field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Preferred Experience:
<ul>
<li>Eclipse, and Oncentra treatment planning systems</li>
<li>HDR planning and treatment.</li>
<li>ARIA ROIS and Mosiaq ROIS</li>
<li>SBRT and SRS procedures</li>
</ul>
?The ideal candidate will have
<ul>
<li>CAMPEP Accredited Residency Program in Medical Physics</li>
<li>Valid Texas Medical Board license</li>
<li>American Board of Radiology certification or board eligible</li>
<li>Preferred two years of experience as a certified medical physicist</li>
<li>Working knowledge of SRS, SBRT, and HDR</li>
<li>Experience with Varian linear accelerators</li>
<li>Experience with Eclipse Planning system</li>
<li>Experience with Oncentra Planning system</li>
<li>Strong organization and oral / written communication skills</li>
</ul>
Required Citizenship / Work Permit / Visa Status US Citizen / Green Card holder
Must-Haves CAMPEP Accredited Residency Program in Medical Physics Valid Texas Medical Board license American Board of Radiology certification or board eligible Preferred two years of experience as a certified physicist Working knowledge of SRS, SBRT, and HDR

Medical Physicist - Plano

<h3>Job Description</h3>
About Civica:
Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports.
Shortages put patients at risk and waste hospital resources.
Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, nearly 60 health systems have joined Civica, representing over 1,400 hospitals and approximately one-third of all U.S. hospital beds. Civica has also supplied the U.S. Department of Veteran's Affairs, the U.S. Department of Defense and the U.S. Strategic National Stockpile with essential medicines. Civica currently supplies medicines to health system members in 49 states.
Civica's mission has expanded beyond the hospital setting to reach consumers directly through CivicaScript, which is dedicated to making quality outpatient generic medicines affordable and available. CivicaScript works with trusted manufacturing partners to develop quality generic medicines and has forged partnerships with like-minded payors, pharmacy benefit managers and pharmacies to enable significant cost savings to be passed along to their customers.
Civica's new 140,000 square foot state-of-the-art manufacturing facility in Virginia will soon produce a steady supply of more than three dozen sterile injectables, all drugs that are currently in or near shortage. The plant will also produce affordable biosimilar insulins, ensuring all Americans have access to lower cost, quality insulins, regardless of their insurance status.
The Civica Foundation is a 501(c)(3) organization that fosters philanthropic support for Civica's work to manufacture and distribute affordable medications. The Foundation's first commitment is to support Civica's efforts to bring affordable insulin to all Americans. Leaders from nearly every corner of the diabetes ecosystem are partners in this initiative. 
Civica is leading a movement for patients, not profits. Because eliminating shortages and stabilizing high prices are in the best interest of patients.
Join us. Learn more at <a href="http://www.civicarx.org" target="_blank">www.civicarx.org</a>
Job Description:
The Microbiologist will join the Civica, Inc. ("Civica") organization and its newly created team at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance. The Petersburg site serves as Civica's new fill-finish facility dedicated to the manufacture and supply of essential generic sterile injectable medications. The responsibilities of the position include supporting facility qualification and equipment validation. 
The role is essential to ensure that the Petersburg site's microbiology laboratory and testing comply with applicable regulatory standards (e.g., Current Good Manufacturing Practices and FDA Guidance documents) and expectations for the development and reliable supply of quality medicines. Responsibilities also include but are not limited to, the generation and/or review of procedures, reports, and other records necessary to support the implementation and maintenance of a microbiology laboratory that meets or exceeds FDA and EU Annex 1 requirements. 
