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field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team The In Vitro Discovery team is a collaborative group driving antibody discovery and optimization using cutting-edge technologies. We work cross-functionally to advance therapeutic solutions, maintaining scientific rigor and efficiency in a fast-paced environment. The Role As an Associate Scientist, you will contribute to antibody discovery and optimization campaigns using state-of-the-art in vitro platforms. This role requires a highly motivated and detail-oriented individual with a strong background in molecular biology and antibody discovery techniques. You will collaborate closely with cross-functional teams to advance projects and deliver high-quality results. This role will report to the head of in vitro discovery and optimization, with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.&nbsp; How You’ll Drive Impact
<ul>
<li>Advance antibody discovery and optimization efforts through innovative in vitro strategies</li>
<li>Deliver high-quality experimental data supporting lead identification and engineering.</li>
<li>Foster effective cross-functional collaboration and communication.</li>
<li>Manage multiple projects with scientific rigor and organizational efficiency.</li>
<li>Contribute to Alloy’s culture of innovation and teamwork.&nbsp;</li>
</ul>
Principle responsibilities
<ul>
<li>Design, execute, and analyze experiments to support antibody discovery and engineering.</li>
<li>Collaborate closely with cross-functional teams to align project goals and timelines.</li>
<li>Document and communicate experimental findings clearly to stakeholders and teams.</li>
<li>Contribute to the development and optimization of in vitro platforms and workflows.</li>
<li>Manage multiple projects simultaneously, maintaining high scientific standards.</li>
<li>Provide technical expertise in molecular biology and related techniques.</li>
<li>Support high-throughput screening and assay development efforts.</li>
<li>Participate in regular team meetings and contribute to strategic planning.</li>
<li>Stay up to date with emerging technologies and scientific advances in the field.</li>
<li>Maintain an organized and efficient laboratory environment.</li>
</ul>
Qualifications
<ul>
<li>Minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree</li>
<li>Hands-on experience in molecular biology techniques (e.g., cloning, PCR, sequencing).</li>
<li>Hands-on experience with yeast/phage/mammalian display platforms</li>
<li>Strong organizational and communication skills to work effectively in collaborative settings.</li>
<li>Demonstrated ability to manage timelines and contribute to multiple projects in parallel.</li>
<li>Preferred experience with cell culture, flow cytometry,&nbsp;NGS sequencing and high-throughput screening</li>
<li>&nbsp;Ability to work across various US and international time zones.</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $94,500 - $104,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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7DYUTtBc3V

Associate Scientist, In Vitro Discovery

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite in Woods Hole, MA 
*Proposal Effort, Position is Subject to Contract Award
POSITION DESCRIPTION:
Think Tank is seeking a Biological Aquarium Technician to support animal care, life support systems, medical procedures, and visitor services in Woods Hole, MA. Working as part of the aquarium team, this role assists in daily husbandry tasks, habitat maintenance, public engagement, and educational activities that advance NOAA's mission of ocean literacy.
RESPONSIBILITIES:
<ul>
<li>
Prepare, monitor, and restock animal food and supplies.
</li>
<li>
Feed animals and document health indicators (injury, illness, stress, breeding, aggression, food intake).
</li>
<li>
Use biological lab and medical testing/sampling equipment as instructed.
</li>
<li>
Maintain habitats and exhibits, including cleaning and light repair work.
</li>
<li>
Support life support system monitoring and animal medical care.
</li>
<li>
Assist with visitor services: reservations, tours, school groups, VIPs, and special events.
</li>
<li>
Greet visitors, answer questions, and maintain educational materials.
</li>
<li>
Safely operate government vehicles as needed.
</li>
<li>
Keep back-of-house workspaces clean and organized.
</li>
</ul>
REQUIREMENTS:
<ul>
<li>
Education: High School Diploma/GED plus 2 years of college coursework (12+ semester hours in biology, chemistry, animal husbandry, or related sciences).
</li>
<li>
Experience: Lab or fieldwork experience applying biological methods, processes, and procedures.
</li>
<li>
Knowledge of aquarium husbandry, life support systems, and basic fish biology.
</li>
<li>
Ability to follow instructions, adhere to procedures, and maintain a reliable schedule.
</li>
<li>
Physical ability to stand, walk, bend, stoop, and lift light objects for extended periods.
</li>
<li>
Skilled in safe use of knives, food prep tools, and basic hand tools.
</li>
<li>
Familiarity with computers and ability to comply with cybersecurity protocols.
</li>
<li>
Strong teamwork and communication skills; able to interact positively with the public.
</li>
<li>
Valid driver's license; must qualify to operate a Government vehicle.
</li>
</ul>

