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<h3>Job Description</h3>
Job Description
STR's Sensors Division is at the forefront of developing advanced signal processing algorithms and prototyping systems for next-generation radar and electronic warfare technologies. The group fosters a culture of innovation and collaboration. You will be a member of a dynamic group of research engineers across STR, academic researchers, and industry partners to develop practical and effective solutions to RF sensing and counter-sensing challenges. Together, we're dedicated to tackling some of the toughest problems faced by our national security-focused clients.
If you're seeking an opportunity to apply your deep technical knowledge and creativity to make a lasting impact in national security, we invite you to join us. 
The Role:
As a Principal Algorithm &amp; Signal Processing Researcher, you will develop and apply state-of-the-art algorithms and techniques for signal detection, classification, autonomous sensor decision-making, sense making, radar electronic warfare, and electronic support measures. You'll engage directly with our customers to understand and address their most critical challenges. You'll lead a team of researchers in creating innovative systems while collaborating closely with our engineering teams to demonstrate state-or-the-art system capabilities.
What you will do: 
<ul>
<li>Engage directly with customers to understand their unique requirements and national security needs, and shape our solutions to meet their objectives</li>
<li>Design and apply cutting-edge signal processing and machine learning techniques to solve complex radar and RF sensing and counter-sensing challenges </li>
<li>Collaborate with diverse teams, bringing together different perspectives to develop and deploy prototype systems that demonstrate our ability to extend the boundaries of what's possible</li>
<li>Lead and inspire multi-disciplinary teams, guiding them towards success with your technical expertise and leadership skills</li>
<li>Drive business development initiatives and support proposal writing efforts, playing a key role in shaping the future direction of our projects and organization</li>
</ul>
Who You Are: 
<ul>
<li>This position requires the ability to obtain a secret security clearance, for which U.S. citizenship is needed by U.S. Government</li>
<li>PhD, MS, or BS in Electrical Engineering, Applied Mathematics, Physics, or related technical discipline</li>
<li>8+ years of experience on EW or Radar programs, including the development of sensor system modes and advanced signal- and data-processing algorithms from mathematical/analytical derivation through testing and verification of system performance</li>
<li>2+ years experience in two or more of the following areas:</li>
<ul>
<li>RF/radar signal processing, optimization, waveform design, electronic warfare, machine learning, adaptive signal processing, AI/ML algorithm development, algorithm development, model &amp; simulation, systems engineering, test engineering, radar modelling,</li>
</ul>
<li>Experience providing technical briefs to subcontractors, senior level executives, and customers</li>
<li>Proficiency in in one or more scientific or mathematical programming languages, such as MATLAB, Python, and C/C++</li>
<li>Experienced researcher and team member who is excited to work with mission partners to leverage cutting-edge technology and research for immediate impact</li>
<li>Excellent communicator and briefer, who is comfortable communicating with both technical and non-technical audiences</li>
<li>Strong mathematical, troubleshooting, written, and verbal communication skills</li>
</ul>
Even Better:
<ul>
<li>Active Secret or TS/SCI Clearance</li>
<li>Demonstrated leadership of complex research, development, and engineering efforts   </li>
<li>Advanced degree in Electrical Engineering, Applied Mathematics, Physics, or a related technical discipline </li>
<li>Experience with:</li>
<ul>
<li>Radar and RF technologies in the defense sector, particularly for RF sensing and electronic warfare applications including electronic attack, electronic protection, cognitive EW, and advanced ESM techniques and algorithms </li>
<li>Machine learning tasks such as natural language processing, image recognition, semantic segmentation, reinforcement learning, approaches such as Bayesian, deep convolutional and graph neural network methods, and tools such as PyTorch, Ray, TensorFlow/board, and MLflow   </li>
<li>Interacting with decision-makers and customers to translate mission needs into an end-to-end solution   </li>
</ul>
<li>Ability to apply novel, innovative and interdisciplinary approaches to challenging engineering problems  </li>
</ul>
Join us and be part of a team that's making an impact at the forefront of technology and innovation.
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Principal Algorithm & Signal Processing Researcher

