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<h3>Job Description</h3>
Job Description
EnSafe is seeking a Senior Hydrogeologist to join our team of environmental professionals working on complex and rewarding projects across the countrybased out of any of EnSafe’ soffices listed: Jacksonville, Tampa, Pensacola, FL; Houston, TX; Memphis, Knoxville, Nashville, TN; or Hartford, CT
EnSafe is an employee-owned global environmental consulting and engineering firm. We strive to provide cutting-edge, creative solutions for our clients. EnSafe specializes in custom solutions in Environmental Management and Planning, Civil Design Engineering, Environmental Restoration, Natural &amp; Water Resources, Health &amp; Safety, and Technology, with offices operating within the U.S. 
What We Are Looking For
As Senior Hydrogeologist, you will lead and contribute to multidisciplinary projects involving environmental site investigation, remediation, groundwater modeling, and regulatory compliance. We offer a workplace culture that promotes autonomy, continuous learning, and professional growth. 
What You Will Be Doing: 
<ul>
<li>Designing, directing, and executing complex site investigations, including the planning and implementation of drilling, geophysical logging, aquifer testing, sampling of various media, and installation of monitoring and recovery wells.</li>
<li>Leading project teams in developing conceptual site models and conducting contaminant fate and transport evaluations.</li>
<li>Managing and overseeing field activities, ensuring health and safety compliance, subcontractor coordination, and efficient scheduling.</li>
<li>Interpreting hydrogeologic data and synthesizing field and analytical results to support reporting, risk assessments, remedial design, and regulatory decision-making.</li>
<li>Practical use of advanced groundwater models to support site characterization and remediation/optimization strategies.</li>
<li>Writing and reviewing technical reports, work plans, sampling plans, and standard operating procedures (SOPs).</li>
<li>Serving as a technical advisor, mentoring junior staff, performing quality control reviews, and helping the next generation of hydrogeologists grow.</li>
<li>Interfacing with clients and regulatory agencies as a subject matter expert, providing strategic guidance, presenting findings, and supporting negotiations.</li>
<li>Performing optimization of passive and active remedial alternatives, including LTM.</li>
<li>Building, calibrating, and validating analytical and numerical soil, groundwater, surface water, sediment, and indoor air (attenuation) modeling.</li>
<li>Providing litigation support for discovery, affidavits, deposition, and trial.</li>
<li>Performing sequence stratigraphy evaluations and reporting.</li>
<li>Performing statistical evaluations, background studies, and associated reporting.</li>
<li>Travel up to approximately 30% may be required, including occasional overnight trips.</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's or Master’s degree in Hydrology, Hydrogeology, Geology, Engineering, or a closely related field.</li>
<li>15–20 years of professional experience, preferably in environmental consulting. </li>
<li>Professional Geologist or Engineer licensure (by exam).</li>
<li>Strong background in hydrogeologic site characterization, groundwater flow and transport modeling and analysis, and environmental remediation/remedy optimization.</li>
<li>Proficiency with regulatory programs including CERCLA, RCRA, and state-specific programs.</li>
<li>Demonstrated ability to lead projects and teams, manage multiple priorities, mentor/supervise employees, and communicate effectively with diverse audiences.</li>
<li>Advanced skills in data analysis, report writing, and preparation of maps, tables, charts, and figures.</li>
<li>Experience using hydrogeologic modeling tools, including but not limited to MODFLOW, MT3D codes, VISTAS, EVS, etc. </li>
<li>Familiarity with GIS applications.</li>
<li>Excellent verbal and written communication skills. </li>
<li>Current 40-hour HAZWOPER certification.</li>
</ul>
About EnSafe
EnSafe began as a two-person firm in 1980, navigating complex regulatory compliance issues on behalf of our clients. We nurture our people with growth and development opportunities. We build enduring, trustful relationships with each of our clients, with a focus on high ethical and safety standards. We build this reputation by attracting high-quality people and retaining them for the long term.
At EnSafe, we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this or other roles at our company.
EnSafe is committed to being an EEO employer and all qualified candidates will receive consideration without regard to race, color, religion, national origin, citizenship, age (except for bona fide occupational qualifications), sex, disability, sexual orientation, gender identity, marital status, military or veteran status, any other status protected by federal, state, or local law, or association with a person on the basis of one or more of the foregoing.
Check us out on the web at <a href="http://www.ensafe.com" target="_blank">www.ensafe.com</a>

Senior Hydrogeologist

<h3>Job Description</h3>
Introduction
 
“Quality and safety above everything”. That is the unassailable theme that guides everything that we do, every day. We have an unwavering commitment to quality and the production of safe and effective products. Our science and risk-based compliant quality culture is innovative, and healthcare oriented. Whether you are involved in development, operations, maintenance, compliance or analysis, through research and manufacturing programs, your contribution will directly impact our success.
 
