field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute aiming to &nbsp;catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians.&nbsp;Why?&nbsp;Protein dysfunctions directly cause many diseases, such as Alzheimer’s disease. Yet, proteins remain understudied because of technological hurdles.&nbsp;How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org.&nbsp;PTI’s new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists, and mass spectrometrists. Alzheimer’s disease and aging will be among the first focuses of this technology-driven research organization.&nbsp;New career opportunitiesMembers of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals.&nbsp;&nbsp;Summary of PositionWe are looking for an experienced Mass Spectrometrist who will be working on maintaining MS instruments for running multitudes of samples for a variety of projects in addition to other responsibilities such as advancing and executing hypothesis-driven experiments.&nbsp;In order to be seriously considered for this position, we require a cover letter as part of the candidate’s application.Responsibilities
<ul>
<li>You will setup, operate, and maintain (i.e. vent and clean) mass spectrometers from multiple major vendors (Thermo, Bruker, Sciex, etc.).</li>
<li>Analyze experimental data and interpret results for internal and public presentation.</li>
<li>Training team members to use instruments independently.</li>
<li>Designing relevant proteomic experiments.</li>
<li>Perform protein sample preparation.</li>
<li>Preparation of lab reagents and media.</li>
<li>Inventory management and preparation reagents and samples.</li>
<li>Communication with purchasing and may be responsible for negotiating with various vendors.</li>
<li>May manage MTAs, software licenses, service contracts, and other documentation.</li>
</ul>
Required Qualifications
<ul>
<li>Masters or PhD in Biology, Biochemistry, or Chemistry.</li>
<li>5+ years of experience maintaining mass spectrometers.</li>
<li>Demonstrated experience optimizing LC-MS/MS methods for bottom-up proteomics (e.g. DDA/DIA/prioritized approaches).</li>
<li>Demonstrated mastery of chemistry techniques or molecular &amp; cellular biology techniques.&nbsp;&nbsp;</li>
<li>Demonstrated enthusiasm &amp; interest in bioanalytical chemistry.</li>
<li>High level of initiative and flexibility, excellent communication and teamwork skills.</li>
<li>Attention to detail and good time management skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience with mass spectrometry technological development (hardware or software).</li>
<li>Proficiency with statistical and computational methods (e.g. coding in Python/R).</li>
</ul>
We Offer
<ul>
<li>An opportunity to change the world and work with some of the smartest and the most talented experts from different fields.</li>
<li>Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from.</li>
<li>Company-paid group life, AD&amp;D, long- and short-term disability insurance.</li>
<li>15 days PTO + 10 sick days per year.</li>
<li>18 company holidays + your birthday off.</li>
<li>$5,000 per year educational reimbursement.</li>
<li>Up to 16 weeks paid parental leave.</li>
<li>Industry competitive salary.</li>
</ul>
We aim to help fill a structural gap in today's R&amp;D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&amp;D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations.&nbsp;We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Mass Spectrometrist

<h3>Job Description</h3>
Job Description
GEOTECHNICAL SUPERINTENDENT - SAFETY SPECIALIST - GROUND IMPROVEMENT
Minimum of 5 years of geotechnical experience preferred and experience operating specialty equipment a plus. 
Job Duties and Responsibilities 
<ul>
<li>Assuring that all project and Company safety requirements are met. </li>
<li>Conducting weekly safety meetings and daily JSA meetings. </li>
<li>Conducting site safety orientation for employees working on a project site. </li>
<li>Monitoring and completing equipment inspections reports and taking corrective action as needed. </li>
<li>Reporting all incidents, near misses and good catches on job sites in an accurate and timely manner. </li>
<li>Coordinating all safety concerns with site safety representatives of our clients, general contractors &amp; subcontractors. </li>
<li>Acting as a strong Safety leader at all times. </li>
<li>Conducting and participating in safety audits. </li>
<li>Attending all scheduling and coordination project meetings. </li>
<li>Coordinating all equipment and material deliveries to the job site. </li>
<li>Supervising and managing all daily work assignments of job site crews. </li>
<li>Working effectively with Field Engineers, Project Managers, and Construction Managers. </li>
<li>Coordinating travel of field personnel, lodging and approving crew expense reports. </li>
<li>Quality control with respect to installation reports and specific design requirements. </li>
</ul>
Knowledge, Skills and Abilities 
<ul>
<li>Excellent verbal and written communication skills. </li>
<li>Ability to work well under pressure. </li>
<li>Ability to oversee and coordinate a variety of people in different roles. </li>
<li>Extremely detail oriented. </li>
<li>Ability to read, understand and execute blueprints, drawings, and plans. </li>
<li>Thorough understanding of legal requirements relating to construction and building sites. </li>
<li>Ability to quickly identify problems and efficiently solve them.</li>
</ul>
#libertyjobs
#midsenior

