field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Our client is a provider of flavorings and ingredient solutions to the food, beverage, and nutraceutical industries. This position is responsible for formulating, testing, and evaluating flavor compounds and blends to meet the diverse needs of our clients and products. You will collaborate closely with cross-functional teams, including product development, quality assurance, and regulatory compliance, to ensure that all flavor formulations align with industry standards and consumer preferences.
 
Job Responsibilities:
<ul>
<li>Create and formulate new flavor profiles for a variety of food and beverage products, ensuring they meet customer specifications and market trends.</li>
<li>Conduct sensory testing and analysis of flavors to evaluate their performance in different applications, using both quantitative and qualitative methods.</li>
<li>Work directly with customers to finalize customer projects as is required</li>
<li>Maintain accurate records of formulations, experimental data, and sensory evaluations, and prepare comprehensive reports summarizing findings and recommendations.</li>
<li>Work closely with cross-functional teams, including product development, marketing, and production, to support the successful launch and optimization of new flavors.</li>
<li>Provide technical support and training to internal teams and clients on flavor properties, applications, and trends.</li>
<li>Collaborate with ingredient suppliers and vendors to source high-quality raw materials and explore new flavor ingredients.</li>
<li>Ensure that all flavor formulations adhere to safety standards and regulatory compliance, including labeling and allergen management.</li>
<li>Aid in training Flavor Apprentice(s) in preparation for testing with the Society of Flavor Chemists</li>
</ul>
 
The Ideal Candidate Will Have:
<ul>
<li>Degree in food science, physical sciences, or related field required</li>
<li>Desired 7+ years of flavor development experience and a certified member of the Society of Flavor Chemists</li>
<li>Experience with the creation and scaling of reaction flavors</li>
<li>Preferred experience in Flavor formula entry in Sage X3, E-Book File, and Product Vision is highly desirable</li>
</ul>
 
What we will offer:
<ul>
<li>An attractive salary, and benefit package</li>
<li>An amazing opportunity to grow your career with an industry leader</li>
</ul>

If you are someone that is ideal for this position, please submit your resume in Microsoft Word format. We look forward to hearing from you.

Certified Flavor Chemist

<h3>Job Description</h3>
Please note: For confidentiality purposes, this position is not located in Blue Bell. The role is based in the tri-state area.
 
This role will focus on the validation of analytical methods for products in development or for commercial products when needed. This position involves executing validation studies and optimizing or developing analytical methods when needed to support drug product applications. In addition to analytical method validation, this position will involve R&amp;D T0 and Stability testing for 2-3 drug products in development
 
Key responsibilities. 
<ul>
<li>Develops analytical methods that are accurate, precise, and specific for use in both the Quality Control department and the Research department. Methods primarily include HPLC and GC but also include ICP-MS, Karl Fisher, solid-state characterization, and others.</li>
<li>Documents the development of the method in the appropriate notebooks for future reference. Performs pre-validation work ahead of transfer to the Validation Department to demonstrate suitability for use.</li>
<li>Prepares test method procedures and supporting documentation for use in the Quality Control laboratory.</li>
<li>May be required to develop validation protocols and validate analytical methods used in the testing of raw materials, intermediate products, final products, and cleaning samples.</li>
<li>Assists in the maintenance and calibration of laboratory analytical instrumentation including, but not limited to HPLC and GC. Maintains accurate records regarding the maintenance and calibration activities.</li>
<li>May support manufacturing operations with testing of raw materials, intermediate products, final products, and cleaning samples. The incumbent is expected to operate in a neat and orderly manner and to provide accurate and timely test results.</li>
<li>Assists in the maintenance of the QC Laboratory. In addition to routine housekeeping and glassware cleaning, maintains and appropriate inventory of supplies and chemicals.</li>
<li>Documents sample preparation, equipment set-up and test results in Laboratory Notebooks or on the appropriate test record form. Documentation must be complete and verified by a second member of the quality group. In addition, laboratory log sheets, those related to equipment usage, calibration, and maintenance, reference standard inventory, QC chemical inventory, or those related to retention samples will be properly maintained.</li>
</ul>
 
