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<h3>Job Description</h3>
Powerwell is a leading recruitment firm helping our clients discover top talent. We’re recruiting for a Lead Food Scientist I. 
 
About Our Client:
Our client’s purpose is unlocking the potential of people, nature, and science to nourish the world. We consistently incorporate social and environmental impact into decision making given its importance to the success and profitability to our business. Our client is committed to creating a diverse and inclusive environment by embracing the wisdom and strengths that diversity brings.
 
Job Summary:
Our client’s Taste and Sensory Innovation team is the foundation and driving force of our client’s business through developing new food concepts and flavor formulations to gain new businesses. As a core team member, you will focus on the development and optimization of savory flavors, including reactions, top notes and EU compliant flavors to ensure that our client remains a leader in delivering high-quality and customized flavor solutions. The successful candidate support both product innovation and customer-specific projects.
 
Essential Job Responsibilities:
<ol>
<li>Utilize knowledge of flavor science to create complex and authentic savory flavors to meet customer and market demands.</li>
<li>Conduct research to explore and understand the functionalities of raw materials and processes that allow the creation of natural flavors for the US, EU and APAC.</li>
<li>Stay abreast of the latest trends and innovations in the flavor world, bringing concepts from ideation to commercialization.</li>
<li>Ensure compliance with regulatory requirements, customer specifications, and food safety standards during the development of flavor products.</li>
<li>Manage innovation projects by collaborating with cross functional teams such as Regulatory, Marketing, Sales, and the Business Unit Leadership teams, and to plan, prioritize, communicate, and execute multiple tasks efficiently.</li>
</ol>
 
Required Education/Experience:
<ul>
<li>Must be a certified Flavorist or in process of obtaining.</li>
<li>Master’s Degree in Food Science or Chemistry or related field.</li>
<li>Experience in developing and enhancing top note profiles for savory applications.</li>
<li>Experience in designing and optimizing reaction flavor systems, including ingredient interactions, thermal processing, and yield efficiency improvements.</li>
<li>Experience in balancing top notes with reaction flavors to achieve complex, authentic flavor profiles.</li>
<li>Ability to analyze and interpret data, communicate, and provide recommendations for research projects.</li>
<li>Excellent communication skills</li>
<li>Excellent project management skills with strong attention to detail.</li>
</ul>
 
Equipment Operation:
<ul>
<li>Standard and Advanced laboratory equipment and instrumentation</li>
<li>Lab scale grinding and extraction equipment</li>
</ul>
This job description is not intended to cover every detail or every aspect of the job identified. Other duties may and will be assigned based upon the workload and needs of the department. Our client is committed to providing safe food to its customers. This position requires completing annual food safety training. Food safety training is conducted through our client’s electronic training program and on-the-job training in each department.
 
Benefit Information:
<ul>
<li>Benefits are effective Day 1 of employment.</li>
<li>Blue Cross Blue Sheild of MI, Delta Dental &amp; VSP Vision</li>
<li>5% direct contribution to 401(k) by our client.</li>
<li>128 hours of PTO/10 Federal Holidays/4 hours volunteer time.</li>
<li>Eligible for 10% Administrative Bonus based on company performance annually.</li>
<li>Paid weekly.</li>
</ul>

Lead Food Scientist I

<h3>Job Description</h3>
LanceSoft is seeking a travel Physicist for a travel job in Vista, California.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 02/23/2026</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>

Under the direction of the Director of Physics, the Radiation Physicist participates in all aspects of the operations of the physics services in Radiation Therapy departments including treatment machine commissioning and acceptance testing, calibration and maintenance of dosimetry and imaging systems, implementing treatment procedures and providing physics consultations in direct patient care activities. Responsible for establishing and maintaining quality assurance, quality control and safety programs in accordance with the standards as determined by regulatory agencies. Responsible for developing, implementing or revising safety or patient care policies and procedures, and contribute to performance improvement activities. Position requires the ability to travel to any site within the system on an as needed basis. Demonstrates age-specific care and excellent problem-solving skills.
They do not perform patient care and this usually falls under an allied role. They mainly perform calibrations and mathematical assessments to assist the dosimetrist.\n\nREQUIRED: ABR board certified, current CA radiation physics license\nREQUIRED: Varian machines/software(Truebeam/IX/Aria/Eclipse), familiarity with Sun Nuclear\nREQUIRED: Looking for 02/09 starts! Please confirm if candidate can start 02/09 with your submittal. If not, please acknowledge candidate can't start 02/09 and indicate the soonest available start date.\nREQUIRED: Interview availability\n\nNo call required. Position is M-F.\n\n(PB)
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>
Job Description
M-F, 8 am to 5 pm 
 
