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<h3>Job Description</h3>
Job DescriptionJob Title: GC Chemist Job Description
Independently perform advanced laboratory testing of raw materials using Gas Chromatography (GC), following approved test methods and in full compliance with QC procedures, company SOPs, and cGMP standards. Operate a range of GC instruments, including those equipped with headspace and direct injection capabilities. Develop GC methods autonomously as needed.
Responsibilities
<ul>
<li>Execute method validation, process validation, and cleaning validation testing, along with all associated verification, validation, optimization, and transfer activities as required.</li>
<li>Support lab management in conducting investigations and handling deviations; assist in preparing for and responding to audits and regulatory inspections.</li>
<li>Perform internal laboratory audits as necessary.</li>
<li>Maintain accurate, organized, and cGMP-compliant documentation for all testing activities, including lab notebooks, chromatograms, report forms, Certificates of Analysis (C of A), specification sheets, and glassware labeling.</li>
<li>Provide training, guidance, and mentorship to Level 1 and Level 2 chemists.</li>
<li>Promote and adhere to all laboratory health, safety, and housekeeping protocols; take a leadership role in lab clean-up efforts and related initiatives.</li>
<li>Ensure proper handling and documentation of controlled substances in strict accordance with federal and company regulations.</li>
<li>Complete assigned projects with precision and timeliness, minimizing errors, repeats, and analyst-related deviations; follow management directives to meet deadlines and priorities.</li>
<li>Actively participate in laboratory and company meetings and training sessions.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor’s degree in Chemistry or a closely related scientific discipline required.</li>
<li>A minimum of 4–5 years of laboratory experience is preferred, ideally within a pharmaceutical setting focused on solid dosage forms.</li>
<li>Proven expertise in analytical testing within a cGMP-compliant laboratory environment.</li>
<li>Demonstrated proficiency in operating advanced laboratory instrumentation and associated software.</li>
<li>Exceptional time management and attention to detail to ensure accurate project completion with minimal errors.</li>
<li>Fluent in English with strong command of both verbal and written communication.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Excellent verbal and written communication skills, including proficiency in technical writing for reports and the ability to interpret technical documents, instructions, diagrams, and schedules.</li>
<li>Excellent interpersonal skills for effective collaboration with colleagues and supervisors.</li>
<li>Ability to consistently deliver high-quality work in a pharmaceutical environment regulated by agencies such as the FDA and DEA.</li>
<li>Capable of working under pressure, following detailed instructions, and managing priorities in a deadline-driven setting.</li>
</ul>
Work Environment
The work environment involves working with chemicals, reagents, and solvents, requiring physical activity in the laboratory. The facility is FDA-approved, employing approximately 200 people, with the QC Lab having about 20 staff members.
Job Type &amp; Location
This is a Permanent position based out of Laurelton, NY.
Pay and Benefits
The pay range for this position is $80000.00 - $85000.00/yr.
Epic Pharma offers benefits including medical, dental, and vision insurance, a 401k with company match, and various paid time off options. Other benefits can include life insurance, short and long-term disability, tuition reimbursement, and employee activities.
Workplace Type
This is a fully onsite position in Laurelton,NY.
Application Deadline
This position is anticipated to close on Nov 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

GC Chemist

<h3>Job Description</h3>
Job Description
About Us Reliance Vitamin is a trusted leader in the manufacturing of high-quality nutritional supplements. We are committed to excellence, innovation, and integrity in every product we produce. Join a company where quality isn’t just a standard, it’s our promise.
 
About the Role We’re seeking a motivated and detail-oriented Quality Control Chemist to join our team. Reporting to the Quality Control Supervisor, this role is responsible for testing raw materials, in-process products, and finished goods to ensure compliance with specifications and Good Manufacturing Practices (GMP). You’ll play a critical role in maintaining our commitment to quality and regulatory excellence.
 