EDUCATION/EXPERIENCE. 
<ul>
<li>A Bachelor’s Degree in Chemistry (Master's or PhD Degree is preferred)</li>
<li>A minimum of 7 years of experience in small molecule pharmaceutical laboratories, with a strong background/proficiency in LC, GC, Dissolution and chromatographic method validation and development.</li>
<li>Proficient with Empower software. </li>
<li>Strong organizational skills.</li>
<li>Good communication skills</li>
<li>Good writing skills.</li>
</ul>

Research And Development Chemist

<h3>Job Description</h3>
Analytical Chemistry- Senior Research Chemist
Exemplify BioPharma, Inc. a Symeres Company, is a global partner research organization (PRO) based in New Jersey, USA.&nbsp;We are a team of biopharma industry experts focused on delivering end-to-end Chemistry, Manufacturing and Controls (CMC) throughout the drug development and regulatory market application processes. Using a unique combination of program management, coupled with our New Jersey based process development laboratories we are ideally positioned to deliver CMC success to partner organizations.&nbsp;We are talent based team and our key asset is our experience, multidisciplinary expertise and proven track record.&nbsp;We strive to bring tangible value to our partners through provision of strategic, tactical and technical leadership to solve complex problems focused on reducing program timelines and costs.
&nbsp;
Position &amp; Responsibilities
 Exemplify BioPharma is seeking a scientific leader to serve as Senior Analytical Chemist at our R&amp;D laboratory located in Cranbury, New Jersey. The ideal candidate will have 0-3 years’ experience and a proven record of sustained laboratory achievement and innovation.
&nbsp;
The professional in this position will lead analytical development for high priority drug candidates. You will identify and characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. tablets, injectable solutions).
&nbsp;
As an innovator, you will develop, validate and implement new analytical methods to guide product development and solve challenging technical problems related to purity, stability, packaging, and manufacturing.
&nbsp;
You will define strategies to address quality-related objectives, and will recommend the methods and specifications used to monitor pharmaceutical materials and/or the formulated product. You will then lead the transfer of these technologies to CRO, CMO manufacturing sites.
&nbsp;
This professional will lead and/or participate on multi-disciplinary product development teams and will supervise the studies and professional development of one or more laboratory professionals. You will develop new scientific ideas, methods and technologies that contribute to the responsibilities described above.
&nbsp;
Other responsibilities include statistical data analysis, compliance with pharmaceutical good manufacturing practices and the completion of technical reports and external publications (as appropriate). This visible and business-critical role demands excellent oral and written communication skills.
&nbsp;
This is an exceptional opportunity for motivated candidates who wish to be exposed to all aspects of CMC drug development in a fast moving, collaborative and learning environment.
&nbsp;
Qualifications 
 A Ph.D. degree in analytical chemistry or a related discipline is preferred. The candidate must have a demonstrated ability to conduct independent research, solve scientific problems, and lead other professionals in a highly collaborative environment.
&nbsp;
 
Application
If you are interested in applying for this exciting opportunity at Exemplify BioPharma please e-mail a cover letter and resume to <a href="mailto:careers@exemplifybiopharma.com" target="_blank">careers@exemplifybiopharma.com</a>.

