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<h3>Job Description</h3>
Shift:
Tuesday through Saturday, 2:00 PM - 10:30 PM
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
This is an onsite, full-time Scientist 1 position located in Fairfield, NJ, Tuesday - Saturday, from 2:00 p.m. - 10:30 p.m.
Compensation: $22.00 per hour
Make an impact. Build a career.
At Pace®, everything we do is built upon an unwavering commitment to making the world a safer, healthier place. We continually work to develop innovative practices that drive sustainability and empower our partners with accurate, quality data at every critical moment and milestone.
That's why we need you -- your curiosity, your talents, and your drive -- to help us advance this important work, and your career.
Find your place at Pace®
Join us as a Scientist I, where you'll put your love of science to work performing and overseeing projects within the microbiology department of our environmental testing laboratory.
What you'll do
<ul>
<li>
Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard microbiology/biology policies, programs, and practices
</li>
<li>
Clean, maintain and calibrate instruments
</li>
<li>
Maintain detailed and organized documentation on all laboratory work
</li>
</ul>
What you'll bring
<ul>
<li>
Bachelor's degree in Microbiology/Biology or a closely related field, or an equivalent combination of education, training and experience
</li>
<li>
Ability to perform work in a lab or office setting, remain standing for long periods while conducting tests, work around strong smells, and wear personal protective equipment while handling samples (e.g., lab coat, safety glasses and gloves; all PPE provided by Pace®).
</li>
</ul>
What we promise
<ul>
<li>
Comprehensive benefit program, including medical, vision and dental insurance, 401(k) matching and tuition reimbursement
</li>
<li>
Opportunities to build a rewarding career
</li>
<li>
An inclusive culture that stands for integrity, innovation and growth
</li>
</ul>
PHYSICAL/MENTAL REQUIREMENTS: The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
 Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.
WORKING ENVIRONMENT:
Work is performed in a lab and office setting. Work is subject chemicals, fumes, gasses, noxious odors and related items in a lab and samples setting.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
Benefits When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Scientist 1 - Microbiology

<h3>Job Description</h3>
The R&amp;D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. This position combines hands-on laboratory research with product development responsibilities, including experimental design, material characterization, prototype development, and compliance with design control requirements. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing. This role bridges early discovery and applied development, requiring both strong scientific skills and practical problem-solving.
Key Responsibilities
<ul>
<li>Plan, execute, and analyze laboratory experiments involving biomaterials, regenerative matrices, and medical device components. </li>
<li>Contribute innovative ideas for new products, testing methods, or process improvements to enhance R&amp;D capabilities. </li>
<li>Develop, build, and refine prototypes to meet defined specifications and clinical needs. </li>
<li>Generate accurate technical documentation, reports, and protocols in compliance with FDA, ISO, and Design Control requirements. </li>
<li>Characterize materials and prototypes using analytical, biochemical, and mechanical testing methods. </li>
<li>Perform risk assessments, troubleshoot technical issues, and propose solutions to improve product performance or process robustness. </li>
<li>Support technology transfer from R&amp;D to manufacturing, including process documentation, validation support, and training of personnel. </li>
<li>Collaborate with cross-functional teams (Manufacturing, Quality, Regulatory, Marketing, and Clinical) to align product development with business and clinical requirements. </li>
<li>Engage with external consultants, and customers to gather feedback and translate needs into product features.</li>
<li>Mentor and provide technical guidance to junior staff on laboratory practices, data analysis, and project tasks.</li>
<li>Present findings and project updates to management, peers, and cross-functional stakeholders. </li>
<li>Maintain laboratory operations, including equipment calibration, safety compliance, and method updates. </li>
</ul>
 
Qualifications
<ul>
<li>MS with 1–2 years or BS with 3–5 years in Biomedical Science, Materials Science, Chemistry, or related field.</li>
<li>Experience in medical device research and development, biomaterials, or regenerative technologies preferred. </li>
<li>Knowledge of laboratory techniques for material characterization, tissue-derived biomaterials, or device testing.</li>
<li>Familiarity with Design Controls, GLP/GMP, and ISO standards. </li>
<li>Proficiency with experimental design, data/statistical analysis, and technical problem-solving. </li>
<li>Experience with CAD, prototyping tools, or modeling software is a plus. </li>
<li>Strong organizational skills with the ability to manage multiple studies and projects simultaneously. </li>
<li>Excellent communications and presentation skills for cross-functional collaboration. </li>
</ul>
Demonstrated ability to work independently, manage multiple priorities, and deliver high-quality results.