Geotechnical Superintendent

<h3>Job Description</h3>
Job Description
Description Introduction
Paragonix Technologies markets organ transportation devices that safeguard organs during the journey between donor and recipient patients. Our devices incorporate clinically proven and medically trusted hypothermic preservation techniques in a novel suspension system to provide unprecedented physical and thermal protection. Our product portfolio spans cardiac, thoracic, and abdominal preservation devices to improve donor organ quality and extend donor organ transport time. Paragonix also markets transplant procurement services to the transplant community.
As Clinical Research Statistician you will be responsible for the design, validation, analysis and interpretation of clinical data from multiple registries in support of product development and business objectives. The position is based out of our Waltham office in the greater Boston area. There is an option to work in a hybrid environment, at least 3 days in-office is expected.
Position Responsibilities
<ul>
<li>Use advanced statistical methods to validate and analyze data</li>
<li>Write efficient code for processing data utilizing R statistical software.</li>
<li>Create processes for validating quality and accuracy of data.</li>
<li>Perform statistical programming and data analysis, as well as database cleaning, verification and validation, and quality review of statistical analyses</li>
<li>Manage resources, timelines and priorities for assigned projects</li>
<li>Work with clinical affairs staff and clinical investigators to determine appropriate study and protocol design</li>
<li>Provide statistical expertise to clinical affairs staff to ensure that the CRFs and database meet the study design needs</li>
<li>Responsible for statistical analysis plans (SAP) and development of tables/listings/figures for statistical reports</li>
<li>Prepare statistical methods and results sections for presentations, reports, and peer-reviewed manuscripts</li>
<li>Participate in preparing and writing statistical content for 501k and other FDA required reports</li>
<li>May be involved in analyses of 'big data' for market assessments, as well as from public sources (such as UNOS)</li>
<li>Organized, self-starter; ability to work in a fast-paced environment with a "roll up your sleeves" attitude</li>
<li>Ability to work independently and as part of a team</li>
<li>Excellent oral and written communication, and interpersonal skills necessary to interact with a wide range of individuals and cross-functional stakeholders.</li>
</ul>
Experience
<ul>
<li>At least 2-4 years of statistical work experience in a biomedical life science or medical device company, including programming using SAS or R statistical software.</li>
<li>Comprehensive knowledge of statistical methods</li>
<li>Prior healthcare or medical device industry experience</li>
<li>Proficiency in R programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming languages such as SAS, Python etc. is a plus.</li>
<li>Prior experience working with research and/or healthcare data.</li>
</ul>
Education
<ul>
<li>Bachelor's degree in biostatistics, statistics, epidemiology or similar area of study, required.</li>
<li>Master's degree or higher in biostatistics or relevant area of study preferred.</li>
<li>Proficient in Microsoft Office Suite.</li>
<li>Transplant surgery /medical knowledge is a plus.</li>
<li>Experience or knowledge of FDA regulations or submissions is a plus.</li>
</ul>
Salary range is $73,000 to $85,000 depending on experience.
Description Conclusion