Analytical Chemistry- Senior Research Chemist

<h3>Job Description</h3>
Job Descriptionjob summary: 
<ul>
<li>As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in nutrition, health, and wellness. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the food and beverage industry. This company is dedicated to innovation and sustainability, investing in cutting-edge research and development to create products that enhance quality of life and contribute to a healthier future. With a strong legacy of excellence and a mission to improve lives worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!</li>
<li>Precision and innovation go hand-in-hand in our client's mission to advance nutritional science. We are seeking a proactive Analytical Chemist to join a premier Research and Development laboratory in St. Louis. In this role, you will be a key contributor to R&amp;D efforts, executing and interpreting complex experimental protocols that drive product development and quality. We are looking for a self-starter who thrives in a collaborative lab environment and is eager to take the lead on method development and process improvements. This is an exciting opportunity to utilize your technical expertise in chromatography and mass spectrometry to ensure the highest standards of scientific integrity while mentoring other laboratory professionals.</li>
</ul>
 location: Saint Louis, Missouri job type: Contract salary: $25.00 - 27.38 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Experimental Execution: Execute and interpret complex procedures and protocols within defined project goals, delivering timely and accurate results.</li>
<li>Method &amp; SOP Development: Learn and implement method development, drive process improvements, and draft comprehensive Standard Operating Procedures (SOPs).</li>
<li>Equipment &amp; Validation: Perform analytical equipment validation and ensure routine calibration and preventive maintenance are conducted at required intervals.</li>
<li>Troubleshooting: Act as a technical lead in troubleshooting assay performance and instrumentation issues to minimize downtime.</li>
<li>Technical Reporting: Prepare and interpret detailed reports for complex experiments, ensuring data is clear and actionable for the broader R&amp;D team.</li>
<li>Collaboration &amp; Mentorship: Work independently while contributing to a high-performing team, providing guidance and mentorship to junior team members.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Education: Bachelor's degree in Chemistry or a related scientific field.</li>
<li>Industry Experience: 3+ years of experience in an analytical laboratory or industry setting.</li>
<li>Technical Expertise: 2+ years of hands-on experience with chromatography and/or mass spectrometry (e.g., HPLC, GC, GCMS, LCMS).</li>
<li>Instrumentation: Proven experience with analytical instrumentation, including the ability to troubleshoot equipment and assay issues.</li>
<li>Location &amp; Environment: Must be able to work on-site in St. Louis and be comfortable with exposure to the Top 14 Allergens.</li>
</ul>
Preferred:
<ul>
<li>Regulatory Knowledge: 1+ years of experience working in an ISO 17025 accredited laboratory.</li>
<li>Professional Attributes: Strong initiative and the ability to work independently in a fast-paced research and development environment.</li>
</ul>
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionLCMS Lead Scientist
Job Description
As a LC-MS Lead Scientist, you will play a pivotal role in overseeing bioanalytical studies, ensuring that all methods meet regulatory and client requirements. You will not be working directly in the lab but will be responsible for reviewing data, signing off on reports, and acting as the primary scientific point of contact. Your expertise will guide the bioanalytical study work, and you will coordinate with regulators and stakeholders, both internally and externally.
Responsibilities
<ul>
<li>Oversee studies and ensure all methods are prepared, validated, executed, and documented to meet regulatory and client requirements.</li>
<li>Sign off on reports and approve raw data.</li>
<li>Act as the primary scientific point of contact for studies.</li>
<li>Coach and indirectly guide a team of up to 20 members.</li>
<li>Coordinate across internal and external stakeholders, including discussions with regulators for clinical or pre-clinical studies.</li>
<li>Travel up to 10% for cross-site or client visits.</li>
</ul>
Required Skills
<ul>
<li>B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.).</li>
<li>2-3 years of LCMS experience.</li>
<li>Experience as a Lead Scientist with 1-5 years (LS1) or 7-9 years (LS2) of experience.</li>
<li>Must have experience as a Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector (GLP or GCP regulations).</li>
<li>Full responsibility over the study, with experience in BioA CRO regulated space.</li>
<li>LBA (Ligand Binding Assay) experience, including data review/approval, protocol/sample analysis plan development, and method validation readiness.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with Sciex Mass Spec and analysis software.</li>
<li>Familiarity with LIMS, Nautilus, and Analyst software.</li>
<li>Knowledge of ICH or 28BMV regulatory guidance protocols and FDA internal standards.</li>
</ul>
Work Environment
The role is based in a lab setting within the Bioanalytical team, consisting of approximately 100 employees, including 60 chemists. This is a hybrid position, requiring 2-3 days onsite per week, with flexibility on the days but consistency each week. The role involves indirect reporting from method development chemists, validation chemists, sample analysis, and report writing. The work is workload-based rather than project-based, with a varying number of projects depending on client needs. The team is expanding, with current plans to increase from 16 to 18 members in Madison. Travel is limited, with a maximum of 10% required for client visits or conferences.
Job Type &amp; Location
This is a Permanent position based out of Madison, WI.
Pay and Benefits
The pay range for this position is $85000.00 - $110000.00/yr.
Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&amp;D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&amp;D Employee Stock Purchase Plan (ESPP)
Workplace Type
This is a hybrid position in Madison,WI.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

