field_job_employment_type

field_job_occupational_field_parents_all

field_job_experience

job_organization_name

city

state

<h3>Job Description</h3>
Now hiring a part-time Lab Analyst for our premier client in Salt Lake City, UT! \n \nPay: $17.50-22/hr \nHours: 20 hrs/week (days and times are very flexible) \nLocation: Salt Lake City, UT 84123 \nPosition Type: Temporary (through 2025, likely will continue into mid Q1 2026) \n \nResponsibilities
\n\n
<ul>\n\t
<li>Creating scenarios to confirm the sterility standards in a newly created Cleanroom for Sterile testing\n\t</li>
<li>Prepping/working with various organisms\n\t</li>
<li>Inoculating organisms/infecting various surfaces with the organisms\n\t</li>
<li>Disinfecting the surfaces\n\t</li>
<li>Testing to see how effective the disinfectant was\n</li>
</ul>
\n\n
Qualifications
\n\n
<ul>\n\t
<li>Bachelor’s degree in biology, chemistry, or related field preferred but NOT required&nbsp;\n\t</li>
<li>Experience in a laboratory performing testing\n\t</li>
<li>Must have experience with sterile and aseptic techniques and standards\n\t</li>
<li>Must have experience with pipette use\n</li>
</ul>
 \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\tAs part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. 
Trust the office staffing pioneer.
 Finding the right job isn’t always easy. Kelly® Professional &amp; Industrial takes the guesswork out of your job search by connecting you with great opportunities that work for you. That means your schedule, your interests, and your career plan. In fact, our company created the staffing industry with the goal of connecting people with great office jobs—so you could say we’re pretty good at it!\n\t\t\t \n\t\t\t \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t
About Kelly
 Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. \n\t\t\t \n\t\t\t

Lab Analyst

<h3>Job Description</h3>
Job DescriptionSalary: 
Why DelRicht Research?
Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position with sustainable opportunities for professional growth? DelRicht Research might be the right opportunity for you! 
Who We Are
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states. 
DelRicht Research has been recognized as a Top Workplace for 2023, 2024, and 2025! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction. 
Healthcare Project Coordinators Main Objective: Overall, the Healthcare Project Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies:
<ul>
<li>Patients have a fun, positive and comfortable experience at our clinic</li>
<li>Patient visits are completed accurately and efficiently seeing to it that all clinical trial protocols are being adhered to 100% of the time</li>
<li>Patient recruitment and enrollment into clinical trials</li>
<li>Ensuring patients come to and complete their clinical trial visits throughout the study</li>
<li>Data Entry timely and accurately entered for clinical visits into multiple online systems</li>
<li>Lead and main point of contact for Pharmaceutical Sponsors and Contract Research Organizations for all clinical trials</li>
<li>Ensuring Sponsors and Clients have amazing customer service when they are onsite at our clinic and assuring we are always providing clear, constant communication with them when they are off site</li>
<li>Maintaining Physician Trust - You are seen as a go to, knowledgeable resource to our physicians including ensuring the physician is well informed of their schedule and updated on all current clinical trial patients and protocols</li>
</ul>
 Skills needed to win:
<ul>
<li>Required: Minimum of 2 years professional working experience with one being directly within a healthcare setting.</li>
<li>Nursing, Radiology Technician, Respiratory Therapist, or medical assistant experience highly desirable!</li>
<li>Prior clinical research experience is not required (but wonderful if you have it, of course!)</li>
<li>Coffee drinkers preferred. Tea drinkers accepted.</li>
</ul>
 The Right Candidate Will:
<ul>
<li>Be self motivated! Energetic! Positive!</li>
</ul>
<ul>
<li>Focus on providing exceptional patient care and creating memorable experiences</li>
</ul>
<ul>
<li>Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals</li>
</ul>
<ul>
<li>Believe in high quality and have a high standard of compliance to our study protocols</li>
</ul>
<ul>
<li>Be remarkably organized</li>
</ul>
<ul>
<li>Be skilled at problem solving, planning and being proactive</li>
<li>Accept ownership of tasks from inception through completion and assume responsibility for personal success</li>
</ul>
 DelRicht Researchs Core Values: Production, Humility, Consistency
Production:
<ul>
<li>We deliver on our promises</li>
<li>We have a bias towards action: we value independent problem solving</li>
<li>We proactively over deliver: we can act without being told what to do and we always have new ideas that will be heard and will improve the company </li>
</ul>
Humility:
<ul>
<li>We support each other relentlessly</li>
<li>We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a can do attitude</li>
<li>We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us</li>
<li>Coachable: we all love to learn, we are willing to be taught and will adapt quickly </li>
</ul>
Consistency:
<ul>
<li>We always are able to execute: we get it right the first time and promote touch it once accuracy</li>
<li>We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done</li>
<li>We are calm under pressure: we can maintain stable performance when under heavy pressure or stress</li>
</ul>
Team Perks &amp; Benefits at DelRicht Research:
<ul>
<li>Medical, Dental, Vision with generous employer paid contributions</li>
<li>Short and Long Term Disability and Group Life Coverage</li>
<li>Paid Time Off that builds throughout your career with the company</li>
<li>401K (+ discretionary match/profit sharing)</li>
<li>Exceptional quarterly bonus plan that clearly outlines your bonus potential per quarter and giving the team the visibility and control to maximize earnings by hitting team goals </li>
</ul>
Job Type: Full-Time 40+ hrs
 Visit our website linked below to learn about our company and current clinical trials, see patient testimonials, and check out our careers page!
Website: <a href="http://www.delrichtresearch.com" target="_blank">www.delrichtresearch.com</a>
Patient Testimonials: <a href="https://delrichtresearch.com/testimonials/" target="_blank">https://delrichtresearch.com/testimonials/</a>
 We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Healthcare Project Coordinator

