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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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Associate Scientist, In Vitro Discovery

<h3>Job Description</h3>
Job Description
John Turner Consulting (JTC), an environmental and engineering consulting firm serving New England, is seeking an experienced Senior Geologist to join our Portsmouth, NH office.
This is a strategic hire for a senior-level environmental professional ready to lead, mentor, and grow a team, with flexibility to work in a hybrid schedule.
Your Role
In this leadership role, you will oversee site investigation and remediation projects, supervise junior technical staff, and contribute to business development. You will bring a strong command of regulatory compliance at local, state, and federal levels, and have the potential to generate up to $1 million in annual revenue through project leadership and client management.
Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lead environmental site assessments, investigation, and remediation projects throughout New England
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prepare and review technical documents, including sampling plans, remedial action plans, and regulatory reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Manage and mentor junior staff, promoting professional development and safety
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Interface with regulatory agencies such as NHDES, MassDEP, MEDEP, and EPA
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support and drive business development, including proposal writing and client outreach
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain responsibility for project scope, budget, and schedule
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Contribute to strategic planning and help grow JTC’s environmental practice
Qualifications
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 15+ years in environmental consulting with increasing technical and leadership responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; New Hampshire Professional Geologist (PG) required; multi-state licensure is a plus
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrated ability to maintain and grow a portfolio of work worth $1M+ annually
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong knowledge of environmental programs (RCRA, CERCLA, TSCA)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience with New England environmental regulations and permitting
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Successful collaboration with local, state, and federal regulatory agencies
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience managing and mentoring junior staff
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong organizational and communication skills
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bachelor’s degree in Geology, Environmental Engineering, or a related field required; Master’s degree preferred
Why Join JTC?
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Competitive 401(k) plan with company match
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Comprehensive medical, dental, vision, and prescription coverage
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Generous vacation, sick leave, holidays, and family medical leave
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hybrid work environment with a balance of office, home, and field time
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Opportunities for advancement, mentorship, and professional development
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Collaborative, supportive culture committed to quality and safety

Senior Geologist

<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 Description
Cultivation Technician
Location: Berkley, MA
 
About Renew Cannabis Co.
At Renew Cannabis Co., people are at the heart of everything we do. Our team members are the foundation of our success, and we are committed to fostering a positive, supportive workplace. By joining our team, you'll contribute to our mission of delivering quality cannabis products while advancing the industry.
 
Job Summary
We are seeking motivated Cultivation Technicians to join our team. In this role, you will be responsible for executing cultivation tasks according to our operating procedures. This includes all aspects of the cannabis production cycle, such as cloning, plant care, harvesting, and facility maintenance.
 
Key Responsibilities
<ul>
<li>Cultivation: Perform tasks such as cloning, transplanting, pruning, watering, and monitoring plant health during vegetative and flowering phases.</li>
<li>Harvesting: Assist in cutting plants, trimming, weighing, and entering inventory data into our tracking system.</li>
<li>Monitoring: Ensure plants are growing under optimal conditions, including pest and disease control, and address any quality concerns.</li>
<li>Facility Maintenance: Operate and maintain cultivation systems (lighting, irrigation, climate control), and ensure all equipment and workspaces are clean and sanitized.</li>
<li>Maintain compliance with state regulations, security protocols, and company policies.</li>
<li>Perform other duties as assigned to support the team and meet company goals.</li>
</ul>
 
Qualifications
<ul>
<li>Strong work ethic, reliability, and flexibility.</li>
<li>Ability to work in a fast-paced, team-oriented environment.</li>
<li>Excellent communication skills and attention to detail.</li>
<li>Physical ability to perform tasks such as standing for long periods, climbing ladders, and lifting up to 50 pounds.</li>
<li>Previous experience in cannabis or agriculture is preferred but not required.</li>
<li>Working Conditions</li>
<li>Exposure to bright lights, moderate heat and humidity, and background noise from environmental systems.</li>
<li>Frequent use of tools and equipment, with occasional heavy lifting.</li>
<li>Regular cleaning and handling of cultivation supplies and materials.</li>
</ul>
 
Why Join Us?
Renew Cannabis Co. offers a collaborative work environment where team members are valued and supported. We are passionate about providing opportunities for growth and contributing to a positive workplace culture.
 