Research And Development Scientist

<h3>Job Description</h3>
PURPOSE
Primary role is to perform chemical analysis of pharmaceutical products and routine laboratory operations in a cGMP environment.
 
Reports to the Quality Control Manager. Internal relationships include Manufacturing, Research &amp; Development, Analytical Development and Quality Assurance.
 
DUTIES AND RESPONSIBILITIES
Analytical Testing &amp; Review
<ul>
<li>Conduct and review routine and non-routine analysis of raw materials, in-process materials, APIs, and finished products in compliance with SOPs, cGMPs, and cGLPs.</li>
<li>Perform testing using HPLC, GC, GC-MS, ICP-MS, FTIR, UV-Vis, and wet chemistry methods.</li>
<li>Participate in method validation and method transfer activities.</li>
</ul>
 
Equipment &amp; Instrumentation
<ul>
<li>Calibrate, maintain, and troubleshoot laboratory equipment to ensure operational readiness.</li>
<li>Proactively prevent production delays through scheduled maintenance.</li>
<li>Maintain expert knowledge of instrument components and functionality.</li>
</ul>
 
Documentation &amp; Compliance
<ul>
<li>Compile and interpret data, document test procedures, and prepare reports.</li>
<li>Administer quality control systems in compliance with FDA guidelines.</li>
<li>Write and revise Standard Operating Procedures (SOPs).</li>
<li>Investigate and document Deviations and Out of Specification (OOS) events. Provide guidance on CAPAs related to adverse quality events where applicable. </li>
<li>Ensure thorough cGMP/cGLP documentation and maintenance of quality records.</li>
</ul>
 
Leadership &amp; Team Development
<ul>
<li>Provide clear direction, coaching, and mentoring to team members to enhance skills and performance.</li>
<li>Foster a culture of accountability, integrity, and continuous improvement.</li>
<li>Demonstrate strong decision-making skills in prioritizing work under changing deadlines.</li>
<li>Lead by example in quality, safety, and compliance standards.</li>
<li>Encourage cross-functional collaboration to resolve technical challenges.</li>
<li>Take ownership of special analytical projects, including authoring protocols and reports.</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Bachelor’s degree (B.S.) in Chemistry or a closely related scientific discipline with a minimum of five (5) years of experience in FDA-regulated laboratories, or Master’s degree (M.S.) in Chemistry or a closely related scientific discipline with a minimum of three (3) years of experience in an FDA-regulated laboratory environment.</li>
<li>Strong background in principles of separation using analytical instrumentation such as HPLC and GC in a GMP environment.</li>
<li>Expert knowledge of ICH and FDA guidelines.</li>
<li>Expertise in Chromatographic Data Acquisition and LIMS Systems experience such as ChemStation (OpenLab), Chromeleon, or Empower 3.</li>
<li>Attention to details in collecting data and accurately maintaining laboratory notebooks required.</li>
<li>Drug Screen and DEA Background check required.</li>
</ul>
 
WORKING CONDITIONS/PHYSICAL REQIUREMENTS
<ul>
<li>Must be able to conduct visual inspections of incoming materials to verify appearance and printed content (e.g. product labels) meet product specifications.</li>
<li>Must accurately distinguish different colors for reporting of appearance and colorimetric tests.</li>
<li>Occasional lifting of up to 50 lbs.</li>
<li>Annual occupational medical assessment required to ensure ability to meet position requirements and based on site requirements.</li>
</ul>
 
WORKING HOURS
<ul>
<li>Monday - Friday</li>
</ul>
 
LOCATION
This position is located in Round Rock, Texas. Rock Round is located 15 miles north of Austin, TX.
 
