field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Eastridge Workforce Solutions is seeking a Co-Op Applied Research Associate for our client in Burlington, MA. This is an opportunity to contribute to innovative medical device development with a company dedicated to transforming ophthalmic care.
<ul>
<li>Location: Burlington, MA</li>
<li>Pay: $28.15/hour (Bachelor’s Jr/Sr) – $35.40/hour (Master’s)</li>
<li>Shifts Available: Full-time, 6-month Co-Op | Onsite</li>
</ul>
Why Join Us?
<ul>
<li>Competitive Pay – Gain valuable experience with strong hourly compensation</li>
<li>Career-Defining Projects – Contribute to next-gen ophthalmic technology</li>
<li>Cross-Functional Exposure – Work alongside top-tier scientists and engineers</li>
</ul>
What You’ll Do:
<ul>
<li>Collaborate on R&amp;D efforts in corneal crosslinking and vision system technologies</li>
<li>Collect lab data, test algorithms, and support AI model development</li>
<li>Analyze data, identify failure modes, and communicate findings effectively</li>
<li>Assist with software, image processing, and biomedical modeling projects</li>
<li>Participate in experimental setup and ongoing research initiatives</li>
</ul>
What We’re Looking For:
<ul>
<li>Enrolled in a BSc or MSc program in Computer Science, Engineering, or related field</li>
<li>Coursework or project experience in computer vision, ML, or medical imaging</li>
<li>Proficiency in Python, MATLAB, or C++</li>
<li>Hands-on lab and data analysis experience</li>
<li>Strong communication and problem-solving skills</li>
</ul>
Ready to Jumpstart Your Career in Applied Research? Apply Today!
 
Benefits: Use this link bit.ly/4cGUQSh to learn more about benefits available to Eastridge’s temporary employees.From time to time Eastridge’s clients may offer additional benefits to Eastridge employees while on assignment.Information about those benefits will be communicated when applicable.
 
Eastridge Workforce Solutions is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We celebrate diversity and are committed to creating an inclusive environment for all employees. Please note that Eastridge is unable to provide visa sponsorship to applicants.
 
Certain clients require Eastridge to perform background checks and Eastridge will consider qualified applicants with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
 
#IPROPLUS
#LI-SM3

Co-Op Applied Research Associate

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.
Responsibilities Include:&nbsp;
<ul>
<li>Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment</li>
<li>90% Method development,&nbsp;qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
<ul>
<li>May include technology transfer activities, regulatory support, and possible project team participation</li>
</ul>
</li>
<li>10% Analytical testing
<ul>
<li>Liquid Chromatography&nbsp;and Plate-Based&nbsp;</li>
</ul>
</li>
<li>Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.&nbsp;</li>
<li>Experience working in a GMP/GLP environment&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives</li>
<li>Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>BS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>2 years of demonstrated work experience with cell-based assays</li>
</ul>
</li>
<li>Or MS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>6 months of Demonstrated experience with cell-based assays&nbsp;</li>
</ul>
</li>
<li>Experience with&nbsp;experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioassay Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We're looking for someone to support routine lab testing and help maintain a well-organized QC environment. This role involves working with various instruments, preparing samples, and following established procedures. A great fit would be someone detail-oriented, eager to learn, and comfortable working in a team setting.
Job Duties Include:&nbsp;
<ul>
<li>Perform routine testing of pharmaceutical samples by following analytical compendial methods (pH, osmolality, concentration, break-loose extrusion force, etc.)</li>
<li>Prepare standards and samples for analysis</li>
<li>Monitoring and replenishing lab reagents and solutions</li>
<li>Maintain, calibrate, and operate instrumentation in the QC laboratory</li>
<li>Document work as required for GMP compliance</li>
<li>Execute work in accordance with standard operating procedures, with attention to detail, and with strong organizational skills</li>
<li>Interact effectively with peers and leaders as part of a multi-disciplinary team</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry or other science related degree concentration</li>
<li>0-2 years of QC analytical experience</li>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>30 Minute Virtual Interview with Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, first shift, Monday-Friday from 8 am-5 pm. Candidates must be flexible to adapt to schedule&nbsp;changes requiring shift changes and/or weekend work, and overtime may be required as needed.&nbsp;Candidates living within a commutable distance of Andover, MA&nbsp;are encouraged to apply.&nbsp;&nbsp;
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

