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<h3>Job Description</h3>
Job Description
Harrison Gray Search has partnered with a prominent Boston-based multi-family office and investment advisory firm.
 
Job Description
 
The Associate role reports to the Managing Director of Investment Research and works in conjunction with the Portfolio Advisory and Family Office Management groups. The successful candidate will have some knowledge of financial markets and third-party managers, including traditional and alternative investments, as well as programming and database management experience.
 
Primary Responsibilities
 
The responsibilities are equally split, focusing on core investment research and crucial engineering/automation tasks.
 
Investment Research (~50%)
<ul>
<li>Maintain, update, and QA the research and manager databases, ensuring completeness, timeliness, and integrity of documents and data.</li>
<li>Source, screen, and monitor third-party managers/funds across traditional and alternative strategies (SMAs, mutual funds, ETFs, LPs).</li>
<li>Support thematic research aligned with the firm's macro views; draft concise research notes and contribute to Due Diligence Memoranda.</li>
<li>Participate in weekly research meetings; assist Portfolio Advisory with portfolio analysis and client-facing materials.</li>
</ul>
 
Engineering, Data &amp; Automation (~50%)
<ul>
<li>Build research tools, including scripts, notebooks, and lightweight apps that automate data intake, validation, transformation, and reporting.</li>
<li>Create reusable models and analytics, including screeners, factor/peer comps, performance/attribution and risk dashboards with clear documentation and an easy UI.</li>
<li>Systematize processes and codify recurring workflows (intake to diligence to approval to monitoring) and reduce manual steps via automation.</li>
<li>Produce dashboards and templates for investment memos, DD checklists, KPI trackers, and monitoring reports.</li>
</ul>
 
Qualifications
<ul>
<li>1-3 years of experience in investment research, manager due diligence, data analytics, or a related role (buy-side, allocator, consultant, data/research engineering).</li>
<li>Strong coding ability in Python, or similar, and SQL or comparable database management skills.</li>
<li>Proficiency in Excel (advanced formulas; Power Query or VBA a plus).</li>
<li>Experience building simple tools/dashboards (e.g., Power BI/Tableau or Python-based).</li>
<li>Familiarity with APIs, CSV/XLSX/PDF ingestion, and basic data QA/validation practices.</li>
<li>Solid grasp of investment concepts (returns, risk, factor exposures, benchmark construction, fees, share classes, liquidity terms), or willingness to take the time to learn.</li>
<li>Detail-orientation, strong organization, and the ability to own projects end-to-end.</li>
<li>Ability to write and present technical topics in a clear and effective manner.</li>
<li>Exposure to alternative investments and investment diligence a plus, but not required.</li>
<li>Experience with Bloomberg, FactSet, or CapIQ a plus, but not required.</li>
<li>Basic systems architecture and cloud literacy a plus, but not required.</li>
<li>Progress or interest toward CFA or CAIA.</li>
</ul>