Essential Functions
<ul>
<li>Conduct analytical testing of raw materials, in-process, and finished products using HPLC, GC, wet chemistry, FTNIR, Atomic Absorption, ICP, and other laboratory methods.</li>
<li>Manage and maintain independent verification testing programs with third-party laboratories.</li>
<li>Investigate Out of Specification (OOS) results and deviations; document corrective and preventive actions (CAPA).</li>
<li>Develop and validate testing methods and specifications for raw materials and finished products.</li>
<li>Maintain and troubleshoot laboratory equipment, ensuring calibration and proper functioning.</li>
<li>Write and maintain SOPs related to laboratory procedures and quality testing.</li>
<li>Collaborate with R&amp;D, Product Development, and Purchasing teams to ensure product and raw material compliance.</li>
<li>Maintain accurate testing records, calibration logs, and environmental monitoring data.</li>
<li>Support microbiological testing, inspections, and other QC functions as needed.</li>
</ul>
 
Knowledge, Skills and Abilities
<ul>
<li>Bachelor’s degree in Chemistry, Biology, or related scientific discipline.</li>
<li>Minimum of 3 years of experience in a GMP-regulated laboratory environment.</li>
<li>Hands-on experience with analytical instrumentation (HPLC, GC, titrations, spectroscopy).</li>
<li>Strong organizational and documentation skills with attention to detail.</li>
<li>Proficiency in Microsoft Office (Word, Excel, Outlook).</li>
<li>Ability to lift up to 25 lbs and stand for extended periods during testing.</li>
</ul>
 
Why Join Reliance Vitamin Company?
<ul>
<li>Be part of a team that values science, integrity, and continuous improvement.</li>
<li>Competitive compensation and comprehensive benefits package.</li>
<li>Opportunities for professional growth in a stable and expanding industry.</li>
<li>A collaborative environment that recognizes your contributions.</li>
</ul>
 
Schedule: Full-time, Monday–Friday Work Location: On-site in Edison, NJ
Company DescriptionReliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions: · Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 Patented and Trademarked raw materials. · Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics and plant proteins. Customer base is branded, domestic and international companies. With over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance. 
<h3>Company Description</h3>
Reliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions:\r\n\r\n· Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 \r\n Patented and Trademarked raw materials.\r\n\r\n· Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics \r\n and plant proteins. Customer base is branded, domestic and international companies. \r\n\r\nWith over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance.

QC Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: GC Chemist Job Description
Independently perform advanced laboratory testing of raw materials using Gas Chromatography (GC), following approved test methods and in full compliance with QC procedures, company SOPs, and cGMP standards. Operate a range of GC instruments, including those equipped with headspace and direct injection capabilities. Develop GC methods autonomously as needed.
Responsibilities
<ul>
<li>Execute method validation, process validation, and cleaning validation testing, along with all associated verification, validation, optimization, and transfer activities as required.</li>
<li>Support lab management in conducting investigations and handling deviations; assist in preparing for and responding to audits and regulatory inspections.</li>
<li>Perform internal laboratory audits as necessary.</li>
<li>Maintain accurate, organized, and cGMP-compliant documentation for all testing activities, including lab notebooks, chromatograms, report forms, Certificates of Analysis (C of A), specification sheets, and glassware labeling.</li>
<li>Provide training, guidance, and mentorship to Level 1 and Level 2 chemists.</li>
<li>Promote and adhere to all laboratory health, safety, and housekeeping protocols; take a leadership role in lab clean-up efforts and related initiatives.</li>
<li>Ensure proper handling and documentation of controlled substances in strict accordance with federal and company regulations.</li>
<li>Complete assigned projects with precision and timeliness, minimizing errors, repeats, and analyst-related deviations; follow management directives to meet deadlines and priorities.</li>
<li>Actively participate in laboratory and company meetings and training sessions.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor’s degree in Chemistry or a closely related scientific discipline required.</li>
<li>A minimum of 4–5 years of laboratory experience is preferred, ideally within a pharmaceutical setting focused on solid dosage forms.</li>
<li>Proven expertise in analytical testing within a cGMP-compliant laboratory environment.</li>
<li>Demonstrated proficiency in operating advanced laboratory instrumentation and associated software.</li>
<li>Exceptional time management and attention to detail to ensure accurate project completion with minimal errors.</li>
<li>Fluent in English with strong command of both verbal and written communication.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Excellent verbal and written communication skills, including proficiency in technical writing for reports and the ability to interpret technical documents, instructions, diagrams, and schedules.</li>
<li>Excellent interpersonal skills for effective collaboration with colleagues and supervisors.</li>
<li>Ability to consistently deliver high-quality work in a pharmaceutical environment regulated by agencies such as the FDA and DEA.</li>
<li>Capable of working under pressure, following detailed instructions, and managing priorities in a deadline-driven setting.</li>
</ul>
Work Environment
The work environment involves working with chemicals, reagents, and solvents, requiring physical activity in the laboratory. The facility is FDA-approved, employing approximately 200 people, with the QC Lab having about 20 staff members.
Job Type &amp; Location
This is a Permanent position based out of Laurelton, NY.
Pay and Benefits
The pay range for this position is $80000.00 - $85000.00/yr.
Epic Pharma offers benefits including medical, dental, and vision insurance, a 401k with company match, and various paid time off options. Other benefits can include life insurance, short and long-term disability, tuition reimbursement, and employee activities.
Workplace Type
This is a fully onsite position in Laurelton,NY.
Application Deadline
This position is anticipated to close on Nov 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
Actalent is urgently hiring for a Clinical Laboratory Technologist
**Microbiology experience is a must for this role**
Start Date: ASAP
Shift: Tuesday and Thursday 7am-5pm, &amp; Friday or Saturday 7am-5pm 30 hours weekly 
Department: Microbiology
Pay Rate: Up to $52 an hour, depending on experience
Location: Hicksville, NY 
Must Haves: 
<ul>
<li>Minimum 1 year of recent microbiology experience </li>
<li>NYS CLT License (NO exceptions) </li>
<li>VITEK preferred </li>
</ul>
Please apply to this posting for immediate consideration!
#LPN25
Job Type &amp; Location
This is a Permanent position based out of Hicksville, NY.
Pay and Benefits
The pay range for this position is $52.00 - $52.00/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 Hicksville,NY.
Application Deadline
This position is anticipated to close on Nov 27, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Medical Technologist Microbiology URGENT

