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<h3>Job Description</h3>
Job Title: Winter, Spring 2026 Co-op-Intern- Oncology Research
Location: Cambridge, MA
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
The Immunomodulation &amp; Cell Reprogramming cluster within Sanofi Oncology is seeking a highly motivated co-op student. The successful candidate will work in a Cambridge MA state of the art facility within a multi-disciplinary team. The candidate will learn and utilize cutting-edge technologies to impact existing portfolio. &nbsp;The candidate will use molecular, cellular, and biochemical techniques to interrogate novel cancer therapeutics in human cancer models with an aim to bring the best new therapies to the correct patients.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
<ul>
<li>
Perform, analyze, and present the results of experiments.
</li>
<li>
Develop and execute cell-based assays to evaluate functional changes in human cancer models.
</li>
<li>
Evaluate signaling cascades to understand the biology of novel candidate therapeutic molecules.
</li>
<li>
Organize and communicate effectively, both orally and in writing
</li>
</ul>
About You
Basic Qualifications:
<ul>
<li>
Currently enrolled and pursuing&nbsp;a bachelor's degree in biology, biochemistry, molecular biology, cellular biology, chemistry, or related field at an accredited college or university with the expectation that you will complete your current degree by the Spring of 2029
</li>
<li>
Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
</li>
<li>
Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship
</li>
</ul>
Preferred Qualifications: 
<ul>
<li>
Previous lab experience is preferred &nbsp;
</li>
</ul>
Why Choose Us:&nbsp;
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.&nbsp;
</li>
<li>
Discover endless opportunities to grow your talent and drive your&nbsp;career, whether it’s through a promotion or lateral move, at home or&nbsp;internationally.&nbsp;
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your&nbsp;contribution and amplifies your impact.&nbsp;
</li>
<li>
Exposure to cutting-edge technologies and research methodologies.&nbsp;
</li>
<li>
Networking opportunities within Sanofi and the broader biotech community.&nbsp;
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.&nbsp;
#GD-SA ​ #LI-SA #LI-Onsite &nbsp;#vhd&nbsp;
null

Winter/Spring 2026 Co-op - Oncology Research

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face.
About Fapon Biotech
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
We are seeking a scientific contributor to develop validated analytical assays for LNP and drug product characterization. This role will be responsible for designing, developing and validating analytical assays for a targeted LNP drug product to support the platform and pipeline development. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams and provide analytical support to the discovery and PD teams. The ideal candidate is a sciences major with strong exposure to analytical techniques and who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
<ul>
<li>Designing, developing and validating analytical assays for LNP and targeted LNP drug product characterization</li>
<li>Develop assays for LNPs including lipid raw material QC, composition assessment, Lipid/cargo profiling and LNP/tLNP characterization using HPLC (SEC, Reverse Phase), fluorescence-based methods and other analytical techniques</li>
<li>Work with cross-functional groups including LNP discovery, PD and CMC team to support needs of analytical method development, characterization, and transfer</li>
<li>Perform CRO outreach including experimental planning, work coordination and data interpretation for as analytical SME</li>
<li>Support technology transfer to Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed)</li>
<li>Author technical documents, including SOPs for analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in life sciences, pharmaceutical sciences, or related field, preferably with 7/5 years of relevant experience. The title will be commensurate with experience.</li>
<li>Hands on experience developing analytical methods for complex biological therapeutics</li>
<li>Prior experience in developing analytical methods for LNP characterization is a must and will be key for this role</li>
<li>Knowledge of ICH/USP guidelines</li>
<li>Experience in analytical methods with HPLC (IPRP, SEC, IEx), UV-vis, colorimetric and fluorescence-based</li>
<li>Must be eligible to work in the United States</li>
</ul>
&nbsp; Preferred Qualifications:
<ul>
<li>Experience in developing validated analytical assays</li>
<li>Experience in advanced analytical methods for LNP characterization such as LC-MS, MALS, SEC-MALS etc</li>
<li>Strong communication skills and ability to present complex technical topics to diverse audiences with varying technical depth.</li>
<li>Strong collaborative instinct with good time and resource management skills to match the fast-paced start-up work culture.</li>
<li>Able to collaborate on and execute multiple parallel studies</li>
</ul>
 Additional Information 
What We Offer:
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior/Principal Research Associate (LNP Analytics)