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, a place to call home, apply with us today
Job Description 
<ul>
<li>Prepare complex cell culture media at various scales with precision and consistency to support iPSC differentiation workflows, ensuring timely and accurate formulation execution.</li>
<li>Interpret, follow, and execute standard operating procedures (SOPs) for the preparation of reagents, stock solutions, and media formulations.</li>
<li>Monitor and manage expiration dates of stock solutions and media batches to maintain compliance and quality standards.</li>
<li>Maintain a detailed and up-to-date media inventory database for raw material tracking, lot usage, forecasting, and performance monitoring.</li>
<li>Accurately document all work in the electronic lab notebook (ELN) system, perform independent data analysis, and communicate results clearly in both written and verbal formats.</li>
<li>Adhere strictly to safety protocols and technical procedures, completing all required training within designated timelines.</li>
<li>Perform advanced algebraic calculations to determine critical formulation parameters such as molarity, molality, and solution concentrations with a high degree of accuracy.</li>
<li>Calculate precise component volumes using complex formulas to ensure exact proportions in both experimental and production settings.</li>
<li>Identify and troubleshoot issues related to media preparation and address deviations as needed to maintain workflow continuity.</li>
<li>Collaborate with process development teams to optimize media formulations for scalability, reproducibility, and cost-effectiveness in high-throughput environments.</li>
<li>Utilize automated systems (e.g., liquid handlers, robotic mixers, and automated dispensers) to enhance the efficiency, consistency, and traceability of media preparation processes.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s or Master’s degree in biological sciences, biochemistry, or a related field
<ul>
<li>Bachelor’s degree with 1–2 years of relevant experience, or</li>
<li>Master’s degree with less than 1 year of relevant experience</li>
</ul>
</li>
<li>Proven proficiency in aseptic techniques and preparation of reagents, stock solutions, and complex cell culture media</li>
<li>Strong command of algebraic calculations, including molarity, percentages, and solution component volumes</li>
<li>Strict adherence to safety protocols and laboratory best practices</li>
<li>Demonstrated attention to detail and commitment to delivering high-quality work with an understanding of its impact on downstream processes</li>
<li>Ability to thrive in a collaborative, team-based laboratory environment and contribute effectively to cross-functional project teams</li>
<li>Authorization to work in the United States without restrictions or the need for sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with automated laboratory systems such as liquid handlers, robotic mixers, or automated dispensers</li>
<li>Background supporting or operating in high-throughput or high-volume laboratory settings</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting with Team</li>
</ul>
Additional Details:&nbsp;
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (once every 1-2 months) to support cell culture.Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Reagent and Media Preparation Associate

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, a place to call home, apply with us today
Job Description 
<ul>
<li>Meticulously prepare complex media at various scales to support cell culture for various iPSC differentiation workflows, ensuring timely and accurate execution of requested formulations.</li>
<li>Read, review, and execute SOPs for preparation of reagents, stock solutions, and media handling and formulation.</li>
<li>Track expiry of corresponding stock solutions and complete complex media.</li>
<li>Maintain an updated media inventory database for forecasting, tracking raw material use &amp; stock, lot usage, and overall material performance.</li>
<li>Maintain accurate and meticulous record keeping with internal ELN system, independent data analysis, and reporting of data in written and oral formats.</li>
<li>Perform work in full compliance with safety policies and technical protocols and complete all required training activities in the timeframe specified.</li>
<li>Perform complex algebraic mathematical calculations with high accuracy to determine critical parameters such as molarity, molality, and percentages.</li>
<li>Precisely calculate volumes of solution components based on intricate mathematical formulas, ensuring exact proportions for experimental and manufacturing processes.</li>
<li>Troubleshoot media preparation challenges and deviations when necessary.</li>
<li>Collaborate with process development scientists to support high throughput optimization of media formulations for scale-up, reproducibility, and cost-efficiency.</li>
<li>Operate automation platforms (e.g., liquid handlers, automated dispensers, robotic mixing systems) to support streamlined media preparation, increasing throughput, reproducibility, and data traceability.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>B.S. and/or M.S. in biological or biochemical sciences (or a related field). B.S., 1-2 years of experience or M.S., less than 1 year of experience.</li>
<li>Demonstrated proficiency in aseptic technique and reagent, stock solution, and complex cell culture media preparations.</li>
<li>Advanced skills in algebraic calculations: molarity, percentages, solution component volumes.</li>
<li>Unwavering commitment to safety protocols and procedures</li>
<li>Proven capacity to ensure work product quality and understand the impact on downstream processes.</li>
<li>Work within a team-oriented lab environment and work within cross-functional project teams.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Exposure to automated systems (e.g., liquid handlers, automated dispensers, robotic mixing systems).</li>
<li>Track record of working in or supporting high-throughput or high-volume laboratory environments. &nbsp;</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting</li>
</ul>
Additional Details:&nbsp;
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (once every 1-2 months) to support cell culture.Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Media Preparation Scientist

