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field_job_employment_type

job_organization_name

city

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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 
We are seeking a highly motivated Senior Scientist I to join the Purification Process Development group within the Operations Product Development Science &amp; Technology -Biologics organization.&nbsp; Our group is responsible for purification process development across early- and late-stage of therapeutic proteins at AbbVie Bioresearch Center in Worcester, MA.&nbsp; As one of leaders in the Purification Development group, this is a dynamic role which will drive the development and transfer of robust and effective purification processes for IND and BLA-enabling programs.&nbsp; In addition, the ideal candidate will develop and apply next generation technologies (i.e. laboratory automation / robotics, modeling, advanced data analysis) and outside-of-the-box thinking to drive efficiency of the purification lab, platforms, and strategies.&nbsp; The candidate will also coordinate and lead purification development activities within cross-functional CMC teams with a collaborative and progressive mindset. &nbsp;
This position is an onsite role in a lab-based function. To be successful candidates must enjoy and thrive in an onsite, highly collaborative lab environment with daily face-to-face cross-functional interactions between scientists.
Responsibilities
<ul>
<li>Development, optimization, scale-up, and tech transfer of purification processes for biologics candidates to support early and late-stage development &nbsp;</li>
<li>Maintain a high level of productivity and accuracy in the lab&nbsp;</li>
<li>Demonstrate creative 'out of the box' thinking to solve difficult problems and champion new technologies to achieve project goals.&nbsp;</li>
<li>Proactively seek out new tools, techniques, and strategies to implement into the overall downstream platform, specifically with respect to the use of lab automation, robotics, and the use of next gen data analytics tools (ML/AI). &nbsp;</li>
<li>Represent purification development team and actively influence development strategy on cross-functional CMC teams &nbsp;</li>
<li>Work efficiently, collaboratively, and cross-functionally toward project timelines and goals&nbsp; &nbsp;</li>
<li>Transfer processes to pilot and GMP manufacturing</li>
</ul>
<ul>
<li>Work with contract labs and carry out viral clearance studies &nbsp;</li>
</ul>
<ul>
<li>Write technical publications, reports, presentations, and regulatory filings including publishing research in peer-reviewed journals and presenting work at scientific conferences &nbsp;</li>
<li>Mentor and train junior scientists&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Degree in Chemical Engineering, Biochemistry, Chemistry or other sciences</li>
<li>Bachelor’s degree + typically 10 or more&nbsp;years of experience OR Masters + typically 8 or more years of experience, OR a PhD&nbsp;with no experience</li>
</ul>
<ul>
<li>Must have expertise in developing standard bioprocess unit operations such as chromatography separations (resin/membrane: affinity, CEX, AEX, HIC, MM) and/or filtration operations (depth filtration, virus filtration, sterile filtration, TFF)&nbsp;</li>
</ul>
<ul>
<li>Able to independently design, execute, and interpret laboratory experiments to answer scientific questions&nbsp;</li>
</ul>
<ul>
<li>Able to independently learn, understand and execute novel/advanced scientific techniques&nbsp;</li>
</ul>
<ul>
<li>Must have excellent attention to detail and ability to keep detailed electronic lab notebook records&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Proven record of authoring publications, technical reports, regulatory documents, and presentations&nbsp;</li>
</ul>
<ul>
<li>Has strong communication skills including verbal, written, and scientific data presentation&nbsp;</li>
<li>Has proficiency with Microsoft Office software, ability to learn new software applications &nbsp;</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Proficient in writing methods and operating AKTA chromatographic instruments (such as AKTA Avant, AKTA Purifier, AKTA Pure, AKTA Ready or similar)&nbsp;</li>
<li>Experience with automated or robotic liquid handling systems (TECAN, Hamilton, or other) for high-throughput experimentation or sample handling and capable of driving the design of experiments using these systems.</li>
<li>Experience with analytical techniques, such as HPLC or ELISA and integration of these methods with automation tools.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist I, Purification Process Development

