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job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Title: Chemist Location: St. Louis, Missouri Company: Fortune 100 Food &amp; Beverage Manufacturing (FuseGlobal has worked with this company for 20 years) Initial term: 12 months (position expected to run longer) 
POSITION SUMMARY:
This department is comprised of talented individuals who possess a genuine love for pets and their families. We thrive on being at the forefront of research, contributing to the innovation and advancements in pet nutrition and quality that sets us apart. Ensuring the delivery of safe ingredients and sustainable practices to our factories and beyond, we are invigorated by the extensive research and development that goes into our products. Bring your impact to the table, and together we will continue to work towards being one of the most trusted companies in pet care.

 PRIMARY RESPONSIBILITIES:
As an Analytical Chemist, you will execute and interpret complex procedures and protocols within a project or goal. You'll be a great fit if you are a self-starter who takes initiative and works independently while collaborating with others. You'll be expected to learn method development, make process improvements, and help draft standard operating procedures (SOP's) in addition to mentoring other team members.
<ul>
<li>Prepare and interpret reports of complex experiments</li>
<li>Follow established methods and procedures to deliver timely results</li>
<li>Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals</li>
</ul>
QUALIFICATIONS AND SKILLS:
<ul>
<li>
Bachelor's degree in Chemistry or a related field
</li>
<li>
3+ years of analytical lab or industry experience, analytical instrumentation experience, and troubleshooting of assay and equipment issues
</li>
<li>
2+ years of experience with chromatography and/or mass spectrometry (HPLC, GC, GCMS, LCMS, etc.)
</li>
<li>
1+ years of experience working in an ISO 17025 accredited laboratory is preferred
</li>
</ul>
<ul>
<li>
Please note: Environment includes exposure to Top 14 Allergens.
</li>
</ul>

COMPENSATION AND BENEFITS:
<ul>
<li>$27.00 per hour + overtime</li>
<li>Medical insurance</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>401(k)</li>
<li>Disability insurance </li>
</ul>
ABOUT FuseGlobal: FuseGlobal is a partnership of people and brand-leading companies, working together to make things run better. For 25 years we have brought functionality to complex business and production processes and supply chains, resulting in enterprises that run smarter and more sustainably. Interested in digital manufacturing, industrial engineering, supply chain management, all-things tech, and energy &amp; the environment? This is where we live. Engage with us! #LI-Onsite #LI-FG

Chemist

<h3>Job Description</h3>
Job Description
Join an exciting, multidisciplinary PhD program that offers hands-on training from day one, bridging cutting-edge laboratory science with clinical research. We are seeking motivated and dedicated doctoral students for the Neuroscience Ph.D. program at the Roskamp Institute, which currently has openings for a 4-year Ph.D. project in Traumatic Brain Injury (TBI) research. 
Roskamp Institute projects are all focused on translational research, with analysis of clinical samples to define the conditions under investigation, and extensive characterization of relevant preclinical models in order to identify and develop diagnostic strategies and therapeutic targets. 
This PhD student will join our translational team investigating a brain-penetrant bioactive neurotherapeutic, as an anti-inflammatory treatment for traumatic brain injury (TBI). Our research integrates PK/PD modeling, dose optimization, therapeutic time-window analysis and acute-to-chronic efficacy studies in a mouse model of TBI, complemented by cell-based systems that model inducible inflammatory signaling.
Techniques associated with this Roskamp Ph.D. project include:
<ul>
<li>Analysis of rodent and human TBI tissue samples </li>
<li>Cell- and tissue-specific isolation and culturing</li>
<li>Cre-LoxP and inducible mouse models and CRISPR/Cas9 editing of glial cell cultures</li>
<li>Antibody-based analytical approaches - Immunoblotting, ELISA, transactivation assays</li>
<li>Rodent manipulation including TBI surgeries, behavioral testing and therapeutic studies. </li>
<li>Neuropathological analyses – Microscopy, Immunohistochemistry</li>
<li>Mass spectrometry analyses – Kp, uu drug concentration levels in the brain </li>
<li>Spatial transcriptomics and proteomics approaches </li>
<li>Pharmacokinetics, pharmacodynamics and physiologically based pharmacokinetic modeling</li>
</ul>
The Roskamp Institute is a leader in the field of neuroscience, with a strong reputation for developing novel therapies for conditions such as traumatic brain injury (TBI), Alzheimer’s disease and Gulf War Illness. The Institute’s cutting-edge research environment offers unmatched opportunities for multidisciplinary training and hands-on experience, working with experts in translational neuroscience. Sarasota, Florida, is known for its beautiful, pristine beaches and pleasant weather year-round, making it an ideal place to live and work. As part of the Roskamp Institute, you will not only advance your career but also enjoy the benefits of living in a vibrant coastal community. Qualifications Required ·Master’s degree in a scientific field, or a Bachelor’s degree with demonstrated scientific laboratory experience.
Please visit The Roskamp Institute – About Us – Ph.D. Program section of the website located at the following weblink, and select the Blue ‘Download Application form’: <a href="https://www.roskampinstitute.org/ph-d-program/" target="_blank">https://www.roskampinstitute.org/ph-d-program/</a>. 
The deadline for submission of applications is January 31st, 2026