Essential Duties and Responsibilities:
<ul>
<li>Support establishing and maintaining the microbiological testing laboratory to ensure compliance with cGMPs and industry standards for best practices.</li>
<li>Perform microbiological testing methods consistent with USP testing requirements. Including but not limited to the following microbiological testing and procedures: bioburden, bacterial endotoxin, identification of microbial isolates and objectional organisms, viable/non-viable particulate monitoring, and growth promotion studies.</li>
<li>Conduct and maintain qualifications of laboratory equipment as well as ongoing maintenance and calibration.</li>
<li>Establish and coordinate test sampling plans.</li>
<li>Perform microbiological testing and sample collection to support environmental monitoring (EM) and utility systems.</li>
<li>Author and participate in the verification of microbiological methods and method transfers.</li>
<li>Participate in the development of training programs for microbiologists.</li>
<li>Lead and/or participate in investigations related to laboratory operations and non-conforming results.</li>
<li>Identify, track, and facilitate resolution of technical issues.</li>
<li>Proactively identify and work collaboratively to resolve problems, taking risk-based and compliant approaches to solutions.</li>
<li>Author and/or review SOPs, protocols, reports, test methods, and product specification documents as applicable.</li>
<li>Create and/or revise Risk Assessments.</li>
<li>Promote a quality mindset and quality excellence approach to all activities.</li>
<li>Travel (up to 10%) may be required.</li>
</ul>
Basic Qualifications and Capabilities:
<ul>
<li>Bachelor's degree in a scientific discipline (microbiology degree preferred) with a minimum of 4 years of Quality/cGMP experience in the pharmaceutical industry. </li>
<li>Strong project management, organization, and execution skills.</li>
<li>Microbiology testing and environmental monitoring experience.</li>
<li>Participation in activities to support regulatory agency inspections required.</li>
<li>Excellent interpersonal and written communication skills and experience using various software/electronic applications required.</li>
<li>Self-motivated, flexible, and able to work in a small, fast-paced, dynamic environment.</li>
<li>Ability to work autonomously and within established guidelines, procedures, and practices.</li>
<li>Committed to delivering high-quality results, working with others to overcome challenges, and focusing on what matters.</li>
<li>Continuously look for opportunities to learn, build skills and share knowledge with others.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience in sterile injectable manufacturing, aseptic processing, and facility qualification.</li>
<li>Environmental monitoring in isolators and cleanrooms per Annex 1 requirements.</li>
<li>Experience with the following microbiological testing and procedures.</li>
<li>Sterility testing and method suitability testing per USP &lt;71&gt;.</li>
<li>Acceptance testing and use of biological indicators.</li>
</ul>
Physical Demands and Work Environment:
The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions.
While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls, and stand, walk, sit, and reach with hands and arms. Specific vision abilities required by this position include color vision, close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. 
The employee must have the ability to lift approximately 40 lbs, stand for 2 to 3 hours at a time, and walk long distances. Vision screening may be required.
The employee must have the capability to don gowning/PPE for entry into the aseptic core and supporting areas for extended periods of time. This will include standing, bending, reaching, kneeling, etc.
The company is an equal opportunity employer, a drug-free workplace, and complies with ADA regulations as applicable.
PandoLogic. Keywords: Microbiologist, Location: Petersburg, VA - 23803

