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<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 work with an innovative medical device company focused on advancing therapies in Ophthalmology.
<ul>
<li>Location: Burlington, MA</li>
<li>Pay: $22/hr</li>
</ul>
Why Join Us?
<ul>
<li>Competitive Pay &amp; Benefits – Health, Dental, Vision &amp; 401(k) Match</li>
<li>Innovative Culture – Collaborate with cutting-edge research teams in medical device development</li>
</ul>
What You’ll Do:
<ul>
<li>Support applied research efforts across multiple projects in ophthalmic technologies</li>
<li>Assist in designing, developing, and executing lab experiments</li>
<li>Contribute to photochemical, biomechanical, and mathematical modeling</li>
<li>Develop and apply data analysis techniques for research findings</li>
<li>Aid in algorithm development and medical device automation</li>
</ul>
What We’re Looking For:
<ul>
<li>Experience with modeling tools such as COMSOL and programming in Python, MATLAB, or C++</li>
<li>Familiarity with CAD software (e.g., SolidWorks) and lab-based research</li>
<li>Strong communication skills and a collaborative mindset</li>
<li>Background in scientific, biomedical, or engineering disciplines</li>
<li>Currently pursuing a PhD, MSc, or BSc in a related field</li>
</ul>
Ready to Get Started? 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.
#IPRO

Co-Op Applied Research Associate

<h3>Job Description</h3>
Job Description
Hillstar Bio, is a precision immunology company that recently completed a sizable Series A financing with a syndicate of blue-chip investors. Our passionate team of drug developers is based in Boston’s Seaport neighborhood. 
Hillstar is advancing a portfolio of programs against autoimmune diseases with unmet or underserved medical needs. Its lead program is an antibody designed to selectively target a root cause of Cold Agglutinin Disease (CAD) and other autoimmune diseases. CAD is a chronic, rare (incidence 15/million) but debilitating condition with high morbidity (anemia, fatigue, cold-induced circulatory symptoms). Existing treatment options for CAD have limited effectiveness, carry considerable safety risks, and fail to address key disease symptoms in a large proportion of patients, leading to significant chronic morbidity and excess mortality. By bringing this new precision modality to patients, Hillstar aims to improve on safety and efficacy, as well as durability of response, setting a new gold standard for the management of CAD, and other serious autoimmune conditions with a common biological origin.
Job Description
Join Hillstar Bio as a Scientist/Senior Scientist Immunology overseeing the design and execution of in vitro and in vivo mechanistic, proof-of-concept and safety studies, provide scientific and technical expertise in immune cell biology, and support regulatory filing with authoring of technical reports. 
This pivotal role offers a chance to shape our company culture, make a meaningful impact on patient care, and contribute to the growth of a pioneering organization. We seek a passionate, hands-on scientist with a collaborative spirit, ready to thrive in a dynamic, close-knit team environment.
Requirements
Essential Duties and Responsibilities
<ul>
<li>Design, execute, and analyze in vitro and in vivo experiments to investigate disease-causing mechanisms and generate proof-of-concept studies. </li>
<li>Establish and validate in vitro models of autoimmune diseases; support the design and execution of in vivo experiments such as PK, tox, dosing</li>
<li>Develop and perform biochemical and biological assay (ELISA, flow cytometry, immunofluorescence, cell sorting)</li>
<li>Provide scientific guidance to external academic collaborations, vendors, CROs.</li>
<li>Assist in authoring technical reports for regulatory filing.</li>
<li>Catalyze emerging scientific breakthroughs in precision immunology into new discovery programs. </li>
<li>Play a key team role in building and fostering Hillstar’s culture and contribute to its growth.</li>
<li>Collaborate on various aspects of general business and people operations, as needed.</li>
</ul>
Qualifications
<ul>
<li>PhD in Immunology or related field.</li>
</ul>
<ul>
<li>A minimum of 2 years of experience in drug development in biotech or pharma setting, with research experience in autoimmune diseases.</li>
<li>Demonstrated experience in humoral and cell-mediated immunology, experience with B and T cell biology is highly preferred. </li>
<li>Demonstrated experience with biochemical and cell-based assays (flow cytometry, cell sorting, and microscopy is required).</li>
<li>Relevant experience is reflected by a track record of patents and high impact publications.</li>
<li>Self-motivated, collaborative, excellent time management and interpersonal skills.</li>
<li>Experience with antibody development is a plus.</li>
</ul>
Benefits
Hillstar Bio offers a competitive compensation and benefits package that includes unlimited vacation and market-leading parental leave.
Additional Information
This is a full-time position located in our Boston, MA office. Hillstar is committed to creating a diverse work culture and we are seeking individuals of all backgrounds, orientations, and identities. We are an equal opportunity employer and do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Senior Scientist Immunology