RESEARCH ASSOCIATE/STUDENT

<h3>Job Description</h3>
Job Description
Fuel Your Career with Oberto Snacks!
 
 
Position: Raw Processor 1 - 2nd Shift
Type: Onsite
Location: Kent, WA 
If you’re looking for a dynamic workplace with exciting opportunities, consider joining Oberto Snacks, Inc. 
 
Here’s why you should apply:
 
Innovative Environment:
<ol>
<li>At Oberto, we thrive on innovation. Be part of a team that constantly pushes boundaries and creates unique snack experiences.</li>
</ol>
Quality-Driven Culture:
<ol>
<li>We’re passionate about delivering top-notch products. Join us if you’re committed to excellence and quality.</li>
</ol>
Team Collaboration:
<ol>
<li>Our collaborative work environment fosters creativity and teamwork. You’ll collaborate with talented individuals across various functions.</li>
</ol>
Career Growth:
<ol>
<li>Oberto offers growth opportunities. Whether you’re starting your career or seeking advancement, we’ve got you covered.</li>
</ol>

OBERTO HISTORY &amp; MISSION:
Founded in Seattle by Constantino Oberto in 1918, Oberto Snacks Inc’s future is brighter than ever. With its growing portfolio of brands, each with its own mission, purpose and army of passionate fans, Oberto continues to be one of the nation’s leading and most innovative meat snacks companies. Employing more than 700 food professionals, Oberto’s mission is to empower people to make better choices for a healthier and happier life. As a part of that mission, we strive to provide innovative, delicious, healthy, and convenient protein-packed snacks.

ABOUT THE POSITION:
Responsible for Raw Processor is to maintain steady workflow of raw processing lines by performing prescribed procedures accurately and timely.
 
SCHEDULE:
<ul>
<li>2nd Shift </li>
<li>8 hours per day with possible daily overtime and during peak summer/fall production.</li>
</ul>

WAGE: Hourly range for this position is $19.00 - $20.00 per hour, with a starting range of $19.00 per hour, also included is $1.00 per hour for shift differential. 

PRIMARY RESPONSIBILITIES:
May do any one of the following:
 
Defrost:
<ul>
<li>Unload trailers full of palletized meat using a pallet jack.</li>
<li>Remove frozen meat from boxes, bag and seal the individual bags of meat using the M-tec sealing machine and stack the bagged and sealed meat onto racks. </li>
<li>Remove fresh meat from boxes and stage the meat in tubs for slicing.</li>
<li>Load racks in to defrost tempering houses. </li>
<li>Set up and start the houses to begin the thaw process and continue to monitor the houses throughout the thawing process until the house is thawed and ready for slicing.</li>
<li>Responsible for unloading the houses and staging thawed meat for slicing.</li>
<li>Clean the racks and tempering houses with chemicals to meet SSOP and food safety standards.</li>
</ul>
Spice/Batching:
<ul>
<li>Prepare work area by assembling and setting up workstations.</li>
<li>Ensure that correct spices are used and properly recorded in a timely manner.</li>
<li>Maintain housekeeping standards and account for all inedible products.</li>
<li>Assist in the production of jerky/sausage by removing batches from tempering room to kitchen. Bring in the correct spices for product production and add spices following standard mixing procedures.</li>
<li>Stage meat to be used by removing meat from carton, making sure that all foreign material (cardboard, plastic, etc.) is removed and that all proper handling procedures are followed.</li>
<li>As directed, perform basic maintenance to equipment, maintain cleanliness of equipment and clean equipment as necessary.</li>
<li>Prepare meat samples for lab by drilling meat for fat analysis following standard A.M.I. drilling procedures and providing all necessary identification of sample (purchase order number, lot number, brand, etc.).</li>
</ul>
Continuous Line/Hanging/Screening:
<ul>
<ul>
<li>Ensure proper identification of product by recording weights of tubs/totes with proper batch number and ingredient ticket weights.</li>
<li>Responsible for monitoring manual and continuous line workstations to ensure that each station has adequate meat supplies to ensure production flow.</li>
<li>Load carts with meat filled tub and bring to workstations to supply meat as needed.</li>
<li>Track each tub that is dumped at the workstation to ensure that employee efficiencies are accurately recorded.</li>
<li>Responsible for performing job duties in compliance with all GMP's and following all company safety standards.</li>
<li>Assist with Raw Processor 1 functions when necessary.</li>
</ul>
<li>Assist with the sanitation of the room at the end of shift or due to a certified start up during the shift. QUALIFICATIONS:</li>
</ul>
<ul>
<li>High School (minimum)</li>
<li>6 months manufacturing experience preferred. </li>
<li>Pallet Jack experience preferred.</li>
<li>Familiarity with HACCP (OJT).</li>
<li>Understanding and compliance with all GMPs (OJT)</li>
<li>Understanding and compliance with all personal safety rules (OJT)</li>
<li>Able to understand and follow instructions.</li>
<li>Ability to work with people to accomplish team goals.</li>
</ul>
 
