Trabajos scientist en White Plains, New YorkCrear alertas

You will design and write programs for data extraction, segmentation and statistical analysis on large population datasets using languages such as R, Python, SQL, Hive, and Pig on Linux, PC, and mainframe computing platforms. At TransUnion, this team reports to a Director of Data Science & Analytics

Medical Solutions Direct Hire is seeking a Clinical Lab Scientist (CLS) for a job in Hartsdale, New York. Job Description & Requirements • Specialty: Clinical Lab Scientist (CLS), • Discipline: Allied Health Professional, • Start Date: ASAP, • Duration: Ongoing, • 37 hours per week, • Shift: 12 hours, days, • Employment Type: Staff Medical Solutions Direct Hire Job ID #1119462. About Medical Solutions Direct Hire At Medical Solutions, we’re people who care, helping people who care. No matter how you look at it, there’s a whole lot of care going on in our world and that’s just the way we like it. What do we do? Medical Solutions is one of the nation’s largest providers of total workforce solutions in the healthcare industry, connecting nurses and allied health clinicians with hospitals and healthcare systems across the country and around the corner. Through our family of brands, we also serve a segment of clients outside of the healthcare space. And we’re the very best at what we do. You’ll love our culture that’s filled with heart and soul. As a company and employer, we’re sincerely and unabashedly us. We lead as humans first and believe the unique qualities of each team member make us better together. We share a purpose for helping others and the drive to make a difference. And we offer endless opportunities for personal and professional growth, throughout your career. At Medical Solutions, you’ll find a great place to work and a career home. We’ve received Best Places to Work awards, landed top industry awards, and received accolades for the impact we’ve made in business and within our community. But the only way to really get to know us, is to join us. We think you’ll fit right in.

Job Description Melissa Owens| President P: (386)339-0839 |E: melissa@alliedsearchpartners.com Schedule a Meeting: https://calendly.com/melissaowens Allied Search Partners Allied Search Partners is back by two decades of healthcare staffing excellence. We are a trusted healthcare staffing firm supporting medical and dental offices nationwide. We partner with private practices and corporate healthcare organizations to provide reliable, well-supported temporary professionals—while prioritizing fair pay, consistency, and respect for our workers’ time. Our team offers 24/7 scheduling support and access to shifts through our efficient temp scheduling application. Unlike traditional staffing agencies that push one-off shifts to large candidate pools, we focus on long-term relationships with both our healthcare facilities and our workers. Job Description Job ID: 3563480 Job Title: Histotechnician Location: South Westchester County, NY Shift: • Per Diem: Varied, • Full Time: Monday to Friday 2pm to 10pm Job Summary: Performs Histological technical procedures using manual and automated techniques to achieve high-quality Pathology slides for review by Pathologists. Job Responsibilities: If Clinical Laboratory Scientist • Understands and adheres to the performance standards, policies, and behaviors, • Laboratory testing personnel responsibilities include:, • Following the laboratory’s pre-analytic and analytic procedures and maintaining records of these tests, • Maintaining records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens, • Adhering to the laboratory’s quality assurance procedures, including documenting all:, • Quality control activities including quality control testing and calibrations, • Instrument and equipment verifications, • Maintenance and preventative maintenance, • Following the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established performance specifications, • Identifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratory’s established performance specifications, • Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing., • Notifies and documents clinicians and patient units of all critical values and maintains the laboratory STAT turn around time requirements., • Participates in regulatory readiness for CAP, AABB, NYSDOH, and Joint Commission., • Maintains 12 Continuing Education credits per year., • Understands and participates in standard operating procedures, proficiency testing, inspection audits, quality program including reporting non-conformances., • Evaluates test results for abnormalities and confirms those results per department protocols where required., • Participates in validations, training, and competency assessments as required., • Responsible for inventory management of lot numbers, expiration dates, labeling, and QC requirement., • Completes all annual mandatory training, in-services, and ongoing education as required., • Performs other duties as assigned., • Section testing training and competency assessments are maintained by the section laboratory supervisor for all assigned disciplines If Histotechnician: • Understands and adheres to the Performance Standards, Policies and Behaviors., • Performs all other related duties as assigned., • Performs embedding and sectioning of tissue blocks following section protocol as to biopsies, routine, etc., • Evaluates routine stain daily (H&E), reviews for inconsistencies and confirms and/or corrects before releasing slides., • Performs Special Stains and evaluates for inconsistencies and confirms and/or correct before releasing slides, Checks positive controls and documents on run log(s)., • Performs Immunohistochemistry, and evaluates for inconsistencies and confirms and/or correct before releasing slides, Checks positive and negative controls and documents on run log(s). Qualifications: If Clinical Laboratory Scientist • Current NYS License as a Clinical Laboratory Technologist, NYS PA License required., • Education in accordance with the NYS Office of Professions and CLIA requirements of testing personnel., • Preferred with ASCP Certification. If Histotechnician • NYS Clinical Laboratory Technician License or NYS histotechnician license required., • Degree in Medical Technology or related science preferred with one year of relevant hospital experience in Histology., • ASCP preferred Core Competencies: • Flexibility, • Organized, • Adaptability, • Attention to Detail, • Stress Tolerance Work Environment: May be exposed to chemicals necessary to perform required tasks. Any hazardous chemicals the employee may be exposed to are listed in the hospital’s SDS (Safety Data Sheet) data base and may be accessed through the hospital’s Intranet site (Employee Tools/SDS Access). A copy of the SDS data base can also be found at the hospital switchboard, saved on a disc. Required Skill: • Must be able to remain stationary for extended/prolonged periods, • Must be able to constantly operate computer, equipment and other devices, • Position requires ability to concentrate on fine detail with interruptions and attend to tasks for more than sixty (60) minutes at a time. Note: The responsibilities and tasks outlined in this job description are not exhaustive and may change as determined by the needs hospital.