Microbiologist

<h3>Job Description</h3>
Job Description
American Battery Technology Company (ABTC) provides technical development and commercialization of domestic, sustainable sourcing of critical battery materials through lithium-ion battery recycling and battery metal extraction technologies for use in batteries that power electric cars, grid storage applications, and consumer electronics and tools. Our first of kind systems produce commercial-scale battery materials that are sold into the battery manufacturing supply chain.
In the role of Chemical Process Engineer, you will enhance and refine our chemical processes related to our proprietary technologies for lithium-ion battery recycling and primary resource extraction. The successful candidate will work closely with our R&amp;D team, plant operations team, and a range of internal and external specialists to guarantee effective design, construction, and operation of our facilities. The ideal applicant will possess experience in research &amp; development, as well as the design, installation, commissioning, and operation of first-of-a-kind facilities. A strong enthusiasm for creating, executing, and sustaining efficient chemical manufacturing processes is essential, along with ensuring quality control of outputs, specifying equipment, developing and implementing monitoring and sampling protocols, and thriving in a high-performance, fast-paced environment. The candidate should be a creative problem-solver with a strong interest in scaling processes from bench-scale to pilot or pre-commercial levels. This includes a consistent emphasis on assessing existing processing steps and proposing and developing innovative solutions to continually enhance system performance and operability. This position will report directly to our Chemical Engineering Lead.
Requirements
<ul>
<li>Design and implement battery recycling &amp; primary resource extraction systems from a laboratory scale basis into pilot and commercial scale systems. </li>
</ul>
<ul>
<li>Iterate technical improvements to novel processing routes for extracting high purity battery materials consistently from various feedstocks. </li>
<li>Support operations and R&amp;D teams by providing technical feedback and test plans for continuous improvement. </li>
<li>Size and select process engineering equipment. Coordinate technical requirements to equipment vendors and review equipment and process submittals. </li>
<li>Develop and update mass and energy balances for improved chemical processing systems. </li>
<li>Complete process system designs leveraging various solids, liquid, and gas processing technologies. </li>
<li>Collaborate with program management and construction teams to safely and quickly implement efficient designs. </li>
</ul>
Qualifications 
<ul>
<li>Background in Chemistry/Chemical Engineering </li>
<li>3+ years of engineering/design experience </li>
<li>Ability to translate fundamental design principles and equations into functional equipment systems </li>
<li>Able to interpret and produce Process Flow Diagrams (PFD) and Piping and Instrumentation Diagrams (P&amp;ID) </li>
<li>Chemical processing background (Oil, Gas &amp; Chemicals, Metals &amp; Mining, Mineral Processing, etc.) </li>
<li>Ability to positively collaborate in a team environment </li>
<li>Licensed Professional Engineer: Chemical or Mining </li>
<li>Strong understanding of both organic and inorganic chemistry </li>
<li>Experience with Autodesk CAD programs (Plant3D, Revit) </li>
<li>Experience with chemical process modeling software </li>
<li>Experience developing Basis of Design documentation and process / control narratives </li>
<li>Experience in water treatment, extraction, and purification system designs </li>
</ul>
Physical Demands 
<ul>
<li>Ability to stand and sit for prolonged periods. </li>
<li>Ability to walk throughout the plant. </li>
<li>Ability to bend at the waist. </li>
<li>Ability to lift assisted over 50 lbs. </li>
<li>Ability to climb stairs and ladders </li>
<li>Ability to wear PPE which includes but is not limited to the following: eye and face protection, hearing protection, respirators, and protective shoes and shoe coverings. </li>
<li>Must have 20/20 or corrected vision. </li>
<li>Ability to perform repetitive duties. </li>
<li>Ability to work in environments that may include exposure to noise, dust, and chemicals for extended periods of time. </li>
</ul>
Benefits
<ul>
<li>Competitive salary </li>
</ul>
<ul>
<li>Company-sponsored health, dental, vision, and life insurance </li>
<li>Parental Leave</li>
</ul>
<ul>
<li>Company-sponsored Employee Assistance Program </li>
</ul>
<ul>
<li>Stock options </li>
</ul>
<ul>
<li>401(K) </li>
</ul>
<ul>
<li>Flexible paid time off </li>
</ul>
<ul>
<li>Monthly phone stipend </li>
</ul>
Equal Opportunity Employer 
American Battery Technology Company is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. 
Americans With Disabilities Act 
American Battery Technology Company does not discriminate based upon disability in its hiring or employment practices and complies with the ADA title I employment regulations. If you need assistance or an accommodation due to a disability or a special need, please contact Human Resources.