ABOUT OBERTO: We offer a creative, diverse, and inclusive workplace environment. We are committed to rewarding our teammates for their hard work, enthusiasm, and professional excellence.
BENEFITS:
<ul>
<li>Excellent benefits including medical, dental, vision, prescription coverage, short term and long-term disability, life insurance and wellness program, Flex spending account.</li>
<li>401K Plan with a generous company match </li>
<li>Quarterly performance incentive.</li>
<li>10 Paid holidays, generous paid time off, and paid sick leave.</li>
<li>Employee Stock Ownership Plan Oberto with contribution match. </li>
</ul>
 EXTRA BENEFIT:
<ul>
<li>Tuition Reimbursement, and career growth opportunities</li>
<li>Discount commuter benefits</li>
<li>Safety Shoe program, and Safety Glasses program</li>
<li>Paid Jury Duty, and Bereavement Leave</li>
<li>Employee Assistance Program</li>
<li>Legal Services, and Pet Insurance</li>
<li>Employee Referral Program </li>
<li>Service Award Recognition program, and Employee Recognition program</li>
<li>Matching Charity Donations </li>
<li>Pet Insurance</li>
<li>Oberto Product Discounts</li>
<li>Basic membership reimbursement to Costco or Sam’s Club.</li>
<li>First-class onsite fitness center</li>
</ul>
Ready to Join Our Snack-Tastic Team? Apply Now! 
Oberto Snacks is committed to a diverse and inclusive workplace. Oberto Snacks is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veterans’ status, disability, age, or other legally protected status. Should you have a disability that requires assistance and/or reasonable accommodation with the job application process, please contact the Human Resources department at (253) 437-6100 or by applying directly on our website at <a href="http://www.oberto.com/careers.com" target="_blank">www.oberto.com/careers.com</a>
EEO/E-Verify Statements: Oberto Snacks, Inc. is an Equal Opportunity Employer. All qualified applicants are encouraged to apply. Oberto Snacks, Inc. participates in the E-Verify program.
**Please note, we do not engage with outside recruiters. All recruitment processes are managed internally by our Talent Acquisition team. Thank you.