<h3>Job Description</h3>
Overview A challenging and exciting career is waiting for you! General Dynamics Electric Boat has a proud history dating back to its incorporation on February 7, 1899, and the delivery of the first practical submarine to the U.S. Navy the following year. During the ensuing century, Electric Boat has been at the forefront of every innovation in submarine technology. Today, we are the nation's premier designer and builder of nuclear submarines. We deliver the advantage that protects our sailors, our families and our freedom! Benefits 
<ul>\n
<li>Medical, Dental, Vision</li>
\n
<li>Prescription Coverage</li>
\n
<li>Health and Wellness Programs</li>
\n
<li>401K</li>
\n
<li>Commuter/Van Services</li>
\n
<li>Paid Vacation and holidays</li>
\n
<li>Paid training</li>
\n
<li>Shift Differential for 2nd and 3rd shifts</li>
\n
<li>Advancement Opportunities</li>
\n</ul>
\n Learn more at gdeb.com/careers The 3D Metrologist in the Accuracy Control Group of the Quonset Point Engineering Department performs 3-dimensional measurement and analysis services for the facility. Responsibilities include, but are not limited to: 
<ul>\n
<li>Providing technical measurement support for construction activities, structural, mechanical and piping manufacturing at Quonset Point</li>
\n
<li>Performing 3-dimensional surveys, processing the data within a graphical analysis software package and develop analysis reports to identify specific measurement points relative to drawing specifications</li>
\n
<li>Ability to learn new instrumentation and software associated with 3-dimensional measuring as new technologies emerge</li>
\n
<li>Collection of high precision datasets via laser tracker, industrial photogrammetry, and various CMM / scanning technologies</li>
\n</ul>
\n Click this link to learn more: <a href="https://youtu.be/oirjeZxpF50" target="_blank">https://youtu.be/oirjeZxpF50</a> This is position is located at the Quonset Point facility in North Kingstown, RI. Qualifications Required: 
<ul>\n
<li>High School Diploma or equivalent</li>
\n
<li>Minimum 1 year of experience using 3-dimensional measurement equipment (Total Stations, photogrammetry, laser tracker, laser scanner, CMM) or Robotic programming</li>
\n
<li>Strong math background including strong knowledge of geometry and trigonometry</li>
\n
<li>Able to read and interpret blueprints, Geometric Tolerance, specifications and procedures</li>
\n
<li>Willing to support occasional travel to vendor sites</li>
\n
<li>Able to obtain and maintain a security clearance through the Department of Defense</li>
\n</ul>
\n Preferred: 
<ul>\n
<li>Associate Degree in Surveying Technology or Engineering Technology</li>
\n
<li>Experience in land surveying or as a Metrology Technician</li>
\n
<li>Experience with a graphical analysis software package such as Spatial Analyzer</li>
\n
<li>Relevant Navy/Military experience </li>
\n</ul>
 Skills 
<ul>\n
<li>Strong mathematical, oral and written communication, computer and interpersonal skills</li>
\n
<li>Ability to work in a collaborative and team environment to meet organizational goals</li>
\n
<li>Independent thinking and problem solving abilities </li>
\n</ul>
 Physical Qualifications Climbing, Color Vision, Crawling, Kneeling, Light Lifting, Medium Lifting, Pulling, Pushing, Reaching, Stooping, Twisting Environmental Attributes Cold, Dry, Dusty, Fumes, Hot, Inside, Noise, Oily, Outside