Biological Aquarium Technician

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting to the Associate Director of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of research operations focused on pipeline advancement and evaluation. The Senior Research Associate I / II will be responsible for conducting immunogenicity assays to measure the efficacy of clinical vaccines and work closely with teammates on the organizations Translational Medicine team. Additional functions of the role include performing in vivo mouse experiments to characterize the immune response to the companys lead vaccine candidates.
Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts, with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States.
 Major Duties/Responsibilities
<ul>
<li>Execute immunogenicity and/or biomarker assays to evaluate correlates of response to therapeutic vaccination, such as ELISPOT/Fluorospot, ICS, and other flow cytometry-based assays</li>
<li>Complete experimental documentation and data analysis following appropriate SOPs for investigations on clinical samples</li>
<li>Perform PBMC isolations from whole blood and leukopak for research and clinical studies</li>
<li>Review and author compliant documents as part of the organizations document life cycle management</li>
<li>Assist with clinical sample management, including sample receipt and maintenance of the clinical sample chain of custody</li>
<li>Perform murine handling, injections, and blood/organ collections</li>
<li>Communicate findings in various forums and interact collaboratively with other team members</li>
<li>Willingness to learn new analytical assays and assist with the advancement of novel T cell and antibody-based assays</li>
<li>Perform job responsibilities in compliance with GCLP guidelines, where applicable</li>
</ul>
Education &amp; Professional Experience
<ul>
<li>BS with 3-5+ years of relevant work experience OR MS with 1-3+ years of experience</li>
<li>Ability to take initiative and produce in a fast-paced environment</li>
<li>Ability to prioritize tasks and consistently demonstrate strong decision-making and judgment skills</li>
<li>Strong attention to detail, organizational skills, and the ability to manage multiple projects</li>
<li>Outstanding communication (written and verbal) and interpersonal skills</li>
<li>This position is based in our Boston office and requires on-site presence</li>
</ul>
Working Conditions
<ul>
<li>Busy office/laboratory environment with frequent deadlines and interruptions</li>
</ul>
 
Travel
<ul>
<li>Travel is not required</li>
</ul>
 
Physical Requirements
<ul>
<li>Subject to periods of sitting or standing, vision is required to monitor data. Work is performed exclusively in an office/laboratory environment.</li>
</ul>
 
About Elicio Therapeutics
Elicio Therapeutics, Inc. (Nasdaq: ELTX) is a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of high-prevalence cancers, including mKRAS-positive pancreatic and colorectal cancers. Elicio intends to build on recent clinical successes in the personalized cancer vaccine space to develop effective, off-the-shelf vaccines. Elicios Amphiphile (AMP) technology aims to enhance the education, activation and amplification of cancer-specific T cells relative to conventional vaccination strategies, with the goal of promoting durable cancer immunosurveillance in patients. Elicios ELI-002 lead program is an off-the-shelf vaccine candidate targeting the most common KRAS mutations, which drive approximately 25% of all solid tumors. Off-the-shelf vaccine approaches have the potential benefits of low cost, rapid commercial scale manufacturing, and rapid availability of drug to patients especially in neo-adjuvant settings and for prophylaxis in high-risk patients, contrary to personalized vaccines approaches. ELI-002 is being studied in an ongoing, randomized clinical trial in patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. ELI-002 also has been studied in patients with mKRAS-positive colorectal cancer (CRC) in Phase 1 studies. The updated AMPLIFY-201 Phase 1 data for PDAC and CRC was presented at the ESMO Immuno-Oncology Congress 2024 and included a 16.3-month median recurrence-free survival and 28.9-month median overall survival for the full study population. In the future, Elicio plans to expand ELI-002 to other indications including mKRAS positive lung cancer and other mKRAS positive cancers. Elicios pipeline includes additional off-the-shelf therapeutic cancer vaccines candidates, including ELI-007 and ELI-008, that target BRAF-driven cancers and p53 hotspot mutations, respectively. For more information, please visit <a href="http://www.elicio.com" target="_blank">www.elicio.com</a>.
 
