field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionDescription:
RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team. 
Requirements:
If this sounds interesting to you, it’s probably because up to this point you have:
<ul>
<li>Bachelor of Science of higher</li>
<li>0-3 years of quality Control experience, preferably in a pharmaceutical, manufacturing, or regulated environment.</li>
<li>Familiarity with cGMP, GDP, and standards.</li>
<li>Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint) and experience with ERP or document management systems (e.g., SAP, Master Control).</li>
<li>Excellent organization, time management, and communication skills.</li>
</ul>
 
The main responsibilities for this position are:
<ul>
<li>Perform daily verification /performance check of the QC analytical instruments such as Analytical balance, Microbalance, KF titrator, KF coulometer, Auto titrator etc.,</li>
<li>Perform calibrations of all the QC analytical instruments/equipment’s as per the calibration calendar schedule or when required.</li>
<li>Perform Instrument/ equipment performance qualification as and when required.</li>
<li>Maintain inventories of chemicals, Standards, samples etc.,</li>
<li>Operation, calibration, maintenance and qualification of all analytical instruments such as HPLC, GC, TOC, UV, IR, automatic titrator, dissolution equipment, etc.</li>
<li>Follow the procedures as per the SOP’s/ guidelines.</li>
<li>Perform Sampling of raw materials, drug substance, packaging components, stability samples, cleaning samples, In-process samples and finished products.</li>
<li>Perform analytical tests and wet chemistry tests on raw materials, drug substance, packaging components, stability samples, cleaning samples, In- process samples and finished products in compliance with the STP and SOP’s.</li>
<li>Follow and document all test results under GLP, GDP, GMP and Lab Safety guidelines.</li>
<li>Document test results, problems and other issues, perform troubleshooting of issues that arise during analysis.</li>
<li>Logging various samples received to QC as per the SOP into their respective log books.</li>
<li>Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc.</li>
<li>Performs Stability samples loading/charging and pull-out according to the stability calendar.</li>
<li>Record the results and prepares CoA to be released in a timely manner.</li>
<li>Perform analysis using various software’s such as Empower, Tiamo, Spectrum two, Flex etc.</li>
<li>Write and perform investigation of out of specification results.</li>
<li>Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods.</li>
<li>Preparation and review of Standard Operating Procedures, specifications and STP’s for Raw materials, Packaging components, drug substances and finished products (based on ICH/Pharmacopeial reference).</li>
<li>Preparation and execution of protocols for Method Validations, Method Transfers, Cleaning Validation, Raw material qualifications, Stability studies and any other studies.</li>
<li>Maintains lab, instruments, logbooks and notebooks at all times.</li>
<li>Maintains lab instruments and performs calibration/preventive maintenance to ensure proper working order and troubleshoot when necessary.</li>
<li>Perform additional duties and responsibilities designated by the supervisor on the need basis after receiving the required training.</li>
</ul>
RK Pharma Inc is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

QC Chemist

<h3>Job Description</h3>
Job Title: Process Chemist
Department: Process R&amp;D
Location: Onsite, Cranbury or South Plainfield Site (NJ)
Job Type: Full Time
Position Reports to: Director of Process Chemistry
 
Job Summary:
We are seeking a highly motivated and skilled Process Chemist to join our Process R&amp;D Department at Porton J-STAR. In this role, you will be responsible for the development, optimization, and scaling of chemical processes for pharmaceutical production. You will collaborate with cross-functional teams to ensure that our processes are efficient, cost-effective, and compliant with regulatory standards. This job description applies to activities and responsibilities associated with the process chemistry development group and support of GMP Operations.
 