Applicants must be legally authorized to work in the U.S. Visa sponsorship is not available at this time.
 
Positions posted for Benuvia Operations are not open to third party recruiters or agencies. Unsolicited resumes for these positions will be considered to be free referrals.

Quality Control Chemist III / Lab Lead

<h3>Job Description</h3>
Essential Job Duties:&nbsp;
<ul>
<li>Responsible for accurate measurement, sampling, operations, and custody transfer of various crude oil types being gathered and transported; following measurement manual procedures and guidelines.</li>
<li>Responsible to reconcile system/segment line balance, batch changes, and system utilization and quality control.</li>
<li>Performs (L) ACT and tank inspections with associated documentation.&nbsp;</li>
<li>Responsible for measurement security at field locations and stations within area of responsibility.</li>
<li>Responsible for monitoring SCADA/HMI interface, generating tickets (internally/externally)</li>
<li>Read and understand station flow diagrams, gate maps, and pipeline drawings.</li>
<li>Perform duties with “One-Call” pipeline response system as needed, to include identifying/locating company pipelines/assets by probing, mapping, and/or flagging methods.</li>
<li>Responsible for launching/receiving scrapers/pigs, valve inspections, and ROW maintenance including line marker replacement.&nbsp;&nbsp;</li>
<li>Position requires manual dexterity and visual acuity, ability to lift 50 lbs., and work outside in all weather conditions, and extended hours.</li>
<li>Other duties as required </li>
</ul>
Education and Ability
<ul>
<li>High School Diploma or GED.</li>
<li>Strong computer skills (Microsoft Suites, STAR)</li>
<li>Strong interpersonal and communication (verbal and written) skills.</li>
<li>Valid driver’s license and clean driving record.</li>
<li>Self-motivated and able to work with little supervision.</li>
</ul>
Experience
<ul>
<li>2 years of oilfield pipeline/station measurement experience.</li>
<li>Preferred experience with (L) ACT meter operations and station equipment, and meters calibration.</li>
<li>Preferred experience with crude oil analyzing equipment.</li>
<li>Preferred experience with flow computers, Coriolis Meters, and displacement meters.</li>
</ul>
 
Physical Demands
<ul>
<li>Position requires manual dexterity and visual acuity, ability to lift 50 lbs., and work outside in all weather conditions, and extended hours.</li>
<li>Must be able to climb large storage tank stairs, with measurement equipment, and work at elevated heights.&nbsp;</li>
</ul>

Measurement Technician

<h3>Job Description</h3>
About Us
At One Physics, our mission is to transform the health and safety of our communities by providing comprehensive medical physics and radiation safety solutions to our clients. Our organization is comprised of leading technical and diagnostic professionals in the medical physics field, coupled with a best-in-class business and client services support team behind the scenes. We share a passion for excellence, dedication to client and patient care, and a commitment to industry leadership.
 
The Role
We are searching for a highly skilled Chief Therapy Medical Physicist to join our dedicated team of experts. Our candidates must be well-trained in Radiation Oncology and be able to work in a collaborative team environment.
 
Clinic Information:
<ul>
<li>This position is located in Norfolk, VA market and will be also supporting surrounding areas.</li>
<li>This clinics you will support have both Varian and Elekta equipment.</li>
<li>Treatment planning systems include Mosaiq, Monaco, Aria &amp; Eclipse.</li>
<li>This role will lead a great team of several physicists, dosimetrist (onsite and remote), and physicians.</li>
</ul>
 
What You’ll Do
<ul>
<li>Perform weekly and monthly radiation measurements, as well as yearly calibration on all treatment units.</li>
<li>Monitor equipment in the Radiation Oncology Department to ensure that it is functioning correctly and safely.</li>
<li>Maintain regulatory agency records and reports.</li>
<li>Analyze alternative treatment plans and supervise dosimetry treatment planning functions.</li>
<li>Implement assessment/treatment and care based on the developmental stages of the patient.</li>
<li>Perform additional duties, as needed.</li>
</ul>
 
