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<h3>Job Description</h3>
Job DescriptionDescription:
Join us at GEOKON Inc (est. 1979), a proud 100% ESOP company and The World Leader in Vibrating Wire Technology®, in the manufacturing of instrumentation and data logger used in civil, mining and structural engineering projects throughout the world. We continuously seek new and experienced talent to assist us in not only creating and implementing great products that our customers need, but also, to maintain and grow our fantastic culture built on integrity and respect. If our goals and values resonate with you, we would love to connect!
 
We are seeking an Engineer-Geotechnical SVCS who will partner with various stakeholders to provide solutions and technical support to our customers. 
Requirements:
The Engineer – Geotechnical SVCS will provide: 
 
Technical/Field Service Customer Support
<ul>
<li>Assist customers with instrumentation selection, installation practices based on project requirements/RFQ’s. Liaise with Sales and Engineering departments to realize compelling and competitive solutions to monitoring challenges.</li>
<li>Provide technical troubleshooting and support for existing installations via phone/email.</li>
<li>Provide data analysis to assess proper functionality and installation of instrumentation.</li>
</ul>
Field Service Coordination
<ul>
<li>Manage Field Service activities, coordinating requests from customers with GEOKON personnel, and providing field services as needed.</li>
<li>Prepare quotes and sales orders for field services, and occasional instrumentation products as needed.</li>
</ul>
Sales/Training Support
<ul>
<li>Assist with providing training on the overview and application of GEOKON products and instrumentation in general. This includes in-house training, on-site training, and webinars.</li>
</ul>
 
Your Contributions
 
Technical Skills/Knowledge
<ul>
<li>Pile design and pile testing</li>
<li>Slope stability</li>
<li>Groundwater hydrology</li>
<li>Understanding and use of various field instrumentation</li>
<li>Awareness of soil and concrete testing procedures</li>
<li>Familiarity with multiple aspects of geotechnical engineering</li>
</ul>
Other Requirements
<ul>
<li>Managing and interpreting customer requirements and project applications</li>
<li>General knowledge of a wide range of Civil Engineering projects and terminology</li>
<li>Exceptional analytical and problem-solving skills</li>
<li>Strong writing capabilities and the skill to write clear, concise technically correct technical documents with high attention to detail</li>
<li>Ability to exercise a high degree of independent judgment and professionalism</li>
<li>Comfortable presenting in front of others and fielding technical questions</li>
<li>Ability to travel 10-20% per year</li>
<li>Fluent English language required</li>
<li>Fluent Spanish languish/speaking preferred</li>
</ul>
 
What to expect with GEOKON:
<ul>
<li>100% Employee-Owned Company ---When the company does well, so do you, with Employee Stock Ownership</li>
<li>Dynamic and supportive culture built on innovation, integrity and respect</li>
<li>Flexible work schedules</li>
<li>Educational Reimbursement</li>
<li>Wellness Reimbursement </li>
<li>Generous Time Off Policy including 9 paid holidays and up to 24 hours of volunteer time, to support the communities and organizations that matter to you!</li>
</ul>

