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<h3>Job Description</h3>
Job DescriptionDescriptionUnder general supervision, responsible for the synthesis of chemicals through various routine manufacturing procedures including the operation of high-pressure reactors. Responsible to work safely with process equipment and hazardous chemicals. Key Responsibilities·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to execute tasks on the manufacturing floor through various routine manufacturing procedures including the operation of high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to operate safely process equipment and work with hazardous chemicals.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for assembling, configuring and leak testing high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for maintaining in good operational condition production equipment, including high-pressure reactors, process piping and process valves.·&nbsp; Responsibleformaintainingacleanandorderlyworkareawhileobservingstringentsafety requirements.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for recording and maintaining accurate production, quality and safety records.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to follow and sustain company`s policies, internal procedures, systems and programs.·&nbsp; &nbsp; &nbsp; &nbsp;May perform computer-based tasks as necessary such as working with Excel and Word software. May perform other facilities duties of a similar complexity as requested, including support of building maintenance, support issues troubleshooting, housekeeping activities, assist Lab activities, and assisting with company`s environmental and safety programs. Minimum Qualifications·&nbsp; &nbsp; &nbsp; &nbsp;Mechanical aptitude and the ability to work with hand tools.·&nbsp; &nbsp; &nbsp; &nbsp;Passing&nbsp; medical evaluation for, and the wearing of a respirator while working is required.&nbsp;&nbsp;Educational Requirements: ·&nbsp; &nbsp; &nbsp; &nbsp;High school diploma or equivalent required ·&nbsp; &nbsp; &nbsp; &nbsp;Previous experience on checmical manufacturing floor or handling chemicals is a plus.&nbsp; Benefits
<ul>
<li>Medical, Dental, Vision - effective day one of employment.</li>
<li>401(k) with company match with immediate vesting - effective first of the month, following date of hire.
<ul>
<li>First 3% is matched dollar-for-dollar.&nbsp;</li>
<li>Second 3% is matched at 70 cents on the dollar.&nbsp;</li>
</ul>
</li>
<li>3 Weeks' Vacation.</li>
<li>12 Paid Holidays.</li>
<li>Basic Life, AD&amp;D, STD, and LTD provided at no cost to employee.</li>
</ul>

Chemical Facilities Technician I

<h3>Job Description</h3>
Job Description
At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). 
Position Summary: 
This role is primarily responsible for calibrating and coordinating the calibration of a diverse range of electrical and mechanical equipment while adhering to good manufacturing practices. The role may also perform and/or assist with the installation, maintenance, testing and repair and of the equipment.
Schedule: This position is in-office Monday-Friday.
Position Scope:
<ul>
<li>Manage vendors and calibrates instruments such as, RO systems, clean steam generators, autoclaves, parts washer systems, lab equipment, and manufacturing equipment. </li>
<li>Develop and maintain the Blue Mountain Regulatory Asset Manager (BMRAM) system.</li>
<li>Maintain all calibration records and instrument tagging. </li>
<li>Write/develop Standard Operating Procedures (SOPs), and/or protocols.</li>
<li>Write initial deviations using the QMS system.</li>
<li>Assist in change control documentation and deviation notifications.</li>
<li>Serve as information resource for validation technicians, contractors and vendors.</li>
<li>Perform scheduled, new and emergency calibrations activities with vendors on all critical process equipment and lab instrumentation ensuring compliance with SOPs and cGMPs.</li>
<li>Troubleshoot instrument control loops like temperatures, pressure, flow controllers, etc.</li>
<li>Follow all environmental, health, and safety requirements and protocols.</li>
<li>Understand schematics, logic ladder diagrams, and P&amp;IDs.</li>
<li>Identify/coordinate inventory for spare parts used on critical instruments.</li>
<li>Support operations during 1st shift and be available after hours as needed to support the business.</li>
<li>Assist in equipment selection, specification and commissioning.</li>
<li>Other duties as assigned.</li>
</ul>
Qualifications: 
<ul>
<li>Bachelors degree in STEM or High School degree with equivalent years of experience.</li>
<li>Minimum 6+ years related experience in the areas such as temperature, pressure, flow (liquid &amp; gas), pH, conductivity, humidity, lab instrumentation controllers, depyrogenation oven, steam generators, steam boilers, air compressor, vacuum pumps, and lab instrumentation.</li>
<li>Knowledge of pharmaceutical manufacturing process equipment and lab instrumentation.</li>
<li>Basic knowledge on cleanroom classifications.</li>
<li>Familiarity with FDA, cGMP, SOPs, ASNI/NCSL, EU and ISO standards.</li>
<li>Good organizational skills.</li>
<li>Experience utilizing quality manage systems like Trackwise and BMRAM preferred.</li>
<li>Excellent verbal, writing and interpersonal communication skills.</li>
<li>Ability to gown and gain entry to manufacturing areas wearing personal protection equipment - safety glasses, gloves, gowns, etc. </li>
<li> Ability to be available after hours as needed to support the business.</li>
<li>Ability to lift up to 25 lbs.</li>
</ul>
Why Vericel?
<ul>
<li>Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.</li>
<li>Career Growth: Be a part of a growing organization with opportunities to expand your impact.</li>
<li>Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.</li>
</ul>
EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.
Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Metrology Lead

