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<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 Summary:
We are seeking a detail-oriented and proactive Analytical Associate Scientist or Scientist to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards.
Key Responsibilities:
<ol>
<li>Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required.</li>
<li>Prepare reagents, standards, and samples according to established protocols.</li>
<li>Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation.</li>
<li>Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations.</li>
<li>Assist in method development, validation, and troubleshooting of analytical procedures.</li>
<li>Collaborate with cross-functional teams to support project timelines and deliverables.</li>
<li>Participate in the review and update of SOPs, batch records, and other quality documentation.</li>
<li>Support continuous improvement initiatives and additional tasks as assigned by the supervisor.</li>
</ol>
Qualifications:
<ol>
<li>BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization.</li>
<li>Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred.</li>
<li>Strong attention to detail, organizational skills, and commitment to data integrity.</li>
<li>Ability to work independently and collaboratively in a fast-paced team environment.</li>
<li>Good communication skills and the ability to clearly document and present data.</li>
<li>Experience working in a CRO or CDMO setting is an advantage.</li>
</ol>
#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.

Analytical Associate Scientist/Scientist

<h3>Job Description</h3>
Job DescriptionQuality Control Microbiology Engineer(s) I, II, III Quality Control Microbiology Engineer I The “Quality Control (QC) Microbiology Engineer I” will support two local sites serving as a support role to clinical and/or commercial production. The QC Microbiology Engineer will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of QC Microbiology, responsibilities of the QC Microbiology Engineer I will include but are not limited to: Microbiological Testing:
<ul>
<li>Growth Promotion</li>
<li>Microbial Identification</li>
<li>Sterility Testing</li>
<li>Gram Stain</li>
<li>Endotoxin</li>
</ul>
Equipment Monitoring:
<ul>
<li>Ensure equipment is in proper working conditions</li>
<li>Ensure all equipment is properly maintained/calibrated</li>
<li>Shipping of test samples and equipment to contract laboratories for testing</li>
<li>Complete all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).</li>
</ul>
REQUIREMENTS
<ul>
<li>Associates degree in a science or relevant field required</li>
<li>Training in GxP/ GDP, Safety</li>
<li>Minimum 0-2 years of experience or equivalent experience.</li>
<li>Microbiology testing or within the biopharmaceutical industry experience preferred.</li>
<li>Proficient with computer software; Microsoft Office</li>
<li>Strong written and oral communication skills</li>
<li>Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities</li>
<li>Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels</li>
<li>Must be able to work during the weekend, holidays and as required by the company</li>
<li>Duties, responsibilities, and activities may change at any time with or without notice.</li>
</ul>
QC Microbiology Engineer II The Quality Control Microbiology Engineer II will support two local sites serving as a support role to clinical and commercial production. The QC Microbiology Engineer II will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of Microbiology, responsibilities of the QC Microbiology Engineer II will include but are not limited to: Microbiological Testing:
<ul>
<li>Growth Promotion</li>
<li>Microbial Identification</li>
<li>Sterility Testing</li>
<li>Gram Stain</li>
<li>Endotoxin</li>
</ul>
Equipment Monitoring:
<ul>
<li>Ensure equipment is in proper working conditions</li>
<li>Ensure all equipment is properly maintained/calibrated</li>
<li>Shipping of test samples and equipment to contract laboratories for testing</li>
<li>Produce documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).</li>
<li>Writing/conducting investigations pertaining to microbiological testing</li>
<li>Develop and train QC Microbiology Engineer I personnel on relevant business processes</li>
</ul>
REQUIREMENTS
<ul>
<li>BA/BS in a science or relevant field required or equivalent experience</li>
<li>Minimum 2-4 years of experience with microbiological testing or within the biopharmaceutical industry.</li>
<li>Training in GxP/GDP, Safety</li>
<li>Proficient with computer software such as; Microsoft Office</li>
<li>MODA/LIMS</li>
<li>Familiarity with ISO and EU standards</li>
<li>Strong written and oral communication skills</li>
<li>Technical writing skills</li>
<li>Technical training ability</li>
<li>Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities</li>
<li>Supervisory Responsibility</li>
<li>Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels.</li>
<li>Employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.</li>
<li>Must have the ability to work in a team-oriented environment and with clients</li>
<li>Must be able to work during the weekend, holidays, and as required by the company</li>
<li>Occasionally personal protective equipment may be required including lab coat, latex gloves, safety glasses and/or respirator.</li>
<li>Duties, responsibilities, and activities may change at any time with or without notice.</li>
</ul>
QC Microbiology Engineer III The Quality Control Microbiology Engineer III will support two local sites. Serving as a support role to clinical and/or commercial production. The QC Microbiology Engineer III will coordinate data for batch release, participate in project/client meetings, and author/revise microbiological testing procedures. Additionally, the incumbent will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of Microbiology, responsibilities of the QC Microbiology Engineer III will include but are not limited to:
<ul>
<li>Documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).</li>
<li>Coordinates microbiological testing data for batch release</li>
<li>Participation in project/client meetings and communications, providing scientific and technical expertise</li>
<li>Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols</li>
<li>Review of investigations and documentation of non-confirming events and environmental excursions.</li>
<li>Apply expertise of compliance requirements to maintain an inspection-ready state.</li>
<li>Participate and act as subject matter expert during audits/inspections</li>
<li>Develop and train QC Microbiology Engineer II on relevant business processes</li>
<li>Processing of purchase orders for outsourced testing and lab supplies</li>
<li>Coordinates work orders</li>
<li>Other duties as assigned</li>
</ul>
REQUIREMENTS
<ul>
<li>BA/BS in a science or relevant field required or equivalent experience</li>
<li>Minimum 5-7 years of experience with environmental monitoring or within the biopharmaceutical industry</li>
<li>Minimum required training; GxP/GDP Training, Safety Training </li>
<li>Proficient with computer software such as; Microsoft Office, MODA/LIMS; Microsoft Visio (preferred); Netsuite (preferred); Maximo Asset Management System (preferred)</li>
<li>Proficient knowledge of ISO and EU standards</li>
<li>Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review.</li>
<li>Strong written and oral communication skills</li>
<li>Strong technical writing skills</li>
<li>Technical training experience</li>
<li>Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities</li>
<li>Supervisory Responsibility; Direct reports</li>
<li>While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.</li>
<li>Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels.</li>
<li>Must have the ability to work in a team-oriented environment and with clients. </li>
<li>Must be able to work during the weekend, holidays and as required by the company</li>
</ul>

