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<h3>Job Description</h3>
Job DescriptionSalary: 
Formulation Chemist-Research and Development
 
About Rowe Casa Organics:
From the beginning, Rowe Casa Organics has been on mission to provide safe, natural, and non-toxic products that you can trust.
 
In 2017, sisters Jill and Alicia embarked on a mission seeking greater health and wellness for their families. Frustrated by the lack of transparency and truly safe, effective options, Jill Rowe took matters into her own hands by making our very first product, Elderberry Immune Support. Today, Rowe Casa Organics produces over 300 products to help people thrive in their health, wellness, and lifestyle. From wellness necessities and household essentials to the finest of self-care, each product that we offer is crafted with the utmost quality, care, and love.
 Job Summary:
 
The Formulation Chemist is a hands-on, in-lab research and development roleresponsible for formulating, testing, and supporting the development of clean-labelcosmetic products dietary supplements. This position focuses on lab bench work tosupport the companys product innovation pipeline as well as continuous improvementon existing products, formulations, scaling for mass production and technical transfer.The Formulation Chemist plays a critical role in creating prototypes, preparing samples,conducting experiments, and recording detailed formulation data to support compliance,quality, and innovation efforts. 
 
This role is essential to developing stable, effective, and scalable formulations that alignwith the companys natural and organic standards.
 Reports to: Director of Product Innovation
 
Key Responsibilities:
 
Development of cosmetics, personal care products and dietary supplement development in various formats, using organic and natural ingredients.
<ul>
<li>Assist in weighing, blending, and mixing sample batches using liposomes, emulsions, or standard blending techniques.</li>
<li>Prepare and test formulas for taste, texture, and dispersion.</li>
<li>Record theoretical yield, ingredient weights, and processing conditions for all test batches.</li>
<li>Help identify ingredient compatibility or solubility issues and communicate findings to directors.</li>
<li>Maintain detailed lab notebooks and digital records for all formulation trials and revisions.</li>
<li>Assist in creating batch record data, sample tracking sheets, and formulation change documentation.</li>
<li>Follow all cGMP lab procedures and support readiness for internal or external audits.</li>
<li>Assist in developing a wide range of cosmetic products, including lotions, serums, oils, cleansers, scrubs, balms, deodorants, and shampoos/conditioners.</li>
<li>Weigh, mix, and prepare lab batches based on provided formulation guidelines.</li>
<li>Adjust formulations based on lab observations and feedback from the R&amp;D team.</li>
<li>Record formulation data and observations including pH, viscosity, color, texture, and separation.</li>
<li>Support testing of formulations for performance, stability, and compatibility with packaging.</li>
<li>Maintain clean and organized lab space, ensuring proper labeling and retention of all samples.</li>
<li>Perform other duties as assigned. </li>
</ul>
Qualifications:
<ul>
<li>Bachelors degree in chemistry, Nutritional Sciences or a related scientific field.</li>
<li>25 years minimum of hands-on formulation experience in dietary supplements, cosmetics, personal care. Natural and organic formulation experience. </li>
<li>Understanding of emulsion systems, pH, natural preservatives, surfactants, botanical extracts, and supplement bioavailability. </li>
<li>Familiarity with good lab practices (GLP), cGMP manufacturing requirements, and cosmetic/supplement regulations.</li>
<li>Strong attention to detail and a disciplined approach to documentation.</li>
<li>Proficient in Excel and lab software/tools for formulation tracking, and calculations.</li>
<li>Comfortable working independently in a lab setting and experience operating R&amp;D Laboratory equipment used in formulation development.</li>
<li>Strong communication skills, self-motivated, curious, and excited to work with natural, organic, and innovative ingredients.</li>
</ul>
 
Bonus Skills (Preferred, not required):
<ul>
<li>Knowledge of functional fragrance/aromatherapy principles or essential oil compatibility.</li>
<li>Familiarity with global cosmetic regulations (EU, Canada, Australia) and supplement market trends.</li>
</ul>
Rowe Casa Organics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, or any other legally protected status.