<h3>Job Description</h3>
Job DescriptionFisheries Biological ScientistCooperative Research Branch (CRB) Support ServicesFalmouth, MA (WHOI); Pocasset, MA; and Narragansett, RI
This role participates in all phases of CRB research projects by serving as a team member on cooperative studies and emphasizes collaboration with fishing partners, development of outreach materials, and participation in meetings and conferences for the Northeast Fisheries Science Center (NEFSC) 
Join @Orchard in bridging science and industry to support sustainable fisheries. This role supports the Cooperative Research Branch (CRB) of NOAA’s Northeast Fisheries Science Center (NEFSC), which partners with commercial fishers to generate critical data on fishing effort, catch composition, and marine ecosystems.
As part of this collaborative mission, @Orchard is seeking a Fisheries Biological Scientist team membertocontribute to field-based research projects spanning trawl, gillnet, scallop dredge, lobster trap, longline, and hook-and-line fisheries across the Northeast. From Atlantic wolffish to environmental monitoring, your work will help fill key data gaps and drive science-based management decisions.
In this role, you’ll work side-by-side with NOAA scientists and fishing partners to collect, analyze, and communicate biological and environmental data. You’ll participate in cooperative surveys, support community engagement, and help translate field results into actionable scientific outputs for assessments and outreach.
If you're passionate about marine research, enjoy engaging with the fishing community, and bring strong skills in field science and data interpretation, this opportunity puts you at the heart of impactful ecosystem science.
Key Responsibilities
As a Fisheries Biological Scientist, your primary duties will include:
<ul>
<li>Participating in all phases of research investigation, including problem definition, planning, execution, analysis, interpretation, and reporting of findings, and analyzing and preparing data for use in stock and ecosystem assessments and fisheries management.</li>
<li>Serving as a team member on cooperative research projects that bring the science and fishing communities together to address research questions and data needs. </li>
<li>Coordinating with research and industry partners in defining and refining research approaches and providing regular updates to project teams. </li>
<li>Developing and maintaining project documentation to ensure reproducibility of research, including metadata to support data processing. </li>
<li>Assisting in the documentation and development of research-related permit applications. </li>
<li>Communicating with and collaborating with fishing industry members about project goals, approaches, implementation, and results. </li>
<li>Providing logistical and at-sea support for industry participants in cooperative research programs, including recruitment with community leaders, program introductions, port visits to identify setup requirements and constraints, equipment deployment and training, troubleshooting support, and data collection, and participating in research cruises, as necessary.</li>
<li>Participating in the observation, collection, sorting, and processing of fish catch, biological samples, oceanographic dynamics, and other fisheries information for use in scientific research.</li>
<li>Extracting relevant data sets, creating data summaries, graphs, tables, charts, or data visualizations for technical publications, outreach documents, and leadership briefings. </li>
<li>Conducting statistical analysis and modeling exercises to understand fisheries, population, and ecosystem dynamics </li>
<li>Fulfilling internal and external data requests, as needed.</li>
<li>Producing technical documentation of research goals, methods, results, and applications for dissemination to the public, scientific community, and fishing industry. </li>
<li>Developing and maintaining collaborations with other scientists to progress the utility, application, and impact of cooperative research data in stock assessments, ecosystem-based fisheries science, fisheries oceanography, and other disciplines and management </li>
<li>Participating in industry meetings, scientific symposia, workshops, and conferences to support and present NOAA projects</li>
<li>Providing operational support for cooperative research field work.</li>
<li>Assisting in developing outreach materials, including user manuals, troubleshooting guides, newsletters, and articles on Cooperative Research accomplishments, challenges, and objectives.</li>
<li>Providing logistical and at-sea support for cooperative research field research programs. (possibly)</li>
</ul>
Required Qualifications &amp; Experience
To be successful in the role, candidates must possess the following qualifications:
<ul>
<li>B.S. degree in a field directly related to the task requirements. </li>
<li>Minimum of 2-3 years of experience in the field or in a related area, or of progressively higher-level graduate education leading to a master’s degree or equivalent graduate degree. </li>
<li>Served as a researcher or member of a research team performing research on fisheries or related marine science. </li>
<li>Ability to work collaboratively with members of the commercial fishing industry, including working at sea and at the dock. </li>
<li>Experience with identifying and applying technical solutions within fisheries research settings. </li>
<li>Experience manipulating complex (i.e., fisheries) data sets. </li>
<li>Experience writing scientific documentation. </li>
<li>Experience in the identification, collection, sorting, and processing of fish samples, biological samples, and oceanographic data. </li>
<li>Familiarity with data analysis tools, such as R.</li>
<li>Proficient in current MS Office software programs.</li>
<li>Proficient in the primary G Suite tools, including Gmail, Drive, Docs, Sheets, Slides, Forms, Calendar, Sites, and Meet.</li>
</ul>
Essential Conditions of Employment
<ul>
<li>Driver's License: Must hold a valid state driver’s license with the ability to operate a federal motor vehicle.</li>
</ul>
This position includes authorized overtime, travel, and training as required by the project scope. If you are ready to contribute to a vital environmental mission, we encourage you to apply.
Established in 2010, @Orchard LLC has an exceptional reputation, providing staffing solutions to time-sensitive, talent scarcity issues to deliver better talent management ROI. Our specialty lies in the critical area of program talent acquisition and resource management, not in one narrow skillset, but across many areas of technical and functional delivery. To learn more about our other exciting opportunities, visit our Jobs Page at <a href="http://www.atOrchard.com" target="_blank">www.atOrchard.com</a>.