If you're looking to build a career in cannabis and are excited about hands-on work in cultivation, we encourage you to apply!

Cultivation Technician

<h3>Job Description</h3>
Job DescriptionDescriptionPrecision Neuroscience is pioneering a brain implant, known as a brain-computer interface (BCI), to restore communication and independence for people with neurological conditions. Our cutting-edge technology is designed to empower people with paralysis to control digital devices—such as computers and smartphones—with their thoughts alone, opening new possibilities for daily life.&nbsp;&nbsp;Precision’s multidisciplinary team brings together leading experts in diverse fields such as neurosurgery, artificial intelligence, machine learning, microfabrication, electrical engineering, and more. We are committed to turning breakthrough scientific advancements into real-world solutions for people affected by conditions such as spinal cord injury, stroke, and ALS. &nbsp; As a Precision employee, you will be joining one of the fastest moving and best-capitalized companies in the emerging field of BCI. Since our founding in 2021, Precision has secured over $155 million in funding, developed and validated our technology, and initiated human trials in collaboration with some of the nation’s top hospitals.&nbsp; We are seeking a highly experienced and detail-oriented Staff Scientist, Preclinical Surgical Research to lead the design, execution, and analysis of preclinical animal studies at our Massachusetts-based Contract Research Organization (CRO). This is a senior-level, cross-functional role central to our scientific, technical, and regulatory efforts. The ideal candidate will bring deep large animal surgical expertise, scientific rigor, and operational leadership to the development of innovative neurosurgical and implantable systems. This position will be based in our Boston office. We are unable to consider remote workers or people not currently based in the United States, with working rights. Key Responsibilities
<ul>
<li>Design and execute preclinical animal studies to evaluate medical device systems and answer key scientific, technical, and regulatory questions. Define study objectives, endpoints, and methodology in alignment with R&amp;D and regulatory strategy.</li>
<li>Lead the drafting, refinement, and execution of surgical protocols aligned with experimental goals, animal welfare standards, and regulatory requirements. Maintain strict version control and support protocol review and approval processes (e.g., IACUC, GLP).</li>
<li>Coordinate closely with R&amp;D, Regulatory, and Quality teams to ensure that studies are designed and conducted to support system-level verification and validation (V&amp;V), meet regulatory submission needs, and withstand technical and scientific scrutiny.</li>
<li>Perform and oversee complex surgical procedures, with an emphasis on large animal models. Ensure procedural consistency, sterility (where required), and surgical quality across studies.</li>
<li>Manage day-of-study execution, including experimental setup, surgical logistics, team coordination, and intraoperative troubleshooting.</li>
<li>Collect, analyze, and interpret experimental data to extract meaningful insights, inform system development, and support formal reporting. Collaborate with internal stakeholders to contextualize results within broader product development.</li>
<li>Own inventory and procurement of all experimental and surgical supplies, ensuring readiness and compliance with procedural requirements.</li>
<li>Maintain meticulous surgical and experimental records, including intraoperative observations, procedural deviations, and postoperative outcomes.</li>
<li>Lead cross-functional debriefings after surgical sessions and produce detailed technical reports to inform design iteration and future studies.</li>
<li>Organize and lead planning meetings for in vivo experiments, ensuring timely decisions, clear documentation, and alignment across research, veterinary, and operational stakeholders.</li>
</ul>
 Skills, Knowledge and Expertise
<ul>
<li>Minimum of 5 years of experience conducting and analyzing in vivo surgical research, preferably with large animal models.</li>
<li>Strong experience in the design and execution of preclinical studies supporting medical device development.</li>
<li>Familiarity with GLP principles, V&amp;V requirements, and regulatory expectations related to animal studies.</li>
<li>Proven ability to work across functions to translate experimental findings into design, risk, and regulatory documentation.</li>
<li>High proficiency in sterile surgical technique, operating room setup, instrumentation, and procedural execution.</li>
<li>Demonstrated excellence in data analysis, technical documentation, and communication with cross-functional teams.</li>
<li>Outstanding organizational skills and attention to detail.</li>
</ul>
Preferred Qualifications
<ul>
<li>Advanced degree (MS, PhD, DVM) in biological sciences, biomedical engineering, veterinary science, or a related field.</li>
<li>Direct experience conducting complex surgeries in large animal models (e.g., pigs, non-human primates).</li>
<li>Prior involvement in GLP or regulatory-submission-enabling preclinical studies.</li>
</ul>
Diverse workforces create the best culture, company, and products. We at Precision are committed to an inclusive culture that celebrates the uniqueness and contributions of everyone. As an equal opportunity employer, Precision does not discriminate on the basis of sex, race, religion, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Staff Scientist, Preclinical Surgical Research

