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<h3>Job Description</h3>
Job Description
SUMMARY 
We are looking for a self-motivated Chemical Plant Operator. The Chemical Operator can expect to work as an integral part of the production team and may be responsible for retrieving, weighing, and mixing chemical ingredients, monitoring equipment during the chemical process, repairing machinery if problems arise, recording information about equipment and compounds, and assisting in the planning and improvement of processes or products. They will also be expected to comply with all company, local, state, and federal safety and quality regulations and report any concerns, violations, or accidents. This is a full time, career-oriented job with benefits. The work is both physically and technically challenging. Hazardous chemical handling in a chemical manufacturing environment. Experience with chemicals or manufacturing is preferred, but not required. Strong physical skills needed also, with handling of 55-gallon barrels, tools, etc. We manufacture in accordance with ISO 9001 standards.
ESSENTIAL DUTIES AND RESPONSIBILITIES include but are not limited to the following:
<ul>
<li>Responsible for complying with all environmental regulations including hazardous waste</li>
<li>Ensure hazardous waste containers are properly labeled, covered, and staged</li>
<li>Using information on work order and batch sheets, collects all required materials and measures or weighs as required for proper formulation</li>
<li>Work from written, verbal or visual instructions</li>
<li>Load chemical process equipment with necessary materials</li>
<li>Observe rate of speed and process to insure proper operation</li>
<li>Observe and follow all safety related procedures while in the work environment</li>
<li>Gather raw materials</li>
<li>Check completed batches for compliance with formulation specifications</li>
<li>Make minor mechanical adjustments or assess malfunctions and notify supervisor</li>
<li>Observe and follow all safety related procedures while in the work environment</li>
<li>Drive a forklift</li>
</ul>
 QUALIFICATIONS 
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The demonstration of regular attendance and punctuality is essential.

Chemical Operator

<h3>Job Description</h3>
Job DescriptionDent Neurologic Institute is committed to excellence in all we do. Our culture is built on 4 key pillars: respect, quality, productivity, and well-being. By remaining dedicated to these values and the overall mission, we are dedicated to making a difference for both patients and colleagues. When you join the Dent team, you can take advantage of a variety of benefits: 
<ul>
<li>Work-Life Balance (no overnight shifts)</li>
<li>Medical, Dental &amp; Vision Plans</li>
<li>Life Insurance</li>
<li>401(k) Retirement Plan</li>
<li>Critical Illness, Accident, &amp; Legal Plans</li>
<li>Wellness Program</li>
<li>Learning &amp; Development Opportunities</li>
<li>Paid Time Off</li>
<li>Paid Holidays </li>
<li>Free Onsite Parking at All Locations</li>
</ul>
 
Schedule: Monday - Friday 8:00am - 4:30pm
Location: Amherst
 
Position Summary: To serve as a research analyst involved in initiating organizing, analyzing, reporting results in regards to investigator initiated research. To coordinate study protocols and initiate new ideas for research as well as maintaining a database and facilitate statistical analysis.

Responsibilities of Position: 
<ul>
<li>Managing the research database on their designated topic</li>
<li>Coordinating study protocols and implementing them within the database</li>
<li>Writing and submitting investigator initiated protocols</li>
<li>Statistical analysis background for data analysis by the means of
<ol>
<li>Excel</li>
<li>Access</li>
<li>SYSTAT</li>
</ol>
</li>
<li>Writing and submitting abstracts and papers to be presented or published</li>
<li>Presenting paper and research results</li>
<li>Performs other duties assigned by Principal Investigator and Supervising Certified Clinical Research Coordinator</li>
<li>May have duties that fall under “Clinical Research Coordinator” job description on a per project basis</li>
</ul>

Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Skills &amp; Experience Necessary: 
<ul>
<li>Proficiency in Excel and PowerPoint</li>
<li>Experience in statistical analysis</li>
<li>Experience in ACCESS and statistical packages such as SYSTAT or SPSS are a plus</li>
<li>All personnel drawing blood must be credentialed by hospital phlebotomy; CPR certification preferred</li>
<li>All personnel handling/packaging/shipping hazardous good must become IATA certified </li>
<li>Strong interpersonal and communications skills</li>
<li>Excellent organizational skills</li>
<li>Must have a flexible schedule according to business need</li>
</ul>
Preferred Education and Experience
<ul>
<li>College degree or technical training preferred</li>
<li>Prior research or lab experience preferred but not required</li>
</ul>