Formulation Chemist-Research and Development

<h3>Job Description</h3>
Job Description
QC Microbiologist specialist is responsible for review of microbiological method validation, microbiological testing of raw materials, in-process samples, finished product. The incumbent is also responsible for Autoclave Validation/revalidations and work with R&amp;D Staff on New product sterility and Endotoxin LAL validation.
Reporting to: Director of Quality Assurance and Regulatory affairs
Qualifications: 
Bachelor of Science in Microbiology from a recognized Institution /University
Experience: 
<ul>
<li>One year experience in the pharmaceutical industry with microbiological testing such as sterility/bioburden, new product validation, raw material /finished product testing, LAL testing and validation, microbial identification, gram staining, purified water testing as per USP (membrane filtration, endotoxin and TOC), bacteriostasis and growth industry</li>
<li>Experience in environmental monitoring of cleanroom, environmental excursion investigations, DET, and the evaluation of aseptic media fills </li>
<li>Experience with QC test scheduling</li>
<li>Experience with GMP, GLP regulations and ISO standards</li>
<li>Experience with Microsoft suite</li>
<li>Excellent communication skills</li>
</ul>
Job description
<ul>
<li>Perform bioburden, endotoxin and TOC testing of Water including water for injection (WFI) per USP method.</li>
<li>Assist with review and approval of Standard Operating Procedures</li>
<li>Train and review the work of microbiological technicians</li>
<li>Review environmental class 5 to 8 cleanroom areas, maintain data on environmental monitoring of the facility.</li>
<li>Track and trend environmental monitoring and working with Quality Assurance Management on continuous improvement activities of facilities contamination control.</li>
<li>Assist with the development and validation of Microbiological methods</li>
<li>Review and approval of microbiological validation record</li>
<li>Perform internal audit per schedule or assist Quality Assurance with external audits.</li>
<li>Other duties may be assigned</li>
</ul>

QC Microbiologist specialist

<h3>Job Description</h3>
Job Description
TITLE: CHEMIST I
Job Summary:
Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures
Primary Responsibilities:
<ul>
<li>Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.</li>
<li>Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.</li>
<li>Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.</li>
<li>Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.</li>
<li>Ensure that equipment and working areas are maintained with good safety and housekeeping practices.</li>
<li>Re-stock chemicals and consumables used in analysis.</li>
</ul>
Education and Experience Requirements:
<ul>
<li>Must have a BA or BS degree in Chemistry or closely related science.</li>
<li>Minimum of 1-year relevant experience preferred.</li>
</ul>
Necessary Knowledge, Skills, and Abilities:
<ul>
<li>Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE).</li>
<li>Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.</li>
</ul>
Physical and Environmental:
<ul>
<li>Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.</li>
<li>Shift hours: Monday thru Thursday - 6am-6:00pm EST (flexibility)</li>
</ul>
Company DescriptionAbout The Rockridge Group: TRG is a privately held Limited Liability Company committed to connecting businesses with job seekers. We deliver high quality contingent personnel to our clients using our 3-step collaborative engagement model: Collaborate. We partner with you to understand the unique needs of your business before we propose a solution. Strategize. Based on your goals and staffing challenges, we develop high impact solutions designed for your industry. Engage. We work with your team before, during, and after every engagement to deliver 100% satisfaction. With over ten (10) years experience in the resource solutions sector, principals Greg Donner [link to bio] and Ronald Lom [link to bio] leverage the power of strategic partnership to create a powerful staffing model that improves your quality of hire. 
<h3>Company Description</h3>
About The Rockridge Group:\r\n\r\nTRG is a privately held Limited Liability Company committed to connecting businesses with job seekers. We deliver high quality contingent personnel to our clients using our 3-step collaborative engagement model:\r\nCollaborate. We partner with you to understand the unique needs of your business before we propose a solution.\r\nStrategize. Based on your goals and staffing challenges, we develop high impact solutions designed for your industry.\r\nEngage. We work with your team before, during, and after every engagement to deliver 100% satisfaction.\r\nWith over ten (10) years experience in the resource solutions sector, principals Greg Donner [link to bio] and Ronald Lom [link to bio] leverage the power of strategic partnership to create a powerful staffing model that improves your quality of hire.

