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

Senior Hydrogeologist

<h3>Job Description</h3>
Job Description
GENERAL FUNCTION: The Research Manager will drive data-informed strategies by analyzing audience behaviors, content performance and industry trends to inform programming, marketing, partnerships and fundraising strategies. The ideal candidate will have a strong analytical mindset, deep understanding of news and information media analytics and consumption trends, and the ability to translate complex data into actionable insights that support content development and audience engagement.
RESPONSIBILITIES:
<ul>
<li>Conducts in-depth research on audience behaviors, content performance and media consumption trends across TV, digital, social media, audio and emerging platforms. </li>
<li>Tracks and analyzes key performance indicators (KPIs) such as engagement rates, viewership and retention metrics to provide data-driven insights. </li>
<li>Analyzes audience and market data to identify opportunities for business development, sponsorships and fundraising initiatives, providing insights that support revenue growth and strategic partnerships. </li>
<li>Creates and delivers comprehensive research reports and visualizations to inform decision-making across content, programming, marketing and partnerships. </li>
<li>Identifies emerging trends and opportunities by analyzing competitor content strategies and industry best practices. </li>
<li>Collaborates with cross-functional teams to provide insights that enhance content development, programming and distribution strategies. </li>
<li>Utilizes analytics tools such as Comscore, Google Analytics, social media insights and other audience measurement platforms to assess content performance. </li>
<li>Prepares monthly competitive analysis reports on audience engagement, platform effectiveness and media trends. </li>
<li>Stays up to date on evolving media technologies, new content platforms and industry shifts to ensure the organization remains competitive. </li>
<li>Supports audience segmentation and targeting strategies to optimize content reach and engagement. </li>
<li>Presents findings and strategic recommendations to leadership in a clear, concise manner.</li>
<li>Performs other duties as assigned.</li>
</ul>
BACKGROUND SKILLS:
<ul>
<li>Bachelor's degree in Marketing, Data Science, Analytics, Media Studies or a related field. </li>
<li>Minimum of six years in research, content analytics or strategic initiatives, preferably in media or communications. </li>
<li>Strong ability to synthesize complex data, identify key insights and translate them into actionable recommendations. </li>
<li>Understanding of content consumption patterns across linear TV, digital, social and audio platforms. </li>
<li>Proficiency in linear TV analytics (Comscore), Google Analytics, social media analytics (Facebook, Instagram, X, TikTok, YouTube), podcast analytics platforms (Megaphone), Excel, PowerPoint and other data visualization tools. </li>
<li>Passion for media, journalism and the evolving digital landscape, with a keen awareness of audience engagement trends. </li>
<li>Strong interest in and awareness of public policy, politics and government, with the ability to contextualize media trends within the broader political and public affairs landscape. </li>
<li>Excellent verbal and written communication skills with the ability to convey data-driven insights to non-technical audiences. </li>
<li>Self-starter with strong problem-solving skills and the ability to work independently while managing multiple projects. </li>
<li>Ability to work effectively with executives and various teams, including content creators, marketing, partnerships and fundraising. </li>
<li>Comfortable working in a fast-paced environment with changing priorities and deadlines. </li>
</ul>

Research Manager

<h3>Job Description</h3>
Job Description
A-Line Staffing is now hiring a Quality Management Associate Scientist (QMAS). The Quality Management Associate Scientist (QMAS) would be working for a major company and has career growth otential.
If you are interested in this Quality Management Associate Scientist (QMAS) position, please apply today for immediate consideration!
Quality Management Associate Scientist (QMAS) Compensation
<ul>
<li>Pay rate: 27.10 per hour</li>
<li>Full shift description: 7am to 3:30 pm (OT might be needed)</li>
</ul>
Quality Management Associate Scientist (QMAS) Responsibilities:
<ul>
<li>Performs microbiological tests on a variety of plated/liquid culture media products and interprets data to ensure product quality.</li>
<li>Visually inspects physical samples and paper records and employs standard microbiology laboratory technique, including but not limited to pipetting, streak/spread plate inoculations, methods, pour plate methods, serial dilutions, stab inoculation technique, among others.</li>
<li>Maintains aseptic technique, is detailed-oriented, and organized, possesses good time management skills, and can succeed working in a team setting as well as independently.</li>
<li>Operates stationary instruments of low to moderate complexity, such as pH meters, analytical balances, and spectrophotometer, among others.</li>
<li>Performs non-routine tasks, such as supporting product inspection for ongoing investigations and projects.</li>
<li>Works with computer systems and software.</li>
<li>Seats, walks, and stands for extended periods of time and up to 4 continuous hours, lifts and carries items weighing up to 15 pounds independently, and keeps constant handwritten records.</li>
<li>Uses personal protective equipment, such as lab coats, respirator masks, gloves, non-permeable full cover shoes, and safety glasses, for extended periods of time.</li>
</ul>
Quality Management Associate Scientist (QMAS) QUALIFICATIONS:
Critical Information
<ul>
<li>May perform testing of Mycobacterium tuberculosis TB and other similar organisms requiring Biosafety Level 3 Laboratory containment with strict adherence to safety policies associated with this manner of testing.</li>
</ul>
Education/Licenses Needed
<ul>
<li>Education - Science microbiology; Bachelor's preferred, Associates with relevant experience is acceptable.</li>
</ul>
If you think this Quality Management Associate Scientist (QMAS) position is a good fit for you, please reach out to me - feel free to call, e-mail, or apply to this posting!
Heather Horkenbach Staffing Manager (586) 588-9799 Local (877) 782-3334 Toll Free (877) 782-3444 Fax