ENGINEER - GEOTECHNICAL SVCS

<h3>Job Description</h3>
Job Description
Description
To perform experiments organize data and analyze results under minimal supervision. With minimal supervision plans conducts or monitors experiments records and organizes data analyses results generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 
Responsibilities include: 
<ul>
<li>Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision </li>
<li>Plans monitors or conducts analyzes and records experiments and provides interpretation of data </li>
<li>Effectively transfers experimental methods from literature to the lab and makes modifications as necessary </li>
<li>Develops and implements new protocols with moderate review </li>
<li>Works efficiently in a matrix team environment and collaborates with coworkers </li>
<li>Communicates data and interpretation to work group </li>
<li>Skilled at developing systems to ensure quality data </li>
<li>Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques HPLC CE physical property testing... </li>
<li>Effectively trouble-shoots equipment and experimental difficulties </li>
<li>Contributes to internal/external reports papers presentations regulatory documents invention disclosure submissions and/or patents </li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Cambridge, MA.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Cambridge,MA.
Application Deadline
This position is anticipated to close on Nov 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Associate 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 
Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops.
The Science &amp; Technology (S&amp;T) organization within AbbVie Operations leads the optimization, validation, implementation, continuous improvement, and global technical support for therapeutic proteins. The S&amp;T Co-Op program provides students with robust projects based on business need. Students will do meaningful work that has a real impact on our business and patients worldwide. Possible 2026 Fall Co-Op assignments are in the following departments:&nbsp;
Bio-Process Development: The department’s mission is to design, deliver and support the biologics manufacturing process for AbbVie’s pipeline and partnered products through clinical development and commercial life cycle with quality, speed, and manufacturing excellence. This is achieved through a focus on targeted product quality, CMC acceleration, people development, and efficient workflows. Key groups include: Cell line development, Cell culture process development, Purification process development, Scale-up lab, and Analytical development.
Cell Line Development: Responsibilities include performing manual and automated processes to generate monoclonal cell lines and to execute various studies on these cell lines leading to the collection of a comprehensive data package for the final clone selection. The team utilizes state-of-the-art automation instrumentation and cutting-edge molecular biology tools at various stages of cell line expansions and performance evaluation. The group also carries out the design and quality control of the vectors used for cell line generation as well as the genetic characterization of the cell lines.
Key Responsibilities Include:
<ul>
<li>Executes experiments in bioprocess development and manufacturing support with supervision.</li>
<li>Performs basic data acquisition and analysis in a timely manner. Assists in experimental designs and data interpretation.</li>
<li>Documents work appropriately in lab notebooks and technical memos; contributes to writing technical reports</li>
<li>Maintains lab equipment and optimizes lab operations for efficient use of time and resources.</li>
<li>Troubleshoots equipment and experimental problems.&nbsp;</li>
<li>Assists in continuous improvement activities.</li>
</ul>
Qualifications 
Minimum&nbsp;Qualifications&nbsp;
<ul>
<li>Must be currently seeking a&nbsp;Master’s degree&nbsp;&nbsp;in a scientific or engineering discipline (preferably Chemistry/Chemical Engineering, Biosciences/Bioengineering).</li>
<li>Must be enrolled in university for at least one semester following the co-op</li>
<li>Expected graduation date&nbsp;between December 2026 – June 2027</li>
<li>Aseptic technique, transfection, Nucleic acid extraction, PCR, gene editing, Next Generation Sequencing, Western blotting, Immuno Precipitation, data analysis using Excel, Graphpad Prism.</li>
</ul>
Preferred Qualifications
<ul>
<li>Exposure to molecular biology techniques including DNA/RNA extraction, PCR, gene editing, Next Generation Sequencing</li>
<li>Aseptic technique</li>
<li>Cumulative GPA of 3.00 or higher preferred</li>
<li>Excellent problem-solving, written, and verbal skills</li>
<li>Exceptional interpersonal, leadership and project management skills</li>
<li>Proven track record of teamwork, adaptability, communication, innovation, initiative, and integrity</li>
<li>Desire to learn and execute scientific experiments</li>
<li>Keep update with published literature</li>
<li>Good time management</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​
Benefits and Amenities:​
<ul>
<li>
Competitive pay​
</li>
<li>
Relocation support for eligible students​
</li>
<li>
Select wellness benefits and paid holiday / sick time&nbsp;​
</li>
</ul>
​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the timeof this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, andwe may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus,commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolutediscretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