Chemical Process Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SPECIFICATIONS:
Ability to adequately do the following:
 Perform the duties of a medical technologist (generalist).
 Work under the direction of the administrative and medical laboratory directors.
 Work closely with the administrative director, the technologists, technicians, and
assistants.
 Work in all areas of the laboratory and in patient areas.
 Supervise the overall technical operations of the laboratory.
 Be subject to frequent interruptions.
 Be willing to work beyond normal working hours, take emergency call when
necessary and be available either on site or by electrical means.
 Cope with possible subjection to infectious diseases and substances.
 Perform certain clerical duties.
 Assist administrative director in maintenance and implementation of laboratorys ongoing quality assurance/quality improvement program.
 Meets regularly with the Administrative Director of the Laboratory. Reports problems in a timely manner.
 Report laboratory results to those individuals who are authorized to receive results.
 Communicate effectively and deal tactfully with physicians, other hospital personnel , fellow department personnel, patients, and the general public.
 Maintain adequate stock and supply levels.
 Attend appropriate inservice activities and meetings
 Other miscellaneous duties as directed by the administrative or medical director, within the scope of training and ability.
Education and experience:
 Successful completion in an accredited college or university, of a course of study which meets all academic requirements for a bachelors degree in Medical Technology or one of the chemical, physical, or biological sciences.
 Must have at least four years experience as a registered or certified medical technologist and preferably two additional years in a supervisory capacity.
 
Education and experience continued:
 Must possess adequate knowledge to work in and supervise the following areas:
1. Specimen collection 5. Microbiology 9. Routine &amp; Preventive maintenance
2. Chemistry 6. Parasitology 10. Hematology
3. Urinalysis 7. Serology 11. Quality Control
4. Blood Bank 8. Coagulation 12. Quality assessment/Quality improvement

LABORATORY SUPERVISOR

<h3>Job Description</h3>
Job Description
Company Summary: 
Radienz Living is a leading North American manufacturer of home and personal care products, 
including unit-dose dish and laundry detergents, refillable applications, facial wipes, and baby wipes. 
With manufacturing plants and warehouses located in Illinois and New York, we provide private label 
solutions and contract manufacturing services for products found in both retail and institutional 
markets. At Radienz Living, we are passionate about delivering exceptional manufacturing 
capabilities through our commitment to agility in innovation, trust and reliability, and sustainable 
practices that support a cleaner way of living. 
Background: 
As a Chemical Compounder at Radienz Living, you will play a vital role in the manufacturing process 
by handling chemicals, chemical substances, and operating specialized machinery to process and 
produce chemical-based products. This role involves both powder and liquid blending, including 
loading and unloading materials safely and efficiently in accordance with established procedures 
and safety guidelines. 
Work Environment: Exposed to hazardous materials and airborne particulates 
Key Responsibilities: 
Additional responsibilities include, but are not limited to: 
<ul>
<li>Competently operate blending machinery both independently and as part of a team.</li>
<li>Match all labels accurately with the corresponding batch records.</li>
<li>Document blending process information in accordance with Standard Operating Procedures (SOPs).</li>
<li>Load and unload materials into blending machines safely and efficiently.</li>
<li>Monitor blending operations periodically and promptly report any abnormal conditions to the supervisor.</li>
<li>Ensure compliance with Good Manufacturing Practices (cGMP), established procedures, safety regulations, and SOPs.</li>
<li>Consistently produce high-quality finished goods in accordance with quality standards.</li>
<li>Maintain a clean, organized, and safe work environment at all times.</li>
<li>Perform additional duties as assigned to support departmental and organizational goals.</li>
<li>Communicate effectively and regularly with personnel in production, maintenance, quality control, and scheduling.</li>
<li>Verify that all incoming materials align with the Bill of Materials (BOM)</li>
<li>Must consistently meet productivity expectations, including yield and volume targets.</li>
</ul>
Requirements &amp; Qualifications: 
<ul>
<li>Must be clean-shaven at all times to comply with blending department safety standards.</li>
<li>High school diploma or GED preferred.</li>
<li>Physically capable of lifting, pushing, and pulling a minimum of 50 pounds.</li>
<li>Flexible schedule availability based on production volume and shift demands.</li>
<li>Prior experience in consumer packaged goods (CPG), manufacturing, packaging, or pharmaceutical environments preferred.</li>
<li>Strong understanding and compliance with Good Manufacturing Practices (GMP) and adherence to all defined safety procedures.</li>
<li>Comfortable working in a fast-paced and loud production setting.</li>
<li>Strong attention to detail and the ability to follow instructions precisely.</li>
<li>Ability to work effectively as part of a team.</li>
<li>Must wear steel-toe boots </li>
<li>Must wear all required Personal Protective Equipment (PPE) at all times.</li>
<li>Must be able to pass all pre-employment fitness and pulmonary function tests.</li>
<li>Will be exposed to hazardous materials and airborne particulates as part of daily responsibilities.</li>
</ul>
Physical Demands: 
<ul>
<li>Constant manual dexterity use.</li>
<li>Required to stand for long period of time.</li>
</ul>