Quality Management Associate Scientist (QMAS)

<h3>Job Description</h3>
Health Advocates Network - Allied is seeking a travel Physicist for a travel job in Wilmington, North Carolina.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 09/25/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
HANStaff Allied Job ID #463238. 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: Physicist - None
About Health Advocates Network - Allied
Health Advocates Network was founded on the basis of a shared aspiration, to improve the way healthcare staffing is done. We are a company established and led by nurses. Our flexible approach enables us to develop solutions customized to your specific needs. From short- and long-term travel contracts to local and per diem assignments and more, we are here to get you to your next adventure! By solving challenges, providing the best placements, and advocating for you, we stand to help you thrive and pave the path forward in your career.

Travel Physicist

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

Quality Control Scientist - Chemistry Supervisor/Manager

<h3>Job Description</h3>
The Immunology R&amp;D organization is looking to fulfill a short-term need with mesoscale discovery (MSD) analysis through December, 2025 with a highly motivated Associate Scientist to join our Immunology Department. Our team is dedicated to discovering new targets for treating autoimmune and chronic inflammatory diseases through computational analysis of human disease tissue-derived datasets and validating these targets using in vitro and in vivo experimental methods to positively impact patient lives. In addition to supporting MSD needs within the Department of Immunology, the candidate will assist with various assays within dermatology, including RNA isolation and PCR. The ideal candidate will have MSD experience, but experience with ELISA is acceptable.
We are seeking an enthusiastic, skilled, and dedicated individual to join a team that validates targets. This position requires passion, attention to detail, prior hands-on experience and teamwork.
 
Key Responsibilities:
<ul>
<li>Demonstrated ability to perform protein/cytokine measurements using MSD and ELISA</li>
<li>Demonstrated ability to perform RNA isolation and run quantitative PCR</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in molecular biology, immunology or other biological sciences with 1-4 (BS/BA) years of experience</li>
</ul>
 
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit <a href="http://www.ustechsolutions.com" target="_blank">www.ustechsolutions.com</a>.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Recruiter- Jyoti Bhargav
Email ID <a href="mailto:jyoti.bhargav@ustechsolutionsinc.com" target="_blank">jyoti.bhargav@ustechsolutionsinc.com</a>
Job ID # 25-45773

Associate Scientist

<h3>Job Description</h3>
Overview
 
We are seeking a Biologist to support the National Institutes of Health’s (NIH), world renowned National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, MD. Our NIAID professional, technical, and scientific support personnel are part of a preeminent team focused on positively impacting millions of lives around the world with groundbreaking research. Candidates will work at a prominent and vibrant NIAID worksite to directly support exciting ongoing research activities as a contractor team member. Accelerate your career and apply below to help us make a difference.
 
CAMRIS International is a dynamic clinical research and international development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today’s most effective, evidence-based best practices. Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs. 
 
Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.
 
Responsibilities
<ul>
<li>Support the Analytical Development department of the Vaccine Production Program (VPP) in the Vaccine Research Center.</li>
<li>Independently perform UPLC-based content and identification assays for virus vaccines, recombinant proteins and virus-like particles that may be used as clinical vaccine candidates.</li>
<li>Contribute to the clinical development of a variety of vaccine candidates by independently performing multiple bioassays as required for project success.</li>
<li>Provide assay support and assay development for cGMP product release and characterization.</li>
<li>Participate in the development the following assays for protein characterization.</li>
<li>Protein A-UPLC.</li>
<li>SE-UPLC.</li>
<li>Bioassay development for a virus-like-particle vaccine.</li>
<li>Develop, characterize and transfer assays to the VRC pilot plant’s QC group for product release.</li>
<li>Write technical protocols and reports documenting analytical development studies pertaining to his work and the work of the group. </li>
<li>Performs other duties as assigned.</li>
</ul>
 