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development.&nbsp;
We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects.&nbsp;
Job Responsibilities and Requirements:&nbsp;
<ul>
<li>Experience with protein chemistry, protein analytics, and bioprocess technology is required&nbsp;</li>
<li>Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process&nbsp;</li>
<li>Hands on experience and working knowledge on techniques including but not limited to&nbsp; liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet&nbsp;</li>
<li>Hands on experience with SDS-PAGE, ELISA, and&nbsp;experience with protein purification/chromatography at the lab scale is a plus&nbsp;</li>
<li>A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred&nbsp;</li>
<li>Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data&nbsp;</li>
<li>Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices&nbsp;</li>
<li>Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline&nbsp;</li>
<li>BS + 4-6 years or MS + 2-4 years of relevant experience&nbsp;</li>
<li>Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet&nbsp;</li>
</ul>
<ul>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, on-site Monday-Friday 8AM-5PM.&nbsp;</li>
<li>Pay range: $27.00 - $31.00 based on degree level and years of relevant experience with the skills utilized in the role.&nbsp;</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>#LI-EB1</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioprocess Analytical Chemist (Purification Process Support)

<h3>Job Description</h3>
Job DescriptionDescription:
Work Where it Matters
 
LDRM, a joint venture comprised of Lockwood Hills Federal, an Akima company, and DTSV, is not just another technical support contractor. As an Alaska Native Corporation (ANC), our mission and purpose extend beyond our exciting federal projects as we support our shareholder communities in Alaska.
 
At LDRM, the work you do every day makes a difference in the lives of our 15,000 Iñupiat shareholders, a group of Alaska natives from one of the most remote and harshest environments in the United States.
 
For our shareholders, LDRM provides support and employment opportunities and contributes to the survival of a culture that has thrived above the Arctic Circle for more than 10,000 years.
For our government customers, LDRM provides technical, operational, and administrative support services to federal agencies, including Department of State and the U.S. Patent and Trademark Office.
As an LDRM employee, you will be surrounded by a challenging, yet supportive work environment that is committed to innovation and diversity, two of our most important values. You will also have access to our comprehensive benefits and competitive pay in addition to growth opportunities and excellent retirement options.
 
Here’s why we want you to consider LDRM:
<ul>
<li>Tuition reimbursement program.</li>
<li>Platinum-level New Hampshire Veteran Friendly Business</li>
<li>Daytime hours, and no weekends</li>
<li>401(k), health, dental and vision plans, and other insurances you can use</li>
<li>An Employee Assistance Plan that’s ready when you need it</li>
<li>Paid training and paid time off</li>
</ul>
This is an external pipeline posting. The successful candidates will get an active offer, be taken through the federal security clearance process, and will then wait for a vacant position to start work. 
 
 
Job Summary:
 
As our Operations Research Analyst, you are responsible for making assessments after reviewing and evaluating information presented to you. You handle data set research and evaluation to draw conclusions, ensure compliance, and identify trends. You’ll team with multiple stakeholders to achieve optimal results. One of your primary responsibilities includes record keeping and report generation. As the person in this critical investigative position, you will gather domestic and international assignment information. Once you’re here, our benefits package helps take care of you and your family in many ways, including an excellent Employee Assistance Program. Career development is as important to us as it is to you, which is why we love to promote from within.
 
 
In this role you will:
<ul>
<li>Conduct research on cases prior to these being sent for adjudication by gathering information from a variety of sources, including but not limited to: petitions, applications, and supporting documents, the internet, telephone calls, government, commercial and open-source databases</li>
<li>Evaluate data sets and interpret the relevance of data gathered including numerical statistics, legal documents, and open-source material with regard to cases</li>
<li>Perform analyses on research conducted and information received from various locations to identify possible fraudulent activity related to cases</li>
<li>Ensure the integrity of recordkeeping systems and the veracity of data collected prior to entering the data into the record keeping systems</li>
<li>Write reports in a clear and concise manner that summarize the information gathered and identified during research</li>
<li>Coordinate and network with agency personnel, other government agencies, and coworkers to facilitate information sharing on cases that involve fraud or potential criminal activity</li>
<li>Handle appropriately any Law Enforcement Sensitive (LES) information</li>
<li>Perform analyses on petitions being returned to identify trends that may be useful in future research that is being conducted prior to the cases being sent overseas. Identify errors and areas for improvement in memos associated with these petitions</li>
<li>Maintain a working knowledge of a variety of resources related to eligibility requirements</li>
<li>Make phone calls to collect information on a personalized basis, and create reports based on the information provided</li>
<li>Evaluate the case at hand, analyze the specific and adapted questions that need to be asked, and communicate in an unscripted manner</li>
</ul>
You may be required to perform other duties as assigned to advance the unit’s mission of supporting case pre-adjudication.
 
