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<h3>Job Description</h3>
Job DescriptionContract Research Associate – Virology (contract 3-4 months) &nbsp;Why Work for Us?At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. We are a high performing team, showing up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.Our Science: Advancing Cancer ImmunotherapiesCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: <a href="http://www.candeltx.com" target="_blank">www.candeltx.com</a>Position Summary:We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment.Key Responsibilities:
<ul>
<li>Support the design, production, and testing of novel HSV-based viral vectors.</li>
<li>Conduct classical virology techniques such as virus production, purification (e.g., ultracentrifugation), and titering.</li>
<li>Execute virology-specific assays including plaque assays, TCID50, viral titration, and viral genome quantification using qPCR.</li>
<li>Contribute to viral vector engineering and optimization of workflows.</li>
<li>Maintain mammalian cell culture operations, including cryopreservation, routine culture, and cell banking.</li>
<li>Perform in vitro to evaluate viral vector transduction and biological activity.</li>
<li>Document experiments in electronic laboratory notebooks, analyze data, and prepare reports for internal review.</li>
<li>Contribute to a scientific culture that values creativity, rigor, and innovation.</li>
</ul>
Qualifications:Education:
<ul>
<li>MS in Virology, Biotechnology, or related field with 1–3 years of industry experience, or</li>
<li>BS with 3–5 years of relevant experience.</li>
</ul>
Experience and Skills:
<ul>
<li>Hands-on experience with virus production, purification, and quantification techniques (e.g., plaque assays, TCID50, qPCR) required.</li>
<li>Solid foundation in mammalian cell culture and aseptic technique.</li>
<li>Familiarity with viral vector design and characterization, particularly HSV-based systems.</li>
<li>Strong analytical and organizational skills with attention to detail.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency in Microsoft Office, GraphPad Prism, and SnapGene (preferred).</li>
</ul>
&nbsp;Work Environment:This is a lab-based position in Needham, Massachusetts. &nbsp;
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dtiN9KRel3

Contract Research Associate - Virology

<h3>Job Description</h3>
Job DescriptionJob Title: Analytical Chemist Job Description
We are seeking an analytical chemist to support, lead, and develop the R&amp;D team in creating innovative new products. This role involves performing field testing, scaling up processes, and developing new polymers, adhesives, epoxies, and coatings.
Responsibilities
<ul>
<li>Lead the R&amp;D team in developing new products and processes.</li>
<li>Perform field testing and scale-up of new product developments.</li>
<li>Support the development of new polymers, adhesives, epoxies, and coatings.</li>
<li>Drive all R&amp;D activities and determine new products for the marketplace.</li>
<li>Manage product development projects and drive continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>Strong knowledge of analytical chemistry and polymer chemistry.</li>
<li>Expertise in research and development, scale-up, and raw material testing.</li>
<li>Experience in epoxy, polymer, and adhesive development.</li>
<li>Proven track record in leading R&amp;D teams and managing product development projects.</li>
<li>5+ years of experience in R&amp;D for coatings, adhesives, and regulatory standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Masters or PhD in Chemistry, Materials Science, or Chemical Engineering.</li>
<li>Knowledge of regulatory standards related to coatings and adhesives.</li>
</ul>
Work Environment
The position is 100% onsite at the Westwood facility, working Monday to Friday from 9:00 am to 5:00 pm. The production schedule is 7:00 am to 3:00 pm, allowing for alignment with this schedule.
Job Type &amp; Location
This is a Permanent position based out of Westwood, Massachusetts.
Pay and Benefits
The pay range for this position is $125000.00 - $140000.00/yr.
They have full vision, dental, health, and vacation. They have great benefits for medical leave as well.
Workplace Type
This is a fully onsite position in Westwood,MA.
Application Deadline
This position is anticipated to close on Oct 2, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Chemist