Working Conditions:
<ul>
<li>Moderate physical activity required at times which may include occasional movement of studies supplies or equipment, not in excess 25 pounds</li>
<li>Occasional exposure to human body fluids/secretions</li>
<li>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions</li>
</ul>

Travel
<ul>
<li>Travel possible between Dent Neurologic Institute sites</li>
</ul>
Compensation:
<ul>
<li>Most candidates will start within the first quartile of the pay range</li>
<li>Rates are commensurate with experience</li>
</ul>
AAP/EEO Statement
Dent Neurologic Institute provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
 Monday - Friday 8:00am - 4:30pm 40 hours/week

Research Assistant

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing analytical testing and characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques as well as supporting laboratory operations and maintenance. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, report authoring, and department documentation support.
 RESPONSIBILITIES: The responsibilities of this position include, but are not limited to:
<ul>
<li>Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, mRNA and vaccines.</li>
<li>Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques.</li>
<li>Provide general laboratory support, including ordering/replacement of reagents and consumables, general maintenance of equipment, continuous improvement activities, and participating in periodic lab inspections.</li>
<li>The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression.</li>
<li>This position will be responsible for preparing data summary presentations, providing data verification support, compiling data, and using lab-based systems for data collection such as Empower and electronic laboratory notebooks.</li>
<li>Effective communication skills are required for interactions with laboratory scientists, project managers and colleagues from numerous functions.</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>At least a BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent</li>
<li>1+ years of hands-on experience with chromatography, preferrably with HPLC</li>
<li>Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, mRNA, or antibody drug conjugates and how to characterize them with analytical techniques</li>
<li>Must be eligible to work in the United States indefinitely without restriction or sponsorship (OPT, H1B, etc.).</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques</li>
<li>Strong computer skills and experience with lab-based computer systems</li>
<li>Ability to collect and analyze data sets</li>
</ul>
 Additional Information 
Positions are full-time, working&nbsp;Monday-Friday 8am-5pm,&nbsp;overtime as needed.&nbsp; Candidates currently&nbsp;living within commutable distance to St. Louis, MO&nbsp;are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
<ul>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Characterization Scientist

<h3>Job Description</h3>
We’re thrilled to share an exceptional opportunity with a highly reputable outpatient primary care group in Mobile, AL. This state-of-the-art facility is dedicated to delivering Value-Based Care to the senior population, offering unparalleled support for both patients and providers.
Why This Role Stands Out:
<ul>
<li>Work-Life Balance: Monday-Friday schedule, 8 AM-5 PM.</li>
<li>Manageable Patient Load: Average of 10-13 patients per day, allowing for quality care.</li>
<li>Competitive Compensation: Starting at $250,000+, with increases based on experience.</li>
<li>Incredible Bonuses: $15,000 sign-on bonus and significant performance-based incentives.</li>
<li>Comprehensive Benefits: A package designed to support you and your family.</li>
</ul>
The practice is equipped with in-house amenities to ensure seamless care delivery, empowering you to focus on what matters most—your patients.
If you’re passionate about making a meaningful difference in senior care, this could be the perfect fit for you!

Transform Senior Care in Mobile, AL: Exciting Primary Care Opportunity!