Job Description Melissa Owens| President P: (386)339-0839 |E: melissa@alliedsearchpartners.com Schedule a Meeting: https://calendly.com/melissaowens Allied Search Partners Allied Search Partners is back by two decades of healthcare staffing excellence. We are a trusted healthcare staffing firm supporting medical and dental offices nationwide. We partner with private practices and corporate healthcare organizations to provide reliable, well-supported temporary professionals—while prioritizing fair pay, consistency, and respect for our workers’ time. Our team offers 24/7 scheduling support and access to shifts through our efficient temp scheduling application. Unlike traditional staffing agencies that push one-off shifts to large candidate pools, we focus on long-term relationships with both our healthcare facilities and our workers. Job Description Job ID: 3563563 Job Title: Clinical Laboratory Scientist - Microbiologist Location: South Westchester County, NY Shift: Clinical Laboratory Scientist • Per Diem: Every other weekend, 8am-4pm Clinical Laboratory Scientist-Microbiology • Full Time: Monday to Friday. 8am - 4pm, Alternate Weekends & Holidays Job Summary: The Clinical Laboratory Scientist performs laboratory testing using both manual and automated techniques. Performs Bacteriology, Parasitology, Virology, Mycology, Mycobacteriology, Susceptibilities, and Molecular testing and other duties as assigned. Job Responsibilities: • Understands and adheres to the performance standards, policies, and behaviors, • Laboratory testing personnel responsibilities include:, • Following the laboratory’s pre-analytic and analytic procedures and maintaining records of these tests, • Maintaining records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens, • Adhering to the laboratory’s quality assurance procedures, including documenting all:, • Quality control activities including quality control testing and calibrations, • Instrument and equipment verifications, • Maintenance and preventative maintenance, • Following the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established performance specifications, • Identifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratory’s established performance specifications, • Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing., • Notifies and documents clinicians and patient units of all critical values and maintains the laboratory STAT turn around time requirements., • Participates in regulatory readiness for CAP, AABB, NYSDOH, and Joint Commission., • Maintains 12 Continuing Education credits per year., • Understands and participates in standard operating procedures, proficiency testing, inspection audits, quality program including reporting non-conformances., • Evaluates test results for abnormalities and confirms those results per department protocols where required., • Participates in validations, training, and competency assessments as required., • Responsible for inventory management of lot numbers, expiration dates, labeling, and QC requirement., • Completes all annual mandatory training, in-services, and ongoing education as required., • Performs other duties as assigned., • Section testing training and competency assessments are maintained by the section laboratory supervisor for all assigned disciplines Qualifications: • Current NYS License as a Clinical Laboratory Technologist required., • Education in accordance with the NYS Office of Professions and CLIA requirements of testing personnel., • Preferred with ASCP Certification. Core Competencies: • Flexibility, • Organized, • Adaptability, • Attention to Detail, • Stress Tolerance Work Environment: May be exposed to chemicals necessary to perform required tasks. Any hazardous chemicals the employee may be exposed to are listed in the hospital’s SDS (Safety Data Sheet) data base and may be accessed through the hospital’s Intranet site (Employee Tools/SDS Access). A copy of the SDS data base can also be found at the hospital switchboard, saved on a disc. Note: The responsibilities and tasks outlined in this job description are not exhaustive and may change as determined by the needs hospital.