Responsibilities
Follow existing synthetic routes, making processing improvements where necessary, while conducting multi-step organic synthesis
Plan and organize routine operations to maximize production output.
Design novel synthetic routes and carry out multi-step organic synthesis.
Operate simple open access HPLC/UV, LC/MS, MS, NMR, GC/MS, and other analytical instruments required to monitor reaction processes.
Consult with management, the Analytical Department, the Director of GMP Operations and others on issues concerning experiments prior to and during GMP production.
Accurately make and check calculations, prepare raw materials, reagents and solutions in accordance with company SOP's.
Faithfully record procedures and results in Batch Records or Solution Preparation Forms, notebooks, or other appropriate forms in an organized manner as dictated by departmental SOP and GMP regulations.
Write reports on research as required.
Promote compliance with cGMP regulations. Attend GMP training sessions.
Support management and maintenance of the SOP and Document Control system.
Work with clients to develop material release tests and specifications for materials supplied by J‑STAR.
Help ensure that client project needs, requirements, and timelines are communicated to, and coordinated between, GMP Operations and Quality Control.
<ul>
<li>Conduct process chemistry R&amp;D for clients as an individual contributor, which includes, but is not limited to, research on synthetic routes to active pharmaceutical ingredients and chemical intermediates by route discovery, process optimization, safety evaluation, enabling technologies, high throughput screening and chemo/biocatalytic reaction discovery and optimization. This will include R&amp;D under c-GLP and potentially under c-GMP conditions.</li>
<li>Develop safe, timely and efficient chemical processes by using established, new and/or novel chemical methodologies and processes.</li>
<li>Coordinate analytical chemistry methodology to process and/or catalysis discovery, development optimization and problem solving.</li>
<li>Maintain an uncompromising focus on quality, documentation, confidentiality and scientific execution.</li>
<li>Participate in idea generation for selective quotes/proposals to clients as well as successfully execute against accepted quotes.</li>
<li>Initiate cross-department communication and develop coordinated R&amp;D, processing schedules and deliverables</li>
<li>Lead and contribute to scientific and technical discussions with co-workers and clients to plan, execute, resolve issues and problem solve.</li>
<li>Communicate candidly, clearly and timely with clients, management and peers.</li>
<li>Participate in weekly client updates as needed, prepare weekly reports, contribute to and lead campaign reports and participate in process chemistry technology transfer.</li>
<li>Coordinate and author professional campaign reports, research summaries, and tech packages.</li>
<li>Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices.</li>
<li>Maintain a clean and well-organized hood, bench, glove-box and common work area that is free of clutter, excess chemicals/samples. Advocate for these principals and positively influence others in this regard.</li>
</ul>
Qualifications
<ul>
<li>Required MS, PhD degree in Organic Chemistry.</li>
<li>Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects.</li>
<li>Knowledge and experience base of working in a c-GMP environment is preferable, but not required</li>
<li>Excellent written, verbal and presentation skills.</li>
<li>Experience in small molecule drug development is preferable, but not required.</li>
<li>Track record of scientific success as measured by publications and presentations.</li>
<li>Ability to prioritize and manage numerous activities simultaneously.</li>
<li>Ability to interact in an effective and appropriate manner with diverse population sets.</li>
<li>Experience in working on and positively contributing to scientific teams.</li>
<li>Ability to perform the physical requirements of the position.</li>
</ul>

Process Chemist

<h3>Job Description</h3>
Job Description
Job Title: Sr Scientist
Book here for more information/immediate interests: <a href="https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl" target="_blank">https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl</a>
Job Description
In this role, you will develop antibody-based biologic drug products and assess their quality and stability. As a Senior Scientist, you will collaborate with various teams to move drug products from pre-clinical through commercial stages. Your responsibilities will include designing, executing, and documenting stability studies and other experiments to support formulation development and stability testing across various phases.
Responsibilities
<ul>
<li>Design, write, execute, and document stability studies and other experiments to support formulation development and stability testing in various phases.</li>
<li>Characterize candidate molecules using various biophysical and biochemical analytical techniques.</li>
<li>Develop drug product formulations and support process development and manufacturing of clinical drug substances and drug products.</li>
<li>Develop fit-for-purpose analytical methods to support biophysical characterization, formulation and process development, and research stability testing.</li>
<li>Collect, process, and analyze data by following the organizational standard methodologies and policies.</li>
<li>Document experiments, results, and findings in electronic laboratory notebook.</li>
<li>Present work at group and department meetings; contribute to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li>
<li>Contribute to general laboratory and equipment maintenance.</li>
</ul>
Essential Skills
<ul>
<li>Protein characterization expertise</li>
<li>Experience with HPLC and UPLC</li>
<li>Background in chemistry</li>
<li>BS/MS with 5+ years of experience or PhD with 0+ years of experience in relevant fields</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Knowledge about protein structure and function is required.</li>
<li>Expertise in protein chemistry/biochemistry and characterization.</li>
<li>Analytical and problem-solving skills are a must.</li>
<li>Experience with protein stability, structure, or biophysics is highly desirable.</li>
<li>Hands-on experience and trouble-shooting proficiency with chromatographic methods (HPLC, UPLC, column chromatography), capillary electrophoresis, and/or biophysical techniques.</li>
<li>Experience with statistical analysis software such as JMP is beneficial.</li>
<li>BS with 5+ years of exp OR MS with 3+ years of exp</li>
</ul>
Work Environment
This role operates within a laboratory environment, requiring onsite work five days a week. You will be part of the Formulation Development Group with a schedule from Monday to Friday, 8:00 am to 5:00 pm. The company is known for its excellent culture, recognized as a top employer, with significant growth expected over the next five years. Amenities include an onsite gym and cafeteria, with plans for a fully staffed daycare. Employees enjoy comprehensive packages including stock options, bonuses, and a 401k match, with contract employees accruing sick and vacation time alongside paid holidays.
Job Type &amp; Location
This is a Contract position based out of Tarrytown, NY.
Pay and Benefits
The pay range for this position is $45.00 - $60.00/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 Tarrytown,NY.
Application Deadline
This position is anticipated to close on Dec 18, 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.