<h3>Job Description</h3>
Job Description
<ul>
<li>Will be working in a cleanroom assembling consumables the size of a cell phone</li>
<li>Process involves taking very thin &nbsp;thin film adhesives off the machine, laying them all out on a vacuum table, making sure no wrinkles etc.</li>
<li>Putting some epoxy on the plastic shell, peeling off the adhesive from the table using fingers or tweezers, lining it up and putting it on the shell.&nbsp; Finish the assembly, visually inspect for defects, putting in a bag and putting the label on it.&nbsp; Total process takes about 4 minutes.</li>
</ul>
Keys to the role
<ul>
<li>Comfortable working in a cleanroom all day</li>
<li>Good dexterity</li>
<li>Reliable, lives in city and can take public transportation</li>
<li>There’s a free shuttle from North and South stations</li>
</ul>
Company DescriptionBlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers. 
<h3>Company Description</h3>
BlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers.

Cleanroom Consumable- Hiring ASAP ($25-26/hr)!!!

<h3>Job Description</h3>
Job Description
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 seeking a highly creative and broadly skilled laboratory Research Associate to help us build our growing menu of diagnostic assays for veterinary medicine and the in vitro device (IVD) market. You will play a key role in development and validation of new techniques and laboratory methods for this next generation clinical diagnostic system.
RESPONSIBILITIES:
<ul>
<li>
Design, develop and validate new clinical chemistry, hematology and immunoassays on our point-of-care instrument using human and animal blood samples.
</li>
</ul>
<ul>
<li>
Independently design and execute laboratory experiments to optimize assay and instrument performance in close collaboration with our design engineers.
</li>
</ul>
<ul>
<li>
Complete statistical data analysis and evaluate assay and instrument performance to guide our analytical validation, regulatory clearance and commercial product launch.
</li>
</ul>
<ul>
<li>
Author experimental protocols, standard operating procedures and R&amp;D reports.
</li>
</ul>
<ul>
<li>
Perform quality assurance through control protocols, instrument calibration and proficiency testing.
</li>
</ul>
<ul>
<li>
Practice safe laboratory methods complying with safety, health, and environmental rules and regulations.
</li>
</ul>
<ul>
<li>
Work safely with human and veterinary specimens under health and environmental regulations.
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor's or advanced degree in biotechnology, biomedical engineering, clinical laboratory science or related fields.
</li>
</ul>
<ul>
<li>
2 to 5 years commercial, hospital, veterinary or academic laboratory experience for bachelor's degree.
</li>
</ul>
<ul>
<li>
Experience independently designing and performing experiments, developing test protocols/procedures, and creating detailed reports with data processing and statistical analysis.
</li>
</ul>
<ul>
<li>
Experience with pipetting, basic chemistry formulations, biosafety cabinets.
</li>
</ul>
<ul>
<li>
Experience with clinical instrumentation (e.g., flow cytometry, hematology, clinical chemistry, immunoassays) preferred.
</li>
</ul>
<ul>
<li>
Exposure to quality control protocols and instrument calibration.
</li>
</ul>
<ul>
<li>
Ability to work under minimal supervision with high degree of technical competence and organizational attention to detail.
</li>
</ul>
<ul>
<li>
Excellent communication skills, verbal and written.
</li>
</ul>
<ul>
<li>
Competency with clinical (human) laboratory practices (e.g., GLP, CLIA, CAP), fundamental health principles and clinical interpretation of test values preferred. Veterinary experience a plus.
</li>
</ul>
<ul>
<li>
Concise communication of scientific concepts, data analysis, clinical interpretation and reporting.
</li>
</ul>
<ul>
<li>
Desire to learn and develop new technologies in a biotech R&amp;D start-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 DescriptionContract Research Associate – Virology (contract 3-4 months) &nbsp;Why Work for Us?At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. We are a high performing team, showing up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.Our Science: Advancing Cancer ImmunotherapiesCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: <a href="http://www.candeltx.com" target="_blank">www.candeltx.com</a>Position Summary:We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment.Key Responsibilities:
<ul>
<li>Support the design, production, and testing of novel HSV-based viral vectors.</li>
<li>Conduct classical virology techniques such as virus production, purification (e.g., ultracentrifugation), and titering.</li>
<li>Execute virology-specific assays including plaque assays, TCID50, viral titration, and viral genome quantification using qPCR.</li>
<li>Contribute to viral vector engineering and optimization of workflows.</li>
<li>Maintain mammalian cell culture operations, including cryopreservation, routine culture, and cell banking.</li>
<li>Perform in vitro to evaluate viral vector transduction and biological activity.</li>
<li>Document experiments in electronic laboratory notebooks, analyze data, and prepare reports for internal review.</li>
<li>Contribute to a scientific culture that values creativity, rigor, and innovation.</li>
</ul>
Qualifications:Education:
<ul>
<li>MS in Virology, Biotechnology, or related field with 1–3 years of industry experience, or</li>
<li>BS with 3–5 years of relevant experience.</li>
</ul>
Experience and Skills:
<ul>
<li>Hands-on experience with virus production, purification, and quantification techniques (e.g., plaque assays, TCID50, qPCR) required.</li>
<li>Solid foundation in mammalian cell culture and aseptic technique.</li>
<li>Familiarity with viral vector design and characterization, particularly HSV-based systems.</li>
<li>Strong analytical and organizational skills with attention to detail.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency in Microsoft Office, GraphPad Prism, and SnapGene (preferred).</li>
</ul>
&nbsp;Work Environment:This is a lab-based position in Needham, Massachusetts. &nbsp;
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dtiN9KRel3