Raw Processor 1 - 2nd Shift

<h3>Job Description</h3>
Job DescriptionOur Story
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow.
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program (ESOP) and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage — with medical premiums either paid by Superior or highly subsidized — so you and your family can access great benefits with minimal cost.
You’ll also join a supportive team, where paid training and experienced coworkers help you learn, grow, and succeed from day one. 
At SUPERIOR, you get more than a job — you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to success.
What We’re Looking For
We are currently seeking a Chemical Handler to work at our Louisville, KY location.
This role is responsible for:
<ul>
<li>Daily production</li>
<li>Unloading raw materials</li>
<li>Completing paperwork</li>
<li>Maintaining a safe operation</li>
</ul>
Schedule:
<ul>
<li>Full-time, 1st shift</li>
<li>Monday–Friday, 8:00 a.m. – 4:30 p.m.</li>
<li>Additional hours may be required</li>
</ul>
What You’ll Do
You will:
<ul>
<li>Transfer products into and out of pails, drums, and totes using transfer pumps and hoses</li>
<li>Read paperwork with chemical amounts and blending instructions</li>
<li>Pull product samples and submit them to the Lab for quality control</li>
<li>Label containers and secure closures</li>
<li>Inspect, label, store, and prepare products for shipment</li>
<li>Stage, load, and unload pails, drums, and totes</li>
<li>Operate a forklift</li>
<li>Wear required PPE for safety</li>
<li>Keep your work area safe, clean, and orderly</li>
<li>Lift and/or move 55 lbs</li>
<li>Cross-train in areas such as shipping/receiving, bulk handling, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventive maintenance, and yard truck spotting</li>
</ul>
Candidates Should Possess
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Effective verbal and written communication skills to work with co-workers, chemists, administrative staff, delivery personnel, and management</li>
</ul>
What We Offer
At Superior, we take care of our people. Our comprehensive benefits package includes:
<ul>
<li>Medical Insurance – 100% company-paid HDHP or a low-cost PPO option</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>401(k) Retirement Plan</li>
<li>Flexible Spending Accounts (FSA)</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Dental, Vision &amp; Life Insurance</li>
<li>Short-Term &amp; Long-Term Disability (STD &amp; LTD)</li>
<li>Paid Training from day one</li>
</ul>
Join a company that invests in you — personally, professionally, and financially.
EOE including disability/veteran/drug free

Chemical Handler

<h3>Job Description</h3>
Job Descriptionjob summary: 
External Research Solutions (ERS) supports scientific innovation by managing external screening partnerships and ensuring seamless data integration between internal teams and external vendors. Our mission is to enable high-quality, efficient research through robust data operations, strong vendor collaboration, and disciplined data governance.
 location: Groton, Connecticut job type: Contract salary: $28.00 - 30.02 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Support external screening data operations and vendor coordination to ensure accurate, timely data delivery for scientific decision-making.</li>
<li>Maintain and update external screening data repositories and vendor-specific portals.</li>
<li>Process screening requests, validate and QC data deliverables, and distribute accurate data to scientists.</li>
<li>Receive, format, and publish screening data using standardized data-loading tools and templates.</li>
<li>Register and maintain vendor profiles and project records in designated systems.</li>
<li>Maintain and update reference/control compound lists and screening protocols.</li>
<li>Request registration of new control/reference compounds as needed.</li>
<li>Adhere to established data handling standards and maintain clear documentation for audits and reporting.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree in Life Sciences, Data Management, or a related field (or equivalent experience).</li>
<li>1-2 years' experience in scientific data workflows and management</li>
</ul>
Preferred:
<ul>
<li>Lab experience with in vitro screening assays desired</li>
</ul>
 skills: In Vitro, Data Management Plan, Good Laboratory Practices (GLP), Quality Assurance (QA), Quality Control (QC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Research Associate I

<h3>Job Description</h3>
Job DescriptionResearch Associate – Peptide Synthesis &amp; Antibody Conjugation
Location: Thousand Oaks, CA (Fully Onsite)
Overview
The Research Associate will play a key role in supporting discovery research by executing peptide synthesis and antibody conjugation workflows. This position is responsible for delivering high‑quality, well‑characterized materials to project teams and ensuring day‑to‑day laboratory readiness for safe and efficient operations.

Ideal Candidate Profile
<ul>
<li>M.S. degree</li>
<li>B.S. degree with 2 years of relevant experience</li>
<li>Solid‑phase synthesis and solid‑phase peptide synthesis (SPPS) experience strongly preferred</li>
</ul>
Key Responsibilities
<ul>
<li>Plan and execute peptide synthesis under minimal supervision</li>
<li>Perform peptide cleavage and purification using RP‑HPLC</li>
<li>Conduct antibody conjugation experiments</li>
<li>Analyze and confirm peptide and conjugate identity and purity</li>
<li>Accurately document experimental procedures, observations, and results in the electronic laboratory notebook</li>
<li>Communicate data, results, and interpretations to the project team</li>
<li>Operate and maintain specialized laboratory equipment and instrumentation</li>
<li>Perform routine lab housekeeping to maintain a clean and safe workspace</li>
<li>Adhere to all laboratory safety guidelines, SOPs, and regulatory requirements</li>
</ul>
Basic Qualifications
<ul>
<li>Master’s degree in Chemistry, Biochemistry, or a related scientific discipline</li>
<li>OR</li>
<li>Bachelor’s degree in Chemistry, Biochemistry, or a related field with 2+ years of relevant experience</li>
</ul>
Preferred Qualifications
<ul>
<li>Hands‑on experience with solid‑phase peptide synthesis (SPPS)</li>
<li>Experience with RP‑HPLC purification</li>
<li>Familiarity with standard laboratory practices</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Thousand Oaks, CA.
Pay and Benefits
The pay range for this position is $31.00 - $31.00/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 Thousand Oaks,CA.
Application Deadline
This position is anticipated to close on Jan 16, 2026.
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.

