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<h3>Job Description</h3>
Job Description
Nanobiosym is an innovative nanotechnology company in Cambridge, MA, developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. Nanobiosym was awarded the 2013 X-PRIZE- the first X-PRIZE ever awarded for healthcare.
DUTIES
<ul>
<li>Lead molecular diagnostic assay development in a hands-on manner through successful FDA submission</li>
<li>Manage and contribute to regulatory documents</li>
<li>Project management; personnel management skills preferred</li>
<li>Design assay performance specifications</li>
<li>Ensure assay development process meets milestones and timelines</li>
<li>Troubleshoot and solve technical issues</li>
<li>Maintain compliant laboratory documents and procedures</li>
<li>Pro-actively improve efficiency, quality and effectiveness of R &amp; D efforts</li>
</ul>
QUALIFICATIONS
<ul>
<li>PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field</li>
<li>Minimum of 7 years of relevant industry experience and IVD assay development</li>
<li>In depth knowledge and hands on experience with qPCR, sequencing and standard molecular biology techniques</li>
<li>Demonstrated technical, managerial and leadership expertise in assay development</li>
<li>Strong understanding of FDA and global regulatory requirements</li>
<li>Prefer commercial assay experience</li>
<li>Demonstrated experience and understanding of quality systems (e.g., GLP, ISO, etc.)</li>
<li>Prefer experience working in BSL-2 laboratory facilities</li>
<li>Strong work ethic and ability to generate high quality work under tight deadlines</li>
<li>Flexibility in work schedule</li>
<li>Self-motivated, independent and a driving force of efficient execution</li>
<li>Strong organizational and project management skills</li>
<li>Excellent oral and written communication skills</li>
</ul>
 Job Posted by ApplicantPro