QC Chemist

<h3>Job Description</h3>
Job Description
Chemical Technician 1&nbsp;for a power plant in&nbsp;Atlanta, GA. Job Description
<ul>
<li>
The responsibilities of the plant Chemical Technician will include performing technical and analytical services essential to the operation of a fossil fuel power plant, including:
</li>
<li>Working safely and being accountable for your safety and the safety of your coworkers</li>
<li>Provide chemical protection of the steam generating equipment to minimize outages due to corrosion and deposits in the steam/water cycle components</li>
<li>Minimize the loss of efficiency and possible replacement of water treatment, steam generating, condensing and turbine mechanical components</li>
<li>Assist in ensuring compliance with applicable environmental, safety and health regulations: ash pond inspections, dikes and wells reporting, drinking water reporting, etc.</li>
<li>Operate and maintain water treatment plant for production of de-ionized/ultra-pure water</li>
<li>Conduct sampling of water, boiler/turbine cleaning samples, oil, coal ash, and metal deposits</li>
<li>Perform analytical testing and monitor plant effluents</li>
<li>Perform analytical testing and monitoring of Flue Gas Desulphurization (scrubber)</li>
<li>Calibrate and maintain laboratory and on-line equipment and instrumentation</li>
<li>Maintain bulk chemical and laboratory supplies inventory</li>
<li>Assist regulatory compliance personnel to help ensure compliance with applicable environmental, safety and health regulations</li>
<li>Operate condensate polishers</li>
<li>Provide equipment clearances - according to the plant clearance procedure</li>
<li>Operate and maintain sewage treatment plants</li>
<li>Perform duties in the main lab
<ul>
<li>Perform QA/QC on instrumentation</li>
<li>Maintain and calibrate bench top instrumentation</li>
<li>Inventory lab equipment and reagent chemicals</li>
<li>Perform duties in the Water Analysis labs</li>
<li>Generate water quality reports</li>
<li>Collect regulatory water samples</li>
<li>Conduct air in leakage surveys</li>
<li>Ensure all laboratory areas meet housekeeping standards outlined by the plant</li>
</ul>
</li>
</ul>
JOB REQUIREMENTS
Pre-Employment Requirements:
<ul>
<li>Possess a valid driver's license</li>
<li>Drug and background testing</li>
</ul>
Education and Experience Requirements:
<ul>
<li>BS or BA degree&nbsp;in&nbsp;Chemistry, Biology, Environmental Science or a related discipline (minimum of 12 semester hours of chemistry) required</li>
<li>Experience and competency in the use, calibration and maintenance of laboratory instrumentation/equipment</li>
<li>Knowledge of proper analytical methods and techniques is required</li>
<li>Previous experience in large water treatment facility is preferred. This would include operating and maintaining clarification, filtration, reverse osmosis and de-ionization systems</li>
</ul>
Knowledge, Skills &amp; Abilities:
<ul>
<li>Broad knowledge of analytical, inorganic, oil, environmental and water chemistries required</li>
<li>High level of knowledge of chemical treatment methods and operation of water treatment plant is preferred.</li>
<li>Collect samples from inside the power plant and water treatment plant; Analyze water and ash samples.</li>
<li>Ability to troubleshoot mechanical systems, read and understand schematic diagrams and identify plant water process problems is preferred.</li>
<li>Perform QA/QC on instrumentation; Maintain and calibrate bench top instrumentation.</li>
<li>Proficiency in various Microsoft applications including Word, Excel, PowerPoint, Access and Outlook</li>
<li>Ability to understand mechanical and electrical theories and fundamentals</li>
<li>Ability to read and interpret information presented in graphic form (examples are blueprints, diagrams, drawings, graphs and plots)</li>
<li>Understanding handling requirement of hazardous materials (HAZMAT)</li>
</ul>
Behavioral and other Requirements:
<ul>
<li>Safety First – We actively care about the safety and well-being of our employees, customers and communities. Safely approaching every job, every day, always comes first.?</li>
<li>Act with Integrity?- We act with honesty, respect and fairness, demonstrating trustworthiness in all we do. We are true to our word and follow through on our commitments.</li>
<li>Be dependable and punctual</li>
<li>Ability to use proper personal protective equipment (PPE) daily including protective eyewear, natural fiber or fire-retardant clothing and steel-toe or composite-toed shoes</li>
<li>Ability to wear respiratory protection periodically</li>
<li>Ability to work shifts, evenings, nights, weekends, and holidays is&nbsp;required (plant is 24/7 operation)</li>
<li>Ability to work in non-temperature-controlled environments (extreme heat &amp; cold)</li>
<li>Ability to work in an environment that could include fly ash, coal dust, and chemical fumes, toxic or caustic chemicals</li>
<li>Available for call-out and overtime is required</li>
<li>Ability to work with limited supervision in a team environment</li>
<li>Ability to take initiative required to manage projects and address issues</li>
<li>Ability to work in extreme noise and vibration</li>
<li>Ability to work around moving equipment or objects</li>
<li>Ability to perform some physical activities while wearing respirators with filter cartridges or self-contained breathing apparatuses in a power plant environment</li>
<li>Ability to lift and/or carry up to 50 lbs.</li>
<li>Ability to climb ladders, bending, reaching, working at different elevations</li>
<li>Basic mechanical skills and / or knowledge</li>
<li>
Must have at least one year of verifiable driving experience (Must hold a valid driver’s license for the class vehicle to be operated. Driving permits are not typically considered a valid driver’s license).&nbsp;
Must have no revocation of driving privileges within the 36 months prior to application, no convictions of major traffic violations (DUI, hit and run, reckless driving, etc.) within the 12 months prior to application, or any pending charges for a major traffic violation at the time of application.
Must consent to a continuous monitoring of your Motor Vehicle Record&nbsp;
</li>
</ul>
Company DescriptionDynamic Engineering firm with incredible team culture and long term growth opportunities! 
<h3>Company Description</h3>
Dynamic Engineering firm with incredible team culture and long term growth opportunities!