QC Microbiology Engineer(s) I, III

<h3>Job Description</h3>
Job Description
Greenberg-Larraby, Inc. (GLI) is seeking a skilled and dedicated Medical Physicist to join our innovative oncology team at a well-known hospital facility in NJ. 
 In this vital role, you will be responsible for ensuring the safe and effective delivery of radiation therapy through the application of physics principles and techniques.
Your responsibilities will include conducting quality assurance checks on radiation therapy equipment, developing and implementing treatment plans in collaboration with radiation oncologists and dosimetrists, and providing expert guidance on radiation safety protocols. You will also engage in research initiatives aimed at advancing treatment modalities and improving patient outcomes.
At GLI, we highly value the expertise and contributions of our staff, fostering a collaborative environment that encourages professional growth and development.
A Master's degree or higher in Medical Physics or a related field is required, along with board certification by the American Board of Radiology (ABR) or equivalent. Candidates must be U.S. Citizens.
This position offers a Monday to Friday work schedule with no weekend or on-call commitments, promoting a healthy work-life balance.
Requirements
Key Responsibilities:
<ul>
<li>Perform routine quality assurance measurements and evaluations on radiation therapy equipment.</li>
<li>Collaborate with radiation oncologists to develop and implement treatment plans tailored to individual patient needs.</li>
<li>Ensure compliance with all safety standards and regulations related to radiation use.</li>
<li>Conduct patient dosimetry evaluations and treatment plan verification.</li>
<li>Participate in education and training of staff, residents, and students in medical physics topics.</li>
<li>Engage in research activities to advance knowledge in radiation therapy technologies and methodologies.</li>
</ul>
Minimum Requirements:
<ul>
<li>Master's degree or Ph.D. in Medical Physics, Physics, or a closely related field.</li>
<li>2 years plus experience is ideal.</li>
<li>Board certification in Medical Physics by the American Board of Radiology (ABR) or equivalent.</li>
<li>Active and unrestricted license or credentialing to practice in the applicable state.</li>
<li>Strong knowledge of radiation therapy physics and dosimetry.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Strong communication and interpersonal skills.</li>
<li>U.S. Citizenship required.</li>
</ul>
This is a long term contract and qualified individuals are encouraged to apply for immediate consideration. Highly competitve rates and benefits.
Benefits
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
<li>Family Leave (Maternity, Paternity)</li>
<li>Short Term &amp; Long-Term Disability</li>
</ul>
Disclaimer: 
Greenberg &amp; Larraby, Inc. will never send offer letters of employment unless a thorough interview process has taken place and all other internal processing has taken place.
 If you receive one from an outside party and is not from the URL of our firm at @greenberg-larraby.com), please do not respond. If you have further questions, please reach out to your administrator. 
When you apply to our positions, upon our interest, a recruiter will call you directly and will pre-screen prior to an interview. Offers of employment are contingent upon a thorough interview process, background check, and security clearance adjudication processing as applicable. Thank you.

