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<h3>Job Description</h3>
Head of Research
San Mateo, CA | Full-Time
 
About Sankhara
Sankhara is a groundbreaking private equity fund dedicated to collecting, protecting and preserving the human experience through extraordinary physical assets. Rare books, maps, religious artifacts, classic cars, cultural landmarks, iconic sports memorabilia, and more - each with a unique story that shapes history. With a 100-year vision, our mission is to democratize ownership of history, making it accessible to the masses and protected by us, the philosopher-builders fostering a shared world.
 
The Role
Sankhara is hiring a Head of Research - a disciplined, highly capable, and deeply curious research leader who will be responsible for building, leading, and executing the research backbone of the firm.
 
This is not an academic role. This is not theoretical. This is a role for someone who has done serious institutional-grade research before - ideally on rare physical assets. Someone who understands how world-class analysis is constructed, how credibility is earned, and how research must stand up to auditors, LP diligence, skeptics, and historians alike. Someone who can think with commercial judgment and cultural reverence, while maintaining uncompromising standards of truth, rigor, provenance, and documentation.
 
You will work directly with the President and CEO. You will be deeply hands-on, producing research personally while building the frameworks, governance, agentic AI systems, and eventually a research function that scales. You will leverage your own expertise while building a trusted network of cultural, historical, technical, academic, and category experts - knowing when to utilize outside specialists.
 
If you want to help ensure that Sankhara not only acquires treasures, but understands them with depth, integrity, and authority - this is that opportunity.
 
What You Will Do
Asset-Level Research and Diligence
<ul>
<li>Lead research supporting potential acquisitions across all Sankhara verticals.</li>
<li>Develop, maintain, and continuously elevate the firm’s research methodology and standards.</li>
<li>Conduct primary and secondary research on provenance, authenticity, cultural importance, historical relevance, and risk considerations.</li>
<li>Produce structured, defensible research briefs to support investment decisions.</li>
<li>Where necessary, engage, manage, and coordinate subject matter experts, researchers, historians, scientists, and technical authorities.</li>
<li>Ensure research supports responsible decision-making, not storytelling bias.</li>
</ul>
 
Institutional Credibility and Governance
<ul>
<li>Design and maintain research frameworks that withstand institutional scrutiny.</li>
<li>Ensure research is audit-ready, organized, documented, and verifiable.</li>
<li>Support LP diligence needs through clear, high-quality research outputs.</li>
<li>Partner with legal, finance, and operations to ensure alignment between research, compliance, and governance expectations.</li>
<li>Contribute to clear standards around provenance management and authenticity validation.</li>
<li>Build trust and confidence with internal stakeholders by being the steady, disciplined truth source.</li>
</ul>
 
Thought Leadership and Scholarly Rigor
<ul>
<li>Help establish Sankhara as a serious, credible, intellectually grounded institution.</li>
<li>Produce high-quality materials as needed for Board review, executive decision-making, and strategic thinking.</li>
<li>Support the development of internal knowledge infrastructure across categories and themes.</li>
<li>Identify emerging cultural and thematic research areas relevant to future acquisitions.</li>
<li>Where appropriate, support external-facing thought leadership, while always anchoring in substance over hype.</li>
</ul>
 
Execution, Leadership, and Enablement
<ul>
<li>Build and lead the Research function over time.</li>
<li>Build out and maintain agentic AI systems for the Research function. </li>
<li>Be highly hands-on in the near term, personally doing a meaningful portion of research work.</li>
<li>Create documentation systems, workflow tools, and research architecture that scale.</li>
<li>Know when to leverage outside experts and when to execute directly.</li>
<li>Where useful, thoughtfully introduce process improvements, technology, tooling, or automation (including AI where appropriate) to enhance speed and rigor - without compromising standards.</li>
<li>Operate with urgency, but never at the expense of quality or integrity.</li>
</ul>
 
Who We’re Looking For
Required
<ul>
<li>3–5+ years of formal research experience in environments such as Gartner, Sotheby’s, Christie’s, Bonhams, leading consulting research organizations, major museums, or equivalent.</li>
<li>Proven track record producing serious, structured, and defensible research.</li>
<li>Experience working in environments that require accuracy, auditability, and institutional credibility.</li>
<li>Ability to synthesize complex cultural, historical, financial, and contextual information into structured research outputs.</li>
<li>Hands-on, execution-first mentality while capable of building toward a broader function.</li>
</ul>
 
Preferred
<ul>
<li>Experience across cultural assets, rare collectibles, historical objects, museums, or heritage fields.</li>
<li>Experience in research supporting investment, diligence, or risk frameworks.</li>
<li>Exposure to working with CEOs, Boards, or executive leadership.</li>
<li>Comfort operating in a fast-moving, ambitious environment without sacrificing rigor.</li>
</ul>
 
