers, LSRPs, Engineers, and Scientists to ensure projects are completed in accordance with technical standards, regulatory requirements, and client objectives., • Perform technical reviews and support QA/QC efforts to ensure consistency, accuracy, and compliance across project deliverables., • Prepare technical and cost proposals, evaluate project risks, and contribute to development of competitive solutions for client pursuits., • Maintain knowledge of applicable environmental regulations, emerging technologies, and industry best practices. Qualifications • Bachelor's degree in Environmental Science, Environmental Engineering, Geology, Hydrogeology, or related discipline required., • PE, PG, or equivalent professional licensure preferred., • LSRP license or willingness to pursue the LSRP examination preferred., • 8+ years of environmental consulting experience with demonstrated expertise in site investigations, remediation systems, soil and groundwater treatment, environmental compliance, waste management, remediation optimization, and long-term operations and maintenance., • Demonstrated ability to independently manage technical assignments and develop practical solutions to complex environmental challenges., • Experience coordinating project teams and providing technical guidance to junior staff., • Familiarity with SRRA, ARRCS, RCRA, CERCLA, TSCA, and related state and federal regulatory programs., • Strong understanding of local, state, and federal environmental requirements and permitting processes., • Excellent written and verbal communication skills., • 40-Hour OSHA HAZWOPER training with annual refresher preferred., • Occasional travel and collaboration across offices required. T&M Associates is committed to pay transparency and equitable compensation practices in compliance with applicable laws, including the New Jersey Equal Pay Act. T&M estimates that the salary range for this position will fall between $95,000- $120,000. The actual salary offered may vary within this range, depending on a variety of factors including the candidate’s experience, educational qualifications, specific skills and knowledge, as well as internal pay equity and geographic location. T&M Associates offers a competitive and comprehensive benefits package designed to support the health, well-being, and professional growth of our employees. Benefits include comprehensive insurance (medical, dental and vision), a 401(k) with company match, paid time off, flexible work schedules, wellness programs, and professional development opportunities — all within a people-first, award-winning hybrid work environment. See more details about benefits here. If this sounds like a company you want to be part of then apply now! New Hires must have documents indicating they are eligible to work in the United States. EEO/AA Employer. For California based applicants, our CCPA-CRPA Privacy Notice can be found on our Careers page at www.tandmassociates.com LI-HYBRID

We are looking for a Staff Data Scientist to join our Safety Insights Data Science team. In this role, you will partner closely with Safety Product, Engineering, and Machine Learning teams along with fellow Safety data scientists, to shape strategy, product development, define and evolve safety metr

Leadership in data science: experience leading cross-functional teams of data scientists, data engineers, and data or cost analysts, and defining a data strategy aligned to organizational goals. Knowledge and experience performing cost estimating and analysis on major defense systems, including typi

This role will support the assigned Clinical Trial Lead with the design and execution of key elements of the Clinical Development Plan (clinical study or studies) with minimal to moderate level of supervision. This position may support clinical development planning (collaboration with Clinical Devel

Additionally, the Data Scientist is expected to present insights and recommendations to non-technical audiences and explain the benefits and impacts of the recommended solutions. The Data Scientist will be a key member of the.

Our core values define who we are as an organization and serve as the foundation of our code of ethics.Arbor Research expects all employees to embody and demonstrate in our day-to-day work.We expect each staff member to learn from and teach one another and ask each to exhibit curiosity and respect

Job DescriptionScientist – Engineer, MSAT The Scientist-Engineer, MSAT performs process and analytical experimental studies as part of a team that is effectively delivering cell therapy services to clients in accordance with defined scope of work, timelines, and budgets. This includes leading projects in process development, technology transfer and continuous improvement of our client's novel manufacturing processes. Our goal is to support our clients in developing commercially viable cell therapy products, so that they can become accessible to all. • Accountable for the design and execution of experimental studies in the laboratory, for example:, • Perform laboratory experiments for client projects, • Perform analytical testing for client projects, • Preparation and scheduling of laboratory equipment for experiments, • Provide technical leadership of client products during manufacturing and development, for example:, • Direct technical communication with clients during manufacturing and development, • Support manufacturing in identifying and resolving manufacturing process constraints, • Lead the generation of manufacturing and development documentation, for example:, • Generating experiment protocols and reports for development projects, • Generating draft batch records and other manufacturing documentation, • Generating manufacturing risk assessments, such as FMEA, • Perform data analysis to reach actionable conclusions, for example:, • Compile and analyze experimental data, • Present experimental data internally and externally to clients, • Supervise direct reports.REQUIREMENTS, • Bachelor's degree in relevant life science or engineering discipline, • Minimum of 3 years' experience in aseptic cell processing, cell culture and cell analytics under the guidance of scientific protocols, • Demonstrated ability to deliver projects to specific timelines and budgets, • Experience in working effectively and delegating tasks in a team-based environment, • Demonstrated ability in technical writing and the preparation of, protocols and reports, presentations and/or other communications, • Basic understanding of the technical principles, theories and concepts of cell therapy or similar products, • Aseptic processing, Good Manufacturing Practice (GMP), communication skills, specific process and analytical equipment, • This job may require occasional evening and weekend work.