QC Analytical Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Research Scientist Location: Lexington, MA Duration: 18 months+ Pay Rate:$52.84/hr. on w2 Job Summary: TOP SKILL PER MGR (in addition to excellent communication skills):
<ul>
<li>Patient endotype discovery using unsupervised/supervised ML approaches</li>
<li>Omics analysis (primarily proteomics, Olink, Soma, LC-MS) incl differential expression, clinical characterisation, clinical outcomes and pathway analyses</li>
<li>Experience w/clinical data with major human cohort data</li>
</ul>
 Job Description: The Position-
<ul>
<li>We are seeking a highly motivated Research Scientist to play a key role in supporting our Therapeutic Areas (TA) in their efforts to better characterise patients/diseases in a real-world context.</li>
<li>Focused initially on initially on Type 2 Diabetes (T2D) or Obesity, you will be responsible for</li>
<li>using patient-derived molecular and phenotypic data to identify treatment-relevant disease subgroups,</li>
<li>integrating diverse features from clinical trials and externally sourced patient cohorts to define Client endotypes and provide real-world context to our Client drug targets, and</li>
<li>utilise modern machine-learning (ML) methods to derive and communicate insights to non-expert stakeholders in a clear and meaningful way.</li>
</ul>
 In this role you will:
<ul>
<li>Develop and apply advanced but explainable AI/ML methods and statistical models to cardiovascular disease</li>
<li>Collaborate with cross-functional teams across EVP areas to identify and validate new endotypes, biomarkers, and drug targets</li>
<li>Analyse large patient-derived molecular and phenotypic datasets, to identify patterns and trends that can inform future target discovery and development</li>
<li>Present findings with clarity and objectivity in internal presentations and publications in scientific journals.</li>
</ul>
 Qualifications:
<ul>
<li>Master's degree in Bioinformatics, Computational Biology, Computer Science / Machine Learning, Genomics, or related field (PhD candidates will be considered w/min of 1 yr prof exp)</li>
<li>3+ years working/professional experience</li>
</ul>
 Our ideal candidate meets the following criteria:
<ul>
<li>Has proven track record of delivering cohort analyses and clear interpretation of insights derived from machine learning</li>
<li>Has strong knowledge of machine learning algorithms and their application to biomedical data</li>
<li>Has experience with programming languages such as Python or R, version control, and high-performance computing</li>
<li>Has excellent communication and collaboration skills</li>
<li>Has the ability to work independently and drive projects forward</li>
</ul>
 #sczr2

Research Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a detail-oriented and collaborative candidate to join our Quality Control team. This role involves performing analytical testing on pharmaceutical samples using techniques such as Capillary Gel Electrophoresis (CGE) and HPLC with Empower software. The ideal candidate will follow GMP guidelines, maintain laboratory equipment, and contribute to a fast-paced, team-driven environment.
Job Duties Include:&nbsp;
<ul>
<li>Perform Capillary Gel Electrophoresis (CGE)</li>
<li>Operate an HPLC utilizing Empower software</li>
<li>Perform routine testing of pharmaceutical samples by following analytical compendial methods (pH, osmolality, concentration, break-loose extrusion force, etc.)</li>
<li>Prepare standards and samples for analysis</li>
<li>Monitoring and replenishing lab reagents and solutions</li>
<li>Maintain, calibrate, and operate instrumentation in the QC laboratory</li>
<li>Document work as required for GMP compliance</li>
<li>Execute work in accordance with standard operating procedures, with attention to detail, and with strong organizational skills</li>
<li>Interact effectively with peers and leaders as part of a multi-disciplinary team</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry or other science related degree concentration</li>
<li>2-4 years of QC analytical experience</li>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>30 Minute Virtual Interview with Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, first shift, Monday-Friday from 8 am-5 pm. Candidates must be flexible to adapt to schedule&nbsp;changes requiring shift changes and/or weekend work, and overtime may be required as needed.&nbsp;Candidates living within a commutable distance of Andover, MA&nbsp;are encouraged to apply.&nbsp;&nbsp;
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

QC Analytical Chemist II

<h3>Job Description</h3>
Job Description
At Boston Fusion, we recognize diversity is the catalyst for limitless creativity.
 
As a Principal Research Scientist for Boston Fusion, you will have the opportunity to utilize your knowledge of scientific research and software engineering best practices to contribute and drive research efforts in development of systems core to the success of future Intelligence, Surveillance, and Reconnaissance (ISR) activities. This role will lead technical teams as a Principal Investigator, lead and contribute to proposal efforts, and collaborate with project teams to solve complex technical problems that support national security.
 
Every day, we go above and beyond to solve complex problems, making a difference for our nation. We do this by bringing together smart, curious people with diverse life experiences who collaborate creatively to achieve innovative technological breakthroughs. We are proudly building a work environment where you can bring your authentic self to work.
 