Contract Research Associate - Virology

<h3>Job Description</h3>
Job DescriptionSalary: 
Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. GMGI is looking for a Research Associate to join our team studying the biology of exceptionally long-lived marine animals. Our goal is to translate evolutionary insights from these exceptional animals into interventions that promote human healthspan and combat age-related diseases, using zebrafish as a development platform. This position will conduct zebrafish genetics work and husbandry, testing these evolutionary targets to extend healthy functionality. This project will use modern genetic editing techniques and apply new assays to modulate and test the molecular mechanisms of aging.
The ideal candidate will have experience with aquatic husbandry, standard molecular biology techniques, excellent communication skills, attention to detail, and the ability to work with a multi-disciplinary team of collaborators. This is an extraordinary opportunity for a dynamic and motivated individual to learn a powerful genetic model and to advance aging research in an entrepreneurial and exciting work environment.
 
Responsibilities:
<ul>
<li>Standard molecular biology and genetics experimental research.</li>
<li>Contribute to the maintenance of the aquatic facility, including feeding, water quality, and health monitoring.</li>
<li>Contribute to the generation and maintenance of transgenic zebrafish lines, including microinjection, mutant screening, and genotyping.</li>
<li>Apply assays to quantify biological aging in zebrafish, including taking tissue samples, performing histology, and compound neuro-muscular functionality.</li>
<li>Maintain a comprehensive electronic lab notebook.</li>
<li>Contribute to grant proposals and publications, and present results at lab meetings and other venues.</li>
<li>Participate in institutional fund-raising activities and community outreach activities.</li>
</ul>
 
Qualifications:
<ul>
<li>BS or MS in genetics, molecular or cell biology, or related field, with lab experience.</li>
<li>Experience with standard molecular biology techniques such as DNA/RNA isolation, PCR/qPCR, molecular cloning, and CRISPR gene editing.</li>
<li>Experience with the husbandry of aquatic models.</li>
<li>Experience with zebrafish and histology is desirable.</li>
<li>Ability to work independently to design and execute experiments</li>
<li>Strong data analysis skills using standard bioinformatic and statistic software packages</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Excellent organization skills and the ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and teamwork skills.</li>
<li>Enthusiasm and commitment to GMGIs mission for science and education.</li>
</ul>
This position will report to the Research Scientist.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
Health and Dental Insurance
Medical and Dependent Flex Spending Accounts
Long Term Disability
Life Insurance
Paid Time Off
403(b) Retirement Plan
12 Paid Holidays
Applicants must be authorized to work in the US.
 