Fisheries Biological Scientist

<h3>Job Description</h3>
Job Description:
The Role
We are looking to hire a Director, Quant Strategist to strengthen our US team. By combining hands-on quantitative research with team leadership, the successful candidate will be accountable for developing and monitoring strategies, ensuring model robustness, troubleshooting issues, and driving workflow enhancements.
This role will play a central part in driving our DeFi research efforts and requires a strong technical background, excellent problem-solving skills, and the ability to manage and mentor a small team whilst coordinating our team efforts across multiple stakeholders, and cross-regional teams.
Key Responsibilities
Strategy Research &amp; Implementation
<ul>
<li>Conduct research into yield-oriented strategies across of a range of market structures and venues, with an emphasis on identifying risk-adjusted return opportunities</li>
<li>Design and run backtests to evaluate strategy performance, stress-test assumptions, and establish statistical robustness</li>
<li>Help deeply analyze protocols to understand mechanics, risks, and potential drivers of yield. Translate insights into research hypotheses and strategy ideas</li>
</ul>
Monitoring &amp; Troubleshooting
<ul>
<li>Act as a first line of response for alerts, coordinating with global colleagues to escalate and resolve issues quickly</li>
<li>Translate lessons learned from monitoring into research and operational playbook improvements</li>
</ul>
Team Leadership
<ul>
<li>Manage and mentor a team of quants/analysts: run sprints, allocate tasks, and oversee objectives and results</li>
<li>Conduct code and strategy reviews, enforce testing standards, and support professional development</li>
<li>Foster a culture of collaboration, technical excellence, and delivery focus</li>
</ul>
Risk &amp; Stakeholder Interaction
<ul>
<li>Present weekly PnL, risk metrics, and performance attribution to senior management</li>
<li>Ensure transparent communication and reporting to internal stakeholders</li>
</ul>
The Expertise and Skills You Bring
Technical Expertise
<ul>
<li>Proficiency in Python (e.g., Pandas, NumPy, PyTorch, etc.) and SQL with the ability to write production-quality, maintainable code</li>
<li>Strong grounding in portfolio mathematics, risk modelling and statistical methods</li>
<li>Experience building and maintaining research infrastructure, including data pipelines, backtesting frameworks, and related tools</li>
</ul>
Communication &amp; Engagement
<ul>
<li>Able to distill complex models into actionable insights for technical and non-technical stakeholders</li>
<li>Collaborate style and effective at working across teams and time zones, fostering strong engagement with colleagues</li>
</ul>
Analytical &amp; Research Skills
<ul>
<li>Skilled at working with large, complex, and imperfect datasets, extracting signal from noise, and applying methods ranging from classical statistics to machine learning where appropriate</li>
</ul>
Professional Experience
<ul>
<li>Typically, 10+ years of relevant experience in digital assets, and/or quantitative research</li>
<li>Advanced degree (Master’s or PhD) in a quantitative field (e.g. Mathematics, Statistics, Computer Science, Physics, or a related discipline)</li>
<li>Previous experience managing or mentoring a small team of quants, developers, or researchers</li>
</ul>
Preferred Qualifications
<ul>
<li>Prior exposure to DeFi yield strategies (staking, LP, lending, re-staking)</li>
<li>Experience with systematic trading across traditional asset classes (equities, FX, commodities, fixed income etc.)</li>
<li>Demonstrated initiative in generating ideas and improving processes</li>
<li>Comfort working across time zones and collaborating with distributed teams</li>
</ul>
The Team
Fidelity Digital Assets (FDA) is dedicated to building products and services that help institutions adopt digital assets and innovate within the increasingly digital world of finance. Fidelity Investments began researching blockchain technology and digital assets solutions in 2014, and years of research and development have provided us with the deep expertise necessary to build the future of finance.
Come join the Quantitative Strategies team within Fidelity Digital Assets to help grow our business initiatives within DeFi and contribute to our research and product capabilities using your insights.
Certifications:Category:Data Analytics and Insights
Most roles at Fidelity are Hybrid, requiring associates to work onsite every other week (all business days, M-F) in a Fidelity office. This does not apply to Remote or fully Onsite roles.
Please be advised that Fidelity’s business is governed by the provisions of the Securities Exchange Act of 1934, the Investment Advisers Act of 1940, the Investment Company Act of 1940, ERISA, numerous state laws governing securities, investment and retirement-related financial activities and the rules and regulations of numerous self-regulatory organizations, including FINRA, among others. Those laws and regulations may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories.

