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<h3>Job Description</h3>
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These owners, who share the belief that the majority of property loss is preventable, represent many of the world’s largest organizations, including one of every four Fortune 500 companies. They work with FM to better understand the hazards that can impact their business continuity to make cost-effective risk management decisions, combining property loss prevention with insurance protection.
&nbsp;
 
Join a world-class research team dedicated to reducing the impact of natural hazards and climate risks. FM is a market leader in commercial and industrial property insurance and loss prevention, serving over one-third of FORTUNE 1000 companies with engineering-based risk management and property insurance solutions. FM helps clients maintain business continuity through state-of-the-art engineering and research.
&nbsp;
The Structures and Geohazards Research Group at FM is seeking a creative and self-motivated Senior Research Scientist with a strong foundation in wind engineering and a specialized focus on computational wind engineering (CWE). The ideal candidate will possess deep expertise in fluid dynamics, high-performance computing, and wind tunnel testing, along with a demonstrated ability to conduct innovative, high-impact research.
&nbsp;
This role is integral to a strategic research initiative aimed at advancing the understanding of wind-related hazards and developing effective mitigation strategies. The successful candidate will contribute to cutting-edge projects that blend computational modeling with experimental validation to address real-world challenges in wind engineering.
&nbsp;
Responsibilities:
Develop computational fluid dynamics (CFD) models to simulate wind flow around buildings and infrastructure, capturing complex aerodynamic interactions. Analyze wind loading on structures using high-resolution simulations; validate results with wind tunnel experiments or field measurements. Collaborate with interdisciplinary teams to incorporate wind effects into risk models, design standards, and resilience strategies. Publish and present research in peer-reviewed journals and at scientific or industry conferences. Contribute to strategic planning and innovation in wind engineering research initiatives.
 
PhD degree. Mechanical, Civil, Aerospace Engineering or related fields.
Hands-on experience with CFD software, both open-source (e.g., OpenFOAM) and commercial (e.g., ANSYS Fluent). Proficient in programming languages such as C++, Python, R, MATLAB. Skilled in high-performance computing (HPC) and parallel computing environments. Experience with wind tunnel testing or field measurements is highly desirable. Familiarity with relevant building codes and standards is a plus. Proven track record of publishing high-quality research and effectively communicating complex technical concepts to diverse audiences.Strong problem-solving abilities, creativity, and the capacity to work independently as well as collaboratively.
 The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
&nbsp;
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.

Senior Research Scientist - Computational Wind Engineering

<h3>Job Description</h3>
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These owners, who share the belief that the majority of property loss is preventable, represent many of the world’s largest organizations, including one of every four Fortune 500 companies. They work with FM to better understand the hazards that can impact their business continuity to make cost-effective risk management decisions, combining property loss prevention with insurance protection.
 
The purpose of this position is to develop new scientific knowledge, technologies and engineering solutions to problems in material flammability, fire dynamics and Lithium-ion battery safety research, which can be used for the prevention or control of industrial property loss.&nbsp;&nbsp;&nbsp;
&nbsp;
The principal responsibilities are to carry out research projects in the areas of flammability, fire spread, and heat transfer in fires from solid combustible as well as Lithium-ion batteries. Key areas of research include understanding of fire behavior at the medium and large scales via bench-scale experiments and theoretical models on material flammability and flame heat transfer. Projects can also involve advanced flame diagnostic of buoyant turbulent sooty flames and wall fires. The experimental and theoretical studies will be closely integrated with Computational Fluid Dynamic (CFD) model development and validation within the work group.&nbsp;
&nbsp;
The position is responsible for all aspects of project management including project proposals, execution, and reporting.
 