Chemical Compounder

<h3>Job Description</h3>
Job Description
About PFXTM

We engineer leading fluid solutions that keep the world moving and we’re building a better future while we do it. As a vertically integrated global powerhouse, we operate 17 manufacturing facilities and 4 R&amp;D centers across the world, delivering performance from lab to road in over 40 countries.
PFX GroupTM brings together a family of trusted companies including Recochem, Prestone, Adam’s Polishes, B&amp;B Blending, Kost USA, Ultra Clear, POR and Auto-Chem, each with deep expertise, regional insight, and a shared commitment to engineering excellence.
From automotive and heavy-duty thermal management systems to household and industrial solutions, our products are built for performance, reliability, and a commitment to sustainability. Join us and be part of a team that’s redefining what’s possible in fluid technology.
&nbsp;We are seeking a&nbsp;Chemical&nbsp;Blender (Operator)&nbsp;to work on the&nbsp;3rd&nbsp;shift and join our dynamic team! The successful candidate will posses the listed skills and experience.
 
Overview
A&nbsp;Chemical Blender (Operator)&nbsp;is responsible for a variety of tank farm tasks including chemical blending, testing solutions, bulk loading of trucks and off-loading railcars.

&nbsp;Your role at Prestone
<ul>
<li>Unload raw material trucks / railcars and perform incoming inspection, test and COA evaluation.</li>
<li>Blend, test, and transfer antifreeze batches.</li>
<li>Control/maintain Tank Farm raw material tank levels and inventories.</li>
<li>Perform preventative maintenance and minor repairs on Tank Farm equipment.</li>
<li>Inspect, load and test OEM trucks; maintain and calibrate laboratory test equipment and perform analytical tests on antifreeze and raw materials; ordering of supplies for test station; maintain strict adherence to ISO/QS standards.</li>
</ul>

Required Experience and Skills
<ul>
<li>Experience working with and around chemicals to produce antifreeze and windshield washer fluid.</li>
<li>Basic math skills required</li>
<li>Ability to read and write comprehend instructions, correspondence, and memos</li>
<li>Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.</li>
</ul>
 
Qualifications
<ul>
<li>At minimum, a high school diploma or equivalent</li>
<li>Previous chemical blending experience required of 2+ years</li>
<li>Previous experience with bulk loading and off-loading of rail cars preferred</li>
<li>A good portion of the primary activities are performed outdoors; the Tank Farm Blender will be subject to inclement weather therefore, ability to handle all-weather conditions.</li>
<li>Must be able to work with and carry heavy equipment, tools, large industrial valves, chemical hoses, raw material containers, etc.</li>
</ul>

Physical Requirements/Working Conditions
The production facility is within an indoor/outdoor, industrial environment and is not climate controlled. Must be able&nbsp;to perform physically demanding tasks, including lifting and moving heavy objects.&nbsp;
Company DescriptionGreat pay and benefits coupled with a great culture! 
<h3>Company Description</h3>
Great pay and benefits coupled with a great culture!