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate – II Location: Lexington, MA, 02421 Duration: 6+ months Schedule: Monday-Friday, 8:30 am – 5 pm, May need to work outside of standard hours sometimes (evenings/weekends) Pay Range: $45 - 48/Hour. on W2 NOTES: Industry experience is preferred; Pharma experience is a plus. Life sciences degree (Biology, Biochemistry, Biotechnology, etc.) is required. MUST HAVE job-related tissue culture and metabolic assay experience; functional genomics (siRNA/CRISPR) experience a plus. MUST HAVES: 1) Experience in working with scientists to follow required protocols 2) Proficient at tissue culture and cell-based functional assays, with metabolic assays strongly preferred 3) Communication/Organization Purpose: To provide technical laboratory research support of projects focused on target validation using human in vitro models in metabolic functional assays such as Seahorse, lipolysis, and glucose uptake. Essential Functions: Work with scientists to conduct lab-based studies to support project efforts • Perform tissue culture work with human cell lines to develop and optimize workflows for in vitro target validation using mid-throughput (96-384 well plate) assays • Support project management efforts in standard operating procedure creation, sharing knowledge and skills, and fostering cross-functional teamwork • Engage in effective communication with colleagues within Client. Physical Requirements: No overnight travel required: • Work with human cell lines and common molecular biology reagents in a laboratory environment that may include hazardous chemicals and blood borne pathogens • Functions may require some morning, evening, or weekend hours outside of standard business hours Qualifications: • Bachelor's degree with 3-5 years of experience post-degree; relevant experience may be substituted as appropriate. Title is dependent on qualifications. • Tissue culture experience is required—including strong aseptic technique, BSL2 stewardship, and troubleshooting • Experience with cell-based screening systems and lab automation • Metabolic disease understanding is a plus • Experience with human primary cells (adipocyte, skeletal myoblasts) is a plus • Experience with automated laboratory equipment, complex machinery, and familiarity of high throughput data production principles are a plus • Ability to carry out complex protocols required • Experience in basic molecular biology techniques required • Experience working in a team environment required, industry (CRO, pharmaceutical, biotech) experience is preferred • Fluency in spoken and written English is a prerequisite for the role • Role requires proactive communication skills and cross-cultural understanding to interact within a global organization • Must be comfortable in asking for clarification and offering suggestions • Other desirable skills include advanced cellular imaging and/or high throughput data collection skills, and ability to interpret interdisciplinary data • Must love to learn, be ambitious, and be determined to contribute to improving patients' well-being. #sczr2

