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<h3>Job Description</h3>
Job Description
 Job ID: 30926 Contract Length: 1 Year (Renewable) Title: Computational Chemist – Molecular Dynamics Simulation Expert Duration: 12-Months Fixed-Term Location: Waltham, minimum of 60% onsite We are seeking an enthusiastic and talented Computational Chemist for a 12-month fixed-term position to contribute to the modeling of anti-tumor drug candidates.
About You: You have a PhD (or equivalent experience) in computational chemistry, biophysics, structural biology, or a related field. You have a proven track record with molecular dynamics simulation methodologies, including set-up, execution, and analysis Preferably, you bring hands-on experience with coarse-grained MD approaches (such as MARTINI or related frameworks) You are proficient in standard scientific programming/scripting (e.g., Python, Bash, or similar) You communicate scientific concepts clearly, both verbally and in writing Familiarity with other computational biophysics techniques (e.g., protein-protein docking, enhanced sampling) Requirements: PhD Years of experience: up to 10 years of experience is max Phython and SAP skills are required. Teams size: 6 Interview process: 1 virtual screen, then 1 panel interview, onsite if local. You will drive molecular dynamics (MD) simulation to work on anti-tumor drug discovery projects. Your primary responsibility will be to develop, execute, and analyze MD simulations, with a strong emphasis on coarse-grained MD methodologies. You will collaborate closely with experimental scientists and other computational experts to provide structural and mechanistic insights that guide the design and optimization of drug candidates. Key Responsibilities: Design and conduct MD simulations to explore structure, dynamics, and interactions relevant to molecular interactions Apply coarse-grained MD techniques and contribute to methodological improvements where possible Analyze and interpret simulation results; effectively communicate findings to multidisciplinary project teams Collaborate with experimental and therapeutic area colleagues to link modeling data to biological and pharmacological outcomes Document methodologies, results, and best practices to enable knowledge transfer and reproducibility
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Company Description<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a> 
<h3>Company Description</h3>
<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a>

Computational Chemist, PHD (30926)

<h3>Job Description</h3>
Job DescriptionJob Title: Analytical Research Associate Location: Cambridge, MA, 02139 Duration: 12+ months (Possibilities of Extension) Shift: 4 days onsite in the lab, 1 day remote if they like Pay Rate: $43.00/Hour. on W2 Job Description Summary: Responsibilities:
<ul>
<li>Execute experiments to advance analytical method development, method suitability assessments, and method troubleshooting</li>
<li>Perform chemical and physical analyses to inform drug substance process and formulation optimization decisions in collaboration with Pharmaceutical Sciences colleagues</li>
<li>Solve technical issues for methods developed both internally and at an external CDMO partner</li>
<li>Author and/or review data and reports associated with work executed in the BProduct laboratories</li>
<li>Contribute to the coordination and prioritization of internal Analytical Development resources in collaboration with Analytical Development project representatives, Formulation Sciences, and Process</li>
<li>Chemistry</li>
<li>Present scientific data and conclusions to cross functional teams</li>
<li>Proactively participate in instrument maintenance</li>
</ul>
 Education:
<ul>
<li>B.S. in chemistry or related field with 0-3 years of relevant experience or M.S. with 0-1 years of experience,</li>
</ul>
 Skills:
<ul>
<li>Demonstrated knowledge of analytical technologies (HPLC, HRMS, GC, FT-IR, NMR, KF, Dissolution, PXRD and/or knowledge of other techniques used in pharmaceutical analysis).</li>
</ul>
 #sczr2