Job Description Job Title: Senior Associate Scientist Immunology & Inflammation Location: Tarrytown, NY Type: Contract Compensation: Up to $55.00 Work Model: Onsite – onsite Hours: 8 AM- 5 PM M-F Responsibilities • Perform tumor implantation in mice, tumor growth measurement, injections through various routes, general surgical techniques, and collection of blood and tissue samples, • Process tissues and purify immune cells, develop and perform in vitro cell-based bioassays (primary mouse and human cells), • Investigate components of the tumor microenvironment using multi-parameter flow cytometry, • Independently design, plan, and execute experiments, and maintain accurate electronic records, • Analyze, interpret, and communicate results during internal and external meetings, • Collaborate proactively with team members to coordinate complex in vivo experiments and support cross-functional efforts Requirements • A BS or MS degree with 5+ years of experience in immuno-oncology lab research, • Hands-on experience with handling mice, tumor models, tissue processing, flow cytometry, and cell-based bioassays, • Proficient in computer skills including Microsoft Office Excel, GraphPad Prism, and FlowJo/OMIQ, • Experience designing and executing experiments, analyzing data, interpreting results, and presenting findings in an impactful manner System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M3 Ref: #558-Scientific

Job DescriptionClinical Lab Scientist / HistotechnicianRole Summary Join a high-precision diagnostic team dedicated to clinical excellence and patient safety. Whether functioning as a Clinical Laboratory Scientist (CLS) or a Histotechnician, you will play a vital role in the diagnostic process. Histotechnicians will utilize both manual and automated techniques to produce high-quality pathology slides, while Clinical Lab Scientists will oversee the accuracy and quality of results across all phases of testing. This is an inspiring opportunity for a detail-oriented professional to contribute to a life-saving laboratory environment that values continuous learning and rigorous quality standards. Key Duties: Laboratory Operations (CLS): Follow pre-analytic and analytic procedures, maintaining meticulous records for proficiency testing and patient specimens. Histological Excellence (Histo): Perform embedding and sectioning of tissue blocks. Evaluate routine (H&E), special, and immunohistochemistry stains for accuracy before releasing slides. Quality Assurance: Adhere to all quality control activities, calibrations, and equipment verifications. Identify and document any deviations from performance specifications. Regulatory Compliance: Participate in regulatory readiness for CAP, AABB, NYSDOH, and the Joint Commission. Ensure all testing meets CLIA requirements. Clinical Collaboration: Confirm and communicate critical values to clinicians and patient units while maintaining strict STAT turnaround times. Inventory & Maintenance: Manage lot numbers, expiration dates, and labeling. Perform preventative maintenance on laboratory instrumentation. Continuous Growth: Participate in validations, training, and competency assessments, maintaining at least 12 continuing education credits per year. Required Qualifications For CLS Candidates: * Current NYS License as a Clinical Laboratory Technologist or NYS PA License. Education in accordance with NYS Office of Professions and CLIA testing personnel requirements. For Histotechnician Candidates: * NYS Clinical Laboratory Technician License or NYS Histotechnician License. Health & Safety: Flu Vaccine required (No exceptions). Skills: Proficiency in adhering to performance standards, policies, and professional behaviors in a laboratory setting. Desired Qualifications Certification: ASCP Certification is highly preferred for both roles. Education (Histo): Degree in Medical Technology or a related science preferred. Experience (Histo): One year of relevant hospital experience in Histology is preferred. Location and Work Type Setting: Hospital Laboratory Location: White Plains, NY Work Type: Full-Time | Direct Hire Schedule: Varied shifts available; Monday – Friday (9:00 AM – 5:00 PM or 2:00 PM – 10:00 PM). Total Rewards: Full suite of healthcare benefits and a robust retirement plan. If you're interested, please reply to this advertisement or directly email your resume to me at DSalgado@teemagroup.com or by calling/texting (949) 295-5951. I strive to reply within 48 hours. Looking forward to connecting with you soon. Thank you!