Research Associate II

<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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
The&nbsp;Metals Prep Analyst&nbsp;prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP’s.
Metals Prep Analyst&nbsp;responsibilities include, but are not limited to, the following:
<ul>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:
<ul>
<li>Preparation of samples using standard techniques</li>
<li>Performing chemical analysis using standard techniques</li>
<li>Calculating data</li>
<li>Recording and reporting data and any unusual test occurrences to the supervisor</li>
</ul>
</li>
<li>Performing routine instrument maintenance</li>
<li>Responsible for performing job functions in compliance with Eurofins Environment Testing&nbsp;EHS and QA standards</li>
<li>Responsible for general housekeeping in his/her work area</li>
<li>Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems.</li>
<li>Works under close supervision using routine and standard methods</li>
<li>&nbsp;Aliquots and weighs samples</li>
<li>&nbsp;Washes glassware</li>
<li>&nbsp;Conducts all activities in a safe and efficient manner</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>BS or BA in chemistry or related field</li>
<li>1-2 years of previous laboratory experience&nbsp;</li>
<li>Previous production-oriented work helpful (awareness and ability to meet deadlines)</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li>
<li>&nbsp;Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Must be able to pass a pre-employment background check and drug screen</li>
</ul>
The ideal candidate would possess:
<ul>
<li>Ability to use calculator/mathematical formulas and concepts</li>
<li>Ability to complete work within time and quality constraints</li>
<li>Can work independently following written or verbal instructions</li>
<li>Cooperate and coordinate both orally and in writing</li>
<li>&nbsp;Able to follow and learn appropriate protocols in one or more of the following disciplines:
<ul>
<li>&nbsp;Organic preparation</li>
<li>Metals preparation and analysis</li>
<li>Gas Chromatography</li>
<li>Gas Chromatography/Mass Spectrometry</li>
<li>Radio Chemistry</li>
<li>Wet Chemistry</li>
<li>High Resolution preparation and analysis</li>
<li>Low Resolution preparation and analysis</li>
</ul>
</li>
</ul>
Eurofins Environment Testing, Inc. is searching for a Metals Prep Analyst in our Concord, NH laboratory.&nbsp;
Position is full-time, Monday-Friday 1st shift, with overtime as needed.&nbsp;
 Additional Information 
Compensation range: $19-21/hour&nbsp; (DOE)
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.
We support your development!&nbsp;Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity!&nbsp;Eurofins network of companies believe in strength and innovation through diversity, being an&nbsp;Equal Opportunity Employer.&nbsp;We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us!&nbsp;We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company description:&nbsp;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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
We do not offer Visa Sponsorship for this role.
Eurofins is a&nbsp;M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Analyst, (Metals Prep) Environment Testing

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Discovery Biotherapeutics and Genetic Medicine (BGM) at Abbvie is seeking a highly motivated Principal Research Scientist to join the Cell and Functional Biology group at the AbbVie Bioresearch Center (ABC) site based in Worcester, MA. &nbsp;This role will be responsible for the design and execution of screening strategies employed to advance promising biotherapeutics from early exploration through lead optimization. &nbsp;Close partnerships with cross-functional colleagues will be required to drive transformative ideas to the clinic. The ideal candidate should possess experience in large molecule screening strategy design including vitro cell-based assays, with a strong experience in functional assay development and high-throughput screening.
Job Responsibilities:
<ul>
<li>Develop in vitro functional assays leveraging diverse signaling pathways to transition early therapeutic ideas into enabled biotherapeutics campaigns.</li>
<li>Design and employ strategic screening funnels for biotherapeutic discovery campaigns, performing detailed analysis of complex data sets for key insights guiding decision-making processes in research projects.</li>
<li>Identify and integrate cutting-edge technologies and methodologies into screening and assay development, anticipating future trends in drug discovery.</li>
<li>Foster strong cross-functional collaborations with therapeutic area partners to promote the generation of innovative ideas and solutions which support organizational objectives.</li>
<li>Present and explain research findings and strategies clearly and effectively, preparing scientific reports, publications, and presentations for varied audiences.</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment.</li>
</ul>
Qualifications 
<ul>
<li>BS with 12+ years of experience or MS with 10+ years of experience or PhD 4+&nbsp;years of experience in Biology, Molecular and Cellular Biology, or another related field.</li>
<li>Extensive experience in biotherapeutic discovery and screening.</li>
<li>Demonstrated ability to inspire team members to achieve their best performance, fostering a positive and productive team environment.</li>
<li>Proficiency in developing and optimizing high-throughput screening assays for biotherapeutic candidates, including cellular and immunoassays.</li>
<li>Demonstrated ability to lead cross-functional research teams, manage projects, and effectively communicate with stakeholders.</li>
<li>Experience with state-of-the-art screening technologies and data analysis tools.</li>
</ul>
Desirable:
<ul>
<li>Experience with HTS and enabling automation platforms</li>
<li>Experience in managing relationships with Contract Research Organizations (CROs) and external partners.</li>
<li>Experience with enterprise data capture solutions (GeneData, Dotmatics, Benchling)</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II, Cellular/Functional Biology