Your Diligence Means Our Success
 
At Pherros, we combine development and safety to improve the lives of those around us. Our employees bring life-changing medicines to people in need and improve the understanding and management of disease. We give our best to putting people first and we are looking for people who are determined to improve life for everyone.
 
You will be a member of Pherros’ dedicated and highly effective quality control operations team. Our aseptic manufacturing facility for parenteral pharmaceuticals presents an exciting opportunity to be an important part of a state-of-the-art facility and quality system. The Quality Control Laboratory assures patients worldwide that our drug products are safe and effective and of the highest quality and integrity. We exceed these standards through effective execution of process, environmental, supply and product testing.
 
General Requirements
 
As a Quality Control Chemist, you will perform accurate and timely testing of routine and non-routine samples in accordance with appropriate Good Manufacturing Practices (“GMP”), Good Laboratory Practices (“GLP”), and safety guidelines, to support site production and stability requirements. 
 
The Chemist and Chemistry Supervisor roles are focused on the quality control testing of the various pharmaceutical products manufactured at Pherros Biosciences. All testing performed is in accordance with the established drug product specifications. The candidate will participate in and perform development and validation of analytical test methods associated with finished dosage form (FDF) drug products as well as investigate, resolve, and mitigate deviations, non-conformances, and OOS (Out of Specification) events associated with products tested at the facility. The Quality Control Scientist utilizes technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and assist in resolving laboratory investigations of atypical data and results. Additional key objectives and deliverables include the capability to:
 
<ul>
<li>Be an inspirational part of a vibrant and growing group of professionals.</li>
<li>Accurately and safely perform timely testing of routine and non-routine lab samples in accordance with appropriate GMP, GLP, and safety guidelines.</li>
<li>Accurately record data in reports or Laboratory Information Management System (“LIMS”) in accordance with laboratory procedures, Good Laboratory Practices (“GLP”), standards, and GMP requirements.</li>
<li>Recognize deviations from procedures, methods, etc., and initiate an investigation as required.</li>
<li>Verify analytical data generated by other analysts within the lab as required.</li>
<li>Adhere to all Environmental, Health, and Safety (“EH&amp;S”) standards.</li>
<li>Identify and communicate opportunities for improvement initiatives in daily work activities.</li>
<li>Troubleshoot equipment and methods as required.</li>
<li>Provide technical support for non-routine (e.g., deviation) investigations.</li>
<li>Maintain inventory of all supplies and consumables for the laboratory.</li>
<li>Gown for activities within aseptic manufacturing suites typical of a GMP environment.</li>
<li>Engage in training exercises to fulfill compliance requirements associated with the position.</li>
<li>Conduct chemical and physical testing of raw materials, API, in-process, finished products, and stability samples, and other in process samples, using established test methods to provide accurate and reliable data to assure their strength, identity and purity.</li>
<li>Work with materials using safe protocols and participate in and contribute to the maintenance and calibration of analytical instruments within the quality control laboratories.</li>
<li>Collaborate with other facility team members and regulatory colleagues to establish release and stability specifications for starting materials, intermediates, drug substances, and drug products.</li>
<li>Work well in a fast-paced team environment.</li>
<li>Collaborate with management to identify training needs and ensure appropriateness of training plans, creating and assigning curricula as required.</li>
<li>Contribute to the training, education, guidance, and influence of operational and support areas on quality control policy and practices.</li>
<li>Foster a culture of collaboration, partnership, teamwork, and a drive for change and continuous improvement.</li>
<li>Take initiative and have the ability to work independently as well as collaboratively with exemplary enthusiasm amongst other team members.</li>
<li>Perform other duties as assigned.</li>
</ul>
 