Chemical Technician 1

<h3>Job Description</h3>
Job DescriptionSalary: 
Site Description
Childrens Research Triangle (CRT) is a mental health non-profit that seeks to provide therapy to children and families in underserved communities. CRT has also been in the forefront of many issues related to maternal substance abuse in pregnancy, the outcomes of children prenatally exposed to alcohol and drugs, the child welfare implications of substance abuse in families, as well as the treatment of youth who have been exposed to trauma. The staff at CRT has written articles that have been published in Pediatrics, The American Journal of Occupational Therapy, Journal of Developmental and Behavioral Pediatrics, Research in Developmental Disabilities, and numerous other leading medical and psychological journals.
 
Intern description
The CRT research team is offering part-time unpaid research internships to qualified undergraduates in the Chicago area.Most of the work is remote; however,interns are expected to come into the office at least once a week in order to help with tasks on site.The Summer cohort typically starts mid-Mayand goes throughmid-August, although scheduling can be flexible.Interns will be involved in multiple ongoing projects, such as:
<ul>
<li>ongoing evaluation of the Trauma Treatment Program</li>
<li>evaluation of a grant program providing training in Youth Mental Health First Aid</li>
<li>the development of a database about children 0 to 18 who have participated in psychological evaluations at CRT</li>
<li>evaluation of the Youth MIND program, which provides trauma-informed screening, assessment, and therapy to youth and families in the Chicago area</li>
<li>evaluation of a gun violence prevention program being implemented in schools around the city</li>
</ul>
 
Interns will be actively involved in most aspects of the research process including searching for relevant literature, putting together research materials, interviewing families, inputting and cleaning data in Excel and IBM SPSS, and helping with data management and analysis. This internship does not provide any clinical experience, i.e., direct contact with children, but is geared for students who would like to learn more about the research/program evaluation work at a non-profit organization. Students will receive the necessary training to do these tasks on these projects and will receive supervision from research team members led by a licensed clinical psychologist. Interns are expected to work at least 6 hours per week, but more hours can be accommodated. Internships can be set up for one, two, or more semesters.
 
Qualified Applicants will be undergraduate students who have:
<ul>
<li>Completed at least one introductory course in psychology, behavioral science, child development, or social work with a grade of B or above, or enrolled in a pre-medical course of study,</li>
<li>Demonstrated merit in their undergraduate studies up until the present time,</li>
<li>Expressed an interest in pursuing future careers or further education in empirical research or medicine, and</li>
<li>Displayed the ability to work well with other people in a team-oriented atmosphere.</li>
</ul>
 
Compensation
Interns may be offered authorship on submitted papers to which they have contributed substantially.
 
To Apply
The Research Team interviews candidates throughout the year, but it is typically divided into three cohorts: Spring, Summer, and Fall. Interested candidates should fill out the job links for their intended cohort. If there are any questions, please email Lorenz Cabe, the Research Internship Manager, <a href="mailto:atlcabe@cr-triangle.org" target="_blank">atlcabe@cr-triangle.org</a>.
 
Interviewing Timeline
Interviews for our cohorts typically start two months before the cohort begins, based on the availability of space for new interns. Interviews for the Summer cohort will take place from March 1st-April 30th of the year in which you are applying.