Chemical Blender - 3rd Shift

<h3>Job Description</h3>
Job Description
Lighthouse Lab Services has partnered with laboratory in lovely New Haven, CT. We are looking for a talented Clinical Laboratory Technologist / Chemist to join our client's team to be a part of their growing organization.
ABOUT NEW HAVEN, CT:
New Haven, Connecticut, blends Ivy League energy with coastal charm. Home to Yale University, it offers world-class museums, cultural events, and a vibrant arts scene alongside a warm, welcoming community. Known as the pizza capital of America, its food scene rivals major cities, complemented by outdoor escapes at East and West Rock Parks and along Long Island Sound. Conveniently located between New York City and Boston, New Haven combines urban excitement, growing biotech opportunities, and small-town appeal in one dynamic that feels like home.
ABOUT THE CLIENT:
The client is a venture-backed biotech company in New Haven, CT, focused on making advanced functional health insights accessible beyond the research lab. They are developing novel proteomic biomarkers for cardiorespiratory fitness, body composition, and metabolic health and personalized, actionable tools designed to enhance chronic disease prevention. Located in a well-regarded co-working lab incubator, their CLIA-registered lab is developing and commercializing innovative laboratory-developed tests (LDTs) built on proven proteomic technology.
ABOUT THE ROLE:
Clinical Laboratory Technologist / Chemist will manage laboratory operations and serve as Testing Personnel under CLIA guidelines. This is a bench-level position, ideal for someone with 1+ years of clinical laboratory experience who is eager to work hands-on with cutting-edge proteomic technology in a fast-paced, translational environment. You will work closely with organizational leaders and operations teams to process samples, run assays, and maintain quality and compliance as we prepare for CLIA certification and clinical launch. Future opportunities for advancement to General Supervisor or Technical Supervisor roles as organization scales.
TECHNOLOGY: The client's laboratory-developed tests use a high-throughput ELISA-based method on plasma or saliva, employing proprietary fluorescent antibody panels run on a standard flow cytometer. This streamlined process enables multiplexed detection of over one hundred proteomic biomarkers in a single pipetting workflow.
KEY RESPONSIBILITIES
Clinical Laboratory Testing
<ul>
<li>Perform sample processing and proteomic assays (multiplexed, flow cytometry–based high-throughput ELISA).</li>
<li>Operate and maintain benchtop flow cytometer and other clinical chemistry instrumentation.</li>
<li>Follow and refine Standard Operating Procedures (SOPs) for sample preparation, reagent handling, and assay execution.</li>
<li>Ensure accurate documentation and recordkeeping in accordance with CLIA and laboratory quality standards.</li>
</ul>
Operational Support
<ul>
<li>Assist with the shipping, receiving, and accessioning of human plasma and saliva samples.</li>
<li>Help maintain a growing biobank with accurate sample labeling, storage, and retrieval processes.</li>
<li>Support laboratory organization, reagent preparation, equipment maintenance, and inventory management.</li>
<li>Participate in laboratory quality control and troubleshooting processes.</li>
</ul>
Regulatory and Quality
<ul>
<li>Serve as Testing Personnel under CLIA during laboratory startup phase.</li>
<li>Collaborate with consultants and supervisors to support CLIA registration and readiness.</li>
<li>Maintain accurate electronic documentation and assist in preparing quality and audit materials.</li>
</ul>
Collaboration
<ul>
<li>Work closely with PhD scientists, MD consultants, and operations staff to support assay validation and optimization.</li>
<li>Communicate effectively across scientific, operational, and software teams to ensure smooth data flow and sample tracking.</li>
</ul>
REQUIRED QUALIFICATIONS
<ul>
<li>Bachelor's degree in chemical, biological, clinical or medical laboratory science or medical technology</li>
<li>At least 1 year experience in a high complexity clinical laboratory setting</li>
<li>Familiarity with clinical chemistry workflows and laboratory instrumentation.</li>
<li>Be prepared for a fast-growing laboratory development environment– early on there will be few samples per week (&lt;50 per week in first months) and may grow to 500 per week towards 12 month mark. The client will bring in automation and additional hires as needed to support expansion</li>
<li>Strong organizational and recordkeeping skills; attention to detail is essential.</li>
<li>Proficiency with Google Workspace, Slack, and other digital collaboration tools.</li>
<li>Must be based locally in Connecticut (New Haven area) and able to work on-site.</li>
</ul>
PREFERRED QUALIFICATIONS
<ul>
<li>ASCP certification (or eligibility)</li>
<li>Experience operating a flow cytometer or performing multiplexed ELISA assays.</li>
<li>Prior experience in biotech startups or small-scale laboratory environments.</li>
<li>Enthusiasm for technology and ability to work across multiple software and data systems.</li>
<li>Excellent interpersonal skills and ability to adapt in a fast-growing organization</li>
</ul>
SHIFT, SALARY, BENEFITS:
<ul>
<li>First shift M-F</li>
<li>$60-$78K per year (depending on experience)</li>
<li>Health insurance option available.</li>
<li>Equity stake and performance based bonuses possible.</li>
<li>Access to BioLabs New Haven amenities: collaborative workspace, shared instrumentation, stocked kitchen, and on-site showers.</li>
<li>Opportunity to join a venture-backed, early-stage biotech at the ground floor.</li>
</ul>
About Us:
At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has more than 21 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.
It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Lighthouse Lab Services will provide reasonable accommodations for qualified individuals with disabilities.
Lighthouse Lab Services|844-914-0785|lighthouselabservices.com
#LLS2