The position requires a PhD in Mechanical, Chemical Engineering, Fire Protection Engineering, or related fields with a strong fundamental background in combustion, fluid mechanics, heat transfer, material science and applied mathematics.&nbsp; Extensive experience in experimental methods in thermal fluids, material flammability, heat transfer, combustion/fire, and an understanding of associated numerical methods are required. Research experience with advanced laser diagnostics in flame, experimental measurement in turbulent flame, heat transfer and failure analysis of battery is desirable. Also needed are excellent written and verbal communication skills, as well as demonstrated expertise in developing solutions to challenging technical problems.
&nbsp;
&nbsp;
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
&nbsp;
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
&nbsp;
#FMG
&nbsp;
#LI-TA1

Senior Research Scientist - Material Flammability, Fire Dynamics and Lithium-ion Battery Safety

<h3>Job Description</h3>
Job Description
Job Title: Cleanroom Assembler
Job Description
The Cleanroom Assembler will be responsible for assembling high-quality medical devices while working within a controlled, sterile, medical-grade manufacturing area.
Responsibilities
<ul>
<li>Process polymer materials to compose, test, or apply on medical devices per approved manufacturing procedures.</li>
<li>Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures.</li>
<li>Perform in-process quality checks on subassemblies and finished products.</li>
<li>Utilize small hand tools, calibrated instruments, measurement equipment, microscopes, and participate in line meetings as needed.</li>
<li>Work with engineers and technicians to resolve line issues and suggest improvements.</li>
<li>Maintain cleanroom integrity by using proper attire and adhering to cleanroom environment practices and procedures.</li>
<li>Maintain accurate records/documentation related to quality, work in progress, test results, labor, and special projects.</li>
<li>Apply workstation practices and line clearance in daily activities.</li>
<li>Adhere to general safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA regulations.</li>
</ul>
Shifts:
<ul>
<li>2nd shift - 3:30 pm to 11:30 pm</li>
<li>A 5-7 week training period is provided</li>
</ul>
Essential Skills
<ul>
<li>Attention to detail</li>
<li>Hand dexterity</li>
<li>Ability to learn and be trained on new skills and equipment</li>
<li>Experience with microscopes is preferred</li>
<li>Experience in cleanroom, medical device, or manufacturing is preferred - more experience means higher starting pay rate.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Good hand-eye coordination and manual dexterity</li>
<li>Ability to work with small plastic and metal components</li>
<li>Ability to maintain production levels in a high-volume manufacturing setting</li>
</ul>
Why Work Here?
Join a company that values long-term growth and provides ample opportunities for advancement. Enjoy benefits such as overtime availability, paid holidays, medical, dental, and vision insurance, and a 401k plan. Take advantage of the onsite Starbucks and cafeteria with reduced pricing, and outdoor patio seating. Benefit from attractive referral bonuses, stock options after becoming a permanent employee, and various employee appreciation events.
Work Environment
Work in a cleanroom environment wearing PPE all day. Adhere to a professional, clean-cut business casual culture. Jewelry, makeup, eyelash extensions, fake nails, perfumes, or colognes are not permitted. 
Job Type &amp; Location
This is a Contract to Hire position based out of Danvers, MA.
Pay and Benefits
The pay range for this position is $20.00 - $24.20/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Danvers,MA.
Application Deadline
This position is anticipated to close on Jan 12, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Technician