Requirements:
Your Minimum Qualifications to be a Research Analyst:
<ul>
<li>Bachelor’s Degree and experience with research and/or reporting</li>
<li>Ability to effectively communicate orally and in writing</li>
<li>Report preparation and document analysis to establish authenticity and for evaluation against government standards</li>
<li>Ability to establish and maintain effective communications with peers and with government officials</li>
<li>Ability to use databases to obtain and validate information</li>
<li>Ability to comprehend government regulations</li>
<li>Ability to conduct telephonic interviews to obtain and/or validate petition</li>
<li>Ability to analyze and evaluate data and interview responses to prepare concise reports and records of findings</li>
<li>Ability to accept feedback</li>
<li>Ability to think flexibly (open-mindedness with no absolutes), and think outside of the box</li>
<li>Proficient use of Microsoft Office suite of products</li>
</ul>
You must be a U.S. citizen. Additionally, you must successfully complete a credit and criminal background check and be able to obtain a Secret-level federal security clearance. AGAIN, this is a pipeline position which, after you receive a federal clearance, may require a wait to begin work.
 
Physical Demands:
 
While performing the duties of this job, you may occasionally be required to stand; walk; sit; lift up to 20 lbs.; bend; reach; carry; stoop; kneel; use hands and fingers to handle, or feel objects, tools or controls; use fingers and hands to type or write; speak; or hear. Specific vision abilities may be required to perform the job which may include close vision, distance vision, color vision, peripheral vision, depth perception, or the ability to adjust focus.
 
At LDRM, honesty and integrity govern our activities. We fulfill our commitments, and we treat everyone with dignity and respect. As an Alaskan Native company, our mission is to improve the quality of life for our shareholders and our people by maximizing economic growth, protecting and enhancing our environment, and by promoting healthy communities with decisions, actions, and behaviors consistent with our core principles.

Research Analyst - DAYS - PIPELINE

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<h3>Job Description</h3>
Job Description
This is an unpaid internship of 15-29 hours per week in the Corporate Lexington location based on the candidate's availability 
Come join an exciting and innovative company that puts the “care” back in healthcare! 
At KabaFusion, our patients come from all walks of life and so do we. We hire GREAT people, period! Our culture celebrates and supports the differences that make us unique. Here, it doesn’t matter what your role is, your hard work and dedication is not only recognized but celebrated. Join us and find out why this is the place to excel and do your best work. 
About Us: 
What started as a single pharmacy in 2010 has grown into KabaFusion becoming the largest privately held home infusion company in the country. We have a national network of pharmacies and nursing offices strategically placed to service 40+ states. Couple that with over 30 years of combined experience and it’s no wonder why KabaFusion is the industry leader in home infusion. 
This is an exciting time to intern at an industry-leading fast-growing national specialty home infusion company to work with patient datasets and gain exposure to senior leadership. The overarching goal of this internship is to gain an understanding of the ways cutting-edge therapeutics impact patient outcomes with detailed information culled through data analytics techniques. 
Essential Duties
<ol>
<li>Assist with ongoing research projects.</li>
<li>Assist in literature reviews, data collection and presentation preparation.</li>
<li>Accurately and efficiently perform data entry and analysis.</li>
<li>Answer questions about the effectiveness of therapies and patient outcomes.</li>
</ol>
Education and Skills
<ol>
<li>College student or recent graduate preferred, with coursework in data analytics and an interest in health sciences.</li>
<li>Advanced skills in workplace tools, including Microsoft Office, required. </li>
<li>Strong interpersonal, verbal, and written communication skills. </li>
<li>Advanced level of multi-tasking and problem-solving skills, with attention to detail. </li>
<li>Ability to maintain confidentiality. </li>
<li>Ability to work with and analyze large datasets, preferred. 
 To learn more about KabaFusion, please visit our careers page: <a href="https://www.kabafusion.com/careers/" target="_blank">https://www.kabafusion.com/careers/</a>
Join us and find out why this is the place to excel and do your best work.
</li>
</ol>

