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<h3>Job Description</h3>
NEW Microbiology and/or Molecular Technologist opening at a full service clinical laboratory! This laboratory is fully accredited by CAP and CLIA. They are looking to hire a permanent and full time Medical Technologist/MLS on DAY Shift! This laboratory offers a culture where there are ample opportunities for challenge, growth and recognition!
For consideration, applicants must have either a Bachelor's Degree in Medical Technology/MLS and/or an AS Degree in Medical Laboratory Science/Medical Laboratory Technician AND ASCP Certification as a MT/MLS, MB, SM/M or&nbsp;MLT. This position is Monday through Friday Day or Evening Shift! New graduates and experienced candidates are both encouraged to apply!
This laboratory is offering a highly competitive hourly rate and a top notch benefits package! Benefits include medical, dental, vision, prescription drug, generous PTO, life insurance, FSA, 401K and more!
Interested? Apply below or contact Andrea at <a href="mailto:andrea@ka-recruiting.com" target="_blank">andrea@ka-recruiting.com</a> or 617-746-2745.
ACC 10311201

Microbiology and Molecular Technologist OR Technician on Day Or Evening Shift

<h3>Job Description</h3>
Job Description
Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA)&nbsp;
We are seeking a Research Scientist– Oncology Translational Research for a global pharmaceutical client. You will join the Translational Research team within the Oncology Thematic Research Center in Cambridge, MA. You will work broadly with the research organization to support drug discovery programs, by conducting experimental work in a translational setting, including developing and implementing cutting-edge technology and novel cellular, molecular, and biochemical assays in cancer research and deliver data for Oncology TRC programs.&nbsp;
This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Cambridge, MA&nbsp;
Work hours/schedule: M - F, typical work hours are 9:00am to 5:00pm&nbsp; Parking Fee: Candidates must be agreeable with the $20/day parking fee at Cambridge Crossings.&nbsp;
This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.&nbsp;
Responsibilities:&nbsp;&nbsp;
<ul>
<li>
Design, optimize, and set up high-throughput screening cellular assays to characterize drug responses and combinations in various in vitro oncology models.&nbsp;
</li>
</ul>
<ul>
<li>
Conduct molecular, biochemical and related assays including qPCR, ELISA, Western blot, immunostaining and basic microscopy.&nbsp;
</li>
</ul>
<ul>
<li>
Develop biomarker, pharmacodynamic and target engagement assays.&nbsp;
</li>
</ul>
<ul>
<li>
Execute, troubleshoot and interpret scientific experiments with some supervision.&nbsp;
</li>
</ul>
<ul>
<li>
Effectively communicate and document experimental procedures, analyze results and data through study reports and internal meetings.&nbsp; &nbsp;
</li>
</ul>
Requirements:&nbsp;&nbsp;
<ul>
<li>
3+ years of experience in conducting cancer cell line and primary cell culture, expansion and functional assays.&nbsp;
</li>
</ul>
<ul>
<li>
Experienced in the design and development of cell-based and molecular assays in a high-throughput manner.&nbsp;
</li>
</ul>
<ul>
<li>
Drug combination screen&nbsp;
</li>
</ul>
<ul>
<li>
Experience performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to western blot, flow cytometry, qPCR, MSD/ELISA, RNAi, CRISPR.&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in utilizing software such as Graph Pad, Microsoft Office, etc. for data analysis and figure generation is required.&nbsp;
</li>
</ul>
<ul>
<li>
BS or MS Degree.&nbsp;
</li>
</ul>
Please submit your resume to our network at <a href="https://www.stage4solutions.com/careers/" target="_blank">https://www.stage4solutions.com/careers/</a> (please apply to the Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA) role).&nbsp;
Please feel free to forward this project opening to others who may be interested.&nbsp;
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates’ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.&nbsp;
Compensation: $45hr. - $50.91/hr.&nbsp;
#LI-SW1&nbsp;&nbsp;&nbsp;

Research Scientist- Oncology Translational Research (Onsite - Cambridge, MA)