Analytical Research Associate

<h3>Job Description</h3>
Job Description
The experienced Research Associate Scientist II, with a background in in vitro screening, will be part of our dynamic, fast-paced and interdisciplinary lead development team. Our mission is to advance novel RNAi therapeutic programs from target discovery through lead candidate selection. The Associate Scientist II will be technically skilled in molecular and/ or cell biology, and bring a rigorous, analytical approach to research.
Key Responsibilities
<ul>
<li>Perform cell culture (iPSCs, primary cells, immortalized cell lines) to support the research needs of the group and high-throughput screening of siRNAs using qPCR and a variety of cell-based assays</li>
<li>Execute day to day operations for RNASeq sample preparation, including: library preparation, QC and sequencing. Maintain sample tracking &amp; records.</li>
<li>Conduct assays that support in vivo studies (e.g. qPCR, ELISA) for the quantitative analysis of biomarkers or siRNA activity </li>
<li>Support lab maintenance including equipment operation &amp; maintenance , reagent inventory and reagent preparation</li>
<li>Troubleshoot technical problems and participate in the continuing development and optimization of existing and new protocols.</li>
<li>Utilize instrumentation and robotics to aid in high throughput (384-well) screening.</li>
<li>Adapts well to the changing platform needs, in workflow, projects and other tasks as required by the platform.</li>
</ul>
Requirements
Qualifications
<ul>
<li>BS in a biological science with at least 2 years of hands-on laboratory experience in cell or molecular biology are required </li>
<li>Experience in cell culture and purification/quantification of nucleic acids/protein, including qPCR</li>
<li>Experience with NGS workflow is desired</li>
<li>Experienced with laboratory automation including liquid handling systems such as Perkin Elmer JANUS, Beckman i7 or other systems.</li>
<li>Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment.</li>
</ul>
Benefits
<ul>
<li>Contract with possible extension</li>
</ul>

Associate Scientist II

<h3>Job Description</h3>
Job Description
We are seeking a motivated and detail-oriented Analytical Development Senior Research Associate to join our Analytical Development team. This individual will support assay development and analytical testing for biologics and cell therapy products. The ideal candidate is technically skilled, thrives in a fast-paced environment, and demonstrates strong documentation and communication abilities.
Key Responsibilities:
<ul>
<li> Conduct experiments to support analytical method development for biologics and cell therapy products. </li>
<li> Perform sample testing and data analysis with minimal supervision and quick turnaround times. </li>
<li> Maintain meticulous and timely documentation of experiments and findings. </li>
<li> Author and review SOPs, protocols, and reports. </li>
<li> Optimize and troubleshoot assay performance in collaboration with the manager. </li>
<li> Present experimental data and updates in internal meetings. </li>
<li> Carry out routine lab support tasks to maintain lab operations. </li>
<li> Perform additional duties as assigned. </li>
</ul>
Required Skills:
<ul>
<li> Proficient in cell culture and aseptic techniques. </li>
<li> Experience with one or more analytical techniques: Flow cytometry, RT-qPCR, cell migration assays. </li>
<li> Ability to work in a regulated, GMP-like laboratory setting. </li>
<li> Strong analytical and problem-solving skills with attention to detail. </li>
<li> Capable of independently modifying experimental designs for continuous improvement. </li>
<li> Effective communicator, both written and verbal. </li>
<li> Ability to multitask and meet deadlines in a fast-paced environment. </li>
<li> Proficiency in Microsoft Word, Excel, and PowerPoint. </li>
</ul>
Requirements
Education &amp; Experience:
<ul>
<li>Bachelor’s degree in Biology, Chemistry, or a related field with 3–5 years of relevant experience. </li>
<li>Master’s degree in Biology, Chemistry, or a related field with 0–2 years of relevant experience. </li>
<li> Equivalent combinations of education, training, and/or directly related experience will also be considered. </li>
</ul>
Preferred Qualifications:
<ul>
<li> Hands-on experience with analytical method development (e.g., characterization, release assays). </li>
<li> Prior experience working with hematopoietic stem cells. </li>
</ul>
Work Environment:
<ul>
<li> This is a fully onsite position located in Boston, MA. </li>
<li> Must be able to work upright or standing for extended periods. </li>
<li> Ability to operate standard lab and office equipment efficiently. </li>
<li> Comfortable working under pressure and handling multiple projects simultaneously. </li>
</ul>
Benefits
<ul>
<li>Contract</li>
</ul>

Analytical Development Senior Research Associate (Contract)

<h3>Job Description</h3>
Job Description
Scientific Marketing Manager / Director - in vivo Pharmacology
Location: Remote, USA
Salary: $120,000 - $160,000
 
Combine your passion for science with creativity in scientific marketing.
Join our dynamic marketing team at Pharmaron as a Scientific Marketing Manager. We are seeking an individual who is passionate about drug discovery and preclinical development with experience in drug efficacy testing in disease models. Become part of our team to help us elevate our brand and drive sales.
 