About the Amphiphile Platform 
Elicios proprietary AMP platform delivers investigational immunotherapeutics directly to the brain center of the immune system the lymph nodes. Elicio believes this site-specific delivery of disease-specific antigens, adjuvants and other immunomodulators may efficiently educate, activate and amplify critical immune cells, potentially resulting in induction and persistence of potent adaptive immunity required to treat many diseases. In preclinical models, Elicio observed lymph node-specific engagement driving therapeutic immune responses of increased magnitude, function and durability. Elicio believes its AMP lymph node-targeted approach will produce superior clinical benefits compared to immunotherapies that do not engage the lymph nodes based on preclinical studies.
 
Elicios AMP platform, originally developed at the Massachusetts Institute of Technology, has broad potential in the cancer space to advance a number of development initiatives through internal activities, in-licensing arrangements or development collaborations and partnerships.
 
The AMP platform has been shown to deliver immunotherapeutics directly to the lymph nodes by latching on to the protein albumin, found in the local injection site, as it travels to lymphatic tissue.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionJob Description The Role: Title: In vivo research associate, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated in vivo research associate to support in vivo experiment (rodent), including MTD studies, Efficacy studies, PK/PD studies and tissue harvest. You will also be asked to maintain and expand cancer cell lines to support the in vivo tumor model studies and conduct hand-on dosing and procedure support for mice pharmacology studies. In addition, you may need to support all aspects of laboratory operation to maintain a highly productive vivarium/laboratory. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Hand-on execute subcutaneous tumor model studies from cancer cells expansion, implantation (in mice), tumor measurement, group randomization and administration of test articles. </li>
<li>Hand-on support all mice pharmacology study procedures, including but not limiting to dosing and tissue harvest.</li>
<li>Follow PIRC IACUC program/protocols and standard operating procedures (SOPs) for all animal procedures.</li>
<li>Maintain and expand cancer cell lines for human xenograft tumor and mouse syngeneic tumor models. </li>
<li>Data process and graphing for the internal team update presentation.</li>
</ul>
Essential Qualifications:
<ul>
<li>B.S. or higher degree in immunology, pharmaceutical sciences or related scientific field</li>
</ul>
&nbsp;SkillPerformed in the last 2 years (includes training)In vitro assayELISANot required, good to knowMSDNot required, good to knowFACSNot required, good to knowHusbandry&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Aseptic TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Micro-Isolator TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Restraint &amp; HandlingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Room ChecksNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cage ChangeNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Injections/ Administration&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubcutaneousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntraperitonealMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntravenousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntramuscularNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oral GavageNot required, good to knowBlood Withdrawal&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tail BleedMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cardiac PunctureMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubmandibularMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; RO BleedNot required, good to knowEuthanasia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; CO2 OverdoseMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cervical DislocationMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; DecapitationNot requiredAnimal Preparation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ShavingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear TaggingNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear Punching/ NotchingNot requiredImplantation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Xenograft SCMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mammary Fat Pad&nbsp;Good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; TrocarNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Anesthesia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Isoflurane AnesthesiaNot required, good to knowLab OperationsGeneral Organizing lab spaceMustReceiving/stocking suppliesMustAny other duties that may ariseMustMammalian Cell CultureStandard mammalian cell culture procedures and associated aseptic techniques in addition to maintenance of tissue culture facilitiesMustMedia and buffer preparation, culture initiation, propagation, and cryopreservation of cells, including primary human and mouse cells and cell lines as well as adherence to quality control schedules for ensuring consistency of cell culture materials.Must &nbsp; EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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BCuKsdi8dH

In-vivo Research Associate, Immunology and Pharmacology

<h3>Job Description</h3>
Job DescriptionJob Title: Process Chemistry Contractor Location: Cambridge, MA, 02139 Duration:12+ months (Possibilities of Extension) Work Shift: : 5 days onsite in the lab. Pay Rate: $43/Hour on W2 Job Description Summary: Duties: Seeking an exceptional organic chemist to join our 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: • Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member. • Collaborate with cross-functional teams to ensure successful project outcomes. • Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes. • Document and report experimental results and findings. • Draft and review technical documents (development reports, patent applications, tech transfer documents etc.) • Maintain an accurate, timely and compliant laboratory notebook. • Maintain laboratory equipment and ensure compliance with safety regulations. Skills: Qualifications: • Strong knowledge of organic chemistry. • Experience with early phase route development and process optimization • Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software. • Strong analytical and problem-solving skills. • Strong written and verbal communication skills. • Ability to work independently and as part of a team. • Strong organizational and time management skills. Capabilities: • 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. • A team player, who listens effectively and invites response and discussion • A collaborator who communicates in an open, transparent, complete, timely and consistent manner Education: 
<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>
</ul>
 #sczr2