Research Operations Senior Associate

<h3>Job Description</h3>
Job Description
What You'll Be Owning: 
As a Senior Geospatial Research Analyst - Production Manager you will be responsible for supporting DoD geospatial and all-source analysis and production, including supervising analysis, research, and production.
What You Must Have:
<ul>
<li>TS/SCI Security Clearance Required</li>
<li>Bachelor's degree in Geography, Geospatial Science, GIS, Remote Sensing, Environmental Science, Computer Science, Business Analytics or a closely related field; or 5+ years minimal experience creating geospatial analytic products in these fields of study or supporting DoD geospatial and all-source analysis and production, including supervising analysis, research, and production.</li>
<li>Expertise, knowledge, and capability to both apply and lead geospatial analytics and all-source intelligence methodologies, theories, and frameworks; and AI/ML, data quality, enrichment, and stewardship processes and techniques to research to:
<ul>
<li>Solve and articulate complex geospatial and all-source intelligence analytic problems.</li>
<li>Develop and oversee data stewardship techniques and best practices.</li>
<li>Collaborate with other data providers and analysts to improve access to key data.</li>
<li>Leverage the knowledge of peers to better understand analytic trends and initiatives.</li>
<li>Working knowledge of Esri ArcGIS Enterprise systems and data steward tools, catalogs, techniques, and processes.</li>
</ul>
</li>
</ul>
What Would Be Nice to Have: 
<ul>
<li>Certifications or training in Esri GIS or related technologies (e.g., ArcGIS Pro, ArcGIS REST API), Python, R, JSON, HTML/XML, SQL, NoSQL, PostgreSQL, Open-Source Intelligence (OSINT), and All-Source Intelligence analytic methodology are advantageous but not required.</li>
</ul>
Why Choose GRVTY
The toughest national security challenges demand vision and ingenuity, not just resources. We deliver mission and technical expertise to outpace our adversaries. We're purpose-built to tackle the most entrenched, systemic national security issues around the world.
We partner with our customers to help them overcome challenges in every corner of technology and defense—including the ones still being explored. Our growing capabilities create complementary advantages, giving on-the-ground operations the edge they need to succeed. We muster everything we have to answer every challenge presented, every day of our lives.
At GRVTY, we believe that when our employees thrive, our company thrives. That's why we offer a comprehensive and competitive benefits package designed to support your well-being, growth, and work-life balance.
• Robust health plan including medical, dental, and vision 
• Health Savings Account with company contribution 
• Annual Paid Time Off and Paid Holidays 
• Paid Parental Leave 
• 401k with generous company match 
• Training and Development Opportunities 
• Award Programs 
• Variety of Company Sponsored Events

EEO Statement
GRVTY, is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran and will not be discriminated against on the basis of disability. 
Anyone requiring reasonable accommodations should email <a href="mailto:recruiting@grvty.com" target="_blank">recruiting@grvty.com</a> or call 703-544-7930 with requested details.  A member of the HR team will respond to your request within 2 business days. 
Know Your Rights: Workplace Discrimination is Illegal (eeoc.gov)  
Please review our current job openings and apply for the positions you believe may be a fit. If you are not an immediate fit, we will also keep your resume in our database for future opportunities.

Senior Geospatial Research Analyst - Production Manager

<h3>Job Description</h3>
Job Description
Responsibilities
Artificial Intelligence; Advanced Technology; The very best in patient care. With decades of expertise, we are Radiology Forward. With dynamic cross-training and advancement opportunities in a team-focused environment, the core of our success is its people with the commitment to a better healthcare experience. When you join us as a Research Assistant you will be joining a dedicated team of professionals who deliver quality, value, and access in the 21st century and align all stakeholders- patients, providers, payors, and regulators to achieve the best clinical outcomes.