<h3>Job Description</h3>
Job Description
This is a position within Keller Executive Search and not with one of its clients. As the Senior Research Manager in Boston, MA, this senior role is accountable for shaping research strategy and delivering measurable outcomes across the business. The position partners closely with cross‑functional leaders, drives operational excellence, and scales processes to support growth. Key Responsibilities:
<ul>
<li>Set a clear multi‑year strategy and translate it into quarterly plans with accountable metrics.</li>
<li>Lead teams with a focus on coaching, psychological safety, and high performance.</li>
<li>Develop repeatable research frameworks and knowledge assets for decision support.</li>
<li>Build data‑driven operating rhythms, dashboards, and continuous‑improvement loops.</li>
<li>Own budgets and vendor relationships; negotiate contracts that balance value, risk, and speed.</li>
<li>Design compliant processes aligned to local regulations and internal policies.</li>
<li>Partner with Sales, Marketing, and People Operations to execute company priorities.</li>
<li>Represent the function to senior leadership; prepare crisp updates and decision memos.</li>
</ul>
To learn more about Keller, please see: <a href="https://www.kellerexecutivesearch.com/executive-recruiters-headhunters-worcester-and-springfield-massachusetts/" target="_blank">https://www.kellerexecutivesearch.com/executive-recruiters-headhunters-…</a>
Requirements
<ul>
<li>7+ years in progressively senior roles within the relevant discipline; experience leading managers.</li>
<li>Demonstrated success building scalable processes and delivering against OKRs.</li>
<li>Strong analytical and financial acumen; fluency with data tools and business cases.</li>
<li>Excellent stakeholder management and executive communication skills.</li>
<li>Working knowledge of applicable local laws, standards, and industry best practices.</li>
<li>Bachelor’s degree required; advanced degree or certifications are advantageous.</li>
</ul>
Benefits
<ul>
<li>Competitive compensation: $ 150,000–183,000 USD</li>
<li>Opportunities for professional growth and leadership development.</li>
<li>Company culture: Flat management structure with direct access to decision‑makers; open communication environment.</li>
<li>Full medical coverage.</li>
</ul>
Equal Employment Opportunity Statement: Keller Executive Search provides equal employment opportunities to all qualified applicants and employees. Employment decisions are based on merit, qualifications, and business needs, without regard to protected characteristics under applicable law. Commitment to Diversity: An inclusive and equitable workplace is actively fostered. Hiring, development, and advancement practices are designed to broaden representation and ensure fair access to opportunity. Data Protection and Privacy: Personal data is processed solely for recruitment and employment purposes, in accordance with applicable data‑protection laws (including GDPR where relevant). Information may be retained for compliance and legitimate interests, subject to data minimization and security controls. Pay Equity: Compensation practices are reviewed to support pay equity for substantially similar work, accounting for bona fide factors such as experience, education, and performance. Health and Safety: Workplace health and safety obligations are observed in line with applicable national and local requirements. Employees are expected to follow all safety policies and promptly report hazards. Compliance with Law: All recruitment, selection, and employment practices are conducted in compliance with applicable laws and regulations in the jurisdiction of employment. 
Note: This job posting may be for a position with Keller Executive Search or one of our clients. The specific employer will be identified during the application and interview process. Employment laws and requirements may vary depending on the employer and location.

Research Manager

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

Research Associate I - Marine Biomedical Discovery

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is a global leader in life sciences testing, offering a comprehensive range of analytical services to ensure the safety, authenticity, and quality of products across industries. With over 47,000 employees in more than 900 companies worldwide, Eurofins is committed to making life and the environment safer, healthier, and more sustainable.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking an&nbsp;Associate Scientist – Analytical Chemistry&nbsp;to support analytical method development and testing in a dynamic biotech environment. This role is ideal for candidates with hands-on experience in&nbsp;RNA and oligonucleotide analysis, particularly using advanced chromatographic and mass spectrometry techniques. You’ll contribute to product development through rigorous data generation, method optimization, and cross-functional collaboration.
Key Responsibilities
<ul>
<li>Develop and execute analytical methods using HPLC, UHPLC, and LCMS to support RNA and oligonucleotide characterization.</li>
<li>Perform analytical testing to assess purity, potency, and stability of nucleic acid-based therapeutics.</li>
<li>Collaborate with cross-functional teams to transfer and implement robust analytical methods.</li>
<li>Troubleshoot and maintain analytical instrumentation to ensure high-quality data output.</li>
<li>Support material testing through coordination with specialized characterization groups.</li>
<li>Uphold safety and compliance standards while contributing to continuous improvement initiatives.</li>
</ul>
Qualifications 
Qualifications&nbsp;Minimum Requirements:
<ul>
<li>B.S. with 3–4 years or M.S. with 1-2 years of relevant industry experience in Analytical Chemistry, Biochemistry, or related field.</li>
<li>Strong hands-on experience with liquid chromatography techniques (HPLC, UPLC, LC-MS).</li>
<li>Familiarity with analytical tools such as FTIR, UV-Vis, KF, ICP, DSC, and XRPD.</li>
<li>Experience with instrumentation, including Waters I-Class, Thermo Vanquish Flex, and AKTA Pure 150 M.</li>
<li>Proficiency in software such as Empower, Xcalibur, Unicorn, and&nbsp; BioPharma Finder.</li>
<li>Solid understanding of method characterization (e.g., linearity, precision, LOD/LOQ).</li>
<li>Strong communication skills and ability to work effectively in dynamic, cross-functional teams.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Direct experience with&nbsp;RNA workflows, including purification, quantification, and stability testing.</li>
<li>Familiarity with&nbsp;oligonucleotide characterization&nbsp;and analytical methods.</li>
<li>Working knowledge of IPRP, AEX/IEX, and HILIC chromatography.</li>
<li>Experience with mass spectrometry for nucleic acid analysis.</li>
<li>Knowledge of lean lab practices (e.g., 5S methodology).</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>60 Minute In-Person Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.
Hourly Rate:&nbsp;$41–$43, based on education and experience
Benefits Include:
<ul>
<li>Comprehensive medical, dental, and vision coverage</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Scientist - Analytical Chemistry