Senior Scientist: IVD Assay Developer

<h3>Job Description</h3>
Job Description
Location: Manchester, NH
Job Type: Full-time
Job Title: Senior Lab Personnel Specialist - PCR &amp; NGS
Salary: $110,00 - $140,000 annually
Shift: Day, Monday - Friday
About the Role:
We are seeking a driven, experienced, and detail-oriented Senior Lab Personnel Specialist to join our innovative genetics lab team. Our lab is dedicated to accelerating the diagnosis of numerous genetic diseases through leading-edge genetic sequencing technologies. In this key role, you will provide advanced technical expertise and mentorship across cutting-edge projects involving PCR and Next Generation Sequencing (NGS). You will help lead lab operations, balancing the execution of CLIA-validated tests for routine diagnostic workflows with the development and optimization of new sequencing technologies and molecular assays that drive our mission forward. Tasks will include a combination of hands-on assay execution and technician supervision, all while demonstrating a devotion to total quality and continuous improvement.
Key Responsibilities:
- Perform, oversee, and troubleshoot complex molecular workflows for both diagnostic and research projects, including PCR assay design, optimization, validation, and routine testing, with a mix of hands-on execution and supervision of lab technicians.
- Conduct and supervise Next Generation Sequencing (NGS) sample preparation, library construction, sequencing runs, and data analysis, ensuring seamless integration between CLIA-validated diagnostic tests and innovative technology development while directly executing assays and guiding team members.
- Act as a technical lead and resource for troubleshooting PCR and NGS protocols, instrumentation, software tools, and bioinformatics pipelines.
- Train and mentor lab personnel on advanced molecular techniques, experimental design, SOPs, best practices, and emerging genetic sequencing technologies, including direct supervision during hands-on assay performance.
- Support cross-functional teams by providing input on experimental design, assay development, data interpretation, and the execution of CLIA-validated tests to ensure accurate and timely genetic disease diagnoses.
- Review, analyze, and interpret sequencing results to guarantee accuracy, validity, and compliance with regulatory standards.
- Draft, review, and update SOPs, work instructions, and protocols in line with internal quality standards, industry best practices, and regulatory requirements (e.g., CLIA, CAP), emphasizing continuous improvement and total quality management.
- Ensure rigorous quality control, compliance with lab safety, research integrity guidelines, and GLP in a combined diagnostic and R&amp;D setting, with a commitment to ongoing process enhancements.
- Collaborate with scientists, bioinformaticians, and project managers to meet timelines, share findings, drive innovation, and accelerate genetic disease diagnostics.
- Maintain and troubleshoot lab instrumentation, ensuring calibration, preventative maintenance, and proper documentation.
- Contribute to process improvements, new method development, and continuous learning within the lab team, with a focus on advancing sequencing technologies for genetic applications and upholding devotion to total quality.
-Ensuring the laboratory takes remedial action when test systems deviate from the laboratory's established performance specifications
- Assuring patient test results aren't reported until all corrective actions have been taken and the test system functions properly
- Making sure that all testing personnel receive orientation and training.
- Evaluating and documenting the competency of all testing personnel
Qualifications:
- Bachelor's degree in Molecular Biology, Genetics, Biotechnology, or a related life sciences field required; Master's degree preferred.
- Certification as a Molecular Biology Technologist (MB) or equivalent (ASCP or similar) strongly preferred.
- 4+ years of hands-on experience in a molecular biology lab environment, with significant expertise in PCR and NGS workflows, including both R&amp;D and diagnostic settings.
- Direct experience working with NGS platforms (e.g., Illumina, Oxford Nanopore, PacBio, or Thermo Fisher) and associated bioinformatics tools and pipelines.
- Strong grasp of molecular assay development, troubleshooting, optimization, validation processes, and the execution of CLIA-validated tests.
- Familiarity with data analysis software, bioinformatics for NGS data, and regulatory guidelines (e.g., CLIA, CAP) is highly desirable.
- Proven leadership and training abilities with strong communication, collaborative, and problem-solving skills, including experience in technician supervision.
- Demonstrated ability to work independently, manage multiple projects simultaneously, and adapt to evolving priorities in a fast-paced genetics lab.
- Knowledge of good laboratory practices (GLP), research integrity standards, and lab safety requirements.
Why Join Us:
- Be part of a dynamic and collaborative genetics lab environment tackling challenging and impactful questions in genetic disease diagnosis, with a strong devotion to total quality and continuous improvement.
- Work with state-of-the-art molecular technologies and contribute to the development of innovative sequencing solutions that accelerate diagnoses.
- Competitive salary and comprehensive benefits package.
- Ample opportunities for growth, skill development, scientific contribution, and professional advancement.
About us:
At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 18 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.
It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities.
If at any time during the application process, you need an accommodation, please contact <a href="mailto:recruiting@lighthouselabservices.com" target="_blank">recruiting@lighthouselabservices.com</a> for assistance.
Lighthouse Lab Services | 844-974-1929 | lighthouselabservices.com
#LLS2