<h3>Job Description</h3>
Job Description
Job Title: Biologist Location: Boston, MA 02210 Work Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Job Overview:
We are seeking a highly motivated Biologist to join our Downstream Process Development team. The candidate will contribute to the purification and characterization of viral vectors, biologics, or recombinant proteins, supporting process development and manufacturing activities.
Key Responsibilities:
<ul>
<li>
Execute purification processes including affinity chromatography (e.g., AVB, CaptureSelect) and ion-exchange chromatography (AEX, CEX).
</li>
<li>
Operate AKTA systems (Avant, Pure, or Pilot) for small- to large-scale purification runs.
</li>
<li>
Perform tangential flow filtration (TFF) for buffer exchange and product concentration.
</li>
<li>
Support experimental design, data collection, and documentation following GMP/GLP guidelines.
</li>
<li>
Troubleshoot and optimize purification processes.
</li>
<li>
Analyze samples using relevant methods (UV, SDS-PAGE, ddPCR, ELISA, HPLC).
</li>
<li>
Collaborate cross-functionally with upstream, analytical, and manufacturing teams.
</li>
<li>
Maintain lab equipment, buffers, column inventory, and compliance with safety standards.
</li>
</ul>
Qualifications:
Education:
<ul>
<li>
Master’s degree in Biochemistry, Chemical Engineering, Biotechnology, or related field.
</li>
</ul>
Experience:
<ul>
<li>
Minimum 2 years of hands-on purification experience in academic or industry settings.
</li>
</ul>
Technical Skills:
<ul>
<li>
Strong experience with ion-exchange and affinity chromatography.
</li>
<li>
Familiarity with buffer preparation.
</li>
<li>
Knowledge of basic analytical methods for product characterization.
</li>
</ul>
Soft Skills:
<ul>
<li>
Strong attention to detail and excellent documentation habits.
</li>
<li>
Effective communication and teamwork skills.
</li>
<li>
Ability to manage multiple tasks and meet project timelines.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience in AAV or other viral vector purification.
</li>
<li>
Experience with AKTA systems and Unicorn software.
</li>
</ul>

Purification Scientist - Biologics / Viral Vectors

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<h3>Job Description</h3>
Job DescriptionSalary: $50K - $55K 
Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. GMGI is looking for a Research Associate to join our team studying the biology of exceptionally long-lived marine animals. Our goal is to translate evolutionary insights from these exceptional animals into interventions that promote human healthspan and combat age-related diseases, using zebrafish as a development platform. This position will conduct zebrafish genetics work and husbandry, testing these evolutionary targets to extend healthy functionality. This project will use modern genetic editing techniques and apply new assays to modulate and test the molecular mechanisms of aging.
The ideal candidate will have experience with aquatic husbandry, standard molecular biology techniques, excellent communication skills, attention to detail, and the ability to work with a multi-disciplinary team of collaborators. This is an extraordinary opportunity for a dynamic and motivated individual to learn a powerful genetic model and to advance aging research in an entrepreneurial and exciting work environment.
 
Responsibilities:
<ul>
<li>Standard molecular biology and genetics experimental research.</li>
<li>Contribute to the maintenance of the aquatic facility, including feeding, water quality, and health monitoring.</li>
<li>Contribute to the generation and maintenance of transgenic zebrafish lines, including microinjection, mutant screening, and genotyping.</li>
<li>Apply assays to quantify biological aging in zebrafish, including taking tissue samples, performing histology, and compound neuro-muscular functionality.</li>
<li>Maintain a comprehensive electronic lab notebook.</li>
<li>Contribute to grant proposals and publications, and present results at lab meetings and other venues.</li>
<li>Participate in institutional fund-raising activities and community outreach activities.</li>
</ul>
 
Qualifications:
<ul>
<li>BS or MS in genetics, molecular or cell biology, or related field, with lab experience.</li>
<li>Experience with standard molecular biology techniques such as DNA/RNA isolation, PCR/qPCR, molecular cloning, and CRISPR gene editing.</li>
<li>Experience with the husbandry of aquatic models.</li>
<li>Experience with zebrafish and histology is desirable.</li>
<li>Ability to work independently to design and execute experiments</li>
<li>Strong data analysis skills using standard bioinformatic and statistic software packages</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Excellent organization skills and the ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and teamwork skills.</li>
<li>Enthusiasm and commitment to GMGIs mission for science and education.</li>
</ul>
This position will report to the Research Scientist.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
Health and Dental Insurance
Medical and Dependent Flex Spending Accounts
Long Term Disability
Life Insurance
Paid Time Off
403(b) Retirement Plan
12 Paid Holidays
Applicants must be authorized to work in the US.
 