<h3>Job Description</h3>
Job Description
Title: Chemical Biology Research Scientist
Hiring Organization: Connexion Systems &amp; Engineering
Compensation, Benefits, and Employment Type
<ul>
<li>Duration: 6+ month contract, with potential for extension or conversion</li>
<li>Pay rate: $64-$68/hr </li>
<li>Job Location: Boston, MA</li>
<li>Schedule: M-F, 1st shift</li>
<li>Job#: bh17622</li>
</ul>
Description:
We are seeking a Research Scientist to join our Chemical Biology group. We aim to treat serious diseases, many with targets difficult to drug. In this lab-based role, this scientist will help deploy novel covalent drug discovery techniques to the identification and validation of ligands for hard-to-target proteins. The ideal candidate is a motivated, detail oriented, life-long learner with expertise in covalent drug discovery and compound screening.
Top requirements: 
<ul>
<li>Skilled in proteomics workflow</li>
<li>Mammalian cell culture</li>
<li>Affinity capture or immunoprecipitation skills</li>
<li>Sample preparation for Mass Spec analysis</li>
</ul>
Key Duties and Responsibilities:
· High throughput compound screening
· Designing, executing and troubleshooting novel screening approaches for covalent ligand discovery
· Proactive verbal and written communication to effectively engage with scientists from different disciplines on the team.
· Collaboratively work with members of the team to coordinate screening staging and timing
Knowledge and Skills:
· Expertise in covalent chemoproteomics and data analysis
· Knowledgeable about concepts of compound binding affinity, selectivity, reactivity and kinetics
· Automation for liquid handling
· Affinity capture methods including immunoprecipitation
· Western analysis
· Cell biology (cell culture, lentiviral based expression)
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

Chemical Biology Research Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Discovery Biotherapeutics and Genetic Medicine (BGM) at Abbvie is seeking a highly motivated Principal Research Scientist to join the Cell and Functional Biology group at the AbbVie Bioresearch Center (ABC) site based in Worcester, MA. &nbsp;This role will be responsible for the design and execution of screening strategies employed to advance promising biotherapeutics from early exploration through lead optimization. &nbsp;Close partnerships with cross-functional colleagues will be required to drive transformative ideas to the clinic. The ideal candidate should possess experience in large molecule screening strategy design including vitro cell-based assays, with a strong experience in functional assay development and high-throughput screening.
Job Responsibilities:
<ul>
<li>Develop in vitro functional assays leveraging diverse signaling pathways to transition early therapeutic ideas into enabled biotherapeutics campaigns.</li>
<li>Design and employ strategic screening funnels for biotherapeutic discovery campaigns, performing detailed analysis of complex data sets for key insights guiding decision-making processes in research projects.</li>
<li>Identify and integrate cutting-edge technologies and methodologies into screening and assay development, anticipating future trends in drug discovery.</li>
<li>Foster strong cross-functional collaborations with therapeutic area partners to promote the generation of innovative ideas and solutions which support organizational objectives.</li>
<li>Present and explain research findings and strategies clearly and effectively, preparing scientific reports, publications, and presentations for varied audiences.</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment.</li>
</ul>
Qualifications 
<ul>
<li>BS with 14+ years of experience or MS with 12+ years of experience or PhD +6 years of experience in Biology, Molecular and Cellular Biology, or another related field.</li>
<li>Extensive experience in biotherapeutic discovery and screening.</li>
<li>Demonstrated ability to inspire team members to achieve their best performance, fostering a positive and productive team environment.</li>
<li>Proficiency in developing and optimizing high-throughput screening assays for biotherapeutic candidates, including cellular and immunoassays.</li>
<li>Demonstrated ability to lead cross-functional research teams, manage projects, and effectively communicate with stakeholders.</li>
<li>Experience with state-of-the-art screening technologies and data analysis tools.</li>
</ul>
Desirable:
<ul>
<li>Experience with HTS and enabling automation platforms</li>
<li>Experience in managing relationships with Contract Research Organizations (CROs) and external partners.</li>
<li>Experience with enterprise data capture solutions (GeneData, Dotmatics, Benchling)</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Principal Scientist I, Cellular/Functional Biology