Summary
The Research Coordinator will support and oversee the execution of multiple clinical research studies across inpatient and outpatient units at The Menninger Clinic. This position may contribute to clinic-wide outcomes research as well as focused research projects examining topics such as mental health, predictors of treatment response, resilience, recovery and relapse, and emerging and innovative interventions.
The role involves direct interaction with patients and clinical staff, coordination with academic and institutional partners, and administrative responsibilities related to regulatory compliance, data quality, and reporting. Depending on the study, the Research Coordinator may also accompany participants to off-site locations (e.g., academic medical centers) for study procedures such as neuroimaging.
This position offers a unique opportunity for meaningful patient-facing research experience within a nationally recognized psychiatric hospital and is particularly well-suited for individuals seeking advanced training in medicine, psychology, social work, public health, or related fields.
Key Functions
Study Coordination &amp; Operations
<ul>
<li>Oversee day-to-day execution of multiple research protocols across Menninger Clinic units (inpatient and/or outpatient).</li>
<li>Serve as a primary point of contact between research teams and Principal Investigator(s).</li>
<li>Track study progress and communicate recruitment, retention, and milestone updates to investigators.</li>
<li>Coordinate research workflows and, when applicable, supervise research assistants or trainees.</li>
<li>Prepare and maintain study-related documentation, including protocols, manuals of procedures, consent forms, and correspondence.</li>
</ul>
Regulatory &amp; Compliance
<ul>
<li>Prepare, submit, and manage Institutional Review Board (IRB) applications, amendments, continuing reviews, and related correspondence.</li>
<li>Ensure adherence to institutional policies and federal and sponsor regulations.</li>
<li>Maintain accurate and up-to-date regulatory binders and study records.</li>
</ul>
Participant Interaction &amp; Clinical Research Activities
<ul>
<li>Recruit, screen, consent, and enroll patients across inpatient and outpatient programs into research studies.</li>
<li>Communicate with participants via face-to-face interactions, phone calls, and email throughout their participation.</li>
<li>Conduct standardized assessments and clinically complex research or diagnostic interviews, as appropriate to training and protocol requirements.</li>
<li>Schedule and coordinate research-related appointments, tests, and procedures (e.g., laboratory tests, imaging, behavioral tasks).</li>
<li>Coordinate and attend off-site study visits when required (e.g., MRI scans at Baylor College of Medicine or other partner institutions).</li>
<li>Communicate relevant study participation information to clinical teams to support coordinated and safe patient care.</li>
</ul>
Data Management &amp; Outcomes Research
<ul>
<li>Ensure timely and accurate data collection across studies.</li>
<li>Perform data cleaning and quality assurance checks, to ensure data are analysis-ready.</li>
<li>Generate and distribute research and outcomes reports for participants, clinicians, investigators, and other stakeholders in a timely manner as appropriate given the study.</li>
<li>Support longitudinal follow-up and retention efforts for outcomes research.</li>
</ul>
Research Dissemination &amp; Professional Development
<ul>
<li>Work closely with clinician-scientists and interdisciplinary research teams and receive mentorship in clinical research methods and scientific communication.</li>
<li>Participate, as appropriate and based on interest and performance, in data analysis, abstract preparation, conference presentations, and manuscript development.</li>
<li>Participate, as appropriate and based on interest and performance, in research meetings and contribute to discussions related to study design, interpretation, and dissemination.</li>
</ul>
Administrative &amp; Resource Management
<ul>
<li>Coordinate acquisition and management of research supplies and equipment.</li>
<li>Assist with budget tracking and financial oversight for research projects.</li>
<li>Perform other research-related duties as assigned.</li>
</ul>
Education
Required: Bachelor’ degree.
Preferred: Bachelor’s degree in psychiatry, psychology, social work, neuroscience, public health, or other degrees translational mental health research. This position is ideal for highly motivated early-career professionals seeking hands-on clinical research experience prior to applying to medical school, graduate programs (PhD, PsyD, MPH), or other health-related training programs. 
Why Join The Menninger Clinic Research Team?
The Menninger Clinic is a nationally recognized leader in psychiatric care and research. This role offers exceptional exposure to complex mental health populations, innovative research initiatives, and close collaboration with experienced clinician-scientists. The Research Coordinator position provides a strong foundation for future careers in medicine, psychology, neuroscience, public health, and clinical research.