Director, Quant Strategist

<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 
The Quantitative Translational &amp; ADME Sciences (QTAS) team in Worcester, MA, is seeking a motivated and independent Senior Scientist to support pre-clinical bioanalytical studies in a non-regulated environment. This role focuses on understanding large molecule therapeutics, pharmacokinetics, and immunogenicity in safety and efficacy studies.
The primary responsibilities of a Senior Scientist include developing and executing bioanalytical strategies to support PK, PD, and TK studies using ligand binding assay platforms. This lab-based role emphasizes bioanalytical (PK and ADA) assay design, planning, and data interpretation to support oncology, immunology, and neuroscience portfolios.
The ideal candidate will have a strong background in immunology, biochemistry, and/or pharmacology or related fields. The candidate is expected to mentor and train bench scientists and provide scientific reasoning behind bioanalytical assay design and data interpretation.
This position is onsite and located at the AbbVie Bioresearch Center in Worcester, MA.
Duties &amp; Responsibilities:
<ul>
<li>Design and execute pre-clinical (rodent, NHP) bioanalytical studies using newly developed or existing bioanalytical protocols, using immunoassays, e.g. MSD.</li>
<li>Effectively and clearly communicate assay plans, timelines, results, and data interpretations with study teams and QTAS stakeholders.</li>
<li>Serve as a scientific and technical consultant across teams.</li>
<li>Train and mentor junior scientists.</li>
<li>Archive data in ELN and LIMS systems.</li>
<li>Write and update experimental protocols and procedures.</li>
<li>Initiate, design, interpret, and troubleshoot operational assays independently and efficiently.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in biochemistry, chemistry, or pharmacology with 10+ years industry experience; MS with 8 years of industry experience, or a PhD&nbsp;with 0+ years experience</li>
<li>Previous experience conducting DMPK studies, PK/PD/TK bioanalysis on antibodies, bi/multi-specifics and/or ADCs, including data interpretation is required.</li>
<li>Highly motivated, reliable, and independent contributor with attention to detail and problem-solving skills.</li>
<li>Required experience with assay development and troubleshooting using ligand binding workflows (ELISA, MSD) is a must.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency with computers and data analysis software, including LIMS systems.</li>
<li>Ability to design, summarize, communicate, and interpret bioanalytical results.</li>
<li>Creative leader and collaborative team player, able to work effectively in a highly matrixed environment.</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

<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 Senior 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, troubleshoot, and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the VP 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 junior scientist with prior industry experience and&nbsp;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>
3-6 years of prior industry R&amp;D experience (not academic lab or QC/manufacturing)&nbsp;
</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: onsite presence, 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.