Job DescriptionQuality Control Manager The Quality Control (QC) Manager plays a pivotal role in ensuring that QC is effectively serving in its support role to clinical and commercial production. The QC Manager will ensure that analytical testing for process check points, stability, and release assays are being carried out to certify that quality standards are upheld for all products produced at the facility. The goal is to ensure that the Quality Control group and company is constantly moving towards fulfilling its short-term and long-term objectives and does not diverge from its strategic guidelines. Under the direction of the VP, Global Quality Head, responsibilities of the QC Manager will include but are not limited to: • Leading, hiring, developing, training, and evaluating QC personnel, • Devising sound hiring strategies based on business needs, • Supervising and overseeing QC personnel in their roles for safe and efficient verification, approval, release/disposition of HCATS and/or client products/materials, • Delegating responsibilities and supervising the work of laboratory personnel, while providing guidance and motivation to drive maximum performance, • Ensuring and promoting compliance with applicable cGMP and GTP regulations, while ensuring compliance with company and client methodologies, • Assuring alignment and efficient continuity in laboratory practices between sites, • Serving as approver in investigations while overseeing timely closure of deviation reports, change controls, CAPAs, and applicable batch records, • Ensuring completion of all client QC requirements related to GMP cellular products and/or materials, • Overseeing QC role in material dispositions via deviation reporting system, CoAs, and/or client-based systems, if applicable, • Prioritizing, scheduling, and managing multiple projects and resources simultaneously, • Monitoring effectiveness of quality systems, change control activities and their completion, for both, internal and client audit findings, • Evaluating and investigating customer complaints and deviations; coordinating corrective and preventive actions as they relate to the Quality Control function, • Delegating maintenance, tracking, and trending aspects of the deviation reporting system, • Developing and maintaining Key Performance Indicators (KPIs) for laboratory testing, • Interfacing with vendors, suppliers, and in-house production personnel to ensure effective corrective and preventive actions are implemented for recurring product/process discrepancies, when applicable, • Interfacing with management at all levels for alignment on significant deviation resolution and corrective action implementation, • Delegating development, revisions, and implementation of Standard Operating Procedures as related to Quality Control activities, • Participating in and tracking group budget setting and cost containment drives, • Communicating and maintaining trust relationships with senior management, business partners, and clients, • Ensuring company policies and legal guidelines are communicated top-down in the company and that they are followed at all times, • Completing projects and special tasks as assigned by the Global Quality Head, • Off-schedule shifts during weekends and holidays based on business requirements a possibility, • On-call presence preferred while physical personal presence is not possible, • Candidate will oversee QC Scientist and QC Associate I, II, and III roles. The QC Manager will delegate responsibilities to direct reports to achieve the requisite business needs, while providing ongoing support to Manufacturing processes.REQUIREMENTS, • BA/BS/MS in a science or relevant field required, • Master’s in Business Administration or relevant field will be preferred, • 7 – 10 years’ experience in the pharmaceutical, biologics or related industry, • Prior cGMP experience required, • Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment a must, • Experience in Flow Cytometry is a must, • 5 + Years experience leading a team is a must. Proven ability to lead, coach, and motivate employees, clearly communicate job requirements and effectively manage performance of assigned staff, • Sound understanding of current Good Manufacturing Practices (cGMPs), • Working knowledge of routine QC laboratory procedures such as flow cytometry and CBC analysis, endotoxin testing, equipment and systems, and understanding of production processes and validation, • Prior experience with reviewing Standard Operating Procedures, work instructions, protocols, methods, method validations preferred, • Proven experience in a supervisory or managerial position, • Demonstrable experience in developing strategic plans based on business needs, • Strong understanding of Quality Control in pharmaceutical/biotechnology/biologics industries, • Thorough knowledge of market changes and forces that influence the company, • Proficient with computer software: Microsoft Office, Visio, • Strong written, oral, and presentational skills, • Strong knowledge of QC Analytical testing methodologies, philosophies, method validation and method transfers, • Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review, • Excellent organizational and leadership skills, • Excellent communication, interpersonal, and presentation skills, • Outstanding analytical and problem-solving abilities, • Strong business acumen, • Ability to think strategically, tactically (detail-oriented), and advise personnel in an effective manner, • Candidate must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilitiesWhile performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy. Must have the ability to work in a team-oriented environment and with clientsMust be able to handle the standard/moderate noise of the manufacturing facility Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Shopmonkey has the structured data and workflows to support serious data science work, and you'll have the rare opportunity to help build the analytical and ML foundation from the ground up, shaping how data-driven decision making scales alongside a maturing platform and defining what the future of