<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 DescriptionThe Science Team at Russell Tobin &amp; Associates is supporting a world-class organization that has an opening for “Research and Development Associate I”. This position is split 50/50 between compound management and assay development. Key Responsibilities
<ul>
<li>Prepare assay-ready plates using automation and manage compound inventory.</li>
<li>Coordinate compound shipments and maintain library records.</li>
<li>Develop and run biochemical and cell-based assays in 384- and 1536-well formats.</li>
<li>Support high-throughput screening using liquid handlers and analyze assay data.</li>
</ul>
Qualifications
<ul>
<li>B.S. (up to 4 yrs exp.) or M.S. (up to 2 yrs exp.) in Biology, Chemistry, or related field.</li>
<li>Experience with plate-based assays and lab automation.</li>
<li>Organized, detail-oriented, and able to work in a fast-paced team environment.</li>
</ul>
Preferred
<ul>
<li>Background in compound management, LIMS, or HTS workflows.</li>
<li>Familiarity with liquid handling systems and basic cell culture.</li>
</ul>
 Additional Information:
<ul>
<li>Location: Cambridge, MA</li>
<li>Assignment Duration: 12 months </li>
<li>Pay range: $30-$34/hr. on W2</li>
</ul>
 Must be authorized to work in the United States. Russell Tobin offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life &amp; disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. APPLY NOW! #LI-RA1 #rta-zr JD-#SCIENCE #RTA Company DescriptionPride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life &amp; disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance and employee discounts with preferred vendors. 
<h3>Company Description</h3>
Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life &amp; disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance and employee discounts with preferred vendors.

Research and Development Associate I

<h3>Job Description</h3>
Job DescriptionDescription:
At Terra Fertility, we are reimagining fertility care by making it more accessible through transparent pricing, innovative technology, and comprehensive patient education. We aim to ensure that everyone—regardless of background, language, or identity—feels informed, empowered, and supported throughout their fertility journey.
 
Role Summary
We are seeking a highly skilled and experienced Senior Embryologist to join our IVF laboratory team in Dedham, Massachusetts. The ideal candidate will bring at least 5 years of hands-on experience in embryology, including advanced techniques such as ICSI, PGTA, cryopreservation, and embryo biopsy. The Senior Embryologist will collaborate with clinical, laboratory, and administrative teams to support excellent patient outcomes and operational excellence.
 