Research Coordinator, Adults

<h3>Job Description</h3>
Job Description

WHO WE ARE
We are a company where people matter.
We are family driven.
We are financially strong.
And we are looking for problem-solvers to join our growing team. 
BENEFITS
<ul>
<li>Up to 10% Retirement Contribution</li>
<li>$3,000 SIGN-ON!</li>
<li>$1.50/hour shift premium on top of hourly pay </li>
<li>$600 per Year Wellness Incentive </li>
<li>Two Weeks Starting Paid Time Off</li>
<li>Medical, Dental, and Vision - Eligible first day of the month following hire date.</li>
</ul>
JOIN A TOP WORKPLACE - <a href="https://www.youtube.com/watch?v=7nlFHnnfvhk" target="_blank">https://www.youtube.com/watch?v=7nlFHnnfvhk</a>

The primary purpose of this position is to address the operational needs such as handling, manufacturing and loading of industrial chemicals to meet customer demand. Through the environmentally safe operations of the facility, in effective and efficient manner, Production Operator plays an important role in helping Hydrite Chemical Company supply its customers with a quality product in a timely fashion. Production Operator always strives for continuous improvement in his performance to achieve a goal of 100% satisfaction for both internal and external customers.
The primary hours of this position are Monday through Wednesday with Alternating Thursday 7pm to 7:30am. 
PRIMARY RESPONSIBILITES 
<ul>
<li>Move bulk trailers to and from the truck bay following safety rules for driving the tractor trailers</li>
<li>Unload raw materials following the Tank Truck Bulk Unloading SOP</li>
<li>Manufacture finished products in the production equipment according to a specific production worksheet</li>
<li>Load bulk trailers following the Tank Truck Bulk Loading SOP</li>
<li>Create schedules for all incoming and outgoing materials, as well as manufactured products</li>
<li>Maintain and update inventory of chemicals on PRISM system</li>
<li>Responsible for following "Good Manufacturing Practices" in manufacturing processes and housekeeping in all interior and exterior areas of the facility.</li>
<li>Comply with company's safety and regulatory programs. Always perform any task in a safe and environmentally sound way.</li>
<li>Participate in mandatory and processes specific</li>
<li>Communicate to your supervisor compliance, safety, and equipment needs</li>
<li>Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers</li>
<li>Perform all duties outlined in relevant SOPs and all other duties to be assigned</li>
<li>Participate in RCRA, regulatory, health &amp; safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant.</li>
</ul>
SECONDARY RESPONSIBILITIES 
<ul>
<li>Perform safety inspections as directed by the supervisor</li>
<li>Actively participate in Preventative Maintenance Program</li>
<li>Perform maintenance tasks during plant shutdowns or on as needed basis </li>
<li>Works with other staff members to maintain workload Provides back-up support as necessary.</li>
<li>Supports effective communication with all Hydrite departments where responsibilities overlap to ensure success of the branch team.</li>
</ul>
REPORTING STRUCTURE
<ul>
<li>This position reports to the Production Supervisor, and under directions of a Shift Leader work closely with members of QC, production and maintenance departments.</li>
</ul>
EXPERIENCE AND EDUCATIONAL CRITERIA
<ul>
<li>2+ years of Delta V experience </li>
<li>Chemical manufacturing experience preferred</li>
<li>Must be self-motivated and be able to work</li>
<li>Must have communication and interpersonal skills, along with the ability to read, write, and speak</li>
<li>Valid drivers license required</li>
</ul>
PHYSICAL REQUIREMENTS
<ul>
<li>Must be able to stand or walk up to 12 hours per</li>
<li>Must be able to lift up to 50 multiple times per shift, lift 100 lbs. on occasion.</li>
<li>Must be able to climb steps and ladders up to 40 feet high several times</li>
<li>Ability to wear a respirator for up to 4 hours a day without restrictions. Please refer to the SOP for facial hair guidelines.</li>
<li>Must meet DOT vision requirements</li>
<li>Due to safety concerns, the wearing of contact lenses is prohibited</li>
</ul>
BENEFITS
Benefits and perks include 401k and profit sharing, medical/dental/vision/life insurance, paid time off, tuition reimbursement, adoption assistance, legal services insurance, scholarship awards for children of employees, summer picnic, community giving events, free family wellness coaching including nutritionist and fitness coach.
WHY HYDRITE? 
Watch this Why Hydrite video to find out: <a href="https://vimeo.com/201673899" target="_blank">https://vimeo.com/201673899</a>
WANT TO STAY CONNECTED? FIND US ON SOCIAL MEDIA
<ul>
<li>LinkedIn: linkedin.com/company/hydrite-chemical-co-</li>
<li>Facebook: facebook.com/hydrite</li>
<li>YouTube:<a href="https://www.youtube.com/watch?v=Bs_493NR8RI" target="_blank">https://www.youtube.com/watch?v=Bs_493NR8RI</a></li>
</ul>
Learn more about Hydrite on our website: <a href="http://www.hydrite.com/careers" target="_blank">www.hydrite.com/careers</a>
Privacy Notice for California Residents: <a href="https://www.hydrite.com/Legal/Privacy-Notice-for-Employees.htm" target="_blank">https://www.hydrite.com/Legal/Privacy-Notice-for-Employees.htm</a>