Job DescriptionJob Title: Associate Scientist Immunology & Inflammation Location: Tarrytown, NY Type: Contract Compensation: $40.00 - $45.00 per hour Contractor Work Model: Onsite Hours: 8 AM - 5 PM Responsibilities • Support respiratory and inflammatory disease research by executing in vivo experiments using mouse lung inflammation models and allorejection models, • Design, plan, and perform in vivo and in vitro assays, including tissue culture, cell-based assays, ELISA, multiplex assays (MSD/Luminex), and flow cytometry, • Process organs for immune cell isolation and analysis, • Maintain, expand, and modulate cells, evaluating results with biological and statistical software, • Analyze data using tools such as FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism, • Collaborate closely with cross-functional teams across the organization, • Document experimental procedures and results accurately Requirements, • BS/MS Degree in Immunology or related field; immunology experience is a plus but open to others, • Minimum of 3 years of industry experience in a relevant role, • Training in handling and care of mice, blood, and tissue sample collection and processing (strongly preferred), • Proficiency in tissue culture, cell-based assays, ELISA, multiplex assays, and flow cytometry, • Ability to independently plan and execute assays, • Experience with FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism, • Enthusiastic, driven, positive attitude, and effective communicator, • Ability to work in an innovative, team-driven environment System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Clinical Laboratory Scientist, Histotechnologist, or Histotechnician White Plains, New York Full-Time | Evening Shift | Monday–Friday A leading hospital laboratory is seeking a detail-oriented Clinical Laboratory Scientist or Histotechnician to join its Anatomic Pathology team. This role is open to candidates from either a Clinical Laboratory Science or Histology background with the appropriate New York State licensure and experience. This role is responsible for performing histological procedures and laboratory testing using both manual and automated techniques to produce high-quality pathology slides and accurate laboratory results that support patient diagnosis and care. This is an excellent opportunity for a licensed laboratory professional who thrives in a fast-paced clinical environment and is committed to quality, precision, and patient safety. Schedule • Full-Time, • Evening Shift, • Monday – Friday, • 2:00 PM – 10:00 PM Compensation • Salary Range: $94,000 – $121,000 annually, • Histotechnologist - $94,000 – $121,000 (based on full-time employment), • Histotechnician - $64,000 - $95,000 (based on full-time employment) Compensation is based on experience, education, certifications, and internal equity. Position Responsibilities Clinical Laboratory Scientist Responsibilities • Perform laboratory testing in accordance with established laboratory procedures and quality standards, • Ensure accuracy throughout pre-analytic, analytic, and post-analytic testing phases, • Maintain quality control, calibration, maintenance, and proficiency testing records, • Identify and troubleshoot testing issues and document corrective actions, • Notify clinicians and patient care units of critical values while meeting STAT turnaround requirements, • Participate in CAP, AABB, NYSDOH, and Joint Commission regulatory readiness activities, • Assist with validations, competency assessments, inspections, and quality improvement initiatives, • Maintain inventory control, lot tracking, expiration monitoring, and quality assurance documentation, • Complete continuing education requirements and mandatory training programs Histotechnologist / Histotechnician Responsibilities • Perform embedding and sectioning of tissue blocks according to established protocols, • Evaluate routine H&E stains and correct inconsistencies prior to slide release, • Perform and evaluate special stains and immunohistochemistry procedures, • Review and document positive and negative controls for all staining procedures, • Maintain adherence to quality standards, sterile practices, and laboratory policies, • Support pathology operations and workflow efficiency Qualifications Clinical Laboratory Scientist Requirements • Current New York State License as a Clinical Laboratory Technologist, Histotechnologist, or Physician Assistant required, • Education meeting NYS Office of Professions and CLIA requirements, • ASCP Certification preferred Histotechnologist / Histotechnician Requirements • Current New York State Clinical Laboratory Technician License or Histotechnician License required, • Degree in Medical Technology or related science preferred, • One year of hospital histology experience preferred, • ASCP Certification preferred Core Competencies • Strong attention to detail and accuracy, • Excellent organizational and multitasking skills, • Adaptability and flexibility, • Strong stress tolerance and focus, • Ability to work independently and collaboratively