Medical Physicist

<h3>Job Description</h3>
Design Research Lead, Manager level
​Capital One’s Experience Design organization is focused on co-creating memorable, meaningful customer and associate experiences that build our brand with humanity and drive business advantage. The goal of Experience Design Research is to accelerate teams’ learning velocity. We do this by conducting primary research studies, assessments, and testing. Additionally, we oversee democratized research/testing conducted by others. A key aspect of our role is to find and synthesize existing research and data to help teams acquire the knowledge they seek to make informed decisions.&nbsp;
Role Overview
As a Design Research Lead, you are responsible for collaborating with product managers, designers, and engineers to articulate learning needs, learning agendas, and research roadmaps. You track research questions and insights within your portfolio. You are well connected to and understand the tower’s strategy and needs in order to prioritize research activities including primary research, knowledge mapping, assessments, and testing. You maintain a close relationship to research peers across the line of business to identify opportunities to re-use learnings and collaborate on research that can serve multiple lines of business.
Role Expectations
<ul>
<li>
Research Expertise: Enabling focus and expectations for design research practice across cross functional portfolio and accelerates learning velocity
</li>
<li>
Leadership: Leads design projects, directing and delegating work for more junior team members while also mentoring &amp; helping to mature the overall research practice at Capital One.
</li>
<li>
Human-Centered: Effectively navigates the needs of partners and stakeholders, leveraging critical-thinking skills that factor in data, research insights, scalability and tech constraints that deliver meaningful, actionable insights and tracking how we influence insights-to-action.
</li>
<li>
Business-Focused: Demonstrates proficiency with products and processes and apply relevant insights on customers, competitors and broader market trends to business challenges that shape a shared point of view for their team, partners and stakeholders
</li>
<li>
Problem-Solving: Has a solid understanding of tech, data capabilities and emerging technologies and uses this knowledge to inform their work and help their cross-functional team move faster and navigate technical limitations in service of the impactful solutions
</li>
<li>
Collaboration: Leverages a rich network of partnerships across lines of business and the organization to foster collaboration and share solutions, incorporating cross-functional perspectives to bridge gaps in information
</li>
<li>
Communication: Presents work across levels and job functions using a human-centered approach that integrates design frameworks, data and research insights to articulate a compelling point of view that influences strategic decision-making and direction at senior levels
</li>
</ul>
Basic Qualifications
<ul>
<li>
At least 5 years of experience conducting quantitative research, qualitative research, or a combination of both
</li>
<li>
At least 4 years of experience conducting data analysis (such as: survey data, behavioral analytics, etc.)
</li>
<li>
At least 3 years of professional experience conducting user experience research in a corporate environment
</li>
</ul>
Preferred Qualifications
<ul>
<li>
7+ years managing user experience research in a corporate environment
</li>
<li>
4+ years experience working and influencing senior level executives
</li>
</ul>
At this time, Capital One will not sponsor a new applicant for employment authorization for this position.
The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked.
McLean, VA: $158,400 - $180,800 for Manager, Design
 &nbsp;
New York, NY: $172,800 - $197,200 for Manager, Design
 &nbsp;
Richmond, VA: $144,000 - $164,400 for Manager, Design
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Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate’s offer letter.
This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan.
Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the&nbsp;Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level.
This role is expected to accept applications for a minimum of 5 business days.No agencies please. Capital One is an equal opportunity employer (EOE, including disability/vet) committed to non-discrimination in compliance with applicable federal, state, and local laws. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City’s Fair Chance Act; Philadelphia’s Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries.
If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at 1-800-304-9102 or via email at <a href="mailto:RecruitingAccommodation@capitalone.com" target="_blank">RecruitingAccommodation@capitalone.com</a>. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations.
For technical support or questions about Capital One's recruiting process, please send an email to <a href="mailto:Careers@capitalone.com" target="_blank">Careers@capitalone.com</a>
Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site.
Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).