<h3>Job Description</h3>
Job DescriptionSalary: 
About Aura:
 
Aura Biosciences is a clinical-stage biotechnology company focused on developing precision therapies for solid tumors that aim to preserve organ function. Our lead candidate, bel-sar (AU-011), is currently in late-stage development for primary choroidal melanoma and in early-stage development in other ocular oncology indications and bladder cancer. Aura Biosciences is headquartered in Boston, MA. Our mission is to grow as an innovative global oncology company that positively transforms the lives of patients.
For more information, visitaurabiosciences.com. Follow us on X (formerly Twitter) @AuraBiosciences and visit us on LinkedIn.
 
Position Summary:
Reporting to the Upstream Process Development Lead, the Associate Scientist/Senior Associate Scientist will be responsible for the development of upstream production processes and the production of material for routine in-house development use. This includes all assays associated with cell culture production. The incumbent will also participate in the transfer of the upstream process to support biopharmaceutical product development at Contract Manufacturing Organizations (CMOs). The Associate Scientist/Senior Associate Scientist will interact with the in-house team and the CRO/CMO to ensure timely progress in technology development, documentation, and manufacturing readiness.
Responsibilities include but are not limited to:
Process development:
<ul>
<li>Design, coordinate, and execute process development studies on seed train, bioreactor production, as well as primary recovery, utilizing multiple approaches including statistically designed experiments (DoE). </li>
<li>Design and coordinate scale-down process verification studies.</li>
<li>Design and support process optimization studies.</li>
<li>Coordinate and carry out in-house production of representative materials for development use.</li>
<li>Develop the companys pipeline by supporting process development of new target indications.</li>
<li>Document studies/lab work in lab notebooks, study plans and reports per company requirements to ensure data integrity and traceability. </li>
<li>Stay compliant with lab safety regulations and build good lab practice in everyday lab operations.</li>
</ul>
 Technology Development and Continuous Improvement:
<ul>
<li>Apply and verify novel manufacturing technologies to Auras unique product.</li>
<li>Improve process performance and quality of product.</li>
<li>Contribute to continuous improvement of the internal data management system.</li>
</ul>
 Tech Transfer and PPQ:
<ul>
<li>Support implementation of new process technologies or significant changes to processes, equipment, or manufacturing instructions as needed. </li>
<li>Support tech transfer tasks and support PPQ-enabling activities such as process risk assessment, process characterization and process control strategy development.</li>
<li>Support evaluation of scale up performance and recommend action items to improve scalability, in collaboration with a cross-functional team.</li>
</ul>
 Manufacturing Support:
<ul>
<li>Generate and implement continuous improvement ideas to improve documentation and business practices. </li>
<li>Support manufacturing by providing technical expertise in the manufacturing area and providing timely support for manufacturing investigations using experiments in Process Development.</li>
<li>Other projects as assigned by management.</li>
</ul>
 Minimum Requirements:
<ul>
<li>Degree in biochemical engineering, biological sciences, biochemistry or related discipline. </li>
<li>B.S. with 2-4 (or M.S. with 0-2) years of experience in pharmaceutical, biologics, viral production, or a related field.</li>
<li>Understanding of biologics manufacturing is required in multiple areas. Knowledge and hands-on experience including cell culture development using bioreactors and conducting transfections at varying scales</li>
<li>Ability to critically analyze data using statistical tools and to compile technical reports. </li>
<li>Ability to accomplish projects by deadline in a dynamic environment </li>
<li>Strong oral and written communication skills.</li>
<li>Motivation in performing and learning novel process methods, and good work ethic is critical. Inventory management experience to ensure material supply for upstream process development</li>
</ul>
 Desired Qualifications
<ul>
<li>Experience with DoE using JMP or similar system is highly desired.</li>
<li>Solid understanding of the Quality-by-Design principle and a track record of implementing it in late-stage development (process FMEA, scale-down model qualification and process characterization) is a strong plus. </li>
<li>Virus production experience is strongly desired.</li>
<li>Cell culture experience with Mammalian, Insect, CHO, or Yeast cell lines for biologics production are highly desired.</li>
<li>Experience working with 1L, 10L, and 50L bioreactors is highly desired.</li>
<li>Experience with optimizing process parameters and supplementation to increase product yield and stability (such as transfection parameters) is strongly desired. </li>
<li>Occasional effort may be needed in downstream purification. Any chromatography (AKTA systems) and filtration experience are a plus.</li>
<li>Experience with various analytical procedures is a plus (SDS-PAGE, western blot, ELISA, HPLC, etc.)</li>
<li>An understanding of current good manufacturing practices (cGMPs) as they apply to the development and qualification of biological manufacturing processes.</li>
<li>Proficient in Excel, PowerPoint, and Word applications.</li>
</ul>
 
