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<h3>Job Description</h3>
Job Description&nbsp;Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect.&nbsp; Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook.&nbsp; &nbsp;
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YmFHsmtNfV

Research Associate I/II/III

<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>
Job Description
Nanobiosym is on the cusp of rewriting the rules of personalized medicine, novel technologies, and healthcare delivery. Founded by a renowned MIT and Harvard trained Physician and Physicist, Nanobiosym's innovative pipeline of products leverage novel advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple other prestigious peer-reviewed funding awards, Nanobiosym is currently adding to its talented team as it expands into a global commercial enterprise.
Nanobiosym is currently seeking a talented research associate with molecular biology experience, to help test our new novel technologies. This role will include a combination of data acquisition, data analysis, statistics and troubleshooting, and the development of testing procedures.
DUTIES
<ul>
<li>Perform novel technology testing, maintain laboratory records, and prepare reports.</li>
<li>Define strategy for testing and optimization.</li>
<li>Create and champion new internal processes of testing, data collection, data acquisition, and data analysis</li>
<li>Expertise with excel and statistics</li>
<li>Exercise technical judgment on test requirements, developing recommendations and translating into course of action</li>
</ul>
QUALIFICATIONS
<ul>
<li>BS degree in Biology, MS in Molecular Biology Preferred, bioinformatics, biostatistics </li>
<li>Prefer 2-5 years of academic or industry experience in molecular biology</li>
<li>Experience in qPCR or PCR preferred but not required</li>
<li>Experience working in a BSL-2 or BSL-2+ facility preferred but not required</li>
<li>Experience working in an ISO 13485 environment, and a working knowledge of ISO documentation &amp; QSR requirements preferred but not required</li>
<li>Experience testing and/or developing life sciences products, including meticulous laboratory notebook skills</li>
<li>Must have an understanding of principles of statistics relevant to product testing</li>
<li>Must have an understanding of failure mode and root cause analysis</li>
<li>Prefer experience working in fast-paced startup environments</li>
<li>Prefer experience with automation tools (i.e., run automation scripts, analyze reports and issues, report bugs)</li>
</ul>
Personal Qualities
<ul>
<li>You are passionate about testing, quality assurance, healthcare, and technology</li>
<li>You are highly organized</li>
<li>You are methodical, detail oriented and effective at time management</li>
<li>You are a self-starter</li>
<li>You have good interpersonal, verbal communication, and documentation skills</li>
<li>You can function well in a challenging and fast-paced environment</li>
<li>You are enthusiastic and positive, with strong skills in the areas of dependability, flexibility, and maturity</li>
</ul>
 Job Posted by ApplicantPro

Sr. Research Associate, Molecular Biology

<h3>Job Description</h3>
Job DescriptionTitle: Research Associate, Antibody &amp; Protein Engineering
 Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 75 have entered clinical trials.&nbsp;&nbsp;
Role Overview: We are seeking a focused and enthusiastic protein engineer to join our Platform Technologies group. In this role, the Research Associate will work in a small, collaborative team to execute Adimab’s platform for the discovery, optimization and characterization of protein-based therapeutics.
Responsibilities:&nbsp;
<ul>
<li>Designing and executing protein engineering experiments</li>
<li>Constructing yeast display libraries and performing FACS selections</li>
<li>Basic protein/DNA sequence and structural analysis</li>
<li>Basic yeast handling and propagation</li>
<li>Collecting, organizing, and analyzing antibody characterization data</li>
<li>Collaborating with colleagues and external partners &nbsp;</li>
</ul>
Needed Upon Hire:
<ul>
<li>B.S., or equivalent practical experience, with training in molecular biology, chemical engineering, or biochemistry</li>
<li>At least 2 years of lab experience in an academic or industry setting&nbsp;</li>
<li>Knowledge of molecular biology, protein engineering, structural biology, and/or flow cytometry</li>
<li>Meticulous approach to benchwork and data analysis &nbsp;</li>
</ul>
Value-added Experience:
<ul>
<li>Experience with protein display technologies (yeast, bacterial and/or ribosomal) desired</li>
<li>Knowledge of protein sequence analysis and next-generation sequencing workflows desired</li>
<li>Experience with protein structural analysis or computational design methods desired</li>
<li>Demonstrated ability to evaluate, interpret, and present scientific data</li>
<li>Internally motivated with proven track record of operating independently at the bench and bringing projects to completion</li>
<li>Excellent organization skills and the ability to manage multiple projects simultaneously</li>
<li>Adaptable and productive in a fast-paced environment</li>
<li>Communicates effectively and openly with colleagues and supervisors</li>
<li>Resourceful with outstanding execution and problem-solving skills</li>
<li>Excellent quantitative skills with a mastery of Excel</li>
</ul>
 Come join us! Our integrated antibody discovery and engineering platform provides unprecedented speed from antigen to purified, full-length human IgGs with exquisite specificity and biophysical behavior. We offer&nbsp;fundamental advantages by delivering diverse panels of antibodies that meet the most demanding standards for affinity, epitope specificity, species cross-reactivity, and developability. We enable our partners to rapidly expand their biologics pipelines through a broad spectrum of technology access arrangements.
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people. We offer individually tailored compensation packages comprised of a competitive salary, meaningful equity, a 2:1 401(k) match, and comprehensive health care benefits.
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the Dartmouth Hitchcock Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, kayaking, and biking.
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DXNnB27kEy

