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<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 
<ul>
<li>Lead and mentor a team of 10-12 scientists specializing in establishing separation-based assays including HPLC (e.g. SEC, IEX, RPLC), capillary electrophoresis (CE, icIEF), etc. for QC lab implementation to support GMP release and stability testing and for sample testing in PDS&amp;T - Analytical Development to support biologics DS process development, characterization, validation as well as GMP manufacturing investigation activities. &nbsp;Develop high-throughput analytical methods and drive timely delivery of high-quality testing results.</li>
<li>Serve as a primary contact for Analytical Development in AbbVie's CMC teams, supporting both early and late-stage biologics pipeline assets. &nbsp;Balance stakeholder expectations between PDST and other AbbVie analytical functions to ensure effective collaboration.</li>
<li>Develop, communicate, and implement analytical strategies with broader PDS&amp;T analytical functions and CMC business partners. &nbsp;Oversee experimental execution, development, qualification, validation, and transfer of robust analytical methods for QC lab as well as analytical control strategy development.</li>
<li>Guide team to evaluate and select effective analytical technologies and methods for meeting program needs.&nbsp; Evaluate and interpret data trends in release and stability assays. &nbsp;Demonstrate scientific excellence in the analytical characterization of biologics and ensure robust documentation of study findings.</li>
<li>Author and review analytical sections of IND/BLA filings for early and late-stage programs, provide response support to agency information request. &nbsp;Ensure all submissions comply with regulatory requirements and industry standard.</li>
<li>Collaborate with other analytical teams in R&amp;D and PDS&amp;T on program transition, workflow and program strategic alignment.&nbsp; Provide guidance to peers in project management, analytical strategy development, and technical skills related to separation techniques.</li>
<li>Communicate project strategies, issues, and risks to relevant teams. &nbsp;Promote proactive risk resolution within and across functional areas to advance project objectives.</li>
<li>Build a high-performing team to proactively seek method and product understanding, build robust product knowledge and new capability, and advance science and innovation.&nbsp; Lead team to actively publish novel study findings at internal and external conferences and journals.</li>
</ul>
Qualifications 
<ul>
<li>MS or PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline. &nbsp;Minimum of 12+ years (MS) or 8+ years (PhD) of professional experience working in biotech/pharmaceutical setting.</li>
<li>Proven experience managing and leading analytical development activities for biologic development, including mAbs, bispecifics, antibody-drug conjugates, and fusion proteins.</li>
<li>Expertise in protein and impurity analysis techniques such as HPLC, capillary electrophoresis, and other relevant methods. &nbsp;Experience with mass spectrometry and ELISA is a Plus.</li>
<li>Familiarity with USP/ICH guidelines for method development, qualification, and validation. Extensive experience in authoring, reviewing regulatory submissions and responding to agency information requests.</li>
<li>Strong technical and people leadership skills, and demonstrated ability to foster an engaging, inclusive and collaborative team environment.</li>
<li>Ability to quickly comprehend and adapt to new situations, with an open mindset and can-do attitude, demonstrating agility where necessary to address evolving project needs.</li>
<li>Excellent communication, organization and inter-personal skills, effectively managing relationships to enhance team decision-making.</li>
</ul>
 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 is 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>

Principal Research Scientist II

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the Head of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
0–2 years post-PhD or 2–5 years of industry/academic R&amp;D experience (not QC/manufacturing).
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: flexible schedule, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Research Associate I / II