Salary &amp; Benefit Information:
 
Salary Range: $60,000/yr - $115,000/yr
(Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity)
Health insurance with FULL premium coverage
401K with company match
Employee Stock Purchase Program (ESPP)
Competitive paid time off (PTO)
Company-paid short &amp; long-term disability insurance and life insurance

(Sr) Associate Scientist, Upstream Process Development

<h3>Job Description</h3>
Job Description
Job Title: Chemist II – Stability Testing (Quality Control) Job Location: Fall River, MA (On-site) Schedule: 8:00 AM – 5:00 PM (May vary based on business needs) Classification: Full-Time, Exempt Relocation Assistance: Up to $6,000 available Work Authorization: US Citizen, Green Card, H1B Transfer, TN Visa, OPT-EAD
About the Role:
We are seeking a QC Chemist II – Stability Testing to join our Quality Control Department. The selected candidate will be responsible for performing and overseeing stability testing for pharmaceutical formulations under various environmental conditions, ensuring data integrity, and compliance with cGMP guidelines.
Key Responsibilities:
<ul>
<li>
Conduct routine and advanced stability testing in a laboratory setting.
</li>
<li>
Operate and maintain instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers.
</li>
<li>
Perform raw material testing and release.
</li>
<li>
Lead investigations into out-of-specification (OOS) or deviations and document findings.
</li>
<li>
Ensure adherence to cGMP, Good Documentation Practices (GDP), and data integrity principles.
</li>
<li>
Prepare and review documentation, including lab notebooks and reports.
</li>
<li>
Participate in audits and ensure inspection readiness.
</li>
<li>
Collaborate with cross-functional teams, including QA and manufacturing.
</li>
<li>
Support training and mentoring of junior team members.
</li>
<li>
Execute additional duties as assigned by departmental leadership.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Bachelor’s degree (BS/BA) in Chemistry or a related physical science.
</li>
<li>
Minimum 3 years of experience in formulation stability testing in a pharmaceutical setting.
</li>
<li>
Working knowledge of analytical instruments including HPLC, GC, ICP, Karl Fischer, and particle size analyzers.
</li>
<li>
Familiarity with MDI (Metered Dose Inhaler) testing is a strong plus.
</li>
<li>
Experience with various dosage forms (liquid, solid, tablets, capsules) is desirable.
</li>
<li>
Strong command of English – spoken and written.
</li>
<li>
Proficiency with Microsoft Office and scientific software.
</li>
<li>
Excellent analytical, documentation, and communication skills.
</li>
<li>
Must be authorized to work in the United States and be available to work on-site full-time.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience working with inhalation products (MDIs).
</li>
<li>
Previous work in a fast-paced, regulated pharmaceutical QC lab environment.
</li>
<li>
Experience leading or contributing to laboratory investigations.
</li>
</ul>
Work Environment Physical Requirements:
<ul>
<li>
Work in a cGMP laboratory or manufacturing environment requiring the use of personal protective equipment (PPE).
</li>
<li>
Regular exposure to solvents, powders, and chemical substances.
</li>
<li>
Must be able to stand or walk for 75% or more of an 8-hour shift.
</li>
<li>
Must be able to lift up to 10 kg unassisted.
</li>
<li>
Must be able to sit and work at a computer for extended periods.
</li>
</ul>
Compensation Benefits:
<ul>
<li>
Competitive salary based on experience ($75K–$105K)
</li>
<li>
Bi-weekly pay
</li>
<li>
Paid Time Off (PTO)
</li>
<li>
Health Insurance (Medical, Dental, Vision) – starts on Day 1
</li>
<li>
Disability Insurance
</li>
<li>
Overtime and shift differential as applicable
</li>
<li>
401(k) with company match
</li>
<li>
Career advancement opportunities and ongoing training
</li>
<li>
Company-sponsored events
</li>
</ul>
Important Notes:
<ul>
<li>
Candidates must have prior pharmaceutical (not biopharma) experience.
</li>
<li>
Chemistry background is highly preferred.
</li>
<li>
Candidates should clearly indicate experience with formulations including MDI, liquid, solid, tablets, and capsules in their resume.
</li>
<li>
No Green Card sponsorship available; H1B transfers are acceptable.
</li>
</ul>