About GMGI 
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization and building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

Research Associate I - Marine Biomedical Discovery

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Principal Scientist, CMC Radiochemistry
Description:
We are seeking an experienced Scientist I/II, CMC Radiochemistry to join Mariana Oncology's CMC organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for radiochemistry development through validations of pipeline projects leading to and enabling production, development, and advancement of radiotherapeutics and nuclear imaging probes. You will join the development efforts in support of the next generation radiotherapeutics for Mariana Oncology's clinical trial programs.
Illustrative Breadth of Responsibilities:
<ul>
<li>Radiolabeling/ coordination chemistry process, analytical development and troubleshooting with a broad range of radioisotopes, including but not limited to: Lu-177, Ac-225, Zr-89, Cu-64, In-111, Ga-68 and Pb-212.</li>
<li>Early formulation development, process and analytical method optimization to ensure drug product stability.</li>
<li>Participate in the development and process validation of radiopharmaceutical productionprocedures for use in preclinical and clinical studies.</li>
<li>Support CMC drafting and executing Master Batch Records, protocols for validation of manufacturing processes of radiopharmaceuticals, validation of analytical methods.</li>
<li>Participate and support CMC analytical development, method validation, and reporting activities, including but not limited to Identity, Purity, Impurities and Assays.</li>
<li>Support CMC in preparation of method validation protocols, execution of method validations, and authoring/review of reports, SOPs, and other technical documents for technical correctness, quality, and regulatory compliance.</li>
<li>Perform analysis, tabulating and gathering data for CMC sections (Module 3), development reports for IND and IMPD, to regulatory agencies including FDA and EMEA.</li>
<li>Support team communications in disseminating results, which may come in the form of presentations or reports.</li>
<li>Contribute to the organization and maintenance of the laboratory.</li>
</ul>
Requirements/Skills:
<ul>
<li>A Ph.D. in Inorganic Chemistry, Organic Chemistry, Radiochemistry, or related discipline and 0+ years of Biotech or Pharmaceutical industry experience; BS or MS in Chemistry or related discipline and 4 6+ years of Biotech or Pharmaceutical industry experience.</li>
<li>Radiopharmaceutical drug substance and drug product development experience is a plus.</li>
<li>Development experience for the biologics and peptides GMP manufacturing is a plus.</li>
<li>A strong background and in-depth working knowledge of biologics and peptides andconjugates analysis, including but not limited to: Assay and Purity (RP-HPLC, IP-RP-HPLC,AEX/CEX-HPLC), with LC-MS and LC-ICP-MS experience being a plus.</li>
<li>Knowledgeable in regulatory requirements and guidelines (cGMP, ICH, FDA, and USP, EP) with the ability to apply to the Phase appropriate pharmaceutical development. GMP pharmaceuticals validation experience is a plus.</li>
<li>Experience with regulatory documentation is preferred. </li>
<li>Understanding of chemistry manufacturing and controls (CMC) documentation for novelcompounds consistent with requirements for IND, NDA, or other regulatory pathways.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Strict adherence to data integrity is required. </li>
<li>Proven ability to adhere to good documentation standards and maintain detailed records of all work performed.</li>
<li>Excellent verbal and written communication skills.</li>
</ul>
Mariana Oncologys Values
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Scientist I/II, CMC Radiochemistry

