field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Mercor is hiring on behalf of a leading AI-enabled research lab seeking a Sell-Side Equity Research Analyst / Associate to produce data-backed insights, forecasts, and coverage reports for institutional investors. The role blends traditional equity research with exposure to automation and AI-driven analytics, supporting the delivery of high-quality research across key market sectors.
Responsibilities
<ul>
<li>
Lead sector coverage by monitoring companies, market trends, and industry developments.
</li>
<li>
Develop and maintain detailed financial models and forecasts.
</li>
<li>
Prepare and publish research notes, coverage reports, and earnings summaries for institutional clients.
</li>
<li>
Collaborate with data teams to integrate automation, AI tools, and quantitative signals into research workflows.
</li>
<li>
Present findings and insights to senior analysts, clients, and internal teams.
</li>
</ul>
Qualifications
<ul>
<li>
2+ years of experience in sell-side equity research, covering a specific sector (e.g., tech, industrials, healthcare, etc.).
</li>
<li>
Proficiency in Excel modeling, valuation, and financial statement analysis.
</li>
<li>
Strong writing, presentation, and client communication skills.
</li>
<li>
Familiarity with Bloomberg, FactSet, and exposure to data visualization or automation tools.
</li>
<li>
Quantitative mindset — able to blend traditional analysis with structured data insights.
</li>
<li>
Degree in Finance, Economics, or STEM preferred; CFA or progress toward it a plus.
</li>
</ul>
Why Join
<ul>
<li>
Gain exposure to AI-enhanced research workflows, working alongside engineers, data scientists, and sector experts.
</li>
<li>
Build deep sector expertise while experimenting with new tools for forecasting and modeling automation.
</li>
<li>
Collaborate with top-tier investors and institutional research teams worldwide.
</li>
<li>
Flexible hours (20-30 hrs/week available) — ideal for analysts looking to expand into AI-driven finance.
</li>
<li>
Flexible remote schedule.
</li>
</ul>

Sell-Side Equity Research Associate

<h3>Job Description</h3>
Job Description
1. Role Overview
Mercor is partnering with a leading AI lab on a collaborative research project featuring top global superforecasters. We're seeking experts with deep knowledge of economics to contribute to high-stakes forecasting challenges aimed at advancing AI reasoning capabilities. This is a unique opportunity to contract with a curated forecasting cohort driving the next generation of AI systems.
2. Key Responsibilities
<ul>
<li>
Generate probabilistic forecasts on macroeconomic and financial indicators
</li>
<li>
Document forecasting rationale with clear, structured reasoning
</li>
<li>
Analyze trends and data sources to inform high-quality predictions
</li>
<li>
Engage with other domain experts to calibrate and refine outputs
</li>
<li>
Provide feedback on forecast design and methodology
</li>
</ul>
3. Ideal Qualifications
<ul>
<li>
Demonstrated experience in economic forecasting, data science, or related fields
</li>
<li>
Strong understanding of global macroeconomic trends and financial systems
</li>
<li>
Proven track record in prediction competitions (e.g., Metaculus, GJ Open) a plus
</li>
<li>
Ability to clearly explain complex economic logic in writing
</li>
<li>
Detail-oriented and intellectually curious
</li>
</ul>
4. More About the Opportunity
<ul>
<li>
Remote and asynchronous — work on your own schedule
</li>
<li>
Expected commitment: ~10–20 hours/week
</li>
</ul>
5. Compensation &amp; Contract Terms
<ul>
<li>
$105–140/hour for U.S.-based applicants
</li>
<li>
You’ll be classified as an independent contractor
</li>
</ul>
6. Application Process
<ul>
<li>
Submit your Mercor profile or resume to get started
</li>
<li>
You’ll complete a brief form
</li>
<li>
We’ll follow up within a few days with next steps
</li>
</ul>
7. About Mercor
<ul>
<li>
Mercor is a talent marketplace that connects top experts with leading AI labs and research organizations
</li>
<li>
Our investors include Benchmark, General Catalyst, Adam D’Angelo, Larry Summers, and Jack Dorsey
</li>
<li>
Thousands of professionals across domains like law, creatives, engineering, and research have joined Mercor to work on frontier projects shaping the next era of AI
</li>
</ul>