Chemical Production Operator - Weekday Nights

<h3>Job Description</h3>
Job Description
Mission Driven, Community Focused About | Charles R. Drew University of Medicine and Science (cdrewu.edu)
Charles R. Drew University is located in the Watts-Willowbrook area of South Los Angeles and was founded in 1966 in the wake of the Watts uprising. CDU was founded to address inadequate medical care in the region and to provide equitable medical education opportunities for underrepresented students. CDU is strongly invested in the local and regional community. The university leads multiple partnerships and programs to provide equitable healthcare resources in a variety of South Los Angeles neighborhoods.
Under the direct supervision of the Project PI/s the Research Associate is responsible for a broad range of routine to moderately complex research duties, including working with mice, perform techniques such as MTT assay, immunohistochemistry, RNA extractions, real time PCR, western blots and biochemical determinations. The long-term goal of our studies is to investigate signaling pathways involved in therapeutic response as well as drug resistance in cancer, and to identify novel agents in cancer chemoprevention and treatment. To achieve these goals, we use multidisciplinary experimental approaches applying both in vitro and in vivo animal models, and high-throughput screening approaches through collaboration with experts in the field.
Essential Duties and Responsibilities:
<ul>
<li>Duties assigned to this title will require an in-depth knowledge of a specialized field, process, or discipline and may involve organizing and implementing complex research plans, the development of methods of research, testing and data collection, analysis and evaluation, and writing reports (weekly reports and progress reports) containing descriptive, analytical and evaluative content.</li>
<li>The duties will require the exercise of independent discretion and judgment in carrying out research activities within the predetermined research scope and methodology.</li>
<li>Participates in research studies to include molecular biology, immunohistochemistry, flow cytometry, MTT assay, RNA extractions, real time PCR, western blots, biochemical determinations, cell transfections, anesthesia, injections, aseptic work, animal handling, and tissue excision.</li>
<li>Maintains inventory and supplies needed for the research lab.</li>
<li>Coordinates from various collaborating departments and collaborates with</li>
<li>Responsible for statistical analyses of data and writing up</li>
<li>Demonstrates leadership in presentation materials and manuscript</li>
<li>Assists divisional staff members and other collaborators in the</li>
<li>Analyzes and records research data, submit weekly reports to the</li>
<li>Maintains related correspondence and regulatory paperwork.</li>
<li>Presents research papers at</li>
<li>Assist the program in mentoring and providing oversight for student</li>
</ul>
Other Duties and Responsibilities:
<ul>
<li>Perform other related duties as</li>
</ul>
Qualifications/Requirements:
 EDUCATION:
<ul>
<li>Regionally accredited doctoral degree (Ph.D., ) or master’s degree required in biomedical science related area.</li>
</ul>
EXPERIENCE:
<ul>
<li>Three years related experience in molecular biology, immunohistochemistry, RNA extractions, real time PCR, western blots, biochemical determinations, plasmid preparation and analysis, cell transfections; anesthesia, injections, aseptic work, animal handling, and tissue excision.</li>
<li>Prior statistical experience with quantitative data analysis and proficiency with commonly used statistical/numerical</li>
<li>Animal self-administration experience is a</li>
</ul>
KNOWLEDGE/ABILITY/SKILLS:
<ul>
<li>Laboratory skills needed including ability to perform biochemical assays and molecular biology</li>
<li>Computer</li>
<li>Written and oral communication</li>
<li>Able to troubleshoot and resolve technical</li>
<li>Committed to a career in biomedical</li>
</ul>
COMPLEXITY:
<ul>
<li>The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position.</li>
</ul>
PHYSICAL DEMANDS:
<ul>
<li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Occasional stooping. Frequent standing. Constant walking, sitting, climbing, reaching high/low levels, finger movement, feeling, speaking clearly, hearing conversationally, and seeing far and near.</li>
</ul>
WORK ENVIRONMENT:
<ul>
<li>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
</ul>
MENTAL DEMANDS:
<ul>
<li>The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent work on a variety of unrelated tasks. Constant calculating interrupted work, work on a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity.</li>
</ul>
SPECIAL REQUIREMENTS:
<ul>
<li>Ability to work effectively with a diverse</li>
<li>The ideal candidate will be seeking a career in Biomedical Science and able to make a long-term commitment.</li>
</ul>
Compensation:
<ul>
<li>$70,304.00</li>
</ul>
Position Status: 
<ul>
<li>Exempt, Full-time </li>
</ul>
Work Location: 
<ul>
<li>On-site</li>
</ul>
Conditional Employment:
The employment status of this position is classified as “Conditional.” Conditional employment means that the job exists contingent upon continued funding and limitations of restricted funds or, the duration of a specific program, project, grant, or contract. Since your salary is funded by: Signaling Mediators, G0075520, End Date: April, 30, 2026, and ACS Pilot Project, End Date: April 30, 2026, your position is contingent upon the continued receipt of these funds. Continuation of your position is dependent, in part, upon funding availability. Furthermore, no work may be performed after the grant end date(s) unless you have received an extension in writing from a Dean, Division VP, or Human Resources.
EEO Statement: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status.
Fair Chance Statement: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws.