2026 Product Development Science & Technology Cell Line Development Co-Op (June - Dec) (Masters)

<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 and experienced scientist to join the Protein Sciences Analytical Team in Worcester, MA. This position provides a unique opportunity to directly impact multiple Discovery Research Therapeutic Areas (TAs) and projects by delivering in-depth analytical and functional characterization of biologics and biopharmaceutical products—including complex protein antigens, monoclonal antibodies, multi-specifics, and other antibody-like biologics. The ideal candidate will have a strong background in protein analytical characterization, with expertise in structural mass spectrometry, including hydrogen-deuterium exchange mass spectrometry (HDX-MS), crosslinking mass spectrometry (XL-MS), and covalent labeling mass spectrometry (CL-MS) to characterize epitopes and antigen-antibody interactions. The successful candidate will foster productive collaborations across functional groups and therapeutic areas. This is an excellent opportunity for a motivated scientist to make a significant impact in a collaborative and innovative environment. Join us in bringing innovative medicines to patients!
Key Responsibilities:
<ul>
<li>Independently develop and execute high-throughput HDX-MS workflows for epitope mapping analysis of biotherapeutics to support discovery pipeline projects.</li>
<li>Develop, optimize, validate, and apply innovative structural MS methods (including XL-MS and CL-MS) to characterize epitopes and antigen-antibody interactions.</li>
<li>Demonstrate scientific initiative and creativity by establishing novel workflows and strategies for the characterization and screening of biologics—including non-traditional modalities such as multi-specifics, alternative scaffolds, and fusion proteins—to support BGM and TA projects.</li>
<li>Collaborate with external partners, CROs, or vendors to advance project objectives.</li>
<li>Analyze, document, and report data concisely; formulate conclusions and design follow-on experiments based on multidisciplinary inputs.</li>
<li>Resolve key project challenges by leveraging analytical tools, information, and technical expertise.</li>
<li>Communicate project progress, data analyses, and technical recommendations clearly and promptly to cross-functional teams and senior management.</li>
<li>Present original research and findings internally and at external scientific conferences; contribute to scientific papers, patents, and technical reports as an author or co-author.</li>
</ul>
Qualifications 
<ul>
<li>BS or MS or PhD in biology, chemistry, biochemistry or related field with typically 10-12+ (BS), 8-10+ (MS) or 0-4+ (PhD) years of experience.</li>
<li>Extensive hands-on experience with HDX-MS platforms (e.g., Trajan’s LEAP HDX automation) and use of HDX-MS data analysis software (e.g., HDExaminer) for epitope mapping analysis.</li>
<li>Strong knowledge of structural mass spectrometry technologies, including covalent labeling MS, and crosslinking MS.</li>
<li>Advanced proficiency with multiple mass spectrometry platforms (such as Orbitrap and Q-ToF), including MS workflows for protein characterization and expertise with relevant data analysis software.</li>
<li>Familiarity or experience with coding/programming (e.g., Python, R, or relevant scripting languages) and in developing automated data workflows or solutions is preferred.</li>
<li>Familiarity with biophysical and structural methods, such as DLS, DSF, SEC-MALS, SEC-SAX, X-ray crystallography, etc. is a plus&nbsp;</li>
<li>Demonstrated theoretical and hands-on expertise in scientific disciplines, with a proven ability to rapidly learn and apply new technologies.</li>
<li>Excellent organizational skills and ability to manage multiple projects and tasks concurrently while meeting deadlines.</li>
<li>Collaborative, goal-driven professional with strong verbal and written communication skills, a proactive attitude, and success operating in fast-paced, cross-functional environments.</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance.</li>
<li>Learns fast, grasps the “essence” and can change course quickly when indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</li>
</ul>
Position will be filled at level commensurate with extent of education, experience, and accomplishment - Senior Scientist I or Senior Scientist II
 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 may be&nbsp;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, Protein Analytical Characterization

<h3>Job Description</h3>
Job Description
*3 YEAR CONTRACT*
 
To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities:
<ul>
<li>Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision,</li>
<li>Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data,</li>
<li>Effectively transfers experimental methods from literature to the lab and makes modifications as necessary,</li>
<li>Develops and implements new protocols with moderate review,</li>
<li>Works efficiently in a matrix team environment and collaborates with coworkers,</li>
<li>Communicates data and interpretation to work group,</li>
<li>Skilled at developing systems to ensure quality data,</li>
<li>Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing...),</li>
<li>Effectively trouble-shoots equipment and experimental difficulties,</li>
<li>Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents,</li>
<li>Participates in department-wide support efforts such as safety, recruiting and committees,</li>
<li>May train staff and/or supervise others,</li>
<li>Coordinates and organizes resources needed to complete the task,</li>
<li>Understands when to seek input and when to make independent judgments.</li>
</ul>
Requirements / Qualifications:
<ul>
<li>Minimum BS degree (MS is preferred) in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and at least 2 year experience in a Biopharmaceutical working environment.</li>
<li>BioPharma lab experience is a plus</li>
<li>HPLC expertise - able to operate, process data, and report findings into electronic lab notebook.</li>
<li>Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently.</li>
<li>Experience working in a biopharmaceutical lab showing analytical skills (compendial assays such as pH, osmolality, protein concentration, particle sizing etc).</li>
</ul>
Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search. 
<h3>Company Description</h3>
The Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search.