Job Description Associate Scientist – Mass Spectrometry (LC-MS) Book here for more information: https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl This Associate Scientist role offers the opportunity to work in an innovative mass spectrometry laboratory, executing LC-MS methods to characterize biotherapeutic products across all stages of drug development, from early-stage candidate selection through late-stage regulatory submissions. You will perform routine and advanced analytical tasks to support a diverse R&D pipeline, focusing on protein and modality characterization, and will collaborate closely with cross-functional teams to solve complex drug development challenges. Responsibilities • Execute established LC-MS-based analytical protocols to characterize biotherapeutic products, including monoclonal antibodies, bispecific antibodies, Fc-fusion proteins, adeno-associated virus (AAV), siRNA, and other emerging modalities., • Perform detailed LC-MS characterization activities to elucidate protein structures, post-translational modifications, sequence variants, and glycan profiles that support all phases of drug development., • Provide analytical support to cross-functional teams such as formulation development, upstream and downstream process development, and manufacturing, contributing data and insights to address drug development challenges., • Independently conduct sample preparation for LC-MS analyses, ensuring compliance with standard operating procedures (SOPs) and best practices for analytical chemistry and protein chemistry., • Operate LC-MS instrumentation and associated liquid chromatography systems to generate high-quality, reproducible analytical data., • Document experimental procedures, data, and interpretations accurately and comprehensively in an electronic laboratory notebook (ELN)., • Manage, organize, and visualize analytical data using appropriate software tools, ensuring data integrity and traceability., • Plan and prioritize daily and weekly laboratory work using strong organizational and time-management skills to meet project timelines and deliverables., • Communicate experimental progress, results, and conclusions clearly and in a timely manner to project teams and stakeholders, both verbally and in written reports., • Support the maintenance of a safe, compliant, and well-organized laboratory environment, including adherence to SOPs and relevant laboratory standards., • Contribute to continuous improvement of analytical methods and workflows by sharing observations, troubleshooting issues, and collaborating with colleagues in the analytical development team. Essential Skills • Bachelor’s or Master’s degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field., • 0–2 years of industry experience, ideally in a biotechnology or pharmaceutical environment., • Foundational knowledge of chemistry and protein chemistry, including principles relevant to biotherapeutic characterization., • Hands-on experience with liquid chromatography (LC) techniques, particularly in the context of protein and peptide analysis., • Basic experience or strong academic exposure to LC-MS methods and their application to protein or biotherapeutic analysis., • Ability to follow and execute established laboratory protocols and standard operating procedures with high attention to detail., • Proficiency in documenting experiments, procedures, and results accurately in an electronic laboratory notebook (ELN) or similar system., • Strong organizational skills with the ability to plan, prioritize, and manage multiple tasks in a fast-paced R&D environment., • Effective written and verbal communication skills to deliver clear, timely updates and present analytical findings to project teams., • Demonstrated ability to work independently at the bench while collaborating effectively within a team-focused environment. Additional Skills & Qualifications • Industry experience in a biotech or pharmaceutical setting supporting drug development programs is highly desirable., • Familiarity with advanced mass spectrometers such as Q Exactive Plus, Exploris, or similar high-resolution instruments., • Experience with or exposure to liquid-handling systems and automated liquid-handling platforms (e.g., Bravo) for sample preparation., • Working knowledge of data processing and analysis software such as Skyline, Protein Metrics, or comparable tools used for LC-MS data., • Experience with LC-MS-based protein mass spectrometry in an analytical development or R&D environment., • Ability to interpret complex protein mass spectrometry data, including post-translational modifications, sequence variants, and glycan profiles., • Comfort working within cross-functional teams and contributing analytical expertise to formulation, process development, and manufacturing discussions., • Motivation to learn new technologies and analytical approaches as the organization and pipeline continue to expand., • Interest in long-term growth opportunities, including potential progression within analytical development or related scientific functions. Work Environment This is a full-time, onsite bench/laboratory role in an analytical development environment focused on protein mass spectrometry (LC-MS). The standard schedule is Monday through Friday, approximately 8:30 a.m. to 5:00 p.m. You will work in a modern mass spectrometry lab equipped with advanced LC-MS systems, high-resolution mass spectrometers (such as Q Exactive Plus and Exploris), liquid chromatography systems, and automated liquid-handling platforms. The team supports a broad drug development pipeline, applying LC-MS-based protein mass spectrometry throughout all stages of development. The work environment emphasizes collaboration, scientific rigor, and continuous learning, with strong company culture and significant growth planned over the next several years. Onsite amenities include a gym and cafeteria, with a fully staffed daycare planned in the coming years. Employees benefit from opportunities for professional growth and development, and contract roles include accrued sick and vacation time as well as access to observed holidays. Job Type & Location This is a Contract position based out of Tarrytown, NY. Pay and Benefits The pay range for this position is $38.00 - $42.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Tarrytown,NY. Application Deadline This position is anticipated to close on Jul 15, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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

