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<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.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionDescription:
About Lux
Lux Research is a leading research and advisory firm, helping clients navigate emerging technologies and drive growth through science-driven innovation. We sell to C-level executives in the world’s largest companies. Our culture is high-energy, detail-obsessed and relentlessly focused on performance. If you thrive in a fast-paced, demanding environment where results, accountability and engagement matter, join our team for what may be the most rewarding job you have ever had.
 
Role Description
Lux Research is seeking a Research Associate specializing in Utilities to help define and advance our vision for the future of innovation in transmission and distribution networks for the power grid. The ideal candidate will possess a strong foundation in a STEM discipline related to utilities—such as electrical engineering, mathematics, power systems engineering, energy systems, or a related technical field—and a passion for applying scientific and technical expertise to strategic innovation questions.
As a Research Associate at Lux, you will conduct and lead research that guides clients in understanding technological transformation within grid modernization including technologies enabling the power grid to carry more capacity with increased efficiency. You will develop thought leadership through writing analytical reports on emerging technologies and companies in the transmission and distribution system to deliver actionable insights which support investment, partnership, and strategy decisions for global electric utility leaders.
 
Salary Range: $65,000 - $75,000
 
Responsibilities:
· Lead research on emerging technologies shaping the utilities sector, including renewable integration, grid resilience, storage, electrification, and decarbonization technologies.
· Develop and test research hypotheses, synthesize data from diverse sources, and produce findings that help clients navigate innovation opportunities.
· Advise and support clients through written deliverables, direct consultations, and presentations, providing clear, evidence-based perspectives on technology and market trends.
· Produce high-quality research reports and analyses that connect innovation in utilities to broader sustainability, regulatory, and consumer dynamics.
· Represent Lux Research at industry conferences, webinars, and client events as a recognized thought leader in utilities and sustainable energy systems.
· Collaborate with analysts across disciplines and geographic regions to deliver integrated insights on cross-sector innovation challenges, including digitalization, infrastructure modernization, and circular resource management.
Requirements:
Minimum Qualifications:
· Bachelor’s degree in a STEM field related to utilities (e.g., electrical engineering, energy systems engineering, environmental science, applied physics, or related discipline).
· 1-2 years of experience in the utilities, energy, or sustainability sectors, ideally involving technology analysis, R&amp;D, or strategic consulting.
· Demonstrated ability to analyze technical and market data, develop original insights, and communicate them effectively to business and technical audiences.
· Exceptional writing and presentation skills, with experience crafting incisive, data-driven reports and delivering client presentations.
· Strong quantitative and qualitative analytical skills, with the ability to translate complex scientific concepts into business implications.
 
Desired Qualifications
<ul>
<li>A Master’s degree is highly preferred, especially with a STEM background in electrical engineering, energy systems, or related disciplines focusing on utilities processes.</li>
<li>Intellectual curiosity and a deep interest in innovation, energy transition, and the future of utilities.</li>
<li>Entrepreneurial and collaborative mindset, with a willingness to go the extra mile in a fast-paced environment.</li>
<li>High degree of organization, attention to detail, and commitment to delivering high-quality research that drives impact.</li>
</ul>
 
Lux Research is an Equal Opportunity Employer
Lux Research is an equal opportunity employer. In accordance with anti-discrimination law, Lux prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Lux Research conforms to the spirit as well as to the letter of all applicable laws and regulations. law. Lux Research conforms to the spirit as well as to the letter of all applicable laws and regulations.