Research Associate, Antibody & Protein Engineering

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face.
About Fapon Biotech
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
We are seeking a scientific contributor to develop validated analytical assays for LNP and drug product characterization. This role will be responsible for designing, developing and validating analytical assays for a targeted LNP drug product to support the platform and pipeline development. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams and provide analytical support to the discovery and PD teams. The ideal candidate is a sciences major with strong exposure to analytical techniques and who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
<ul>
<li>Designing, developing and validating analytical assays for LNP and targeted LNP drug product characterization</li>
<li>Develop assays for LNPs including lipid raw material QC, composition assessment, Lipid/cargo profiling and LNP/tLNP characterization using HPLC (SEC, Reverse Phase), fluorescence-based methods and other analytical techniques</li>
<li>Work with cross-functional groups including LNP discovery, PD and CMC team to support needs of analytical method development, characterization, and transfer</li>
<li>Perform CRO outreach including experimental planning, work coordination and data interpretation for as analytical SME</li>
<li>Support technology transfer to Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed)</li>
<li>Author technical documents, including SOPs for analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in life sciences, pharmaceutical sciences, or related field, preferably with 7/5 years of relevant experience. The title will be commensurate with experience.</li>
<li>Hands on experience developing analytical methods for complex biological therapeutics</li>
<li>Prior experience in developing analytical methods for LNP characterization is a must and will be key for this role</li>
<li>Knowledge of ICH/USP guidelines</li>
<li>Experience in analytical methods with HPLC (IPRP, SEC, IEx), UV-vis, colorimetric and fluorescence-based</li>
<li>Must be eligible to work in the United States</li>
</ul>
&nbsp; Preferred Qualifications:
<ul>
<li>Experience in developing validated analytical assays</li>
<li>Experience in advanced analytical methods for LNP characterization such as LC-MS, MALS, SEC-MALS etc</li>
<li>Strong communication skills and ability to present complex technical topics to diverse audiences with varying technical depth.</li>
<li>Strong collaborative instinct with good time and resource management skills to match the fast-paced start-up work culture.</li>
<li>Able to collaborate on and execute multiple parallel studies</li>
</ul>
 Additional Information 
What We Offer:
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior/Principal Research Associate (LNP Analytics)