Associate Investment Research Analyst

<h3>Job Description</h3>
Job Description
Why Choose Editas?
At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor!
Decoding The Role:
Editas Medicine is seeking a highly motivated biomarker scientist to join our DMPK, Nonclinical Safety and Translational Sciences (DSTS) team. In this role, you would report to the Sr. Director of Bioanalytical and Biomarker Sciences and developing and executing stage-appropriate protein biomarker assays in support of translational biomarkers, non-clinical safety, and PK/PD studies. 
The ideal candidate will have strong technical skills in regulated and non-regulated LBA, PD Biomarker assays, a broad understanding of drug development, IND-enabling activities and ability to work in a matrix team structure. The individual in this role should be an independent thinker, possess a positive and team-centered mindset, and an ability to thrive in a fast-paced environment. Prior experience in gene therapy and with lipid nanoparticle based (LNP) delivery systems and/or nucleic acid therapeutics is highly preferred.
Characterizing Your Impact:
As the Senior Scientist, you will:
<ul>
<li>Establish and execute routine workflows for method development using techniques such as LBA assays (ELISA/MSD, Flow cytometry) to support PD and safety biomarker development and apply innovative solutions to solve complex problems in order to advance the pipeline.</li>
<li>Develop and execute LBA-based methods, sample analysis, data generation, and report writing for preclinical (IND-enabling) and clinical samples. </li>
<li>Develop and execute cell-based assays in support of translational in vitro studies to highlight MOA or hypothesis-driven nonclinical translational safety questions. </li>
<li>Design and execute in vitro studies to address efficacy and PD response questions aligned with our overall scientific strategy. </li>
<li>Execute protein assay strategies to characterize PK/PD, and biodistribution properties of the drug product and address key scientific questions.</li>
<li>Ensure that the data obtained is of the highest quality, and stage appropriate. </li>
<li>Write biomarker assay protocols and reports that are suitable for inclusion in registration dossiers.</li>
<li>Model behaviors of a strong leader and mentor to staff members as appropriate. </li>
<li>Establish strong partnerships across sites and across functions; Work cross-functionally within the R&amp;D organization. </li>
<li>Ensure compliance with electronic notebooks (ELN), high data integrity and company policies. </li>
</ul>
Requirements
The Ideal Transcript:
To thrive in this role, you’ll need:
<ul>
<li>PhD in pharmaceutics, medicinal chemistry, analytical chemistry, or a relevant discipline, with a minimum of 5 years of drug discovery experience; Bachelor’s/Master’s degrees with 11+ years and relevant industry experience will also be considered.</li>
<li>Extensive knowledge and experience in conducting regulated biomarker analysis using LBA techniques such as ELISA/MSD, Flow cytometry, to support discovery and development projects.</li>
<li>Demonstrated knowledge and experience in establishing biomarker methods, PK/PD for a variety of therapeutic modalities, ideally in preclinical environment.</li>
<li>Experience with primary cell cultures, patient-derived specimens, in vitro models to answer disease-relevant questions. </li>
<li>Experience with formulating and executing forward- and reverse translational questions to address clinically relevant hypothesis. </li>
<li>Experience in leading and developing strong, technical, delivery-focused teams is a plus.</li>
<li>Experience with gene editing or gene delivery technologies and lipid nanoparticle delivery is highly desired.</li>
<li>Excellent communication skills and proven ability to collaborate with interdisciplinary teams, along with exceptional scientific thinking and problem-solving skills.</li>
<li>Ability to multi-task to meet research and development goals in a fast-paced environment.</li>
</ul>
Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Salary Range: 
$150,000 - $170,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Senior Scientist, Translational Biomarkers