Research Internship(Summer 2026)

<h3>Job Description</h3>
Job DescriptionAre you ready to be part of a team that’s revolutionizing an entire industry? At Supportworks, we don’t just create high-quality, proprietary products, we build innovative solutions that redefine what’s possible. We’re seeking a&nbsp;Geotechnical Project Engineer&nbsp;with expertise in Geotechnical to join our mission-driven team. In this pivotal role, you’ll act as the bridge between our cutting-edge products and the contractors who rely on them. By understanding our customers’ evolving needs, you’ll help deliver tailored solutions that drive their success, as well as our own. Location:&nbsp;This will be an&nbsp;on-site&nbsp;position based in Omaha, NE, with occasional travel to project sites for hands-on collaboration, product installations, and field testing.&nbsp; Who We Are Supportworks is more than a company, we’re a family of brands dedicated to transforming the contractor industry:
<ul>
<li>Foundation Supportworks:&nbsp;A leader in foundation and concrete repair products, empowering a network of contractors across North America.</li>
<li>SolutionView:&nbsp;A software innovator creating digital tools that redefine the contractor-homeowner experience.</li>
</ul>
 When you join Supportworks, you become part of a team committed to making a real difference, both for our customers and the industries we serve. Qualifications As a&nbsp;Geotechnical Project Engineer, you will: Be the Go-To Technical Expert
<ul>
<li>Work closely with Supportworks customers to analyze project needs, problem solve and design/recommend tailored solutions.</li>
<li>Consult with design engineers, architects, and contractors to ensure job requirements are met with precision.</li>
<li>Champion Supportworks products, providing guidance and support to our customer network.</li>
</ul>
 Educate &amp; Train Stakeholders
<ul>
<li>Develop technical documents, specifications, case studies, training materials, and more.</li>
<li>Share your expertise through webinars and in-person presentations for design professionals and customers.</li>
<li>Assist with training our network of installing contractors on how to be successful on commercial projects, including bidding, equipment needs, understanding contracts, etc.</li>
<li>Travel to trade shows and industry events to represent and spread awareness about Supportworks products and engineering methodologies.</li>
</ul>
 Drive Product Innovation &amp; Compliance
<ul>
<li>Collaborate with third-party agencies to secure and maintain product evaluation reports.</li>
<li>Work with vendors and testing labs on product sampling, documentation and validation.</li>
<li>Manage renewals and ensure compliance with industry standards.</li>
</ul>
 Education and Experience We’re looking for someone who’s both innovative and has the necessary technical expertise.
<ul>
<li>BS degree in Geotechnical or Civil&nbsp;Engineering and 5+ years of relevant experience.</li>
<li>Possession of a Professional Engineer (P.E.) license is required.</li>
<li>Proficiency in design software.</li>
<li>Familiarity with commercial and residential construction codes.</li>
<li>Extensive knowledge of soil mechanics, deep foundation design and residential/commercial construction.</li>
<li>Strong communication skills and ability to communicate complicated subject matter to internal stakeholders and customers in a meaningful way.</li>
<li>A collaborative mindset and a knack for managing projects effectively.</li>
<li>Ability and willingness to travel occasionally across the U.S. and Canada.</li>
</ul>
 Why Supportworks? At Supportworks, you won’t just be another engineer, you’ll be a part of a dynamic team that values creativity, innovation, and impact. We believe in fostering a collaborative, supportive work environment where your ideas can thrive, and your contributions will directly shape our industry. Join us in redefining what’s possible in-home services. Apply today and be part of something truly transformative! Supportworks is proud to be an Equal Opportunity Employer (EOE). &nbsp;
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Project Engineer - Geotechnical

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking a highly motivated and skilled Microbiologist to join our Quality Control team at Medivant Healthcare. The ideal candidate will have a strong background in microbiological testing, laboratory techniques, environmental monitoring, and personnel monitoring, all focused on ensuring the safety and quality of healthcare products. The Microbiologist will be responsible for conducting routine and non-routine microbiological tests, performing environmental and personnel monitoring, identifying pathogens, and ensuring compliance with industry standards and regulations. This role is essential in maintaining the highest quality standards and supporting the production of safe and effective pharmaceutical products.
 