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Overview: The Laboratory Supervisor is responsible for overseeing and guiding the daily operations of the laboratory, ensuring that the work is conducted efficiently and accurately. This position requires a background in laboratory studies or work and extensive team management experience. The candidate should be able to set and break down team goals, establish employee performance assessment criteria (PBC/KPI), and drive the team towards achieving its objectives.
This role has an estimated salary range of $80,000 - $90,000 dependent upon experience. 
Key Responsibilities:
Team Management:
<ul>
<li>Lead and manage the laboratory team, assign tasks, and monitor progress.</li>
<li>Set annual and quarterly team goals and break them down into actionable tasks.</li>
<li>Conduct employee performance evaluations, set PBC/KPI, ensuring alignment of employee goals with team objectives.</li>
</ul>
Communication and Coordination:
<ul>
<li>Maintain open communication channels, regularly communicate with team members, and provide feedback and guidance.</li>
<li>Resolve internal team conflicts and issues, fostering a positive work environment.</li>
<li>Coordinate with other departments to ensure laboratory work aligns with organizational objectives.</li>
</ul>
Employee Development:
<ul>
<li>Identify training and development needs of employees, develop and implement training plans.</li>
<li>Mentor and cultivate employees, helping them improve skills and advance their careers.</li>
<li>Support employee career growth through regular performance evaluations.</li>
</ul>
Lean Management and Site Management:
<ul>
<li>Apply lean principles to optimize laboratory processes, enhancing efficiency and quality.</li>
<li>Implement site management practices to ensure effective use of laboratory equipment and resources.</li>
<li>Monitor laboratory safety and compliance, ensuring adherence to relevant standards and regulations.</li>
</ul>
Development and Improvement of SOP (Standard Operating Procedures):
<ul>
<li>Develop and maintain laboratory SOPs, ensuring all operations comply with industry best practices and regulatory requirements.</li>
<li>Regularly review and update SOPs to adapt to new technologies and methods.</li>
<li>Ensure team members are familiar with and follow SOPs, providing necessary training.</li>
</ul>
Problem Analysis and Resolution:
<ul>
<li>Apply comprehensive thinking to analyze problems from perspectives such as personnel, equipment, materials, methods, and environment.</li>
<li>Identify potential issues and develop preventive measures to reduce impacts on laboratory operations.</li>
<li>Implement solutions and monitor their effectiveness to ensure problems are effectively resolved.</li>
</ul>
Goal Achievement:
<ul>
<li>Represent the team in developing and executing strategies to achieve laboratory goals.</li>
<li>Monitor project progress, make necessary adjustments to ensure goals are met.</li>
<li>Regularly report team performance and project progress, providing improvement suggestions.</li>
</ul>
Qualifications:
<ul>
<li>Possess a degree in a relevant field and laboratory work experience.</li>
<li>Extensive team management experience with the ability to set and achieve goals.</li>
<li>Familiarity with lean management principles and site management practices.</li>
<li>Excellent communication and coordination skills, able to effectively resolve issues.</li>
<li>Ability to mentor and develop employees, supporting the team's continuous growth.</li>
</ul>
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Lab Supervisor