<h3>Job Description</h3>
Job Description
KOMAN Government Solutions, LLC (KGS), a wholly-owned 8(a) subsidiary of the Natives of Kodiak, is an Alaska Native Corporation, providing environmental investigation, remediation, munitions and explosives of concern support, operations and maintenance, long-term monitoring, and construction services to our clients.
We have an immediate need for a Senior Environmental Project Chemist to support our diverse portfolio of DoD, USEPA, other federal agencies, and private sector projects. This position can be full or part-time depending on the candidate’s availability. This is a hybrid position reporting to either our Marlborough, MA or Exton, PA office locations. However, remote candidates will also be considered.
In this leadership role, you’ll serve as principal contact to internal and external customers for all chemistry-related activities and will manage and direct all internal requests for chemistry support. You will be responsible for mentoring and oversight to our part-time data validator and to additional chemistry and data validation staff as we grow the business. You will assign work and review chemistry and data validation work products for completion and accuracy prior to client submittal. You will be responsible for managing laboratory products and determining which validation assignments may need to be subcontracted, as well as monitoring laboratory and validation subcontracts to ensure they are compliant with the project requirements.
Why Work Here?
<ul>
<li>Competitive salary with Paid Time Off and Holidays</li>
<li>Benefits selected start first of month after hire.</li>
<li>Robust benefit options: medical, vision, dental, additional life insurance, critical illness, additional hospitalization coverage, pet insurance, and identity theft offerings.</li>
<li>Company paid 1X salary life insurance, short term disability and long-term disability insurance.</li>
<li>Company match up to 4% on 401K</li>
</ul>
Typical work assignments include:
<ul>
<li>Proposal support: identify preferred environmental analytical laboratories, create requests for price proposals, and obtain competitive pricing.</li>
<li>UFP-QAPP and work plan support: prepare chemistry portion of UFP-QAPPs. Ensure that all work plans prepared by junior staff correctly identify analytical methods, preservation requirements, bottleware, and number and frequency of required QA/QC samples.</li>
<li>Resolve chemistry-related client or regulatory comments on plans and reports.</li>
<li>Laboratory procurement and coordination: Support preparation of analytical laboratory scopes of work; procurement of those laboratories; and coordination with laboratories prior to, and following, sampling events.</li>
<li>Auditing laboratory operations when needed.</li>
<li>Laboratory data report review: ensure reports meet criteria for completeness, correctness, sensitivity, and conformance with requirements. Ensure data received meets the requirements of the UFP-QAPP.</li>
<li>Data validation: follow established DoD and USEPA guidelines to determine the analytical quality of laboratory data. Ensure data validation meets the requirements of the UFP-QAPP. Review all data validation reports prepared by junior staff.</li>
<li>Database management: Follow established procedures for management of analytical data in NIRIS, various USACE chemistry databases (including FUDSChem, ERPIMS, and EDMS), and state-specific databases.</li>
<li>Implementation and monitoring of corrective action, as needed.</li>
</ul>
Required qualifications:
<ul>
<li>Bachelor of Science degree (Master’s preferred) in Chemistry or Environmental Chemistry.</li>
<li>Minimum 10 years of experience supporting federal projects.</li>
<li>Expertise in chemical data quality management of environmental analytical data, including working knowledge of industry-standard procedures for environmental data verification and data validation.</li>
<li>Working knowledge of Microsoft Office Suite and Adobe.</li>
<li>Excellent communication skills, both verbal and written.</li>
</ul>
The ideal candidate will have:
<ul>
<li>Commercial environmental analytical laboratory experience.</li>
<li>Experience with validation of data using current DoD QSM requirements for various methods including explosives, perchlorate, PFAS, PCBs, in addition to more common environmental analytical methods.</li>
<li>Experience working on DoD, USEPA, and other federal agency projects and/or state environmental/department of health agencies.</li>
<li>Experience directing and mentoring junior staff/chemists.</li>
</ul>
As a Federal Contract Employer, KOMAN Families of Companies follows Federal Laws as it pertains to drug testing. All candidates who receive a written offer of employment will be required to undergo drug testing for commonly abused controlled substances in accordance with Federal Law. It is important to note although a State may have legalized a controlled substance, if the controlled substance is illegal per Federal Law, it is then considered to be illegal. KOMAN Families of Companies is a Drug-Free Workplace. Successful completion of a background and DMV record check also must be completed prior to hire.
Preference will be given to Natives of Kodiak, Inc. Shareholders and Descendants of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i)
KGS is an Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities

Senior Environmental Chemist - Marlborough, MA

<h3>Job Description</h3>
Job DescriptionEfficient Foundation Models for Edge Intelligence
We are seeking passionate and skilled interns to join our cutting-edge research team at Mitsubishi Electric Research Laboratories (MERL), focusing on efficient and sustainable AI. This internship offers a unique opportunity to contribute to next-generation machine learning techniques that enable real-time, edge, and energy-efficient AI systems — with the ultimate goal of publishing at top-tier AI venues.
Research Focus Areas
<ul>
<li>Edge AI, real-time AI, and compact neural architectures</li>
<li>Energy-efficient and hardware-friendly AI</li>
<li>On-device, on-premise, and embedded-system AI</li>
<li>Generative and multi-modal foundation models with resource constraints</li>
</ul>
Qualifications
<ul>
<li>Advanced research experience in generative models, efficient architectures, or foundation models (LLM, VLM, LMM, FoMo)</li>
<li>Strong understanding of state-of-the-art machine learning and optimization techniques</li>
<li>Proficiency in Python and PyTorch, with familiarity in other deep learning frameworks</li>
<li>Proven research record and motivation for publication in leading AI conferences</li>
</ul>
Internship Details
<ul>
<li>Duration: Approximately 3 months</li>
<li>Start Date: Flexible</li>
<li>Objective: Conduct high-quality research leading to publications in premier AI conferences</li>
</ul>
If you are a highly motivated researcher eager to push the boundaries of efficient and sustainable AI, we encourage you to apply. Join us in shaping the future of intelligent systems that are not only powerful but also responsible and sustainable.
The pay range for this internship position will be 6-8K per month.
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL’s employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions. 
In addition to base pay, interns receive a relocation stipend, covered travel to and from MERL, and a monthly Charlie Card for local commuting. Interns are invited to participate in weekly social gatherings and professional development opportunities, including research talks by both internal and external speakers. Interns who meet the 90-day waiting period are also eligible for health insurance coverage. MERL provides immigration support for qualified candidates as needed. Employment is considered “at-will,” and the Company reserves the right to modify base salary or any other compensation program at any time, including for reasons related to individual performance, departmental or Company performance, and market conditions.