<h3>Job Description</h3>
Job DescriptionTumor Ex-vivo Research Associate (6 month contract role) Position Summary We are seeking a highly motivated Research Associate on a 6 month contract basis to join the Primary Cell Platform (PCP) Team within the Immunology and Pharmacology Department at PIRC. The candidate will be part of a collaborative and fast-paced team driving preclinical research focused on human tumor biology and immune function. The role offers the opportunity to work with clinically relevant human samples and contribute to translational research efforts that support early-stage therapeutic discovery. A strong candidate will have a background in immunology and/or cell biology, with prior hands-on experience in cellular assays, tissue culture, or immunoassays. The ability to work effectively within multidisciplinary teams, follow complex protocols, and deliver high-quality experimental data is essential. This is an excellent opportunity to gain experience in advanced tumor modeling and immunoprofiling techniques while supporting impactful, real-world research. This is a 6 month contract with potential to transition to a full-time permanent role based on performance and project success. Upon conversion, the employee will be eligible for our full benefits package. &nbsp;Main Responsibilities
<ul>
<li>Perform in vitro and ex vivo experiments focused on tumor-immune interactions using primary human models</li>
<li>Support the culture and maintenance of primary tumor tissues, including tumor slice assays, spheroids/organoids, and immune co-cultures</li>
<li>Process tumor/blood specimens: e.g. tissue dissociation, PBMC isolations from whole blood, viability assessment, and assay preparation</li>
<li>Execute immunological assays such as:
<ul>
<li>Flow cytometry, ELISA, MSD, cytokine profiling</li>
<li>T cell activation, proliferation, and cytotoxicity assays</li>
</ul>
</li>
<li>Culture primary human immune cells (e.g., PBMCs, T cells, macrophages)</li>
<li>Analyze and interpret experimental data and present findings to the team</li>
<li>Maintain detailed, timely, and compliant documentation using an electronic lab notebook (ELN)</li>
<li>Follow lab safety and quality standards</li>
<li>Be available for occasional after-hours work to support time-sensitive tumor sample processing</li>
</ul>
Basic Qualifications
<ul>
<li>Bachelors/Masters degree in Immunology, Cell Biology, Biomedical Sciences, or a related life science field with 2-3 years of industrial experience</li>
<li>Available to work full-time, onsite for the 6 months duration without needed work authorization/sponsorship from the company</li>
</ul>
Preferred Qualifications
<ul>
<li>Previous relevant laboratory experience is highly preferred</li>
<li>Skilled in aseptic technique and primary human cell culture</li>
<li>Experience with tumor tissue handling, 3D culture systems, or ex vivo tumor models</li>
<li>Familiarity with flow cytometry, immunoassays, and related technologies</li>
<li>Experience using an electronic lab notebook for experimental documentation</li>
<li>Excellent communication, time management, and organizational abilities</li>
<li>Collaborative, flexible, and motivated to work in a fast-paced translational research environment</li>
</ul>
 &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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erzebwIriX

Tumor Ex-vivo Research Associate (6 month contract role)

<h3>Job Description</h3>
Job DescriptionSenior/Principal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated and experienced senior or principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond. In this position, you will utilize your expertise in pharmacokinetics, pharmacodynamics, and biomarker discovery to guide drug development and biomarker strategies, optimize dosing regimens, and ensure the safety and efficacy of investigational drugs. You will also contribute to translational activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms. These efforts include indication expansion, novel combinations, and refining/improving biomarker approaches to guide dosing and patient selection. Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. 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), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities:
<ul>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Further Exploration of BESREMi: Collaborate with clinical development team to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally and be involved in investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Regulatory Interaction: Work with regulatory affairs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, new drug applications (NDAs), and marketing authorization applications (MAAs). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>3+ (for senior scientist) or 8+ (for principal scientist) years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via contract research organizations and academic collaborations.</li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism of action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models is preferred.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials is strongly desirable.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Experience working closely with academic collaborators via sponsored research agreements or IITs is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
Conclusion: As a Senior/Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward and ultimately improving patient outcomes at PIRC.
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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o8966sEgdk

Senior/Principal Scientist, Translational Sciences

<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.
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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>
Job Description
GEOTECHNICAL PROJECT MANAGER
Award-winning environmental engineering firm is seeking a senior level project manager to add to its team. Candidate will lead commercial projects in New England. The role involves managing proposals, budgets, schedules, technical deliverables, and client relationships, while also mentoring supporting business development.
This is a full-time, permanent opportunity to grow with one of the area's best outfits.
Company offers excellent compensation and benefits packages, flexible work schedules, 401k, PTO, and more!
<ul>
<li>Bachelor's degree in environmental engineering or related with 5+ years of industry experience.</li>
<li>EIT or PE license highly preferred.</li>
<li>Oversee full scope of projects - interact with clients, track projects and provide technical support, mentor junior staff, keep tabs on financials, etc.</li>
<li>Experience with soil and groundwater remediation, evaluations, site investigations, safety practices.</li>
<li>OSHA certified with strong written and oral communication skills.</li>
</ul>
610-684-8680
Keywords
Environmental Engineer, Environmental, Remediation, Environmental Investigation, Remediation, Project Manager, Site Investigations, OSHA, HAZWOPER, LSRP

Geotechnical Project Manager

<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.
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