<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist, Cell Therapy
Location: 100% on-site in Cambridge
&nbsp;
Remote Flexibility: No; 100% Onsite
&nbsp;
Contract Term: 6 months to start; 40 hours/week (potential to extend)
Experience required:
<ul>
<li>Background in immunology – especially in NK cell, TCR-T and CAR-T cell biology</li>
<li>This role will be a lot of time in the lab performing experiments towards building a donor section criteria for our Allogenic CAR-T call program.</li>
</ul>
&nbsp;
As an Immunologist, you will join our Cell Therapy group, where we leverage top-notch CRISPR technology to fully unleash the power of cell-based therapy for autoimmune and Immuno-Oncology indications. Your main responsibilities will include:&nbsp;
<ul>
<li>Designing, implementing, and troubleshooting experiments, both independently and in collaboration with colleagues, to reach desired goals&nbsp;</li>
</ul>
<ul>
<li>Establishing and performing in vitro/in vivo assays to support NK cell, TCR-T and CAR-T related projects&nbsp;</li>
</ul>
<ul>
<li>Using technical and literature knowledge to analyze and interpret results. Communicate research and development findings with internal and external teams/partners in a clear and concise manner&nbsp;</li>
</ul>
&nbsp;
&nbsp;
About You&nbsp;
Are you an Immunologist with a strong interest in genomic editing and cell therapy? Our ideal candidate will have a M.S. in Immunology, cell biology or related field with a solid background in immunology, especially in NK cell, TCR-T and CAR-T cell biology. If you are a team player looking to work with a highly motivated and energetic team, we encourage you to apply
&nbsp;
<ul>
<li>Team spirit and can-do attitude are must-to-have in an individual who thrives and enjoys working in a collaborative environment</li>
</ul>
<ul>
<li>Ability to isolate immune cells from leukopak using magnetic based isolation methods, in vitro culture of primary T cells and perform in vitro assays, T cell killing assay, and cytokine profiling assay by ELISA or MSD is a must.</li>
<li>Ability to perform multi-color FACS profiling assay,&nbsp; cell proliferation assay, Incucyte based assays, and mixed lymphocyte reaction (MLR) assay is required.&nbsp;Experience with cell metabolic assays using instruments like Agilent Seahorse Analyzers is a plus.&nbsp;</li>
</ul>
<ul>
<li>Experience with CRISPR gene editing and lentiviral transduction / AAV insertion in primary T cells and primary NK cells&nbsp;</li>
</ul>
<ul>
<li>Experience with Electronic Lab Notebook (ELN) to record detailed protocols and data in a timely manner.&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Publication of original scientific work in peer-reviewed journal(s) is a plus&nbsp;</li>
</ul>
&nbsp;
Meet your future team:&nbsp;
&nbsp;
The Cell Therapy team are a group of bright, fun and team-first individuals. Eager to move cool projects forward, we are motivated at the opportunity to make an impact for patients. The breadth of exposure to cutting edge gene therapy development will provide you with exposure to the full spectrum of gene and cell-based therapies, starting from CRISPR guides to patients who we try our best to support. Your future hiring manager is the Senior Scientist, Cell Therapy. The team is currently working mostly onsite in a wet-lab environment. Therefore, we hope you are currently local to Cambridge MA, or open to relocating. While much of the day-to-day operations require wet-lab work, our team is focused on building not just technical expertise but fostering an environment for growth of scientists interested in a career in therapeutic biotechnology. If you join our team, you can expect to join fast, fun, exciting and collaborative environment. We look forward to fostering your skills, learning from your experiences, and building a larger team together.&nbsp;&nbsp;
The team is currently working mostly onsite in a wet-lab environment. Therefore, we hope you are currently local to Cambridge MA, or open to relocating. While much of the day-to-day operations require wet-lab work, our team is focused on building not just technical expertise but fostering an environment for growth of scientists interested in a career in therapeutic biotechnology. If you join our team, you can expect to join fast, fun, exciting and collaborative environment. We look forward to fostering your skills, learning from your experiences, and building a larger team together.
&nbsp;
&nbsp;
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Associate Scientist, Cell Therapy

<h3>Job Description</h3>
Job Description
Our client is seeking an individual to work closely with the RNA Chemistry Team responsible for synthetic oligonucleotides. This individual will be involved in a complete production process for the identification, implementation &amp; fulfillment of synthesis, purification and reaction scheme analytical characterization and method development of oligonucleotides.
&nbsp;RESPONSIBILITIES:
<ul>
<li>Hands-on position in an oligonucleotide chemistry lab inclusive of operating, maintaining &amp; calibrating synthesis platforms and other scientific equipment.</li>
<li>Handling automated oligo synthesizer (Expedite, Dr.Oligo, Mermaid, Akta OP-100, etc) using solid-phase.</li>
<li>Knowledge of oligonucleotide purification techniques (using Akta system) and Unicorn software.</li>
<li>Synthetic oligonucleotide method and process development participation.</li>
<li>Demonstrate basic lab competency in preparing reagents and buffers &amp; handling chemicals.</li>
<li>Follow operating procedures and process improvement documents.</li>
<li>Documentation of results and data analysis</li>
<li>Ensure safety and product quality are paramount throughout the laboratory environment.</li>
<li>Capable of repetitive tasks and performing other duties as assigned.</li>
<li>Perform general lab-operation activities.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>B.S. or B.A. equivalent in Organic Chemistry, Biochemistry or related field with 2+ yrs general laboratory experience or M.S. in Organic Chemistry, Biochemistry</li>
<li>Basic computer skills including MS Office Suite.</li>
<li>More experienced candidates with oligonucleotide chemistry experience will be strongly considered.</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Research Associate, RNA Oligonucleotide Chemistry