Are you looking to join an organization that is growing and dynamic? What about a high-energy, collaborative environment that rewards hard work?.Held is a global consulting firm that combines technical, scientific, financial, and strategic expertise to advise clients seeking to realize value and mit

We are looking for a skilled Data Scientist who will help us analyze large amounts of raw information to find patterns and use them to optimize our performance. Data Scientist or Data Analyst position.

Stira Pharmaceuticals, LLC, located in Fairfield, NJ, seeks a motivated and detail-oriented Analytical Scientist for a full-time, on-site role.

Stira Pharmaceuticals, LLC, located in Fairfield, NJ, seeks a motivated and detail-oriented Analytical Scientist for a full-time, on-site role.

The team is seeking a Data Scientist with strong MLOps and full-stack data experience, capable of both developing models and supporting production deployment within an AWS environment. Senior Data Scientists (peer mentors and project leads). Background or understanding of insurance or healthcare dat

Join a leading investment firm as a Lead Data Scientist, partnering with Machine Learning Engineers, Data Engineers, Data Analysts, and cross-functional teams to build AI and Machine Learning products. Provide deep technical leadership across a portfolio of high-impact data science initiatives. Data

The team is seeking a Data Scientist with strong MLOps and full-stack data experience, capable of both developing models and supporting production deployment within an AWS environment. Senior Data Scientists (peer mentors and project leads). Strong understanding of business processes and ability to

Join a leading investment firm as a Lead Data Scientist, partnering with Machine Learning Engineers, Data Engineers, Data Analysts, and cross-functional teams to build AI and Machine Learning products. Provide deep technical leadership across a portfolio of high-impact data science initiatives. Data

Stira Pharmaceuticals, LLC, located in Fairfield, NJ, seeks a motivated and detail-oriented Analytical Scientist for a full-time, on-site role. The successful candidate will develop, validate, and transfer analytical methods for drug substance and drug products with a specific focus on related subst

Company DescriptionSonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services.Job DescriptionRequired Skills:Overall Responsibilities:• 10 to 15 years of experience with PhD or MS. • Hands on experience on machine learning algorithms (Neural Networks, Support Vector Machines, Random Forest, logistic regression, clustering, classification, Naive Bayes, association rules, Collaborative Filtering, recommendation techniques, pattern recognition etc.) Qualifications• Strong experience in Text Mining, NLP – Natural Language Processing • Hands on experience on model development lifecycle • Strong hands on experience on R, Python, IBM SPSS • Excellent communication skills and ability to express the statistical model output properly to senior management • Logistics experience desired – shipment processing • Cognitive computing desirable Additional Information** U.S. citizens and those who are authorized to work independently in the United States are encourage to apply. We are unable to sponsor at this time.Note:-This is a Contract job opportunity.Only US Citizen, Green Card Holder, GC-EAD, H4-EAD, L2-EAD, H1B and TN Visacan apply.No OPT-EAD candidates please.Please mention your Immigration Status while applying .All your information will be kept confidential according to EEO guidelines.SummaryType: Full-timeFunction: Information TechnologyExperience level: AssociateIndustry: Information Technology And Services

Stira Pharmaceuticals, LLC, located in Fairfield, NJ, seeks a motivated and detail-oriented Analytical Scientist for a full-time, on-site role. Exceptional problem-solving capabilities and experience in leading analytical investigations. We offer comprehensive services including Analytical R&D, Pref

You will mentor scientists, shape toxicology solutions, and drive validation in a fast-paced startup setting.