Due to the nature of our project work, we can only consider candidates with a current US Citizenship.
 Day to Day Responsibilities
 
<ul>
<li>Investigate fundamental topics in a scientific field such as signal processing, artificial intelligence, machine learning, data science, physics and/or math</li>
<li>Lead teams of two or more Scientists, Engineers, and Programmers, including identifying, assigning, and completing research and development tasks appropriate to each member of the team</li>
<li>Provide a strategic leadership role in working with a project / proposal team to identify the research approach, hypotheses to be tested, and program milestones to achieve all program objectives</li>
<li>Facilitate collaboration in large, complex teams to ensure resulting technology (algorithms, software, frameworks) achieves all research objectives</li>
<li>Select, improve, or design computational models</li>
<li>Identify relevant research approaches, hypotheses to be tested, and program milestones to achieve all program objectives with project and/or proposal teams</li>
<li>Provide scientific, technical and software design support to projects and proposals</li>
<li>Design statistically valid experiments to test and validate resulting computational models</li>
<li>Provide leadership and guidance in the analysis of results of the experiments using sound scientific principles</li>
<li>Design experiments to test and validate computational models</li>
<li>Establish and maintain a professional rapport with all project stakeholders (internal and external)</li>
<li>Additional project and proposal duties as assigned</li>
</ul>
 
Additional Responsibilities
<ul>
<li>Occasional travel to attend and present at customer meetings and essential industry conferences</li>
<li>Prepare technical briefing materials/summarize technical work and progress of projects</li>
<li>Collaborate with company leadership and senior technical staff to conduct proposal research and proposal writing</li>
<li>Publish technical reports based on original or improved algorithms created to solve the application challenges</li>
<li>Maintain high standards at work, continuously looking for solutions to improve processes and products</li>
<li>Develop, maintain, and strengthen partnerships with others inside and outside the organization to achieve Boston Fusion business goals</li>
<li>Demonstrate personal accountability, effective work habits, integrity, and ethical behavior that align with Boston Fusion corporate values</li>
<li>May perform other duties as required</li>
</ul>
 
This Job is Right for You if you Have:
 
<ul>
<li>Bachelor’s degree in computer science, engineering, mathematics, physics, or related field, with 15+ years of experience; Master’s degree with 13+ years of experience; PhD with 10+ years of experience</li>
<li>Excellent analytical and problem-solving skills</li>
<li>Ability to prioritize and manage time effectively</li>
<li>Excellent communication, writing and presentation skills</li>
<li>Ability to work both collaboratively and independently</li>
</ul>
 
Demonstrates strong competency in every category and a mastery of at least one category
<ul>
<li>Demonstrated competency in radar, signal processing, human-machine systems, computer vision, AI/ML, or other technical discipline</li>
<li>Experience implementing modeling and analysis techniques, including machine learning, operations research, optimization, control theory, probabilistic modeling, etc.</li>
<li>Understanding of mathematical principles which underlie these modeling methods</li>
<li>Experience in implementing algorithms in standard programming languages such as Python, Java, C++</li>
<li>Experience in using sound software development techniques, e.g., testing, documentation, source control</li>
</ul>
 
Preferred Technical Qualifications
<ul>
<li>Classical applied probabilistic, mathematical, and/or artificial intelligence methods (planning, searching, logic, uncertain knowledge, probabilistic reasoning, natural language processing)</li>
<li>Radar signal processing techniques</li>
<li>Machine learning frameworks (e.g., Scikit-learn, Tensorflow, PyTorch, Keras) and concepts (e.g., supervised, unsupervised, active, and reinforcement learning; neural networks; generative, discriminative models)</li>
</ul>
 
Preferred Domain Knowledge
<ul>
<li>6+ years of experience applying technology to US Department of Defense and/or Intelligence Community problems, including but not limited to the following: intelligence analysis, command and control, logistics, ISR, information operations, missile defense, operations in the cyber, space, or maritime domains</li>
<li>8+ years of experience in a research leadership role</li>
<li>Work Authorization/Security Clearance Requirements</li>
<li>U.S. citizenship and DoD security clearance (REQUIRED)</li>
</ul>
 