Research Associate

<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>
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 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>
Yoh presents an excellent long-term&nbsp;Internal Laboratory Testing Coordinator&nbsp;opportunity with a trusted, long-term client located in Waltham, MA. Scientist/Sr. Research Associate -ESI&nbsp;Multiplex assays/Flow Cytometry Scientist/Sr. Research Associate The Yoh resource is expected to apply expertise across several areas in support of Sanofi Vaccines R&amp;D Global Immunology function developing innovative vaccine solutions for infectious diseases. Key Responsibilities:
<ul>
<li>Design and execute complex immunological experiments to evaluate vaccine candidates</li>
<li>Analyze immune responses using state-of-the-art techniques including multiparameter flow cytometry, ligand-binding, and cell-based assays</li>
<li>Support optimization of the automation of protocols and testing of the samples in automated immune assays as needed</li>
<li>Develop novel immunological assays to support vaccine development programs</li>
<li>Generate, analyze, visualize, and interpret scientific data sets, record experimental procedures and raw and analyzed data in electronic laboratory notebook</li>
<li>Author technical reports, SOPs, and contribute to regulatory submissions as required</li>
<li>Prepare and present findings to internal stakeholders</li>
<li>Provide technical guidance to junior team members as required</li>
<li>Collaborate within immunology and cross-functional teams across R&amp;D</li>
<li>Comply with the company HSE policies and minimize risk to self, others, and the environment, consistent with the community and industry standards.</li>
</ul>
Required Responsibilities:
<ul>
<li>Expertise in cellular and molecular immunology techniques</li>
<li>Proven experience with:</li>
<li>Spectral flow cytometry or flow cytometry with primary mammalian cells</li>
<li>Primary cells isolation and culture</li>
<li>Immunological assays development and implementation (ligand binding, multiplex (Luminex, MSD), cell-based)</li>
<li>Data visualization and analysis</li>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent documentation and record-keeping abilities</li>
<li>Proficiency in standard laboratory software and data analysis tools</li>
<li>Strong written and verbal communication skills</li>
</ul>
Preferred Responsibilities:
<ul>
<li>Experience with vaccine development or infectious disease research</li>
<li>Working knowledge of Good Research Practices (GRP) and electronic note booking</li>
<li>Proficiency in advanced data analysis tools (FlowJo, OMIQ, GraphPad Prism, &amp; other)</li>
<li>Experience with automated/semi-automated platforms/ liquid handlers</li>
</ul>
Education Experience:
<ul>
<li>Data Review</li>
<li>Training</li>
<li>Scheduling</li>
<li>GDP</li>
<li>GRP, compliance requirements for clinical trial samples</li>
<li>Master's degree in Immunology, Microbiology, or related field with 2+ years of relevant industry or academia experience</li>
<li>Bachelor's degree with 4+ years of relevant experience</li>
<li>Experience in pharmaceutical or biotechnology industry preferred. </li>
</ul>
 Estimated Min Rate: $31.50 Estimated Max Rate: $45.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities </li>
</ul>
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:&nbsp;<a href="https://www.yoh.com/privacy-notice" target="_blank">https://www.yoh.com/privacy-notice</a>

Scientist/Sr. Research Associate-ESI Multiplex assays/Flow Cytometry

<h3>Job Description</h3>
Central Processing Supervisor, Core Laboratory - Evening Shift
Location: Boston Teaching Hospital
 
<ul>
<li>Evening Shift: 3p – 11:30p ($3/hr evening diff).</li>
<li>Must be ASCP certified (or equivalent).</li>
<li>Sign-on bonus eligible.</li>
</ul>
 
Responsibilities:
<ul>
<li>Responsible for coordinating the daily operation of the front office of the core laboratory.</li>
<li>Oversees all Pre and Post analytic activity on the evening shift, in close conjunction with the day shift MT Operations Coordinator, reference lab staff, and other individuals who oversee areas that have an overlapping operating relationship with Central Processing.</li>
<li>Ensures that all activities, processes and policies are carried out in strict compliance with governmental regulations, licensing agency standards, and hospital policies and procedures.</li>
<li>Responsible for day-to-day general management including staffing, schedules, payroll, performance management, training, education, development of policy and protocol, compliance, and safety.</li>
<li>FTE's: 25+/-.</li>
<li>Reports to the Technical Director of Pre/Post Analytics in the Core Laboratory.</li>
</ul>
 
Qualifications:
<ul>
<li>MT (ASCP) or equivalent.</li>
<li>Bachelor’s Degree in Medical Technology or physical sciences.</li>
<li>4+ years of hospital laboratory experience, including knowledge of &amp;/or experience with pre/post analytics &amp;/or central processing.</li>
<li>1+ years of leadership experience.</li>
<li>Preferred: experience overseeing non-exempt hourly staff.</li>
</ul>

Central Processing Supervisor, Core Laboratory

<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>

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