Accuracy Control 3D Metrologist

<h3>Job Description</h3>
Job Description
VCS is looking for a computational chemistry/Toxicology Scientist for one of our client
Job Title -&nbsp;Computational Chemistry/Toxicology Scientist
Job Location -&nbsp;Indianapolis, IN 46077
Contract- 12+ Months with possible extension
Shift- Day M-F 40 hrs./week
Pay- 57/Hr. 
Description: The client has an exciting and challenging opportunity in the Predictive Safety Center within Regulatory Science for a Computational Scientist Contractor with expertise in c/Bioinformatics. The individual will partner with a multidisciplinary team to design, develop, and implement machine learning models to predict safety profiles of chemicals to support the discovery, development and registration of novel crop protection products. This position is located in Indianapolis, IN, while strong candidates working remotely will be considered. Responsibilities:
<ul>
<li>Develop and apply chemistry structure-based predictive models for assessing safety profiles of early-stage discovery molecules</li>
<li>Assess potential mechanisms of toxicity by assessing ligand-protein binding affinity using protein structure alignment, binding pocket evaluation, and molecular docking</li>
<li>Work collaboratively with internal and external cross-functional multidisciplinary teams, collaborators, and consultants to implement in silico models to meet business needs</li>
<li>Serve as a subject matter expert on in silico modelling for the team and other partners in R&amp;D sub-functions</li>
<li>Present the development and application of cheminformatics/bioinformatics approaches and novel ML/DL models internally and externally including scientific conferences</li>
<li>Keep abreast of the latest scientific development in the areas of machine learning, cheminformatics, bioinformatics, and related fields and identify technologies to be applied internally</li>
<li>Analyze complex datasets using machine learning approaches and interpret results to improve data-driven decision-making processes</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. degree in Cheminformatics, Computational Chemistry, Computational Biology, Bioinformatics, Toxicology, or a related field</li>
<li>3+ years of experience in developing machine learning models and applying cheminformatics/bioinformatics and AI for structure-based drug design, toxicology assessment, mechanism prediction</li>
<li>Strong technical background in machine learning, deep learning, and statistical modeling with prior experience in applying these techniques to process, analyze and draw insights from complex datasets involving chemical compound structures and toxicity endpoints</li>
<li>Demonstrated programming proficiency in Python and experience in utilizing machine learning libraries</li>
<li>Demonstrated in-depth knowledge in toxicology, chemistry, chemical structure, QSAR, protein structure</li>
<li>Knowledge in omics analysis and systems biology is a plus</li>
<li>Demonstrated teamwork and project leadership skills to manage multiple projects on different timelines for stakeholders across the business</li>
<li>Excellent communication and presentation skills to different stakeholder audiences</li>
</ul>
Thank You!
Bhanendra S Singh Vish Consulting Services(VCS) Bhanendra @vishusa.com