Clinical Research Statistician

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Location: Marlborough, MA 01581 Duration: 6 Months+ (possibilities of Extension) Pay Range: $43 - $48/hr. on w2 Summary: We are seeking a highly motivated Research Associate to support the development of cell therapy products, with a primary focus on formulation development. The successful candidate will contribute to development work on drug product, such as formulation design, manufacturing process development, product characterization, and evaluation of administration method. This role involved hands-on laboratory work including cell culture, preparation of drug product, other wet lab experiments, data analysis, and documentation such as drafting protocols and reports. The Research Associate will work under the guidance of a Scientist II. Key Responsibilities:
<ul>
<li>Support formulation development for cell therapy products, including process optimization and product evaluation.</li>
<li>Conduct cell-based experiments in a laboratory setting under supervision.</li>
<li>Perform basic cell culture and aseptic techniques within a biosafety cabinet (BSC).</li>
<li>Assist with formulation, analytical, and manufacturing tasks involving non-cellular components as needed.</li>
<li>Contribute to the development and evaluation of administration procedures simutated at clinical settings.</li>
<li>Maintain accurate compliant experimental records in accordance with Good Documentation Practice.</li>
<li>Draft study protocols and reports with guidance.</li>
</ul>
 Qualifications: Required:
<ul>
<li>BS degree with 5+ years of laboratory experience or MS with 2 years.</li>
<li>Hands-on experience with aseptic tissue culture techniques in a BSC.</li>
<li>Solid understanding of cell biology and cell-based assays.</li>
<li>Strong attention to detail and organizational skills.</li>
<li>Ability to work independently and collaborative within a team.</li>
<li>Self-motivated and proactive in learning new skills.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to analyze experimental data and summarize findings clearly.</li>
<li>Flexibility to work variable hours as needed.</li>
<li>Knowledge and experience of CMC (Chemistry Manufacturing and Control) development.</li>
</ul>
 Preferred:
<ul>
<li>Prior experience working in a GMP-regulated environment is highly desirable.</li>
<li>Knowledge and hands-on experience in drug product development.</li>
<li>Familiarity with GMP standards, ICH guidelines, and global compendial regulations including USP, JP and EP.</li>
<li>Prior experience with flow cytometry and plate-based assays.</li>
<li>Familiarity with data analysis and visualization tools such as GraphPad Prism and JMP.</li>
<li>Flexibility to work on weekends as needed.</li>
</ul>
 #sczr2

Research Associate

<h3>Job Description</h3>
Job Description
We’re seeking a Senior Dam Safety Engineer with deep expertise in geotechnical engineering and dam safety evaluations. This leadership role is ideal for someone with FERC Part 12 Independent Consultant approval—or the experience to qualify—and a passion for risk-based analysis and infrastructure resilience.
You’ll play a pivotal role in guiding project teams, mentoring junior staff, and shaping the future of our dam safety services. This is your opportunity to work on meaningful, high-impact projects in clean energy and environmental restoration. Ready to make a difference? Let’s build something lasting—together!
**Remote work options available for highly qualified candidates
 
 
Key Responsibilities
<ul>
<li>Lead and coordinate design teams for FERC and state-regulated dam safety projects</li>
<li>Conduct dam safety evaluations, including FERC Part 12 inspections</li>
<li>Design earthen embankments and perform geotechnical assessments for dams and civil works</li>
<li>Develop and analyze geotechnical monitoring and testing programs</li>
<li>Review construction sequencing, design plans/specs, and permitting documents</li>
<li>Represent the firm in technical discussions with regulators, clients, and public forums</li>
<li>Author and review technical reports and project documentation</li>
<li>Mentor engineers in technical execution and career development</li>
<li>Support proposal writing, cost estimating, and project scheduling</li>
</ul>
Qualifications
<ul>
<li>B.S. in Civil or Geotechnical Engineering (M.S. preferred)</li>
<li>Licensed Professional Engineer (PE) with willingness to maintain multi-state registrations</li>
<li>FERC Part 12 Independent Consultant approval or eligibility</li>
<li>Comprehensive Assessments expert</li>
<li>Strong communication skills and attention to detail</li>
<li>Experience with risk-based analysis preferred</li>
<li>15+ years of experience in:
<ul>
<li>Dam safety evaluations and geotechnical design</li>
<li>Project management and client engagement</li>
<li>Earthquake response analysis for embankments</li>
<li>Proposal development and team mentoring</li>
<li>Familiarity with federal/state dam safety standards</li>
</ul>
</li>
<li>Some travel required to project sites</li>
</ul>
Benefits
We offer a competitive and comprehensive benefits package, including:
<ul>
<li>Medical, dental, and vision insurance</li>
<li>Generous vacation, comp time, and flexible holidays</li>
<li>Paid sick leave and extended medical leave account</li>
<li>Educational assistance and professional development support</li>
<li>Parental leave and Dependent Care FSA</li>
<li>Short and long-term disability coverage, Life Insurance</li>
<li>401K and profit-sharing program</li>
<li>Relocation provided and supported</li>
</ul>