<h3>Job Description</h3>
Job Description
Nanopath is a well-funded Series A-stage company working to develop a first-in-class in vitro diagnostics platform to revolutionize the way we diagnose disease. Nanopath works to disrupt existing lengthy molecular testing methodologies by bringing them closer to the patient. We aim to improve the lives of patients, starting with women, using our purpose-built tool that provides actionable information within a single office visit.
The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. As a company, we are committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social - is at the forefront of our decision making.
About the Role
<ul>
<li>Support and manage a variety of assay development tasks. We are happy to tailor key responsibilities to the candidate ranging from molecular biology, cell culture, biomanufacturing, and bioinformatics. </li>
<li>Participate in critical team discussions, meetings, and presentations. Our co-ops are given critical and important projects!</li>
<li>Work directly with our tight-knit team of scientists and engineers to drive our product forward.</li>
<li>Learn more about cutting edge biophysics and interdisciplinary medtech development.</li>
</ul>
Qualifications:
<ul>
<li>Ability to commit to 15+ weeks of full-time and onsite work in Cambridge, MA</li>
<li>Sophomore or above with demonstrated experience through past internships or research projects</li>
<li>Excellent communication and presentation skills, highly organized with demonstrated curiosity, scientific rigor and creative problem-solving</li>
<li>Proactive self-starter with eagerness to adapt to a fast-paced, dynamic startup environment</li>
<li>Passion for technology translation and willingness to shape Nanopath's future</li>
<li>Current enrollment in a relevant academic program - we are open to undergraduate and graduate degree opportunities</li>
</ul>
This is a full-time onsite role in Cambridge, MA starting in early January, lasting no less than 5 months.
Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles!
Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

Research Associate Co-op (January '26 Start)

<h3>Job Description</h3>
Job DescriptionRole Overview
We're looking for a Director of Research &amp; Development to lead the modernization and expansion of our software products for the alternative financial services industry. This is a hands-on leadership role that merges software engineering expertise with forward-thinking AI integration and rapid product innovation.
As Director of R&amp;D, you will manage a talented engineering team and collaborate closely with our Product Manager and Operations teams. You’ll take ownership of delivering modern, scalable software—while embedding cutting-edge AI technologies into our workflows, user experience, and development process.
What You'll Do
Full-Stack Leadership
<ul>
<li>Take technical ownership across the entire stack: APIs, databases, cloud infrastructure, CI/CD, frontend apps, and internal tools.</li>
<li>Promote best practices in testing, observability, documentation, and code quality.</li>
<li>Ensure platform reliability and performance across services, products, and AI components.</li>
</ul>
Team Management &amp; Mentorship
<ul>
<li>Lead and grow a cross-functional engineering team with a strong culture of innovation, delivery, and continuous learning.</li>
<li>Mentor developers in AI-assisted development tools (e.g., GitHub Copilot, Cursor) and encourage experimentation to increase team productivity.</li>
<li>Support individual and team performance through feedback, pairing, code reviews, and professional development.</li>
</ul>
AI-Driven Innovation &amp; Product Development
<ul>
<li>Design, build, and deploy AI-powered features across the platform—including agent-based workflows, retrieval-augmented generation (RAG), predictive tools, and automated decision systems.</li>
<li>Drive the rapid prototyping of new features, turning ideas into working proof-of-concepts in days and production-ready tools in weeks.</li>
<li>Apply LLMs and AI orchestration frameworks (e.g., LangChain, LlamaIndex) to real-world problems like compliance automation, document analysis, and fraud prevention.</li>
<li>Lead platform modernization by refactoring legacy components and building scalable cloud-native services.</li>
</ul>
Cross-Functional Execution
<ul>
<li>Work in close partnership with Product Management and Operations to align development work with customer needs and business priorities.</li>
<li>Communicate technical vision and architectural decisions across departments.</li>
</ul>
<ul>
<li>Bring a pragmatic approach to balancing innovation, speed, and technical debt</li>
</ul>
What You Bring
<ul>
<li>5+ years of experience leading software engineering or R&amp;D teams, ideally in SaaS or fintech environments.</li>
<li>Proven success delivering production-ready, customer-facing software across the full stack—from backend services to web frontends.</li>
<li>Strong architectural skills and comfort with modern cloud platforms (AWS, Azure) and DevOps workflows.</li>
<li>Experience applying AI or automation tools to enhance product features or streamline development workflows.</li>
<li>Familiarity with emerging AI/LLM frameworks (e.g., LangChain, LlamaIndex) and enthusiasm for exploring how they can support product innovation.</li>
<li>A track record of rapid iteration: launching prototypes quickly, gathering feedback, and refining based on real-world use.</li>
<li>A leadership style grounded in mentorship, collaboration, and elevating team performance.</li>
</ul>
<ul>
<li>Strong communication and project management skills—able to align cross-functional stakeholders and keep teams focused</li>
</ul>
Bonus Points
<ul>
<li>Experience revamping or re-platforming legacy systems into modern microservice or serverless architectures.</li>
<li>Understanding of compliance and regulatory demands in financial software or MSBs.</li>
<li>Background in intelligent automation, ML ops, or AI infrastructure.</li>
</ul>
Why This Role Matters
This role is central to how we design, build, and scale our software platform. As Director of R&amp;D, you’ll lead the engineering team responsible for delivering the features, systems, and tools that power our products and support our customers. Your work will directly influence product quality, development velocity, and the overall experience we deliver to the financial services industry.
From modernizing core systems to guiding the next phase of platform growth, your leadership will shape the future of our technology and the success of the teams behind it.