Computational Chemistry/Toxicology Scientist

<h3>Job Description</h3>
Job DescriptionFor further inquiries regarding the following opportunity, please contact our Talent Specialist Prawin at 224 369 2969&nbsp;&nbsp;Title: Research Associate Scientific II Location: Onsite/Hybrid in Round Lake, IL, 3 days onsite and 2 days remoteDuration: 18 Months contract Work Schedule: 8-hour workdays (between 7-5)&nbsp;Top 3-5 Must-Have Non-Negotiable Skills Required 1. Basic technical understanding of sterilization (Moist Heat, Aseptic, Irradiation) 2. Basic technical understanding of microbiological method validations (sterility, bioburden and bacterial endotoxin) (specific for the Research Associate II) 3. Ability to write, execute and review validation and qualification protocols and reports. 4. Ability to evaluate and interpret technical data and test resultsBachelor’s degree required&nbsp;These roles would be geared towards a Sterility Assurance support role will focuses on Microbiology. 2-4 years of recent experience preferred&nbsp;Nice to Have Skills 1. Understanding of aseptic technique (RAII) 2. Ability to conduct experiments with minimal assistance 3. Knowledge and understanding of GxP and related regulations and guidance&nbsp;&nbsp;
<ul>
<li>Effectively contribute solid technical knowledge to a variety of projects within the sterility assurance discipline with minimal assistance.</li>
<li>Display basic technical understanding of related sterility assurance disciplines, specifically sterilization modalities and/or microbiological test method validation.</li>
<li>Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.</li>
<li>Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines.</li>
<li>Maintain knowledge of relevant Quality System Regulations and safety requirements while building knowledge of other regulatory requirements related to R&amp;D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.</li>
<li>Recommend appropriate designs, techniques and processes for a specified sequence of tasks where needed.</li>
<li>In-depth knowledge and understanding of GxP and related regulations and guidance.</li>
<li>Provide support to the Sterility Assurance Focal Point for product development or on change controls.</li>
<li>Write, execute and review validation and qualification protocols and reports.</li>
<li>Evaluate and interpret technical data and test results.</li>
<li>The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills.</li>
<li>Bachelor's Degree &nbsp;in a scientific discipline with at least 2-4 years lab experience.</li>
<li>Background in microbiology</li>
<li>somebody that knows the basics of microbiology, aseptic technique has worked with organisms in a lab.</li>
<li>Ideally would be somebody that has a sterile assurance.</li>
<li>Understanding a little bit of the micro methods and validations required for a pharmaceutical company.</li>
<li>it's a research associate 2 level, so has a few years of experience in the lab.</li>
<li>And also looking for them to help with report generation. So analyzing data and putting it into a template for report.</li>
<li>word, excel basic general understanding of the Microsoft platform would be enough.</li>
<li>work will be report generation and data analysis, probably 80% 20%.</li>
<li>Bachelors degree 2 years will be ideal</li>
<li>Looking for biology or microbiology, but any really of those extensions, if they have lab skills or have done plating and dilution working with microorganisms.</li>
<li>Masters, if they have maybe one year of experience would probably be OK, but PHD may be overqualified for this level.</li>
<li>Academic lab experience be considerable</li>
</ul>
 Interview process: 2 interviews &nbsp;(Teams and Onsite, Length, Rounds, Team involved) Teams, one round, two team members involved, 30-45 minutes.

Research Associate Scientific II

<h3>Job Description</h3>
Job DescriptionSalary: $19.50 - $ 22 per hour 
Integrated Environmental Solutions, LLC (IES) is seeking to immediately hire multiple archeological field technicians to assist with projects within Arkansas, Oklahoma, and Texas.IES is in the process of surveying approximately 4,000 acres for the U.S. Army Corps of Engineers Little Rock District and will be starting survey for a major fiber optic line project in the coming weeks. We also have ongoing Phase III excavation at a prehistoric habitation site and cemetery. We have sufficient work underway and planned to keep applicants busy continuously for the next 6 to 8 months, which could be extended or lead to permanent positions.Applicants with Phase III experience will be given priority ranking to assist with the Phase III project. 
To find out more about IES, please visit our website at <a href="http://www.intenvsol.com" target="_blank">www.intenvsol.com</a> or find us on social media: @IntegratedEnvironmentalSolutions on Facebook, @i.e.solutions on Instagram, or Integrated Environmental Solutions, LLC on LinkedIn. 
Compensation
<ul>
<li>Initial pay will be $19.50 to $22/hr based on experience.</li>
<li>Per diem will be based on GSA rate for project location. </li>
<li>Overtime beyond 40hrs per week is expected and will be paid at time and half</li>
<li>Single occupancy lodging will be provided</li>
<li>Typical Schedule 10 days rotations and standard Monday through Friday schedules will be required.</li>
<li>Maximum 8 to 10hr days anticipated </li>
<li>401k available after 6 months of employment. </li>
</ul>
Qualifications:
To apply for this position the applicant must meet the following qualifications:
<ul>
<li> Hold a bachelors degree in anthropology, archeology, or a closely related field</li>
<li> Have a minimum of 12 months field experience or have completed an accredited archeology field school required</li>
<li> Experience conducting archeological monitoring and/or survey </li>
<li> Experience recording sites, completing field notes and paperwork, and familiarity with GPS and GIS technology</li>
<li> Must be able to mobilize quickly </li>
<li> Must have a valid drivers license and clean driving record</li>
</ul>
Physical Demands:
Physical requirements for project will included: 
<ul>
<li> Regularly required to use hands, walk, sit, talk, and listen, stand; climb, balance; stoop, kneel, crouch, or crawl </li>
<li> Survey work will require hiking long distances daily over rugged terrain while shovel testing</li>
<li> Work is less than favorable environmental conditions</li>
<li> The employee must occasionally lift and/ or move up to 50 pounds.</li>
</ul>