Internship, Department of Clinical Affairs

<h3>Job Description</h3>
Job Description
Our client is seeking an organic chemist to join their Process Chemistry group. This contract position resides within the Pharmaceutical Sciences organization. The candidate will work full-time onsite and execute laboratory activities related to the development of robust drug substance manufacturing processes across various phases of drug substance development. The ideal candidate will conduct multi-step organic synthesis, route scouting and optimization, purification and characterization of intermediates and final compounds to support drug substance scale-up activities.
An ideal candidate will have a strong foundation in modern synthetic organic chemistry and analytical techniques such as NMR, LCMS, UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments. Experience in small-molecule process development and scale up is highly desired, however not required.
Responsibilities&nbsp;
<ul>
<li>Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member.</li>
<li>&nbsp;Collaborate with cross-functional teams to ensure successful project outcomes.</li>
<li>Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes.</li>
<li>Document and report experimental results and findings.</li>
<li>Draft and review technical documents (development reports, patent applications, tech transfer documents etc.) Maintain an accurate, timely and compliant laboratory notebook.</li>
<li>Maintain laboratory equipment and ensure compliance with safety regulations.</li>
</ul>
Requirements&nbsp;
<ul>
<li>An ideal candidate would have a B.S. or M.S. in Chemistry, or a related field with 3+ years of experience in pharmaceutical research or laboratory setting or, Ph.D. with 0-3+ years of experience.</li>
<li>Strong knowledge of organic chemistry.</li>
<li>Experience with early phase route development and process optimization Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Strong written and verbal communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Strong organizational and time management skills.</li>
<li>Ability to effectively prioritize and manage multiple tasks and compounds Ability to adapt to change and to work optimally within a variety of situations Ability to build productive working relationships across functions and highly diverse groups of individuals Self-motivated and willing to “learn on the job” and ask for assistance when needed Ability to make a significant impact in a results-driven environment where accountability is key.</li>
<li>A team player, who listens effectively and invites response and discussion A collaborator who communicates in an open, transparent, complete, timely and consistent manner</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Process Chemist