Senior Scientist

<h3>Job Description</h3>
Job Description
Job Title: Sr Scientist
Book here for more information/immediate interests: <a href="https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl" target="_blank">https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl</a>
Job Description
In this role, you will develop antibody-based biologic drug products and assess their quality and stability. As a Senior Scientist, you will collaborate with various teams to move drug products from pre-clinical through commercial stages. Your responsibilities will include designing, executing, and documenting stability studies and other experiments to support formulation development and stability testing across various phases.
Responsibilities
<ul>
<li>Design, write, execute, and document stability studies and other experiments to support formulation development and stability testing in various phases.</li>
<li>Characterize candidate molecules using various biophysical and biochemical analytical techniques.</li>
<li>Develop drug product formulations and support process development and manufacturing of clinical drug substances and drug products.</li>
<li>Develop fit-for-purpose analytical methods to support biophysical characterization, formulation and process development, and research stability testing.</li>
<li>Collect, process, and analyze data by following the organizational standard methodologies and policies.</li>
<li>Document experiments, results, and findings in electronic laboratory notebook.</li>
<li>Present work at group and department meetings; contribute to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li>
<li>Contribute to general laboratory and equipment maintenance.</li>
</ul>
Essential Skills
<ul>
<li>Protein characterization expertise</li>
<li>Experience with HPLC and UPLC</li>
<li>Background in chemistry</li>
<li>BS/MS with 5+ years of experience or PhD with 0+ years of experience in relevant fields</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Knowledge about protein structure and function is required.</li>
<li>Expertise in protein chemistry/biochemistry and characterization.</li>
<li>Analytical and problem-solving skills are a must.</li>
<li>Experience with protein stability, structure, or biophysics is highly desirable.</li>
<li>Hands-on experience and trouble-shooting proficiency with chromatographic methods (HPLC, UPLC, column chromatography), capillary electrophoresis, and/or biophysical techniques.</li>
<li>Experience with statistical analysis software such as JMP is beneficial.</li>
<li>BS with 5+ years of exp OR MS with 3+ years of exp</li>
</ul>
Work Environment
This role operates within a laboratory environment, requiring onsite work five days a week. You will be part of the Formulation Development Group with a schedule from Monday to Friday, 8:00 am to 5:00 pm. The company is known for its excellent culture, recognized as a top employer, with significant growth expected over the next five years. Amenities include an onsite gym and cafeteria, with plans for a fully staffed daycare. Employees enjoy comprehensive packages including stock options, bonuses, and a 401k match, with contract employees accruing sick and vacation time alongside paid holidays.
Job Type &amp; Location
This is a Contract position based out of Tarrytown, NY.
Pay and Benefits
The pay range for this position is $45.00 - $60.00/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 Tarrytown,NY.
Application Deadline
This position is anticipated to close on Dec 13, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description
Quantitative Developer
Equity Quantitative Research, Portfolio Monetization 
Location: New York 
Citadel is a worldwide leader in finance that uses next-generation technology and alpha- driven strategies to transform the global economy. They tackle some of the toughest problems in the industry by pushing themselves to be the best. They offer demanding work for the brightest minds, and wouldn’t have it any other way. At Citadel, great ideas can come from anyone. Everyone. You. Team: Equity Quantitative Research (EQR) provides portfolio construction, risk management, and execution services for Citadel’s Fundamental Equities businesses. Embedded within EQR, the 
Engineering team is responsible for providing consistent, highly scaled services, environments, curated datasets, and libraries, to deliver a robust platform upon which users from several key Citadel businesses can efficiently research, trade, and run analytics. By building analysis tools into a common platform, we empower our colleagues to work more effectively and to easily share their research and collaborate on ideas. In addition to providing shared frameworks, we also help to make research and ideas production-ready and scalable, so they can be applied in Citadel’s systematic trading environment. 
Responsibilities: 
The Portfolio Monetization team works on various central portfolios within the EQR team, with responsibilities spanning engineering, research, and trading. The investment mandate of these strategies span enhanced alpha capture/portfolio construction, optimal order execution, and risk management for the equities business. 
The team works on: 
• Building out and maintaining the end-to-end trading engines and back-testing platforms that drive these strategies: from data gathering to, portfolio construction, and order submission
• Work on post-trade analytics and pricing models 
• Partnering with quantitative researchers to work on portfolio construction and trading research 
• Partnering with traders to manage the portfolios on a day-to-day basis. Qualifications: 
• BS or MS in a relevant and highly technical field (computer science, math, or other quantitative field) 
• 4-15 years professional experience (finance industry experience not required) 
• Strong coding skills required; Python preferred 
• Strong interest in quantitative research (especially optimization techniques) 
• Demonstrated interest in understanding business needs 
• Ability to own end-to-end engineering processes in a highly collaborative environment