You Will:
<ul>
<li>Greet, register, collect copays, and verify all patient information. Assist team members by notifying patient arrival. Communicate delays in appointments in a timely fashion and offers rescheduling for timely and effective care of patients;</li>
<li>Obtain proper insurance/authorizations and patient information, collects signatures and ensures accuracy and completion of necessary documentation.</li>
<li>Schedules, reschedules or cancels new or current patients, confirms appointments and notifies staff of changes when necessary.</li>
</ul>

If You Are:
<ul>
<li>Passionate about patient care and exercise sound judgement and an ability to remain professional in all situations.</li>
<li>You demonstrate effective and professional communication, interpersonal skills and respect with patients, guests &amp; colleagues.</li>
<li>You have a structured work-approach, understand complex problems are and you are able to prioritize work in a fast-paced environment.</li>
</ul>

To Ensure Success in This Role, You Must Have:
<ul>
<li>High School Diploma</li>
<li>1 year of previous medical office experience and intermediate computer skills</li>
<li>Medical terminology knowledge and recent medical/radiology office work experience is preferred.</li>
</ul>

We Offer: 
<ul>
<li>Comprehensive Medical, Dental and Vision coverages.</li>
<li>Health Savings Accounts with employer funding.</li>
<li>Wellness dollars</li>
<li>401(k) Employer Match</li>
<li>Free services at any of our imaging centers for you and your immediate family.</li>
</ul>
#corpwest

Research Assistant

<h3>Job Description</h3>
Job Description
About AIRCO AIRCO is a world leader in carbon conversion technology, paving the way to global energy security by transforming CO₂ into a valuable resource. Its proprietary AIRMADE™ Technology is an adaptable platform that allows any industry to efficiently produce high-demand, fully-formulated synthetic fuels from waste CO₂ and hydrogen.
The company has commercial partnerships with airlines including JetBlue and Virgin Atlantic, amongst others, and has been awarded multiple government contracts, including with NASA and the United States Department of Defense's Defense Innovation Unit. The company has received industry recognition through awards such as Time Best Inventions, Inc. Best in Business, Fast Company World Changing Ideas, and the XPrize for Carbon Removal.
AIRCO's many accolades include winning the prestigious Green Chemistry Challenge Award from the Environmental Protection Agency in October 2023, an award given to organizations that reinvent processes to reduce the generation of hazardous substances and byproducts. AIRCO was also declared a winner for the World Economic Forum UpLink Sustainable Aviation Challenge, which accelerates the development of promising technology pathways that enable widespread uptake of SAF.
The Position
AIRCO is seeking a Senior Scientist to join our team. This role will report to the Director, Research, and will contribute to the development of heterogeneous catalysts for the production of Sustainable Aviation Fuel (SAF) from CO2, supporting AIRCO's business Growth. This role is based in New Britain, PA with travel as needed to Brooklyn, NY.
What you get to do
<ul>
<li>Design and execute experiments independently with minimal supervision to meet the project goals</li>
<li>Synthesis, characterization, and testing of heterogeneous catalysts</li>
<li>Catalyst stability testing and scale-up support </li>
<li>Record, analyze, interpret, and present data to stakeholders</li>
<li>Supervise and mentor chemists and technicians involved in catalyst synthesis and testing</li>
<li>Collaborate cross functionally with Development and Engineering teams</li>
</ul>
What you bring to AIRCO
<ul>
<li>PhD in Chemistry or Chemical Engineering</li>
<li>0-5 years of post-doctoral, academic, or industrial experience in heterogeneous catalyst development in academic or industrial setting </li>
<li>Ability to work in a hands-on laboratory setting with minimal supervision</li>
<li>Ability to learn new techniques related to catalyst synthesis and testing</li>
<li>Maintain a safe and compliant working environment, adhering to all relevant regulations, standards, and guidelines</li>
<li>Good communication and presentation skills, with the ability to effectively communicate technical information to both technical and non-technical audiences</li>
<li>Ability to work independently and collaboratively in a fast-paced, multidisciplinary team environment</li>
</ul>
Bonus Points
<ul>
<li>Prior experience in fixed-bed reactor set-up and maintenance</li>
<li>Experience in characterization techniques such as BET, TPR, TGA, SEM, Mercury Porosimetry </li>
</ul>
 Working at AIRCO - In addition to standard medical and dental benefits, that kick in Day 1, we provide:
Comprehensive Health Benefits
<ul>
<li>Full coverage for employee base premiums on health, dental, and vision insurance.</li>
<li>70% coverage for spouse and dependent base premiums.</li>
<li>Choose between base plans or enhanced options to fit your needs.</li>
</ul>
Health Savings &amp; Flexibility
<ul>
<li>Access company-sponsored HSA and FSA accounts to save on healthcare and dependent care expenses.</li>
</ul>
Income Protection &amp; Insurance
<ul>
<li>Company-paid Short-Term Disability insurance.</li>
<li>Optional Long-Term Disability and Life Insurance plans.</li>
</ul>
Time Off &amp; Leave
<ul>
<li>Flexible and generous paid time off, including national holidays and sick leave.</li>
<li>Paid family leave to support you during important life moments.</li>
</ul>
Retirement Savings
<ul>
<li>Tax-deferred 401(k) plan with a 3% company match to help you invest in your future.</li>
</ul>
Commuter Benefits
<ul>
<li>Pre-tax savings on transit and parking, plus monthly company contributions.</li>
</ul>
Additional Perks
<ul>
<li>Ancillary benefits through Sequoia, including pet insurance and financial wellness programs.</li>
<li>Employee wellness program to support your well-being.Inclusive of Wellhub &amp; One Medical. </li>
<li>Company-sponsored events and programs that promote an inclusive and values-driven workplace.</li>
<li>In person weekly catered lunch every Wednesday.</li>
</ul>
At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
Don't meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIRCO we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles
This position requires access to technology, software and other information that is subject to governmental access control restrictions, due to export controls, security classification and/or designation as Controlled Unclassified Information. Employment in this position is conditioned on the candidate's ability to obtain and maintain appropriate government authorization to access technology or information, to the extent required, including without limitation a security clearance, export license, or other documentation required to establish authorization to receive access to such items technology or information.
We may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to Company facilities and information systems, as we deem appropriate, in order to ensure compliance with applicable government access control restrictions.
I consent to transfer my data to Air Company in the U.S. and to its use in accordance with the Air Company Privacy Policy, and I opt in to receiving information from Air Company. Air Company does not sell or share personal information to third parties within the meanings given under applicable laws.