PI05b2235a508a-25405-36297946

Principal Research Scientist

<h3>Job Description</h3>
Job Description
About GrapheneDx: GrapheneDx is a new diagnostics technology company with a mission to transform consumer diagnostics. Our employees gain experience in a multidisciplinary, fast-paced start-up and have ample opportunities to acquire new skills, engage with emerging technologies, and collaborate closely with an accomplished team, all within in a supportive and energetic environment. 
GrapheneDx offers a competitive compensation package including base salary, performance bonuses, paid time off, health and dental benefits, and excellent growth opportunities. 
GrapheneDx is seeking a Research Scientist who will apply their expertise to advance our R&amp;D efforts in biosensor development and communicate valuable insights to a highly collaborative and dynamic team. 
Summary: The Research Scientist in Assay Development will design and execute experiments to functionalize sensors with nucleic acid or antibody probes for biomarker detection, contributing to the development of a groundbreaking, point-of-care diagnostic platform. Collaborating closely with a senior scientist and a cross-functional team of materials scientists, electronics engineers, and data scientists, this role drives forward a disruptive diagnostic technology poised to redefine the field. 
Key Duties and Responsibilities: 
<ul>
<li>Drive the development of a novel GFET-based point-of-care diagnostic platform. </li>
<li>Design, execute, and optimize experiments for biomarker detection, including feasibility, pilot, and process optimization studies. </li>
<li>Perform data analysis, critically interpret results, and prepare reports and presentations tailored to the needs and expertise of internal and external stakeholders.</li>
<li>Collaborate with a cross-functional team of scientists and engineers to design experiments aligned with R&amp;D objectives, ensuring sensor technology integration into scalable diagnostic solutions.</li>
<li>Document, refine, and optimize protocols, creating actionable plans to improve processes and advance R&amp;D milestones</li>
<li>Identify and troubleshoot technical challenges, contributing to regulatory documentation, and ensure protocol compliance where relevant.</li>
</ul>
Essential Experience:
<ul>
<li>Ph.D. in Biochemistry, Biology, Chemistry, Electrochemistry, Biophysics, or a related discipline, or a Master’s degree with 1-5 years of relevant academic or industry experience.</li>
<li>Proven experience in creating and developing biosensor immunoassays and/or nucleic acid detection assays through probe hybridization.</li>
<li>Strong problem-solving skills, with the ability to identify challenges and propose alternative approaches.</li>
<li>Excellent organizational and analytical skills, including the ability to summarize and translate data into actionable plans.</li>
<li>Effective oral and written communication skills to convey technical information to both supervisors and team members.</li>
</ul>
 
Desirable Experience:
<ul>
<li>Experience with non-optical-, electrical-, or electrochemical-based sensors, especially graphene-based or carbon nanotube-based sensing platforms.</li>
<li>Experience functionalizing GFETs with biological probes, such as nucleic acids or antibodies, to enable biomarker detection.</li>
<li>Experience defining and improving biosensor performance metrics, such as sensitivity, specificity, limit of detection (LOD), and other industry-standard used to quantify biosensor efficacy and reliability.</li>
<li>Proficiency in coding or data visualization using Python, Origin, and/or Minitab for data analysis and visualization. </li>
<li>Working knowledge of statistical analysis and design of experiments.</li>
<li>Ability to coordinate effectively across multiple functional areas.</li>
<li>Highly motivated and adaptable, with the flexibility to thrive in a dynamic and interdependent environment.</li>
</ul>