Clinical Laboratory Technologist / Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
JOB SUMMARY
The Computational Scientist III will design, develop, and maintain robust systems and system models (i.e., Digital Twins) for opto-mechanical sensor systems that detect and identify biological threats. These models will be leveraged for requirements and concept generation, design and development, manufacturing, system troubleshooting, and logistical analysis.
 
ESSENTIAL JOB FUNCTIONS
<ul>
<li>Build from the ground up (and maintain) digital twins using Model-Based Systems Engineering (MBSE) methodologies.</li>
<li>Develop digital twins to support troubleshooting and repair of production systems.</li>
<li>Develop virtual representations of physical systems to support new technology development.</li>
<li>Provide key contributions to system requirements development, trade studies, and architecture definition.</li>
<li>Leverage Artificial Intelligence and Machine learning tools to maximize the accuracy and effectiveness of developed models.</li>
<li>Prepare and maintain documentation related to computer code/scripts, including end-user guides and instructions.</li>
<li>All employees are expected to be in compliance with government and corporate laws, rules, regulations, policies, and procedures.</li>
</ul>
SUPERVISORY RESONSIBILTY 
No supervisory responsibilities
Requirements:
EDUCATION
Minimum Master’s degree in Physics, Chemistry, Computer Science, Systems Engineering, Electrical Engineering, Software Engineering, Optical Engineering, or a related field, Ph.D. Preferred
 
EXPERIENCE
3-5 years of related experience or 0 - 3 years experience with applicable Ph.D. level research in Biology, Chemistry, Physics or a related field.
 
SKILLS and QUALIFICATIONS
<ul>
<li>Must be eligible to obtain and/or maintain a U.S. Government Security Clearance commensurate with the level of facility clearance.</li>
<li>Proficiency in systems engineering processes and principles</li>
<li>Experience in developing a digital twin for spectroscopic, spectrometric, or electrochemical-based instrumentation</li>
<li>Working-level knowledge of one or more of the following areas: optical spectroscopy, surface immobilization, molecular recognition, molecular biology, or aerosol physics</li>
<li>Software programming/scripting proficiency in C, C#, Python, and/or MATLAB</li>
<li>Optical modeling proficiency with Zemax or equivalent</li>
<li>Working knowledge of software development practices such as version control systems (e.g., Git, Azure DevOps, Synergy CM) </li>
<li>Working knowledge of statistics, experimental error, Design of Experiments, and quantification as it applies to scientific data</li>
<li>Excellent written and verbal communication skills</li>
<li>Working knowledge of Artificial Intelligence/ Machine Learning tools, as their application to physics-based models</li>
<li>Ability to communicate technical information to non-technical audiences</li>
<li>Ability to work independently and to interact effectively with individuals on multi-disciplinary teams</li>
<li>Team player with a positive attitude</li>
</ul>
Preferred
<ul>
<li>Experience in developing detailed optical specifications for spectroscopic instrumentation</li>
<li>Development of interface software required to command and control excitation and imaging subsystems</li>
<li>Ability to define, assemble, and test optical component breadboards for spectroscopic applications</li>
<li>Previous research and development experience related to chemical, biological, radiological, nuclear, and/or explosive (CBRNE) threats</li>
</ul>
PHYSICAL AND OTHER REQUIREMENTS
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
 
