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<h3>Job Description</h3>
Job DescriptionSalary: $160,000 - $180,000 
About Acrivon Therapeutics
 Acrivon is a clinical stage biopharmaceutical company discovering and developing precision medicines utilizing its proprietary Generative Phosphoproteomics AP3 platform. The platform allows the company to interpret and quantify compound specific, drug-regulated pathway activity levels inside the intact cell in an unbiased manner, yielding terabytes of proprietary data and delivering rapid, actionable insights. The Generative Phosphoproteomics AP3 platform is comprised of a growing suite of powerful, internally-developed tools, including the AP3 Data Portal, converting multimodal data into structured data for generative AI analyses, the AP3 KaiSR Kinase Substrate Relationship Predictor, and the AP3 Interactome. These distinctive capabilities enable the company to go beyond the limitations of traditional drug discovery, as well as current AI-based target-centric drug discovery, and rapidly design highly differentiated compounds with desirable pathway effects through intracellular protein network analyses and advance these agents into the clinic for streamlined development.
 
Acrivon is currently advancing its lead program, ACR-368 (also known as prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2b trial for endometrial cancer. The company has received Fast Track designation from the Food and Drug Administration, or FDA, for the investigation of ACR-368 as a monotherapy based on OncoSignature-predicted sensitivity in patients with endometrial cancer. The FDA has granted a Breakthrough Device designation for the ACR-368 OncoSignature assay for the identification of patients with endometrial cancer who may benefit from ACR-368 treatment. In addition, the company has initiated a third arm to the Phase 2b study without the need for a pre-treatment biopsy to evaluate ACR-368 with ultra-low-dose gemcitabine (ULDG) sensitization in all-comer, biomarker-unselected 2nd line patients with endometrial cancer who have all received prior treatment with chemotherapy and anti-PD-1.
 
Acrivon is also leveraging its proprietary Generative Phosphoproteomics AP3 platform for developing its co-crystallography-driven, internally discovered pipeline programs. These include ACR-2316, the companys second clinical stage asset, a novel, potent, selective WEE1/PKMYT1 inhibitor designed for superior single-agent activity through strong activation of not only CDK1 and CDK2, but also of PLK1 to drive pro-apoptotic cell death, as observed in preclinical studies against benchmark inhibitors. The Phase 1 trial of ACR-2316 is advancing with enrollment in the first three dose-escalation cohorts completed. Drug target engagement was observed at DL1 and 2 using the companys clinical mass spectrometry-based AP3 profiling, with evidence of approximate dose proportionality based on plasma pharmacokinetic analyses, and initial clinical activity and confirmed partial response. In addition, the company is advancing a preclinical program directed against an undisclosed cell cycle regulatory target.
Position Overview:
This position will apply technical expertise to support biomarker assaysprimarily digital imaging, analysis and associated workflows, data analysis, scripting and LIMSwithin our CLIA/CAP framework, and work closely with our biomarker platform team to advance our precision medicines in oncology.
Location:
This position will report to the CLIA Laboratory Director and be based at least 60% in our Watertown, MA facility, with no more than 40% in a home office.
Duties and Responsibilities:
<ul>
<li>Execute validated slide scanning and quantitative image analysis protocols for highcomplexity tests, including IHC and multiplex immunofluorescence assays.</li>
<li>Develop and execute validation plans for equipment and assay procedures including software and electronic workflow.</li>
<li>Collaborate with cross-functional teams to develop image analysis algorithms, scripts and workflows to support clinical and research assay development.</li>
<li>Lead all LIMS efforts including configurations, validations, document support and training.</li>
<li>Provide technical guidance on laboratory automation, data tracking and workflow optimization.</li>
<li>Assist with biostatistics for validation protocols and result analysis.</li>
<li>Collaborate with Quality, Regulatory, and IT teams to maintain a compliant, efficient laboratory.</li>
<li>Participate in proficiency testing and regulatory compliance.</li>
<li>Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.</li>
<li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.</li>
<li>Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, or Laboratory Director.</li>
<li>Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.</li>
<li>Work on special projects as assigned by management.</li>
</ul>
Required Skills/Abilities:
<ul>
<li>Minimum of masters degree in computer science, medical technology, histology, biology, or related field.</li>
<li>Minimum of 5 years of experience in clinical or research pathology laboratory.</li>
<li>Expertise in digital pathology platforms including multispectral imaging systems.</li>
<li>Familiarity with histology and IHC (including both bright field and fluorescence techniques).</li>
<li>Proficiency in Python, RStudio, HTML and laboratory information systems.</li>
<li>Familiarity with machine learning/AI applications</li>
<li>Detailoriented, precise, and adept at working in regulated environments.</li>
<li>Excellent communication, problem-solving, and leadership skills.</li>
<li>Ability to participate constructively on cross-functional and diverse teams.</li>
<li>Visual acuity for microscopic examination and computer use.</li>
</ul>
Acrivon Therapeutics is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation, or genetics. In addition to federal law requirements, Acrivon Therapeutics complies with applicable state and local laws governing nondiscrimination in employment.