Key Responsibilities
<ul>
<li>Perform ICSI, embryo biopsy (e.g., trophectoderm biopsy), and vitrification with high accuracy and success rates.</li>
<li>Support daily operations of the embryology lab including quality control, media preparation, equipment maintenance, and documentation.</li>
<li>Assist with oocyte retrievals, including assessment and preparation of oocytes and semen samples.</li>
<li>Perform fertilization assessments, embryo culture, grading, and cryopreservation.</li>
<li>Adhere to strict quality assurance, double-verification, and safety protocols to maintain lab integrity.</li>
<li>Support embryo transfer processes and communicate with physicians and nursing teams as needed.</li>
<li>Maintain accurate and timely records in laboratory information systems.</li>
<li>Ensure compliance with all regulatory requirements (e.g., CLIA, FDA, OSHA).</li>
<li>Participate in data review, protocol optimization, and lab performance improvement initiatives.</li>
<li>Provide mentorship and training to junior embryology staff.</li>
<li>Support research and validation projects as needed.</li>
</ul>
Work Schedule and Compensation
 
<ul>
<li>This is a full-time, salaried, exempt position. This role is 40 hours/week. </li>
<li>The compensation for this role is $120-170,000, commensurate with experience and qualifications.</li>
<li>Eligible for a generous bonus based on individual and clinic performance. </li>
<li>Comprehensive health, dental, and vision insurance. </li>
<li>401(k) with employer match beginning on day one. </li>
<li>Paid Time off </li>
<li>Support for professional development and ongoing education. </li>
<li>Inclusive, mission-driven workplace environment. </li>
</ul>
Accessibility and Inclusion 
Terra Fertility is committed to fostering an inclusive, diverse, and equitable work environment. We are proud to be an equal opportunity employer. Reasonable accommodations are available upon request during the hiring process or on the job for individuals with disabilities. 
As a condition of employment, Terra Fertility requires all team members to be fully vaccinated against COVID-19 and influenza. Reasonable accommodations will be considered in accordance with applicable laws. 
 
Accommodations
Terra Fertility is committed to providing equal employment opportunities to all individuals. If you require a reasonable accommodation during the application or interview process, or to perform the essential functions of this role, please contact our team at <a href="mailto:info@terrafertility.com" target="_blank">info@terrafertility.com</a>. We will work with you to meet your needs in accordance with applicable law.
 
 
Requirements:
<ul>
<li>Bachelor’s degree in Biology, Biomedical Sciences, or related field required.</li>
<li>Minimum of 5 years of hands-on embryology lab experience, preferably in a high-volume IVF setting.</li>
<li>Proficiency in ICSI, embryo vitrification/warming, egg vitrification embryo biopsy, and embryo culture techniques.</li>
<li>PGT-A biopsy experience strongly preferred.</li>
<li>Strong working knowledge of embryology laboratory equipment, regulatory standards, and best practices.</li>
<li>Detail-oriented with exceptional accuracy and problem-solving skills.</li>
<li>Excellent communication and collaboration with multidisciplinary teams.</li>
<li>Flexible and reliable, with availability for early mornings and occasional weekend or holiday shifts if needed.</li>
</ul>

Senior Embryologist

<h3>Job Description</h3>
Job Description
Title: Undergraduate HTE Research Co-op (Spring - Summer 2026)
Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 75 have entered clinical trials.&nbsp;&nbsp;
Role
We are seeking a motivated student&nbsp;to join our High Throughput Expression Group for approximately 40 hours per week, with the potential for minimum (2-4 hours) weekend work. The successful candidate will provide support on the following tasks:
Responsibilities
<ul>
<li>Media formulation</li>
<li>Yeast culture maintenance</li>
<li>Routine platform affinity purification</li>
</ul>
Needed upon hire
<ul>
<li>Working towards degree in Biotechnology, Bioengineering, or a related field</li>
<li>Detail oriented</li>
<li>Ability to commit to a 6-month term starting in January 2026</li>
<li>Knowledge of basic wet bench skills and laboratory safety</li>
<li>Adaptable and productive in a fast-paced environment</li>
<li>Ability to communicate effectively and openly with colleagues and supervisors&nbsp;</li>
<li>Willing to work weekends as needed</li>
</ul>
Come join us!
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people.&nbsp;
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the&nbsp;Dartmouth Hitchcock&nbsp;Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, and biking.
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