LCMS Lead Scientist

<h3>Job Description</h3>
About the Role
Our client - one of the most ambitious AI research labs is hiring ML Research Scientists, Cheminformatics! With offices based in California and New York, this team is unlocking groundbreaking therapies for patients with severe diseases. They work at the intersection of machine learning, physics, and computational chemistry to advance the development of small molecule drug discovery. Backed by top investors and founded by ex-Google/Stanford Scientists, they are scaling their Cheminformatics team.
 
 
Why Join?
<ul>
<li>World-Class Research - Work alongside AI pioneers from the most elite institutions and industry labs - Google/Meta/OpenAI/Stanford/Harvard/MIT</li>
<li>Massive Compute - Unparalleled access to cutting-edge infrastructure</li>
<li>Research - this is about making fundamental advances in deep learning, representation learning, and generative models. Developing SOTA models within active drug programs, taking the lead on model validation, deployment to drive the discovery of new medicines</li>
<li>Real-World Impact - Your work won’t sit in a paper; it will be deployed in groundbreaking AI systems</li>
</ul>
 
 
Who We're Looking For:
We’re seeking top-tier ML research scientists, Cheminformatics with a strong track record of applying machine learning methods to advance small molecule drug discovery.
 
 
Your Responsibilities:
<ul>
<li>Cheminformatics expert skilled in molecular data and tools like RDKit and OpenEye.</li>
<li>Experienced in experimental drug discovery assays and CADD workflows, from docking to ADME prediction.</li>
<li>Proficient data scientist and applied ML engineer, fluent in Python, scikit-learn, and PyTorch.</li>
</ul>
 
 
What We’re Looking For:
<ul>
<li>PhD in Cheminformatics, Computational Chemistry, Computer Science</li>
<li>Expert in advanced modelling techniques, including GNNs, multitask modelling, active learning, and Bayesian optimisation.</li>
<li>Experienced in large-scale data management, SQL, data pipelines, and robust approaches to molecule featurisation and model validation.</li>
</ul>
 
 
Locations:
San Francisco, New York City
 
 
Package:
Salary up to $350,000K + benefits and equity options.
 
 
Ready to shape the future of AI? Apply now and join a team redefining intelligence.

ML Research Scientist

<h3>Job Description</h3>
R&amp;D Manager 
Job Summary
The Research and Development (R&amp;D) Manager at CP Foods North America will lead the planning, execution, and completion of new product development and existing product optimization projects, from concept through commercialization. This role requires a blend of scientific expertise, project management skills, and innovative thinking to ensure products meet market demands, quality standards, and regulatory requirements. The R&amp;D Manager will foster a culture of innovation and collaborate closely with cross-functional teams including Marketing, Sales, Quality Assurance (QA), Operations, and Supply Chain.
Key Responsibilities
<ul>
<li>Product Development &amp; Innovation: Drive the development of new and innovative food products and improve existing formulations to meet consumer needs and market trends.</li>
<li>Project Management: Oversee the R&amp;D projects supported by the Columbus R&amp;D team, ensuring projects are completed on time, within budget, and align with company objectives.</li>
<li>Team Leadership: Manage and mentor a team of food technologists and technicians, fostering a collaborative and innovative work environment.</li>
<li>Technical Expertise &amp; Analysis: Provide technical leadership and support, including formulation, shelf-life stability testing, and sensory evaluation, for the projects supported by the R&amp;D team. Strong knowledge of scientific process and application of experimental design in lab experiments and plant trials, including statistical analysis of results. </li>
</ul>
 