<h3>Job Description</h3>
Job Title: Associate Scientist
Location: Cambridge MA – 100% Onsite
Duration: 3 Years Contract
Terms: Contract W2
 
Description:
 
Fully onsite 8-5. Cambridge site. Must be able to commute to site. Open to relocation candidates but must be willing to start ASAP.
 
Must have: HPLC expertise and hands on lab experience.
M.S. and 1 YOE would be ideal.
 
B.S. and 3 YOE would be acceptable but a M.S is preferred.
 
Managers ideal candidate: Someone who has a couple of years experience in biopharma working on bioanalytical assays such as SEC HPLC, Ion Exchange HPLC, and some basic assays like pH, osmolality, protein concentration etc. Good communication skills are also a must as they will work with a big group of people.
 
Job Details:
 
1+ Years w/ Relevant MS OR equivalent 3+ Years w/ Relevant BS
 
To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
 
Responsibilities include:
1 Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision,
2 Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data,
3 Effectively transfers experimental methods from literature to the lab and makes modifications as necessary,
4 Develops and implements new protocols with moderate review,
5 Works efficiently in a matrix team environment and collaborates with coworkers,
6 Communicates data and interpretation to work group,
7 Skilled at developing systems to ensure quality data,
8 Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing...),
9 Effectively trouble-shoots equipment and experimental difficulties,
10 Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents,
11 Participates in department-wide support efforts such as safety, recruiting and committees,
12 May train staff and/or supervise others,
13 Coordinates and organizes resources needed to complete the task,
14 Understands when to seek input and when to make independent judgments.
 
Requirements: Minimum BS degree (MS is preferred) in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and at least 2 year experience in a Biopharmaceutical working environment.
 
Top 3 Must Have Skill Sets: 
BioPharma lab experience is a plus
HPLC expertise - able to operate, process data, and report findings into electronic lab notebook.
Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently.
Experience working in a biopharmaceutical lab showing analytical skills (compendial assays such as pH, osmolality, protein concentration, particle sizing etc).
 
Day to Day Responsibilities: 
Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance and communicated with the study owners.

Associate Scientist/Chemist (HPLC experience)

<h3>Job Description</h3>
Job description:
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery based in Cambridge MA. In this role, the candidate will collaborate with multiple cross-functional teams to advance portfolio projects, with a particular emphasis on supporting in vitro data generation. Responsibilities include performing and adapting cell-based in vitro protocols in a timely manner across diverse cell systems, data analysis and effective communication of results, and collaboration across multiple teams. The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery. The position requires ability to work independently, demonstrate excellent technical, written and oral communication skills and work very well in a collaborative team environment.
 
Key responsibilities
<ul>
<li>Human colon organoid culture, passaging, and plating for experiments to support the group</li>
<li>Perform cell-based assays using cell lines and mammalian primary cells</li>
<li>Test biologic and small molecules in cell-based assays for functional readouts including cell proliferation, cytokine release, and gene expression</li>
<li>Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF, qPCR)</li>
<li>Responsibilities may include processing animal tissue ex vivo and isolation of immune cells from human and animal tissue or blood</li>
<li>Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need</li>
<li>Maintain close communication with multiple groups to support human colon organoid cell needs</li>
<li>Implement and innovate new experimental protocols/techniques as needed</li>
<li>Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment</li>
<li>Impact projects mostly through lab-based activities</li>
</ul>
 
Qualifications and requirements:
<ul>
<li>Bachelor’s degree in Biological Science or related field with 2+ years of experience in biotech or pharma setting (industry experience)</li>
<li>Experience with human organoid culture</li>
<li>In vitro assays with primary human immune cells (ie myeloid, PBMCs)</li>
<li>Molecular and cellular analysis techniques including qPCR, MSD, ELISA, flow cytometry</li>
</ul>

Biologist

<h3>Job Description</h3>
Role:- Chemical Engineer
 Location:- Lexington/Cambridge, MA – onsite 
 