What Success Looks Like
<ul>
<li>Sankhara develops an institutional-grade research backbone that is highly respected internally and externally.</li>
<li>Research materially strengthens investment decisions and institutional confidence.</li>
<li>LPs, auditors, advisors, and partners trust Sankhara’s depth, seriousness, and documentation.</li>
<li>The firm’s narrative becomes stronger because its foundation is unassailably true.</li>
<li>The executive team sleeps better knowing research is disciplined, responsible, and world-class.</li>
</ul>
 
Compensation
Competitive base compensation, performance-based bonus opportunity, and long-term upside participation potential (including equity, carry, and/or token-linked economics depending on structure).
 
Why This Role Matters
Sankhara is building something designed to last centuries. This role ensures that what we collect, protect, and share with the world is deeply understood, properly honored, defensible, and documented - preserving not only treasures themselves, but the truth and meaning behind them.
 
If that excites you - we’d love to meet you.
 
How to Apply
Interested candidates should apply through LinkedIn and/or submit their resume and a cover letter detailing their qualifications and experience to <a href="mailto:blake@sankhara.com" target="_blank">blake@sankhara.com</a>.
 
Join us at Sankhara and help us on this incredible journey!

Head of Research

<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. 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 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>
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>
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\n#11
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>
Soloh Partners is seeking a travel Physicist for a travel job in Atlanta, Georgia.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 02/16/2026</li>
<li>Duration: 12 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
Job Title: Medical Physicist No local candidates within 50 miles. Schedule 730a-430p M-F 13 weeks 725A Cancer Center - Medical Physicist Min of 2 years of experience within specialty. Required BLS 
Soloh Partners Job ID #T31418662. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Medical Physicist
About Soloh Partners
WHO WE ARE&nbsp;
How you project yourself in the world says a lot about you. So, what do we think is important for you to know about us? Soloh Partners is proud to be a certified women-owned business. We are committed to diversity, equity and inclusion. We are driven by our passion for service: service to our clients &amp; their mission and service to our candidates and employees. We believe in making things personal. It isn’t just business for us. This is about shaping careers and building an engaged workforce. To be successful at either you, need to be invested in both.
 
OUR MISSION&nbsp;
Our mission is to be recognized by our clients as an indispensable partner in their pursuit of high-impact Talent. We succeed by creating and maintaining intensely caring and mutually rewarding relationships with our internal employees, candidates and contingent workforce. We aren’t just a staffing agency; we fancy ourselves creatives. We create opportunity. We create excitement. We create and foster relationships built on trust, and partnerships based on mutual respect and understanding.
 
Benefits
<ul>
<li>Medical benefits</li>
<li>Dental benefits</li>
<li>Vision benefits</li>
<li>401k retirement plan</li>
<li>Weekly pay</li>
<li>Sick pay</li>
<li>Referral bonus</li>
<li>Wellness and fitness programs</li>
</ul>

<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;

Chemical Technician/Driver Southfield

<h3>Job Description</h3>
Job Description
COMPANY OVERVIEW:
Certerra provides technology-enabled testing, inspection, and certification services for new product development, engineering solutions to manage assets, and quality assurance for project delivery.
Working in partnership, we help you bring code compliant products to market faster, move into construction with confidence, keep your projects moving forwards and extend the life of your infrastructure assets.
With a nationwide office network and an expert team of over 1,000 people, we have the resources to deliver materially better outcomes, along with local knowledge that ensures the communities we serve are built to last.
JOB RESPONSIBILITIES:
As a Project Geotechnical Engineer at Certerra, you will be responsible for managing small projects as well as managing discrete tasks within larger projects. In this role, you will be expected to:
<ul>
<li>Scoping geotechnical investigations and preparing draft proposals and cost estimates;</li>
<li>Managing and conducting field investigations; reviewing samples/core; ordering laboratory tests and preparing/reviewing/editing boring logs for investigations of any scale;</li>
<li>Working directly with and managing sub-consultants;</li>
<li>Performing and/or supervising engineering analyses;</li>
<li>Preparing geotechnical investigation and geologic hazard reports;</li>
<li>Reviewing plans and specifications for conformance with the intent of A3GEO’s geotechnical recommendations;</li>
<li>Assisting in the managing, training, mentoring and supervision of staff-level engineers;</li>
<li>Managing construction-phase services for projects; and</li>
<li>Conducting onsite construction observation for engineering-related activities, if needed.</li>
</ul>