$80 - $150/hourpayPhysics MasteryWritten Technical CommunicationCritical Evaluation & Error DetectionCalibrated Technical JudgmentVerification & Cross-Checking Fluencymicro1 is the leading 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. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform. Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI. Role Title: Physics Expert (Postdoc / Junior professor) Role Type: Contractor Location: Remote (US, Canada, UK focused) micro1 is engaging Physics Experts (Postdoc / Junior professor) to participate in a high-impact project supporting a customer in the science and technology sector. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. Scope of Work • Critically evaluate and review physics solutions, mathematical derivations, and theoretical arguments generated by researchers or AI platforms., • Detect errors, unjustified steps, missing assumptions, dimensional inconsistencies, and weaknesses in logic or methodology., • Delineate between substantive scientific issues and stylistic or cosmetic matters, providing technically precise written feedback., • Articulate and document the reasoning behind any identified flaws, ensuring actionable guidance for improvement., • Recognize when correct reasoning can be optimized, and offer suggestions to sharpen or clarify the argument., • Utilize LaTeX, SymPy, Python, and Jupyter to independently verify or counter-check scientific claims as appropriate., • Deliver structured feedback designed to support iterative enhancement of submitted work and project outcomes. Preferred Qualifications • PhD in physics and an active record of independent research within a specialized subfield (e.g., High Energy/Mathematical Physics, Biophysics/Statistical Physics, Condensed Matter, AMO/Quantum Optics, Gravitation/Cosmology, Quantum Information, or Optical Materials)., • Experience as a postdoctoral researcher, research fellow, junior/assistant professor, or senior research scientist., • Recent (last ~5 years) representative publications in the relevant subfield, with arXiv or DOI links., • Advanced proficiency with LaTeX, SymPy, Python, and Jupyter for theoretical modeling and computational validation., • Demonstrated skill in reviewing the work of others—through peer review, supervision, dissertation committees, or group seminars., • Exceptional written communication skills with the ability to convey nuanced, constructive feedback with technical rigor., • Reliable access to high-speed internet and a computer suitable for rigorous technical work.

In this role, you will contribute to the development and evaluation of novel bispecific antibody therapeutics, working at the intersection of tumor biology and immune modulation.

About Mercor’s talent network Join our Physical Scientist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in our network contribute to: - Training and evaluating AI models in Physical Sciences - Creating tasks and deliverables

What You'll Do** - Access primary sources (papers, patents) to verify protein target assignments against UniProt records - Flag and classify target assignment errors using a structured taxonomy - Propose correct UniProt accessions where assignments are wrong - Write concise, evidence-grounded notes

Looking for a new Med Tech job? My name is Leah and I'm a healthcare recruiter, I'm here to help!.I have an awesome Med Tech position available near Cos Cob, Connecticut!.Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc).Click apply or email your resume to / cal

The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director Clinical Sciences, and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. • May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical SubTeam, • Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments, • Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape, • Applies proficient scientific expertise to propose, design, and complete clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature, • Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments, • Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support, • Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety, • Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders, • Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety, • Applies proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies, • Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program, • May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate, • Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally, • Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements, • Resolves novel problems requiring creative application of advanced skill, training, and education, • Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs., • Strong cross-functional management, interpersonal and problem-solving skills with a proven track in clinical trial process improvements., • Considerable organizational awareness, including significant experience working cross-functionally To be considered for this role, you must have ? 10 years of pharmaceutical clinical drug development experience. We are seeking experience in managing clinical trials in one or more of the following therapeutic areas cardiovascular, renal, metabolic disease. Demonstrate proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. Other levels considered depending on experience. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.