Key Responsibilities:
<ul>
<li>Perform microbiological testing of raw materials, finished products, and environmental samples to ensure quality and safety.</li>
<li>Conduct routine microbiological assays including sterility testing, endotoxin testing, microbial limit testing, environmental monitoring, and personnel monitoring.</li>
<li>Interpret test results, analyze data, and document findings in a clear and concise manner.</li>
<li>Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and relevant regulatory standards.</li>
<li>Maintain laboratory equipment and perform calibration, maintenance, and troubleshooting as needed.</li>
<li>Assist in the development and validation of microbiological testing methods and protocols.</li>
<li>Participate in investigations of out-of-specification (OOS) results and provide support for corrective actions.</li>
<li>Collaborate with cross-functional teams, including R&amp;D, production, and quality assurance, to support product development and ensure compliance with regulatory requirements.</li>
<li>Ensure proper documentation and reporting of test results and assist with regulatory audits and inspections as needed.</li>
<li>Stay current with industry trends, regulatory updates, and advancements in microbiological testing technologies.</li>
</ul>
Qualifications:
<ul>
<li>Education: Bachelor’s degree in microbiology, Biology, or a related field. Master’s degree is a plus.</li>
<li>Experience: Minimum of 2 years of experience in microbiological testing, preferably within the pharmaceutical or healthcare industry.</li>
<li>Skills:
<ul>
<li>Strong knowledge of microbiological testing methods and laboratory equipment.</li>
<li>Experience with microbiological techniques such as PCR, ELISA, and sterility testing.</li>
<li>Familiarity with GMP, GLP, FDA, USP, and other regulatory guidelines.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Strong attention to detail and accuracy in laboratory practices.</li>
<li>Ability to work independently and as part of a team in a fast-paced environment.</li>
</ul>
</li>
</ul>

Microbiologist

<h3>Job Description</h3>
Job DescriptionClinical Lab Analyst
Job Description
As a Clinical Lab Analyst, you will perform newborn screening testing on blood spot specimens to help identify infants at risk for inherited conditions. Your role involves using various methods such as immunoassay, enzyme assay, electrophoresis, HPLC, tandem mass spectrometry, and molecular methods to ensure accurate screening results.
Responsibilities
<ul>
<li>Perform daily operation and routine maintenance, calibration, and assist in troubleshooting of laboratory instruments and equipment.</li>
<li>Document and review newborn screening test data, procedures, and results.</li>
<li>Release data and reports for use by physicians, health care professionals, and newborn screening medical follow-up personnel.</li>
<li>Develop and maintain standard operating procedures and prepare documentation for test verification or validation studies.</li>
<li>Perform quality control and quality assurance procedures in accordance with established standard operating procedures and policies.</li>
<li>Recognize basic problems and assist troubleshooting of laboratory method and performance issues.</li>
<li>Assemble quality control data for further analysis; recognize problems; document issues; perform root cause analysis; and initiate corrective actions.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemistry, biology, genetics, HPLC, mass spectrometry, and biochemistry.</li>
<li>Bachelor’s degree in Chemistry, Biochemistry, Biology, Genetics, or related field, or equivalent combination of education and experience.</li>
<li>Meet Clinical Laboratory Improvement Amendments (CLIA) qualifications for high complexity testing (6 semesters of Biology and 6 semesters of Chemistry).</li>
<li>At least 3 months of hands-on laboratory experience.</li>
<li>Consideration given to certified Medical Lab Technologist or MLT.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Six months to one year of newborn screening laboratory experience.</li>
<li>Basic experience with immunoassay, mass spectrometry, and molecular biology techniques.</li>
<li>Completion of human genetics college coursework.</li>
<li>Quality Assurance and Quality Control (QA/QC) experience.</li>
</ul>
Work Environment
Work in a lab where newborn blood samples are tested for potential inherited disorders. This department operates 24/7 to ensure timely testing. The lab, located in Ankeny, tests samples from Iowa, North Dakota, South Dakota, and Alaska. The job involves working the 1st shift from 8 AM to 4:30 PM with rotating weekends and holidays, where weekend shifts are 7 AM to 3:30 PM. The position is a 4-month contract during a leave of absence. Dress code includes long pants and closed-toed shoes.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/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 Ankeny,IA.
Application Deadline
This position is anticipated to close on Sep 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Clinical Lab Analyst