<h3>Job Description</h3>
Job Description
The Research Associate (RA) is a key member of the R&amp;D team, supporting important research projects and ongoing scientific activities. The RA brings 3-5 years of experience at a life sciences company, academic or medical research organization and is comfortable working in a fast-paced environment. The RA plays an important role assisting the CSO and other team members' conduct of the Company's clinical studies, technical validations, and scientific initiatives associated with CND's suite of neurodiagnostic products and services. The RA helps define research plans in collaboration with team members and performs secondary research on assigned topics. The RA provides key facts and figures for peer-reviewed publications and helps review and ensure all data is accurate and checked. The individual is a strong collaborator and is comfortable interfacing across multiple departments and communicating effectively with various team members. The RA has excellent attention to detail and provides effective written summaries of complex information. The individual also offers key insights on analyses and has experience discussing methods and conclusions with senior leaders in the organization.
Job Responsibilities:
Research Design and Execution
<ul>
<li>Contribute to the design and implementation of research projects </li>
<li>Conduct literature reviews to identify relevant research and methodologies</li>
<li>Support the development of research protocols and procedures </li>
<li>Help collect, analyze, and interpret data from various sources </li>
<li>Maintain accurate records of research activities and data </li>
</ul>
Data Analysis and Reporting
<ul>
<li>Support statistical analyses and other data analysis techniques</li>
<li>Develop figures for effective display of information</li>
<li>Help prepare reports, posters, presentations, and publications summarizing research findings </li>
<li>Aid in publication of manuscripts, abstracts and protocols</li>
</ul>
Collaboration and Communication
<ul>
<li>Work collaboratively with project teams, principal investigators(PIs), other researchers, and team members</li>
<li>Communicate research progress and findings effectively, both orally and in writing </li>
<li>Assist with grant writing and securing funding for research projects </li>
</ul>
Other Duties
<ul>
<li>Play a key role in maintaining the Company's scientific publications library and providing summaries of specific publications when needed</li>
<li>Stay current with advancements in the field and communicate to Company leaders</li>
<li>Assist with laboratory or field research activities when requested</li>
<li>Help manage research budgets and resources Perform literature searches as required and communicate relevant publications and findings to the research team.</li>
<li>Review agendas and abstracts from upcoming or previous scientific meetings and share relevant insights with the research team.</li>
<li>Contribute to additional activities, as needed, that support the goals of the research or study team</li>
<li>Perform other duties as assigned.</li>
</ul>
Knowledge, Skills &amp; Experience:
<ul>
<li>Experience in a research lab focused on innovative scientific advancements</li>
<li>Familiarity with moderately complex statistical methods that apply to applicable clinical studies</li>
<li>Ability to effectively manage multiple tasks and projects</li>
<li>Proficiency in relevant software, statistical packages, and laboratory techniques </li>
<li>Strong analytical and problem-solving skills are essential</li>
<li>Excellent written and verbal communication skills are necessary for effective collaboration and reporting </li>
<li>Strong organizational and time-management skills are needed to manage multiple projects and deadlines.</li>
<li>Ability to work effectively in a team environment.</li>
</ul>
Education, Certifications &amp; Licensures:
<ul>
<li>Master's degree or Ph.D is neuroscience required</li>
</ul>
Other:
<ul>
<li>This position is based in our Boston office (Coolidge Corner, Brookline) and is expected to be in-office at least 3-4 days/week.</li>
</ul>

Research Associate

<h3>Job Description</h3>
Job Description
We are seeking a motivated and detail-oriented Analytical Development Associate to support HPLC method development and analytical assay optimization. This role is essential in developing, improving, and qualifying analytical methods that ensure the quality and consistency of pharmaceutical products. The successful candidate will work closely with a collaborative team to support analytical initiatives while maintaining compliance with regulatory expectations.
Responsibilities
<ul>
<li> Support the development and improvement of HPLC methods for purity and impurity analysis. </li>
<li> Assist in the qualification of new and existing analytical assays. </li>
<li> Troubleshoot instrumentation and method-related challenges. </li>
<li> Design experiments and document procedures in accordance with good laboratory practices. </li>
<li> Maintain accurate and detailed laboratory records. </li>
<li> Collaborate with cross-functional teams to support technical and regulatory goals. </li>
<li> Contribute to initiatives that enhance the group’s technical capabilities.</li>
</ul>
Requirements
Qualifications
<ul>
<li> Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline from an accredited institution. </li>
<li> 1–3 years of hands-on experience with HPLC methods and assays. </li>
<li> Strong understanding of analytical chemistry techniques and method development. </li>
<li> Excellent problem-solving, communication, and documentation skills. </li>
<li> Proven ability to work independently and in team-oriented environments. </li>
<li> Strong organizational skills and a keen attention to detail. </li>
<li> A sense of urgency and ability to manage multiple priorities.</li>
</ul>

Senior Associate Scientist

<h3>Job Description</h3>
Job DescriptionSalary: $1,634 to $1,814/week commensurate with experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Easton, 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.

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