Senior Research Associate

<h3>Job Description</h3>
The Dimensional Inspection Technician helps measure and inspect material and supports calibration activities for the organization working closely with our engineering teams General Responsibilities 
<ul>\n
<li>Interprets mechanical prints.</li>
\n
<li>Collects data and conveys tests results to stakeholders</li>
\n
<li>Document and record data in accordance with lab procedures.</li>
\n
<li>Prepares technical reports with recommendations for solutions to technical problems.</li>
\n
<li>Performs precise calibrations and preventative corrective maintenance on measuring and test equipment and tools.</li>
\n
<li>Develops calibration operating procedures and documentation for all instruments.</li>
\n
<li>Identify and perform preventative maintenance on equipment.</li>
\n
<li>Perform preventative maintenance on equipment.</li>
\n</ul>
\n Experience / Qualifications 
<ul>\n
<li>Relevant work experience or knowledge of the role</li>
\n
<li>Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands</li>
\n
<li>Strong organization, planning and time management skills to achieve results</li>
\n
<li>Holds self-accountable to achieving goals and standards</li>
\n
<li>Proficient in Microsoft Office programs (Outlook, Word, PowerPoint, and Excel)</li>
\n</ul>
\n Dimensional Inspection activities include: 
<ul>\n
<li>Mechanical print reading and GD&amp;T interpretation</li>
\n
<li>CMM program development</li>
\n
<li>3D Laser scanning</li>
\n
<li>Hand tool measurement</li>
\n
<li>Data collection and reporting</li>
\n</ul>
\n Calibration activities include: 
<ul>
<li>Process various internal calibrations for Sensata in accordance with documented procedures. Calibration parameters include:</li>
</ul>
\n 
<ul>
<li>
<ul>\n
<li>Resistance</li>
\n
<li>Current</li>
\n
<li>Voltage</li>
\n
<li>Pressure</li>
\n
<li>Temperature</li>
\n
<li>Force</li>
\n
<li>Dimensional</li>
\n
<li>Other</li>
\n</ul>
</li>
</ul>
\n 
<ul>\n
<li>Document and record data in accordance with lab procedures</li>
\n
<li>Communicate with equipment owners &amp; requesters to convey test results and to collect/process equipment</li>
\n
<li>Write and update test procedures</li>
\n
<li>Identify and perform preventative maintenance on equipment</li>
\n
<li>Identify and execute process and equipment improvement opportunities to drive lab efficiencies</li>
\n</ul>
\n #LI-MY1 #LI-Onsite Hourly Base Pay Range: $28.00 - $38.50 At Sensata, our employees are the key to our success and growth. We recognize that each individual brings their own unique experience, therefore the base salary range information shown above is a general guideline only. Sensata considers several factors when extending an offer, including, but not limited to, a candidate's experience and qualifications, as well as internal equity, market and business considerations. In addition to base salary, Sensata offers competitive medical, dental, vision, life and disability insurance plans, along with education reimbursement, wellness programs, a 401(k) retirement plan with Company matching, and a variety of paid time off, such as vacation or flex-time, sick, bereavement, and parental leave. SmarterTogether 
<ul>\n
<li>Collaborating at Sensata means working with some of the world's most talented people in an enriching environment that is constantly pushing towards the next best thing</li>
\n
<li>Employees work across functions, countries and cultures gaining new perspectives through mutual respect and open communication</li>
\n
<li>As OneSensata, we are working together to make things work together</li>
\n</ul>