<h3>Job Description</h3>
Overview The Medical Physicist is responsible for performing all medical physics tasks necessary for the safe and accurate delivery of therapeutic ionizing radiation in collaboration with the radiation oncologists and staff of Carle Health– Methodist. The Medical Physicist will be responsible for maintaining state and federal regulatory requirements specific to the practice of radiation therapy at Carle Health– Methodist. Creates and monitors clinical quality indicators and collaborates with physicians to ensure appropriate treatment guidelines are utilized and/or developed and monitored. Willing to consider partial remote if within driving distance of Peoria. This position qualifies for a Sign on Bonus and Relocation Assistance! Qualifications Certifications: Certified Specialist in Therapeutic Radiology Physics - American Board of Radiology (ABR); Licensed Radiologic Technologist - Radiation Therapy - Illinois Emergency Management Agency (IEMA), Education: Master's Degree: Physics; Master's Degree: Related Field, Work Experience: Related field Responsibilities 
<ul>
<li>Knowledgeable of all aspects of medical physics in radiation therapy including brachytherapy, SRS, SBRT, radiation shielding, treatment planning, radiation safety and regulatory compliance. Purposefully conducts all aspects of the job in an ethical manner in support of the UPH-Methodist commitment to ethical behavior in all areas of personal and professional activity
<ul>
<li>Completes hospital-wide orientation, annual hospital competencies and unit specific competencies.</li>
<li>Demonstrates good verbal and written communication skills with patients, families, healthcare team members and other customers. Verbal communication is clear and precise. Written communication is legible, if handwritten, and done in a timely manner using approved abbreviations.</li>
<li>Completes computer documentation in accordance with hospital policies.</li>
<li>Assures compliance with local, state, and federal guidelines in the acquisition, storage, and application of radioactivity used in therapeutic applications.</li>
<li>Assures compliance with regulatory agencies such as IEMA, JCAHO, ACR, NRC, by adhering to the respective guidelines of each agency.</li>
<li>Assures departmental compliance with outside organizations to maintain compatibility with protocol studies.</li>
</ul>
</li>
</ul>
<ul>
<li>Develops, implements, and reviews the policies and procedures that assure proper functioning of all therapeutic equipment including accelerators, and brachytherapy equipment, insuring smooth and safe operation. Performs required QA activities.
<ul>
<li>Participates in departmental and radiation safety meetings.</li>
<li>Participates in strategic planning for the needs of the radiation oncology department.</li>
<li>Monitors and maintains documentation for radiation monitoring of departmental staff.</li>
<li>Evaluates all equipment for its continued utility, appropriateness, reliability, and condition and makes recommendations on obsolescence and replacement.</li>
<li>Participates in or leads physics projects</li>
<li>Participates in regulatory compliance tasks</li>
<li>Assures performance of an annual output check of each beam to verify their consistency with national standards and prepares a report on this process and its results.</li>
<li>Assures that the daily output and quality assessment checks of radiation producing equipment are performed and that equipment is in proper working order.</li>
<li>Maintains proper output checks on accelerators, simulation, and other radiation therapy associated equipment.</li>
<li>Initiates and routinely reviews all treatment equipment operational logs and service reports.</li>
<li>Performs clinical QA of equipment specifications, acceptance testing, commissioning and calibrations on all new and repaired clinical equipment, and the lead shielding requirements of rooms.</li>
<li>Participates in quality assurance checks and performance improvement initiatives.</li>
<li>Participates in routine QA of patient treatment records.</li>
<li>Develops and performs departmental physics QA program</li>
<li>Maintains and documents the inventory of all radioactive materials and returns used materials in a timely manner.</li>
<li>Acts as Department Radiation Safety Officer and assists in radiation safety tasks.</li>
<li>Develops and implements new radiation oncology projects in coordination with the department manager, as directed by the radiation oncologists.</li>
<li>Maintains and organizes required records, reports and files, and collects necessary statistics.</li>
</ul>
</li>
</ul>
<ul>
<li>Assists dosimetry in treatment planning for External Beam, Stereotactic Radiosurgery and Brachytherapy
<ul>
<li>Evaluates and implements necessary changes and updates in treatment planning computer, radiation calculation and measurement, and record and verification software.</li>
<li>Prepares coordinates and effectively collaborates with the radiation oncologists and technical staff on optimal treatment plans.</li>
<li>Instructs and supervises dosimetrist and technologist in special treatment techniques associated with treatment plan.</li>
<li>Oversees technical aspects of dosimetrist’s and technologist’s activities.</li>
<li>Provides technical in-services as necessary for the demonstration of new techniques and other appropriate subjects.</li>
<li>Assumes responsibility of maintaining proficiency in job skills and seeks opportunities for continued growth and has ability to meet the department work schedule.</li>
<li>Assists radiation oncologists with brachytherapy procedures and maintains all regulatory requirements for all radioactive materials.</li>
<li>Assists with orientation of new employees and students.</li>
<li>Performs other related duties incidental to the work described herein</li>
</ul>
</li>
</ul>
 About Us Find it here. Discover the job, the career, the purpose you were meant for. The supportive and inclusive team where you can thrive. The place where growth meets balance – and opportunities meet flexibility. Find it all at Carle Health. Based in Urbana, IL, Carle Health is a healthcare system with nearly 16,600 team members in its eight hospitals, physician groups and a variety of healthcare businesses. Carle BroMenn Medical Center, Carle Foundation Hospital, Carle Health Methodist Hospital, Carle Health Proctor Hospital, Carle Health Pekin Hospital, and Carle Hoopeston Regional Health Center hold Magnet® designations, the nation’s highest honor for nursing care. The system includes Methodist College and Carle Illinois College of Medicine, the world’s first engineering-based medical school, and Health Alliance™. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Carle Health participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. | For more information: <a href="mailto:human.resources@carle.com" target="_blank">human.resources@carle.com</a>. Compensation and Benefits The compensation range for this position is $84.33per hour - $145.05per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including, but not limited to, the candidate’s experience, qualifications, location, training, licenses, shifts worked and compensation model. Carle Health offers a comprehensive benefits package for team members and providers. To learn more visit careers.carlehealth.org/benefits.