Analytical Chemist-Epoxy

<h3>Job Description</h3>
Job Description
Head of Process Development MSAT Can be based in Philadephlia or Boston
Position Summary: The head of Biologics MSAT will lead the strategic and operational oversight of the Manufacturing Science and Technology function for biologics DS and/or DP manufacturing. This role is responsible for ensuring robust technology transfer, process validation, lifecycle management, and continuous improvement of biologics manufacturing processes across internal and external manufacturing global sites. The ideal candidate will bring deep technical expertise in biologics (e.g., monoclonal antibodies, ADCs, dAbs, fusion proteins), strong leadership capabilities, and a proven track record of cross-functional collaboration.
Key Responsibilities:
<ul>
<li>Lead and develop a high-performing MSAT team supporting clinical and commercial biologics manufacturing.</li>
<li>Oversee technology transfer of biologics processes from development to manufacturing, ensuring scalability, robustness, and compliance.</li>
<li>Drive global process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH).</li>
<li>Provide technical leadership for troubleshooting, deviation investigations, and CAPA implementation.</li>
<li>Partner with Quality, Regulatory, Development, and Manufacturing to ensure seamless product lifecycle management.</li>
<li>Lead initiatives for process optimization, cost reduction, and implementation of new technologies (e.g., PAT, automation, single-use systems).</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Serve as a subject matter expert during regulatory inspections and audits.</li>
<li>Develop and manage MSAT budgets, resource planning, and strategic initiatives.</li>
<li>Foster a culture of innovation, scientific excellence, and continuous improvement.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. or M.S. in Biochemical Engineering, Biotechnology, or related field; Ph.D. preferred.</li>
<li>15+ years of experience in biologics manufacturing, with at least 7 years in a leadership role within MSAT or Technical Operations.</li>
<li>Deep understanding of scale-up, upstream &amp; downstream biologics processes, tech transfers, and regulatory requirements.</li>
<li>Experience with CMO/CRO management and global manufacturing networks.</li>
<li>Demonstrated success in leading cross-functional teams and managing complex projects.</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Extensive experience in structured technical troubleshooting, RCA and CAPA effectiveness</li>
<li>Excellent communication, leadership, and strategic thinking skills.</li>
</ul>
Preferred Experience:
<ul>
<li>Experience with advanced biologics modalities (e.g., bispecifics, fusion proteins, ADCs, monoclonal antibodies).</li>
<li>Familiarity with digital tools for process monitoring and data analytics.</li>
<li>Prior experience in a fast-paced biotech or a global pharmaceutical environment.</li>
</ul>
Company DescriptionA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints. Job Responsibilities: •\tConducting Post Market Activities and Post Market Surveillance •\tManaging Customer and Product Complaint Investigation programs Education and Experience: •\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry •\tBachelor's degree •\tComputer proficiency