Senior Geotechnical Dam Safety Engineer - PE

<h3>Job Description</h3>
Job Description
Notes Short term labeling project utilizing a proprietary interface. Will require contingents to sign the attached additional NDA on their first day of assignment. &nbsp; Job description: Faculty member with course and curriculum development efforts, scholarly research and data collection efforts. Contribute to the faculty member's research in ways that typically include writing and editing, data and information gathering, designing qualitative and quantitative research. Gain understanding of the research subject matter. Plan and conduct interviews, surveys, and literature reviews. Synthesize findings, analyze and interpret results. Assisting with the creation of presentations, summaries and articles on research topics.
Company DescriptionDella Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations. 
<h3>Company Description</h3>
Della Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations.

Research Assistant - Short Term Assignment

<h3>Job Description</h3>
Job Description
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities.
Job Responsibilities:
● Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus.
● Communicate and coordinate with other scientists on a project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks.
● Collect and record data. Prepare summaries of experimental procedures and results and present data in team meetings.
● Develop, perform, interpret, and troubleshoot a broad range of in vitro assays including immune cell profiling, cytokine profiling, functional assays using primary cells, as well as cytotoxicity/apoptosis assays using primary and/or cultured cells. 
● Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company.
Requirements
● Bachelor’s or Master’s degree with 1-3 years of academic or industry research experience. Demonstrated experience in small animal handling and pharmacology is highly preferred. 
● Experience with small animal handling, drug administration, and blood and tissue collection is preferred.
● Experience in cell biology, biochemistry, and/or molecular biology, in particular assay development and execution, is required. This includes cell-based assays, tissue culture, biochemical assay technologies, and protein and RNA expression analysis. 
● Experience with cell culture and in vitro assays is desirable.
● Experience in primary immune cell-based assays is strongly preferred. 
● Experience in flow cytometry (FACS) analysis is preferred.
● Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment.
● Collaborative team player. Be flexible and prioritize tasks based on team and company goals. 
● Communicate effectively at all levels, within teams, with internal and external collaborators. 
● Strong organizational skills. Maintain research data and records with the highest integrity. 
● Ability to multitask in a fast-paced environment.
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>
BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Pharmacology Research Associate

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>
Responsible for generation of stable CHO cell lines, cell banks, and expression assessments as well as the possible scale up of CHO pools in disposable 5-50L bioreactors.
</li>
<li>
Provide logistical support to the lab such as ordering supplies, managing instruments, and other general lab bench activities.
</li>
<li>
Maintain, thaw, and prepare host cell line cultures for all group activities.
</li>
<li>
Independently planning and executing stable cell line generation for both plate-based and at-scale transfections.
</li>
<li>
Receive, track, and disseminate DNA plasmid library serving as liaison between plasmid generation and cell line generation groups.
</li>
<li>
Present formal data packages to portfolio project teams and collaboration teams
</li>
</ul>
PREQUIREMENTS:
<ul>
<li>
BS with 1-2 years of experience in Biology, Chemistry, or related discipline
</li>
<li>
Ability to lift 50 lbs
</li>
<li>
Occasionally lifting such as consumable boxes and 20L (~50lbs)media bags and would need to be able to be independent.
</li>
<li>
Nice to have: gel electrophoresis, Flow Cytometry
</li>
<li>
Must have: Sterile Technique, Mammalian Cell Culture skills
</li>
<li>
Communication skills - Written and Verbal
</li>
<li>
Organizational skills
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Associate Scientist - Cell Line Development