<h3>Job Description</h3>
Job Description
Job Title: Research Billing Specialist
As a Research Billing Specialist, you will manage invoices and track payments from clinical trial sponsors for patient visits and other study-related costs as outlined in clinical trial budgets and contracts. You will perform payment reconciliation for clinical research, process payment requests for patient reimbursement and third-party vendors in accordance with policy, and serve as a financial resource for clinical site staff and research patients. Additionally, you will utilize CTMS or financial software to track clinical trial revenue and attend finance meetings, assisting other departments with patient account discrepancies.
Responsibilities
<ul>
<li>Invoice and track payments from clinical trial sponsors.</li>
<li>Perform payments reconciliation for clinical research.</li>
<li>Process payment requests for patient reimbursement and third-party vendors.</li>
<li>Serve as a financial resource for clinical site staff and research patients.</li>
<li>Utilize CTMS or financial software to track clinical trial revenue.</li>
<li>Attend finance meetings and assist other departments with patient account discrepancies.</li>
<li>Assist with preparation of reports requested by the Finance department.</li>
<li>Troubleshoot internal department billing processes.</li>
<li>Conduct annual billing training for research staff and as-needed for new hire orientation.</li>
<li>Provide cross-coverage with Research Billing compliance specialists.</li>
<li>Review budgets, reports, and transfer charges in hospital billing systems.</li>
<li>Prepare monthly reports capturing and applying research payments to aged accounts.</li>
<li>Maintain DSA forms and documentation for clinical patient accounts.</li>
<li>Resolve outstanding patient bills and disputes with the Finance department.</li>
<li>Develop and maintain tracking metrics for research finance.</li>
<li>Maintain strong communication with ancillary departments and outside vendors.</li>
</ul>
Essential Skills
<ul>
<li>Experience in clinical research and compliance.</li>
<li>Ability to navigate EPIC systems.</li>
<li>Experience with digital accounts for patients.</li>
<li>Knowledge of research and Medicare coverage analysis.</li>
<li>Organizational skills.</li>
<li>Experience with CTMS.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's Degree in Accounting, Sciences, or equivalent HS diploma.</li>
<li>2 years of experience with billing/coding and/or financial business operations.</li>
<li>Experience with billing and collections processes.</li>
</ul>
Work Environment
 The organization offers a hybrid work schedule after 90 days, providing flexibility thereafter. The position is part of an NCI-designated organization
Job Type &amp; Location
This is a 6-month contract position based out of Hackensack, New Jersey.
Job Type &amp; Location
This is a Contract position based out of Hackensack, NJ.
Pay and Benefits
The pay range for this position is $26.71 - $35.01/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 hybrid position in Hackensack,NJ.
Application Deadline
This position is anticipated to close on Nov 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Research Compliance Specialist