Head of Process Development MSAT

<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 
The Senior Scientist I will be an integral part of the Analytical Development team in the Operations – Product Development Science and Technology – Biologics division. The role involves managing all analytical aspects of biologics products at different stages of their drug development lifecycle with a focus on advancing AbbVie’s pre-clinical and early clinical programs. The individual will play a key role in analytical method development, method transfer, troubleshooting, specification setting and justification, stability studies, and regulatory filings. Collaboration with other analytical teams, quality control, bioprocess development, and R&amp;D groups is a crucial part of this role to meet business objectives and program milestones.
Responsibilities:
<ul>
<li>Execute and/or lead method development and analytical testing to support pipeline programs using analytical separation techniques including HPLC/UPLC, electrophoresis, etc.</li>
<li>May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program. Demonstrates high proficiency across a wide range of relevant technologies.</li>
<li>Partner with other groups in the Analytical Development team to provide analytical support for pipeline programs using traditional and advanced analytical techniques, including but not limited to ELISA, bioassays, mass spectrometry, biophysical, spectrophotometric and compendial methods.</li>
<li>Participate in cross-functional, multi-site meetings / projects and coordinate analytical activities that need to be supported in the Analytical Development team for pipeline programs.</li>
<li>Participate in the preparation and review of internal technical documents to ensure compliance.</li>
<li>Author regulatory submissions and provide scientifically sound responses to agency deficiency letters.</li>
<li>Evaluate and implement novel analytical techniques to expand analytical capabilities in the Analytical Development team</li>
<li>Mentor or supervise junior members in the same team.&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>PhD in Chemistry, biochemistry, biological sciences, chemical engineering or related scientific disciplines with 0-2 years relevant experience, or MS or BS with 9-12+ years relevant experience</li>
<li>Proficient in the characterization of proteins, mRNA, DNA, or various other modalities</li>
<li>Experience in analytical method development, validation, and transfer in support of biological products is preferred. &nbsp; Methods including but not limited to HPLC/UPLC, capillary electrophoresis, spectrophotometry, mass spectrometry, biophysical methods, ELISA and bioassays.</li>
<li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</li>
<li>Ability to lead and manage projects of significant scope and complexity, while meeting all deliverables and timelines.</li>
<li>Ability to effectively communicate with stakeholders and collaborate with cross-team partners.</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>

Senior Scientist, I

<h3>Job Description</h3>
Job DescriptionSalary: 
TreeFrog Therapeutics is an innovative, international biotechnology company aiming to bring cell therapies to millions of patients using our C-STEM encapsulation technology, enabling large-scale amplification of iPS and differentiated cell products for patients. Using our C-STEM format, TreeFrog is currently developing multiple cell therapy programs for disease indications including Parkinsons disease and acute liver failure. TreeFrog has also entered into a collaboration with Vertex Pharmaceuticals to incorporate C-STEM in the production of iPS-derived islets for type 1 diabetes. Our US team is newly located in our own, renovated space in Cambridgeport Labs and supports a combination of internal R&amp;D programs as well as collaborations with external partners.Find out more at our website: <a href="https://treefrog.fr" target="_blank">https://treefrog.fr</a>
 
Description of Position
We are seeking a highly motivated and detail-oriented laboratory scientist to support iPS expansion and differentiation activities at TreeFrog. This position will support internal research activities and external collaborations to grow and differentiate iPS cells within the C-STEM platform. The successful candidate will be a collaborative laboratory scientist with a passion for stem cell differentiation and a track record of hPSC differentiation and characterization experience. This position will work in collaboration with scientists across multiple teams and report directly to the cell differentiation group lead at TreeFrog, US.
 
Job Responsibilities :
<ul>
<li>Culture and differentiation of iPS in multiple 2D and 3D formats</li>
<li>Encapsulation and expansion of iPS cells in TreeFrogs C-STEM capsule technology</li>
<li>Testing and optimizing differentiation methods within the C-STEM platform</li>
<li>Routine analysis of differentiated cell products including
<ul>
<li>Flow cytometry</li>
<li>2D cytochemistry</li>
<li>3D immunocytochemistry</li>
<li>Protein analysis (ELISA, western blot, etc.)</li>
<li>RNA analysis (Real Time RT-PCR, RNAseq)</li>
</ul>
</li>
</ul>
<ul>
<li>Support method development efforts involving the C-STEM platform</li>
<li>Routine laboratory maintenance</li>
<li>Diligent record keeping and thorough electronic lab notebook practices</li>
</ul>
 
Required Skills
<ul>
<li>B.S. or equivalent in Biology or a related field</li>
<li>Previous stem cell culture and differentiation experience (industry preferred)</li>
<li>Excellent tissue culture technique and ability to maintain large number of cultures at once</li>
<li>Experience in differentiation protocol optimization and development</li>
<li>Flow cytometry sample preparation and data analysis</li>
<li>Self-motivated, independent laboratory scientist</li>
<li>Ability to work in a larger research team and communicate effectively with other team members</li>
<li>Ability to work limited weekend hours</li>
</ul>
 
TreeFrog is an Equal Opportunity Employer. We comply with all applicable national, state, and local laws governing nondiscrimination in employment, as well as the employment eligibility verification requirements of the Immigration and Nationality Act.
 All applicants must be authorized to work in the United States.