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The PDS&amp;T Parenterals/Eye Care group is seeking a motivated Senior Scientist as a CMC drug product project lead, specifically for parenteral drug product process development and commercial site scale up and tech transfer. The candidate will independently design and execute lab studies to develop robust manufacturing processes for clinical phase and commercial products. This person will generate and analyze precise, reliable, and reproducible data in a timely manner, independently or under the direction of a more senior scientific leader. This position will be an integral part of the product development and CMC teams and is highly collaborative across functions such as analytical, process engineering, internal and external manufacturing, quality assurance, CMC regulatory affairs, &nbsp;supply chain and Operations Manufacturing Sites.
Major Responsibilities:
<ul>
<li>Independently design and conduct critical experiments that further project goals. Implement and may innovate new experimental protocols/techniques for parenteral DP characterization studies to enable process scale up.</li>
<li>Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.</li>
<li>Tech transfer activities for parenteral DP from development scale up to clinical/commercial scale.</li>
<li>Support drug product manufacture at GMP facilities from clinical to PPQ and commercial batches.</li>
<li>Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.</li>
<li>Authoring of comprehensive, scientifically sound reports,&nbsp;e.g.&nbsp;development reports or risk assessments that serve as source documents for regulatory submissions. Author portions of regulatory submissions to designated health authorities related to these reports.</li>
<li>Develop and maintain comprehensive project plans, timelines and development and/or scale up tech transfer strategy; technical projects at all stages of development are included, from phase II clinical through commercial.</li>
<li>Lead cross-functional PDS&amp;T product teams and represent the CMC team and/or PDS&amp;T in interface with PDS&amp;T leadership, other Operations functions, other AbbVie functions and external partners. Participate in or coordinate Governance efforts such as Product Performance Teams or gate reviews.</li>
<li>Prepare and review submissions through registration of the product as well as post-approval life-cycle management. Serve as a peer reviewer for submissions and under stand how regulatory submissions limit operational changes.</li>
<li>Establish and foster partnerships with key customers and counterpart functions to facilitate effective collaboration. Identify and promote best practices among PDS&amp;T CMC leads.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelors, Masters, or PhD in chemical engineering, pharmaceutical sciences, chemistry, pharmaceutics, or related disciplines with 10+ (Bachelors), 8+ (Masters), or 3+ (PhD) years of relevant industry experience.</li>
<li>Strong laboratory skills and experience focused on manufacturing process development for monoclonal antibodies, antibody constructs/conjugates or other parenteral formulations.</li>
<li>Scientific problem solving, experimental design, and trouble shooting skills.</li>
<li>Solid understanding of the various unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized products.</li>
<li>Experience in laboratory documentation systems, including ELN, and demonstrated experience with technical report writing. Technical understanding and experience with small molecule products manufacturing, development, quality and analytics is required.</li>
<li>Knowledge and experience with FDA and global regulatory requirements for CMC issues is required.</li>
<li>Ability to influence internal and external experts on CMC regulatory issues, independently.</li>
<li>Demonstrated excellence in writing, presentation, and overall communication.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II