What You’ll Need
<ul>
<li>Master’s Degree and/or PhD in Medical Physics.</li>
<li>A board certification by the American Board of Radiology in Therapeutic Medical Physics, or board eligibility as demonstrated by graduation from a CAMPEP accredited residency in therapy physics.</li>
<li>7+ years of clinical Therapy Medical Physics experience preferred.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to interpret regulations.</li>
<li>A willingness to go “above and beyond” for clients and fellow colleagues.</li>
<li>Demonstrate initiative, organization, and ownership of daily tasks and projects.</li>
<li>Ability to problem solve by seeking, developing, and implementing viable solutions.</li>
</ul>
 
Physical Requirements
<ul>
<li>Requires ability to use and move equipment.</li>
<li>Requires a variety of physical activities including sitting, standing, walking, stopping, lifting, carrying.</li>
<li>Exposure to radiation, communicable diseases, and other conditions common to radiation therapy setting.</li>
<li>Occasional evening or weekend work.</li>
</ul>
 
Benefits 
<ul>
<li>Competitive compensation.</li>
<li>PTO plan with paid company holidays.</li>
<li>Health Insurance (Medical, Dental, Vision and Prescription).</li>
<li>401(k) Plan with company match after 1 year of employment.</li>
<li>Group Life &amp; Voluntary Life Insurance.</li>
<li>Short Term &amp; Long Term Disability.</li>
<li>Flexible Spending Account (FSA).</li>
<li>Health Spending Account (HSA).</li>
</ul>
 
Final offer amounts are determined by multiple factors, including geographic location, as well as candidate experience, education level and expertise. If you have questions on compensation, please ask your recruiter. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.
 
We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class.

Chief Therapy Physicist

<h3>Job Description</h3>
Fenagh Engineering and Testing provides special inspections, geotechnical engineering, and other materials testing services for a wide array of private and public sector clients.
 
We are seeking a full time Geotechnical Engineer (PE) to work in our Chicago, IL office.
 
Illinois PE License is required
 
Job Description
<ul>
<li>Prepare or assist staff to prepare geotechnical reports.</li>
<li>Respond to geotechnical related requests from job sites.</li>
<li>Delegate tasks, visits, and activities to staff and project geotechnical professionals.</li>
<li>Develop relations with Fenagh Geotechnical staff in your region through weekly video meetings and in person visits with each on a quarterly basis.</li>
<li>Develop relations with other Fenagh Geotechnical Services Managers through weekly video meetings and co attendance at conferences and offices quarterly..</li>
<li>Develop and recruit geotechnical staff with assistance from all leadership to maintain good work-life balance.</li>
<li>Provide review of requests for geotechnical proposals and advise on level of effort.</li>
<li>Comprehend geotechnical proposals by others and prepare schedule of work.</li>
<li>Prepare marketing writeups for new proposals as requested.</li>
<li>Manage the progress of active investigations weekly by discussing ongoing steps with staff.</li>
<li>Attend mandatory pre-drill and post drill meetings with staff and principals as needed.</li>
<li>Prepare and present trainings to staff (and clients) on geological and geotechnical services.</li>
<li>Assess risk of field investigations and travel where appropriate for oversight and training.</li>
<li>Travel may be required to any Fenagh office location, or client location.</li>
</ul>
 
Requirements
<ul>
<li>IL PE required</li>
<li>Bachelor of Science degree in Engineering.</li>
<li>5 plus years of Geotechnical engineering experience.</li>
</ul>

Geotechnical Engineer, P.E.