Limited domestic travel may be required less than 5% of time.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
The incumbent should be able to lift up to 25 pounds without assistance and 50 pounds with assistance to complete laboratory activities.
 
Incumbent may have to wear and function in personal protective equipment, including a respirator for limited periods of time.
 
Incumbent will be required to complete company paid for medical monitoring.
 
DISCLAIMER 
The preceding job description has been designed to indicate the general nature and essential job functions of this position. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Employees will be expected to perform other job functions and duties as may be needed and/or required.
 
EQUAL OPPORTUNITY EMPLOYER
Chemring Sensors and Electronic Systems, Inc. (CSES) is an equal opportunity employer. We evaluate applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. 
 
The “Know Your Rights” Poster is available here:
<a href="https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf" target="_blank">https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRi…</a>
<a href="https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRightsSp6.12.pdf" target="_blank">https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRi…</a>
 
CSES’ EEO Policy Statement is available here: Chemring Sensors and Electronic Systems, Inc. EEO Policy Statement
CSES is committed to working with and providing reasonable accommodations to individuals with disabilities.
If you need a reasonable accommodation because of a disability for any part of the employment process, please send an e-mail to <a href="mailto:HR@chemringsensors.com" target="_blank">HR@chemringsensors.com</a> or call (980) 235-2200, Option 3 and let us know the nature of your request and your contact information. 
 
 
#zr

Computational Scientist III

<h3>Job Description</h3>
Job DescriptionSalary: $60 per Assessment/Admission 
CHEMICAL HEALTH ASSESSOR - INDEPENDENT CONTRACTOR POSITION
 
Chemical Health Assessor Position Overview - Fully Remote**
The Chemical Health Assessor is a professional who plays an important role in the interdisciplinary team at Transformation House. They are responsible for providing comprehensive assessments to patients seeking treatment recommendations or admissions.
Time Allocation: Consulting- minimum of 4 available assessment slots per week/16 per month and a 6 month commitment
Compensation: $60 per assessment/admission
Knowledge, skills and abilities:
<ul>
<li>Must understand the impact of cultural and individual difference within varied populations</li>
<li>Broad knowledge of ASAM Criteria and making placement recommendations</li>
<li>Excellent communication skills</li>
<li>Strong problem solving skills</li>
<li>Demonstrates collaborative relationships with all members of the Transformation House team to support patient care</li>
<li>Familiarity with healthcare technology and software</li>
<li>Ability to collaboratively work with patients, providers, staff, and partners</li>
<li>Works well independently and as part of a team</li>
<li>Strong written and verbal communication skills</li>
<li>Ability to quickly adjust/respond to an evolving workload</li>
<li>Excellent time management and organizational skills, attention to detail</li>
</ul>
Responsibilities:
<ul>
<li>Provide chemical health assessments</li>
<li>Complete timely documentation of assessments provided to meet Minnesota DHS requirements as well asTransformation House policies and procedures</li>
<li>Provide recommendations for appropriate levels of care.</li>
</ul>
Requirements: To qualify, applicants must meet the following criteria:
<ul>
<li>Fully licensed as an LADC (no temporary licenses)</li>
<li>Must pass a State of Minnesota Background Check.</li>
<li>This is a remote position, must live in the state of Minnesota</li>
</ul>
Preferred:
<ul>
<li>Experience working with substance use and co-occurring disorders </li>
</ul>
 
**Will need to provide your own computer

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