<ul>
<li>Scale-Up &amp; Commercialization: Ensure trials have strong technical plans and are designed to ensure a seamless transition from lab to manufacturing. Partner with the Engineering, Quality and Operations teams to enable efficient start-up. </li>
<li>Quality &amp; Regulatory Compliance: Work with quality and regulatory teams to ensure all products and processes comply with industry regulations and food safety standards (e.g., FDA, USDA, HACCP, GMPs, SQF).</li>
<li>Cross-Functional Collaboration: Partner with Marketing to translate consumer insights into project briefs, with Operations to ensure manufacturing feasibility, and with Procurement to source new ingredients and manage costs.</li>
<li>Documentation &amp; Reporting: Maintain comprehensive documentation for product specifications, formulations, processing protocols, and project progress reports. Responsible for accurate documentation and protocol management for lab and pilot plant space in Columbus. </li>
</ul>
Qualifications &amp; Skills
<ul>
<li>Education: Bachelor's or Master's degree in Food Science, Food Engineering, Culinary Science, or a related scientific field.</li>
<li>Experience:</li>
<li>Minimum of 5-10 years of R&amp;D experience in the food manufacturing industry.</li>
<li>Proven experience managing R&amp;D projects and leading cross-functional teams, experience with people management preferred.</li>
<li>Experience with commercializing products from concept to launch.</li>
<li>Technical Skills: Strong knowledge of ingredient functionality, food chemistry, processing techniques, and food safety systems.</li>
<li>Related Skills:</li>
<li>Excellent problem-solving, analytical, and critical thinking abilities.</li>
<li>Strong leadership, communication, and interpersonal skills.</li>
<li>Ability to manage multiple projects, prioritize tasks, and adapt to a fast-paced environment</li>
<li>Champions a “What If” attitude, searches and provides new ideas and solutions</li>
<li>Values collaboration and the power of team</li>
<li>Other job responsibilities as assigned</li>
</ul>
 
Location: Columbus, OH
 
Disclaimer
This job description indicates in general the nature and levels of work, knowledge, skills, abilities and other essential functions (as covered under the Americans with Disabilities Act) expected of an incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of an incumbent. Duties, responsibilities and activities may change at any time with or without notice.

Research And Development Manager

<h3>Job Description</h3>
Job Description
Mount Sinai Services at NYC Health+Hospitals/Queens is seeking a Chief of Hematology/Medical Oncology for the Queens Cancer Center at the Queens Hospital Center. This Center of Excellence is the only state-of the-art comprehensive cancer center in the NYC Health+Hospitals System. This is an excellent opportunity to work in a mission-driven institution whose goal is to deliver exceptional care to the community.
The qualified candidate will join a collaborative team of medical oncologists/hematologists, radiation oncologists, and surgeons to deliver a wide array of oncologic and hematologic services. Offering a range of services, the Queens Cancer Center is strongly committed to caring for the whole patient and places a strong emphasis on providing patient-centered care. The Queens Cancer Center is a Commission on Cancer-designated Community Cancer Program employing a multidisciplinary approach to cancer research and treatment.
The ideal candidate will contribute to the leadership, direction and integration of the oncology/hematology service line at Queens Hospital Center/Queens Cancer Center and participate in the well-established and robust clinical research program. The research mission of the Queens Cancer Center is to advance the field of cancer/hematologic treatments and preventive measures and to facilitate the availability of these advancements to the community we serve.
Minimum Position Qualifications:
· Possess a medical degree (MD/DO) from an accredited university
· Has or has the ability to obtain a New York State Medical License
· Board Certified in Hematology and Medical Oncology
· Minimum of 5+ years of clinical/leadership experience
· Excellent communication, bedside manner, and organizational skills
· Strong work ethic and desire to participate in a team-oriented, collaborative mission-driven institution
&nbsp;
All faculty have an academic appointment at The Icahn School of Medicine at Mount Sinai.
&nbsp;
Responsibilities include:
<ul>
<li>Deliver direct clinical hematology/medical oncology care to patients at the Queens Cancer Center/Queens Hospital Center, including outpatient clinic and in-patient consultation.</li>
<li>Work collaboratively with leadership to optimize effective use of resources and operational performance of the Cancer Center.</li>
<li>Work collaboratively with leadership to create new patient services and define expectations and standards of patient care.</li>
<li>Actively participate in relevant committees and programs, including Cancer Committee and weekly Multidisciplinary Tumor Board Conference, contributing to the overall excellence in hematology/medical oncology services.</li>
<li>Demonstrate high standards of care through collaboration with physicians, surgeons, clinical professionals and staff.</li>
<li>Contribute to medical and surgical education programs, by participating in teaching residents and medical students.</li>
<li>Be committed to a professional and patient-centered care environment that places a high priority on clinical excellence.</li>
</ul>
The Mount Sinai Health System (MSHS) provides equal employment opportunity to all its employees and applicants for employment without unlawful discrimination on the basis of their actual or perceived race, creed, color, religion, national origin, sex, gender, gender expression, gender identity, age, disability, marital or parental status, sexual orientation, veteran, immigration, citizenship, or other protected status. EOE including Veterans and Disabled
Company DescriptionWho We Are: Over 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve. Formed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai. 
<h3>Company Description</h3>
Who We Are:\r\nOver 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve.\r\n\r\nFormed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai.