Physicist - Methodist Radiation Oncology

<h3>Job Description</h3>
Job DescriptionABOUT STRM.BIO STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genentic medicines that target the bone marrow. We’re a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We’re here to do great science and build a company we’re proud of. THE OPPORTUNITY We’re looking for a Senior Scientist to help lead and grow our research engine. You’ll work shoulder-to-shoulder with the VP of R&amp;D and Director of Research to drive key programs forward and manage external collaborations. This is a hands-on, highly cross-functional role ideal for someone who’s ready to lead and execute in equal measure. This is a full-time, on-site role. WHAT YOU’LL DO (Key Responsibilities)&nbsp;
<ul>
<li>Lead day-to-day scientific execution across internal teams and CRO/academic partners</li>
<li>Own program timelines and technical plans; troubleshoot and drive decisions to keep progress on track</li>
<li>Design, run, and refine experiments, hands-on and alongside junior team members</li>
<li>Coordinate with collaborators, ensure data integrity, and maintain clean documentation across projects</li>
<li>Contribute to company strategy through project planning, milestone tracking, and resource scoping</li>
<li>Present internally and externally, including pitch decks, grant applications, and scientific meetings</li>
<li>Stay sharp on emerging EV, gene therapy, and CAR-T technologies to shape R&amp;D direction</li>
<li>Pitch in on lab ops, team culture, and whatever else it takes to get the job done</li>
</ul>
WHAT YOU BRING (Required Qualifications)
<ul>
<li>Ph.D. + 5 years’ postdoc or industry experience in gene therapy/genetic medicines, CAR-T, or related areas</li>
<li>Deep expertise in in vivo gene delivery platforms (viral vectors, LNPs, EVs)</li>
<li>Strong bench skills in molecular/cell biology, including flow cytometry, qPCR, Western, microscopy, NGS</li>
<li>Experience developing ex vivo and in vivo CAR-T or other T-cell based therapies</li>
<li>Solid working knowledge of genome editing tools (CRISPR, Cre-lox, etc.)</li>
<li>Experience managing external partners (CROs, academic labs)</li>
<li>Comfortable navigating ambiguity, shifting priorities, and high ownership environments</li>
<li>Excellent communicator, highly organized, strong attention to detail</li>
<li>Bonus: experience with startup ops, grant writing, or early product development</li>
</ul>
KEY POSITION DETAILS
<ul>
<li>100% on-site in Cambridge, MA</li>
<li>Full time with competitive compensation
<ul>
<li>The salary range for this position is $140,000 to $160,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. &nbsp;</li>
</ul>
</li>
</ul>
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