Educational, Experience and Training Requirements 
 
Bachelors, Masters or Ph.D. degree in Chemistry with three (3) to seven (7) years of relevant experience in a GMP Chemistry Lab environment, including knowledge of analytical chemistry testing, excellent understanding and knowledge of analytical instrumentation technologies, chromatography methods, USP compendial test methods, ICH guidelines, and cGMP, experience with HPLC and LCMS analytical testing, method development, and method validation is required, experience with GCMS, FTIR and ICPMS is required for supervisors, strong communication and organizational skills, proficiency in Microsoft Office suite applications (Excel, Word, PowerPoint), ability to handle multiple tasks simultaneously while meeting deadlines, ability to investigate, collect data, and analyze trends investigations, ability to work as needed for off-hours stability timepoints and potential early start times, excellent communication (written and verbal), interpersonal, organizational and negotiation skills, project management skills, experience in process improvement, and the ability to be solution focused on the design and implementation of quality and process improvements.
 
Additional Preferences:
 
Experience with a LIMS system.
Ability to lead and to inspire others.
Experience with a Quality Management System (“QMS”) such as Master Control.
Demonstrated problem solving and analytical thinking skills.
Understanding of statistical tools and analysis.
Excellent interpersonal skills and networking skills.
Experience in a GMP QC Lab environment.
Demonstrated written and verbal communications skills.
Strong attention to detail.
Ability to organize and prioritize multiple tasks.
Experience with Root Cause Analysis.
Demonstrated ability to work both independently and as a part of a team.
 
Additional Information
 
The position is full-time non-remote, Monday through Friday, with flexibility to support weekends. Applicants will work in various areas within the site. Some allergens may be present in the facility. Exposure to allergens should be considered when applying for this position. Tasks may require repetitive motion (e.g., keyboarding). Minimal travel required.
 
Sunshine Act
 
Pherros reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.&nbsp;These laws and regulations require Pherros to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.&nbsp;Subject to further legal review and statutory or regulatory clarification, which Pherros intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.&nbsp;Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pherros that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.&nbsp;If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
 
EEO &amp; Employment Eligibility
 
Pherros is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.&nbsp;Pherros also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.
 
Quality Control
 
About Us
Careers at Pherros Biosciences are like no other. We believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community in order to bring innovative therapies to market and to make the world a healthier place.

Quality Control Scientist - Chemistry Supervisor/Manager

<h3>Job Description</h3>
Job Description
Murphy Research is a full-service custom market research firm known for our innovative research design and consultative approach. We produce groundbreaking qualitative and quantitative research through our focus on creative design, rigorous execution, and enduring insights. Our team thinks out of the box, follows a steady execution process, and is empowered to produce the highest quality research product that truly matters to our clients.
We are actively seeking a Senior Research Manager to join the Murphy Research team. In this role, you will direct the development, execution, and analysis of projects for a diverse range of Fortune 500 companies. All of our researchers work across industries on diverse projects with clients like, Disney, Gatorade, Waymo, and Visa. This is an exciting opportunity to continue to grow your research career as you support some of the world’s most prominent brands with market assessment, brand strategy, product development, customer loyalty and engagement, and communications research.
About You:
<ul>
<li>You have 3-5 years of market research experience, and familiarity with both qualitative and quantitative methods</li>
<li>You have a B.A., M.A., or PhD in a field with a strong research or business emphasis</li>
<li>You apply strong understanding of research principles to strategic business questions in ways that reflect your excellent problem-solving and advanced analytic skill</li>
<li>You love teamwork, but you’re great at prioritizing and managing multiple projects while you work independently</li>
<li>You demonstrate excellent verbal and written communication, and are comfortable presenting to large groups</li>
<li>Your strong interpersonal skills support your ability to build client relations, effectively delegate, and provide mentorship to others</li>
<li>You are self-motivated to take initiative and maintain high expectations for quality work that delights the clients you serve</li>
</ul>
What You’ll Be Doing:
<ul>
<li>You will oversee and direct research projects directly and/or collaborate with a team, while leading analysis and reporting on all projects under your direction</li>
<li>You will utilize excellent management skills in both project and financial management</li>
<li>You will work with large data sets to discover and share compelling data-driven stories; of course, your proficiency in Word, Excel, &amp; Powerpoint will certainly come in handy! (bonus points for skills in SPSS, R, InDesign, Keynote)</li>
<li>With strong support from senior leadership, you’ll receive on-the-job training in advanced interviewing, management, methodology, and analytics</li>
<li>In a fast-paced environment, you will be challenged to think strategically and learn new things every day! </li>
</ul>
What We Offer:
<ul>
<li>Daily opportunity for variety, challenge, and growth</li>
<li>Great training, career advancement, and mentorship opportunities</li>
<li>A collaborative, team-oriented, and high-performing atmosphere</li>
<li>Salary Range commensurate with experience: $95,000 - $120,000</li>
<li>Competitive benefits package, including medical, dental, vision, 401k matching, paid time off, in-person and virtual social activities</li>
<li>Flexibility to work remotely, with a commitment to a hybrid work model (all new hires must live within commuting distance of our Century City or downtown Minneapolis co-working spaces)</li>
</ul>