Research Associate

<h3>Job Description</h3>
LanceSoft is seeking a travel Physicist for a travel job in Concord, North Carolina.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 02/23/2026</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>

A.C
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>

<h3>Job Description</h3>
Job Description
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As an Associate Research Coordinator, one will assist the research coordinator (CRC/CCRC) in conducting clinical trials. The associate research coordinator is responsible for collecting, processing, storing and handling clinical specimens (as needed), scheduling study subjects for study visits, and collecting, recording, and filing clinical research data. Additionally, the associate research coordinator conducts study visits under the supervision of a study coordinator or senior coordinator.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (<a href="http://www.qps.com" target="_blank">www.qps.com</a>) for more information and to see all current openings.
The Job
<ul>
<li>Ensuring GCP is followed throughout the entire study conduct.</li>
<li>Ensuring subject confidentiality.</li>
<li>Ensuring the subject or subject’s legal representative is provided with a copy of the signed and dated informed consent form.</li>
<li>Possess a sound and in-depth understanding of each protocol that has been assigned</li>
<li>Source document creation per Protocol requirements (if applicable) or as needed</li>
<li>Ensuring compliance with applicable MRA SOP’s/MRA Clinical Research SOP’s, Good Clinical Practice guidelines and regulations</li>
<li>Timely communication of study issues to the study coordinator</li>
<li>Screening, Enrollment, and Ongoing Study Procedures
<ol>
<li>Establish good rapport with potential study subjects</li>
<li>Conduct telephone screening process</li>
<li>Conduct Informed Consent Process (must complete Consenting Process module and quiz prior to consenting)</li>
<li>Clinical data collection such as vital signs, ECG recording, subject height and weight, etc.</li>
<li>Medical records retrieval and review</li>
<li>Laboratory specimen collection, processing and shipment (as needed)</li>
<li>Transporting clinical specimens to the laboratory</li>
<li>Study visits scheduling </li>
</ol>
</li>
</ul>
Requirements
<ul>
<li>Combination of relevant education &amp; experience that provides sufficient knowledge &amp; skills to ensure incumbent’s success in this role, such as: </li>
<li>High School Diploma, and/or </li>
<li>Experience in a similar role </li>
<li>Prior experience as a medical assistant or in an ancillary or allied health specialty a plus</li>
</ul>
Why You Should Apply
<ul>
<li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li>
<li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li>
<li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li>
</ul>

QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Associate Research Coordinator

<h3>Job Description</h3>
Job Description
Join Decypher and make a direct impact on the health and readiness of America’s service members, veterans, and their families. Since 2008 Decypher has offered healthcare industry professionals careers where their expertise is valued, and their work makes a meaningful impact. Decypher partners with the Defense Health Agency to deliver professional services, technology, and management solutions. Our mission is to provide and support quality care for our veterans, servicemembers and their families, across the United States.
Job Summary:
The Medical Physicist provides specialized physics support for radiation oncology services by supporting advanced radiation therapy procedures, treatment planning, equipment acceptance testing, quality assurance, and emergency oncology cases while collaborating closely with physicians, dosimetrists, and clinical staff. The Medical Physicist also supports training, quality improvement initiatives, and coordination of care to ensure safe, accurate, and effective radiation treatment delivery.
Required Qualifications:
<ul>
<li>Education:
<ul>
<li>
Degree/Education: Possess a Master's Degree in Medical Physics, Physics or other related physical science or Engineering disciplines and has at least two (2) years’ experience working in radiation therapy physics documented by a physicist certified by the American Board of Medical Physics or American Board of Radiology. 
</li>
<li>
Possess subspecialty certification as a Medical Physicist by one or more of the following: The American Board of Medical Physics in Radiation Oncology Physics; The American Board of Radiology in either Therapeutic Radiological Physics or Radiological Physics; The Canadian College of Physics in Medicine.
</li>
</ul>
</li>
<li>
Certifications:
<ul>
<li>
Basic Life Support (BLS)
</li>
</ul>
</li>
<li>
Experience:
<ul>
<li>
Possess proficient experience as a Medical Physicist of at least 24 months within the preceding 40 months.
</li>
<li>
Possess at least 24 months experience in treating with intensity modulated radiation therapy (IMRT) including familiarity with various modulation techniques and systems, patient immobilization and data acquisition, treatment planning, treatment plan and machine QA procedures, dosimetry and film QA validation techniques for IMRT treatment plans.
</li>
<li>
Possess supervisory clinical experience as a Medical Physicist for at least 24 continuous months within the preceding 36 months.
</li>
</ul>
</li>
</ul>
Key Responsibilities:
<ul>
<li>
Shall be able to read, write, speak and understand English well enough to effectively communicate with all patients and other health care providers.
</li>
<li>
Shall be knowledgeable of equipment and supply terminology and skill sufficient to identify and use necessary equipment and supplies properly and to communicate proper use with nurses, medical staff, patients, and family members.
</li>
<li>
Shall be sufficiently skilled to teach patients proper self-care and to motivate patients and family members to continue the procedures for promoting rapid healing.
</li>
<li>
Shall be knowledgeable and possess skills necessary to provide care appropriate to any age-related needs of the patients. The Contract Medical Physicist shall demonstrate knowledge of the principles of growth and development appropriate to the appropriate patient population served: Infants, Children, Adolescent, Adults, and Geriatric (&gt;65).Assess, coordinate, facilitate, deliver and evaluate care for infant to geriatric patients using the nursing process.
</li>
<li>
Assess, coordinate, facilitate, deliver and evaluate care for infant to geriatric patients.
</li>
<li>
Possess proficient knowledge of a wide range of medical disorders/conditions, diagnostic studies and treatments related to prevention, and detection of illnesses in adults, is desirable.
</li>
<li>
The contracted Medical Physicist will be knowledgeable in professional care theories, principles, practices, and procedures to perform duties
</li>
<li>
Possess knowledge of computer operations and proficiency in the use of basic word processing, data entry and automated medical records.
</li>
<li>
Be a U.S citizen.
</li>
</ul>
Work Environment and Schedule: Monday-Friday 8:00am-4:30pm at Walter Reed National Military Medical Center.
Decypher is an equal opportunity and affirmative action employer committed to a diverse and inclusive workforce (M/F/D/V)