Research Scientist, Assay Development

<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist location: Andover , MA Duration: 18 months+ Payrate: $20.69/hr on w2 Job Summary (Required): Why Patients Need You Client’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Client’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve : Manufacturing Sciences and Technology (MSAT) Upstream Group at Clients looking for a highly motivated and versatile candidate to join our multidisciplinary team of scientists and engineers in Andover, MA. MSAT supports Client’s portfolio of late-stage development of commercial biopharmaceuticals and vaccines, and is responsible for process troubleshooting, process improvements and second- generation process development. We are looking for someone who is eager to contribute independent thinking and technical excellence to the upstream fermentation team. The Associate Scientist will be a part of a diverse and motivated team of scientists, engineers, and technical professionals that are focused on fermentation processes to produce biotherapeutics. The role is well-integrated into the rest of the MSAT Microbial Team. This role will collaborate with other MSAT scientists to setup bioreactors and execute well-designed experiments, including but not limited to basic analytics, data acquisition and documentation of work. The candidate would also be responsible for user-level maintenance of the relevant equipment and associated documentation. How You Will Achieve It : • Contribute to achievement of the upstream work group goals and collaborate with other team members. • Maintain laboratory area and equipment in clean, safe, and functional order. • Comply with safety and regulatory requirements is expected and documented through the internal training program. • Perform routine laboratory studies. • Qualified candidates will serve as an upstream resource for the department and project teams. • Follow Standard Operating Procedures and Standard Work instructions. Qualifications Required : • Bachelor's Degree or Associate Degree in a relevant discipline (Chemical engineering, Bioprocessing, Biotechnology, Biochemistry, Biology, etc.) with 0 - 3 years of applicable bioprocess experience. • Proficient in aseptic technique (REQUIRED). • Experience in bioreactor operation and associated analytical tools (PREFERRED). • Candidate should have in-depth scientific knowledge and experience in a wide array of upstream techniques. • Ability to perform complex data analysis and work in a dynamic team environment. • Ability to troubleshoot technical issues, plan and carry out experiments independently, and work with complex instrumentation and software. • Excellent oral and written communication skills. • Strong analytical and computer skills. • Biopharmaceutical or pharmaceutical industry experience. • Experience in troubleshooting electrical and mechanical systems. • Experience in executing lab scale microbial fermentation formats and scale-up to pilot/manufacturing scale. • Familiarity with control and data acquisition systems. • Knowledge of cell culture/fermentations. • Experience with industrial scale fermentation scale up, optimization and operations are highly desired. • Curiosity about seeking and applying current relevant scientific literature. Physical/mental requirements : • Involves typical bioprocessing lab activities • Ability to routinely lift 50 lbs. • Standing for prolonged periods of time, walking, bending, and using tools. • Ability to perform mathematical calculations and ability to perform complex data analysis. Non-standard work schedule, travel or environment requirements : • Weekly Schedule is Monday - Friday / First shift • Requires off hours working to support laboratory work on average of two times per week. • This is an on-site laboratory role. What will the resource be working with, or, have exposure to: 
<ul>
<li>Biohazardous Agent work (such as menigiditis, staph </li>
<li>aureus, Lenti Virus, streph pneumoniae)</li>
<li>Strep Pneumoniae</li>
</ul>
 What is the minimum education experience required: 
<ul>
<li>Bachelor's Degree or Associate </li>
<li>Degree in a relevant discipline (Chemical engineering, Bioprocessing, </li>
<li>Biotechnology, Biochemistry, Biology, etc.) with 0 - 3 years of applicable </li>
<li>bioprocess experience.</li>
</ul>
 Interview: • First round: Teams Meeting • Second round: Onsite
<ul>
<li>Position Comments visible to </li>
<li>Supplier: HM open to fresh </li>
<li>grads with lab experience</li>
<li>Candidates MUST be able to understand and speak to true </li>
<li>lab experience.</li>
</ul>
 #sczr2

Associate Scientist

<h3>Job Description</h3>
Job DescriptionThe successful candidate will have outstanding expertise in mouse handling and mouse procedures. They will be responsible for managing mouse colonies, performing project-specific in vivo experiments, intravenous injections of hematopoietic stem cells in humanized murine models, retro-orbital and submandibular blood collection, and blood cell FACS analyses and in vivo imaging. This is a collaborative role that will be partnering with other team members to assist with project-specific- in vivo experiments as well as other needs across the process development function. Role and Responsibilities:
<ul>
<li>Hands-on role with a commitment to designing, conducting and analyzing in vivo studies to assess engraftment of hematopoietic stem cells.</li>
<li>Execute pluripotent stem cell culture and differentiation into hematopoietic stem cells to support process development, optimization, and characterization.</li>
<li>Document experimental procedures and results according to established guidelines; Perform statistical analysis of experimental data.</li>
<li>Collaborate effectively within departmental teams, engage in team discussions to resolve issues, and lead projects with a fully integrated team to facilitate successful outcomes.</li>
<li>Prior experience in bioreactor-based process development for iPSC-derived cell therapies is highly desirable.</li>
</ul>
Qualifications:
<ul>
<li>Advanced degree (M.S. or Ph.D.) in molecular biology or pharmacology, with at least 2 years of industry experience is required</li>
</ul>
<ul>
<li>Experience working with human induced pluripotent stem cells (iPSC), hematopoietic stem cells (HSC), and/or immune cell biology; including scale-up processes utilizing bioreactors such as PBS vertical wheel, Rotea counterflow centrifuge is required</li>
</ul>
<ul>
<li>Proficiency with in-vivo techniques including animal handling, intra-bone and intravenous transplants, blood collection and tissue dissection</li>
</ul>
<ul>
<li>Experience in standard processing techniques including flow cytometry, molecular biology assays such as CFUs, immunological assays, and aseptic cell culture technique is required</li>
</ul>
<ul>
<li>Experience with experiment design tools such as FlowJo and practical knowledge of statistical analysis is required</li>
</ul>
<ul>
<li>Strong organizational, analytical, problem-solving, root-cause-analysis, and trouble-shooting skills are required</li>
</ul>
Powered by JazzHR
acCYiv1F9m

In Vivo Scientist

<h3>Job Description</h3>
Job DescriptionSalary: $1,615 - $1,793/week based on experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Boylston, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

175 Science Jobs