Director of Research & Development

<h3>Job Description</h3>
Job Description
Job Title: Molecular and Cellular Biologist
Duration: 6 months
Location: Cambridge, MA 02139
We are seeking a scientist to join our Systems Immunology Lab in Client’s Inflammation &amp; Immunology Research Unit. The successful candidate will be responsible for generating massive single-cell perturbational data using functional genomics and single cell transcriptomics technologies in collaboration with a small team.
Position Responsibilities: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Generate custom lentiviral libraries and maintain extensive cell cultures. Generate edited pools of cells via lentiviral transduction and arrayed electroporation. Generate single-cell data via several commercial workflows, including from 10x Genomics. Develop, modify, and customize such procedures as needed to succeed in specific cell lines and types, and at large scale.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Reports to a lead scientist in Systems Immunology Lab. Collaborates with and supports several multi-disciplinary experimental teams on a per-project basis.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Education and Experience: Bachelors or Masters + 3 years of experience in Biology, Immunology or a related field
Description:
<ul>
<li>3+ years of hands-on experience with standard cell culture techniques including primary immune cells handling and isolation, maintenance of cell lines and in vitro stimulation of primary immune cells, experience with standard molecular biology techniques including lentivirus infection, qPCR, western blot, and flow cytometry.</li>
<li>Bonus: direct experience in pooled cell screening of immune cells using CRISPRi, CRISPRa, and other methods of in vitro gene editing.</li>
</ul>
Hard Skills:
<ol>
<li>Diverse Cell Types</li>
<li>2. Molecular biology techniques *qPCR</li>
<li>3. Gene Editing</li>
</ol>
Preferred:
Direct experience in pooled cell screening of immune cells using CRISPRi, CRISPRa, and other methods of in vitro gene editing.
Interview Process: 2 Rounds, Video &amp; In person
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Molecular and Cellular Biologist

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Senior Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design, troubleshoot, and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the VP of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a junior scientist with prior industry experience and&nbsp;self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
3-6 years of prior industry R&amp;D experience (not academic lab or QC/manufacturing)&nbsp;
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: onsite presence, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>
Execute experiments in cell line development and characterization with supervision.
</li>
<li>
Extensive cell culture work - both directly and through coordination with the automation sub-team.
</li>
<li>
Perform data acquisition and analysis in a timely manner.
</li>
<li>
Assist in experimental designs, data interpretation and troubleshooting.
</li>
<li>
Document work appropriately in lab notebooks, reports and presentations.
</li>
<li>
Assist with lab operations and continuous improvement activities.
</li>
<li>
Team collaborates closely with other teams, such as Analytical Development, the Genomics Research Center, and Cell Culture Development.
</li>
</ul>
Minimum Qualifications:
<ul>
<li>
Must have completed Bachelor's degree in Biosciences or related field
</li>
<li>
Extensive experience with aseptic technique and mammalian cell culture
</li>
<li>
Microsoft software: Word, Excel, PowerPoint, Outlook
</li>
<li>
Proven track record of teamwork, adaptability, initiative, and integrity
</li>
<li>
Excellent interpersonal and both written &amp; oral communication in English
</li>
<li>
Strong Attention to Detail; Proactive; Fast learner
</li>
</ul>
Preferred Requirements
<ul>
<li>
Experience with Flow Cytometry (e.g., analysis, compensation, sorting)
</li>
<li>
Experience with Molecular Biology (e.g., recombinant DNA, vector construction, PCR, NGS)
</li>
<li>
Experience with Electronic Lab Notebook system (ELN)
</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.

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