\n Click here to view Sensata Recruitment Privacy Statement Click here to view our Sensata Recruitment Privacy Statement for China NOTE: If you are a current Sensata employee (or one of our Affiliates), please back out of this application and log into Workday via the Company Intranet to apply directly. Type "FIND JOBS" in the Workday search bar.

Dimensional & Metrology Lab Specialist

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Assembler Job Description
As a Clean Room Assembler, you will be responsible for assembling product parts on the assembly line in accordance with production guidelines. You will also perform spot checks of products to ensure adherence to approved quality standards.
Responsibilities
<ul>
<li>Assemble assigned product parts on the assembly line following production guidelines.</li>
<li>Perform spot checks of products to ensure adherence to approved quality standards.</li>
<li>Notify management of product discrepancies or equipment malfunctions.</li>
<li>Adhere to established company policies and procedures, paying special attention to safety regulations.</li>
<li>Wear personal protective equipment in accordance with training guidelines.</li>
<li>Perform other related duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Experience in assembly, preferably in a cleanroom environment.</li>
<li>Ability to work with microscopes, hand tools, and perform medical assembly.</li>
<li>Comfortable using tweezers, cutters, wire strippers, and adhesives.</li>
<li>Strong attention to detail and mechanical assembly skills.</li>
<li>Proficiency in work instruction and hand dexterity.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Strong written communication skills.</li>
<li>Physical dexterity.</li>
<li>Reading skills.</li>
<li>Effective time management.</li>
<li>Mechanical skills.</li>
</ul>
Why Work Here?
Join a dynamic team that values safety and quality in a clean and flexible work environment. Enjoy a supportive company culture that emphasizes personal growth and development.
Work Environment
Work in a clean room environment with flexible hours, typically from 7:00 AM to 3:00 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of NASHUA, New Hampshire.
Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in NASHUA,NH.
Application Deadline
This position is anticipated to close on Sep 30, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Cell Line Development Group: The CLD team utilizes state-of-the-art approaches and equipment to generate and characterize production cell lines for Biologics manufacturing. Team collaborates closely with other teams, such as Analytical Development, the Genomics Research Center, and Cell Culture Development.
Position’s key responsibilities will include:
· Execute experiments in cell line development and characterization with supervision.
· Extensive cell culture work – both directly and through coordination with the automation sub-team.
· Perform data acquisition and analysis in a timely manner.
· Assist in experimental designs, data interpretation and troubleshooting.
· Document work appropriately in lab notebooks, reports and presentations.
· Assist with lab operations and continuous improvement activities.
Location: Worcester, Massachusetts; Bio4 Building; Onsite
Minimum Qualifications:
· Must have completed bachelor’s degree in Biosciences or related field
· Extensive experience with aseptic technique and mammalian cell culture
· Microsoft software: Word, Excel, PowerPoint, Outlook
· Proven track record of teamwork, adaptability, initiative, and integrity
· Excellent interpersonal and both written &amp; oral communication in English
Preferred Requirements (Optional):
· Experience with Flow Cytometry (e.g., analysis, compensation, sorting)
· Experience with Molecular Biology (e.g., recombinant DNA, vector construction, PCR, NGS)
· Experience with Electronic Lab Notebook system (ELN)