<h3>Job Description</h3>
Job Description
About Synaptrix Labs Inc.
Synaptrix is on a mission to revolutionize brain-computer interfaces through non-invasive approaches. We believe that the power to diagnose and treat neurological conditions safely, and to expand human potential, will become a reality with the right fusion of deep learning, signal processing, and computational neuroscience.
We're seeking a full time Research Scientist, Artificial Intelligence (PhD) to join our growing team of researchers &amp; engineers. If you're passionate about shaping the future of brain-computer interfaces and excited by the potential of deep learning in neurotechnology, we want to hear from you!
Responsibilities:
<ul>
<li>Design, prototype, and optimize state-of-the-art AI systems for neural decoding, including diffusion models, graph neural networks, contrastive/self-supervised frameworks, and transformer-based sequence models.</li>
<li>Conduct foundational research on neural time-series representation learning: build architectures that extract latent dynamics from EEG, EMG, or related biosignals.</li>
<li>Develop high-fidelity simulation environments for testing decoding algorithms, incorporating stochastic signal noise and realistic biophysical constraints.</li>
<li>Scale model training across multi-GPU and multi-node clusters using PyTorch Distributed, DeepSpeed, or JAX/Flax; profile and tune system performance for sub-10 ms inference latency.</li>
<li>Build and maintain end-to-end research pipelines for large-scale signal datasets, including preprocessing, artifact rejection, and multimodal fusion with video, audio, and IMU data.</li>
<li>Collaborate with neuroscientists and hardware engineers to integrate learned models into real-time BCI control loops and embedded systems.</li>
<li>Contribute to core ML infrastructure: experiment tracking, model versioning, dataset lineage, and reproducibility standards.</li>
<li>Publish at top-tier ML or neurotech venues (NeurIPS, ICLR, Nature Neuro, EMBC) and present findings to the research community.</li>
</ul>
Minimum Qualifications:
<ul>
<li>PhD or equivalent deep technical expertise in Machine Learning, Artificial Intelligence, Computer Science, Computational Neuroscience, or related fields.</li>
<li>Strong command of PyTorch or JAX, with experience implementing custom training loops, loss functions, and model architectures.</li>
<li>Proven ability to conduct end-to-end research, from conceptual design to reproducible experiments and evaluation.</li>
<li>Strong mathematical foundations in linear algebra, probability, optimization, and information theory.</li>
<li>Experience working with high-dimensional time-series or sensory data (EEG, speech, video, motion capture, etc.).</li>
<li>Skilled in Python, NumPy, Pandas, and scientific computing workflows; experience with CUDA or low-level GPU debugging is highly valued.</li>
<li>Demonstrated ability to operate independently on open-ended problems and drive original research with limited supervision.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Deep familiarity with neural signal modeling, neural decoding, or biosignal preprocessing (EEG/MEG/ECoG/EMG).</li>
<li>Experience designing self-supervised or generative models (diffusion, VAEs, contrastive, masked modeling) for noisy, non-stationary data.</li>
<li>Background in reinforcement learning, optimal control, or human-in-the-loop systems, especially in continuous domains.</li>
<li>Publications or preprints in top venues (NeurIPS, ICML, ICLR, CVPR, EMBC, Nature Neuro).</li>
<li>Familiarity with distributed training, mixed-precision, multi-GPU orchestration, and cloud ML infrastructure (AWS/GCP/Azure).</li>
<li>Contributions to open-source ML frameworks or custom CUDA kernels.</li>
<li>Understanding of neural signal acquisition hardware, embedded inference, or edge ML deployment.</li>
<li>Track record of curiosity-driven, independent research resulting in practical systems or open-source codebases.</li>
</ul>
About our Culture:
At Synaptrix Labs, we celebrate curiosity, open collaboration, and scientific rigor. Our interdisciplinary team spans neuroscience, AI, and clinical research, and we are united by the belief that non-invasive BCI is the key to unlocking a new era in healthcare, accessibility, and human augmentation.
Expected Compensation:
The base salary for this role is anticipated to fall within the following range. Actual compensation will depend on your experience, technical expertise, and relevant education or training. In addition to base pay, Synaptrix offers equity to all full-time employees, reflecting our commitment to shared success and long-term company growth.
Base Salary Range:
$85,000 - $150,000 USD
What We Offer:
<ul>
<li>An opportunity to change the world and work with some of the smartest and most talented experts from different fields</li>
<li>Growth potential; we rapidly advance team members who have an outsized impact</li>
<li>Paid holidays, unlimited PTO</li>
</ul>

Research Scientist, Artificial Intelligence (PhD)

<h3>Job Description</h3>
Job Description
Survey &amp; Research Associate - Rating/Rankings/Financial Market Insights
New York, NY
Hybrid (2x per week in office required)
Preference to be given to applicants within a commutable area to the office location.
 
My client, a leader in the investment market insights sector is looking for a Research Associate with an understanding of finance to help with survey data processing.
 
This is not a Financial Analyst or Data Analyst role. This role is focused on survey data processing and research.
 
What will you do?
 