Position: Environmental Scientist Location: White Plains, NY Remote Status: On‑Site Job Id: 1539-122-2026 # of Openings: 1 Tectonic is currently seeking a full‑time Environmental Scientist to work on various projects based in White Plains, NY. This is a great opportunity for professional growth and development in the A/E/C industry and to be mentored by advanced industry professionals! Tectonic rewards its staff with an excellent salary and benefits package. ESSENTIAL FUNCTIONS The essential functions of this position will include traveling to various job sites and utilizing necessary field equipment to complete asbestos and lead investigations, soil and groundwater sampling, site investigations, remedial investigations, phase I and phase II environmental site assessments, receptor evaluations, and related remediation tasks. Essential functions also include the preparation of detailed, concise, and accurate field reports, technical report writing, communicating with project managers, contractors, client representatives and colleagues, performing research, communicating required information for and assisting with various analyses of data using various software, as well as all other duties as assigned. QUALIFICATIONS BS Degree or equivalent in Geology, Environmental Science, Environmental Engineering, or similar 2-6 years of relevant experience; experience conducting phase I and phase II environmental site assessments required Experience with asbestos, lead, and hazardous material is a plus This position requires obtaining OSHA safety training within a reasonable period of time upon commencement of employment Must have excellent written and oral communication skills, as well as strong interpersonal skills and the ability to represent the company in a professional manner Must have strong organizational skills Functional computer skills, including familiarity with Microsoft Outlook, Word and Excel, Nitro/Adobe or similar PDF suite, as well as ability to utilize various software programs, time reporting systems, and other related computer applications; GIS software experience is a plus Open availability for work outside of typical business hours for projects that require alternate working hours Requires a valid, acceptable driver's license and personal vehicle to travel to project sites, as regular daily travel may be required PHYSICAL REQUIREMENTS While performing the essential functions, the employee is frequently required to move around the job site and inspect, observe, move, operate, and/or transport documents, materials and/or field testing equipment relevant to the job and communicate about same. The employee must regularly lift and/or move up to 27 lbs. The employee is constantly working in outdoor weather conditions, including exposure to extreme heat, extreme cold, biological hazards conditions and sometimes working in the office environment. The employee will also communicate with colleagues, supervisors and clients both orally and in writing through corporate communication systems, and occasionally operate a computer and related office machinery such as printers, and fax machines. This position also requires frequent operation of a motor‑vehicle, which sometimes may require remaining stationary for extended periods of time. Employees may also be required to undergo substance abuse testing, Hazwoper Physical, medical surveillance program, respirator clearance, and use of appropriate respirator as per project requirements. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. COMPETITIVE SALARY & BENEFITS PACKAGE Tectonic offers competitive salaries along with a comprehensive benefits package that includes: Opportunities for mentoring, professional development and career advancement Tuition reimbursement to advance education Paid time off, including vacation, sick leave, and personal days Company‑observed, paid holidays 401(k) retirement plan with profit‑sharing opportunities Comprehensive group medical insurance, including health, dental, vision, and life coverage High Deductible Health Plan (HDHP) option paired with a Health Savings Account (HSA) Flexible spending accounts (FSAs) for medical expenses and dependent care Commuter benefits for public transportation costs Short and long‑term disability coverage Employee Assistance Program PAY RANGE Tectonic’s goal is to compensate employees fairly and equitably across all positions companywide. Our advertised pay ranges represent our good faith effort to provide a reasonable anticipated salary range. The offered pay may be outside of the provided salary range based upon the selected candidate’s work location, experience, education, certifications, and capabilities compared to the advertised position. Pay Range: $30.00 - $36.06 per hour. Tectonic is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by law. Employment decisions are based on qualifications, merit, and business needs. Tectonic participates in USCIS E‑Verify to verify employment authorization. #J-18808-Ljbffr

Jobtailor is seeking a field-focused environmental engineer/scientist to assist with planning and executing site investigations, collect diverse samples, and manage data records in support of regulatory compliance and remediation efforts. This role requires independent work, strong teamwork, and attention to detail on complex construction projects. The candidate should have a Bachelor’s degree in Environmental Science or Engineering and 4+ years in contaminated site investigations, with #J-18808-Ljbffr