Clinical Medical Physicists

<h3>Job Description</h3>
Job DescriptionJob Title: R&amp;D Formulation Scientist - Soft GelJob Description
We are looking for an experienced R&amp;D Formulation Scientist specializing in soft gels to join our innovative team. You will partner closely with sales and customers to support product requirements and technical needs, develop formulations for various products, and collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency.
Responsibilities
<ul>
<li>Develop formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations.</li>
<li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li>
<li>Assist with analytical testing and quality assessments.</li>
<li>Perform hands-on work in the Product Development laboratory.</li>
<li>Utilize analytical instrumentation including GC, HPLC, and ICP-MS.</li>
<li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li>
<li>Work effectively with a predominantly Spanish-speaking laboratory team.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of R&amp;D formulation experience.</li>
<li>Bachelor's Degree in Food Science, Chemistry, or related field.</li>
<li>Expertise in soft gels.</li>
<li>Experience in the nutraceutical industry.</li>
<li>Skilled in HPLC, GC, and ICP.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bilingual skills are a plus.</li>
<li>Experience with raw materials and quality control.</li>
<li>Knowledge of analytical chemistry and fish oils.</li>
</ul>
Work Environment
The position will report to the Quality Director until a future R&amp;D Director is hired. Initially, there will be only two R&amp;D formulators on the team until the acquisition expands the team. The work schedule is Monday to Friday, 8 AM to 5 PM, 100% on-site. The dress code is business casual.
Job Type &amp; Location
This is a Permanent position based out of Clifton, NJ.
Pay and Benefits
The pay range for this position is $75000.00 - $90000.00/yr.
401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&amp;D department!
Workplace Type
This is a fully onsite position in Clifton,NJ.
Application Deadline
This position is anticipated to close on Jan 21, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

R&d Formulation Scientist - Soft Gel

<h3>Job Description</h3>
Job Description &nbsp;Job Title – Chemical Technician / Driver Farmington Hills, MI Location &nbsp; We are looking for a candidate with a valid Class A or Class B Commercial Driver’s License (CDL). Existing hazardous materials CDL endorsement is preferred, but not required for hiring. &nbsp; &nbsp;This position will include assisting project managers and field chemists with consolidation/packaging of hazardous wastes, industrial cleaning, spill response and clean-up, recycling activities, and transportation (driving) of hazardous and regulated wastes. This position is based out of our Southfield office with work primarily centered around southeastern Michigan, but will include occasional overnight travel throughout Michigan and the surrounding states. This is a field position, NOT a laboratory position. &nbsp; &nbsp;Work Activities &nbsp;Day-to-day work activities for this position will include, but are not limited to: &nbsp; &nbsp;
<ul>
<li>Packaging, labeling, manifesting, and transport of universal wastes, liquid industrial by-products, medical wastes, and hazardous wastes.</li>
<li>Perform consolidation of hazardous materials/wastes (including bulk packaging and repackaging).</li>
<li>Properly complete regulatory documents for compliant transport and disposal of waste materials.</li>
<li>Assist in preparation of chemical inventories for proper waste handling and/or disposal.</li>
<li>Assist in the safe, compliant, and timely clean-up of chemical spills.</li>
<li>Assist in industrial cleaning projects.</li>
<li>Operate a commercial motor vehicle transporting hazardous materials and wastes for recycling and/or disposal.</li>
</ul>
Hours &nbsp;This is a full time position. Anticipated full-time work hours will be Monday - Friday, typically 7:00 a.m. - 4:00 p.m. or 8:00 a.m. - 5:00 p.m. depending on project commitments. Additional overtime and weekend work may be needed from time to time to support specific project deadlines. This position is also required to have weekend “on-call” commitments two weekends per month. &nbsp; &nbsp;Job Requirements &nbsp;
<ul>
<li>Self-starter, efficient, productive, works well with a team.</li>
<li>Valid Commercial Driver’s License (CDL) – Class A or Class B.</li>
<li>Due to insurance requirements, the candidate must be at least 23 years of age and have a clean driving record.</li>
<li>Successful completion of OSHA/DOT physical examination and drug test.</li>
<li>Clean criminal/security history required to obtain TSA Threat Assessment clearance for CDL Hazardous Materials endorsement.</li>
<li>Must be able to frequently move/lift equipment and supplies weighing 50-100 pounds.</li>
<li>Basic computer experience to handle day-to-day project assignments, use of MS Office.</li>
</ul>
Preferred Experience/Qualifications &nbsp;
<ul>
<li>Current CDL endorsements for Hazardous Materials (H)</li>
<li>Current DOT Medical Examiners (ME) card</li>
<li>Experience in the hazardous waste or emergency response industries</li>
<li>1-3 years' experience preferred</li>
</ul>
 &nbsp; &nbsp;

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