Chief of Hematology/Medical Oncology

<h3>Job Description</h3>
The Staff Scientist will prepare grant applications and other scientific communication materials on a wide range of genomic research topics. This role is deeply immersed in the science of NYGC and supports our research team in building and expanding a successful, independently-funded research base. They collaborate with diverse teams of students, postdoctoral fellows, and principal investigators, and relates scientific and strategic goals to individual grant opportunities and other research communications vehicles. Typical grants include individual investigator, multi-PI and research center grants.
 
Key Responsibilities
<ul>
<li>Takes a lead role in preparation and project management of individual and multi-investigator proposals;</li>
<li>Provides advice on grantsmanship, editorial support and standardized language for administrative sections;</li>
<li>Identifies opportunities for funding</li>
<li>Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables;</li>
<li>Provides draft preparation, review and revision of grants and scientific writing.</li>
<li>Coordinates with and supports Sponsored Research staff to ensure timely, accurate application submission.</li>
<li>Edits manuscripts, fellowship applications, research progress reports, clinical research protocols and other research communications materials.</li>
<li>Interacts with lab members to independently develop new grant proposals.</li>
<li>Organizes small group meetings with lab members to review project progress, plan experiments, and integrate team data.</li>
<li>Assists in the design and planning of functional genomics and genetic perturbation experiments; and,</li>
<li>Assists in analysis and figure preparation of diverse types of data, including high-throughput sequencing, microscopy images, gel images, and schematic diagrams.</li>
</ul>
 
Key Responsibilities include (but are not limited to):
<ul>
<li>PhD in genetics, genomics, cancer biology, neuroscience or related discipline required;</li>
<li>5+ years research experience, including contributing to grant writing, required. NIH experience strongly desirable;</li>
<li>Exceptional written communication skills required to prepare and edit competitive grant applications, publications, administrative materials, and other research communications;</li>
<li>Ability to grasp complicated technical subjects, synthesize diverse lines of evidence and apply these abilities to technical writing required;</li>
<li>Experience handling the scientific writing and project management process for multi-investigator and institutional grant applications strongly preferred;</li>
<li>Experience with standard grant development concepts, practices, and procedures in a research environment preferred;</li>
<li>Applied statistics background required, to perform power calculations and develop quantitative metrics for genomic assays;</li>
<li>Ability to collaborate with diverse teams of investigators and administrative personnel required; and,</li>
<li>Strong project management skills and experience required.</li>
</ul>
 