Design Research Lead, Manager level

<h3>Job Description</h3>
Job Description
Were seeking reliable individuals to support our team with straightforward, entry-level tasks related to our ongoing research on technology products. The role involves general assistant-style responsibilities and does not require prior experience in this field. Requirements:
<ul>
<li>Must be 18 or older</li>
<li>Comfortable with basic English communication</li>
<li>Willingness to learn and follow instructions</li>
<li>Flexible schedule </li>
</ul>

Research Assistant

<h3>Job Description</h3>
Job Description
Reproductive Medicine Associates of New York, one of the top fertility centers in the country, is seeking an experienced Senior Embryologist to work in our brand-new state of the art clinical laboratory in our New York City location.
Responsibilities Include:
<ul>
<li>Quality control procedures</li>
<li>Laboratory set-up</li>
<li>Media and culture dish preparation</li>
<li>Sperm preparation</li>
<li>Conventional insemination</li>
<li>Oocyte retrieval</li>
<li>Fertilization assessment</li>
<li>Embryo cryopreservation and thaw</li>
<li>Biopsies</li>
<li>ICSI</li>
</ul>
What Is Needed:
<ul>
<li>Ph.D., MS or BS in a chemical, physical, biological, or clinical laboratory science with 2-3 years of specific clinical laboratory experience required</li>
<li>Must have the ability to perform concentrated and complex mental activity with frequent involvement in complex and highly technical situations</li>
<li>Must have the ability to make sound, independent judgments based on laboratory protocols, and be able to collaborate with other multidisciplinary team members in an appropriate fashion</li>
<li>Must have the aptitude to learn to make appropriate judgments about the clinical significance of laboratory data</li>
<li>Have skills to access, input, and retrieve information from a computer</li>
<li>Must be able to communicate accurately and concisely</li>
<li>Excellent attention to detail and interpersonal skills are required</li>
</ul>
RMA of New York offers a great team-oriented working environment as well as a competitive salary and health benefits. Please visit our website: <a href="http://www.rmany.com" target="_blank">www.rmany.com</a>
Job Type: Full-time
Pay: $120,000.00 - $170,000 per year
Schedule:
<ul>
<li>4 day work week; at least one weekend day</li>
<li>10 hour shift</li>
<li>Day shift</li>
</ul>
Work Location:
<ul>
<li>In person with potential to float to RMANY - Brooklyn as needed</li>
</ul>
Ability to Relocate:
<ul>
<li>New York, NY 10022: Relocate after starting work (Required)</li>
</ul>
Benefits:
<ul>
<li>Paid time off</li>
<li>Health insurance</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>401(k)</li>
<li>Employee assistance program</li>
<li>Life insurance</li>
</ul>

Senior Embryologist

<h3>Job Description</h3>
Job Description
COMPANY OVERVIEW:
CERTERRA (formerly RMA Companies) is a growing national provider of testing, inspection, and certification services that support innovation in new product development, quality assurance, for project delivery, and engineered solutions for asset management. We are passionate about contributing to the sustainable development of the communities we serve.
We are a national firm with a global reach serving national and international clients from 30+ offices located in 10 states and are ranked on ENR’s Top 500 list alongside the nation’s top firms.
With a 60-year history, CERTERRA has a passion for high-end services, constant innovation, and investment in the development of world-class laboratory facilities, and interactive management technologies. Each member of our staff is committed to service, innovation, and the success of our clients.
 