Your Key Responsibilities:
<ul>
<li>Craft compelling narratives: Translate complex scientific concepts into engaging stories that resonate with our audience.</li>
<li>Create new content: Partner with our scientists to create engaging content that showcases our expertise such as brochures, white papers, flyers, webpage content, etc.</li>
<li>Lead marketing campaigns: Develop and execute multi-channel campaigns that increase brand awareness and generate leads.</li>
<li>Analyze and optimize: Track marketing performance, identify trends, and refine our strategies for maximum impact.</li>
<li>Represent our brand: Manage our presence at industry conferences and events.</li>
</ul>
 Your Profile:
<ul>
<li>Location: Remote, the applicant must be located in Europe or North America.</li>
<li>Scientific background: A degree in biology, pharmacology, veterinary medicine or a related field is essential.</li>
<li>Experience: Minimum of 5 years of industry experience related to animal disease models in drug discovery or drug development.</li>
<li>Exceptional communication skills: A passion for writing and the ability to convey complex scientific ideas to diverse audiences.</li>
<li>Passion for learning: A desire to stay updated on industry trends and best practices.</li>
<li>Collaborative spirit: Enjoy working with cross-functional teams and external partners with a willingness to travel as needed.</li>
</ul>
 
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental &amp; Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare &amp; Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&amp;D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
 
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
 
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
 
#LI-EH1

Scientific Marketing Manager / Director - in vivo Pharmacology / Toxicology

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
As a recognized industry multidisciplinary expert, drives performance of a team of precision medicine leads in psychiatry by setting a strategic vision and achievable roadmap in collaboration with cross-functional stakeholders to inform the design and implementation of studies aimed to derisk, accelerate, or inform creation of new or improved drug products.&nbsp;&nbsp;&nbsp;
Responsibilities:
<ul>
<li>Responsible for direction and execution of the scientific strategy in alignment with cross-functional, cross-disciplinary goals and key scientific goals. Ensures achievement of set goals.</li>
<li>Establishes scientific standards for excellence by collaborating with multi-disciplinary functional leaders and experts to integrate standards into strategies and tactics associated with development of new or improved products or technology.</li>
<li>Leads scientific expertise within the function by mentoring and training colleagues. Proactively advises and shares knowledge and expert opinions with senior management.</li>
<li>Delivers results that meet or exceed expectations of major project plans across function through sound design, early risk assessments, and implementation of fallback strategies.</li>
<li>Anticipates challenges and continually sets approaches to utilize newly proven technology. Proactively establishes scientific standards within AbbVie.</li>
<li>Anticipates and prioritizes emerging scientific trends. Champions the use of innovation sourced both internally and externally and formulates the innovations for widespread organizational use. Integrates innovation into objectives and ensure alignment with customer needs.</li>
<li>Drives advancement of new products by pioneering and implementing breakthrough ideas and novel approaches that are valued by customers across the company. Creates institutional knowledge and patent strategy.</li>
<li>Keeps identified stakeholders informed by presenting scientific concepts and results for functional and non-scientific leaders and potential and existing partners. Maximizes impact and value of expertise.</li>
<li>Maintains an external reputation as multidiscipline expert and leads the industry as invited panelist to senior industry meetings or by authoring and reviewing high-impact articles for peer-reviewed, top-tier publications.</li>
<li>Manages a team of 3-5 precision medicine leads responsible for asset and study level work, providing above-asset strategic vision and support the team to overcome institutional or technical barriers.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's Degree in Science or related field with 20 years or more of related work: Master's Degree in Science or related field or PharmD with 18 years of related work;&nbsp; PhD in Science or related field with 12 years of related work experience</li>
<li>Proven ability to innovate with a history of successful new or improved product releases</li>
<li>Ability to advise discipline experts and leaders within the function on how to manage their particular risks</li>
<li>Interacts well with diverse groups and maintains a strong working relationships with internal and external collaborators</li>
<li>Listens and understands others' point of views and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations</li>
<li>Interpersonal skills capable of negotiating and reconciling interdisciplinary differences, optimizing overall business goals</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Scientific Director II, Precision Medicine Neuroscience