Internship - Efficient Foundation Models for Edge Intelligence

<h3>Job Description</h3>
Job Description
Job description:
<ul>
<li>
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery based in Cambridge MA.
</li>
<li>
In this role, the candidate will collaborate with multiple cross-functional teams to advance portfolio projects, with a particular emphasis on supporting in vitro data generation. 
</li>
<li>
Responsibilities include performing and adapting cell-based in vitro protocols in a timely manner across diverse cell systems, data analysis and effective communication of results, and collaboration across multiple teams. 
</li>
<li>
The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery. 
</li>
<li>
The position requires ability to work independently, demonstrate excellent technical, written and oral communication skills and work very well in a collaborative team environment.
</li>
<li>
Human colon organoid culture, passaging, and plating for experiments to support the group
</li>
<li>
Perform cell-based assays using cell lines and mammalian primary cells
</li>
<li>
Test biologic and small molecules in cell-based assays for functional readouts including cell proliferation, cytokine release, and gene expression.
</li>
<li>
Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF, qPCR)
</li>
<li>
Responsibilities may include processing animal tissue ex vivo and isolation of immune cells from human and animal tissue or blood
</li>
<li>
Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need
</li>
<li>
Maintain close communication with multiple groups to support human colon organoid cell needs
</li>
<li>
Implement and innovate new experimental protocols/techniques as needed
</li>
<li>
Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings
</li>
<li>
Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment
</li>
<li>
Impact projects mostly through lab-based activities
</li>
</ul>
Qualifications 
<ul>
<li>
Must have a bachelor's degree in Biological Science or related field with 2+ years of experience in biotech or pharma setting (industry experience)
</li>
<li>
Experience in in vitro cell culture (sterile techniques, handling challenging cell types) is required.
</li>
<li>
Experience with primary epithelial cells and human colon organoids is required.
</li>
<li>
Experience with immune cells including myeloid cells (monocytes macrophages or dendritic cells) is required.
</li>
<li>
Experience in immunoassays including multi-color flow cytometry and ELISA (or MSD, HTRF) is required.
</li>
<li>
Experience with gene expression analysis by qPCR is required
</li>
<li>
Experience with ex vivo animal tissue processing is a plus.
</li>
<li>
Ability to learn new skills and apply them in a fast-paced research environment.
</li>
<li>
Creativity, problem-solving, and attention to details.
</li>
<li>
Excellent oral and written communication and collaboration skills.
</li>
<li>
Ability to work independently as well as in a team.
</li>
<li>
Proven flexibility to deal with changing timelines and shifting work priorities.
</li>
<li>
Experience with in vitro assays with primary human immune cells (ie myeloid, PBMCs)
</li>
<li>
Experience with molecular and cellular analysis techniques including qPCR, MSD, ELISA, flow cytometry
</li>
<li>
Experience with cell-based assay development is a plus.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologist

<h3>Job Description</h3>
Job Description
Are you detail-oriented and passionate about maintaining high-quality standards in a fast-paced environment? We're looking for a fill-time Post Processing Technician I to join our team in the Processing Department. Available shifts include Monday through Friday 7:30AM - 4:00PM or Friday through Monday 7:00AM - 5:30PM. This position plays a vital role in supporting the post-processing process, ensuring compliance, and maintaining product quality from start to finish. If you're excited to work with a dedicated team in a dynamic setting, this could be the perfect opportunity for you!
As a Post Processing Technician I, you will be responsible for performing routine tasks across all processing areas, working under the guidance of the Processing Supervisor and Post Processing Technician III. Your responsibilities will include conducting green waste disposal processes, trimming batches by hand and machine, and assisting with the dry and cure processes. You'll play a role in maintaining quality control measures, ensuring batches meet product standards, and supporting inventory management by keeping accurate records. In addition, you will be expected to keep your workspaces and machinery clean, sanitized, and organized to maintain operational efficiency.
Previous experience is preferred but not required. The ideal candidate will have a keen eye for detail and the ability to focus on sensitive and complex tasks. Strong verbal and written communication skills, flexibility, and adaptability are essential to succeed in this role. You must be able to stand for extended periods, lift up to 50 lbs occasionally, and perform manual tasks requiring fine motor skills. Safety is a priority, and you will be required to maintain balance while using ladders or performing tasks such as stooping, kneeling, or reaching.
If you're ready to be part of a supportive team in an evolving environment and are excited about contributing to our post-processing process, we encourage you to apply today!