Process Chemistry Contractor

<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
We’re seeking a motivated scientist to support the development of next-generation antibody-drug conjugates (ADCs). In this role, you’ll perform hands-on conjugation and purification experiments with antibodies, peptides, and oligonucleotides, optimizing processes that directly impact the success of innovative therapeutics. Working under the guidance of experienced technical leads, you’ll gain valuable experience while contributing to projects that drive real-world impact.
Core Responsibilities: 
<ul>
<li>Develop and implement phase appropriate bioconjugation development strategies for the attachment of cytotoxic payloads, peptides, oligonucleotides, or other small molecules to antibodies, proteins, peptides, or other therapeutic entities.</li>
<li>Delivers experimental output with a high degree of scientific integrity, schedule and target adherence, and quality with guidance. </li>
<li>Exhibits safety awareness by conducting lab and other operations in a safe manner and holding themselves accountable for safe behavior in the work environment. </li>
<li>Act on feedback and shows continuous commitment to learning and development.</li>
<li>Makes efforts towards independently working and consistently meeting deadlines.</li>
<li>Keeps accurate, legible and complete records of all experiments, observations, and equipment. </li>
<li>Writes high quality reports and delivers presentations to customers and management with some guidance in alignment with the project milestones.</li>
<li>Builds an understanding of process chemistry for developing active pharmaceutical ingredients.</li>
<li>May maintain technical equipment.</li>
<li>Accomplishes other duties which are within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s degree (or equivalent experience) in a chemistry related discipline.</li>
<li> </li>
<li>Experience with bioconjugation lab and analytical techniques desired.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms</li>
<li>Good written and verbal communication skills.</li>
<li>Ability to work independently and in a team environment.</li>
</ul>
Preferred
<ul>
<li>Master’s degree (or equivalent experience) in a chemistry related discipline.</li>
</ul>
Special Factors 
<ul>
<li>While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Must be able to lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include: near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>Regularly works with moving mechanical parts and may work with toxic or caustic chemicals. </li>
<li>The work may be performed in humid areas with low or high temperatures. </li>
<li>This work may need to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Associate Scientist - Bioconjugation

<h3>Job Description</h3>
Job DescriptionAbout Us
Merryfield Investment Management, Inc. is a leading investment management firm that specializes in providing personalized investment solutions to high-net-worth individuals, institutions, and foundations. With a client-centered approach and a team of experienced professionals, we aim to help our clients achieve their financial goals through disciplined and calculated investment strategies.
About the Job
Merryfield Investment Management, Inc. is seeking a highly skilled Quantitative Analyst to join our dynamic team. As a Quantitative Analyst, you will be responsible for conducting in-depth research and analysis of market trends and data to help inform our investment decisions. You will utilize your strong quantitative and analytical skills to provide insights that drive performance and enhance our clients' portfolios.
Responsibilities
<ul>
<li>Develop, maintain and enhance quantitative models and tools for analyzing investment opportunities and tracking portfolio performance.</li>
<li>Conduct extensive research and analysis of market trends, economic indicators, and company financial data.</li>
<li>Collaborate with portfolio managers to identify investment opportunities and make data-driven investment decisions.</li>
<li>Perform statistical and data analysis to identify investment trends and opportunities within various market sectors.</li>
<li>Monitor and evaluate risk metrics, including value-at-risk, stress testing, and exposure analysis, to ensure effective portfolio management.</li>
<li>Utilize programming skills to develop and automate data collection, analysis, and reporting processes.</li>
<li>Present findings and insights to the investment team and assist in the formulation and implementation of investment strategies.</li>
<li>Stay up-to-date with industry developments and best practices to continuously improve our quantitative processes.</li>
</ul>
Requirements
<ul>
<li>Bachelor's or Master's degree in Mathematics, Statistics, Quantitative Finance, or a related field.</li>
<li>3-5 years of experience as a Quantitative Analyst, preferably in the investment management industry.</li>
<li>Strong analytical and problem-solving skills with a keen attention to detail.</li>
<li>Proficient in statistics, econometrics, and programming languages such as SAS, R, Python, or MATLAB.</li>
<li>Excellent communication and presentation skills, with the ability to clearly communicate complex quantitative concepts to non-technical stakeholders.</li>
<li>Knowledge of financial markets and investment products, with a deep understanding of risk management principles.</li>
<li>Ability to work independently and collaboratively in a fast-paced, deadline-driven environment.</li>
<li>CFA or FRM certification is a plus.</li>
</ul>
Bonus Points
<ul>
<li>Paid parental leave</li>
<li>Parental leave</li>
<li>Health insurance</li>
<li>401(k) matching</li>
<li>Paid time off</li>
<li>Vision insurance</li>
<li>Dental insurance</li>
</ul>