Lab ScientistApplylocations: 41 East Post Roadtime type: Per diemposted on: Posted 5 Days Agojob requisition id: JR231213City/State:White Plains, New YorkDepartment:WPH Lab Anatomic Pathology_1Work Shift:EveningWork Days:DAYS VARYScheduled Hours:Hours Vary**Hours Per Pay Period:

Clinical Laboratory Scientist/Histotechnician White Plains Hospital | White Plains Hospital | Posted Feb 16 Full-time White Plains Unknown Position Summary Performs Histological technical procedures using manual and automated techniques to achieve high-quality Pathology slides for review by Pat

Coordinates with Data Engineers to build data environments providing data identified by Data Analysts, Data Integrators, Knowledge Managers, and Intel Analysts. Defines company data assets (data models), spark, sparkSQL, and hiveSQL jobs to populate data models. Coordinates research and analytic act

Professional Engineer and/or Professional Geologist licensure in the State of New York or the ability to obtain licensure within 1-year is highly preferred. Project Manager, Civil/Environmental Engineer, Environmental Scientist, or Geologist/Hydrogeologist. We are looking to add new talent to our gr

Job Responsibilities Manage environmental investigation and remediation projects; Perform complex analyses for specific portions of broader engineering and environmental projects; Supervise field activities and ensure correct interpretations of findings; Manage and deliver on multiple projects a

Qualifications Bachelor’s degree in Environmental Science or Environmental Engineering; 4+ years of related experience in contaminated sites investigation, engineering feasibility studies, remedial and mitigation system design and construction oversight; For engineers, possession of a valid Profes

Job Summary Langan is seeking an Entry‑Level Environmental Engineer, Scientist or Geologist to join its collaborative team in NewYork, NY, White Plains, NY, or Melville, NY.

Requirements Bachelor’s degree in Environmental Science or Environmental Engineering 4+ years of related experience in contaminated sites investigation, engineering feasibility studies, remedial and mitigation system design and construction oversight For engineers, possession of a valid Profess

Langan Engineering & Environmental Services in White Plains, NY seeks a Senior Staff Environmental Engineer or Scientist to join a collaborative team. The ideal candidate holds a bachelor's degree in Environmental Science or Environmental Engineering, 4+ years of related experience, and strong commu

Performs monthly quality control of blood components and tracks amount tested to meet monthly requirements as per regulatory agencies.

As a Research Scientist in Robotic Perception, you will play a key role in solving challenging robot perception problems for various robotic platforms (i.

Senior Manager, Internal Medicine, Clinical Scientist. The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program.

HRP Associates Inc is seeking an Entry Level Geologist/Environmental Scientist for its Clifton Park office.

Tectonic Engineering Consultants, Geologists & Land Surveyors, DPC is seeking a full-time Environmental Scientist based in White Plains, NY.

Role description Arcadis is seeking a Principal Engineer / Scientist to act as the Licensed Site Professional for on‑going and upcoming Massachusetts projects, and to assist with site investigation and remediation for other assessment and remediation projects. Provide mentoring and training to jun

Responsibilities Manage environmental investigation and remediation projects Perform complex analyses for specific portions of broader engineering and environmental projects Supervise field activities and ensure correct interpretations of findings Manage and deliver on multiple projects and task

PepsiCo is seeking an R&D Associate Scientist in the Town of Mount Pleasant, NY, focused on quality-related issues across beverage categories.

The Manager Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program.

Jobtailor in White Plains, NY seeks an experienced environmental project manager to lead investigations and remediation efforts on complex assignments.You will supervise field crews, deliver rigorous analyses, manage budgets and schedules, and coordinate with clients, subcontractors, and office team

Research Scientist (Beverage Ingredient Science) Duration: 08+ Months Contract/Possibility of extension Schedule: Monday-Friday, 8AM-5PM Pay Rate: Negotiable Responsibilities: Support and drive technical evaluation of new ingredient and formulation technologies for the Beverage portfolio (Sports and

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Arcadis is seeking a Principal Engineer / Scientist to act as the Licensed Site Professional for on-going and upcoming Massachusetts projects, and to assist with site investigation and remediation for other assessment and remediation projects. Provide mentoring and training to junior engineers and s