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
The position will support a client team that is responsible for ensuring the consistency, safety, and efficacy of biologics, including cutting-edge cell and gene therapies. The successful candidate will work in close partnership with analytical development, bioprocessing, formulation, and data science groups to support manufacturing and quality control activities across the client’s development pipeline.
We are seeking a skilled analytical development scientist who will contribute to the development of the client’s islet cell therapy platform. This role will involve designing, optimizing, and executing bioanalytical assays for use in process development, in-process testing, and lot release. Knowledge and expertise in mammalian cell culture, flow cytometry, and molecular assays, including PCR, are a must.&nbsp; The successful candidate must be self-motivated and able to work independently to troubleshoot and interpret experimental results and effectively present conclusions.&nbsp;
Job Responsibilities and Requirements
<ul>
<li>Develop, optimize, and execute a range of analytical assays to support product development and batch release.</li>
<li>Perform sample analysis using a broad set of platforms such as flow cytometry, ELISA, PCR, and cell-based assays.</li>
<li>Investigate and resolve assay-related challenges by applying scientific and technical problem-solving skills.</li>
<li>Support assay qualification, validation, and lifecycle management to ensure reliability and regulatory compliance.</li>
<li>Collaborate with cross-functional teams, including R&amp;D, manufacturing, and quality to ensure alignment on analytical goals and timelines.</li>
<li>Contribute to preclinical study support by aligning analytical strategies with experimental objectives.</li>
<li>Interpret experimental data, summarize results clearly, and communicate findings to technical and non-technical audiences.</li>
<li>Support assay transfer and technical communication with CDMOs, including troubleshooting, documentation review, and knowledge transfer.</li>
<li>Maintain laboratory infrastructure, including oversight of reagents, reference materials, and analytical equipment.</li>
<li>Author technical documentation such as protocols, reports, and standard operating procedures.</li>
<li>Continuously evaluate emerging technologies and scientific approaches to improve assay performance and robustness.</li>
</ul>
Qualifications 
Minimum Qualifications
<ul>
<li>Master’s degree in a relevant scientific field with 4+ years of industry experience</li>
<li>Deep expertise in dPCR and qPCR assay development</li>
<li>Proficient in multicolor flow cytometry for phenotyping and functional assays, with the ability to lead assay development efforts</li>
<li>Hands-on experience in mammalian cell culture, including iPSCs, tumor/cancer lines, and primary cell types</li>
<li>Strong background in designing, developing, optimizing, and executing complex bioanalytical assays</li>
<li>Skilled problem-solver with the ability to interpret and troubleshoot complex datasets</li>
<li>Excellent verbal and written communication skills; confident in presenting data and conclusions to diverse audiences</li>
<li>Flexible and dependable; open to variable scheduling, including occasional weekend work</li>
</ul>
Preferred Qualifications
<ul>
<li>Ph.D. in a life science or related field</li>
<li>Specialized experience in dPCR/ddPCR assay design for evaluating marker expression in cell culture systems</li>
<li>Expertise in designing multicolor flow cytometry panels for both marker expression and functional readouts (e.g., apoptosis, proliferation, signaling pathways)</li>
<li>Strong literature research skills for the development of novel bioassays</li>
<li>Hands-on experience with iPSC culture and differentiation is a plus</li>
<li>Knowledge of assay qualification, validation, and regulatory guidelines (e.g., ICH)</li>
<li>Proficient with digital lab tools such as FlowJo, GraphPad Prism, Benchling, SharePoint, and Veeva</li>
<li>Exceptional time-management and organizational skills with the ability to balance multiple priorities under tight deadlines</li>
<li>Highly collaborative, self-driven, and adaptable to dynamic, fast-paced environments</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role</li>
</ul>
ThePosition is Full Time, Monday-Friday, 8am-5pm.Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.&nbsp;
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly rate is between $41 - $43,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Development Scientist

<h3>Job Description</h3>
FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services; tailored risk transfer capabilities; and superior financial strength. To do so, we rely on a dynamic, culturally diverse group of employees, working in more than 100 countries, in a variety of challenging roles.
 
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.
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.
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.
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.
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>
FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services; tailored risk transfer capabilities; and superior financial strength. To do so, we rely on a dynamic, culturally diverse group of employees, working in more than 100 countries, in a variety of challenging roles.
 
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;
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;
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.
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.
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
#FMG
#LI-TA1

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