QC Chemist II

<h3>Job Description</h3>
Job Description
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Marine Biologist!!
A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is looking for Marine Biologists (At-Sea Monitors) to work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Northeast Fisheries Science Center (NEFCS) aboard commercial fishing vessels.
The primary goals of Northeast federal fishery observation programs are to provide quantitative biological, vessel, and gear-selectivity information for various New England and Mid-Atlantic fisheries. The At-Sea Monitor program focuses specifically on the groundfish industry, a grouping of fish that includes many commonly consumed fish such as cod, haddock and various flounder species. Each fishery observer or monitor operates on commercial fishing vessels operating in ports throughout New England and the Mid-Atlantic. If you ever wanted to make a difference, this is how.
Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between fishermen and fisheries management scientists like yourself. In order to facilitate that cooperation, marine biologists collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen. Commit to the journey!
Click to Learn More about Becoming a Fisheries Observer
At-Sea Monitors record detailed information on the gear and fishing activity of the vessels. Monitors work on deck on vessels ranging from 20’ to 100’ on trips roughly ranging from 1 to 14 days collecting data on fish catch and discard and incidental takes such as marine mammals, seabirds, and marine turtles. After attending a 3-week paid training in-person training in Falmouth, MA monitors are deployed from ports throughout New England and Mid-Atlantic states. Gear types assessed include, trawl, gillnet, longline and handline.
Accommodations and meal reimbursement during in person session of training are provided. Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.
This is a challenging job and candidates must be mentally prepared to be away from home for multiple days, and must be physically able to handle heavy lifting, working odd hours, and long days in rough seas. Observing provides an excellent career in marine biology, as observers and monitors are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.
Compensation: Monitors’ starting pay is $19.00/hour. Dependent on enrollment in our H&amp;W benefit, biologists may also be eligible for an additional $4.41/hour for the first 40 hours worked on each calendar week for a total of $23.41 hour. This is a full–time position with benefits. Annually, monitors earn between $35K - $55K a year dependent on their availability to deploy offshore and their personal sea day accomplishments. Monitors will be paid a minimum of 12 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.
AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits. Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.
Travel is reimbursed at an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.
Minimum Qualifications:
<ul>
<li>High school diploma is required.</li>
<li>Experience with data entry on computers.</li>
<li>Monitor candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physician’s certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
<li>Candidates are expected to commit to the program for at least one year.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Bachelor's degree in Biology or a related field from an accredited college or university with 30 credits of biology coursework, 6 credits of marine science is preferred.</li>
<li>At least one undergraduate course in math or statistics preferred.</li>
<li>At-sea experience</li>
<li>Coursework in Dichotomous Keys</li>
<li>Experience collecting Field Data and entering databases.</li>
</ul>
Locations:
<ul>
<li>Applicants must be currently living or be willing to live within 50 miles of Gloucester, Ma.</li>
</ul>
Contact:
If you would like to apply for one of these exciting new openings, please click the following link <a href="http://aisobservers.com/careers/" target="_blank">http://aisobservers.com/careers/</a> to submit the following information.
<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>At least 5 professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts.</li>
</ul>
All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to the Talent Acquisition team at <a href="mailto:talentacquisitionteam@aisobservers.com" target="_blank">talentacquisitionteam@aisobservers.com</a> or 508-990-9055.
An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
Must be able to work in the U.S. • VEVRAA Federal Contractor • Request Priority Protected Veteran Referrals • Equal Opportunity Employer