<h3>Job Description</h3>
Job Description
Are you passionate about creating innovative nutritional beverages and powders that make a real impact on health and wellness? We are seeking a Senior Food Scientist to lead the development and optimization of cutting-edge nutritional products from concept to commercialization. This role is perfect for a creative, detail-oriented scientist who thrives on innovation, quality, and clinical impact.
Key Responsibilities:
<ul>
<li>Develop, optimize, and scale nutritional beverage and powder formulations to meet sensory, nutritional, and stability goals.</li>
<li>Collaborate with Medical Nutrition, Marketing, and Sales teams to align product development with business objectives and patient needs.</li>
<li>Research and evaluate new ingredients and explore novel opportunities in medical nutrition.</li>
<li>Provide scientific and technical expertise to support leadership in product and clinical development initiatives.</li>
<li>Build and maintain strong vendor relationships to source high-quality ingredients that meet product specifications.</li>
<li>Represent the company at scientific meetings, conferences, and industry events.</li>
<li>Ensure protection of intellectual property for new products, formulations, and processes.</li>
<li>Comply with all GMP, food safety, and workplace safety standards.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree in Food Science, Nutrition, or a related field (Master's preferred; PhD or PharmD a plus).</li>
<li>5+ years of product development experience from concept to commercialization in nutrition, food, beverage, supplement, nutraceutical, or biotech industries.</li>
<li>Experience in both basic and applied R&amp;D, preferably in small to mid-sized nutrition, food, beverage, or biotech companies.</li>
<li>Strong expertise in food science, ingredient interactions, and process impact on nutrient stability.</li>
<li>Knowledge of food safety regulations, aseptic processing, and quality standards.</li>
<li>Excellent problem-solving, communication, and project management skills.</li>
</ul>
Why Join Us:
<ul>
<li>Competitive salary with a 12.5% performance-based bonus program</li>
<li>Comprehensive health, dental, and vision insurance</li>
<li>Paid time off and company holidays</li>
<li>401(k) plan with company match</li>
<li>Opportunities for professional growth and career advancement</li>
<li>Employee discounts on company products</li>
</ul>

Senior Food Scientist - Product Development

<h3>Job Description</h3>
Job DescriptionOutstanding Benefits &amp; Hybrid Schedule | Collaborative &amp; Tenured Practice | Growth Track! This Jobot Job is hosted by: Christina Chariott Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $125,000 - $175,000 per year 
A bit about us:
 This full-service regional law firm has deep roots in New England and a longstanding reputation for client-focused legal work. The team values collaboration, integrity, and long-term relationships. Attorneys practice alongside like-minded professionals who care deeply about each other and their clients. The firm offers a supportive platform with full-time resources in IT, HR, accounting, legal writing, and business development -designed to help attorneys grow their practice and thrive. Currently expanding its Concord, NH office, the firm welcomes high-quality attorneys who want to be part of a collegial environment that prioritizes teamwork, professional growth, and meaningful client service. Apply now to learn more! 
Why join us?
 
<ul>
<li>Generous healthcare coverage: 90% paid by firm</li>
<li>Great tenure - most employees have been there 20+ years</li>
<li>Competitive compensation + bonuses + incentive compensation</li>
<li>Lots of growth and training opportunities</li>
<li>Established client base</li>
</ul>
 
Job Details
 Key Responsibilities: Advise high-net-worth individuals, families, and business owners on estate planning strategies and wealth transfer. Draft and review complex estate planning documents, including wills, trusts, powers of attorney, and healthcare directives. Handle probate and trust administration matters with precision and sensitivity. Provide guidance on gift, estate, and generation-skipping transfer tax issues. Collaborate with other attorneys across practice areas to deliver comprehensive client solutions. Maintain and grow client relationships through thoughtful, responsive service. Contribute to firm leadership and mentoring of junior attorneys, if desired. Qualifications: Juris Doctor (JD) from an accredited law school. Minimum of 10 years of experience in trusts and estates law. Admission to the New Hampshire Bar (or ability to waive in). Portable book of business of at least $275,000. Strong drafting, analytical, and communication skills. High ethical standards and professional integrity. Desire to work in a collaborative, team-oriented environment. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policyCompany DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

760 Science Jobs