Senior Research Manager

<h3>Job Description</h3>
FRANdata is looking for an Entry Level Research Analyst to join our fast-paced and growing market research, insights, and consulting&nbsp;firm. The ideal candidate will have a strong background in data analysis, financial statement interpretation, and research methodologies. This is an entry-level role that involves working closely with clients to deliver customized research reports and data-driven insights.
 
FRANdata has more than 30+ years of expertise in researching the franchising business model and providing insights to help our clients operate and succeed. These clients cover the entire spectrum from start-up companies to well-known global brands that have been franchising or serving the franchise vertical for decades.&nbsp;
 
Salary Range is 50K-60K depending on level of experience. 
 
ESSENTIAL FUNCTIONS
<ul>
<li>Conduct in-depth research and data analysis to support custom client projects</li>
<li>Interpret and analyze financial statements (e.g., EBITDA, earnings before tax, depreciation, and amortization)</li>
<li>Manage and maintain databases, ensuring accuracy and timely updates based on client feedback</li>
<li>Collaborate with team members and clients to understand project requirements and deliver high-quality, tailored research reports</li>
<li>Communicate findings and insights to clients, helping them understand the data and make informed business decisions</li>
<li>Lead and participate in client calls to kick off projects, explain the scope of research, and gather necessary information</li>
<li>Produce clear, comprehensive research reports (e.g., bank credit reports) based on client specifications</li>
</ul>
 
This is a hybrid role, with 2 days in-person (Tue and Wed) at our office in Arlington, VA, and 3 days remote.

Research Analyst

<h3>Job Description</h3>
W. R. MEADOWS, INC. designs, manufactures, and markets high quality building materials for today’s construction professionals. Products are sold through our authorized distribution network. We’re a family-owned and operated company focusing on product quality, outstanding service, and business integrity since our founding in 1926.
 
We remain committed to producing high quality products and systems that meet or exceed the latest regulations. From highway construction and repair, building construction and restoration, to waterproofing/vapor-proofing/air barrier products and more, we’ve been satisfying the needs of the public and private sector of the building construction industry for over 95 years.
 
CONSTRUCTION CHEMICALS SCIENTIST
 
JOB SUMMARY:
Immediate need for a Construction Chemicals Scientist based out of our Innovation and R&amp;D Center. Reporting to the Technical Director, the selected individual will provide senior-level research and development expertise to identify, develop, scale up, and commercialize innovative chemical solutions for the construction industry. We seek an experienced individual possessing the ability and creativity to formulate, apply, and evaluate new chemistries for the Concrete Construction Chemicals Market. The successful candidate will collaborate with Product Management to identify trends, market insights, customer needs, new market opportunities, and provide product solutions.
 
ESSENTIAL FUNCTIONS:
<ol>
<li>Development of New Products and assimilation of Acquired Products and Technologies in conjunction with Product Management.</li>
<li>Explore, Identify, and Secure Potential New Technology Platforms.</li>
<li>Provide Technical Support for current Product Lines.</li>
<li>Provide Production Support and Maintenance for current Product Lines.</li>
<li>Provide Coaching, Mentoring, and Leading as appropriate.</li>
<li>Organization, cleaning and recordkeeping.</li>
<li>10% Travel</li>
</ol>
 