About GMGI 
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization and building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

Research Associate I

<h3>Job Description</h3>
Job Description&nbsp;Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect.&nbsp; Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook.&nbsp; &nbsp;
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Research Associate I/II/III

<h3>Job Description</h3>
Job DescriptionDescription:
Hoyle Tanner is seeking a part-time Geotechnical Engineer for our Ground Transportation Services Division. If you have a PE license and 10 years of experience, we would like to offer you a role in design and analysis of infrastructure projects from bridge foundations, retaining walls, treatment plan structures. A perfect opportunity for the retired Engineer who is looking for a part-time project.
We are a welcoming, collaborative, respectful, encouraging, and diverse community where you can achieve your career goals. Our midsize allows you to be visible and heard. Hoyle Tanner offers you a flexible schedule, remote work opportunities and a generous sign-on bonus. See our impressive benefits package for more information.
 
Location: Manchester, NH
Manchester’s historic mill yard, our 30,000 square foot office space sits perched on the 5th floor of the original Amory Mill and is the home of our company’s headquarters. Remnants of the historic charm remain in various locations throughout the mill, while our space has been redesigned with modern lines and architectural accents. 
 
Job Responsibilities:
<ul>
<li>Develop geotechnical investigation requirements for projects and develop scopes of services and budgets for sub-consultant partners including other geotechnical specialists or subsurface investigation companies</li>
<li>Interface with sub-consultant geotechnical engineering firms or subsurface investigation companies to coordinate services and review submissions</li>
<li>Perform fieldwork, as necessary, to subsurface investigation parameters or to observe investigations</li>
<li>Perform/ review design calculations for project components such as abutments, walls, foundations, retaining walls, and tanks</li>
<li>Assist with design of airfield pavements and present alternative pavement solutions that may provide project sustainability and resilience benefits</li>
<li>Mentor team members on aspects of geotechnical engineering including interpretation of subsurface data and designs of civil infrastructure components</li>
<li>Design and evaluate shallow and deep foundation systems including driven piles, micro-piles, integral abutments, reinforced earth structures, and other geotechnical engineering solutions</li>
<li>Prepare geotechnical reports, design calculations, and construction specifications</li>
<li>Collaborate with project managers and other technical team members to ensure the successful completion of projects by communicating the integration of geotechnical investigations into design projects</li>
<li>Perform site visits and inspections to assess soil conditions, evaluate foundation performance, and provide recommendations for rehabilitation</li>
<li>Stay current with industry standards, codes, and regulations related to geotechnical engineering</li>
<li>Participate in project meetings and communicate effectively with clients, contractors, and regulatory agencies</li>
</ul>
Benefits:
<ul>
<li>Competitive salary aligning with experience</li>
<li>Flexible hours and opportunity for a hybrid work environment</li>
<li>Flexibility to work part or full time</li>
<li>Opportunities for professional development and continuing education</li>
<li>Comprehensive benefits package including health insurance, retirement plans and paid time off</li>
<li>Collaborative and supportive work environment</li>
</ul>
Requirements:
Qualifications:
<ul>
<li>BS in Civil Engineering (MS in Geotechnical Engineering preferred)</li>
<li>Professional Engineer (PE) licensure required</li>
<li>Minimum of 10 years' experience in geotechnical engineering, with a focus on the design of bridge foundations, retaining walls, treatment plant structures, and/ or facility foundations</li>
<li>Proficiency in the design and analysis of shallow and deep foundations including driven piles, micro-piles, integral abutments, and reinforced earth structures</li>
<li>Strong understanding of geotechnical engineering principles, soil mechanics, and foundation design</li>
<li>Experience with related geotechnical software, such as LPile, or other similar tools and industry-related applications</li>
<li>Strong communication and interpersonal skills, with the ability to work effectively in a team environment as well as the ability to work independently</li>
<li>Strong problem-solving skills and attention to detail</li>
<li>Salary is contingent on experience</li>
</ul>
Hoyle Tanner is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Hoyle Tanner does not currently offer sponsorship and participates in E-Verify. All offers are contingent upon a successful criminal background check.