Post Processing Technician 1

<h3>Job Description</h3>
Job DescriptionJob Description: Senior Computational Biologist Department: Data Science, PIRC Reports to: Director of AI in Drug Development Job Summary: We are seeking a highly motivated and skilled Senior Computational Biologist to join our dynamic data science team. This individual will apply advanced OMICS-oriented analytical methods, statistical modeling, and ML/AI to accelerate discovery and decision-making in support of PIRC’s expanding research programs. The ideal candidate will leverage their deep expertise in computational biology, deep learning, and data-driven drug discovery to develop state-of-art solutions. This role involves close, cross-functional collaboration with Immunology, Translational Science, and Biologics teams to build sophisticated algorithms and predictive models that drive our pipeline. The Company: It’s not often you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology and oncology, with one approved product and a diversifying pipeline. We believe in the potential to improve both health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese-American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung.&nbsp; This role will be in the PharmaEssentia Innovation Research Center (PIRC), the US R&amp;D center for PharmaEssentia. As PIRC is essentially in startup mode with the full backing of PharmaEssentia HQ, this is an exciting time for PIRC and the Data Scientist will have great influence in developing and growing PIRC from the ground floor up. Key Responsibilities
<ul>
<li>Lead multi-omics data analysis across diverse datasets, including genomics, bulk and single-cell transcriptomics, proteomics, metabolomics and pathway analysis, to address critical questions in target identification, prioritization, and translational science</li>
<li>Design and implement novel computational modules and frameworks to enable seamless integration and interpretation of multi-omics data, driving insights for R&amp;D</li>
<li>Develop and apply machine learning and AI algorithms to uncover patterns and generate predictions from complex biological datasets, and accelerate target discovery and validation efforts</li>
<li>Enhance internal cross-disciplinary collaboration with project teams to align computational strategies with project goals and ensure robust biological interpretation of data</li>
<li>Establish best practices for data management, quality control, and reproducibility in bioinformatics pipelines, and create intuitive visualizations and detail-oriented reports to communicate findings with stakeholders, enabling data-driven decision-making&nbsp;</li>
<li>Continuously evaluate and adopt cutting-edge computational tools, algorithms and technologies to stay at the forefront of the field and enhance data analysis capabilities</li>
<li>Contribute to the strategic planning of computational/AI initiatives, influencing the direction of research programs and technological investments</li>
<li>Contribute to scientific publications, conference presentations, showcasing advancements in bioinformatics and AI, and their impact on drug discovery and translational research</li>
</ul>
 Qualifications
<ul>
<li>Ph.D. in Bioinformatics, Computational Biology, Computer Science or relevant quantitative discipline</li>
<li>At least 3-years work experience in combining bioinformatics/computational biology analysis and cutting-edge computational approaches (including ML/AI) for project support in cross-functional biotech or pharma setting.&nbsp;</li>
<li>Expertise in multi-omics data analysis and result interpretation (genomics, transcriptomics and scRNASeq are must, spatial omics and image are plus)</li>
<li>Proficiency in Python and R, familiarity with database management</li>
<li>A strong understanding of the drug discovery and development, including target identification, lead optimization, translational research, and early clinical development</li>
<li>Experience in a therapeutic area relevant to oncology and immunology</li>
<li>Working knowledge of traditional machine learning algorithms, Deep learning frameworks and LLM, and their applications in drug discovery</li>
</ul>
 EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Senior Computational Biologist

<h3>Job Description</h3>
Job Description
Seeking Senior Summer Camp counselor in Groton Ma. Prefer school teacher.&nbsp; Requires 3 years experience. 8am-4pm M-F. Must be creative, great problem solver, can "think on the go" and work with little direct supervision.&nbsp; Able to lead other counselors.&nbsp; Must be very well organized.&nbsp; Duties include creative planning for the day/week.&nbsp; Excellent compensation with bonuses.