Senior Research Associate

<h3>Job Description</h3>
Embark on a Cutting-Edge Journey in Climate Risk Research with FM! Location: Norwood, MA Are you ready to dive into the thrilling world of climate science and make a tangible impact on global resilience? Join our world-class research team, where exciting technical challenges await as we tackle the pressing issues of weather and climate risks. 
About FM: 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. 
 
As a pivotal member of our research team, you will spearhead groundbreaking studies on extreme weather catastrophes. Your work will initially focus on modeling the evolving risks and impacts of phenomena such as tropical cyclones, severe convective storms, and extreme precipitation. Additionally, you'll have the chance to support regional research initiatives and contribute to our global Climate Risk &amp; Resilience activities. Key Responsibilities:
<ul>
<li>Identify, plan, and conduct innovative research projects focused on extreme weather events.</li>
<li>Develop and implement novel techniques and models to enhance risk analytics and loss prevention.</li>
<li>Collaborate with a global team of scientists across the U.S., Singapore, and Luxembourg.</li>
<li>Contribute to the development of hazard models assessing flood, wind, storms, and wildfire risks.</li>
</ul>
 
Minimum Education and experience:
<ul>
<li>MS in meteorology, data science or an adjacent field, with practical experience in the modelling of extreme weather, plus more than 3 years of professional experience with a good working knowledge of statistical/ dynamical downscaling techniques.</li>
</ul>
or
<ul>
<li>PhD in meteorology, data science or an adjacent field with a good working knowledge of statistical/ dynamical downscaling techniques.</li>
</ul>
Required Skills and Competency Areas
<ul>
<li>Project and Research Management: Proven ability to manage projects and conduct research effectively.</li>
<li>Data Handling: Proficient in collecting, processing, and analyzing large datasets.</li>
<li>Advanced Statistical Analysis: Proficiency in statistical methods, including extreme value analysis and probabilistic modeling.</li>
<li>Data Science Expertise: Strong background in data science techniques, including machine learning (ML), neural networks and artificial intelligence (AI) methods with proven experience in developing machine learning models applied to geospatial or climate data.</li>
<li>Climate Science Knowledge: Understanding of meteorological processes, particularly related to tropical cyclones, severe convective storms, synoptic-scale systems, and/ or extreme rainfall. </li>
<li>Demonstrated experience using or developing global and/or regional climate models, analyzing CMIP6 global climate model output, and combining large atmospheric datasets in various formats (including GeoTIFF, NetCDF, HDF, and GRIB).</li>
<li>Programming Skills: Experience writing shell scripts and using APIs for process automation, excellent programming skills in at least two programming languages including Python, R, Fortran, and/or Matlab.</li>
<li>Communication Skills: Excellent oral and written communication and presentation skills.</li>
<li>Teamwork: Ability to self-start and thrive within a high-performance team environment.</li>
</ul>
Desired Skills and Competency Areas
<ul>
<li>Education: PhD in meteorology or atmospheric/ climate science with a solid research record. </li>
<li>Collaborative development and High-Performance Computing: Proficiency in utilizing Linux/Unix clusters for high performance computing, along with experience in DevOps practices and cloud platforms such as AWS and Azure.</li>
<li>Effectiveness in communicating highly technical and scientific insights to non-technical audiences. </li>
<li>GIS Software: Competence in using GIS software and processing tools, including ArcGIS, QGIS, GDAL and Google Earth Engine.</li>
<li>Stochastic Modeling: Demonstrated expertise in developing and applying stochastic models to simulate natural events.</li>
</ul>
 What We Offer:
<ul>
<li>Competitive salary and comprehensive benefits package.</li>
<li>Opportunities for professional development and career growth.</li>
<li>A dynamic, inclusive work environment that fosters innovation.</li>
<li>The chance to work on impactful projects shaping the future of climate risk resilience. </li>
</ul>
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.
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