Geotechnical Engineer - Manchester, NH

<h3>Job Description</h3>
Job Description
Nanobiosym is on the cusp of rewriting the rules of personalized medicine, novel technologies, and healthcare delivery. Founded by a renowned MIT and Harvard trained Physician and Physicist, Nanobiosym's innovative pipeline of products leverage novel advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple other prestigious peer-reviewed funding awards, Nanobiosym is currently adding to its talented team as it expands into a global commercial enterprise.
Nanobiosym is currently seeking a talented research associate with molecular biology experience, to help test our new novel technologies. This role will include a combination of data acquisition, data analysis, statistics and troubleshooting, and the development of testing procedures.
DUTIES
<ul>
<li>Perform novel technology testing, maintain laboratory records, and prepare reports.</li>
<li>Define strategy for testing and optimization.</li>
<li>Create and champion new internal processes of testing, data collection, data acquisition, and data analysis</li>
<li>Expertise with excel and statistics</li>
<li>Exercise technical judgment on test requirements, developing recommendations and translating into course of action</li>
</ul>
QUALIFICATIONS
<ul>
<li>BS degree in Biology, MS in Molecular Biology Preferred, bioinformatics, biostatistics </li>
<li>Prefer 2-5 years of academic or industry experience in molecular biology</li>
<li>Experience in qPCR or PCR preferred but not required</li>
<li>Experience working in a BSL-2 or BSL-2+ facility preferred but not required</li>
<li>Experience working in an ISO 13485 environment, and a working knowledge of ISO documentation &amp; QSR requirements preferred but not required</li>
<li>Experience testing and/or developing life sciences products, including meticulous laboratory notebook skills</li>
<li>Must have an understanding of principles of statistics relevant to product testing</li>
<li>Must have an understanding of failure mode and root cause analysis</li>
<li>Prefer experience working in fast-paced startup environments</li>
<li>Prefer experience with automation tools (i.e., run automation scripts, analyze reports and issues, report bugs)</li>
</ul>
Personal Qualities
<ul>
<li>You are passionate about testing, quality assurance, healthcare, and technology</li>
<li>You are highly organized</li>
<li>You are methodical, detail oriented and effective at time management</li>
<li>You are a self-starter</li>
<li>You have good interpersonal, verbal communication, and documentation skills</li>
<li>You can function well in a challenging and fast-paced environment</li>
<li>You are enthusiastic and positive, with strong skills in the areas of dependability, flexibility, and maturity</li>
</ul>
 Job Posted by ApplicantPro