Job Summary: We are seeking a Lab Supervisor to oversee our laboratory operations and ensure the highest quality of testing services. The supervisor will be responsible for supervising staff, assisting the Lab Director in developing and implementing lab policies and procedures, and maintaining compliance with regulatory standards. Qualifications
<ul>
<li>Associate’s degree in Engineering (preferred).</li>
<li>Minimum of 3+ years of experience with laboratory testing of construction materials, with at least 1+ years in a supervisory or managerial role</li>
<li>Strong knowledge of laboratory operations, quality control, and regulatory requirements</li>
<li>Excellent leadership, communication, and problem-solving skills.</li>
<li>Must have excellent interpersonal, verbal, and written communication skills.</li>
</ul>
Responsibilities
<ul>
<li>Oversee daily operations of the laboratory, including scheduling, staffing, equipment calibration and verification, and workflow management</li>
<li>Assist Lab Director in developing and implementing lab policies, procedures, and quality assurance programs</li>
<li>Ensure compliance with regulatory standards, accrediting agencies, and best practices</li>
<li>Lead and mentor laboratory staff, providing training and guidance as needed</li>
<li>Collaborate with other departments to ensure seamless integration of lab services</li>
<li>Handle any issues or concerns related to lab services promptly and effectively.</li>
</ul>
Technical Requirements:
<ul>
<li>American Concrete Institute (ACI) Certifications:</li>
<li>Aggregate Testing Technician - Level 1 or 2</li>
<li>Aggregate/Soils Base Testing Technician</li>
<li>Concrete Strength Testing Technician</li>
<li>Concrete Field-Testing Technician - Grade 1</li>
<li>Concrete Laboratory Testing Technician - Level 1 or 2</li>
<li>National Institute for Certification in Engineering Technologies (NICET): Construction Materials Testing: Asphalt, Concrete, Soils (Levels I, II, or III)</li>
<li>NJSAT Certifications: HMA Plant Technologist Level 1</li>
</ul>
Other Miscellaneous Qualities:
<ul>
<li>Familiarity with Lab Information Management Systems (LIMS)</li>
</ul>

Lab Supervisor

<h3>Job Description</h3>
Job DescriptionAt Focused Staffing, we don’t just fill positions,we transform lives, one rockstar talent at a time. Whether you’re eager to make a meaningful difference in behavioral health or dedicated to empowering students in K-12 education, our mission is to connect skilled, passionate professionals with the communities that need them most. As a leader in specialized staffing, we provide exceptional opportunities and support for every member of our team, creating lasting impact for those we serve and those who serve with us. Discover how your unique strengths can help build brighter futures across schools and behavioral health organizations nationwide.
Want to love what you do? Let's make it happen!Check out our candidates' success stories!
Reports To: High School Principal &amp; Vice Principal
Compensation Rate:
$50-$55/h
Qualifications:
<ul>
<li>
Bachelor’s Degree in Science Education, Biology, Chemistry, or related field
</li>
<li>
Valid New Jersey Teaching Certification in Science (Grades 9–12)
</li>
<li>
Knowledge of lab safety protocols and scientific inquiry methods
</li>
<li>
Familiarity with NJSLS Science Standards and Next Generation Science Standards (NGSS)
</li>
<li>
Strong classroom management and communication skills
</li>
<li>
Experience in high school science instruction preferred
</li>
</ul>
Job Summary: The Science Teacher will create engaging, hands-on learning experiences in Biology, Chemistry, and Physical Science, fostering curiosity, critical thinking, and problem-solving skills.
Key Responsibilities Include:
<ul>
<li>
Plan and deliver science lessons aligned with NGSS and district curriculum
</li>
<li>
Design and supervise safe, engaging laboratory experiments
</li>
<li>
Differentiate instruction for diverse learners
</li>
<li>
Use formative and summative assessments to guide instruction
</li>
<li>
Integrate technology and real-world applications into science learning
</li>
<li>
Maintain accurate records of student progress and participation
</li>
</ul>
Apply now!

High School Science Teacher (Biology/Chemistry)

<h3>Job Description</h3>
Job Description
Job Description: The Temporary Microbiology LaboratoryTechnician is responsible for performing general microbiological laboratoryduties as outlined below: 
Prepare microbiological media including QC sterilitychecks and media growth promotion testing 
Prepare specimens and materials, including cleaning theworkspace 
Perform microbiological testing of water in accordancewith standard procedures, using aseptic technique. 
Maintain accurate, up-to-date and concise laboratoryrecords 
General housekeeping/upkeep/cleaning of laboratory
Monitor, clean, and perform calibration checks forlaboratory equipment and machinery 
Dish washing of laboratory glassware 
Autoclave waste 
Stock laboratory supplies and maintain laboratoryinventory
Back up for Lab Analyst with respect to generalmicrobiological duties 
Work in a team environment under minimal supervision 
Participate in laboratory investigations 
Additional responsibilities as needed 
Skills/Experience/Education
Bachelor\'s degree or equivalent in Microbiology/Biologyor working towards said degree, with Microbiology related coursework 
Minimum of 6-12 months experience in a Microbiologylaboratory, preferred
Knowledge of GMP and aseptic techniques preferred 
Strong interpersonal skills 
Works well in a team environment 
Ability to work with minimal supervision 
Strong multi-tasking skills 
Precise, accurate and detail oriented