ADDITIONAL RESPONSIBILITITES:
<ol>
<li>Industry Presence</li>
<li>Grow toward an Outward Facing Voice and Technical Representative of WR Meadows</li>
<li>Provide Participation and Leadership in Technical Associations such as ASTM, CPI, CRC and the like</li>
<li>Travel with Sales Leaders to watch, listen to WRM customers, end users and influencers</li>
<li>Cross Functional Support</li>
<li>Provide ideas and advice to other scientists and lab members as needed</li>
</ol>
 
KNOWLEDGE, SKILLS AND ABILITIES:
<ol>
<li>Excellent formulation skills.</li>
<li>Experience and familiarity in developing and formulating, including, but not limited to, the below:</li>
</ol>
 
<ol>
<li>Water-based and solvent-based Concrete Sealers e. Dispersions and Emulsions</li>
<li>Silicone and Silane Chemistry and Products f.</li>
<li>Concrete Curing Compounds</li>
<li>Concrete Curing Aids, Accelerators, and Retarders</li>
</ol>
 
EDUCATION AND EXPERIENCE:
<ol>
<li>Bachelors Degree in Chemistry</li>
<li>5-10 ten years of experience formulating construction products or similar items.</li>
</ol>

Chemist

<h3>Job Description</h3>
The Center for Innovative Public Health Research is seeking a dynamic, experienced public health professional to fill the role of Research Associate on an adolescent centered, NIH-funded research study.
 
About us: The Center for Innovative Public Health Research (CiPHR) has been quietly growing into one of the most innovative and progressive technology-focused organizations in the technology and public health space. We are a non-profit organization that primarily focuses on understanding how technology is affecting the health and well-being of youth, particularly LGBT+ youth, while also identifying ways we can harness the power of technology to promote healthy behaviors.
 
We are looking for MPH-trained professionals who want to be part of something bigger. The office setting promotes healthy lifestyle choices: We have two walking desks that can be used by the team. Each researcher has a standing desk. We have an outdoor space with an ocean view for breaks and lunch time, and are a 15-minute walk to the beach. Benefits include generous health, dental and vision insurance coverage, and 403b matching.
 
Research Associate Job Description
 
This is an in-office position. The applicant must be local to Orange County and able to work in our San Clemente office Monday-Friday, 40 hours per week. Applicants who need to relocate for the position will not be considered. Some nights and weekends, based on study needs, will be necessary.
 
The RA position provides a range of research/development activities, including the following:
<ul>
<li>Leading a project, including ownership of milestones and deadlines</li>
<li>Designing social media recruitment campaigns to engage young people in research</li>
<li>Promoting participant retention through ongoing communication strategies</li>
<li>Supporting and tracking IRB submissions to ensure ethical compliance</li>
<li>Contributing to our organization’s social media presence by creating professional posts</li>
<li>Assisting with the finalization of research documents, including formatting the document for particular journal requirements, the insertion of references, etc.</li>
<li>Proofreading research documents, including journal articles and grant proposals</li>
<li>Other duties as assigned</li>
</ul>
 
To perform the RA position successfully, an individual must be able to perform each duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required:
<ul>
<li>Strong communication skills, both verbal and written; including the ability to speak clearly to different audiences (e.g., adolescents, parents)</li>
<li>Ability to take ownership of tasks and take them from conception to completion, while communicating and coordinating with the larger research team</li>
<li>Excellent prioritization skills</li>
<li>Ability to complete tasks on time to meet articulated deadlines</li>
<li>Demonstrate high productivity in a fast-paced work environment</li>
<li>Ability to work independently and also cooperatively within a team</li>
<li>Understand and adhere to standard concepts, practices, and procedures related to adolescent public health research and associated human subjects’ research ethics.</li>
<li>Strong attention to detail</li>
<li>Excellent familiarity with Microsoft Word and Excel</li>
<li>A certain degree of creativity and latitude</li>
<li>Flexibility to work on nights and weekends as needed.</li>
</ul>
 
Qualifications:
<ul>
<li>Successful applicants will have a Master’s degree in Public Health or a related field; or an undergraduate degree in Public Health or a related field and at least 2 years of post-graduate research experience.</li>
<li>Experience working with LGBT+ populations is strongly desired.</li>
<li>Applicants who are fluent in both Spanish and English are highly preferred.</li>
<li>Applicants must currently live local to San Clemente and be able to commute to the office each work day. People who need to relocate or work remotely will not be considered.</li>
</ul>
 
CiPHR is an equal opportunity employer. All applicants will be considered for employment without regard to age, race, ethnicity, religion, sex, sexual orientation, gender identity or expression, veteran or disability status. We are committed to fostering a supportive environment for our employees.
 