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY The Metrology Technician will assist Metrology personnel with product, maintenance and equipment calibration issues according to FDA, cGMP and BA Sciences' Standard Operating Procedures. 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Monitors and maintains the water systems.</li>
<li>Installation, maintenance and calibrates stability chambers, incubators, refrigerators and freezers.</li>
<li>On-call Monitoring of stability chambers and controlled rooms.</li>
<li>Calibration of equipment and instrumentation required for tests, including mechanical and chemical tests.</li>
<li>Assists chemists and other company personnel on an as needed basis.</li>
<li>Follows all safety rules and regulations.</li>
<li>Ensures all work performed strictly adheres to cGMP, Company, client and Pharmacopeial methodologies.</li>
<li>Assist in proper management of hazardous waste and compliance with DES hazardous waste rules.</li>
<li>Performs problem solving with minimal rework.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
A high school diploma or GED is required. 0-2 years of related experience. Knowledge of cGMPs and related compliance regulations and guidances is preferred. A Metrology Technician should be willing to attend technical training classes to enhance skills or correct identified deficiencies. Requires the ability to lift and/or move up to 50 lbs.
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>Self-starting motivated person who possesses good interpersonal skills and who is able to effectively interact with all departments with the Company.</li>
<li>Must have good organizational and verbal communication skills.</li>
<li>Basic computer skills required. Experience with cGMP is preferred.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Metrology Technician

<h3>Job Description</h3>
Job DescriptionDescription:
Nobis Group is an integrated consulting firm providing engineering and engineering solutions for public and private projects of all sizes. We are committed to solving the challenges of making the Earth a better place to live - community by community, and project by project.
 
Overview
Do you want to expand your career as a Senior Project Geologist? If so, Nobis wants you! 
 
Nobis is looking for a Senior Project Geologist in our Environmental Engineering group based in Concord, New Hampshire. The ideal candidate will have demonstrated experience and a desire to join our remarkable team of forward thinking committed partners. 
 
What You’ll Do
<ul>
<li>As an experienced member of a project team, collaborate with project team members (internal and external) and others to execute assignments efficiently and effectively. Provide technical support and direction to junior staff members. Collect environmental media samples both individually and as part of a field team; operate necessary field equipment and instruments; perform soil and bedrock characterization; , and perform other field tasks and oversight as needed. Support project manager with cost documentation for project and field work.</li>
<li>As a leader of a field team or project team, direct team members and others to effectively execute assignments, provide value to the project manager (effective management of subcontractors, preparing cost estimates, and leading the team to meet project objectives of schedule and budget), and show strong organizational and managerial skills. Actively provide mentoring of work tasks to less experienced team members.</li>
<li>Oversee and/or prepare, review, and modify, as necessary, technical reports, specifications, plans, engineering calculations, engineering design drawings, construction schedules, and cost estimates for a project. Work with team members to complete environmental and remediation investigation projects, including sampling, drilling, and decontamination tasks.</li>
<li>Oversee, review, evaluate, and/or provide interpretations of engineering design and environmental reports, maps, drawings, specifications, regulations, ordinances, permits, field test results, design manuals, aerial photographs, and other data necessary for environmental projects.</li>
<li>Oversee and/or communicate technical information with vendors, accurately document such communications, and apply the information obtained to the relevant project work.</li>
<li>Oversee and/or prepare a wide range of groundwater and contaminant fate and transport calculations, and cost estimates, hydrogeological assessments, construction cost estimates, and determine the feasibility of a project or project feature based on analysis of the calculation., cost estimates, and other collected data.</li>
<li>Oversee and use scientific software and computer hardware necessary to complete engineering analysis, hydrogeologic analysis, and engineering design projects. Software may include GIS, spreadsheet applications, hydrogeologic software, boring log software, and other applicable software. </li>
<li>Oversee means and methods of collecting necessary field data by working with field personnel. Oversee and/or collect and interpret field data through observation or field data collection techniques using field instruments such as survey equipment, tape measures, flow meters, turbidity samplers, sieve analysis, cameras, pumps, data loggers, remediation equipment, and other instruments as needed.</li>
<li>Oversee and/or perform evaluation of technical data, or direct others to perform evaluations to provide the basis for environmental cleanup; understand permit requirements and can work to obtain needed project permits; and verify and promote compliance with applicable federal, state, and local rules and regulations to project work.</li>
<li>Work with project team members to perform and complete a wide range of projects. Provide mentoring to entry-level and mid-level staff in the application of engineering and/or scientific theory, principles, and practices. </li>
</ul>
What It’s Like Working at Nobis
We are 100% Employee-Owned and that makes you an owner. As a Nobis Employee-Owner, you will become part of a team that thrives on diversity of thought, encourages out-of-the-box ideas, and strives to fulfill our mission to deliver unparalleled engineering and environmental solutions that drive employee-owner, client, and community success.
 