<h3>Job Description</h3>
Job Description
Scientist II/ Senior Scientist – Viral Vector / Discovery &nbsp;
(Hybrid – Greater Boston, on-site lab work required)&nbsp; NOTE: Applicants must be legally authorized to work in the United States on a permanent basis. At this time, the Company does not provide, and will not provide in the future, sponsorship for employment visas.
Why Work With Us?&nbsp;
At Candel, our people drive our mission to transform cancer care. We value curiosity, collaboration, and bold science in a supportive environment where everyone has visibility and impact. You’ll join a team that embraces creativity, trusts its people, and fosters growth through coaching and open discussion. This is the place to bring your ideas forward, dig deep into data, and see your work make a real difference for patients.&nbsp;
Our Science: Advancing Cancer Immunotherapies&nbsp;
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies designed to stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs, advancing novel treatments through discovery, IND-enabling studies, and into clinical development. With positive Phase 3 results for our lead candidate and multiple pipeline programs on the horizon, it’s an exciting time to join us. Learn more: <a href="http://www.candeltx.com&amp;nbsp" target="_blank">www.candeltx.com&amp;nbsp</a>;
Position Summary&nbsp;
This is a highly visible, hands-on role reporting directly to the VP of Research. As Scientist II /Senior Scientist, (We will determine final title and level based on your experience and background.) you’ll balance bench work and strategic contributions to advance novel viral vectors into IND-enabling studies and first-in-human trials. You’ll gain full-spectrum exposure across discovery, development, regulatory, and clinical programs, while contributing to the future of Candel’s viral immunotherapy platform.&nbsp;
We’re looking for a scientist who thrives in a fast-paced biotech with a “can-do” mindset — someone versatile enough to design experiments at the bench, analyze data, and present insights across functions. If you’re inquisitive, data-driven, and energized by the chance to innovate while still being hands-on, this role offers both the challenge and growth you’re seeking.&nbsp;
What You Will Do&nbsp;
<ul>
<li>
Support scientific strategy and execution for viral immunotherapy programs from discovery through IND-enabling studies.&nbsp;
</li>
</ul>
<ul>
<li>
Design and optimize viral vectors (e.g., HSV) for therapeutic applications, including genome engineering and payload design.&nbsp;
</li>
</ul>
<ul>
<li>
Oversee and perform in vitro and ex vivo assays to evaluate vector potency, transduction efficiency, and immunological activity.&nbsp;
</li>
</ul>
<ul>
<li>
Collaborate closely with cross-functional teams including CMC and Regulatory to ensure seamless program progression.&nbsp;
</li>
</ul>
<ul>
<li>
Guide the development and transfer of analytical and process development methods to the CMC team.&nbsp;
</li>
</ul>
<ul>
<li>
Mentor and manage junior scientists and research associates; foster a culture of scientific rigor, innovation, and collaboration.&nbsp;
</li>
</ul>
<ul>
<li>
Contribute to regulatory documentation, including IND-enabling study design and data interpretation.&nbsp;
</li>
</ul>
<ul>
<li>
Stay current with scientific literature and emerging technologies in viral vector design, immunotherapy, and oncology.&nbsp;
</li>
</ul>
What You Will Bring&nbsp;
<ul>
<li>
Ph.D. in Virology, Molecular Biology, Immunology, or related field with 3–5+ years biotech industry experience&nbsp;
</li>
</ul>
<ul>
<li>
Extensive hands-on experience with viral vector systems, including design, production, purification, and characterization; HSV experience a plus&nbsp;
</li>
</ul>
<ul>
<li>
Strong background in mammalian cell culture, transduction assays, and molecular biology techniques (qPCR, ELISA, flow cytometry)&nbsp;
</li>
</ul>
<ul>
<li>
Demonstrated experience developing and implementing platform-based approaches in cell and gene therapy (e.g., scalable vector design, modular assays, standardized workflows)&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with IND-enabling studies, GLP/GMP environments, and regulatory expectations for gene therapy products&nbsp;
</li>
</ul>
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<li>
Comfort running your own bench work while also contributing strategically&nbsp;
</li>
</ul>
<ul>
<li>
Proven ability to thrive in a lean, entrepreneurial environment without big-pharma infrastructure&nbsp;
</li>
</ul>
<ul>
<li>
Curious, data-driven mindset — eager to ask questions, revisit data, and generate new insights&nbsp;
</li>
</ul>
<ul>
<li>
Excellent written and verbal communication skills with confidence to present across levels and functions&nbsp;
</li>
</ul>
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<li>
Must be legally authorized to work in the United States. Sponsorship is not available; U.S. citizenship or permanent residency is required&nbsp;
</li>
</ul>
Preferred Attributes&nbsp;
<ul>
<li>
Desire to grow into leadership, with experience mentoring or guiding junior staff&nbsp;
</li>
</ul>
Work Environment&nbsp;
This is a hybrid role based in Greater Boston, with significant on-site lab work (bench and data analysis). Expect to be onsite most of the week to fully engage with research, team collaboration, and laboratory execution.&nbsp;
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Scientist II / Senior Scientist - - Viral Vector / Discovery

<h3>Job Description</h3>
Job DescriptionJob Title: Associate Scientist – iPSC-Derived Neuron Models Location: Lexington, MA, 02421 Duration: 1 year+ (Possibility of Extension) Onsite, 5 days/wk Pay Rate: $44.72-$51.43/Hour. on W2 TOP SKILLS PER MGR:
<ul>
<li>Human iPSC-derived neuron culture experience</li>
<li>Gene perturbations using siRNA and/or CRISPR</li>
<li>Cell-based molecular and biochemical assays including 1) immunocytochemistry, 2) qPCR, 3) ELISA, 4) micro-electrode array (MEA), and 5) fluorescence microscopy (at least 2-3 of these 5 skillsets).</li>
</ul>
 JOB DESCRIPTION: Position Summary: We are seeking a highly motivated and detail-oriented scientist to join our Humanized In Vitro Model Development team. The successful candidate will contribute to the development of human iPSC-derived neuronal models and assays to support drug discovery and translational research. This is an exciting opportunity to work at the forefront of human-relevant neuroscience in a collaborative and innovative environment. Key Responsibilities: • Culture, differentiate, and maintain human iPSC-derived neurons. • Perform routine cell-based and molecular assays including immunocytochemistry, qPCR, ELISA, MEA, luciferase, western blot, and fluorescence microscopy. • Conduct functional gene perturbations and pharmacological interventions. • Support assay development and optimization for phenotypic screening and mechanistic studies. • Analyze and interpret experimental data, maintain accurate records, and present findings in team meetings. • Collaborate cross-functionally with scientists in different units. • Contribute to protocol development, SOP documentation, and continuous improvement initiatives. Qualifications: • Bachelor’s or Master’s degree in Neuroscience, Cell Biology, Stem Cell Biology, or a related field. • LEVEL II - Minimum of 2 years of hands-on experience with human iPSC-derived neuronal cell models and assays. • LEVEL III - Minimum of 5 years of hands-on experience with human iPSC-derived neuronal cell models and assays. • Proficiency in cell-based assay techniques and fluorescence microscopy. • Strong organizational and communication skills. • Ability to work independently and collaboratively in a fast-paced research environment. • Comfortable working with electronic lab notebooks. Preferred Skills: • Experience with CRISPR editing, RNA-seq, calcium imaging, high-content imaging, or complex co-culture systems is plus. • Knowledge of automated liquid handling systems and high-throughput screening platforms. • Familiarity with cardiometabolic diseases is a plus. #sczr2