?Senior Lab Personnel Specialist - PCR & NGS

<h3>Job Description</h3>
Job Description
Biocytogen Boston Corp is seeking a highly motivated and versatile Pharmacology Scientist to support both in vivo and in vitro preclinical research services in the fields of immunology, immuno-oncology, metabolic disease and neurology. This role is ideal for candidates with broad expertise in pharmacological studies, disease model development, and cell-based assays, who are passionate about evaluating novel therapeutic agents for clients. 
The successful candidate will be a critical member of our fast-paced and expanding CRO team, actively engaging in both hands-on experimental work and strategic project management to support biotech and pharmaceutical partners
Key Responsibilities
In Vivo Pharmacology
<ul>
<li>Design and develop animal models, execute in vivo experiments to evaluate the biological efficacy of novel therapeutic agents.</li>
<li>Independently lead in vivo service projects and preclinical studies, acting as Project Manager or Study Director.</li>
<li>Perform animal handling, tumor inoculation, drug administration via multiple routes, blood and tissue collection, tumor measurements, and PK/PD studies.</li>
<li>Design and execute internal model-building projects and characterize various humanized mouse models.</li>
<li>Provide troubleshooting support and technical guidance to junior associates.</li>
<li>Collaborate closely with the BD/Sales team for client project planning and technical discussions.</li>
<li>Present project results to clients and internal stakeholders; prepare scientific reports and summaries.</li>
<li>Mentor and facilitate the growth of junior research associates.</li>
</ul>
In Vitro and Ex Vivo Pharmacology
<ul>
<li>Independently develop, validate, and perform a broad range of in vitro and ex vivo assays including:</li>
<ul>
<li>Immune cell profiling from blood and tissues.</li>
<li>Functional assays using primary cells (T cells, NK cells, macrophages).</li>
<li>Cytokine profiling, cytotoxicity, and apoptosis assays.</li>
</ul>
<li>Develop new assay technologies by researching scientific literature and adapting methodologies from collaborations and other internal teams.</li>
<li>Perform flow cytometry (FACS), ELISA, Western blot, qRT-PCR, and multiplex cytokine analyses.</li>
<li>Contribute to the design and support of in vivo pharmacology studies from an in vitro perspective.</li>
<li>Present research findings at internal meetings and contribute to external scientific discussions.</li>
</ul>
Requirements
<ul>
<li>PhD in pharmacology, immunology, cancer biology, or related biomedical field.</li>
<li>Extensive hands-on experience in animal models and preclinical in vivo pharmacology.</li>
<li>Proven skills in cell-based immunological assays including T cell activation, NK cell-mediated cytotoxicity, and macrophage functional assays.</li>
<li>Proficiency in PK/PD model establishment and analysis.</li>
<li>Expertise in flow cytometry, cytokine profiling (ELISA, qRT-PCR, multiplex assays), and immune cell isolation from tissues.</li>
<li>Experience with surgical procedures in rodents is highly desirable </li>
<li>Cross-functional knowledge across therapeutic areas is a plus.</li>
<li>Strong communication, organizational, and team collaboration skills with the ability to prioritize in a fast-paced environment.</li>
<li>Demonstrated ability to independently manage projects and work with cross-functional teams.</li>
</ul>
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>
BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Scientist/Senior Scientist for Pharmacology

<h3>Job Description</h3>
Job DescriptionPrincipal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. &nbsp;The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond.&nbsp; You will also drive translational and early clinical activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms, including indication expansion and novel combinations. &nbsp;To this end, you will work cross-functionally with clinical development, clinical operations, regulatory affairs as well as with academic investigators and clinical CROs to explore new applications for BESREMi.&nbsp; Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. The Company: It’s not often that 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, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the 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. Our new research center, PharmaEssentia Innovation Research Center (PIRC), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities: &nbsp;
<ul>
<li>Further Exploration of BESREMi: Collaborate with clinical development to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally or externally via CROs, and drive investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi. </li>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. &nbsp;Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, clinical operations and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration. </li>
<li>Regulatory Interaction: Work with regulatory affairs and CROs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, biologics license applications (BLA), and marketing authorization applications (MAA). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
</ul>
 Qualifications: &nbsp;
<ul>
<li>M.D or Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>8+ years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via CROs and academic collaborations. </li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism-of-action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials. </li>
<li>Experience working closely with academic collaborators and managing all aspects of sponsored research agreements or IITs.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
 Conclusion: As a Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward, maximizing the potential of BESREMi and ultimately improving patient outcomes at PIRC. 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.
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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SymhRGPsqz

Principal Scientist, Translational Sciences

<h3>Job Description</h3>
Job DescriptionSalary: 
A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline.
AIS is looking for a Jr. Sea Turtle Research Ecologist to participate in data collection for the Sea Turtle Ecology research program. This position is part of a contract opportunity we are currently bidding on.
 