Biologist

<h3>Job Description</h3>
Job Description
We’re seeking a Senior Dam Safety Engineer with deep expertise in geotechnical engineering and dam safety evaluations. This leadership role is ideal for someone with FERC Part 12 Independent Consultant approval—or the experience to qualify—and a passion for risk-based analysis and infrastructure resilience.
You’ll play a pivotal role in guiding project teams, mentoring junior staff, and shaping the future of our dam safety services. This is your opportunity to work on meaningful, high-impact projects in clean energy and environmental restoration. Ready to make a difference? Let’s build something lasting—together!
**Remote work options available
 
 
Key Responsibilities
<ul>
<li>Lead and coordinate design teams for FERC and state-regulated dam safety projects</li>
<li>Conduct dam safety evaluations, including FERC Part 12 inspections</li>
<li>Design earthen embankments and perform geotechnical assessments for dams and civil works</li>
<li>Develop and analyze geotechnical monitoring and testing programs</li>
<li>Review construction sequencing, design plans/specs, and permitting documents</li>
<li>Represent the firm in technical discussions with regulators, clients, and public forums</li>
<li>Author and review technical reports and project documentation</li>
<li>Mentor engineers in technical execution and career development</li>
<li>Support proposal writing, cost estimating, and project scheduling</li>
</ul>
Qualifications
<ul>
<li>B.S. in Civil or Geotechnical Engineering (M.S. preferred)</li>
<li>Licensed Professional Engineer (PE) with willingness to maintain multi-state registrations</li>
<li>FERC Part 12 Independent Consultant approval or eligibility</li>
<li>Comprehensive Assessments expert</li>
<li>Strong communication skills and attention to detail</li>
<li>Experience with risk-based analysis preferred</li>
<li>15+ years of experience in:
<ul>
<li>Dam safety evaluations and geotechnical design</li>
<li>Project management and client engagement</li>
<li>Earthquake response analysis for embankments</li>
<li>Proposal development and team mentoring</li>
<li>Familiarity with federal/state dam safety standards</li>
</ul>
</li>
<li>Some travel required to project sites</li>
</ul>
Benefits
We offer a competitive and comprehensive benefits package, including:
<ul>
<li>Medical, dental, and vision insurance</li>
<li>Generous vacation, comp time, and flexible holidays</li>
<li>Paid sick leave and extended medical leave account</li>
<li>Educational assistance and professional development support</li>
<li>Parental leave and Dependent Care FSA</li>
<li>Short and long-term disability coverage, Life Insurance</li>
<li>401K and profit-sharing program</li>
</ul>

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