Laboratory Information and Workflow Manager, CLIA Immunohistochemistry (IHC) Laboratory

<h3>Job Description</h3>
This position is based in Cambridge, Massachusetts or San Francisco, Califonia. Remote work from certain states may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines. Candidates interested in remote work are encouraged to apply.
Purpose and Scope:
The Modality Intelligence Lead is a scientific subject matter expert within the Oncology Research Intelligence group, specializing in the strategic analysis of emerging therapeutic modalities such as next gen ADCs, engineered biologics, or small molecules. Reporting to the Head of CI&amp;RPM, this role provides deep, cross-oncology research portfolio insights on modality trends, competitor activities, platform technologies, and translational relevance to inform Oncology Research strategy. In addition to ongoing landscape monitoring and intelligence synthesis, the Modality Intelligence Lead proactively identifies high-potential external opportunities and leads the development of evaluation proposals for internal consideration. By collaborating closely with External Innovation Partners, Oncology Research Leadership, relevant PF (ie. PF-IO and PF-TPD) and Business Development, the role ensures timely, well-informed assessments that support strategic research alignment and external innovation prioritization.
Essential Job Responsibilities:
Modality Landscape Monitoring &amp; Strategic Foresight:
<ul>
<li>Continuously monitor scientific, clinical, and technological advances across prioritized therapeutic modalities.</li>
<li>Identify emerging trends, breakthroughs, and risks with implications for Astellas' oncology research strategy and modality capabilities.</li>
<li>Develop structured landscape assessments and foresight reports highlighting implications for internal pipeline differentiation and innovation gaps.</li>
</ul>
External Opportunity Assessment &amp; Strategic Framing:
<ul>
<li>Collaborate with External Innovation Partners and Business Development to assess novel platforms, technologies, and innovation opportunities aligned with prioritized therapeutic modalities and the overarching Oncology Research Strategy.</li>
<li>Support nonclinical-stage opportunity assessments by providing strategic modality insights, and lead the development of internal opportunity briefs and evaluation proposals for potential collaborations, partnerships, or in-licensing opportunities.</li>
</ul>
Collaboration &amp; Influence:
<ul>
<li>Act as a trusted advisor to CI&amp;RPM and other sub-function units in Oncology Research, and other scientific stakeholders on modality trends and strategic implications.</li>
<li>Partner with Innovation Intelligence analysts and Research Strategy Leads to ensure data-driven modality insights inform broader Oncology Research Strategy development.</li>
<li>Contribute to the enhancement of intelligence infrastructure (e.g., databases, dashboards, horizon scanning tools) with a modality focus.</li>
</ul>
Qualifications:
Required
<ul>
<li>Advanced degree (PhD, MD, MBA, or equivalent) in life sciences, pharmacology, medicinal chemistry, bioengineering or related field.</li>
<li>Minimum 8 years of experience in pharmaceutical R&amp;D, external innovation, academic collaboration, or scientific partnering.</li>
<li>Deep technical understanding of one or more modality platforms (e.g., engineered biologics, engineered small molecules, next generation ADCs).</li>
<li>Strong analytical skills with the ability to synthesize complex datasets and scientific trends into actionable strategy.</li>
<li>Proven experience influencing research or portfolio decisions through strategic insights.</li>
<li>Familiarity with the external innovation ecosystem including biotech start-ups, platform companies, and academic research.</li>
<li>Experience working closely with Research Leadership and Business Development on strategic evaluations.</li>
<li>High digital literacy and familiarity with CI or analytics tools/platforms.</li>
<li>Effective communication skills, with ability to convey scientific and strategic ideas to both technical and executive audiences.</li>
</ul>
Salary Range
$175K – $240K (NOTE: Final salary could be more or less, based on experience)
Benefits:
<ul>
<li>Medical, Dental and Vision Insurance</li>
<li>Generous Paid Time Off options, including Vacation, Sick time, plus national holidays including Heritage Days, and Summer and Winter Breaks</li>
<li>401(k) match and annual company contribution</li>
<li>Company paid life insurance</li>
<li>Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions</li>
<li>Long Term Incentive Plan for eligible positions</li>
<li>Referral bonus program</li>
</ul>
Category CI &amp; Research Program Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Modality Intelligence Lead, Oncology Research Intelligence

<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 
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 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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