Primary Function:
NOAA fisheries evaluate the status of sea turtle populations within the Greater Atlantic Region of the Northwest Atlantic Ocean. This program assesses the current and anticipated population dynamics of these species, as well as their ecology, distribution, occurrence, health, and habitat usage. 
 
Duties/Responsibilities:
<ul>
<li>Preparation for field work and de-staging</li>
<li>Participate in data collection for land-based or at-sea field research programs</li>
<li>Take photos of species that are able to positively identify sea turtles and other marine species</li>
<li>Interacting with live turtles or turtle carcasses</li>
<li>Record/edit data collected at sea and maintain databases and equipment</li>
<li>Pursue, handle, collect physical measurements (i.e. carapace lengths and width), collect samples, and apply tags to live turtles. Be able to collect physical measurements, tag, and necropsy dead turtles. This includes collecting the following counts/surveys: epibiota removal, laparoscopy, cloacal, gastric lavage, measure, monitor vitals, photograph/video, blood, fecal material, scutes, skin, ultrasound, and weight</li>
<li>Participate in small boat operations deployed from land or sea</li>
<li>Complete project reports</li>
</ul>
 
Compensation: Candidates will be paid an hourly rate to be negotiated, and total compensation will vary depending on the candidates depth of experience. This is a fulltime position. AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.
Minimum Qualifications:
<ul>
<li>Bachelor's Degree in one of the biological sciences and more than 3 months of experience with the tasks listed above.</li>
<li>Have excellent communication skills, both verbal and written (including visual presentations) that may target a variety of audiences including technical, scientific, and the general public, as appropriate.</li>
<li>Have previous experience working as an effective member of a team; adapting to quickly changing priorities and strict timelines; and exhibiting self-motivation to complete assigned tasks; strong time management skills; the ability to work both independently and as part of a team, strong management skills, and attention to detail</li>
<li>Shall have all necessary medical clearance and required safety training certificates before research activities</li>
<li>Shall have corrected 20/20 vision when position is a visual observer</li>
<li>Shall have capability to work outside, including on a small boat, for periods of up to 12 hours at a time</li>
<li>Be able to safely lift 40 lbs. on a rolling vessel</li>
<li>Willingness and ability to work far from home (including far from land) for weeks at a time</li>
<li>Meet the requirements listed under NOAA Small Boat Requirements</li>
</ul>
Preferred Qualifications:
<ul>
<li>At least one (1) year of experience successfully performing the above tasks, or a Masters degree in relevant field.</li>
<li>Demonstrated proficiency with Oracle, R, and R shiny is also required.</li>
<li>Past experience working in offshore research activities</li>
<li>Experience with necropsies, especially performing sea turtle necropsies</li>
<li>Some experience with data management, analytical reporting, and environmental and biological data</li>
</ul>
Travel: 
<ul>
<li>Domestic travel may be required as follows: offshore survey support, attendance at project-related workshops and conferences, in addition to working group meetings.</li>
<li>Anticipated three (3) travel events per year, excluding field work. </li>
</ul>
Location:
<ul>
<li>166 Water St, Woods Hole, Ma, 02543 </li>
</ul>
Contact:
If you would like to apply for this exciting new opening, please visit our Careers Page to submit the required information:
<ol>
<li>Resume</li>
<li>Cover letter detailing relevant experience.</li>
<li>3 professional references (name, email address and phone number),</li>
</ol>
 
All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please reach out to ourTalent Team or call 508-990-9054.
An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

Jr. Sea Turtle Research Ecologist

<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.
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>
Qualifications (What You Bring)
<ul>
<li>PhD in Bioengineering, Molecular Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or related field</li>
<li>5+ years of experience in vitro diagnostics, medical devices, or 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>
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.
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.