Sr. Research Associate, Molecular Biology

<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 
Purpose:
We are seeking a highly motivated and collaborative individual with deep expertise in the LNP field to lead our non-viral delivery efforts. This person will report to the Sr Director, Head of Genetic Medicine, and join the Genetic Medicine leadership team. The successful candidate will lead a group of approximately 10 Scientists and be responsible for delivering a pipeline of mRNA/LNP development candidates in close collaboration with biotherapeutics, bioconjugation, protein science, therapeutic area and development teams.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
Responsibilities:
<ul>
<li>Lead an internal team of experienced scientists and oversee the design, optimization and production of mRNA and targeted LNP to support in vitro and in vivo studies.</li>
<li>Define and implement strategies to develop novel LNP formulations and advance targeted LNP delivery by leveraging internal expertise in lipid chemistry, antibody engineering and bioconjugation for in situ mRNA delivery.</li>
<li>Establish and drive productive collaborations with internal multi-disciplinary project teams and external partners to achieve key milestones.</li>
<li>Stay up to date on latest development in LNP and other non-viral delivery technologies.</li>
<li>Dive deeply into science and present scientific findings internally and externally.</li>
<li>Mentor and coach staff to ensure the team achieve strategic priorities.</li>
</ul>
Qualifications 
<ul>
<li>PhD in biochemistry, chemical engineering, material science or related field.</li>
<li>&gt; 10 years postdoc/industry experience focusing on lipid nanoparticle systems for mRNA delivery.</li>
<li>Strong experience in lipid chemistry, formulation development and analytical techniques.</li>
<li>Deep understanding of conjugation chemistry.</li>
<li>Experience in mRNA/LNP scale up production and process development.</li>
<li>Demonstrated ability to lead a high performing team working in a fast-paced environment.</li>
<li>Proven ability to work collaboratively across teams to meet project deliverables and timelines</li>
<li>Strong communication and decision making skills.</li>
<li>Previous experience in targeted LNP for extra hepatic delivery is highly preferred.</li>
</ul>
Prior experience in leading or co-leading a portfolio project to the stage of candidate selection is highly preferred.
 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>
​
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Director I, Lipid Nanoparticles

<h3>Job Description</h3>
Job Description
Mission:
Woodwell Climate Research Center (Woodwell Climate) conducts science for solutions at the nexus of climate, people, and nature. We partner with leaders and communities for just meaningful impact to address the climate crisis. 
 
Woodwell Climate is a rapidly growing, top-ranked, independent non-profit climate research institute whose mission is to advance science-based climate policies through scientific research and outreach. Our world-leading research and impact helps individuals, organizations, corporations, communities, and nations understand the realities of climate change, recognize the impact on our planet, and embrace the urgent action needed to safeguard the future of life on Earth.
 
Summary:
Join Woodwell Climate’s Rangeland team as a Research Associate on a 2-year project focused on applying ecosystem carbon model simulations for conservation practices within U.S. rangeland systems, including those in Montana and Colorado. The successful candidate will work closely with our partners at the World Wildlife Fund and Columbia University, and will interact with ranch managers and other collaborators. The successful candidate will lead model simulations within a high-performance computing (HPC) environment, and may assist the team with model structural improvements, optimization, and parameterizations. The candidate will help process remote sensing and geospatial data, will lead model verification using field and lab data, will compute change detection analyses and data summary statistics. The successful candidate will develop reports for ranch managers, and will organize/co-lead a workshop in Montana for participating ranch managers. 
 
Responsibilities include but not limited:
<ul>
<li>
Lead RangeSTAR model simulations within a HPC environment
</li>
<li>
Mange very large geospatial datasets with a HPC environment 
</li>
<li>
Refine computing code (Python) and improve model parameter calibration
</li>
<li>
Assist the team in developing an efficient pipeline for implementing the model across millions of acres
</li>
<li>
Lead project reports/presentations
</li>
<li>
Organize and lead a workshop for participating ranch managers
</li>
<li>
Archive project data 
</li>
</ul>
 
Must have the Following Knowledge, Skills and Abilities:
<ul>
<li>
Minimum of 3 years of demonstrated a record of successful original research
</li>
<li>
Cloud computing and HPC 
</li>
<li>
Experience improving and implementing process models
</li>
<li>
Strong data science skills including proficiency in spatial data analysis
</li>
<li>
Familiarity with different gridded geospatial data formats (NetCDF and Zarr)
</li>
<li>
Experience using version control (Git, GitHub)
</li>
<li>
Experience developing code within a Unix/Linux environment
</li>
<li>
Strong coding skills using Python (R, Julia, C/C++ or other languages a plus)
</li>
<li>
Superior oral and written communication and networking skills
</li>
<li>
Ability to work as a member of a highly collaborative team in a fast-paced environment
</li>
<li>
Willingness to travel about 5% of time
</li>
</ul>
 