JOB QUALIFICATIONS:
Certerra is seeking a well-rounded Professional Engineer, with experience on a variety of project types. The following minimum requirements apply to this position.
<ul>
<li>U.S. Citizenship or legal authorization to work in the U.S.</li>
<li>Master of Science (MS) in Geotechnical Engineering.</li>
<li>California Professional Engineer (PE) license.</li>
<li>California Geotechnical Engineer (GE) license.</li>
<li>At least 5-10 years of relevant geotechnical experience.</li>
<li>Demonstrated strong problem-solving skills.</li>
<li>Excellent writing and communication skills.</li>
</ul>

We are an Equal Opportunity Employer. This Company is dedicated to both the letter and the spirit of the equal opportunity employment laws. All applicants and all employees will be evaluated on the basis of their ability, competence, and performance of the essential functions of their positions. There will be no discrimination on the basis of race, sex, national origin, religion, age 40 and over, disability, sexual orientation, marital status, or any other classification which may be protected by federal, state, or local laws. In compliance with the Americans with Disabilities Act, we specifically offer equal opportunity for all employees or job applicants who may have a physical or mental disability. Such persons will be hired on the basis of their ability to perform the essential functions of the job in question. Likewise, their work will be evaluated on their performance of these essential functions. We will offer reasonable accommodation to individuals with disabilities, to the extent that Company resources allow without undue hardship. As part of our equal employment policy, there will be no wage differentials based on gender, between men and women employed in the same establishment, on jobs that require equal skill, effort, and responsibility, and which are performed under similar working conditions.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
COMPANY OVERVIEW:
Certerra is a growing national provider of testing, inspection, and certification services that support innovation in new product development, quality assurance, for project delivery, and engineered solutions for asset management. We are passionate about contributing to the sustainable development of the communities we serve. We are a national firm with a global reach serving national and international clients from 30+ offices located in 10 states and are ranked on ENR’s Top 500 list alongside the nation’s top firms. With a 60-year history, Certerra has a passion for high-end services, constant innovation, and investment in the development of world-class laboratory facilities, and interactive management technologies. Each member of our staff is committed to service, innovation, and the success of our clients.
 
POSITION OVERVIEW:
We are seeking a full-time Staff/Project Geotechnical Engineer to join our Sacramento, CA team. At Certerra, you can look forward to working on a wide variety of interesting projects both in the field and in the office.
 
JOB RESPONSIBILITIES:
As a Staff/Project Geotechnical Engineer at Certerra, your will support lead geotechnical engineers to successfully complete geotechnical projects in ways that satisfy clients and minimize risks. The position, salary, and level of responsibilities assigned to the individual will be based on the experience level of the candidate.
 
Under the supervision of a lead geotechnical engineer, you will be expected to:
<ul>
<li>Supervise subsurface investigations.</li>
<li>Perform engineering analyses including but not limited to settlement, seepage, slope stability, lateral load resistance, deep foundation analyses, soil-structure interaction, seismic deformation, and site-specific seismic hazard analyses.</li>
<li>Develop geotechnical design-level recommendations.</li>
<li>Observe geotechnical construction activities.</li>
<li>Write geotechnical reports, letters, and proposals.</li>
<li>Represent RMA at team and client meetings.</li>
</ul>
 
JOB QUALIFICATIONS:
The following minimum requirements apply to this position.
<ul>
<li>Bachelor’s degree in civil engineering or related field. Master of Science (MS) in Geotechnical Engineering preferred.</li>
<li>At least 3 years of relevant geotechnical experience for the project engineer position.</li>
<li>Excellent writing and communication skills.</li>
<li>Hold a valid driving license with a good standing driving record.</li>
<li>The employee occasionally is required to lift and/or move up to 25 pounds and to walk up to ½ mile daily.</li>
</ul>
 
We are an Equal Opportunity Employer. This Company is dedicated to both the letter and the spirit of the equal opportunity employment laws. All applicants and all employees will be evaluated on the basis of their ability, competence, and performance of the essential functions of their positions. There will be no discrimination on the basis of race, sex, national origin, religion, age 40 and over, disability, sexual orientation, marital status, or any other classification which may be protected by federal, state, or local laws. In compliance with the Americans with Disabilities Act, we specifically offer equal opportunity for all employees or job applicants who may have a physical or mental disability. Such persons will be hired on the basis of their ability to perform the essential functions of the job in question. Likewise, their work will be evaluated on their performance of these essential functions. We will offer reasonable accommodation to individuals with disabilities, to the extent that Company resources allow without undue hardship. As part of our equal employment policy, there will be no wage differentials based on gender, between men and women employed in the same establishment, on jobs that require equal skill, effort, and responsibility, and which are performed under similar working conditions.

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