<h3>Job Description</h3>
Job Description
Earth Systems R&amp;R is not your average environmental consulting firm. We’re hands-on, collaborative, and committed to solving real-world geotechnical and environmental challenges with technical excellence and regulatory know-how. If you want your work to matter—and have the autonomy to lead it—we want you on our Austin-based team.
We are seeking a Geotechnical Engineer with a background in Geology, Environmental Science, or Environmental Engineering who thrives in a multidisciplinary environment. Candidates must reside in or near Austin, TX, and have direct experience with Texas regulations and field conditions. This is a field-forward position with a focus on practical problem-solving and project leadership in the central Texas region.
Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations including site reconnaissance, subsurface explorations, soil/rock classification, and in-situ testing</li>
<li>Analyze data for foundation design, slope stability, settlement analysis, and pavement recommendations</li>
<li>Prepare detailed geotechnical reports with practical engineering solutions</li>
<li>Develop project scopes, proposals, and budgets; assist with project management and client communications</li>
<li>Oversee field exploration programs, coordinate lab testing, and ensure QA/QC on deliverables</li>
<li>Work closely with regulatory agencies to ensure compliance with TXDOT, TCEQ, and other Texas-specific environmental/geotechnical regulations</li>
<li>Mentor junior staff and support business development through local networking and technical presentations</li>
</ul>
Required Qualifications:
<ul>
<li>Bachelor's degree in Geotechnical Engineering, Geology, Environmental Engineering, or related field (master’s preferred)</li>
<li>5+ years of experience in geotechnical engineering or applied environmental consulting</li>
<li>PE or the ability to obtain PE in Texas within 12 months</li>
<li>Proficiency in AutoCAD, gINT, GeoStudio, or similar software</li>
<li>Strong writing skills and experience preparing detailed technical reports</li>
<li>Current driver’s license and willingness to travel to project sites across Central Texas</li>
</ul>
What We Offer:
<ul>
<li>Competitive salary</li>
<li>Medical, dental, vision, and life insurance</li>
<li>401(k) with company match</li>
<li>PTO, holidays, and flexible field scheduling</li>
<li>Mileage reimbursement</li>
<li>Paid training, certifications, and continuing education</li>
<li>Growth-focused culture with a seat at the table</li>
</ul>
Must be authorized to work in the United States. Sponsorship is not available for this position.
Ready to take your career to the next level in a place where your skills are valued and your impact is real? Apply now to join Earth Systems R&amp;R in Austin, TX.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Why We Exist and What We Do:
At Dr. Squatch (<a href="http://www.drsquatch.com" target="_blank">www.drsquatch.com</a>), we're raising the bar on men's personal care with our line of natural, high-performance products. We're on a high-growth, fast-moving ride, continually introducing new product categories, launching into retailers nationwide, and growing internationally. We have been recognized and certified by Great Place to Work® multiple times, and we achieved status as a certified B Corp in 2023. We are looking for passionate, talented people who want to join us in our mission to inspire and educate men to be happier and healthier!
About the Role:
The Associate Scientist will be part of the Research &amp; Development team responsible for bringing new and innovative personal care products to life. This role will research and develop new soap products and work with our operations team to support continuous improvement of existing products. Specifically, this role will work in our R&amp;D laboratory to prototype new products and evaluate new ingredients, fragrances, colorants, and designs.
Dr. Squatch is best known for our bar soaps, and this role will be a key contributor to the development efforts for new soap launches. An interest in contributing to new product ideas and excitement about new product development is key. The ideal candidate will balance the technical and scientific requirements of the role with the creative side of new product development and problem solving.
This role will report to the R&amp;D Senior Scientist.
This is a full-time role with company benefits based in Marina Del Rey, California.
The anticipated base compensation range for this role will be $65,000 - $80,000. Compensation will be commensurate with the candidate's experience and local market rates.
What You'll Do:
<ul>
<li>Identify key gaps in the market for men's soap products from both a conceptual and technical perspective, with a narrow focus on products that fit our brand voice and mission</li>
<li>Become an expert in making cold process soap at the laboratory scale</li>
<li>Create soap batches in our research and development laboratory to test out new concepts for ingredients, design, and fragrance</li>
<li>Research raw materials and build relationships with suppliers to source and test unique ingredients for our products</li>
<li>Manage timelines of research and development laboratory projects to support execution of new product launches</li>
<li>Coordinate with cross-functional partners including Operations, Marketing, and the rest of the Product team to ensure products can be effectively produced at scale and successfully launched via marketing campaigns</li>
<li>Support raw material testing for supply chain projects, including onboarding new suppliers and supporting quality assurance</li>
<li>Ensure laboratory is stocked with necessary raw materials and equipment for batching</li>
<li>Maintain organization and documentation of laboratory according to GLP and GDP standards</li>
</ul>
About You:
<ul>
<li>Bachelor's degree in chemistry, chemical engineering, or similar science</li>
<li>Solid technical background in laboratory work with 1-2 years of laboratory experience</li>
<li>Experience in cosmetic product development, preferably natural products and/or cold process soaps</li>
<li>Familiarity with GLP and GDP, preferably in an FDA-regulated environment</li>
<li>Strong interest in health and wellness</li>
<li>Comfort with a rapidly evolving work environment, and experience taking initiative</li>
<li>Excellent communication and presentation skills</li>
</ul>
Who We Are:
Our core values come naturally and make us a better, more whole, and unique team. We are Bold &amp; Innovative - we are creative, rethink how things are done, and find a way. We Play to Win - we have high standards, we encourage ownership of work, we are scrappy, we act with urgency, and we invest in the outcome of our work. We are Team Squatch - we are humble, help others outside our own wheelhouse, stay positive, have fun, and have approachable and transparent leadership.
We offer a competitive salary in a growth-focused &amp; collaborative team environment. Benefits include medical, dental, vision, 401k with Squatch match, and PTO. We also have great perks like healthy snacks, frequent company events, and of course, free products!
For Applicants with Disabilities. Reasonable accommodation will be made so that qualified applicants with disabilities may participate in the application process. If you need any accommodations during the hiring process, please let us know when you submit your application and we'll do our very best to adjust as needed.
For Information regarding Data Privacy, please review <a href="https://privacy.drsquatch.com/" target="_blank">https://privacy.drsquatch.com/</a>.
Unsolicited Resume Policy. Dr. Squatch ("DRSQ") employs an internal Talent Acquisition department. Exceptionally, DRSQ may choose to supplement that internal team with support from temporary staffing agencies, placement services, and/or recruiting agencies ("Agency"). Agencies are hereby specifically directed NOT to contact DRSQ employees directly in an attempt to present candidates. DRSQ's Talent Acquisition team is responsible for all candidate presentations to our hiring managers.
To protect the interests of all parties, Dr. Squatch will not accept unsolicited resumes from any source other than directly from a candidate. Any unsolicited resumes sent to DRSQ, including unsolicited resumes sent to a DRSQ email address or mailing address, directly to DRSQ employees, or to DRSQ's resume database will be considered property of Dr. Squatch.
DRSQ will not pay a placement, service or other fee for any placement resulting from the receipt of an unsolicited resume. This also includes partial resumes, LinkedIn profiles, general candidate profiles, and/or candidate details or information. DRSQ will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees.
DRSQ's Talent Acquisition team must provide advance written approval to an Agency to submit resumes and/or profiles for a specific job-opening, and the approval must be in conjunction with a valid fully executed staffing, placement or other service agreement. DRSQ will not pay a fee to any Agency that does not have a fully executed agreement in place prior to submission, receipt and placement of candidates.