In Vitro Diagnostics Scientist/Engineer - Redefine Diagnostics

<h3>Job Description</h3>
Job Description
Boston Metal is commercializing cutting­­-edge­ extractive metallurgy technology that will revolutionize primary metals production by improving metal quality while decreasing cost and lowering environmental impact. This fast-paced startup company is looking for a Senior Scientist to join the team. 
The Senior Scientist will collaborate with the R&amp;D team on the laboratory-scale research programs as well as with the process, operations, and engineering teams for the development activities of full-scale industrial experiments.
Responsibilities include but are not limited to:
<ul>
<li>Lead the development of electrometallurgical processes for new products using new feedstocks for our Critical Metals program.</li>
</ul>
<ul>
<li>Carry out thermodynamic and electrochemical calculations to support process development.</li>
</ul>
<ul>
<li>Track metrics such as conductivity, voltage, current efficiency, and specific energy consumption. </li>
</ul>
<ul>
<li>Collaborate with process development, engineering, operations, and supply chain to keep a focus on scalability while optimizing process parameters. </li>
</ul>
<ul>
<li>Conduct experiments and analyze data on existing high temperature electrochemical testing setup.</li>
</ul>
<ul>
<li>Regular presentation and communication of results within the technical team, to senior management, and company-wide.</li>
</ul>
Requirements
Strong theoretical background in electrochemistry with proven ability to perform data analysis and first-principles modeling, track record in novel electrochemical research, demonstrated ability to independently plan and implement research programs.
7+ years of experience with electrochemical research or metallurgy in a technical environment. MS/PhD from accredited university or college in one or more of the following areas: Materials Science, Chemical Engineering, Chemistry, process metallurgy or a closely related field. 
<ul>
<li>Demonstrated technical leadership experience</li>
<li>Experience with experimental electrochemical cell setup and characterization</li>
<li>Familiarity with chemical engineering principles (e.g., mass and energy balances, thermodynamics, transport phenomena)</li>
<li>Experience developing a MATLAB or Python based data analysis pipeline, and using graphical plotting software for data analysis and visualization</li>
<li>Experience in research and working with large datasets </li>
<li>Materials or metallurgical research</li>
<li>Experience with high-temperature setup/system</li>
<li>Experience with thermodynamic modeling and calculations (FactSage preferred)</li>
<li>Analysis Scripting in Matlab or Python</li>
<li>Experience using Labview</li>
<li>Materials characterization</li>
<li>Portuguese language experience preferred</li>
<li>Intermittent travel to our Brazil facility </li>
</ul>
Benefits
Additional Information:
We are people first with a comprehensive benefits package that can be customized to fit your needs. Our full benefits package offers health, dental, vision, life and disability insurance, paid vacation, sick &amp; holidays, health savings account with a company contribution, dependent care account plan, paid parental and bonding leave and a 401k with company matching provision.
You will be working in a small team environment where teamwork and good relationships with other team members is critical. We operate pilot plants and labs and many of our staff members are required to wear Personal Protection Equipment (PPE) and you should be prepared to do so as well when necessary.
Boston Metal is an equal opportunity employer who considers all qualified applicants equally for employment. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender identity, sexual orientation, pregnancy or pregnancy-related condition, disability, ancestry, genetic information, veteran or military status, or any other characteristics protected by applicable federal, state or local law.