<ul>
<li>Project Management:&nbsp;The candidate will be required to assist in the development and execution of project plans and schedules. They must understand project overlaps, track status and provide updates on project progress, and assist in the implementation of project deadlines. Collaboration with cross-functional teams is essential to ensure smooth survey delivery.</li>
</ul>
 
<ul>
<li>Technical Operations: The candidate will be expected to independently use firm systems which include Qlik and Hubspot, to carry out the operational processes.</li>
</ul>
 
<ul>
<li>Client Engagement: Interaction with external contacts to explain voting process and survey methodology, as well as encouraging participation in the surveys. A professional and efficient approach is essential.</li>
</ul>
 
<ul>
<li>Database Operation: Data cleansing to ensure accurate demographic information, eligibility of participants and quality of voting for research projects, working with other project managers and database team. Monitor and maintain accurate contact data in CRM.</li>
</ul>
 
<ul>
<li>Survey Results: Assist with preparation of survey results publication. Review results for processing errors, year-on-year trends, missing information.</li>
</ul>
 
Skills &amp; Experience:
<ul>
<li>1-2 years’ experience in a survey data research role</li>
<li>Robust project planning and coordination skills</li>
<li>Ability to work under pressure and hit deadlines</li>
<li>Demonstrate experience of multi-tasking in a complex environment</li>
<li>Ability to work in a team environment and maintain good communication with cross-functional teams</li>
<li>Exceptional organizational skills, a superior work ethic and extreme attention to detail</li>
<li>Creative and critical thinking skills to analyze data and uncover insights</li>
<li>Some client service experience would be beneficial</li>
<li>IT Literate; knowledge of Microsoft Office (including strong Excel skills)</li>
<li>Understanding of financial markets preferred.</li>
</ul>
 
This is a full time position with benefits. Salary range from $65K-$75K USD and variable bonus.
 
All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you require accommodation, please contact us at <a href="mailto:sabrina@svrecruitment.com" target="_blank">sabrina@svrecruitment.com</a>

Survey Research Analyst - Investment Market Insights

<h3>Job Description</h3>
The New Jersey Attorney General’s office is looking for a Research Analyst 2 for the New Jersey Division of Consumer Affairs, Office of the Director, Drug Affordability Unit in Newark, NJ. Come join the Division of Consumer Affairs as a Research Analyst 2 in the Drug Affordability Unit (DAU). The position will perform analytic review and interpretation of data relevant to the operations and mission of the DAU in order to inform policy decisions related to drug price transparency. The Analyst will develop public-facing static and interactive data reports to promote and improve public understanding of prescription drug affordability, conducting prescription drug price data analysis, including review of drug price increases and new drug notification and reporting requirements. The annual salary for this position ranges from $64,340.11 to $94,061.71. 
 
ABOUT THE DEPARTMENT:
 
The Attorney General has broad oversight of the state’s legal and law enforcement matters. As the head of the Department of Law &amp; Public Safety, the Attorney General supervises a wide range of Divisions, Offices, and Commissions, consisting of over 2,800 sworn law enforcement officers, 600 attorneys, and thousands of other public servants.
 
ABOUT THE DIVISION:
 
The New Jersey Division of Consumer Affairs protects the public from fraud, deceit, misrepresentation and professional misconduct in the sale of goods and services in New Jersey through education, advocacy, regulation and enforcement. The Division pursues its mission through its 51 professional and occupational boards that oversee 720,000 licensees in the state, its Regulated Business section that oversees 60,000 NJ registered businesses, as well as through its Office of Consumer Protection, Bureau of Securities, Charities Registration section, Office of Weights and Measures, and Legalized Games of Chance Control Commission. 
 
ABOUT THE SECTION:
 
Since its creation in 1978, ODCA has played a valuable role in protecting consumer interests. ODCA has been an Office of the Department of Enterprise, Trade and Employment and has primarily concentrated on enforcing consumer legislation and providing information to consumers.
ABOUT THE POSITION:
 
Under the direction of a supervisory official in a State department or agency:
<ul>
<li>Analyze drug pricing databases and external data sets to inform decisions by the DAU.</li>
<li>Use a number of different data sources to develop reports, publications and data visualizations for Drug Affordability Council (DAC), state, legislative stakeholders, and public audiences.</li>
<li>Use available data to create annual pricing and spending trends for annual reports.</li>
<li>Support special projects as assigned.</li>
<li>Manage an interactive dashboard tool for prescription drugs notification and reporting – to ensure pharmaceutical entities submit data to support the price increase and new drug notifications and reporting.</li>
<li>Analyze data to conduct reviews on price increases and new drug notification and reporting.</li>
<li>Support and analyze the database/portal for the Drug Affordability Unit Fee Assessment. And report out the status and updates on fee assessments.</li>
</ul>
 