We offer highly competitive salaries, generous paid time off, and a flexible hybrid schedule that allows our employee-owners to maintain a comfortable balance between life and work. In addition to our extensive benefits package, you will have access to all the advantages that come with working for an ESOP.
 
Nobis is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, veteran status, sexual orientation, or gender identity.
Requirements:
What You’ll Need to Bring With You
<ul>
<li>Bachelor’s degree from an accredited four-year college or university in science or engineering (e.g., Environmental Engineering, Geology, Hydrogeology, Environmental Science, Earth Science, or related field) is required. An emphasis on hydrogeology, aqueous geochemistry, and/or bedrock structural geology coursework is preferred. A Master of Science (M.S.) degree is highly desirable.</li>
<li>A minimum of six years of related experience is required; minimum of 10 year’s professional experience in the investigation and/or remediation of environmentally impacted sites is preferred.</li>
<li>Must have OSHA 40-hour Hazardous Waste Operations and Emergency Response (HAZWOPER) certification and annual 8-hour refresher, as applicable.</li>
<li>Must possess a valid driver’s license, have own transportation, and be able to travel for project site visits, meetings, data collection, and training. Travel is highly dependent upon project work requirements and may be extensive at times.</li>
<li>P.G. license is strongly preferred.</li>
<li>Familiarity with and demonstrated expertise in applicable environmental rules and regulations is required.</li>
<li>Must have working knowledge of word processing and spreadsheet software applications, necessary engineering design software applications, internet searching techniques, electronic mail, and company intranet and servers. Software may include GIS, spreadsheet applications, hydrogeologic software, boring log software, and Microsoft office products.</li>
<li>Knowledge of chemical fate and transport concepts, experience in conducting environmental investigations, bedrock environmental investigations, and experience with interpreting hydrogeologic data in overburden and bedrock. This position also requires experience leading field teams, including overseeing contractors.</li>
<li>Preference will be given to candidates with expertise in one or more of the following areas: development and completion of large field programs, impacted mine sites, numerical groundwater modeling, geostatistics, natural attenuation evaluations, geochemistry, geophysical data evaluation, NHDES regulations, and the CERCLA process.</li>
<li>Experience with ArcGIS and RockWorks is preferred.</li>
</ul>

Senior Project Geologist

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite at a NEFSC Facility
POSITION DESCRIPTION:
Think Tank is a woman-owned small business with more than 27 years of proven success delivering exceptional IT and marine fisheries services to the federal government. We are currently seeking an ideal candidate for the position of Ecologist to support an upcoming proposal with the National Oceanic and Atmospheric Administration. Résumé of successful candidate(s) will be included with our proposal. 
The Ecologist supports the study of protected species by analyzing their ecological relationships, behavior, and habitat use. This role integrates field research, statistical modeling, and data synthesis to inform conservation and management decisions.
RESPONSIBILITIES:
<ul>
<li>Develop models to assess ecological relationships, habitat use, and anthropogenic impacts.</li>
<li>Analyze multi-source datasets including acoustic, visual, environmental, and telemetry data.</li>
<li>Participate in field surveys and biological sampling for marine species.</li>
<li>Support scientific writing, peer-reviewed publications, and outreach.</li>
<li>Contribute to database management and GIS/spatial analysis efforts.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Bachelor's or advanced degree in ecology, environmental science, or related discipline.</li>
<li>Experience with statistical modeling, data analysis, and fieldwork.</li>
<li>Proficiency in GIS, R, and/or Python; knowledge of AI/ML is beneficial.</li>
<li>Understanding of species conservation frameworks and environmental policies.</li>
<li>Excellent communication and teamwork skills; ability to work in remote settings.</li>
</ul>

821 Science Jobs