Senior Scientist Critical Metals

<h3>Job Description</h3>
Job DescriptionDEKA Research &amp; Development has an immediate opening for a Biocompatibility &amp; Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role will work directly with Research &amp; Development, Regulatory &amp; Clinical Affairs and Quality Engineering to formulate and execute biocompatibility and toxicological evaluation strategies that support development objectives and world-wide regulatory approvals.&nbsp; How you will make a difference as a&nbsp;Biocompatibility &amp; Toxicology Senior Scientist:
<ul>
<li>Work in close association with customers and development teams to define and execute biocompatibility/toxicology evaluations, including establishing requirements for biological safety of medical devices and combination products</li>
<li>Lead the preparation and conduct of biocompatibility/toxicology test programs</li>
<li>Lead interactions with external consultants and contract laboratories including in-person meetings, teleconferences, and other communications as needed to support program objectives</li>
<li>Develop and deploy mechanisms to continually maintain state of the art knowledge and understanding related to biocompatibility and toxicological safety of medical devices, including relevant standards and test methods.&nbsp; Insure processes and procedures maximize resource efficiency and minimize time to market</li>
<li>Insure the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through monitoring regulatory authority and industry resources</li>
<li>Coach and mentor internal and external partners on effective strategies and tactics</li>
<li>Interface with customers on biocompatibility and toxicology issues</li>
</ul>
Skills you will need to be successful:
<ul>
<li>MS in a technically related field (toxicology, materials science, chemical engineering, biomedical engineering or related).</li>
<li>Minimum of 7 years direct work experience in a medical device and/or combination product development role with demonstrated success in planning and conducting biocompatibility and toxicological evaluations</li>
<li>Expertise in U.S. and international medical device biocompatibility requirements including ISO 10993 standards, Good Laboratory Practices, and guidance from regulatory authorities</li>
<li>Demonstrated practical knowledge of the laboratory methods and analytical techniques associated with medical device and/or combination product biocompatibility and chemical characterization evaluations</li>
<li>Demonstrated ability to establish consensus and work collaboratively across functions and development teams</li>
<li>Excellent written and verbal communication skills including the ability to effectively communicate at all levels of the organization and with external partners</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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Biocompatibility & Toxicology Senior Scientist

<h3>Job Description</h3>
Job Description
About Seismic
Seismic Therapeutic, a cutting-edge biomedicines company at the intersection of machine learning, protein engineering, and immunology, is seeking a creative, independently-minded machine learning scientist to help accelerate the Impact Platform for the computational discovery and optimization of new biologic drugs. Seismic’s machine learning platform enables on-demand generation and optimization of protein therapeutics to fight diseases of the immune system, using the power of artificial intelligence to translate audacious ideas into breakthrough drugs. Weare dedicated to building a supportive culture around a superstar team, while keeping the unmet needs of patients at the center of our goals. Seismic has the tools, skills, ideas and people to make this vision a reality. 
Working closely with our team of machine learning scientists, structural biologists, immunologists and others, you will develop and apply innovative machine learning approaches to optimize natural proteins for clinical applications and design novel classes of synthetic proteins with therapeutic functions. 
Who you are and what you bring:
<ul>
<li>A rigorous machine learning scientist with a deep understanding of molecular biology, protein biochemistry and structure.</li>
<li>Appreciation of the characteristics that make a robust biologic drug.</li>
<li>Hands-on experience with protein design models incorporating sequence (evolutionary sequence models and large language models) and/or structure (diffusion and inverse folding models).</li>
<li>Ability to communicate complex machine learning and computational concepts to audiences with a wide range of backgrounds and technical familiarity.</li>
<li>Experience working with wet lab teams to bridge the divide from in-silico designs to real-world applications.</li>
<li>Driven and conscientious, thriving in a fast-paced, entrepreneurial environment.</li>
<li>Passionate about improving patients’ lives.</li>
</ul>
Core Responsibilities:
<ul>
<li>Design and train new classes of machine learning models to optimize natural proteins for therapeutic properties and design synthetic proteins with novel therapeutic functions.</li>
<li>Spearhead computational de novo antibody design efforts to create new therapeutics targeting challenging antigens. </li>
<li>Integrate diverse external and internal data sources including protein sequence, structure, function, and molecular characterization data to enable detailed modulation and multi-objective optimization of protein properties.</li>
<li>Work with a diverse team of protein scientists, immunologists, and clinical experts to tailor modeling efforts toward high-impact therapeutic applications.</li>
<li>Establish robust data infrastructure to enable machine learning model training and deployment of data analysis and visualization tools. </li>
<li>Develop production-quality code in a team setting for use by both computational and wet-lab scientists. </li>
<li>Present progress from scientific work in regular meetings and prepare reports and slide decks for broader internal and external communication.</li>
</ul>
Required Qualifications:
<ul>
<li>PhD in Mathematics, Computational Biology, Computer Science, Statistics or a related field. Exceptional candidates with extensive computational experience and a PhD in a non-computational field will also be considered. </li>
<li>3+ years of industry experience with developing and applying machine learning methods to create new biological drugs, using deep learning models such as variational autoencoders and graph neural networks. </li>
<li>Application of ML in the field of drug discovery is essential with hands-on experience in the following: protein engineering, or statistical genetics are especially relevant. </li>
<li>Demonstrated experience collaborating with wet lab scientists to generate and analyze real-world data in an applied setting, especially in the context of pharmaceutical development. </li>
<li>Proficiency in Python and data analysis with Numpy/Scipy, R, or another statistical programming language.</li>
<li>A strong drive to collaborate and communicate with a diverse and vibrant team of both dry and wet lab scientists. </li>
</ul>
It's a plus but not required:
<ul>
<li>Experience with AWS, Google Cloud, or another cloud computing framework. </li>
<li>Familiarity with Dash, R Shiny, or another interactive app development framework.</li>
<li>Application of ML in the fields of genomics and immunology.</li>
<li>Publications in major scientific journals that apply machine learning methods to problems in molecular or structural biology.</li>
</ul>
 