Archeological Field Technician - Long-term

<h3>Job Description</h3>
Job DescriptionSalary: 
Market Research-Quantitative Project Director/Sr. Project Director (temporary role, full-time hours, and potential to become regular staff employee)
Location:Remote (U.S.-based, EST time zone workday)
Lieberman is looking to add a Project Director/Senior Project Directorwith a true passion for consumer insights and storytelling to join our quantitative research team. This individual will work together with our custom research team to execute multiple research projects.
Key Responsibilities
<ul>
<li>Independently manage multiple complex national and international research projects simultaneously</li>
<li>Write questionnaires</li>
<li>Manage fielding of projects</li>
<li>Oversee data processing and data analysis</li>
<li>Proof and post data for toplines and reports</li>
<li>Develop insightful reports and actionable final recommendations in PowerPoint, while having a clear understanding of the market and business implications of the research findings</li>
<li>Manage communication with clients: project updates, problem solving of issues where necessary.</li>
</ul>
 Qualifications
<ul>
<li>3+ years experience in Quantitative Market Research may apply, as there are open quant research positions at a variety of levels .</li>
<li>Experience in the pharma/healthcare sector is preferred.</li>
</ul>
Apply: <a href="https://lieberman.bamboohr.com/careers" target="_blank">https://lieberman.bamboohr.com/careers</a>
Join us in this exciting opportunity to contribute to ourexceptional, growing quantitative practice!

Market Research-Quantitative Project Director/Sr. Project Director (temporary role, full-time hours,

<h3>Job Description</h3>
Job DescriptionLand Research Specialist
Location: GPC Headquarters, Atlanta, GA Contract- 3 Years
Client-&nbsp; Georgia Power
Position Overview
We are seeking a motivated Land Research Specialist to provide research, analysis, and documentation in support of land use, property ownership, and development projects within the utilities sector. This role is critical to ensuring compliance, supporting real estate transactions, and delivering accurate information to stakeholders involved in planning and operating infrastructure projects.
Key Responsibilities
<ul>
<li>
Land &amp; Property Research: Conduct research on land parcels, ownership, and real estate transactions using public records, online databases, and GIS tools.
</li>
<li>
Property Ownership Verification: Review and validate ownership records, legal descriptions, and property boundaries.
</li>
<li>
Title &amp; Records Review: Perform title searches to track ownership history, encumbrances, liens, and legal issues.
</li>
<li>
Land Use &amp; Zoning Analysis: Interpret zoning regulations, land use codes, and planning documents to assess development feasibility.
</li>
<li>
Parcel Mapping: Develop and maintain parcel maps using GIS software to visualize land boundaries and features.
</li>
<li>
Due Diligence Support: Assist in due diligence processes for transactions, evaluating site suitability for development or utility projects.
</li>
<li>
Environmental Impact Research: Investigate environmental conditions (soil, flood zones, hazardous materials) that may impact land use.
</li>
<li>
Market &amp; Valuation Analysis: Research market trends, land values, and rental rates to support investment decisions.
</li>
<li>
Regulatory Compliance: Ensure land use aligns with local, state, and federal regulations. Advise on permits and approvals.
</li>
<li>
Documentation &amp; Reporting: Prepare detailed records, reports, and presentations of findings for leadership, compliance, and legal teams.
</li>
<li>
Stakeholder Communication: Present findings to internal stakeholders, external partners, attorneys, or government agencies.
</li>
</ul>
Qualifications
Education
<ul>
<li>
Required: Bachelor’s degree in Geography, Urban Planning, Land Management, Real Estate, or related field.
</li>
<li>
Preferred: Advanced degree or certification in land use, GIS, or real estate.
</li>
</ul>
Experience
<ul>
<li>
0–5 years of experience in land research, real estate analysis, or property transactions.
</li>
<li>
Prior utilities, energy, or government experience is a plus.
</li>
</ul>
Skills &amp; Expertise
<ul>
<li>
Strong analytical and research skills with ability to interpret complex data and legal documents.
</li>
<li>
Proficiency in GIS software (ArcGIS, QGIS) and mapping tools.
</li>
<li>
Knowledge of real estate law, property rights, and land use regulations.
</li>
<li>
Detail-oriented with excellent organizational and time management skills.
</li>
<li>
Proficiency in MS Office (Word, Excel, PowerPoint, Access) and databases.
</li>
<li>
Excellent written and verbal communication skills.
</li>
</ul>
Work Expectations
<ul>
<li>
Hybrid Schedule: On-site at GPC Headquarters Monday through Thursday; remote work on Fridays.
</li>
<li>
Must be flexible to support emergent work requirements in a fast-paced utility environment.
</li>
</ul>