 
Qualifications
<ul>
<li>Bachelor’s degree in Chemistry or a related discipline is required.</li>
<li>Minimum of three (3) years of experience in chemistry or a related field is required.</li>
<li>Demonstrated experience working in a clinical or research laboratory.</li>
<li>Demonstrated knowledge of principles and operating procedures of general laboratory equipment.</li>
<li>Experience with analytical equipment automation or instrument and method qualification will be highly beneficial.</li>
<li>Confident oral and written communication skills.</li>
<li>Proficiency in writing and reviewing method qualification/validation protocols and reports, method transfers, SOPs, QC data packets and other process documents.</li>
<li>Familiarity with computer software including word processing and data evaluation.</li>
<li>Knowledge and use of statistical design of experiments (DOE).</li>
<li>Demonstrated ability to work on multiple projects.</li>
<li>Strong communications skills, both oral and written.</li>
<li>Excellent analytical, organizational and time management skills.</li>
</ul>
 
Physical Requirements:
The physical requirements described here are representative of those that must be met by a candidate to perform the essential functions of this job. Reasonable accommodations may be provided to enable individuals with disabilities to perform essential job functions.
<ul>
<li>Ability to lift or carry less than 25 pounds, push or pull less than 25 pounds, reach above shoulder level, and use both hands.</li>
<li>Required to stand or walk more than 25 of 30 min., bend repeatedly, climb, and perform repetitive activities.</li>
<li>Required to have depth perception, correctable near vision and distinguish basic colors.</li>
<li>Ability to work alone and closely with others, work on ladders or scaffolding, work with hands in water, and work with solvents.</li>
<li>Required to be in contact with lasers (open or closed) in instrument.</li>
<li>Will work with corrosive substances, inorganic dust and powders, heavy metals, plastics, solvents and sensitizing agents.</li>
<li>Must be able to wear personal protective equipment (PPE), including gloves, face shields/goggles, safety glasses, safety shoes, lab coat, and disposable dust/surgical mask.</li>
</ul>
 
 
Please submit your resume online at <a href="http://www.CAMRIS.com" target="_blank">www.CAMRIS.com</a>. CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.
 
CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&amp;D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability.
 
Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.

Biologist

<h3>Job Description</h3>
Job Description
Project Manager - Geotechnical Full Time | Wall | Newark, NJ, US
________________________________________
Who We Are
At FPA, we are looking for talented and driven professionals to join our commitment to pushing the boundaries of what is possible and providing cutting-edge solutions that make a difference in people's lives. We value individuals who are passionate about their work, who are committed to delivering quality results, and who are eager to learn and grow with us. 
We value candidates of all backgrounds, experiences, skill sets, and walks of life. At FPA, we actively foster a work environment that promotes inclusion and diversity, which is embedded in the foundation of our practice through policies, training, local partnerships with professional and diverse organizations, internal networks, and leadership support. We offer a dynamic and collaborative work environment where employees are encouraged to share ideas, take on new challenges, and contribute to the success of the company. 
As an FPA employee, you will have the opportunity to achieve anything you set your mind to, and to help shape the future. If you are a motivated individual who is looking for an exciting and rewarding career opportunity, we encourage you to apply to be a part of a dynamic and inclusive community of professionals. 
 