Qualifications:
<ul>
<li>
3+ years’ experience with a Masters degree in Environmental Data Science, Earth System Science, Ecology, Geography, Environmental Engineering, Computer Science or a related discipline or 5+ years experience, appropriate for the requirements of the job with a bachelors degree or
</li>
<li>
Ph.D. (granted or expected soon) in Environmental Data Science, Earth System Science, Ecology, Geography, Environmental Engineering, Computer Science or a related discipline
</li>
</ul>
Physical Requirements: 
In the office: 
● Ability to tolerate sustained periods of walking, standing, sitting 
● Ability to lift 25 pounds 
● Ability to communicate, verbally and written 
● Ability to kneel, bend, and carry items 
● Ability to use phone and computers 
● Repetitive movements
Work Environment: 
The functions of this role are primarily conducted indoors, but travel to organize a workshop within Montana is required. .
Hours of Work: 
<ul>
<li>
This role is paid on a salaried, exempt, basis
</li>
<li>
Typically, full-time employees work 40 hours during a Monday through Friday workweek. However, this is a salaried position. Therefore, the individual is expected to work as required to complete the duties of the position. This may mean weekend hours and/or hours beyond 40 per week
</li>
</ul>
Application review will begin ongoing
Desired Start Date: September 2025
 
Fixed-term: 2 years
 
Classification and Compensation: This is a full-time, salaried, exempt position, the annual salary range is $65,000 plus dependent on qualifications/experience. Woodwell offers a generous benefits package and work life balance.
 
Location: Falmouth, Massachusetts, hybrid and/or remote
 
Application Instructions: To apply, please send your cover letter addressing your experience and qualifications in relation to the responsibilities of this position and curriculum vitae as a single PDF to our career’s portal.
Please visit Woodwell's website to learn more about Woodwell’s work.
Located on a 10-acre campus near the village of Woods Hole, the Woodwell Climate Research Center (Woodwell) is a private, non-profit research center. Woodwell is a leading source of climate science that drives the urgent action needed to solve climate change. Woodwell has 100+ staff members and is excited to welcome new employees to this work. 
Woodwell Climate is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, mental, or physical disability, age, sexual orientation, gender identity, national origin, familial status, veteran status, or genetic information. Woodwell is committed to providing access, equal opportunity, and reasonable accommodation for all individuals in employment practices, services, programs, and activities.
 
Diversity, Equity and Inclusion at Woodwell
WE NEED ALL VOICES IN THE FIGHT AGAINST CLIMATE CHANGE
 
Climate change is the greatest challenge of our lifetimes. Woodwell Climate Research Center (Woodwell) understands that the climate crisis—from causes to consequences—is inextricably linked with persistent social injustice. Effectively addressing either requires addressing both. The climate crisis demands that we bring to bear all of the knowledge, expertise, innovation, and creativity that we can collectively muster, and those who have been marginalized and disproportionately impacted must be heard.
 
The work Woodwell Climate does—the questions we ask, the ways we seek answers, and the strategies we put forward—is stronger when shaped by a diversity of knowledge, perspectives, and experiences. We strive to welcome, respect, and amplify differing voices. We value individuals as they are, with all their differences in race, age, ethnicity, gender identity, sexual orientation, religious beliefs, language, and mental and physical abilities.
 
Woodwell Climate acknowledges that our organization, and the scientific community more broadly, have a long way to go in living up to these ideals. We approach the work of improving our organization with the same ambition and commitment to systemic change that we bring to addressing climate change.
 
We will inevitably make mistakes, but we will continue to listen, learn, and do this critical work. We understand that this work requires an ongoing commitment from each and every one of us. We are actively engaged in building and sustaining an equitable and inclusive culture within our organization, and in fostering greater diversity in climate science.

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