Sr. Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Formulation Scientist Location: Lexington, MA 02421 Duration: 6 months+ (Possible Extension) Pay Rate: $37.97/hr. on w2 TOP SKILLS PER MGR: 1. Experience in preparing injectable formulations for animal studies 2. Experience creating ELN entries and managing formulation requests / workflows 3. Highly communicative and able to quickly solve problems as they arise JOB DESCRIPTION: About the Department: Our Research &amp; Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Seattle reflect the full R&amp;D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&amp;D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&amp;D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients. The Position: Client is seeking a highly motivated formulation scientist to join its Pharmaceutical Research Sciences department in Lexington, Massachusetts. The candidate will be responsible for the formulation and characterization of peptides, proteins, small molecules, and bioconjugates. Relationships: This position reports to the Head of Pharmaceutical Formulation Sciences. Internal relationships include project teams and research colleagues in Lexington MA. Individual Contributor: does not manage other employees or contingent workers. Essential Functions:
<ul>
<li>Prepare peptide and protein injectable formulations for in vitro and in vivo studies including selection of buffers, excipients, surfactants and conducting the relevant biophysical characterization and stability studies</li>
<li>Collaborate with cross-functional teams to ensure the selected dosage form meets the desired biophysical and biochemical profile and contribute to early screening strategies and execution</li>
<li>Operate, maintain, and troubleshoot lab instruments such as biophysical and analytical characterization equipment</li>
<li>Conduct laboratory work in a safe, efficient manner that ensures a safe working environment for colleagues</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor's Degree required. Degree within subject matter expertise (biological, biochemical, or pharmacological sciences) preferred</li>
<li>2+ years’ relevant technical experience required</li>
<li>Strong knowledge and expertise in biophysical characterization and injectable formulation development</li>
<li>Experience with spectroscopy, calorimetry, light scattering, and other biophysical methods for peptide and protein injectable formulations is a plus</li>
<li>Proficient in data analysis and interpretation for drawing conclusions and making recommendations</li>
<li>Experience in managing projects and working collaboratively with cross-functional teams</li>
<li>Excellent scientific communication skills and ability to engage with stakeholders effectively</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN)</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical industries a plus.</li>
</ul>
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