Xpertise - Citadel EQR Quant Dev

Quinton Davies - Citadel EQR Quant Developer

<h3>Job Description</h3>
Job Description
JOB DESCRIPTION:
The position provides a rich multidisciplinary environment for postdoctoral training and more advanced career development. The candidate will receive a multidisciplinary training investment in performing multi-'omics expression profiling studies at the single population and subregional level relevant towards understanding the potential pathogenesis of selective neuronal vulnerability during the progression of dementia. The position available involves studies of cellular and animal models and postmortem human brain tissues to investigate vulnerable neuronal populations via single population RNA sequencing (RNA-seq), digital spatial profiling (DSP), and related validation strategies within the hippocampus, basal forebrain, and cortex.
JOB DUTIES:
Job requirements include microaspiration of pyramidal neurons and basal forebrain cholinergic neurons from mouse brain and postmortem human brain tissues via laser capture microdissection (LCM), preparing samples for RNA-seq, cryocutting frozen postmortem human and animal model brains for digital spatial profiling (DSP), and subsequent bioinformatic and pathway analyses of the resultant datasets. Additional technical experience with RNA amplification, siRNA knockdown delivery, surgical manipulations, ELISA, confocal microscopy, Western blotting, and real-time qPCR is strongly recommended.
JOB QUALIFICATIONS
Minimum Qualifications:
Bachelor's degree and two years of professional research experience in an appropriate field or master's degree in an appropriate field may substitute for one year of the experience.
Preferred Qualification:
• Ph.D. in Neuroscience/Molecular Cellular Neuroscience • Experience with human neuroanatomy • Experience with molecular and cellular neuroscience in mouse and/or postmortem human brain tissues • Experience with laser capture microdissection • Experience with RNA-sequencing • Experience with digital spatial profiling • Training in statistics/bioinformatics • Previous work with mice
Background Investigation/Justice Center Review Requirements: 
Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Prospective employees whose names appear on the SEL as having been found responsible for serious or repeated acts of abuse or neglect will be barred from appointment. 2) Screened against the Statewide Central Register of Child Abuse and Maltreatment (SCR). Prospective employees whose names are indicated on the SCR may be barred from appointment.
*The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.
Applications will only be accepted through website at: <a href="http://corporate.rfmh.org" target="_blank">http://corporate.rfmh.org</a> - Click on Employment Opportunities. Applications will be accepted only during the posting dates as listed at the top of the job announcement.
Questions regarding this position please email: <a href="mailto:hrprocessing@nki.rfmh.org" target="_blank">hrprocessing@nki.rfmh.org</a>
 Job Posted by ApplicantPro