Senior Summer Camp Counselor

<h3>Job Description</h3>
Job Description
Engineer Science into Impact
At EmergingDx Inc, we are reimagining diagnostics at the edge of science, engineering, and innovation. As an institution for integrated innovation, we fuse biology, technology, and systems design to build transformative diagnostic tools that improve human health and empower clinicians, patients, and communities.
We’re looking for an In Vitro Diagnostics (IVD) Scientist/Engineer to join our mission-driven team. You’ll help architect, prototype, and validate next-generation diagnostic platforms—from rapid point-of-care assays to integrated microfluidic systems for disease monitoring and early detection.
This role is ideal for someone who thrives at the intersection of biological insight and engineering ingenuity, and who wants to shape the future of healthcare from the bench to the field.
&nbsp;
Responsibilities (What You’ll Do)
<ul>
<li>Design, develop, and optimize IVD assays (immunoassays, molecular diagnostics, or clinical chemistry) for lab-on-chip and point-of-care platforms</li>
<li>Collaborate with cross-functional teams to integrate biological assays with microfluidic, optical, and electronic systems</li>
<li>Lead analytical validation studies including sensitivity, specificity, reproducibility, and regulatory performance metrics</li>
<li>Prototype, test, and troubleshoot diagnostic systems across wet lab and hardware environments</li>
<li>Contribute to product development processes including documentation, risk analysis, quality systems (ISO 13485), and FDA regulatory pathways</li>
<li>Apply systems thinking to challenges in sample preparation, biomarker detection, signal amplification, and data analysis</li>
<li>Effectively communicate results and technical insights to clients and stakeholders through both written reports and oral presentations</li>
<li>Develop and manage fast-paced project timelines while proactively identifying and mitigating risks</li>
<li>Stay current on scientific literature, emerging technologies, and clinical needs in diagnostics</li>
<li>Craft and deliver clear, compelling narratives—both written and oral—conveying technical project progress and proposed initiatives</li>
</ul>
&nbsp;
Qualifications (What You Bring)
<ul>
<li>PhD in Bioengineering, Molecular Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or related field</li>
<li>7+ years of experience in vitro diagnostics, medical devices, genetics, microbiology, synthetic biology, translational research</li>
<li>Strong knowledge of assay formats: ELISA, lateral flow, qPCR, CRISPR-based diagnostics, isothermal amplification, or electrochemical detection</li>
<li>Experience with fluidic handling systems (manual and automated), sample matrices (blood, saliva, urine), and surface functionalization</li>
<li>Familiarity with data acquisition and analysis, including use of MATLAB, Python, or other statistical tools</li>
<li>Comfortable working across disciplines with engineers, designers, and clinicians</li>
<li>Adaptability in fast-paced environments</li>
<li>Detail-oriented, systems-focused, and passionate about delivering health impact through innovation</li>
<li>Proven track record of leading R&amp;D programs to deliver innovative, high-quality outcomes on schedule, aligned with stakeholder expectations and technical goals</li>
<li>Excellent verbal and written communication skills</li>
<li>Bonus: Experience in microfabrication, biosensor integration, point-of-care regulatory submissions, or multiplexed assay development</li>
</ul>
&nbsp;
Why EmergingDx
<ul>
<li>You’ll work on products, platforms, and ventures — not just features</li>
<li>You’ll gain ownership, mentorship, and momentum</li>
<li>You’ll be part of something bigger: a community shaping what’s next</li>
<li>We offer a competitive salary with full benefits package.</li>
</ul>
Ready to redefine diagnostics? Send your resume to <a href="mailto:careers@emergingdx.com" target="_blank">careers@emergingdx.com</a>
Subject: In Vitro Diagnostics Scientist/Engineer – [Your Name]
Due to the nature of our business and information associated with this position, interested candidates must be US Citizens or Permanent Resident.
&nbsp;
At EmergingDx Inc, we are proud to be an Equal Opportunity Employer committed to building and sustaining a talented, inclusive, and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, marital status, national origin, age, veteran status, disability, or any other legally protected status.
Note to recruiters: We are not seeking assistance for this position. Please do not contact us via phone or email regarding this opening.
As a U.S. Government contractor, we are required to collect certain applicant information for federal reporting purposes.

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