<h3>Job Description</h3>
Job Description
Help us change lives
At Exact Sciences, we’re helping&nbsp;change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.
Position Overview
The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as:&nbsp; accessioning, processing, automation usage, sample racking, lab maintenance, and lab cleaning, as well as other lab support tasks.
The Clinical Lab Associate I, Specimen Processing follows all Laboratory policies and procedures and maintains accurate data reporting practices to ensure consistent and diligent execution of Specimen Processing. This role supports the mission and vision of Exact Sciences Laboratories and shares the responsibility of ensuring the Specimen Processing department operates effectively. The function of this position is performed under the guided direction of the Specimen Processing Supervisor or designee.
Shift: Saturday - Monday 6:00am - 6:30pm
Essential Duties
include but are not limited to the following:
<ul>
<li>Perform primary responsibilities listed below completely, timely and accurately:
<ul>
<li>Support and comply with the company’s Quality Management System policies and procedures.</li>
<li>Maintain documentation of problems and problem resolutions following Good Documentation Practices (GDP).</li>
<li>Support department goals that align with organizational priorities.</li>
<li>Work with leadership to identify and progress on individual development goals that align with organizational priorities.</li>
<li>Support operational initiatives including, but not limited to, quality and process improvements, SOP development, department inspections and audits.</li>
<li>Complete all mandatory training assignments and annual competencies within &nbsp;established timelines.</li>
<li>Handle and dispose of all specimens following standard precautions and applicable safety policies.</li>
<li>Understand and comply with all lab and safety regulations.</li>
<li>Support employee engagement initiatives and activities to maintain and improve team morale.</li>
</ul>
</li>
</ul>
<ul>
<li>Meet performance and behavior expectations listed below:
<ul>
<li>Exemplify the core values of Integrity, Teamwork, Accountability, Quality, and Innovation at all times.</li>
<li>Self-motivation with a results-driven approach.</li>
<li>Maintain a high level of professionalism in written and verbal communications.</li>
<li>Act with an inclusion mindset and model these behaviors for the organization.</li>
<li>Maintain regular and reliable attendance.</li>
</ul>
</li>
</ul>
<ul>
<li>Demonstrate the necessary skills and abilities:
<ul>
<li>Ability to work in a fast-paced team environment, adapt to changing workload and circumstances effectively and respond to new information quickly.</li>
<li>Strong critical thinking skills with the ability to make decisions in a fast-paced environment.</li>
<li>Ability to communicate effectively with all levels of the organization through both verbal and written communication.</li>
<li>High level of listening skills and attention to detail with strong organizational and prioritization skills.</li>
<li>Ability to flex hours and work nights and/or weekends as needed to support the success of ES Labs.</li>
<li>Ability to work overtime, as needed.</li>
<li>Ability to lift and move up to 40 pounds for approximately 25% of a typical working day.</li>
<li>Ability to work seated for approximately 50% of a typical working day.</li>
<li>Ability to work standing for approximately 50% of a typical working day.</li>
<li>Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 75% of a typical working day.</li>
<li>Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.</li>
<li>Ability to comply with any applicable personal protective equipment requirements.</li>
<li>Ability to perform repetitive motions.</li>
<li>Understand potential exposure to hazardous materials, tissue specimens and instruments with moving parts, heating and freezing elements.</li>
<li>Tolerate the handling of bodily fluids and solids (e.g., blood, urine and feces).</li>
<li>Ability and means to travel to and work at all other sites within the same city, as needed.</li>
</ul>
</li>
</ul>
Minimum Qualifications
<ul>
<li>High School Degree/General Education Diploma.</li>
<li>Must be 18 years of age or older.</li>
<li>Experience using computers to include Internet navigation, email, Microsoft Office Suite.</li>
<li>Demonstrated ability to perform the Essential Duties of the position with or without accommodation.</li>
<li>Authorization to work in the United States without sponsorship.</li>
</ul>
Preferred Qualifications
<ul>
<li>Associate degree or Bachelor’s degree in Life Sciences, Physical Sciences, or field related to the essential duties of the job.</li>
<li>Experience in a laboratory or similar environment with maintaining sample integrity, following procedures and protocols, and sample collecting/handling.</li>
<li>Knowledge and understanding of CAP, GLP, GDP, CLIA, New York State Department of Health (NYSDOH), and HIPAA.</li>
<li>Experience in troubleshooting automation and performing instrument maintenance.</li>
<li>Lean experience (Kaizen, Kanban, root cause analysis, countermeasure implementation, etc.).</li>
</ul>
#LI-JL2
Salary Range:
$31,000.00 - $52,000.00