Associate Scientist

<h3>Job Description</h3>
Job Description
Earth Systems is not your average environmental consulting firm. We’re hands-on, collaborative, and committed to solving real-world geotechnical and environmental challenges with technical excellence and regulatory know-how. If you want your work to matter—and have the autonomy to lead it—we want you on our Florida-based team.
 
We are seeking a Geotechnical Engineer with a background in Geology, Environmental Science, or Environmental Engineering who thrives in a multidisciplinary environment. Candidates must reside in Florida and have direct experience with Florida regulations and field conditions. This is a field-forward position with a focus on practical problem-solving and project leadership in the Southeastern region.
 
Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations including site reconnaissance, subsurface explorations, soil/rock classification, and in-situ testing</li>
<li>Analyze data for foundation design, slope stability, settlement analysis, and pavement recommendations</li>
<li>Prepare detailed geotechnical reports with practical engineering solutions</li>
<li>Develop project scopes, proposals, and budgets; assist with project management and client communications</li>
<li>Oversee field exploration programs, coordinate lab testing, and ensure QA/QC on deliverables</li>
<li>Work closely with regulatory agencies to ensure compliance with FDEP, FDOT, and other Florida-specific environmental/geotechnical regulations</li>
<li>Mentor junior staff and support business development through local networking and technical presentations</li>
</ul>
 
Required Qualifications:
<ul>
<li>Bachelor's degree in Geotechnical Engineering, Geology, Environmental Engineering, or related field (Master’s preferred)</li>
<li>5+ years of experience in geotechnical engineering or applied environmental consulting</li>
<li>PE or the ability to obtain PE in Florida within 12 months</li>
<li>Proficiency in AutoCAD, gINT, GeoStudio, or similar software</li>
<li>Strong writing skills and experience preparing detailed technical reports</li>
<li>Current driver’s license and willingness to travel to project sites across Central Texas</li>
</ul>
 
What We Offer:
<ul>
<li>Competitive salary </li>
<li>Medical, dental, vision, and life insurance</li>
<li>401(k) with company match</li>
<li>PTO, holidays, and flexible field scheduling</li>
<li>Mileage reimbursement</li>
<li>Paid training, certifications, and continuing education</li>
<li>Growth-focused culture with a seat at the table</li>
</ul>
 
Must be authorized to work in the United States. Sponsorship is not available for this position.
 
Ready to take your career to the next level in a place where your skills are valued and your impact is real? Apply now to join Earth Systems.