Marine Biologist (ASM) - Gloucester, Ma

<h3>Job Description</h3>
Job DescriptionDescription Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology. The company’s proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gases to be captured with up to 80% less energy and 70% less cost than conventional approaches. Verdox is backed by institutional investors and based in Boston. See verdox.com for additional information on our technology and our vision. Verdox seeks a Polymer Chemist to join our R&amp;D team.&nbsp; Key Responsibilities
<ul>
<li> Design and synthesize polymers with specific electrochemical and physico-chemical properties</li>
<li> Examine and develop diverse polymer chemistry, employing various types of polymerizations, polymer backbones, and purification techniques</li>
<li> Focus on developing and optimizing synthetic protocols for cost-effective polymer synthesis and purification at the multi-kilogram scale and beyond</li>
<li> Perform and interpret the physical, chemical, and electrochemical characterization of monomers and polymers</li>
<li> Oversee quality control of polymer products</li>
<li> Use and maintain elements of the chemistry R&amp;D infrastructure</li>
</ul>
 Skills Knowledge and Expertise
<ul>
<li> PhD in Synthetic/Organic/Polymer Chemistry (or equivalent), with focus on polymer synthesis, purification and physical characterization. Some industry experience is preferred</li>
<li> Strong polymer chemistry experience, including the design and preparation of novel polymer structures</li>
<li> Advanced organic synthesis skills – ability to design and synthesize monomers and polymers with desired properties. This includes multistep synthesis, Schlenk line and air-free techniques.</li>
<li> Characterization – chemical: NMR, GPC, GC/LC-MS, MALDI-TOF, FT-IR, UV-Vis, etc.; physical: SEM, TEM, AFM, tensile strength</li>
<li> Purification techniques – experience with various polymer workup and purification techniques, including at the kilogram scale</li>
<li> Scale-up (preferred) – some experience in gram to kilogram scale synthesis</li>
<li> Electrochemistry experience (preferred) – some experience in organic electrochemistry and electrochemical techniques</li>
<li> ChemDraw, NMR analysis software, Excel, MATLAB (or equivalent)</li>
<li> Ability to work in cross-functional teams</li>
<li> Strong oral and written communication skills</li>
<li> Comfortable working in an evolutionary and dynamic startup environment</li>
</ul>

Polymer Chemist

<h3>Job Description</h3>
Job DescriptionDescription . Plans, conducts and performs a variety of chemical productions and process&nbsp; &nbsp; &nbsp; &nbsp;developments under general supervision. · Utilizes or adapts new methods under guided supervision for updating existing synthesis procedures in order to improve yields, reduce production time and waste.&nbsp; · Keeps abreast of most recent technological developments pertaining to new products and applying to new products R/D under guided supervision&nbsp; · Troubleshoots and resolves standard production problems with full understanding of chemistries and analytical tools for progress of reactions&nbsp; · May supervise activities of lower chemists ensuring guided procedures or scale-ups in effective and safe manner&nbsp; · Attends technical meetings, conferences, seminars and reads current literature to keep up with up to date scientific knowledge.&nbsp; Key Responsibilities · Responsible for maintaining a clear and detailed lab book. · Responsible for maintaining neat, clean and safe work area. · Performs other duties of similar complexity as directed. · Ability to define problems, collect data, establish facts, and draw conclusions · Strong organizational, problem-solving, and analytical skills · Ability to manage priorities and workflow · Ability to work independently and as a member of various teams and committees · Proven ability to handle multiple projects and meet deadlines · Strong interpersonal skills Skills, Knowledge and Expertise · Strong understanding of chemistry · Bachelor’s degree in Chemistry with 10-15 years experience or · Master’s degree in Chemistry with 5-10 year of experience or · PhD in Chemistry with 5-7 years of experience.