Representation matters. Researchers who are part of the LGBT+ community are strongly encouraged to apply.
 
Job Type: Full-time
 
Compensation is dependent upon experience.
Pay: $55,000 - 58,000 per year
 
COVID-19 considerations:
CiPHR is a 100% vaccinated and boosted research team. Researchers are required to be fully vaccinated and boosted for COVID-19 unless they have a medical exemption.

Research Associate

<h3>Job Description</h3>
Scientist III (Quantitative, Translational &amp; ADME Sciences)
$52 -$55/hr medical benefits available at a cost
6 month initial contract with possibility of extensions
100% onsite in North Chicago, IL
M-F core hours 9 am to 3 pm (+2 hours at beginning or end of shift based on needs)
 
Orion Group and our largest US client are in immediate need of Scientists looking for new and exciting contract opportunities in North Chicago, IL. We are seeking candidates experienced in quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including extraction, data analysis and interpretation.
 
Don’t pass on the amazing opportunity to join a market leading pharmaceutical company!!!
 
Key Responsibilities Include:
<ul>
<li>Perform high throughput quantitative in vivo and in vitro LC-MS/MS analysis, troubleshooting and problem solving of small molecule and peptides from various bio-matrices.</li>
<li>Operate, perform routine maintenance, and hands-on troubleshooting of AB Sciex LC-MS/MS systems.</li>
<li>Maintain excellent documentation of all work including LIMS, test methods, and protocols.</li>
<li>Work closely with multiple teams across Discovery and DMPK-BA to support bioanalysis.</li>
</ul>
 
Qualifications needed to be successful in this role:
<ul>
<li>Bachelors, Masters, or Ph.D. in Biochemistry, Analytical Chemistry, or related discipline typically with 8+ (BS), 6+ (MS), or 0+ (PhD) years of relevant academia/pharmaceutical experience.</li>
<li>Proven method development experience using various extraction, chromatographic and analytical methodologies.</li>
<li>Proven experience with quantitative bioanalysis of small molecules.</li>
<li>Proven experience operating and troubleshooting Agilent HPLCs, Leap/CTC PAL autosamplers and AB Sciex Mass Spectrometers</li>
<li>The ideal candidate is detail oriented and committed to generating high-quality results within tight deadlines and across different projects.</li>
<li>Strong communication, interpersonal, and presentation skills.</li>
<li>Work experience in regulated bioanalysis and/or CRO Facility settings is a plus.</li>
</ul>

Senior Scientist

<h3>Job Description</h3>
LanceSoft is seeking a travel Physicist for a travel job in Wilmington, North Carolina.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 09/25/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
Minimum Years of Experience: 3 years of Experience Required Traveler Experience: Clinic WILL ACCEPT 1st Time Travelers Locals Accepted / Rate Difference: Yes&nbsp; **Work Setting Skills REQUIRED: Radiation Oncology **Radiation Therapy Skills REQUIRED: External Beam Radiation Therapy (Teletherapy), Intensity Modulated Radiation Therapy (IMRT) &amp; Radiation safety precautions Certs: ABR - Therapeutic Medical Physics&nbsp; JOB DETAILS: RATIOS: 1 Visit/Day SHIFT: *40 Hours Can Be Offered Will Accept 13 Weeks. 8 HOUR DAYS; 08:00 - 17:00, Monday-Friday Call Requirement: NONE Float Requirement: NONE Weekend Requirement: NONE PATIENT DIAGNOSES: Radiation Oncology Patients SPECIAL PROCEDURES / UNIT DETAILS: Cover Physics clinical tasks during clinical hours. The main center comprises 1 Varian Halcyon, 1 Varian TrueBeam, a Varian IX linac, a Nucletron HDR Afterloader, a Siemens CT simulator, and Sun Nuclear QA physics equipment. VisonRT is used for SGRT. Varian Eclipse and Aria are used for treatment planning and Record and Verify, respectively. Several special procedures are offered at the main campus such as MLC based SRS, SBRT, IMRT, VMAT, IGRT, T&amp;O, and Vaginal Cylinder. The group also covers two nearby satellite centers, each comprising of a Varian linac. SPECIAL EQUIPMENT: All Varian equipment. UNIT SYSTEMS: ARIA/Eclipse SCHEDULING TYPE: Per Clinic Needs; Monday - Friday
&amp;#x1F3AF; Why LanceSoft? \n \nWe’re proud to be recognized by Staffing Industry Analysts (SIA) as one of the fastest-growing staffing firms in the U.S. Our mission is simple: to empower healthcare professionals like you with opportunities that support both personal fulfillment and professional growth. \nAs a certified Minority Business Enterprise (MBE) and an Equal Opportunity Employer, we’re committed to diversity, inclusion, and real human connection. \n \n&amp;#x1F3AF; Benefits \nFour options of medical Insurance \nDental and Vision Insurance \n401k Contributions \nOther Employee Perks \nLicense &amp; certification reimbursements
About LanceSoft
Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we’re 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug &amp; Alcohol Facilities, Home Health &amp; Community Health, Urgent Care Clinics, and many other provider-based facilities.
Benefits
<ul>
<li>Weekly pay</li>
<li>Medical benefits</li>
</ul>