Microbiology Lab Technician

<h3>Job Description</h3>
NYU Langone Health is a fully integrated health system that consistently achieves the best patient outcomes through a rigorous focus on quality that has resulted in some of the lowest mortality rates in the nation. Vizient Inc. has ranked NYU Langone the No. 1 comprehensive academic medical center in the country for three years in a row, and U.S. News &amp; World Report recently placed nine of its clinical specialties among the top five in the nation. NYU Langone offers a comprehensive range of medical services with one high standard of care across 6 inpatient locations, its Perlmutter Cancer Center, and over 320 outpatient locations in the New York area and Florida. With $14.2 billion in revenue this year, the system also includes two tuition-free medical schools, in Manhattan and on Long Island, and a vast research enterprise with over $1 billion in active awards from the National Institutes of Health. For more information, go to NYU Langone Health, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter, YouTube and Instagram.
Position Summary: We have an exciting opportunity to join our team as a Physicist - Radiation Oncology (Staten Island + float to other campuses). In this role, the successful candidate will be responsible for maintenance of quality assurance program, supervision and review of dosimetrists tasks, review of planning procedures and oversight of the patient planning and treatment process with brachytherapy or external beam radiation therapy
Job Responsibilities:
<ul>
<li>Treatment Planning: Identifies and evaluates target volumes and critical structures. Generates QA plans as required for IMRT and reference points as needed for physics checks. Follows established policies and procedures as they relate to treatment planning. Demonstrated level of planning capability. Completeness of RT electronic charts: setup fields, DRR, CBCT, ref points, scheduling.</li>
<li>Performs other duties as assigned.</li>
<li>Quality Assurance: Performs assigned quality assurance tasks in a complete and timely fashion (linac monthly and annual QA, IMRT QA, brachytherapy QA). Performs assigned quality assurance tasks in a complete and timely fashion (initial chart checks, weekly chart checks, final chart review). Documents all quality assurance work in a complete and timely fashion and determines compliance in all categories included in the lists; initiates corrective action when necessary.</li>
<li>Participates in in-service programs and conferences. Attends all required department in-service meetings. Attends annual billing/documentation/safety classes. Attends annual Radiation Safety in-service.</li>
<li>Participation in training of Residents and Students: Assists in the training of Residents and Students on use of Eclipse or ARIA and the principle of treatment planning. Participates in research protocols.</li>
<li>Initiative: Makes suggestions for positive changes. Demonstrates ability to understand tasks and creatively apply solutions. Demonstrates ability to adopt and help develop new physics initiatives and policies. Readily accepts new assignments and responsibilities. Recognizes when help is needed by others and offers guidance and assistance. Monitors patient tracker to effect a smooth and orderly process for patients and staff.</li>
<li>Planning and Time Utilization: Work is thought out and planned in advance and successfully implemented. Coordinates own work to achieve efficiency and quality patient care. Work is completed in a timely manner, meeting schedules.</li>
<li>Documentation: All paperwork and electronic forms are complete, signed and labeled accordingly. Procedure codes are complete, timely and accurate. Documents, dates &amp; signs all changes to treatment set-up. Documentation for clinical trials and protocols is coordinated with appropriate parties.</li>
</ul>
Minimum Qualifications: To qualify you must have a Master's of Science degree in physics or engineering and completion of a training/residency program or a Master's Degree in an accredited Medical Physics program. Required license NYS Med Physicist License (Grace period - NA) or NYS Limited Med Physicist Permit (Grace period - NA) Well developed communication and computer skills. Required Licenses: NYS Limited Med Physicist Perm, NYS Med Physicist License
Preferred Qualifications: Certification (ABR);
Qualified candidates must be able to effectively communicate with all levels of the organization. NYU Langone Health provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents.
At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family. NYU Langone Health is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
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NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $213,477.55 - $235,000.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
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680 Science Jobs in New York, NY 10007, USA