<h3>Job Description</h3>
Job Title: Senior Team Leader Statistics
Location: Morristown, NJ Cambridge, MA
&nbsp;
About the Job
&nbsp;
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&amp;D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Our Evidence Generation and Decision Science (EGDS) group at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision making through cutting-edge quantitative science and deliver unparalleled integrated evidence that drives innovation and scientific breakthroughs.

Join our EGDS Biostatistics I&amp;I team as Senior Team Leader Statistics, Biostatistics (Senior Director) and you’ll provide statistical leadership, guidance, and strategic input for clinical studies in large or multiple complexed projects. You’ll manage a team of biostatisticians and will have opportunities to develop innovative statistical solutions to support critical trial decision-making and advance treatment across all phases of drug development. EGDS will support your growth through people development and inclusive career opportunities that value diversity of thought and abilities, cultivating future leaders to shape the next generation of clinical science.

About Sanofi: We’re an R&amp;D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:

<ul>
<li>
Oversee statistical and scientific contribution to clinical development plans, studies and submissions activities (when applicable), and provide strategic statistical leadership for responsible projects.
</li>
<li>
Manage a team of biostatisticians. Define team members priorities, performance review and development areas. Mentor junior project team members and nurture a culture of productive teamwork, quality, operational efficiency, and innovation.
</li>
<li>
Plan, monitor and manage project activities, timelines, processes, and resources to ensure operational excellence and align practices in compliant with Sanofi SOPs and Biostatistics standards.
</li>
<li>
Develop productive collaboration with other functions in the aligned project team, with other statistics project leaders, and in communicating with senior leadership.
</li>
<li>
Lead or play an influential role in EGDS development initiatives and key cross-functional activities; represent statistics in challenging regulatory meetings, key scientific or technology working groups.
</li>
</ul>
&nbsp;
About You&nbsp;

<ul>
<li>
PhD/MS in statistics or related discipline with at least 10 years of pharmaceutical experience in clinical development, including experience with Biotech, Pharma, Clinical Research Organizations (CROs), health authorities and academic clinical research centers.
</li>
<li>
Excellent knowledge and understanding of clinical development and advanced statistical concepts and techniques.
</li>
<li>
Proven successful experience in clinical development or post-marketing activities such as submissions, interactions with regulatory agencies or other external stakeholders.
</li>
<li>
Demonstrated and recognized expertise in operational or statistical or managerial aspects
</li>
<li>
Demonstrated leadership and excellent interpersonal/communication, project and people management skills.
</li>
<li>
Exhibited expertise to represent organizations in cross-company activities (e.g. consortiums or professional associations).
</li>
</ul>

Why Choose Us?

<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SA&nbsp; #LI-SA &nbsp;&nbsp;&nbsp; #LI-Onsite
#vhd &nbsp;&nbsp;
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Senior Team Leader Statistics

<h3>Job Description</h3>
Job Title: Development Scientific Director (DSD)
Location: Cambridge, MA,

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.&nbsp;

