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job_organization_name

city

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<h3>Job Description</h3>
Job Description
Who We Are:&nbsp;CAMBA is a community of staff, volunteers, clients, donors, neighbors and partners who work together to build an inclusive New York City, where all children and adults have access to the resources and supports, they need to thrive.&nbsp; We take a comprehensive approach by offering more than 180 integrated programs in: Education &amp; Youth Development, Family Support, Job Training &amp; Employment Support Services, Health, Housing, and Legal Services. We reach almost 80,000 individuals and families, including almost 13,000 youth.&nbsp;CAMBA serves a diverse cross section of New Yorkers from new mothers in Brownsville to job seekers in the Rockaways. More than half of our clients are immigrants and refugees from around the globe. Over 85% of our families are living in poverty, reflecting the challenges faced by nearly 1.7 million New Yorkers today.
Program Overview
CAMBA subcontracts with Columbia University on the research project P3: “Estimating the Impact of a Multilevel, Multicomponent Intervention to Increase Uptake of HIV Testing and Biomedical HIV Prevention among African American/Black Gay, Bisexual, and Same-gender Loving Men.” CAMBA oversees recruitment for the study and provides substance misuse and HIV/hepatitis prevention navigation, including navigation&nbsp;to PrEP,
for study participants. A Recruitment Coordinator who identifies with the community of focus conducts in-person and online outreach to their peers through dating apps/hook up sites. The Recruitment Coordinator will be responsible for recruitment and delivery of peer navigation&nbsp;to PrEP of P3 study participants.

Position: Research Project Recruitment Coordinator
Reports To: Supervisor II
Location: 1259 Flatbush Avenue, Brooklyn, NY 11226
What The&nbsp;Research Project Recruitment Coordinator Does:
The incumbent will: oversee recruitment of study participants through both online and in-person outreach; conduct risk screening for substance misuse and sexual health; provide navigation to link clients to PrEP and other appropriate services; and assist clients in attaining their goals by locating community resources and making appropriate social service referrals both within and outside CAMBA. This work is carried out in support of the goals and mission of CAMBA.
<ul>
<li>Assume primary responsibility for recruitment strategy&nbsp;and community&nbsp;engagement&nbsp;for P3 study, a partnership between CAMBA and Columbia University.</li>
<li>Identify&nbsp;and engage venues, organizations, and individuals as recruitment partners for P3.</li>
<li>Conduct recruitment activities 2-3 days per week.</li>
<li>Design and execute on-line (Meta, TikTok, dating/hook-up apps, etc.) recruitment strategy&nbsp;to support doubling of enrollments in Year 2 of recruiting.</li>
<li>Deliver peer navigation&nbsp;to enrolled P3 participants and other CAMBA clients.</li>
<li>Prepare marketing materials for the program.</li>
<li>Follow-up with clients and with referral organizations regarding client contact and progress with referral organization.</li>
<li>In collaboration with program staff, work with clients to break through barriers to client goals and to assist clients in advocating for themselves and in moving toward self-sufficiency.</li>
<li>Contact clients via telephone, mail and/or face-to-face home and office visits to ensure adherence to program, and document via progress notes.</li>
<li>Escort clients to appointments (educational, medical, social service, etc.).</li>
<li>Provide all required information for weekly/monthly/quarterly/annual reports.</li>
<li>Create and maintain client files and make copies of all client documents.</li>
<li>Conduct pre- and post-intervention assessments of clients’ knowledge, attitudes, and behaviors regarding HIV risk.</li>
<li>Prescreen clients over the telephone for eligibility and may schedule intake appointments.</li>
<li>Assist clients in completing all CAMBA intake applications and forms.</li>
<li>Schedule appointments for client with referral organizations.</li>
<li>Input client data and client progress information into automated database.</li>
<li>Contact clients for 30- and 90-day follow-up surveys.&nbsp;</li>
</ul>
Minimum Education/Experience Required:
<ul>
<li>Sufficient education (English-speaking, reading, writing, &amp; math abilities) to comprehend oral and written information and to assist callers and visitors and staff.</li>
<li>Two (2) years of relevant experience, preferably in a mid-sized (250+ employees) organization.</li>
<li>Good written &amp; verbal communication.</li>
<li>Computer literacy in Microsoft Office Suite.</li>
<li>Knowledge about, understanding of, and ability to work closely with, persons with HIV/AIDS and related issues.</li>
<li>Experience and/or comfort conducting online outreach via social media and dating/” hook-up” apps and websites.</li>
<li>Required to work occasional evenings/weekend days</li>
</ul>
Preferred Qualifications:
<ul>
<li>Bi-lingual English/Spanish preferred, but not required.</li>
</ul>
Compensation: $50,000 annually
Status: Full-time (35 hours per week)&nbsp; Benefits: CAMBA offers a comprehensive benefits package including health insurance, dental insurance, 403(b) retirement plan with employer match, paid time off (vacation, personal, and sick time), and paid holidays.
CAMBA is an Equal Opportunity Employer. We value a diverse workforce and inclusive workplace. People of color, people with disabilities, and lesbian, gay, bisexual, and transgender people are encouraged to apply. We consider all applicants without regard to race, color, religion, creed, gender, gender identity, gender expression, national origin, age, disability, socio-economic status, marital or veteran status, pregnancy status or sexual orientation.
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Research Project Recruitment Coordinator, P3

<h3>Job Description</h3>
Job Description
Position Summary:
A growing Health and Beauty Company is seeking a Formulation Chemist with past formulation experience related to health and personal care products. The primary purpose of the position is to formulate new products, create product documentation, prepare samples, coordinate R&amp;D trials, support manufacturing operations, and provide training to other members of the R&amp;D organization. The individual must engage with other departments including Quality, Regulatory Affairs, Sales, Manufacturing Operations, and Purchasing, to ensure procedures and specifications are set properly and can be met consistently.
Responsibilities:
● The Formulation Chemist will create and validate new formulas and processes and will support company initiatives regarding efficiency and innovations.
● Develop new and improved formulations including toothpaste, oral care products, lotions, creams, aerosols, capsules, and other personal care and pharmaceutical products.
● Collaborate with process engineering and the Operations team to establish manufacturing specifications and process instructions.
● Responsible for the formula and process transfer from R&amp;D to manufacturing.
● Research, evaluate, and approve raw materials for use in manufactured products.
● Generate and analyze data to validate finished goods and support new products. Monitor product test history and stability data. Ensure formulas are maintained and updated.
● Assess the impact of formula changes with respect to cost, specifications, and labeling.
● Manage multiple projects at one time. Provide regular and timely feedback on project statuses.
● Assist in writing, editing, and training on department SOPs as needed.
Company DescriptionHealth and Natural Beauty USA Corp has 30 years of co-packing and contract manufacturing expertise. Our state-of-the-art facility is cGMP registered and located in Piscataway, NJ. From custom product formulation and design to exclusive package engineering, our technology and development teams have the capabilities and innovative knowledge to deliver. Our patented formula of our own brand "SprinJene Natural toothpaste" is distributed all over the country and abroad. 
<h3>Company Description</h3>
Health and Natural Beauty USA Corp has 30 years of co-packing and contract manufacturing expertise. Our state-of-the-art facility is cGMP registered and located in Piscataway, NJ. From custom product formulation and design to exclusive package engineering, our technology and development teams have the capabilities and innovative knowledge to deliver. Our patented formula of our own brand "SprinJene Natural toothpaste" is distributed all over the country and abroad.

R&D Scientist

<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 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.
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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. 
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