Economics Forecaster

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

GC Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
With over 100 years of experience, Sika is a worldwide innovation and sustainability leader in the development and production of systems and products for commercial and residential construction, as well as the marine, automotive, and renewable energy manufacturing industries.&nbsp; Sika has offices in over 100 countries with over 300 manufacturing facilities and more than 33,500 employees worldwide. With annual sales of 11.5+ billion dollars in 2022, our commitment to quality, innovation, and the environment as well as putting our customer’s needs first, encompasses why Sika is the global leader in our industries.&nbsp;
Job Description 
Develop new products and provide technical support to production plants and customers. Analyze substances to determine their composition and concentration of elements. Conduct tests on materials and other substances to ensure that safety and quality standards are met.
<ul>
<li>Independently develop new specialty chemical products and industrial materials according to customer specifications in the construction and industrial markets.</li>
<li>Develop DOE (Design of Experiments) and design FEMA for product development.</li>
<li>Define new product QA requirements to ensure product quality and performance.</li>
<li>Transfer new products/technologies to the Processing group.</li>
<li>Perform initial material testing and gain material approvals from customers.</li>
<li>Provide technical support to manufacturing plants to assure product quality.</li>
</ul>
Qualifications 
<ul>
<li>Two (2) years of experience in the offered role, or a related position.</li>
<li>Minimum requirement, a Bachelor’s degree (or foreign equivalent) in Chemistry, Polymer Science, Material Science, Chemical Engineering, or a related field plus five (5) years of experience in the offered role, or a related position.</li>
<li>Master’s degree (or foreign equivalent) in Chemistry, Polymer Science, Material Science, Chemical Engineering, or a related field.</li>
<li>Must have two (2) years of experience in each of the following (experience may be gained concurrently):
<ul>
<li>Hands-on industrial experience in polyester concrete overlays, cement-based mortars, and mortar&nbsp;admixtures</li>
<li>Experience with specific laboratory equipment for testing mortars, and normal concrete products; and</li>
<li>Microsoft Word, Excel, PowerPoint, and Project Management.</li>
</ul>
</li>
</ul>
<ul>
<li>Strong presentation skills. Excellent technical and business writing skills.</li>
<li>Excellent skills in DOE, Design FEMA, and other quality programs.</li>
<li>Good computer skills in Microsoft Word, Excel, PowerPoint, and Project Management.</li>
</ul>
 Additional Information 
Building Trust, Every Day
Competitive Benefits: Health Insurance, 401k with company match, year-end profit-sharing bonus, paid time off, and paid holidays. Meaningful Work: Sika products enhance our surroundings and the work every employee completes helps positively impact daily lives by making our world stronger, more durable, and more reliable – every day. Company Culture: Sika centers work culture around entrepreneurship where individuals have the power to make decisions, learn from mistakes, and define their career.
Community Involvement:&nbsp; Sika takes active roles in our community and aims to support volunteer work and charitable endeavors across the United States through rebuilding and giving back. Sustainability Initiatives: Sika is committed to sustainable development, reducing environmental impacts, and assuming social responsibility. The company supports energy efficient projects and implements numerous measures aimed to boost economic, social, and ecological sustainability.
Sika Corporation is committed to a work environment that supports, inspires, and respects all individuals that apply. As an equal opportunity employer Sika will consider all qualified applicants without discrimination on the basis of race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, disability, national or ethnic origin, or other protected characteristics.

Chemist--Resins

<h3>Job Description</h3>
Job DescriptionDescription:
Title: Senior Peer Mentor 
Department: Behavioral Health 
Reports To: Senior Director Client Services 
Location: Next Step Resource &amp; Recovery Center, 56 Bay Street, Staten Island, NY 10301 
Position Status: Full-Time 
FLSA Status: Non-Exempt 
Pay Rate/Benefits: The pay range for this role is generally $37,000 - $42,000 annually, commensurate with relevant experience and qualifications and in alignment with internal equity. Additionally, we offer an excellent benefits package that includes generous paid time off (4 weeks of vacation plus paid holidays, personal, and sick time), medical, dental, vision, supplemental benefits including employer provided basic life insurance and employee assistance programs, tuition reimbursement and fitness reimbursement after 1 year of employment, a retirement plan that includes employer matching, and more! 
 
Community Health Action of Staten Island (CHASI) drives dramatic improvements in the health of New Yorkers by feeding people who are hungry, healing families broken apart by violence, and bridging the gaps between people and the compassionate health care they deserve. CHASI serves the most vulnerable individuals, families, and communities with critical services and programs. CHASI provides outreach, education, prevention, and direct support services for populations most affected by health disparities – the poor and working poor, low income people with chronic illnesses, persons with criminal justice involvement, substance users, domestic violence survivors, people of color, and the LGBTQ community. 
 