Land Research Specialist

<h3>Job Description</h3>
Job DescriptionRidgefield, CTContract Duration: 12-24 monthsRate: Negotiable
Responsibilities:
<ul>
<li>Excellent employment opportunity for a Scientist III/IV in the Ridgefield, CT area.</li>
<li>Develop and execute in vivo studies to qualify exploratory new therapeutic concepts for anti-inflammatory and/or fibrotic mechanisms. </li>
<li>Contribute to the incorporation of new ideas and the development of innovative processes, including technologies such as in vivo siRNA and adeno-associated virus (AAV) delivery. </li>
<li>Contribute to the incorporation of new ideas and contribute to the development of innovative processes, including technologies, presentations &amp; publications. </li>
<li>Independently plan, coordinate, conduct and interpret non-routine in vivo studies to explore mechanism of action and biomarker identification, to support translational biology and deliver clear understanding of new therapeutic concepts. </li>
<li>Be motivated to apply his/her skills to impact project needs and drive key innovative scientific concepts and enjoy working in a fast-paced dynamic team environment with a proven ability to focus and deliver high quality data that support timely decisions for projects. </li>
<li>Candidate must have strong analytical and problem-solving skills with proven track record of high research accountability and productivity both independently, with minimal supervision and within a team setting in a matrix environment. </li>
<li>Continue to develop scientific expertise and drug development knowledge by keeping abreast of relevant literature, and by expanding scientific/technical knowledge and skill sets. </li>
<li>Ensure compliance with all required training, safety, regulatory, HR and intellectual property activities and corporate policies. </li>
<li>Assist in training junior scientists in all areas of laboratory operations. </li>
</ul>
Experience: 
<ul>
<li>Bachelor's Degree up to a PhD from an accredited institution with 3+ years' experience in Immunology or a related field</li>
<li>Scientist III Requirements: </li>
<li>Master's Degree from an accredited institution with three-plus (3+) years of experience in related Scientific discipline, OR </li>
<li>Bachelor's Degree from an accredited institution with seven-plus (7+) years of experience in related Scientific discipline or equivalent experience in related field </li>
<li>Scientist IV Requirements: </li>
<li>Master's Degree from an accredited institution with six-plus (6+) years of experience in a related Scientific discipline, OR </li>
<li>Bachelor's Degree from an accredited institution with 10+ years of experience in a related field or equivalent experience in a related field </li>
<li>Requirements for both levels: </li>
<li>Understanding of basic Scientific principles and research practices in the field of Immunology. </li>
<li>Strong understanding of mouse biology and immunology with extensive hands-on experience conducting rodent experiments including preparation of test compounds, handling and dosing mice by various routes (IP, SC, IV or PO), collection of blood and tissues for PK and PD biomarker analysis. </li>
<li>Experience in techniques such as ELISA, MSD multiplexing, RNA isolation, RT-PCR and western blots. </li>
<li>Experience in using multi-color flow cytometry (FACS) to evaluate immune cell biomarkers and data analysis software is preferred but not required. </li>
<li>Experience or familiarity with in vivo vector delivery (e.g., minicircle DNA, adeno-associated virus (AAV) or si/shRNA) is preferred but not required. </li>
<li>Familiarity with hydrodynamic tail vein injection is a plus but not required. </li>
<li>Experience in use of Microsoft Office tools and GraphPad (Prism). </li>
<li>Team player with exceptional verbal, presentation, and written communication skills, with the ability to propose, articulate, evaluate and defend scientific ideas and data.</li>
<li>Required Skills: ASSAY DEVELOPMENT, COLLECTION, ELISA, FLOW CYTOMETRY, OPTIMIZATION</li>
<li>Additional Skills: VIVO, DATA ANALYSIS, IMMUNOLOGY, MARKETING ANALYSIS, PHARMACOLOGY, THERAPEUTIC, TOXICOLOGY</li>
</ul>