The&nbsp;Development Scientific Director (DSD)&nbsp;role in the Neurology Clinical Development department provides clinical scientific leadership for Alzheimer’s disease clinical trials. The DSD contributes to the &nbsp;protocol development, study feasibility and risk assessment, regulatory submissions, protocol training, scientific review of data, and cross-functional collaboration to ensure scientific integrity and operational excellence. This role requires a scientifically and operationally focused, organized, and emotionally intelligent professional with strong analytical, communication, and leadership skills.
&nbsp;
At Sanofi we chase the miracles of science. Sanofi believes that the more we understand about disease pathogenesis in the human nervous system, the greater the chance we can produce life-changing therapies. Sanofi has a large internal research team including the Genomic Medicine Unit (GMU), which are committed to building the future pipeline in various neurological and ophthalmological diseases.&nbsp;Over the next five years, the Neurology &amp; Ophthalmology Development (NOD) group plans to regularly test in the clinic potentially disease-modifying treatments for Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculopathy (CIDP), Alzheimer’s disease, Parkinson’s disease, Amyotrophic Lateral Sclerosis (ALS), as well as other CNS diseases, with therapeutic modalities encompassing Small Molecules, Biologics, and Gene Therapy.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
&nbsp;
Main Responsibilities:
&nbsp;
Clinical Study Leadership
<ul>
<li>
Provide scientific expertise for study protocols, data interpretation, and clinical study reports.
</li>
<li>
Ensure scientific relevance and quality of clinical data throughout study execution.
</li>
<li>
Support feasibility assessments, risk management, and validation of clinical data.
</li>
<li>
Participate in internal governance and regulatory meetings.
</li>
</ul>

Cross-Functional Collaboration
<ul>
<li>
Serve as the scientific reference for study teams, investigators, and internal stakeholders.
</li>
<li>
Collaborate with Global Project Heads, Clinical Research Director, Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs, Biostatistics, Clinical Study Units, Medical Affairs, and CROs to optimize study design and execution.
</li>
</ul>

Study Document Development
<ul>
<li>
Author, review, and validate study-related documents including trial protocols, informed consent forms, case report forms, risk management plans, training materials, clinical study reports, and publications.
</li>
<li>
Develop materials for and organize investigator meetings, steering committees, and independent data monitoring committees.
</li>
<li>
Contribute to regulatory submissions and respond to health authority queries.
</li>
</ul>

Scientific Expertise &amp; Strategy
<ul>
<li>
Maintain deep knowledge of Alzheimer’s disease pathophysiology, biomarkers, disease staging, clinical management, and drug development.
</li>
<li>
Contribute to biomarker strategy and mechanism-of-action understanding.
</li>
<li>
Support clinical development plans and integrated development strategies.
</li>
<li>
Provide scientific input for in-licensing evaluations and strategic initiatives as needed.
</li>
</ul>

Operational Oversight
<ul>
<li>
Define study timelines, budgets, and risk mitigation plans in collaboration with clinical operations and project management.
</li>
<li>
Ensure harmonization of study documents and alignment across projects.
</li>
<li>
Escalate and resolve study-level issues, sharing lessons learned across teams
</li>
</ul>

QUALIFICATIONS
<ul>
<li>
Advanced degree (PhD, PharmD, or equivalent in Life/Health Sciences); MPH or Master’s with extensive drug development experience may be considered.
</li>
<li>
Minimum 5 years of clinical development experience in academic, biopharma, or CRO.
</li>
<li>
Strong scientific and clinical development expertise, especially in neurology. Clinical research and drug development expertise in Alzheimer’s disease is highly desired.
</li>
<li>
Excellent communication, teaching, and cross-functional collaboration skills.
</li>
<li>
Fluent in English (spoken and written).
</li>
<li>
Experience working in a matrixed environment with global teams.
</li>
</ul>

Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SA&nbsp; #LI-SA &nbsp;&nbsp;&nbsp; #LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Development Scientific Director, Neurology (Early Development)

<h3>Job Description</h3>
$15,000 sign on bonus (external candidates only)

Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others?&nbsp; Are you looking for an industry leading company that offers growth and stability?&nbsp; LabCorp is seeking a Clinical Laboratory Team Leader to join our team at Tuft Medical Center in Boston, MA.&nbsp; In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives".

**Pay Range: $90,000 - $120,000 annually
All job offers will be&nbsp;based on a candidate’s skills and prior relevant experience, applicable&nbsp;degrees/certifications,&nbsp;as well as internal equity and market data.&nbsp;

Work Schedule: Monday-Friday 3:00pm-11:30pm; rotating weekends.