Competencies
<ul>
<li>Technical and Professional Skills: Consistently demonstrates skills and knowledge relevant for current role; strives to expand the depth and breadth of technical and professional skills; works with a high level of integrity; exhibits focus and discipline; appropriately prioritizes, manages expectations, and delivers on commitments.</li>
<li>Collaborative &amp; Communicative: Models collaboration and teamwork; brings out the best in others; effectively works with all levels, internally and externally; respects and embraces diversity of perspective; communicates clearly and listens carefully; uses good judgment as to what to communicate and when to do so.</li>
<li>Adaptable &amp; Innovative: Adaptable and embraces change; develops new insights and pursues improvements and efficiency; fosters exchange of new ideas and willing to challenge the status quo; takes initiative and is solution-oriented; engages in work with passion and curiosity.</li>
</ul>
 
Salary
The salary range for this position is $62,000-78,000 per year. Base pay offered may vary depending on job-related knowledge, skills, and experience. In addition, NYGC offers a full range of medical, financial, and other benefits as well as generous time off.
 
About the New York Genome Center
The New York Genome Center (NYGC) is an independent, nonprofit, academic research organization dedicated to advancing genomic research. NYGC scientists and staff are furthering new approaches to diagnosing and treating neurological diseases and cancer through their unique capabilities in whole genome sequencing, RNA sequencing, state-of-the art analytics, and the development of genomic tools. NYGC concentrates specifically on disease-based research in the following areas: neuropsychiatric disease (autism, schizophrenia, bipolar); neurodegenerative disease (ALS, Alzheimer’s, Parkinson’s, Huntington’s), and cancer.
Located in Lower Manhattan, the New York Genome Center was founded by and remains closely affiliated with the leading academic medical centers and research universities in the New York region, engaging in research projects with and for these institutions. Essential to our collaborative work is an outstanding faculty, whose members typically hold a joint appointment at NYGC and a partner university. They support our scientific mission by conducting independent research in areas of mutual interest to us and the wider scientific community.
 
Equal Opportunity
We are committed to fostering a workplace environment that is welcoming and fair to all, ensuring that every employee has the opportunity to thrive. We believe that bringing together individuals with diverse backgrounds, experiences, and perspectives leads to greater collaboration, innovation, and discovery. Valuing and supporting each employee in reaching their full potential strengthens our organization and enhances our collective success. We recognize that creating an environment where all employees feel valued and included requires sustained effort and dedication from the entire organization.
The New York Genome Center is a VEVRAA Federal Contractor. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, creed, color, gender, religion, national origin, sexual orientation, age, disability, genetic predisposition or carrier status, protected veteran or military status, domestic violence victim status, partnership status, caregiver status, alienage or citizenship status, marital status, or any other characteristic protected by applicable law. NYGC takes affirmative action in support of its policy to hire and advance in employment individuals who are protected veterans and individuals with disabilities. 
 
FLSA Status – Exempt
This position is eligible for visa sponsorship and relocation assistance.

Staff Scientist / Grant Writer, Sanjana Lab

<h3>Job Description</h3>
Job Description
Description
Work closely with the Senior Chemist and/or Technical Director to improve the functionality, performance, and application of chemical products. Adjust, refine, or optimize existing product formulations based on feedback from sales engineers, field service personnel, and customers. Replicate specific water qualities and system conditions to conduct testing of new and existing products, ensuring accuracy and relevance to real-world applications. Review, perform, and verify quality control parameters to support consistent production standards. Prepare documentation, technical reports, and presentations as required by the Senior Chemist and/or Technical Director. Maintain accurate laboratory records, test data, and research files in accordance with internal documentation standards. Collaborate with the R&amp;D and QC teams to support product troubleshooting, root-cause analysis, and continuous improvement initiatives. Follow all laboratory safety protocols and maintain clean, organized, and compliant laboratory workspaces. Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
The Research &amp; Development Chemist supports the development of new products, enhancement of existing formulations, and testing efforts required for innovation and continuous product improvement. This role also supports Proton Software by providing accurate data, application insights, and testing results that inform internal and external stakeholders.
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of Plant City, FL.
Pay and Benefits
The pay range for this position is $24.00 - $26.00/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 &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;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 Plant City,FL.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

15,007 Science Jobs