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<h3>Job Description</h3>
Job Description
Dynamis is seeking a Junior Open-Source Intelligence Analyst to support Immigration and Customs Enforcement in Williston, VT and Santa Ana, CA by performing analysis of information sources to obtain real-time and mission critical person-specific information.
Responsibilities:
<ul>
<li>Analysts will perform research and analysis on a myriad of data sources and initiate leads. </li>
<li>Screen, prioritize, and develop leads on incoming cases.</li>
<li>Enter leads into the leads management system of record.</li>
<li>Identify key targeting data (e.g., addresses, vehicles, places of employment, associates, etc.); collect and include additional intelligence of value to officer and operational safety, pattern(s) of travel, and potential criminal activity/criminal indicators.</li>
<li>Ensure data fields in the system of record are updated, accurate, and complete. Attach pertinent photographs, reports, and correspondence. Once entered, leads will be reviewed by PERC or NCATC federal staff for accuracy, quality, and completeness before disseminating them to ICE Field Offices.</li>
<li>Develop and/or enhance leads as directed by TOD staff or according to established priorities.</li>
<li>Use digital methods to conduct all source and open-source research and analysis on matters of national security in support of ongoing investigations.</li>
<li>Assess foreign and domestic-based, publicly available information to identify trends, patterns, and relationships that provide unique insights to address intelligence requirements.</li>
<li>Exploit data from specific sources and raw intelligence and compile them to validate intelligence collection requirements.</li>
<li>Identify trends, detect high-risk areas for weapons proliferation, and prioritize enforcement approaches by applying research and advanced analytics.</li>
<li>Deliver accurate, complete, and timely data to users across the organization.</li>
<li>Work with sensitive information within the guidelines of statutes, regulations, and policies governing the customer. As detailed in the Terms and Conditions, all personnel will be required to obtain at least a Public Trust High adjudication.</li>
<li>Answer and track incoming phone calls and elicit details from the caller to identify possible allegations and specific actionable information. </li>
<li>Maintain confidentiality of information.</li>
<li>Review web tips received online to identify possible allegations and specific actionable information. </li>
<li>Compare viable tips to existing information and process as necessary. </li>
<li>Analyze content of phone and web tips to determine if allegation is within ICE jurisdiction; as dictated by current procedure, policy, or instruction. </li>
<li>Perform research in sensitive, law enforcement, DHS, and open-source databases to identify reported subjects, immigration status, and criminal history. </li>
<li>Accurately document information received from a tipster and reference findings obtained from law enforcement or open-source systems. </li>
<li>Write detailed reports to document research results, identify the appropriate field office for report dissemination and upload the report into the required database.</li>
</ul>
Requirements:
<ul>
<li>U.S. Citizenship</li>
<li>Ability to obtain ICE suitability (current ICE or DHS suitability is preferred).</li>
<li>Education/Experience:
<ul>
<li>Bachelor's degree or higher and one year of experience performing primarily social media, and open-source information research, targeting, and analysis; or,</li>
<li>Associate's degree and two years of experience performing primarily social media and open-source information research, targeting, and analysis; or, </li>
<li>High school diploma or GED and three years of experience performing primarily social media and open-source information research, targeting, and analysis.</li>
</ul>
</li>
<li> Shall provide support in accordance with NCATC duty hours (i.e., Monday through Friday 7:00 am to 6:30 pm (Eastern Time) or PERC duty hours (24x7, 365 days per year). </li>
<li>Work hours are to be aligned with the NCATC's and PERC's established hours.</li>
<li>Work is deemed mission essential and will be expected to continue during government shutdowns. </li>
<li>Telework and remote work are not generally authorized. However, in extenuating circumstances, telework and remote work may be authorized on a case-by-case basis with written telework authorization by the COR in accordance with agency policies.</li>
</ul>
Preferred:
<ul>
<li>Current or recent experience providing open-source analytical support for DHS or other US Government clients</li>
<li>Watch Center or similar threat monitoring experience</li>
<li>Federal law enforcement experience</li>
</ul>

Open-Source Intelligence Analyst

<h3>Job Description</h3>
Medical Laboratory Supervisor – Contract-to-Hire (6 Months)
Bedford, IN (On-site; some travel to Paoli)
 Schedule: Monday–Friday, normal business hours
 No regular weekends (may be required occasionally for coverage/bandwidth)
Position Summary
We are seeking a Medical Laboratory Supervisor to support and lead day-to-day laboratory operations for a large healthcare provider. This is a people-focused leadership role, ideal for someone who enjoys supervising teams, improving workflows, and supporting staff success rather than working primarily on the bench. This is a 6-month contract-to-hire opportunity supporting a new hire initiative.
The supervisor will be on-site primarily in Bedford (3 days/week) with additional support in Paoli (2 days/week).
Key Responsibilities
<ul>
<li>Supervise daily laboratory operations, including staff scheduling, coverage planning, and workflow coordination.</li>
<li>Act as a people leader by conducting weekly check-ins, supporting PTO planning, and promoting team engagement and morale.</li>
<li>Provide administrative and operational guidance to laboratory staff; serve as a point of escalation for workflow or personnel issues.</li>
<li>Support quality assurance, compliance, and documentation standards in alignment with hospital, state, and federal regulations.</li>
<li>Oversee supply inventory, equipment readiness, and general lab operations to ensure continuity of service.</li>
<li>Lead team development efforts including onboarding, training coordination, performance feedback, and team-building initiatives.</li>
<li>Collaborate with leadership to identify process improvements and operational efficiencies.</li>
<li>Bench work is not required, but available if the supervisor chooses to support during high-volume periods.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Medical Technology, Chemical, Physical, or Biological Science required.</li>
<li>Master’s degree in Medical Technology, Clinical Laboratory Science, or related field preferred.</li>
<li>3–5 years of experience in a high-complexity laboratory environment.</li>
<li>Certification through ASCP, AMT, NCA, or equivalent required.</li>
<li>Prior supervisory or leadership experience strongly preferred.</li>
<li>Strong communication, organization, and team leadership skills.</li>
<li>Proficiency with laboratory information systems (LIS) and standard computer applications.</li>
<li>Working knowledge of laboratory regulations, SOPs, and quality standards.</li>
</ul>
Additional Details
<ul>
<li>On-site role with travel between Bedford and Paoli locations</li>
<li>Focused on leadership, staffing, and operations rather than technical bench work</li>
<li>Contract-to-hire after 6 months based on performance and business needs</li>
</ul>

Medical Laboratory Supervisor

<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
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>
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>
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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