This Opportunity
FPA is currently searching for a full-time Geotechnical Project Managerfor our Newark, New Jersey office or Wall, NJ office. This position offers an excellent opportunity for a professional with a strong geotechnical background to manage complex projects, mentor junior staff, and work on a variety of challenging infrastructure projects across diverse sectors including transportation, commercial, residential, and industrial developments. The ideal candidate will be a licensed Professional Engineer (PE) with a master’s degree in Geotechnical Engineering or a related field and at least 8 years of relevant experience.
At FPA, our unwavering commitment to dedicated service and innovative solutions has empowered us to build thriving communities and expand our horizons. The ideal candidate will work alongside other talented engineers from various disciplines, collaborating to design, develop, and deliver projects that make a real difference in people's lives. They will bring a fresh perspective, a passion for engineering, and a commitment to excellence. Joining our team will provide you with an excellent opportunity to unlock your full potential, gain invaluable experience, and create a meaningful impact on the world.
 Core Responsibilities
<ul>
<li>Lead and manage geotechnical engineering projects from inception through completion, ensuring they are delivered on time, within budget, and meet client expectations.</li>
<li>Establish and maintain strong relationships with clients, stakeholders, and regulatory agencies, providing technical advice and strategic direction as needed.</li>
<li>Oversee the design and analysis of geotechnical aspects of projects including foundation design, slope stability, soil mechanics, earth retaining structures, and groundwater management.</li>
<li>Supervise and mentor junior engineers, geologists, and technicians, ensuring their professional development and adherence to company standards.</li>
<li>Prepare and review geotechnical investigation reports, feasibility studies, and technical specifications for clients and contractors.</li>
<li>Ensure high standards of quality control, review project deliverables, and provide constructive feedback to team members.</li>
<li>Develop project budgets, track project costs, and monitor schedules, proactively addressing any issues that could impact project delivery.</li>
<li>Assist in identifying new business opportunities, preparing proposals, and supporting marketing initiatives to grow the geotechnical division.</li>
<li>Ensure all projects comply with local, state, and federal regulations and maintain the highest standards of safety and environmental responsibility.</li>
</ul>
Required Qualifications 
<ul>
<li>Bachelor’s degree in Civil Engineering, Geotechnical Engineering, or a related field required.</li>
<li>Master's degree in Geotechnical Engineering or related discipline preferred.</li>
<li>Professional Engineer (PE) license in New Jersey required (or the ability to obtain licensure within a reasonable time frame).</li>
<li>Additional certifications such as Geo-technical Engineer-in-Training (EIT) or related are a plus.</li>
<li>At least 8 years of progressive experience in geotechnical engineering, with a focus on project management and leadership.</li>
<li>Experience with geotechnical site investigations, foundation design, soil-structure interaction, and remedial solutions.</li>
<li>Prior experience managing multiple projects simultaneously and interacting with clients.</li>
<li>Strong technical expertise in geotechnical engineering, including software tools for analysis </li>
<li>Proficient in project management software</li>
<li>Excellent verbal and written communication skills.</li>
<li>Strong problem-solving and critical-thinking abilities.</li>
<li>Ability to work both independently and collaboratively within a multi-disciplinary team</li>
<li>Willingness to travel to project sites as needed (including occasional overnight stays).</li>
<li>Strong organizational skills and the ability to handle multiple priorities simultaneously.</li>
</ul>
Benefits
As a valued member of our team, we provide you with a flexible benefits package that reflects our respect for your workplace contributions, professional goals, and personal priorities. FPA offers an extensive range of benefits, including medical, dental, vision, disability, life, and retirement savings, aimed at ensuring the physical well-being and financial security of employees throughout their careers. The personal benefits program at FPA includes the following:
<ul>
<li>Medical, Dental, Vision insurance</li>
<li>401(k) Retirement Plan with Employer Matching &amp; Roth 401(k) Option</li>
<li>Individual and Dependent Life Insurance</li>
<li>Short and Long-Term Disability Insurance and Supplemental Insurance Plans</li>
<li>Employee Assistance Program (EAP) and Wellness Benefits</li>
<li>Tuition Reimbursement</li>
<li>Training and Professional Development</li>
<li>Corporate sponsored events, outings &amp; activities, including community outreach opportunities.</li>
<li>Competitive Personal Time Off Program (PTO)</li>
<li>Transit/Parking Program</li>
<li>Summer Hours</li>
<li>Employee Discounts</li>
<li>Corporate Events, Outings &amp; Activities</li>
</ul>
Compensation
The projected compensation range for this position is $120,000 to $150,000. Actual compensation will depend on factors such as experience, education and skill set. 
________________________________________
About FPA
Since 1974, French &amp; Parrello Associates (FPA) has partnered with clients to address the ever-changing challenges of the world around us. Nationally and locally ranked among Engineering News - Record’s Top Firms, FPA has the staff and resources to provide innovative engineering services to clients in both the public and private sectors across a growing network of locations in New Jersey, New York, Pennsylvania, and Georgia. From modernizing the aging infrastructure, to designing state-of-the-art facilities and serving as stewards to our environment, FPA improves quality of life.
At our core, we are a dedicated group of professionals focused on servicing our clients and improving our world. Our team’s technical resources include site/civil, water, wastewater, water resources/dams, geotechnical, structural, bridge, highway, mechanical and electrical engineers, licensed land surveyors and landscape architects, as well as environmental professional and LSRPs, materials testing technicians, and construction oversight professionals and technicians. Our ability to service our clients is bolstered by a highly motivated team of marketing, business development, accounting, information technology, and administrative staff. Our professionals’ daily contributions play a crucial role in achieving client objectives, meeting goals, and improving our world.

Geotechnical Project Manager

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

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