Scientist III/IV

<h3>Job Description</h3>
Job DescriptionSalary: $100K - $130K 
Senior Formulation Scientist (Full-time)
 
Join Us in Revolutionizing Agriculture!
 
Are you ready to be at the forefront of agricultural innovation? AgXelerators Inc. is a bold, fast-moving start-up on a mission to transform crop protection, crop health, soil regeneration, and sustainable agriculture. Were not just developing products - were redefining whats possible. Our team thrives on creativity, risk-taking, and an entrepreneurial mindset, pushing the boundaries of science to create cutting-edge solutions for the future of farming. 
 
We are looking for a Formulation Scientist to help shape the future of agriculture. Based at the Purdue Technology Center in West Lafayette, Indiana, this role is a rare opportunity to work alongside some of the greatest minds in formulation science. If youre passionate about innovation and want to see your work make a real impact, this is your chance to join a high-energy start-up where your contributions will directly drive our success. 
 
Key Responsibilities:
<ul>
<li>In consultation with company experts, lead the formulation development efforts of new active ingredients, including both biologicals (micro-organisms, proteins, peptides, plant extracts, viruses) and chemistry (naturally-derived or synthetic).</li>
</ul>
<ul>
<li>Collaborate with our customers to ensure alignment between formulation development, regulatory requirements, and commercial objectives.</li>
</ul>
<ul>
<li>Design and optimize formulation compositions to improve product performance, stability, and efficacy.</li>
</ul>
<ul>
<li>Conduct laboratory experiments and tests to evaluate the physical and chemical properties of formulations.</li>
</ul>
<ul>
<li>Stay abreast of industry trends, emerging technologies, and regulatory developments in agricultural formulations and actively contribute to innovative ideas and new approaches.</li>
</ul>
<ul>
<li>Follow established protocols and standard operating procedures (SOPs) for safe and efficient laboratory practices.</li>
</ul>
<ul>
<li>Record and document all experimental information and organize, analyze, summarize, and report the final results.</li>
</ul>
<ul>
<li>Communicate effectively with other team members and our customers. Present experimental results and progress in group discussions and project updates.</li>
</ul>
<ul>
<li>Provide technical guidance and mentorship to junior team members as needed.</li>
</ul>
 
Qualifications:
<ul>
<li>PhD or Master's degree in chemistry, chemical engineering, material science or related field.</li>
</ul>
<ul>
<li>5+ years of experience in agricultural formulation development (industry or research).</li>
</ul>
<ul>
<li>Proven success in bringing innovative agricultural products to market.</li>
</ul>
<ul>
<li>Strong understanding of regulatory frameworks for agricultural formulations.</li>
</ul>
<ul>
<li>A curious, hands-on scientist eager to push boundaries and explore new frontiers.</li>
</ul>
<ul>
<li>Excellent communicator who thrives in a collaborative, fast-paced environment.</li>
</ul>
<ul>
<li>Excellent problem-solving skills and the ability to work independently as well as part of a team.</li>
</ul>
<ul>
<li>Entrepreneurial spirit with a passion for solving big problems and taking bold risks.</li>
</ul>
<ul>
<li>Enthusiastic about the opportunity to contribute to the growth of a small start-up team.</li>
</ul>
Why Join Us?
<ul>
<li>Game-changing impact Play a key role in transforming the future of agriculture.</li>
</ul>
<ul>
<li>Equity ownership Share in the companys growth and success.</li>
</ul>
<ul>
<li>Dynamic start-up environment Work on exciting, high-stakes projects with top industry experts.</li>
</ul>
<ul>
<li>Flexibility &amp; autonomy A work environment that values creativity, adaptability, and independence.</li>
</ul>
<ul>
<li>Competitive benefits package Designed to reward your talent and expertise.</li>
</ul>
 
If youre excited about making a real difference in sustainable agriculture and thrive in a start-up environment where innovation is at the core, wed love to hear from you!

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