Research Scientist, Level I - Center for Dementia Research

<h3>Job Description</h3>
Job DescriptionJob Title: Aseptic Technician Job Description
We are looking for an Aseptic Technician to assist with the validation of new areas, including manufacturing equipment and processes. You will collaborate with cross-functional teams such as Quality Assurance, Quality Control, and Maintenance to troubleshoot issues and resolve deviations. Your role will involve participating in aseptic process simulations, media fills, and equipment qualifications, as well as conducting in-process inspections and quality control checks to ensure product quality. You will also be responsible for completing necessary documentation, adhering to cGMP and Good Documentation Practices, and contributing to continuous improvement initiatives.
Responsibilities
<ul>
<li>Assist with initial and subsequent validation of new manufacturing equipment and processes.</li>
<li>Collaborate with cross-functional teams to troubleshoot issues and resolve deviations.</li>
<li>Participate in aseptic process simulations, media fills, and equipment qualifications.</li>
<li>Conduct in-process inspections and quality control checks to verify product integrity.</li>
<li>Complete logbook, form, and batch record documentation as required.</li>
<li>Contribute to continuous improvement initiatives.</li>
<li>Maintain qualification to work within Grade A and Grade B cleaning environments.</li>
<li>Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable cGMPs.</li>
<li>Perform other duties as required and assigned by management.</li>
</ul>
Essential Skills
<ul>
<li>Experience in cleanroom and aseptic environments.</li>
<li>Knowledge of aseptic techniques, cGMP, and cleanroom protocols.</li>
<li>Ability to read and comprehend work instructions and standard operating procedures.</li>
<li>Understanding of equipment alarms and escalation procedures.</li>
<li>Exceptional attention to detail, accuracy, and documentation skills.</li>
<li>Good communication and teamwork abilities.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High school diploma or equivalent; additional technical or vocational education is a plus.</li>
<li>Minimum 1 year of experience in the pharmaceutical/biopharma/biotech industry within aseptic cleanroom environments.</li>
<li>Flexibility to work shifts, including evenings, nights, weekends, and holidays, as required.</li>
</ul>
Work Environment
You will work in a controlled Grade A and B cleanroom environment where aseptic gowning is crucial. This position requires flexibility to work during various shifts, including evenings, nights, weekends, and holidays, as needed by production schedules.
Job Type &amp; Location
This is a Contract to Hire position based out of Parsippany, NJ.
Pay and Benefits
The pay range for this position is $28.00 - $28.00/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 Parsippany,NJ.
Application Deadline
This position is anticipated to close on Dec 9, 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.

Aseptic Technician

<h3>Job Description</h3>
Job DescriptionOverview Ansible Government Solutions, LLC (Ansible) is currently recruiting a Therapeutic Medical Physicist to provide onsite services to eligible beneficiaries of the East Orange VA New Jersey Healthcare System located at 385 Tremont Avenue, East Orange, NJ 07018.&nbsp; If you accept employment with Ansible, you must also acknowledge that any assigned schedule is subject to change at the direction of either Ansible or its customers. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities&nbsp;
<ul>
<li>Radiation treatment planning and dose delivery optimization.</li>
<li>Radiation protection for patients and staff.</li>
<li>Presence during complex procedures (SRS, SBRT, IGRT).</li>
<li>Weekly and final chart reviews for all radiation therapy patients.</li>
<li>Dosimetry and QA for treatment planning systems and equipment.</li>
<li>Peer review participation and documentation.</li>
<li>Support for direct patient care (90–95% involvement for radiation therapy technologists).</li>
<li>Calibration and testing of radiation therapy equipment.</li>
<li>Maintenance and QA of treatment planning software and hardware.</li>
<li>Documentation of QA activities and performance metrics.</li>
<li>Support for acquisition and evaluation of radiation-producing machines.</li>
<li>Network and computer support for radiotherapy systems.</li>
<li>Participation in quality improvement meetings and staff meetings.</li>
<li>Compliance with VA patient safety and incident reporting protocols.</li>
<li>Documentation in VA’s CPRS system with proper coding and electronic signatures.</li>
<li>Attendance tracking and invoice verification.</li>
</ul>
Qualifications
<ul>
<li>Master's degree in Medical Physics or related field&nbsp;</li>
<li>Board Certification in Medical Physics or Therapeutic Medical Physics by the American Board of Radiology (ABR)&nbsp;</li>
<li>Minimum 2 years of continuous working experience within the last 3 years in therapeutic medical physics&nbsp;</li>
<li>Experience with:&nbsp;
<ul>
<li>Varian Linear Accelerators (TrueBeam with Brain Lab Accessories)&nbsp;</li>
<li>Image Guided Radiation Therapy (IGRT) including Cone Beam CT&nbsp;</li>
<li>Eclipse treatment planning system and ARIA record &amp; verify system&nbsp;</li>
<li>Treatment modalities including 2D/3D Conformal, SRS, SRT, SBRT, and IMRT/VMAT&nbsp;</li>
<li>IMRT QA systems (e.g.,&nbsp;MapCheck)&nbsp;</li>
<li>CT Simulators&nbsp;</li>
<li>Superficial X-ray machines&nbsp;</li>
</ul>
</li>
<li>Experience in a healthcare system with ACR or&nbsp;APEx&nbsp;certification preferred&nbsp;</li>
<li>Strong analytical and problem-solving skills&nbsp;</li>
<li>Excellent communication and teamwork abilities&nbsp;</li>
<li>Proficiency&nbsp;in computer systems and networking related to radiation oncology&nbsp;</li>
<li>Ability to pass a government background check and complete required VA training&nbsp;</li>
</ul>
All candidates must be able to:
<ul>
<li>Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift</li>
<li>Lift up to 50 lbs from floor to waist</li>
<li>Lift up to 20 lbs</li>
<li>Carry up to 40 lbs a reasonable distance</li>
<li>Push/pull with 30 lbs of force</li>
</ul>
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. 
Powered by JazzHR
6FuC94Pd8m