Technical Expertise:
<ul>
<li>Enablon Metrics Module Experience</li>
<li>Green House Gas Protocol (reviewing, evaluating, editing)</li>
<li>Enablon compliance or sampling (nice to have)</li>
<li>Carbon Emissions calculations for Scope 1 &amp; 2</li>
<li>Familiar with Water and Waste management reporting</li>
</ul>
Educational Background
<ul>
<li>Environmental / Chemical Engineer</li>
</ul>
Work Outline:
<ul>
<li>Day to day management of all Scope 1, 2, Water &amp; Waste data for Takeda Globally</li>
<li>Creating, updating campaigns, formulas, creating, versioning of indicators etc. in the Enablon Metrics Module</li>
<li>Ability to verify carbon emissions calculations, run re-calc scripts and perform data analysis based on formulas, as required</li>
<li>Work with Takeda Site users globally</li>
<li>Enablon System admin experience a plus</li>
</ul>

Chemical Engineer

<h3>Job Description</h3>
Scallop Bay Shellfish Company (SBSC) is a vertically integrated aquaculture company based out of Pocasset, MA on Cape Cod.
 
SBSC is currently seeking a highly motivated research technician, with proficiency in microalgae techniques and lab-based research experience. The candidate will be responsible for conducting research that contributes to our understanding of microalgal biology within the context of commercial aquaculture. The desired candidate will have a strong background in laboratory techniques, proficient in microalgae culture, as well as experience in independently performing lab based research and data analysis.
 
Standard tasks: 
<ul>
<li>Conduct laboratory and field research on microalgae species, focusing on their growth, nutritional requirements, and production in bioreactors.</li>
<li>Analyze the biochemical composition of microalgae and assess their potential for scalable production.</li>
<li>Prepare detailed reports and presentations on research findings for both internal stakeholders and external publications.</li>
</ul>
<ul>
<li> </li>
Preferred qualifications:
<ul>
<li>A MS or Ph.D. in Microbiology, Marine Biology, Environmental Science, or a related field is preferred.</li>
<li>Experience with laboratory techniques such as microscopy, spectrophotometry, and bioreactor production methods is highly desirable.</li>
<li>Proficiency in data analysis and statistical analysis of experimental results.</li>
<li>Excellent written and verbal communication skills for effective collaboration and reporting.</li>
</ul>
<li> </li>
The typical work schedule is Monday-Friday 7am-3pm, though this is subject to change seasonally. Depending on the needs of the research plan, work on weekends and/or holidays is required intermittently.
 
All full time employees are eligible for health and dental 50% company paid, HCA company funded 100%, all Federal holidays, 3 weeks paid vacation, paid sick time, and a competitive salary. Health and dental may start day 1 of full time employment, vacation time accrues based on hours worked. Part time employees receive paid Federal holidays and a competitive wage.
</ul>

Research Assistant

<h3>Job Description</h3>
Job Description
Greater Lynn Senior Services, Inc has a great opportunity for a hands-on experience that would be ideal for a Math, Business, Economics, Healthcare Administration or Social Work major!
Summary
This internship will assist the CEO and Senior Leaders in data collection and analysis focused on the Strategic Planning efforts. In addition, this internship will provide administrative support and research for the Lynn Non-Profit Leadership Group as requested.
Qualifications
<ul>
<li>College level aptitude in data collection and analysis</li>
<li>Professional demeanor with the ability to handle confidential information and documents with discretion and according to GLSS policy and HIPAA guidelines</li>
<li>Must be proficient in the use of Microsoft Word, Excel and Outlook</li>
<li>Ability to meet established deadlines and demonstrate excellent time management and efficiency</li>
<li>Excellent interpersonal skills with the ability to ask questions to obtain detailed and complete information</li>
<li>Ability to work both independently and as part of a team</li>
<li>Well-developed listening skills</li>
</ul>
Responsibilities
<ul>
<li>Assist strategic planning work groups with date gathering and administrative support as requested</li>
<li>Assist with community based needs surveys for strategic planning work groups</li>
<li>Assist CEO with research and support for Lynn Non-Profit Leadership initiatives</li>
<li>Research and identify funding mechanisms to support innovation capacities across strategic planning work groups</li>
</ul>
Hours: 20 hours per week - Starting January 2026
*GLSS is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age (40 or older), disability or genetic information.*
*GLSS will provide reasonable accommodations to applicants with disabilities upon request*

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