Travel Physicist

<h3>Job Description</h3>
Next-gen optical hardware for Space/Earth Observation and Advanced Manufacturing.
Backed by VCs, Government Agencies and top Universities.
Equity options in a brand-new startup as a founding team member!
 
We’ve teamed up with a next-gen optical hardware startup, who are revolutionizing AI imaging with intelligent vision developed through breakthrough quantum technology. Backed by VC, DARPA, NASA and founded through MIT &amp; Harvard research, they provide the world’s highest resolution imaging system, capable of seeing 20x further than any camera in known existence.
 
Having launched earlier this year, they’re looking for a Lead Research Scientist to build a first-of-its-kind hardware prototype that will be shot into Low Earth Orbit. They’re building their hub near Cambridge (MA), with this position likely to evolve into a senior technical leadership role as the business scales up.
 
Please note that this position can only support US Green Card holders, and cannot offer sponsorship.
 
What will I do?
 
As their first algorithms hire, you will require an extensive background in quantum optics and information theory. Working closely with the CTO and eventual optical engineering team, you’ll build simulations and algorithms to optimize the imaging &amp; sensing systems for their initial prototype. This involves calculating fundamental quantum limits of various imaging/sensing scenarios, building &amp; testing models, conducting simulations and developing/optimizing algorithms to ensure a functional prototype. You’ll develop ML and statistical tooling for object classification, state detection or parameter estimation, as well as developing algorithms to extract data from photons. Whilst the initial project is focused on Space/Earth observation, long-term, they will expand into areas like robotics and advanced manufacturing, so adaptability and pace is key.
 
What skills do I need?
<ul>
<li>PhD (or Masters with industry experience) in Physics, Electrical/Optical Engineering, Computer Science, Mathematics or similar, with a focus on quantum optics and/or quantum information theory.</li>
<li>5+ years of experience in the research of Quantum Optics or Quantum Information Theory.</li>
<li>Strong proficiency in programming languages for simulations (Python, MATLAB, R).</li>
<li>Deep understanding of quantum optics concepts (photon statistics, entanglement, interferometry).</li>
<li>Deep understanding of information theory and communication protocols.</li>
<li>Experience developing and implementing numerical algorithms.</li>
<li>Experience with machine learning algorithms.</li>
<li>Desirable Skills:</li>
<li>Experience with optical neural networks modeling and simulation.</li>
<li>Experience with optical hardware and experimental work.</li>
<li>Experience in Defense and/or Space technologies. </li>
</ul>
 
What do I get in return?
 
On top of a competitive salary in line with your experience (+ equity), the business offers a matched 401(k), medical, dental and vision coverage from day one, private health insurance, as well as generous PTO. They have a mature approach to flexible working, supporting personal circumstances where possible, and also offer fantastic equity options, as an early-stage member of the team and technical leader for their first functional prototype. 
 
Not only that, but you’ll be a part of truly transformative technology for the Defense and Space industries!
 
Where do I apply?
 
Interested? Please send your resume to <a href="mailto:joe@enable-technology.io" target="_blank">joe@enable-technology.io</a> to be considered!

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