Principal Production Chemist

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
And we’re looking for a Research Chemist!
About the position: E Ink is seeking a creative chemist to join a team making innovations in electrophoretic ink materials systems. This opportunity is for a full-time scientist to work under the supervision of Senior Research Scientists. The successful candidate will be responsible for the development of color pigments and the new electronic ink formulations. This position is with E Ink’s Research Department.
Responsibilities:
<ul>
<li>Work with senior technical staff to conduct laboratory experiments primarily in the area of pigment surface modification and ink formulations</li>
<li>Collaborate with analytical scientists to characterize pigments and materials</li>
<li>Perform electrical and electro-optical measurements for new color displays</li>
<li>Document processes and results</li>
<li>Participate in group and project meetings</li>
<li>Work safely in the laboratory adhering to the company’s safety protocols and policies</li>
</ul>
Qualifications:
<ul>
<li>BS/BA in Chemistry, Chemical Engineering, Materials Science and engineering or relevant science fields</li>
<li>0-3 years of experience working in a laboratory environment with a variety of equipment</li>
<li>Effective oral and written communication skills and the ability to write scientific reports/technical updates</li>
<li>Self-directed, motivated, and hands-on personality</li>
<li>Ability to multitasking, work independently as well as in a team environment</li>
<li>Aptitude in acquiring new knowledge and skills, flexible to adapt to changes</li>
<li>Local address</li>
</ul>
Preferences:
Knowledge of and experience in polymer and colloid science
Benefits:
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

Research Chemist 1060S-BFAC

<h3>Job Description</h3>
Job Description
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Chemist I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.
The Senior Chemist I will be responsible for the de novo synthesis, route development, and final product characterization of a wide variety of complex isotopically labeled targets (13C, 15N, 18O, and D isotopes). This role demands the production of high-quality, finished products in accordance with established specifications, while adhering to CIL’s safety and general policies. The Senior Chemist I will operate with a high degree of autonomy, ensuring that production requirements for safety, yield, time, and quality are consistently met.
Responsibilities 
<ul>
<li>Adhere to CIL’s general and safety policies to maintain a safe work environment</li>
<li>Synthesize complex, non-routine, and routine target compounds containing isotopes such as 15N, 18O, D, and/or 13C, utilizing established SOPs where applicable</li>
<li>Design and develop new synthetic routes when required to achieve optimal results</li>
<li>Contribute to the optimization of chemical processes for targeted molecules, intermediates, and scalable, cost-effective production methods</li>
<li>Analyze and interpret data using various techniques, including Nuclear Magnetic Resonance (NMR), Ultraviolet (UV) Spectroscopy, Mass Spectrometry (MS), High-Performance Liquid Chromatography (HPLC), and Infrared (IR) Spectroscopy</li>
<li>Employ a variety of purification techniques, including chromatography, distillation, recrystallization, and sublimation</li>
<li>Maintain accurate and detailed records in the laboratory notebook</li>
<li>Mentor and assist junior team members, offering guidance on experimental techniques and troubleshooting</li>
<li>Ensure all work is conducted with strict adherence to safety protocols and good laboratory practices, in line with CIL’s safety manual</li>
<li>Perform additional related duties as needed</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Synthetic Organic Chemistry or a closely related field, or a Master's degree with significant relevant experience (e.g., 5+ years in organic chemistry and/or synthesis)</li>
<li>Alternatively, a Bachelor's degree in Chemistry or a related field with extensive hands-on experience in organic synthesis and chemical processes may be considered</li>
<li>1-3 years of professional experience in organic chemistry and/or synthesis, or equivalent practical training as a Research Assistant or Postdoctoral Researcher</li>
<li>Expertise in organic synthetic methods, chemical separation, and compound identification, with strong analytical skills</li>
<li>Proficiency in laboratory techniques, including synthesis, purification, and characterization of organic compounds</li>
<li>Excellent verbal and written communication skills. Additionally, strong documentation and collaboration skills are essential</li>
<li>Ability to perform hands-on bench chemistry, which may involve standing, bending, and stooping</li>
<li>Familiarity with working in a controlled, hooded lab environment, as required by safety protocols</li>
<li>Comfortable working with both hazardous and non-hazardous chemicals</li>
<li>Physical ability to lift 50 lbs regularly and transport drums of chemicals, including up to 55-gallon drums, using appropriate equipment (e.g., drum dolly)</li>
</ul>
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
Cambridge Isotope Laboratories is an Equal Opportunity Employer. 
Learn more about us on our website: <a href="http://www.isotope.com" target="_blank">www.isotope.com</a>
About Us: Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of stable isotopes and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website: <a href="http://www.isotope.com" target="_blank">www.isotope.com</a>

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