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.&nbsp; Casual, PRN &amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.&nbsp;For more detailed information, please&nbsp;click here.&nbsp; 

Job Responsibilities
<ul>
<li>Supervise the day to day operations of the Blood Bank department</li>
<li>Ensure laboratory tests are accurately performed and results are reported in a timely manner</li>
<li>Directly supervise, train, and mentor laboratory personnel of the department</li>
<li>Monitor daily workflow in the lab and schedule adequate assay coverage</li>
<li>Responsible for ensuring all shifts in the department are properly staffed</li>
<li>Research and resolve any production errors while escalating when necessary</li>
<li>Engage in continuous process and service level improvements</li>
<li>Ensure all equipment is being properly maintained through Quality Control</li>
<li>Prepare and maintain Quality Assurance records and documents</li>
<li>Evaluate new process improvements and make appropriate recommendations</li>
<li>Meet regularly with direct reports to provide coaching and feedback for their development</li>
<li>Perform bench work as needed and maintain proficiency/competency in technical operations</li>
<li>Ensure all work is in accordance with state and Federal regulations</li>
<li>Responsible for administering and managing policies and procedures</li>
<li>Process and maintain payroll and personnel files</li>
<li>Perform administrative duties as needed</li>
</ul>

&nbsp;Requirements
<ul>
<li>Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA &amp; State) requirements – Bachelor’s degree is a plus</li>
<li>Minimum 5 years of experience as a Technologist/Technician </li>
<li>Previous Senior or Lead Technologist experience is highly preferred</li>
<li>ASCP or AMT certification is preferred</li>
<li>Strong working knowledge of CLIA, CAP and relevant state regulations</li>
<li>Understanding of laboratory operations as well as policies and procedures</li>
<li>Proficient with Laboratory Information Systems and Microsoft Office</li>
<li>Strong communication skills; both written and verbal</li>
<li>High level of attention to detail with strong organizational skills</li>
<li>Comfortability making decisions in a changing environment</li>
<li>Ability to handle the physical requirements of the position</li>
</ul>

If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.&nbsp;

We encourage all to apply
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Laboratory Supervisor - Blood Bank

<h3>Job Description</h3>
Date Posted:
2025-11-11
Country:
United States of America
Location:
MA102: Andover MA 362 Lowell Plymouth 362 Lowell Street Plymouth, Andover, MA, 01810 USA
Position Role Type:
Onsite
U.S. Citizen, U.S. Person, or Immigration Status Requirements: 
U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.
Security Clearance: 
DoD Clearance: Secret

At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend freedoms and deter aggression.&nbsp; We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead of tomorrow’s threat.&nbsp; Our team solves tough, meaningful problems that create a safer, more secure world.&nbsp;

Job Summary:
An opportunity exists in the Advanced Microelectronics Solutions (AMS) Department, a part of Raytheon, for a 2nd Shift Metrology Process Support Engineer. AMS develops, designs, and manufactures compound semiconductor devices, millimeter/microwave integrated circuits, focal plane arrays, and modules for defense and commercial applications.&nbsp;

The individual in this role will serve as a process engineer within the Metrology Workcenter, which will focus primarily on supporting the production line through measurement techniques such as CDSEM and overlay. The ideal candidate will have experience in both electron and optical microscopy and a general understanding of measurement systems analysis.&nbsp; They would also demonstrate the ability to analyze data and clearly communicate results with process and development engineers. Further, they would have experience leading or contributing to process improvement projects.&nbsp; The candidate will support the operational goals of the facility through the collection of reliable data to support the other process areas.

The candidate should have a general understanding of the overall techniques involved in semiconductor wafer fabrication and integration, with some experience of analog device processing.&nbsp; Experience with statistical analysis software such as JMP, Minitab, R, etc. is preferred.

This position is 100% onsite and will be based in Andover, MA.