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job DescriptionAbout Amigo
Amigo builds AI agents for healthcare—systems that handle patient conversations, take clinical actions, and escalate to humans when needed.
Clinical research focuses on healthcare-specific problems: evaluation frameworks for clinical safety, methods for learning what works across patient populations, and ensuring agent behavior meets the standards healthcare organizations require.
Series A from leading investors. Clinical validation and evidence generation in partnership with leading academic medical institutions.
About this role
As a Clinical Research Scientist at Amigo, you'll lead research on clinical AI safety, evaluation frameworks, and evidence generation. You'll design studies that validate agent performance across patient populations, develop metrics for clinical quality, and publish findings that advance the field. Your clinical expertise ensures our agents meet the standards required for autonomous operation in healthcare.
This role bridges clinical practice and AI research. You'll work directly with our agent engineering and data science teams to translate clinical knowledge into measurable evaluation criteria and safety guardrails.
What you'll do
<ul>
<li>
Design and lead clinical validation studies for AI agent performance
</li>
<li>
Develop evaluation frameworks and metrics for clinical safety and quality
</li>
<li>
Publish research on clinical AI safety and agent evaluation methodologies
</li>
<li>
Collaborate with academic medical institutions on research partnerships
</li>
<li>
Define clinical protocols and escalation criteria for agent behavior
</li>
<li>
Review agent outputs and failure modes from a clinical perspective
</li>
<li>
Contribute to regulatory submissions and compliance documentation
</li>
<li>
Advise on clinical workflow design and patient safety considerations
</li>
</ul>
What we're looking for
<ul>
<li>
MD or equivalent medical degree with active clinical license
</li>
<li>
Clinical experience in primary care, internal medicine, or relevant specialty
</li>
<li>
Track record of clinical research and peer-reviewed publications
</li>
<li>
Understanding of clinical quality metrics and patient safety frameworks
</li>
<li>
Experience with clinical study design and IRB processes
</li>
<li>
Ability to translate clinical expertise into technical requirements
</li>
<li>
Strong communication across clinical, research, and engineering teams
</li>
<li>
Interest in AI/ML applications in healthcare
</li>
</ul>
Nice to have
<ul>
<li>
Fellowship or additional training in clinical informatics
</li>
<li>
Experience with digital health or health technology companies
</li>
<li>
Background in quality improvement or patient safety initiatives
</li>
<li>
Familiarity with FDA guidance on clinical decision support and AI/ML
</li>
<li>
Experience with EHR systems and clinical workflow optimization
</li>
<li>
Publications in clinical AI, digital health, or health informatics
</li>
</ul>
BenefitsHealth &amp; Wellness
<ul>
<li>
Comprehensive health, dental, and vision insurance
</li>
<li>
Mental health support and wellness coaching
</li>
<li>
Flexible wellness stipend for fitness, therapy, or personal growth
</li>
<li>
Daily catered lunch and dinner
</li>
</ul>
Growth &amp; Development
<ul>
<li>
Annual learning budget for courses, books, or conferences
</li>
<li>
Conference attendance budget for professional development
</li>
<li>
Development setup of your choice
</li>
<li>
Academic collaboration opportunities
</li>
</ul>
Compensation Range: $150K - $300K

641 Science Jobs in New York, NY, USA