Associate Scientist iPSC-Derived Neuron Models

<h3>Job Description</h3>
Job Description
JOB SUMMARY
The Cultivation Technician will perform manual labor to assist in the upkeep, stocking, and fulfillment of growing cannabis, including, but not limited to; watering, feeding, pruning, cloning, cleaning, and transplanting. This position will report to the Cultivation Manager. 
PRIMARY RESPONSIBILITES 
<ul>
<li>Daily care of cannabis plants, including watering, pruning and trimming, inspecting the plants. </li>
<li>Fertilizing and providing nutrients to the plants according to cultivation protocols</li>
<li>Careful monitoring of the plants for any signs of growing issues or problems; treatment for disease or infestation.</li>
<li>Ensure the appropriate information is accurate and listed clearly in accordance with the state regulations and company standard operating procedures.</li>
<li>Carefully follow directions as provided by the Cultivation Department</li>
<li>Willingness to continue to learn best practices of cannabis cultivation with a strong interest in horticulture, agriculture and greenhouse operating systems.</li>
<li>Sweeping, mopping and all other required cleaning</li>
<li>Cleaning of the plant housing devices</li>
<li>Maintenance and cleaning of the plant tables</li>
<li>Maintenance of the plant pots</li>
<li>Reporting any issues to management to ensure a timely fix</li>
</ul>
JOB REQUIREMENTS 
<ul>
<li>Must be 21 years or older</li>
<li>Well organized and ability to keep deadlines</li>
<li>Ability to work in a team environment to achieve company goals</li>
<li>Effective time-management skills and ability to multi-task</li>
<li>Ability to work in a fast-paced, changing, and challenging environment</li>
<li>The willingness to continue to learn and grow with the company, improve cultivation skills and gain greater knowledge of cultivation processes.</li>
<li>Basic Excel, Word, and general computer knowledge</li>
<li>Full knowledge of all applicable law, regulations, and requirements; maintaining facility at 100% compliance at all times; this includes being up to date on any changes to current applicable laws/regulations </li>
<li>Must be and remain compliant with all regulatory requirements for working in the cannabis industry</li>
<li>Must be able to obtain and retain a Registered Agent Card issued by the state of operation</li>
<li>Must be focused, pay close attention to detail</li>
<li>Must be able to internalize training and follow instructions </li>
<li>Must be able to communicate clearly and effectively</li>
<li>Other duties and responsibilities</li>
</ul>
COMPANY OVERVIEW
Ascend Wellness Holdings (AWH) is a vertically integrated cannabis cultivator, processor and provisioning center operator with assets in Illinois, Maryland, Massachusetts, Michigan, New Jersey, Ohio and Pennsylvania. We seek to foster a robust and inclusive cannabis industry through a premium, unmatched customer-focused retail experience. We are looking to build a world-class team that will help carry out our mission of helping to shape the future of cannabis as a leading healthcare solution. We are committed to improving the quality of our patient's lives by offering unrivaled quality, consistency and meticulously curated products that satisfy our customers unique, individual needs. When it comes to customer service experience, our dispensaries will set a new standard of excellence, emphasizing health and wellness by a highly knowledgeable team. A team that is committed to our values, our people, and our communities; we are looking for people who are inspired by our vision and stay dedicated to our mission as we continuously expand.
EEO STATEMENT 
Ascend Wellness Holdings, Inc. ("AWH") and its subsidiaries is an equal opportunity employer and celebrate the population of differences and does not discriminate in its hiring / hiring practices, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. #LetsAscend

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