What You Will Do:
<ul>
<li>Supporting the production line through custom job writes, lot disposition, and data validation.</li>
<li>Collaborating with Engineering, Operations, and Quality to troubleshoot efforts with production processes</li>
<li>Working with the Metrology lead engineer to drive efforts to improve measurement and data quality.</li>
<li>Supporting capital qualification efforts.</li>
</ul>

Qualifications You Must Have:
<ul>
<li>Typically, a Bachelor’s in Science, Technology, Engineering, or Mathematics (STEM) and 5+ years of prior work experience OR a STEM Master's and 2+ years of prior work experience related to semiconductor metrology techniques such as automated optical inspection, CDSEM, overlay, reflectometry, ellipsometry, or others.</li>
<li>Experience troubleshooting production process equipment.</li>
<li>The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance.</li>
</ul>

Qualifications We Prefer:
<ul>
<li>Master’s in Science, Technology, Engineering, or Mathematics (STEM).</li>
<li>Experience supporting process improvement projects</li>
<li>Experience working with SQL databases</li>
<li>Experience with statistical analysis software (JMP, Minitab, R, SPSS, MATLAB, etc)</li>
<li>Experience with compound semiconductor devices.</li>
<li>Experience in statistical process control (SPC) and/or advanced process control (APC)</li>
<li>Strong communication skills and the ability to clearly present data and analyses</li>
</ul>

What We Offer:
Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation.


As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend&nbsp;select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote.

The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate’s work experience, location, education/training, and key skills.


Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.

Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company’s performance.

This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.

RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.

RTX 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, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans’ Readjustment Assistance Act.

Privacy Policy and Terms:
Click on this link to read the Policy and Terms

2nd Shift Metrology Process Support Engineer

<h3>Job Description</h3>
UII America, Inc., a subsidiary company of Shanghai United Imaging Intelligence Healthcare Co. Ltd. (UII), is building an organization of highly-motivated, talented and skillful AI experts and software developers to strengthen our R&amp;D power and address the need of our innovative products in the USA market. United Imaging Intelligence (UII) is committed to providing AI solutions for medical devices, imaging, and diagnosis – to helping clients better understand and embrace AI. United Imaging Intelligence is led by two world-renown leaders in the AI industry. Together, they will lead UII in focusing on “empowerment” and “win-win.” UII empowers doctors and equipment in order for doctors and hospitals to win, for research institutions to win, and for third-party companies to win. UII America, Inc. is building a world-class research and development team in Boston, MA.
 
We have immediate openings for LLM Research Interns with the following qualification requirements:
[ Responsibilities ]
<ul>
<li>Research and develop automated evaluation pipelines for Large Language Models (LLMs) in the medical domain, integrating clinical logic and bioinformatic standards;</li>
<li>Implement and optimize evaluation frameworks using LLM/Agent-as-a-judge techniques and reward models to assess complex clinical reasoning capabilities;</li>
<li>Conduct deep-dive analysis on model performance from both technical (NLP) and clinical perspectives, identifying failure modes and providing actionable insights for model alignment;</li>
<li>Extend and improve the company's existing algorithms and evaluation libraries;</li>
<li>Work closely with colleagues and management to develop company assets in NLP/LLM and Conversational AI;</li>
<li>Be ambitious to lead the changes in future Healthcare with innovations.</li>
</ul>
[ Qualifications ]
<ul>
<li>Currently pursuing a PhD or Master’s degree in Computer Science (AI/ML), Bioinformatics, Medical Informatics, Computational Biology, or a related quantitative/medical field;</li>
<li>Strong interest in the intersection of AI and Healthcare, with the ability to bridge technical model evaluation and clinical domain knowledge;</li>
<li>Strong programming skills with Python and familiarity with deep learning frameworks such as PyTorch;</li>
<li>Understanding of the LLM life cycle, including data preparation and reinforcement learning (RLHF/RLAIF);</li>
<li>Proven track record of publications in top-tier conferences and journals (e.g., NeurIPS, ICML, ACL, EMNLP, etc.) is a plus;</li>
<li>Passion for applying AI to make a positive impact in the healthcare domain;</li>
<li>Ability to develop practical solutions to challenging problems;</li>
<li>Strong writing, communication, and cross-discipline collaboration skills</li>
</ul>

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