As a member of our diverse and growing team, you’ll help shape Seismic into a company that takes its scientific mission seriously while providing a positive and supportive workplace environment and culture. With your insights, passion, and talent - we’ll bring novel therapeutics to the patients who need them the most.
Seismic Therapeutic is an equal opportunity employer. We will not tolerate discrimination on the basis of race, color, national origin, sex, sexual orientation, gender identity, religion, age, disability, veteran's status, pregnancy, genetic information or on any basis prohibited by federal, state or local law.

Scientist / Senior Scientist, Machine Learning

<h3>Job Description</h3>
Job Description
John Turner Consulting (JTC), an environmental and engineering consulting firm serving New England, is seeking an experienced Senior Geologist to join our Portsmouth, NH office.
This is a strategic hire for a senior-level environmental professional ready to lead, mentor, and grow a team, with flexibility to work in a hybrid schedule.
Your Role
In this leadership role, you will oversee site investigation and remediation projects, supervise junior technical staff, and contribute to business development. You will bring a strong command of regulatory compliance at local, state, and federal levels, and have the potential to generate up to $1 million in annual revenue through project leadership and client management.
Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lead environmental site assessments, investigation, and remediation projects throughout New England
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prepare and review technical documents, including sampling plans, remedial action plans, and regulatory reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Manage and mentor junior staff, promoting professional development and safety
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Interface with regulatory agencies such as NHDES, MassDEP, MEDEP, and EPA
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support and drive business development, including proposal writing and client outreach
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain responsibility for project scope, budget, and schedule
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Contribute to strategic planning and help grow JTC’s environmental practice
Qualifications
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 15+ years in environmental consulting with increasing technical and leadership responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; New Hampshire Professional Geologist (PG) required; multi-state licensure is a plus
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrated ability to maintain and grow a portfolio of work worth $1M+ annually
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong knowledge of environmental programs (RCRA, CERCLA, TSCA)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience with New England environmental regulations and permitting
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Successful collaboration with local, state, and federal regulatory agencies
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience managing and mentoring junior staff
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong organizational and communication skills
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bachelor’s degree in Geology, Environmental Engineering, or a related field required; Master’s degree preferred
Why Join JTC?
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Competitive 401(k) plan with company match
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Comprehensive medical, dental, vision, and prescription coverage
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Generous vacation, sick leave, holidays, and family medical leave
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hybrid work environment with a balance of office, home, and field time
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Opportunities for advancement, mentorship, and professional development
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Collaborative, supportive culture committed to quality and safety

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