REQUIRED QUALIFICATIONS:
NOTE: Applicants must meet one of the following or a combination of both experience and education. Thirty (30) semester-hour credits are equal to one (1) year of relevant experience.
<ul>
<li>Six (6) years of professional experience in legal or legislative research or similar administrative experience involving public contact with an emphasis on the review and analysis of operating and legislative methods, procedures, and policies. OR</li>
<li>Graduation from an accredited college or university with a bachelor's degree; and two (2) years of the above-mentioned professional experience. OR</li>
<li>Possession of a master’s degree in public administration, Political Science, Government, or other relevant area from an accredited college or university; and one (1) years of the above-mentioned professional experience. OR</li>
<li>Possession of a Juris Doctor degree or bachelor of laws degree from an accredited law school,</li>
<li>Appointees will be required to possess a driver's license valid in New Jersey. </li>
</ul>
 
OTHER KEY FACTORS:
 
<ul>
<li>All offers of employment are conditional subject to the applicant agreeing to and then passing a background check that may include fingerprinting.</li>
</ul>
 
BENEFITS: Appointees may be eligible for a comprehensive benefits package that includes health, dental, and life insurance; a prescription drug plan; and vision care reimbursement. Participation in retirement and deferred compensation plans, as well as flexible spending and health savings accounts may also be available. Eligible employees receive annual paid sick and vacation leave as well as paid State holidays. Positions may offer telework or an Alternate Work Week (AWP) schedule. Benefit eligibility may vary based on job duties, operational needs, and funding. For more information, visit NJDPB.
 
HOW TO APPLY: : If qualified, please send a cover letter indicating interest in job vacancy announcement #25-256, a current resume and a copy of your final unofficial transcripts and/or foreign degree evaluation (for education credit) to the Recruitment Coordinator at <a href="mailto:Recruit@dca.njoag.gov" target="_blank">Recruit@dca.njoag.gov</a> on or before the closing date on or before the closing date of November 28, 2025.
 
 
For more information, please visit <a href="https://www.njoag.gov/careers/all-job-postings/" target="_blank">https://www.njoag.gov/careers/all-job-postings/</a>

DCA #25-256: Research Analyst 2 (Data Analyst -Drug Affordability Unit) Newark

<h3>Job Description</h3>
Job DescriptionSalary: $75K-$95K, depending upon experience 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation.
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values:
 Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients.
 
We currently have a role available for a Molecular Biologist to join our New York City team.
 
Job duties include, but are not limited to, the following:
<ul>
<li>Demonstrating laboratory expertise with biologic assays aimed at drug development including monoclonal antibodies (mAb), antibody-drug conjugates (ADC) and T-Cell Engagers (TCE) platforms.
<ul>
<li>Must be proficient in cell culture techniques, ELISA, and flow cytometry (antibody selection, method optimization, analysis).</li>
<li>Must be able to maintain multiple cell lines simultaneously (approx. 2-10).</li>
</ul>
</li>
<li>Performing functional antibody screening and profiling (including tumor cell signaling assays, internalization, tumor cell killing assays, cytokine release assays).</li>
<li>Conducting potential drug candidate evaluation in both in vitro (Pharmacokinetic-Pharmacodynamic (PK/PD), receptor occupancy, density, cytokine release), and ex vivo assays (tumor isolation, analysis of blood cells).</li>
<li>Designing and executing studies to select and deliver potential drug candidates.</li>
<li>Communicate results at project team meetings, be involved in the coordination and preparation of presentations as needed.</li>
</ul>
Job requirements include, but are not limited to:
<ul>
<li>MS-Molecular/Cellular Biology or related field with 1+ years of lab experience, preferably pharma. BS-Molecular/Cellular Biology or related field with 3+ years of lab experience outside of academia will also be considered.</li>
<li>Proficient in Microsoft Office Suite as well as GraphPad Prism, Spotfire, and Benchling.</li>
<li>Team player mentality with strong written and verbal communication skills. Will be required to work collaboratively with cross-functional teams including structural biology, molecular biology, biochemistry, and biophysics.</li>
<li>The ideal candidate will be enthusiastic, self-motivated and details oriented, with the skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.</li>
</ul>
 This job posting will close by February 28th 2026 or when a candidate is identified, whichever comes first.

638 Science Jobs in New York, NY 10007, USA