The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible.
Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.
Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.
Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law.
To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.
PandoLogic. Keywords: Medical Laboratory Technician (MLT), Location: Madison, WI - 53725 , PL: 600368317

Lab Processing Associate - Weekend AM

<h3>Job Description</h3>
Lead Microbiology Technologist OR Microbiology Lead Opening at an Award Winning Hospital in Georgia!
This large hospital offers over 50 specialties and is a Magnet Designated hospital for nursing excellence. This hospital is also a teaching hospital and offers residency-training programs as well advanced training for nursing students. This hospital is looking to hire a permanent and full time, experienced Lead Microbiology Technologist on DAY Shift.&nbsp;This facility also has bench level openings in core laboratory and microbiology. For consideration, applicants must have a Bachelor's Degree in Medical Technology (or a related field) as well as previous experience in a microbiology laboratory. In addition, applicants MUST have a certification as a MT,&nbsp;MLS, M or SM by the Board of Registry of&nbsp;ASCP. Compensation package includes a highly competitive hourly rate, fantastic benefits package as well as a sign on bonus or relocation assistance! Benefits includes (but is not limited to) Basic, Standard, and Choice Health Plans, Dental and Vision Plans,&nbsp;FSA, Short and Long Term Disability, 403B Plans and Tuition Reimbursement!
Interested in learning more? Contact Andrea at&nbsp;<a href="mailto:andrea@ka-recruiting.com" target="_blank">andrea@ka-recruiting.com</a>&nbsp;or call/text 617-746-2745.&nbsp;
ACC 02111741

Senior Microbiology Technologist OR Microbiology Lead at Top Hospital

<h3>Job Description</h3>
Medical Physics Consulting (MPC), an ONE Physics Partner, is seeking a full time Therapy Medical Physicist based in St. Louis, Missouri to join our growing team located in the Midwest. MPC is a new ONE Physics Partner and is an innovative and growing medical physics consulting practice servicing clients throughout Oklahoma, Kansas, Missouri and Illinois.
 
The Role
We are searching for a highly skilled, compassionate Therapy Medical Physicist to join our dedicated team of experts. Our candidates must be well-trained in Radiation Oncology and be able to work in a collaborative team environment. 
 
Clinic Information:
<ul>
<li>This position is located in St. Louis, Missouri but will be also supporting surrounding areas. </li>
<li>This clinics you will support have both Varian and Elekta </li>
<li>Treatment planning systems include Mosaiq, Monaco, Aria &amp; Eclipse.</li>
<li>This role will join a great team of several physicists, dosimetrist (onsite and remote), and physicians. </li>
</ul>
 
What You’ll Do
<ul>
<li>Perform weekly and monthly radiation measurements, as well as yearly calibration on all treatment units.</li>
<li>Monitor equipment in the Radiation Oncology Department to ensure that it is functioning correctly and safely.</li>
<li>Maintain regulatory agency records and reports.</li>
<li>Analyze alternative treatment plans and supervise dosimetry treatment planning functions.</li>
<li>Implement assessment/treatment and care based on the developmental stages of the patient.</li>
<li>Perform additional duties, as needed.</li>
</ul>
 
What You’ll Need
<ul>
<li>Master’s Degree and/or PhD in Medical Physics.</li>
<li>A board certification by the American Board of Radiology in Therapeutic Medical Physics, or board eligibility as demonstrated by graduation from a CAMPEP accredited residency in therapy physics. </li>
<li>2+ years of clinical Therapy Medical Physics experience preferred.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to interpret regulations.</li>
<li>A willingness to go “above and beyond” for clients and fellow colleagues.</li>
<li>Demonstrate initiative, organization, and ownership of daily tasks and projects.</li>
<li>Ability to problem solve by seeking, developing, and implementing viable solutions.</li>
</ul>
 
Physical Requirements
<ul>
<li>Requires ability to use and move equipment.</li>
<li>Requires a variety of physical activities including sitting, standing, walking, stopping, lifting, carrying.</li>
<li>Exposure to radiation, communicable diseases, and other conditions common to radiation therapy setting.</li>
<li>Occasional evening or weekend work.</li>
</ul>
 