<h3>Job Description</h3>
Job DescriptionYU &amp; Associates, Inc., an awarding winning engineering firm located in Elmwood Park, New Jersey is seeking a Supervising Project Engineer to join our team. The successful candidate will manage aspects of important projects including proposal development, budget, project execution, scheduling and client communications. Participates in conducting engineering investigations and planning work by completing well-defined tasks. These tasks may include collection and analysis of data using established procedures, performance of routine calculations, and participation in evaluating the feasibility of alternate solutions. Requirements/Responsibilities
<ul>
<li>Bachelor's degree in civil engineering&nbsp;(master's&nbsp;preferred) and a Registered Professional Engineer in the State of New York&nbsp;required.</li>
<li>Minimum of 5 years of&nbsp;experience.</li>
<li>Demonstrated ability to manage multi-discipline projects and utilize technical support&nbsp;staff.</li>
<li>Ability to develop and maintain strong relationships with clients, must possess the desire to develop new clients and expand the services of existing clients while maintaining strong&nbsp;billability.</li>
<li>Record and report all work performed, including deviations from approved work plans, contract documents, poor quality of work, unforeseen conditions, unsafe conditions, etc.;</li>
<li>Interface with Senior Inspector to maintain and track various logs, reports and field records for the designated area of&nbsp;responsibility.</li>
<li>Monitor the contractor’s timely execution and quality of&nbsp;work.</li>
<li>Interact with contractor’s superintendent for on-site resolution of construction&nbsp;issues.</li>
<li>Review and proof contractor submittals and respond to&nbsp;RFIs.</li>
<li>Prepare proposal cost estimates, technical approach and scope of work&nbsp;write-ups.</li>
<li>Perform review of responses to RFPs for project subcontracts, materials and&nbsp;equipment.</li>
<li>Prepare thorough documentation of site activities, monitor project schedules and subcontractor performance and correct issues when needed.</li>
<li>Assist with preparing project reports, correspondence and cost tracking/status.</li>
<li>Provide technical assistance to engineering oversight staff as required.</li>
</ul>
Qualifications
<ul>
<li>Experience in managing large field programs as a team leader is a&nbsp;plus.</li>
<li>Geotechnical analytical and design&nbsp;experience.</li>
<li>Technical report writing&nbsp;skills.</li>
<li>Project and safety&nbsp;management.</li>
<li>Field documentation&nbsp;skills.</li>
<li>Excellent reading, writing, and verbal communication&nbsp;skills.</li>
<li>Strong computer&nbsp;skills.</li>
<li>Field and office assignments, as required.</li>
</ul>
We offer employees competitive compensation packages, medical/dental/vision, life insurance, short, and long-term disability, paid holidays, paid time off, and&nbsp;401k retirement plan with company match. YU &amp; Associates' is an Equal Employment Opportunity employer fully committed to providing equal opportunity in all areas of employment practices.&nbsp;No employee or applicant for employment is discriminated against because of race, creed, color, religion, gender, gender identity or expression, sexual or affectional preference, sexual orientation, sex, ancestry or national origin, citizenship status, age, disability, marital or domestic status, veteran status, atypical hereditary cellular or blood trait, genetic information or testing, or any other legally protected category in all employment decisions. We foster a work environment that’s inclusive as well as diverse, where our employees can be themselves.&nbsp; Every idea and perspective are valued to meet our common goals. YU &amp; Associates is committed to supporting our employees’ well-being by providing benefits that are a valuable part of the compensation package. We partner with our employees to foster a healthy, safe and rewarding lifestyle both at work and at home. The Y&amp;A benefits program for full-time employees include: ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Benefits:&nbsp;&nbsp;
<ul>
<li>Medical-National plan with low out of pocket costs to members.</li>
<li>Dental-National plan.</li>
<li>Vision-National plan with the largest vision network.</li>
<li>Life/AD&amp;D-Benefit available should an employee pass away while employed.</li>
<li>Short-Term Disability-Benefit in the event an employee is unable to work for a short period of time.</li>
<li>Long Term Disability-Benefit in the event an employee&nbsp;is unable to work for an extended period.</li>
<li>Employee Assistance Program-Employee 3rd&nbsp;party support available when needed.</li>
<li>ADP Retirement Plan with company match.</li>
<li>Bonus Program – based on individual and company performance.</li>
<li>Yearly review – based on individual and company performance.</li>
</ul>
Tax Savings Tools:&nbsp;&nbsp;
<ul>
<li>&nbsp; &nbsp; &nbsp; Healthcare Reimbursement Accounts-Tax Free benefit to employees.</li>
<li>&nbsp; &nbsp; &nbsp; Flexible Spending Accounts-Tax Deductible benefit for employees.</li>
<li>&nbsp; &nbsp; &nbsp; Dependent Care and Commuter Program-Tax Deductible benefit for employees.</li>
</ul>
Value Adds:&nbsp;&nbsp;
<ul>
<li>&nbsp; &nbsp; &nbsp; Will Preparation</li>
<li>&nbsp; &nbsp; &nbsp; Beneficiary Grief Support</li>
</ul>
 &nbsp;SALARY RANGE:&nbsp; $90,000 - $100,000 &nbsp;
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79LL92278Q

Geotechnical Supervising Project Engineer

<h3>Job Description</h3>
Dynamic start-up medical device firm seeks individual to join its r&amp;d organization. Responsibilities will be broad based, sharing responsibilities with the VP of R&amp;D. This may include overseeing early feasibility study submission and submissions for the European Union. 
This is a hands-on technical management role. The technology consists of implants and catheter delivery systems to treat mitral valve regurgitation. This firm has about 20 employees and is currently conducting clinical trials OUS.

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