Quantitative Analyst

<h3>Job Description</h3>
FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services; tailored risk transfer capabilities; and superior financial strength. To do so, we rely on a dynamic, culturally diverse group of employees, working in more than 100 countries, in a variety of challenging roles.
 
Provide technical support in the performance of Research and Approvals tests conducted at the FM Research Campus, primarily in the Large and Small Burn Laboratories, under the direction of the General Foreman. Day-to-day activities includes test setup, instrumentation and equipment troubleshooting as well as firefighting and cleanup efforts.
 
High School/Trade School or Military specialist training with 3 years general mechanical or electrical experience.
1 year laboratory experience preferred.
Experience with or knowledge of product assembly, equipment repair, use of hand and power tools, welding/fabrication, use of instrumentation and sensors and computer literacy.&nbsp;
Must be able to commute to the FM Research Campus in West Glocester, RI.
Must be able to fulfill the physical requirements of the job (applies to all Labs, LBL, SBL, Remote Test Site, Earthquake Lab,&nbsp;and Campus Work Areas) including:
<ul>
<li>Ability to lift 50 pounds</li>
<li>Ability to climb stairs and ladders</li>
<li>Ability to work at heights</li>
<li>Ability to operate vehicles, lift trucks, fork trucks,&nbsp;other vehicles</li>
<li>Must be able to work while wearing full Firefighter’s Turnout gear with SCBA for an extended period of time in a wet and smoky environment</li>
<li>Must be able to obtain certification&nbsp;for using a personal respirator and work while wearing one for an extended period of time in a wet and smoky environment</li>
<li>Must not be claustrophobic and be able to work in tight and cramped spaces</li>
<li>Must have a current US Driver’s License</li>
<li>Must be able to communicate effectively in English</li>
<li>Must be able to work while wearing a Fall Protection Harness</li>
<li>Candidate must have the ability to read, write and speak English proficiently and the ability to understand and follow English instructions.</li>
</ul>
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.&nbsp;
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
#LI-TA1

Research Technician-Large Burn Laboratories

<h3>Job Description</h3>
FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services; tailored risk transfer capabilities; and superior financial strength. To do so, we rely on a dynamic, culturally diverse group of employees, working in more than 100 countries, in a variety of challenging roles.
 
The purpose of this position is to develop new scientific knowledge, technologies and engineering solutions to problems in material flammability, fire dynamics and Lithium-ion battery safety research, which can be used for the prevention or control of industrial property loss.&nbsp;&nbsp;&nbsp;
The principal responsibilities are to carry out research projects in the areas of flammability, fire spread, and heat transfer in fires from solid combustible as well as Lithium-ion batteries. Key areas of research include understanding of fire behavior at the medium and large scales via bench-scale experiments and theoretical models on material flammability and flame heat transfer. Projects can also involve advanced flame diagnostic of buoyant turbulent sooty flames and wall fires. The experimental and theoretical studies will be closely integrated with Computational Fluid Dynamic (CFD) model development and validation within the work group.&nbsp;
The position is responsible for all aspects of project management including project proposals, execution, and reporting.
 
The position requires a PhD in Mechanical, Chemical Engineering, Fire Protection Engineering, or related fields with a strong fundamental background in combustion, fluid mechanics, heat transfer, material science and applied mathematics.&nbsp; Extensive experience in experimental methods in thermal fluids, material flammability, heat transfer, combustion/fire, and an understanding of associated numerical methods are required. Research experience with advanced laser diagnostics in flame, experimental measurement in turbulent flame, heat transfer and failure analysis of battery is desirable. Also needed are excellent written and verbal communication skills, as well as demonstrated expertise in developing solutions to challenging technical problems.
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
#FMG
#LI-TA1

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