POSITION SUMMARY: CHASI’s Next Step Resource and Recovery Center is a hub for people and families struggling with drug and alcohol addiction and substance use. The Next Step Center is a caring, energetic recovery support community for Staten Islanders in all stages of recovery from dependency on drugs or alcohol. 
The Senior Peer Mentor provides outreach, engagement, and accompaniment to individuals and families using Next Step programs on-site as well as in the community. The Senior Peer Mentor also engages individuals who have survived an opioid overdose at partnering hospital emergency rooms to provide support, collaborate on tailored strategies to reduce future overdose, train on and dispense naloxone, and assist with connection to any needed community-based services. The Senior Peer Mentor conducts telephone and office-based follow up with individuals recently seen in the precinct or the hospital. 
 
DUTIES &amp; RESPONSIBILITIES:
 
Relay Overdose Response Initiative
<ul>
<li>Receive and reply rapidly to notifications from participating hospital emergency room when notified of an individual being treated for an opioid overdose </li>
<li>Travel to partnering hospital emergency room within 45 minutes of notification to meet with, support, and engage into the Relay program the individual who has survived an opioid overdose </li>
<li>Discuss Relay program benefits and service approach with each individual and explain the evaluation model and informed consent process. </li>
<li>Collaborate with each individual to develop personalized strategies to reduce future opioid overdose risk, including discussion of safer drug using behaviors </li>
<li>Partner with the Emergency Department Warm Handoff Recovery Coach to address the service needs agreed to by each individual, which may include substance use treatment, harm reduction, benefits, or other supportive services </li>
<li>Provide each individual and any accompanying friends/family members with naloxone (Narcan) kit and training or ensure its provision by emergency department staff </li>
<li>Arrange with each individual a 24-48 hour follow up plan </li>
</ul>
Next Step Recovery Community Center Services
<ul>
<li>Welcome and engage individuals who are seeking assessment and linkage to services responsive to their individual needs and readiness for change </li>
<li>Provide overview of on-site services and orient Recovery Center members to program guidelines </li>
<li>Conduct naloxone (Narcan) training and dispensing </li>
<li>Accompany participants to other provider sites to provide support and navigation assistance </li>
<li>Reach out to participants to follow up on referrals made and to reengage them into programming </li>
<li>Facilitate on-site recovery-oriented groups or social activities, as assigned </li>
<li>Assist with community outreach and program promotion to inform the public of available resource and recovery center services </li>
<li>Align all activities with CHASI’s mission, core values, and culture </li>
<li>Other duties as assigned </li>
</ul>
QUALIFICATIONS: 
<ul>
<li>High school diploma or high school equivalency required </li>
<li>Recovery Coach Certification or Certified Recovery Peer Advocate (CRPA) required. Individuals currently holding a Certified Alcohol and Addiction Counselor (CASAC) or CASAC-Trainee may be considered but must complete Recovery Coach or CRPA programs within 90 days of hire </li>
<li>Must be able to complete all required background and medical clearances within 90 days of hire, including COVID and Flu vaccination </li>
</ul>
 
Requirements:
QUALIFICATIONS: 
<ul>
<li>High school diploma or high school equivalency required </li>
<li>Recovery Coach Certification or Certified Recovery Peer Advocate (CRPA) required. Individuals currently holding a Certified Alcohol and Addiction Counselor (CASAC) or CASAC-Trainee may be considered but must complete Recovery Coach or CRPA programs within 90 days of hire </li>
<li>Must be able to complete all required background and medical clearances within 90 days of hire, including COVID and Flu vaccination </li>
</ul>
CHASI is an equal opportunity employer and is committed to hiring and supporting a diverse staff. People of color, LGBTQ, women, and people with disabilities strongly encouraged to apply. All qualified applicants will be afforded equal employment opportunities without discrimination because of race, religion, color, national origin, sex, sexual orientation, gender identity, age, genetic information, disability or marital status.

Senior Peer Mentor

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

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

QC Chemist

<h3>Job Description</h3>
Job Description
Actalent is urgently hiring for a Clinical Laboratory Technologist
**Microbiology experience is a must for this role**
Start Date: ASAP
Shift: Tuesday and Thursday 7am-5pm, &amp; Friday or Saturday 7am-5pm 30 hours weekly 
Department: Microbiology
Pay Rate: Up to $52 an hour, depending on experience
Location: Hicksville, NY 
Must Haves: 
<ul>
<li>Minimum 1 year of recent microbiology experience </li>
<li>NYS CLT License (NO exceptions) </li>
<li>VITEK preferred </li>
</ul>
Please apply to this posting for immediate consideration!
#LPN25
Job Type &amp; Location
This is a Permanent position based out of Hicksville, NY.
Pay and Benefits
The pay range for this position is $52.00 - $52.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hicksville,NY.
Application Deadline
This position is anticipated to close on Nov 27, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Medical Technologist Microbiology URGENT

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

688 Science Jobs in New York, NY 10007, USA