Benefits 
<ul>
<li>Competitive compensation.</li>
<li>PTO plan with paid company holidays.</li>
<li>Health Insurance (Medical, Dental, Vision and Prescription).</li>
<li>401(k) Plan with company match after 1 year of employment.</li>
<li>Group Life &amp; Voluntary Life Insurance.</li>
<li>Short Term &amp; Long Term Disability.</li>
<li>Flexible Spending Account (FSA).</li>
<li>Health Spending Account (HSA).</li>
</ul>
 
Final offer amounts are determined by multiple factors, including geographic location, as well as candidate experience, education level and expertise. If you have questions on compensation, please ask your recruiter. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.
 
We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class.

Therapy Medical Physicist

<h3>Job Description</h3>
Yoh presents an excellent long-term&nbsp;Internal Laboratory Testing Coordinator&nbsp;opportunity with a trusted, long-term client located in Waltham, MA. Scientist/Sr. Research Associate -ESI&nbsp;Multiplex assays/Flow Cytometry Scientist/Sr. Research Associate The Yoh resource is expected to apply expertise across several areas in support of Sanofi Vaccines R&amp;D Global Immunology function developing innovative vaccine solutions for infectious diseases. Key Responsibilities:
<ul>
<li>Design and execute complex immunological experiments to evaluate vaccine candidates</li>
<li>Analyze immune responses using state-of-the-art techniques including multiparameter flow cytometry, ligand-binding, and cell-based assays</li>
<li>Support optimization of the automation of protocols and testing of the samples in automated immune assays as needed</li>
<li>Develop novel immunological assays to support vaccine development programs</li>
<li>Generate, analyze, visualize, and interpret scientific data sets, record experimental procedures and raw and analyzed data in electronic laboratory notebook</li>
<li>Author technical reports, SOPs, and contribute to regulatory submissions as required</li>
<li>Prepare and present findings to internal stakeholders</li>
<li>Provide technical guidance to junior team members as required</li>
<li>Collaborate within immunology and cross-functional teams across R&amp;D</li>
<li>Comply with the company HSE policies and minimize risk to self, others, and the environment, consistent with the community and industry standards.</li>
</ul>
Required Responsibilities:
<ul>
<li>Expertise in cellular and molecular immunology techniques</li>
<li>Proven experience with:</li>
<li>Spectral flow cytometry or flow cytometry with primary mammalian cells</li>
<li>Primary cells isolation and culture</li>
<li>Immunological assays development and implementation (ligand binding, multiplex (Luminex, MSD), cell-based)</li>
<li>Data visualization and analysis</li>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent documentation and record-keeping abilities</li>
<li>Proficiency in standard laboratory software and data analysis tools</li>
<li>Strong written and verbal communication skills</li>
</ul>
Preferred Responsibilities:
<ul>
<li>Experience with vaccine development or infectious disease research</li>
<li>Working knowledge of Good Research Practices (GRP) and electronic note booking</li>
<li>Proficiency in advanced data analysis tools (FlowJo, OMIQ, GraphPad Prism, &amp; other)</li>
<li>Experience with automated/semi-automated platforms/ liquid handlers</li>
</ul>
Education Experience:
<ul>
<li>Data Review</li>
<li>Training</li>
<li>Scheduling</li>
<li>GDP</li>
<li>GRP, compliance requirements for clinical trial samples</li>
<li>Master's degree in Immunology, Microbiology, or related field with 2+ years of relevant industry or academia experience</li>
<li>Bachelor's degree with 4+ years of relevant experience</li>
<li>Experience in pharmaceutical or biotechnology industry preferred. </li>
</ul>
 Estimated Min Rate: $31.50 Estimated Max Rate: $45.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities </li>
</ul>
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, 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. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:&nbsp;<a href="https://www.yoh.com/privacy-notice" target="_blank">https://www.yoh.com/privacy-notice</a>

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